Anda di halaman 1dari 14


published: 14 May 2013

doi: 10.3389/fmicb.2013.00096

A brief multi-disciplinary review on antimicrobial

resistance in medicine and its linkage to the global
environmental microbiota
L. Cantas 1*, Syed Q. A. Shah 1 , L. M. Cavaco 2 , C. M. Manaia 3 , F. Walsh 4 , M. Popowska 5 , H. Garelick 6 ,
H. Brgmann 7 and H. Srum 1
Department of Food Safety and Infection Biology, Norwegian School of Veterinary Science, Oslo, Norway
Research Group for Microbial Genomics and Antimicrobial Resistance, National Food Institute, Technical University of Denmark, Kgs Lyngby, Denmark
Centro de Biotecnologia e Qumica Fina, Escola Superior de Biotecnologia, Centro Regional do Porto da Universidade Catlica Portuguesa, Rua Dr. Antnio
Bernardino Almeida, Porto, Portugal
Bacteriology, Agroscope Changins-Wdenswil, Wdenswil, Switzerland
Department of Applied Microbiology, Institute of Microbiology, University of Warsaw, Warsaw, Poland
Department of Natural Sciences, Middlesex University, London, UK
Department of Surface Waters - Research and Management, Eawag, Swiss Federal Institute for Aquatic Science and Technology, Kastanienbaum, Switzerland

Edited by: The discovery and introduction of antimicrobial agents to clinical medicine was
Stefania Stefani, University one of the greatest medical triumphs of the 20th century that revolutionized the
of Catania, Italy
treatment of bacterial infections. However, the gradual emergence of populations of
Reviewed by:
antimicrobial-resistant pathogenic bacteria resulting from use, misuse, and abuse of
Aixin Yan, The University of
Hong Kong, Hong Kong antimicrobials has today become a major global health concern. Antimicrobial resistance
Ingeborg M. Van Geijlswijk, (AMR) genes have been suggested to originate from environmental bacteria, as clinically
Utrecht University, Netherlands relevant resistance genes have been detected on the chromosome of environmental
*Correspondence: bacteria. As only a few new antimicrobials have been developed in the last decade, the
L. Cantas, Department of Food
further evolution of resistance poses a serious threat to public health. Urgent measures
Safety and Infection Biology, Section
for Microbiology, Immunology and are required not only to minimize the use of antimicrobials for prophylactic and therapeutic
Parasitology, Norwegian School of purposes but also to look for alternative strategies for the control of bacterial infections.
Veterinary Science, PO Box 8146 This review examines the global picture of antimicrobial resistance, factors that favor its
Dep. NO-0033 Oslo, Norway.
spread, strategies, and limitations for its control and the need for continuous training of
all stake-holders i.e., medical, veterinary, public health, and other relevant professionals as
well as human consumers, in the appropriate use of antimicrobial drugs.
Keywords: antimicrobial resistance, human and veterinary medicine, environment, soil, wastewater, resistance

BACKGROUND antimicrobials have been extremely important corner stones of

Arguably one of the greatest examples of serendipity in science modern medicine since the last half of the previous century.
was the discovery of natural antimicrobials between Alexander Antimicrobial drugs have saved millions of people from life-
Fleming and Ernest Duchesne. Although Fleming generally holds threatening bacterial infections and eased patients suffering.
the reputation of the discovery of penicillin in 1928, a French Today, the treatment of bacterial infections is once again becom-
medical student, Ernest Duchesne (18741912), originally dis- ing increasingly complicated because microorganisms are devel-
covered the antimicrobial properties of Penicillium earlier, in oping resistance to antimicrobial agents worldwide (Pouillard,
1896. He observed Arab stable boys that kept their saddles in 2002; Levy and Marshall, 2004; Alanis, 2005; Pallett and Hand,
a dark and damp room to encourage mold to grow on them, 2010).
which they said helped heal saddle sores. Curious, Duchesne A causal relationship has been demonstrated between the
prepared a suspension from the mold and injected it into dis- increased use of antimicrobials in both human and veteri-
eased guinea pigs along with a lethal dose of virulent typhoid nary medicine, the greater movement of people, as well as
bacilli and still all animals remained healthy. His work, how- domestic and wild animals, the increased industrialization
ever, was ignored because of his young age and unknown status and the increased prevalence of antimicrobial-resistant bacte-
(Pouillard, 2002). In a way, with the success of the natural antibi- ria (Holmberg et al., 1987; Cheng et al., 2012). Antimicrobial
otic penicillin and the synthetic antimicrobial sulfonamides in resistance (AMR) was identified in pathogenic bacteria concur-
the first half of the 20th century, the modern antimicrobial rev- rently with the development of the first commercial antibiotic
olution began. Since then, new natural antimicrobial compounds produced by microorganisms, penicillin (Abraham and Chain,
were discovered and many semi-synthetic and synthetic antimi- 1940). Although the first concerns about drug-resistant bacteria
crobial drugs were created to combat bacterial infections. Thus, appeared in hospitals, where most antimicrobials were being used May 2013 | Volume 4 | Article 96 | 1

Cantas et al. The problem of antimicrobial resistance: a multi-disciplinary review

(Levy, 1998), the importance of AMR was already recognized in different ecological locations (Figure 1), aiming to unify the many
1969 both in humans and veterinary medicine as stated in the important aspects of this problem. Finally we advocate the need
Swan Report (Swann, 1969). Further research showed that the for teaching and continuous training of all stake-holders (i.e.,
origin and spread of AMR is, in fact, a very complex problem. medical, veterinary, public health, and other relevant profession-
Hence, there cannot be a single solution for minimizing AMR; als) as well as human consumers of antimicrobial drugs, in the
rather a coordinated multi-disciplinary approach will be required appropriate use of antimicrobials.
to address this issue (Serrano, 2005; Smith et al., 2009). We must
also recognize that wherever antimicrobials are used, AMR will THE HUMAN MEDICINE AND ANTIMICROBIAL RESISTANCE
The purpose of this review is to highlight the problem of In human medicine AMR is as old as the clinical usage of antimi-
resistance to antimicrobials with its consequences, including how crobial compounds. Antimicrobial-resistant pathogens have been
the spread of AMR could be limited. We highlight how the observed soon after the introduction of new drugs in hos-
numerous useful applications of antimicrobials led to AMR in pitals where antimicrobials are intensively used (Levy, 1998).

FIGURE 1 | Schematic representation of the complexity of the potential genetic links between the microbiotas of the various reservoirs are showed
bacterial genetic web of communication between the various by arrows. Thick arrows show major selective pressures for selection of
microbiotas that are impacted by the use of antibiotics in a wide antibiotic resistance genes, thin arrows show the significant directions of
context. The reservoirs where antimicrobials are applied are also suggested gene flow. Future research may document unique arrows that must be
as hot spots for horizontal gene transfer. The potentially most important integrated in the web drawn.

Frontiers in Microbiology | Antimicrobials, Resistance and Chemotherapy May 2013 | Volume 4 | Article 96 | 2
Cantas et al. The problem of antimicrobial resistance: a multi-disciplinary review

Consequently, AMR in the context of human medicine has dom- of defense against the non-Enterobacteriaceae pathogens, such
inated the literature for a long time (Figure 2). Over the years, as Pseudomonas aeruginosa and Acinetobacter baumannii (Brown
and continuing into the present, almost every known bacterial et al., 1998). However, since the first description of the blaOXA
pathogen and numerous human commensals have developed genes, there has been a worldwide increase in the dissemi-
resistance to one or more antimicrobials in clinical use (Table 1). nation of new resistance determinants conferring carbapenem
Extended-spectrum -lactamases (ESBL) are the ones most often resistance. For example, the Klebsiella pneumoniae carbapene-
encountered in the hospital (intensive care) setting. Methicillin- mase (KPC) type enzymes, Verona integron-encoded metallo--
resistant Staphylococcus aureus (MRSA) and vancomycin-resistant lactamase (VIM), Imipenemase Metallo--lactamase (IMP) and
enterococci (VRE) have also been found to have a signifi- New Delhi metallo--lactamase (NDM), and the OXA-48 type
cant nosocomial ecology (Otter and French, 2010). In addition, of enzymes have been isolated from a number of bacterial gen-
ESBL positive bacteria and MRSA infections are increasingly era irrespective of their geographical distribution (Kumarasamy
detected in the community. Furthermore, the increase in flu- et al., 2010; Walsh et al., 2011). Carbapenemase resistance mech-
oroquinolone resistance due to target-site mutations and the anisms are found among Escherichia coli and Klebsiella isolates in
worldwide emergence of plasmid-mediated quinolone resistance hospital settings, and to a lesser extent also in the community,
genes may represent a major challenge in future given the crit- thus healthy human carriers begin to be a concern (Nordmann
ical importance of this antimicrobial therapy (Cattoir et al., et al., 2012). Furthermore, carbapenemase-producing organisms
2007; Strahilevitz et al., 2009). Carbapenems are the last line have also been isolated from farm animals (Fischer et al., 2012).

FIGURE 2 | The change in number of antimicrobial resistance related Hospital, (hospital OR patient OR clinic ); Animal, (animal OR veterinary
published research papers in different subdisciplines and covering OR livestock OR pig OR cow OR chicken OR poultry); Wastewater,
different environments. The data for the graphs were obtained by searching (wastewate OR sewage); Natural water, (wate OR lake OR river OR ocean
the ISI web of science for publications with titles matching the query terms OR sea); Soil, (soil OR sediment OR rhizosphere ) (Source: http://apps.
(antibioti OR antimicro ) AND resistan AND the following specific terms: The search was performed on 06/03/2013. May 2013 | Volume 4 | Article 96 | 3

Cantas et al. The problem of antimicrobial resistance: a multi-disciplinary review

Table 1 | Antimicrobial resistance detection in some important pathogens soon after arrival of the magic bullets into the market.

Year Bacteria Drug resistance Comments References

1948 Staphylococcus aureus Penicillin In British civilian hospitals soon Barber and
after the introduction of penicillin Rozwadowska-Dowzenko, 1948
1948 Mycobacterium tuberculosis Streptomycin In the community soon after the Crofton and Mitchison, 1948
clinical usage of this antimicrobial
1950s1960s Escherichia coli, Shigella spp., and Multiple drugs Watanabe, 1963; Olarte, 1983;
Salmonella enterica Levy, 2001
1960s VRE- Enterococcus spp. Multiple drugs Levy and Marshall, 2004;
ESBL- E. cloacae, K. pneumoniae, E. coli, Nordmann et al., 2011
MRSA, QR - Enterobacteriaceae
MDR- Acinetobacter baumannii,
Pseudomonas aeruginosa

VRE, Vancomycin-Resistant Enterococcus; ESBL, Extended-spectrum -lactamase; MRSA, methicillin/oxacillin-resistant Staphylococcus aureus; QR , Quinolone
resistant; MDR, Multi-drug resistant.

HUMAN MOBILITYTHE DIRECT AND INDIRECT IMPACT ON HUMAN human diseases from the mid-1940s (Gustafson and Bowen,
PATHOGENS 1997; McEwen, 2006). Even though some drugs are exclusively
The increasing cross-border and cross-continental movements of designed for veterinary use, most belong to the same antimicro-
people has a major impact on the spread of multi-resistant bac- bial classes as those used in human medicine with identical or very
teria (Linton et al., 1972; Arya and Agarwal, 2011; Cheng et al., similar structures (Swann, 1969; Heuer et al., 2009).
2012). The emergence and global spread of the international clone Annually, large quantities of drugs are administered to ani-
1 of penicillin-resistant Streptococcus pneumoniae (Klugman, mals in the agricultural sector worldwide to secure a sufficient
2002) and the recently occurring New Delhi Metallo--lactamase amount of food (meat, eggs, and dairy products) to feed a rapidly
(blaNDM -1) producing Enterobacteriaceae, which inactivates all growing world human population (Vazquez-Moreno et al.,
-lactam antimicrobials, including carbapenems, are good exam- 1990; Roura et al., 1992; Rassow and Schaper, 1996). As data
ples. The blaNDM -1 appears to have originated in the Indian sub- collection on antimicrobial use in animals was not harmonized
continent and subsequently could be found in North America, the to provide reliable and comparable information, and following a
United Kingdom, and other European countries by the movement request from the European Commission the European Medicines
of people (Arya and Agarwal, 2011; Walsh et al., 2011). Agency (EMA), the European Surveillance of Antimicrobial
The AMR problem remains a growing public health concern Consumption (ESVAC) programme has been created. The
because infections caused by resistant bacteria are increasingly ESVAC programme is responsible for collecting, analyzing, and
difficult and expensive to treat. The consequences of this problem reporting sales data from European countries and developing
are: longer hospital stay, longer time off work, reduced quality of an organized approach for the collection and reporting of data
life, greater likelihood of death due to inadequate or delayed treat- on antimicrobial use for animals including annual reporting
ment, increases in private insurance coverage and an additional from EU member states (
costs for hospitals when hospital-acquired infections occur in jsp?curl=pages/regulation/document_listing/document_listing_
addition to the increased overall healthcare expenditure (Roberts 000302.jsp). During 2007, in 10 European countries the sale of
et al., 2009; Filice et al., 2010; Korczak and Schffmann, 2010; antimicrobial drugs for therapeutic use as veterinary medicine
Wilke, 2010). Thus, in order to calculate the full economic bur- varied from 18 to 188 mg/kg biomass (Grave et al., 2010).
den of AMR we have to consider the burden of not having The administration of antimicrobials to food producing
antimicrobial treatment options at all, which in the extreme case animals can have other purposes than treatment, such as:
would probably cause a breakdown of the entire modern medi- growth promotion (although now totally banned in Europe and
cal system (Alanis, 2005; Falagas and Bliziotis, 2007; Pratt, 2010). quinolones for the poultry industry are banned in the USA), pro-
In short, everyone will be at risk when antimicrobials become phylaxis, and -metaphylaxis (Anthony et al., 2001; Anderson et al.,
ineffective and the threat is greatest for young children, the 2003; Casewell et al., 2003; Cabello, 2006). Approximately 70% of
elderly, and immune-compromised individuals, such as cancer all the antimicrobials administered in animal farming are used for
patients undergoing chemotherapy and organ transplant patients non-therapeutic purposes (Roe and Pillai, 2003).
(Tablan et al., 2004). In the European Union (EU) the use of avoparcin was banned
in 1997. Furthermore spiramycin, tylosin, and virginiamycin for
THE VETERINARY MEDICINE AND AGRICULTURE SECTOR growth promotion were banned from use in 1998. All other
CONSUMPTION AND REGULATION OF ANTIMICROBIAL USE IN growth promoters in the feed of food-producing animals were
ANIMALS banned in the EUcountries from January 1, 2006 (http://
The antimicrobials, used in veterinary medicine were intro- Data from Denmark showed that animals could be
duced soon after they became available for the treatment of produced at a large scale without the use of growth promoters,

Frontiers in Microbiology | Antimicrobials, Resistance and Chemotherapy May 2013 | Volume 4 | Article 96 | 4
Cantas et al. The problem of antimicrobial resistance: a multi-disciplinary review

without adversely affecting the production (Aarestrup et al., 2001; underlying allergic reactions result in an increasing use of semi-
Aarestrup, 2005; Hammerum et al., 2007). In the United States synthetic penicillins because of the ineffectiveness of penicillin
of America, politicians are discussing the introduction of a sim- against penicillinase producing Staphylococcus pseudintermedius
ilar ban on the use of antimicrobials in animal husbandry for (Yoon et al., 2010). Moreover, emerging methicillin-resistant
growth promotion ( Staphylococcus pseudintermedius (MRSP), methicillin-resistant
s742). Despite these bans, in some parts of the world, medically Staphylococcus aureus (MRSA), and ESBL producing E. coli dis-
important antibiotics are still routinely fed to livestock prophy- playing multidrug resistance has led to increased concern related
lactically to increase profits and to ward-off potential bacterial to AMR in companion animal practice (Bannoehr et al., 2007;
infections in the stressed and crowded livestock and aquaculture Wieler et al., 2011). Increased antimicrobial resistance devel-
environments (Cabello, 2006; Smith et al., 2009; Ndi and Barton, opment and spread in companion animals due to irrational
2012). Because stress lowers the function of the immune system antimicrobial usage, especially overprescribed broad spectrum
in animals, antimicrobials are seen as especially useful in intensive antimicrobials without precise diagnostics, inevitably cause (1)
confinements of animals (Halverson, 2000). The non-therapeutic animal health problem (increased mortality and morbidity), (2)
use of antimicrobials involves low-level exposure through feed economical problem to the owner (more visits-therapies and
over long periodsan optimal way in which to enrich resistant prolonged hospitalization), (3) economical problem to the vet-
bacterial populations (Sharma et al., 2008; Kohanski et al., 2010; erinarian (possible loss of customers and high costs for hospital
Alexander et al., 2011; Gullberg et al., 2011). decontamination), and (4) human health problems (risks of
Various monitoring programs around the world have started zoonotic transmission). Because of this threat small animal veteri-
monitoring AMR and a range of research activities and inter- narians should prescribe broad spectrum antimicrobials after cul-
ventions have shown that antimicrobial usage has a large effect turing and educate pet owners to handle infected-antimicrobial
upon selection of AMR in animal production. A rapid and par- treated animals with precaution.
allel decrease in resistant Enterococcus faecium from pig and However, emergences of resistance toward antimicrobials
poultry has been reported in Denmark after the ban of growth which are critically important for human therapy are the most
promoters in livestock (Aarestrup et al., 2001). The Norwegian worrisome. These include the recent emergence of ESBL pro-
aquaculture industry has produced over one million tons of ducing and carbapenemase positive Enterobacteriaceae bacteria in
farmed fish ( by using only animal production (Horton et al., 2011), the emergence of farm
649 kg of antimicrobials in 2011 (NORM/NORM-VET, 2011). associated MRSA ST398 (the main pig associated clone) (Cuny
It is evident from the Danish integrated AMR monitoring and et al., 2010; Kluytmans, 2010; Weese, 2010) and of plasmid-
research program (DANMAP) and NORM/NORM-VET Report mediated quinolone resistance in animal isolates and food prod-
(NORM/NORM-VET, 2011) that reduction of antimicrobial ucts (Poirel et al., 2005; Nordmann et al., 2011). Unfortunately,
usage with strict policies may still be the safest way to control the there are several examples in the literature that show that these
development and spread of AMR in this sector in the future. are already widespread in Europe and other parts of the world
and have a large impact on human health (Angulo et al., 2004;
AND ANIMAL HUSBANDRY Aquaculture (fish, shellfish, and shrimp farming industries)
The use of antimicrobials in animal husbandry has for many has developed rapidly in the last decade and has become an
years actively selected for bacteria which possess genes capable important food source (FAO, 2010). Fish pathogenic bacteria
of conferring AMR (Bastianello et al., 1995; Sundin et al., 1995). often produce devastating infections in fish farms where dense
Consequently, this aspect has also seen much attention in the populations of fish are intensively reared. Although modern
literature (Figure 2). Despite large differences in methodology, fish farming relies increasingly on vaccination and improved
the results of most relevant scientific studies demonstrate that management to avoid infections (Markestad and Grave, 1997;
not long after the introduction of antimicrobials in veterinary Midtlyng et al., 2011), still many bacterial infections in fish
practice, resistance in pathogenic bacteria, and/or the fecal flora are regularly treated with antimicrobials in medicated feed or
was observed (Caprioli et al., 2000; Jean-Louis et al., 2000). In by bath immersion. The most widely used drugs are fluoro-
particular an increased emergence of pathogenic bacteria resis- quinolones, florfenicol, oxytetracyclines amoxicillin and sulfon-
tant to antimicrobials has occurred in members of the genera amides (Cabello, 2006; Grslund et al., 2003; Holmstrm et al.,
Salmonella, Campylobacter, Listeria, Staphylococcus, Enterococcus, 2003; Primavera, 2006; Soonthornchaikul and Garelick, 2009).
and Escherichia coli. Some resistant strains of these genera are By now, most of the fish pathogenic bacteria from fish farms
propagated primarily among animals but can subsequently infect with a history of infections have developed AMR (Colquhoun
people as zoonotic agents (Levy, 1984; Corpet, 1988; Marshall et al., 2007; Lie, 2008; Srum, 2008; Farmed Fish Health Report,
et al., 1990; Gigure et al., 2007). 2010; Shah et al., 2012a). Furthermore, in some areas of the
In veterinary medicine the use of antimicrobials in compan- world, particularly in South-East Asia, integrated farming is a
ion animals such as pets and horses is restricted to therapeutic common practice where organic wastes from poultry and live-
purposes only. Companion animals are increasingly treated as stock are widely used in manuring the fish farms (Hoa et al.,
family members, in the context of applying advanced antimi- 2011; Shah et al., 2012b). It has been reported that antimicrobial
crobial treatments to their infectious diseases. For instance, skin residues present in the poultry and livestock waste has pro-
infections caused by staphylococci in dogs with or without vided sufficient selection pressure for the selection of AMR genes, May 2013 | Volume 4 | Article 96 | 5

Cantas et al. The problem of antimicrobial resistance: a multi-disciplinary review

increasing the complexity of transmission of bacteria, and resis- harbor-resistant bacteria (Zhang et al., 2009; Glad et al., 2010;
tances between the livestock and aquatic environment (Petersen Lang et al., 2010).
et al., 2002; Agers and Petersen, 2007; Hoa et al., 2011; Shah
AMR has been detected in different aquatic environments MICROBIAL COMMUNITIES IN SOIL AND ANTIMICROBIAL
and some resistance determinants have been found to originate RESISTANCE
from aquatic bacteria. A good example is the recently emerging Research data shows that in diverse soils from various regions of
plasmid-mediated quinolone resistance determinants from the the world, there is a wide dispersion of AMR. One explanation
qnr family (Ash et al., 2002; Picao et al., 2008) and CTX-M from for this phenomenon is the existence of antimicrobial produc-
aquatic Kluyvera spp. (Decousser et al., 2001; Rodriguez et al., ing bacteria in soil. The Actinomycetes, which are common
2004; Ma et al., 2012). In addition, epidemiological and molecular soil bacteria (Streptomyces, Micromonospora, Saccharopolyspora
data indicate that some fish pathogens such as Aeromonas are able genus), synthesize over half of all known most clinically rele-
to transmit and share AMR determinants with bacteria isolated vant antimicrobials e.g., tetracycline, gentamicin, erythromycin,
from humans such as E. coli (Rhodes et al., 2000; Srum, 2006). streptomycin, vancomycin, and amphotericin. Bacteria of the
Similarly, the fish pathogen Yersinia ruckeri have been reported to genus Bacillus also produce antibiotics, e.g., Bacillus brevis which
share AMR plasmid and AMR genes with the bacterium causing producing gramicidin (Baltz, 2007). These antimicrobials now
human plague (Welch et al., 2007). also reach the environment from human and animal therapeu-
tics, through manure, sewage, agriculture, etc. Many retrospective
ANTIMICROBIAL USE IN PLANT AGRICULTURE and prospective studies have been performed to assess the emer-
Streptomycin and oxytetracycline are routinely used for the pro- gence and selection of AMR in environmental bacteria. The
phylaxis of fire blight disease (causative agent Erwinia amylovora) environment is eventually the largest and most ancient reservoir
in apple and pear orchards. Streptomycin use is strictly controlled of potential AMR, constituting the environmental resistome
within the EU and is only authorized for use on a yearly basis. (Aminov and Mackie, 2007; Allen et al., 2010; DCosta et al.,
However, streptomycin use in plant agriculture in the USA has 2011). Under such powerful selection pressure, it is not surpris-
been replaced by oxytetracycline, due to streptomycin resistance ing that the soil resistome is so diverse (Knapp et al., 2010).
development among E. amylovora in the apple orchards. Oxolinic The best example illustrating this is the tetracycline resistome.
acid had been reported to be used in Israel against fire blight and Tetracyclines are an important class of antimicrobials with desir-
against rice blight in Japan (Shtienberg et al., 2001). Gentamicin able broad-spectrum activity against numerous pathogens and
is used in Mexico and Central America to control Fire Blight and the widespread emergence of resistance has had a massive impact
various diseases of vegetable crops (Stockwell and Duffy, 2012). on these drugs (Thaker et al., 2010). Opportunistic pathogens
However, the role of antimicrobial use on plants is, knowing the ubiquitous in the soil for example, Pseudomonas aeruginosa,
AMR crisis in human medicine, the subject of debate (McManus Acinetobacter spp., Burkholderia spp., and Stenotrophomonas spp.
et al., 2002). can combine intrinsic resistance to several antimicrobials with a
remarkable capacity to acquire new resistance genes (Popowska
DISSEMINATION OF ANTIMICROBIAL-RESISTANT BACTERIA et al., 2010). Still, little is known about the diversity, distribution,
THROUGH FOOD AND FOOD PRODUCTION and origins of resistance genes, particularly among the as yet non-
Resistant bacteria can be transferred from animals and plants cultivable environmental bacteria. In uncultured soil bacteria,
to humans in many different ways, which can be catego- identified resistance mechanisms comprise efflux of tetracycline
rized into three major modes of transmission: (1) through the and inactivation of aminoglycoside antimicrobials by phosphory-
food chain to people (Roe and Pillai, 2003; Soonthornchaikul lation and acetylation (Popowska et al., 2012). In addition, bacte-
and Garelick, 2009), (2) through direct or indirect contact ria resistant to macrolides including the new drug telithromycin
with livestock industry or animal health workers (Levy et al., have been reported from soil (Riesenfeld et al., 2004a). In a study
1976), (3) through environments which are contaminated by (DCosta et al., 2006), 480 strains of Streptomyces from soil
with manure in agriculture ( were screened against 21 antimicrobials. Most strains were found
integration/research/newsalert/pdf/279na4.pdf) and aquaculture to be multi-drug resistant to seven or eight antimicrobials on
(Petersen et al., 2002; Shah et al., 2012b). The environment con- average, with two strains being resistant to 15 of the 21 drugs. It
tains a great variety of bacteria creating an immense pool of AMR was also reported that soil is a reservoir for -lactamases and these
genes that are available for transfer to bacteria that cause human genes, if transferred to pathogens, can then impact human health
disease (Riesenfeld et al., 2004b; DCosta et al., 2006). The real- (Allen et al., 2010). It is supposed that the presence of antibiotics
ization of these links sparked the recent interest in the role and in the environment has promoted the acquisition or independent
dynamics of environmental AMR (Figure 2). evolution of highly specific resistance elements. These determi-
In addition, other sources are available. For instance, wild nants are located mainly on mobile genetic elements such as
animals may also be carriers of antimicrobial-resistant bacte- plasmids and conjugative transposons, which ensure their spread
ria (Literak et al., 2011). These animals may have close contact by horizontal gene transfer. Conjugative, broad-host-range plas-
to human or farming areas and/or waste and become colo- mids play a key role in this process (Martinez, 2009; Stokes
nized with resistant strains (Literak et al., 2011; Nkogwe et al., and Gillings, 2011). Numerous studies have demonstrated that
2011). Interestingly, animals in remote areas have been found to the prevalence of such resistance plasmids in soil is very high

Frontiers in Microbiology | Antimicrobials, Resistance and Chemotherapy May 2013 | Volume 4 | Article 96 | 6
Cantas et al. The problem of antimicrobial resistance: a multi-disciplinary review

(Gtz et al., 1996). Among the plasmids conferring resistance to sewage treatment plants (Segura et al., 2009; Michael et al., 2013).
antimicrobials, representatives of the incompatibility groups P, Although proportion of the antimicrobial compounds are trans-
Q, N, and W have been identified. An example of this type of formed and degraded in the environment, the occurrence of
mobile genetic elements may be the IncP-1 plasmids (Popowska these micropollutants is reported worldwide, with antimicrobials
and Krawczyk-Balska, 2013). Results from the scientific literature of all classes being detected in wastewater habitats in concen-
show that plasmids carrying resistance genes have been identi- trations ranging from ng1 to mgL1 (Michael et al., 2013).
fied in pathogenic bacteria of the genus Escherichia, Salmonella, Simultaneously, urban sewage and wastewater contain AMR bac-
Shigella, Klebsiella, Aeromonas, and Pseudomonas, the genera that teria and other pollutants, such as pharmaceutical and personal
can be found in soil and water (Stokes and Gillings, 2011). hygiene products and heavy metals, whose effects on AMR selec-
These plasmids carry determinants for resistance to at least one tion are still not very clear (Graham et al., 2011; Oberl et al.,
heavy metal (Ni, Cd, Co, Cu, Hg, Pb, Zn) and antimicrobials 2012; Patra et al., 2012; Novo et al., 2013). Often, wastewater
of different groups, i.e., tetracyclines, quinolones, aminoglyco- treatment is not enough to eliminate the antimicrobial residues
sides, sulfonamides, -lactams, and chemotherapeutics (Sen et al., entering the system (Michael et al., 2013). The consequence
2011; Seiler and Berendonk, 2012). Overall these data indicate is that such micropollutants, exerting selective pressures, may
that soil bacteria constitute a reservoir of resistance determinants facilitate the selection of AMR bacteria or the acquisition of
that can be mobilized into the microbial community including resistance genes by horizontal gene transfer (Martinez, 2009).
pathogenic bacteria. Recent studies also indicate a different mech- Indeed, the relevance of wastewater habitats to the dissemina-
anism of AMR in soil-derived actinomycetes, by engendering tion of AMR among human pathogens as well as commensal
mutations in genes encoding the transcriptional and translational and environmental bacteria is increasingly emphasized (Baquero
apparatus that lead to alterations in global metabolism. This ver- et al., 2008; Marshall and Levy, 2011; Czekalski et al., 2012; Rizzo
tically selected AMR includes increased production of secondary et al., 2013). Wastewater treatment plants reduce the load of AMR
metabolites (Derewacz et al., 2013). Very recently evidence for bacteria, but treated water still carries elevated levels of AMR
recent exchange of AMR genes between environmental bacteria bacteria, and may select for strains with high levels of multidrug-
and clinical pathogens was presented using a high-throughput resistance (Czekalski et al., 2012). Resistance gene abundance in a
functional metagenomic approach (Forsberg et al., 2012). In stream system could be linked to the input of (treated) wastewater
this study it was shown that multidrug-resistant soil bacteria and animal husbandry, demonstrating landscape-scale pollution
contain resistance gene cassettes against five classes of antimicro- of natural aquatic systems with AMR (Pruden et al., 2012). The
bials (-lactams, aminoglycosides, amphenicols, sulfonamides, currently available literature demonstrates that most of the AMR
and tetracyclines) with high nucleotide identity to genes from genetic elements found in clinical isolates are also detected in
diverse human pathogens. Therefore, it is important to study this wastewater habitats, even shortly after they have been reported
reservoir, which may contribute to the detection of new clini- in hospitals (Szczepanowski et al., 2009; Rizzo et al., 2013). The
cally relevant AMR-mechanisms and/or the multidrug-resistant occurrence of the same AMR genetic elements in different habi-
pathogens that should be avoided from entering medically impor- tats demonstrates the uniqueness of the resistome, mainly due to
tant bacteria (Torres-Corts et al., 2011). rapid dissemination processes, demonstrating the urgent needs
for an integrated approach.
ANTIMICROBIAL RESISTANCE IN AQUATIC ENVIRONMENTS Ubiquitous bacteria that can live in the environment and
Water is one of the most important habitats for bacteria, hold- are also able to colonize humans are particularly relevant to
ing complex microbial communities. Not surprisingly, water the spread of AMR in the environment and the implications
also contains AMR bacteria. From natural fresh water systems to human health. Indeed, numerous studies have reported
to drinking water, or from sewage to human-engineered water the occurrence of AMR in ubiquitous bacteria isolated from
infrastructures, AMR, either intrinsic or acquired, have been wastewater habitats, which are also recognized as opportunistic
reported in aquatic environments worldwide (e.g., Goi-Urriza pathogens, mainly nosocomial agents. AMR bacteria of clinical
et al., 2000; Volkmann et al., 2004; Schwartz et al., 2006; Ferreira relevance which may be found in the environment comprise,
da Silva et al., 2007; Bckelmann et al., 2009; Vaz-Moreira et al., among others, members of the genera Acinetobacter, Enterococcus,
2011; Falcone-Dias et al., 2012). In this respect, given their Escherichia, Klebsiella, Pseudomonas, and Shigella (Blanch et al.,
characteristics, wastewater habitats are particularly important. 2003; Reinthaler et al., 2003; Ferreira da Silva et al., 2006, 2007;
Watkinson et al., 2007; Novo and Manaia, 2010; Czekalski et al.,
WASTEWATER HABITATS AS RESERVOIRS OF ANTIMICROBIAL 2012). In addition, non-cultivable bacteria may also be important
RESISTANCE either for AMR spread or selection. Indeed, over the last years,
Among the aquatic environments, wastewater habitats repre- the use of culture independent approaches brought additional
sent the most important reservoir of AMR bacteria and genes. insights into the abundance and diversity of resistance genes in
This type of water contains human and animal excretions with wastewaters and into the effects of antimicrobials on the bacte-
abundant doses of commensal and pathogenic antimicrobial- rial communities (Volkmann et al., 2004; Czekalski et al., 2012;
resistant bacteria (Yang et al., 2011; Ye and Zhang, 2011, 2013; Oberl et al., 2012; Novo et al., 2013). In particular, several stud-
Novo et al., 2013). Since antimicrobials are not fully degraded ies presented evidence that in wastewater habitats there is a high
in the human and animal body, antimicrobial compounds, their potential for horizontal gene transfer, mediated by plasmids and
metabolites and transformation products are abundant in urban facilitated by integrons (Tennstedt et al., 2003; Szczepanowski May 2013 | Volume 4 | Article 96 | 7

Cantas et al. The problem of antimicrobial resistance: a multi-disciplinary review

et al., 2008; Moura et al., 2010; Zhang et al., 2011). Despite the Table 2 | Degradation rates of various antimicrobials in soil.
importance of wastewater as a reservoir for AMR genes, and the
Class of Degradation Time References
relevance of wastewater treatment to control resistance spread,
antimicrobial [%] [d]
to date the number of studies that have been published remains
relatively low (Figure 2). Macrolides 050 530 Thiele-Bruhn, 2003*
Nevertheless, over the last decades the knowledge in this Sulfonamides 050 2264 Thiele-Bruhn, 2003
area has increased considerably and the importance of wastew-
Fluoroquinolones 030 5680 Hektoen et al., 1995;
ater treatment systems for the spread of AMR is unequivocally Thiele-Bruhn, 2003
demonstrated. Therefore, it is now possible to address some spe-
Tetracycline 050 10180 Bjrklund et al., 1991;
cific questions which we expect to be a focus of the research in
Thiele-Bruhn, 2003
this area in the coming years. Examples of these issues are (1)
the identification of the conditions that may enhance or mit- Aminoglycosides 0 30 Thiele-Bruhn, 2003
igate the occurrence of horizontal gene transfer and selection -lactams 050 30 Thiele-Bruhn, 2003
of AMR (which pollutants, which concentrations, temperature, Imidasoles 50 1475 Thiele-Bruhn, 2003
pH, hydraulic residence time of wastewater treatment, etc.);
Polypeptides 1290 2173 Thiele-Bruhn, 2003
(2) the classification and quantification of risk, e.g., the likelihood
that an AMR bacterium or gene from wastewater habitats reach
This reference does not include the modern macrolides with very long
humans and causes issues for human health; (3) the improvement
elimination half-lives. For instance, Tulathromycine has an half live (so 50%
of wastewater treatment processes in order to minimize the loads
degraded, not nearly 100%) in soil of 99 days (Pfizer, personal communication
of antimicrobial-resistant bacteria and genes in the final effluent
(Dodd, 2012).

THE ANTIMICROBIAL RESISTANCE GENE POOL physicians in reducing antimicrobial overuse should be imple-
AMR genes can be differentiated depending on the genetic event mented. Following the analysis more than 500 scientific articles, it
that is required for acquiring an AMR phenotype. These include has been suggested that the elimination of non-therapeutic use of
genes that are acquired by horizontal gene transfer and genes that antimicrobials in food animals, will lower the burden of AMR in
are present in the bacterial genome and that can encode AMR the environment, with consequent benefits to human and animal
following gene mutations or activation (Olliver et al., 2005). health (FAAIR Scientific, 2002; Swartz, 2002).
AMR features evolve as a consequence of permanent exchange Better management techniques and strict legislation in the
of and ever new recombinations of genes, genetic platforms, and use of antimicrobials for therapeutic use in humans and in ani-
genetic vectors. Many of these genes are not primarily resistance mals will reduce the risk of development of AMR (Cunha, 2002;
genes, but belong to the hidden resistome, the set of genes able to Defoirdt et al., 2011; Midtlyng et al., 2011). For example, the
be converted into AMR genes (Baquero et al., 2009). As evidenced prevention of nosocomial transmission of multi-drug resistant
by our discussion above, microbial organisms harboring these bacteria is possible with active routine surveillance programs that
genes are present naturally in all kinds of environments, but also can identify colonized patients. Numerous studies have demon-
released into water and soil from organisms, including humans, strated that such a search and containment approach and/or
where they evolve or increase in abundance under direct selection a search and destroy approach in which an attempt is made
from exposure to antimicrobials. At the same time, antimicrobials to eliminate carriage of the organism can reduce the incidence
(often at low concentrations), disinfectants, and heavy metals are of hospital-acquired infections and be cost-saving (Muto et al.,
disseminated into the water as well, and may act as selective fac- 2003).
tors fostering the evolution of new AMR features (Cantas et al., New management techniques in the animal husbandry, such
2012a,b,c; Cantas et al., unpublished). The rate of degradation as organic farming, need to be thoroughly investigated to ensure
of antimicrobials in the environment varies and is dependent on that these are viable alternatives that help to reduce the potential
a range of environmental conditions, for example: temperature, for selection of AMR bacteria. Samples from organically farmed
available oxygen, pH, presence of alternative sources of organic poultry showed a significantly lower level of AMR in intestinal
and inorganic discharges as described in Table 2. bacteria such as E. coli and Campylobacter (Soonthornchaikul
et al., 2006). However from organically farmed cattle no signifi-
HOW TO SLOW DOWN THE SPREAD AND EVOLUTION OF AMR? cant differences were obtained in microbiological contamination.
In this review we have emphasized that the problem of AMR E. coli and S. aureus isolates were found to have significantly lower
evolution and dissemination is multifaceted and involves clinical, rates of AMR in organically raised cattle (Sato et al., 2005). More
agricultural, technical, and environmental systems. Similarly studies are needed (1) to determine the reasons of antimicrobial
strategies to deal with the impending AMR crisis have to take this usage in the farms by veterinarians, (2) to compare and update
complexity into account. the recommended treatment protocols for veterinarians through-
The overuse of antimicrobials needs to be limited or reduced out different countries, (3) to evaluate the impact of other factors
in human medicine, veterinary medicine, agriculture, and aqua- other than AMR development in bacteria: e.g., immune response-
culture. Ideally, the use of antimicrobials in agriculture should stress has been indicated to correlate with resistance genetic ele-
be eliminated. Intensive programs to educate both patients and ment shuffling among gut microbiota in different animal models,

Frontiers in Microbiology | Antimicrobials, Resistance and Chemotherapy May 2013 | Volume 4 | Article 96 | 8
Cantas et al. The problem of antimicrobial resistance: a multi-disciplinary review

such as: atlantic salmon, zebrafish, neonatal piglets, and cats or contact with the environment. Introduction of antimicrobial
(Cantas et al., 2011, 2012a,b,c, 2013). Animal welfare parameters compounds into the aquatic environment via medical therapy,
under intensive production such as stress should be investigated agriculture, animal husbandry and companion animals has
in future studies with regards to control of resistance development resulted in selective pressures on resident environmental bacteria.
in animal husbandry. Development of AMR in environmental bacteria has a great
Vaccination and improved hygienic measures are among the impact and may help in explaining how human and animal
important cornerstones in controlling infectious diseases and pathogens acquire resistance features. Besides the role of clinical
consequently aid in reducing AMR (Potter et al., 2008). The microbiology laboratories with rapid and accurate detection of
Norwegian aquaculture may serve as a good example by reduc- a diverse number of pathogens and its drug resistance profiles,
tion in the use of antimicrobials from around 50 tons in the late robust routine surveillances in an epidemiological frame-work
1980s to less than 1000 kg per annum after introduction of effec- covering the whole livestock food chain and the environment
tive vaccines against devastating fish diseases like furunculosis and need to be taken into consideration. Due to this complexity
vibriosis (Midtlyng et al., 2011; NORM/NORM-VET, 2011). the control of AMR has to include numerous actions at diverse
The use of pre- and probiotics to improve the health and levels. Future research should focus on finding unknown routes
performance of livestock might be a good alternative to growth of transfer of AMR between microbiotas of relevance to the
promoters. This is an important biological control aiming to food chain and to all microbiotas of importance for bacterial
reduce outbreaks of infectious diseases and which in turn would pathogens when they acquire antibiotic resistance genes laterally.
minimize the use of antimicrobials in livestock and aquaculture Ultimately, even a successful integrative approach on all aspects,
for therapeutic purposes (Verschuere et al., 2000; Callaway et al., can probably only help to slow down the spread of AMR, not
2008). prevent it. The development of new generations of antimicrobial
The issue of dissemination and possible long-term enrich- should therefore receive equal attention. This is summarized
ment of AMR and AMR genes in the environment (Knapp and emphasized in a 12-point action plan against the rising
et al., 2008) needs to be studied further, with specific regards threats of AMR implemented by the European Commission
to the actual risks associated with it. However, taking action is which includes actions in the field of human medicine, animal
already possible today. For example, several treatment methods husbandry, veterinary medicine, authorization requirements
for waste and wastewater disinfection and removal of microp- for commercialization of human and veterinary drugs and
ollutants, including antimicrobials, are available. These include other products, on research, on scientific opinions, and under-
various chemical disinfections, UV treatment, and membrane fil- taking also actions on the international level in collabora-
tration. Disinfection and DNA degradation of community based tion with the WHO and Codex (
and hospital wastewater may be effective means to reduce AMR consumer/does/communication_amr_2011_748_en.pdf, Bush
release, although more research is required to fully assess the inac- et al., 2011).
tivation of resistance genes (i.e., DNA released from lysed cells The problem of AMR is widespread all over the world, there-
that may be available for horizontal gene transfer) by these mea- fore it is not eradicable, but can be managed. Concerted efforts
sures (Dodd, 2012). The combined removal of pollutants that between medical doctors, dentists, veterinarians, scientists, fun-
are potential selective agents, disinfection, and deactivation of the ders, industry, regulators, and multi-disciplinary approaches are
genetic material, may be a useful strategy to reduce the pollution needed to track resistance. Furthermore, global monitoring of
of environments with resistance factors. the antimicrobial drug consumption in human and veterinary
medicine and AMR, is an essential part of an overall strategy
CONCLUSIONS to inform, educate and get commitment of all parties, includ-
Inevitably, AMR in medicine has become common place. ing farmers and patients (American Academy of Microbiology,
Bacteria have evolved multiple mechanisms for the efficient 2009). All these are important measures for the efficient future
evolution and spread of AMR. Meanwhile the new developments use of antimicrobials in medicine. All members of society should
of quick and adequate molecular diagnostic techniques for be conscious of their role and take on responsibility for main-
the identification and epidemiological surveillance of genetic taining the effectiveness of current and future antimicrobials. We
determinants of AMR in different hosts and in the environment believe that future interventions can be successful in minimizing
will enhance the number of control options. We have outlined this problem.
above a number of potential measures that are enabled by our
improved ability to track AMR. However, there seems to be a AUTHOR CONTRIBUTIONS
clear need for action and policy changes. This includes drug L. Cantas defined the review theme, established the interdis-
licensing, financial incentives, penalties, and ban or restriction ciplinary coordination and the collaborations, designed the
on use of certain drugs. Similarly, the prescriber behavior needs manuscript, contributed to the data collection, data analysis,
to be altered. Animal health and hygiene needs to be improved. and drafting and writing of the manuscript. Syed Q. A. Shah,
In addition, the implementation of microbiological criteria L. M. Cavaco, C. M. Manaia, F. Walsh, M. Popowska: draft-
for the detection of certain types of resistant pathogens would ing, writing, and editing the manuscript. H. Garelick and H.
be important to control the trade of both food animals and Brgmann: contributed to data analysis, drafting, and writing the
food products. The problem of AMR in human medicine will manuscript. H. Srum: contributed to manuscript design, data
not be solved if nothing is done to limit the constant influx of collection, data analysis, drafting, and writing the manuscript. All
resistance genes into the human microbiota via the food chain authors have contributed to, seen and approved the manuscript. May 2013 | Volume 4 | Article 96 | 9

Cantas et al. The problem of antimicrobial resistance: a multi-disciplinary review

ACKNOWLEDGMENTS AND FUNDING responsible for the use which might be made of the information
contained in this publication. The COST Office is not respon-
sible for the external websites referred to in this publication.
C. M. Manaia acknowledges National Funds from FCT
Fundao para a Cincia e a Tecnologia through projects PEst-
OE/EQB/LA0016/2011 and PTDC/AAC-AMB/113840/2009. F.
Walsh acknowledges funding from the Swiss Federal Office for
All authors acknowledge DARE TD0803 (Detecting Agriculture, the Swiss Federal Office for the Environment and the
Antimicrobial Resistance in Europe) COST Action. (http:// Swiss Expert Committee for Biosafety (SECB). Finally L. Cantas This publication is supported by COST. extend his thanks to, for helpful support in reviewing
Neither the COST Office nor any person acting on its behalf is the manuscript.

REFERENCES resistance genes. FEMS Microbiol. Baquero, F., Martinez, J.-L., and a growing problem for human
Aarestrup, F. M. (2005). Veterinary Lett. 271, 147161. Canton, R. (2008). Antibiotics and and animal health and for the
drug usage and antimicrobial resis- Anderson, A. D., Nelson, J. M., antibiotic resistance in water envi- environment. Environ. Microbiol. 8,
tance in bacteria of animal origin. Rossiter, S., and Angulo, F. J. ronments. Curr. Opin. Biotechnol. 11371144.
Basic Clin. Pharmacol. Toxicol. 96, (2003). Public health consequences 19, 260265. Callaway, T. R., Edrington, T. S.,
271281. of use of antimicrobial agents in Barber, M., and Rozwadowska- Anderson, R. C., Harvey, R. B.,
Aarestrup, F. M., Seyfarth, A. M., food animals in the United States. Dowzenko, M. (1948). Infection by Genovese, K. J., Kennedy, C. N.,
Emborg, H. D., Pedersen, K., Microb. Drug Resist. 9, 373379. penecillin-resistant staphylococci. et al. (2008). Probiotics, prebi-
Hendriksen, R. S., and Bager, F. Angulo, F. J., Nargund, V. N., and Lancet 2, 641644. otics and competitive exclusion for
(2001). Effect of abolishment of Chiller, T. C. (2004). Evidence Bastianello, S. S., Fourie, N., Prozesky, prophylaxis against bacterial dis-
the use of antimicrobial agents for of an association between use L., Nel, P. W., and Kellermann, ease. Anim. Health Res. Rev. 9,
growth promotion on occurrence of anti-microbial agents in food T. S. (1995). Cardiomyopathy of 217225.
of antimicrobial resistance in fecal animals and anti-microbial resis- ruminants induced by the litter Cantas, L., Fraser, T. W. K., Fjelldal, P.
Enterococci from food animals tance among bacteria isolated from of poultry fed on rations con- G., Mayer, I., and Srum, H. (2011).
in Denmark. Antimicrob. Agents humans and the human health taining the ionophore antibiotic, The culturable intestinal micro-
Chemother. 45, 20542059. consequences of such resistance. maduramicin.2. macropathology biota of triploid and diploid juve-
Abraham, E. P., and Chain, E. (1940). J. Vet. Med. B 51, 374379. and histopathology. Onderstepoort nile Atlantic salmon (Salmo salar)
An enzyme from bacteria able to Anthony, F., Acar, J., Franklin, A., J. Vet. Res. 62, 518. a comparison of composition and
destroy penicillin. Nature 146, 837. Gupta, R., Nicholls, T., Tamura, Y., Bjrklund, H. V., Rbergh, C. M. I., drug resistance. BMC Vet. Res. 7:71.
Agers, Y., and Petersen, A. (2007). The et al. (2001). Antimicrobial resis- and Bylund, G. (1991). Residues of doi: 10.1186/1746-6148-7-71
tetracycline resistance determinant tance: responsible and prudent use oxolinic acid and oxytetracycline in Cantas, L., Le Roux, F., Mazel, D.,
Tet 39 and the sulphonamide resis- of antimicrobial agents in veteri- fish and sediments from fish farms. and Srum, H. (2012a). Impact
tance gene sulII are common among nary medicine. Rev. Sci. Tech. 20, Aquaculture 97, 8596. of Antibiotics on the Expression
resistant Acinetobacter spp. iso- 829839. Blanch, A. R., Caplin, J. L., Iversen, of the tra Genes and on the Host
lated from integrated fish farms in Arya, S. C., and Agarwal, N. (2011). A., Khn, I., Manero, A., Taylor, Innate Immune Gene Activity
Thailand. J. Antimicrob. Chemother. International travel with acquisition H. D., et al. (2003). Comparison during SXT Element Bearing
59, 2327. of multi-drug resistant Gram neg- of enterococcal populations related Aeromonas salmonicida Infection in
Alanis, A. J. (2005). Resistance to ative bacteria containing the New to urban and hospital wastewater Atlantic Salmon (Salmo salar L.).
antibiotics: are we in the post- Delhi metallo-beta-lactamase gene, in various climatic and geographic PSN-ICAAC12PS1-B-1330. San
antibiotic era? Arch. Med. Res. 36, bla(NDM-1). Travel Med. Infect. European regions. J. Appl. Microbiol. Francisco, CA.
697705. Dis. 9, 4748. 94, 9941002. Cantas, L., Torp, J. R., Alestrm, P.,
Alexander, T. W., Yanke, J. L., Reuter, Ash, R. J., Mauck, B., and Morgan, Bckelmann, U., Dorries, H. H., Srum, H. (2012b). Cultureable gut
T., Topp, E., Read, R. R., Selinger, B. M. (2002). Antibiotic resistance of Ayuso-Gabella, M. N., Maray, M. microbiota diversity in zebrafish.
L., et al. (2011). Longitudinal char- gram-negative bacteria in rivers, S., Tandoi, V., Levantesi, C., et al. Zebrafish 9, 2637.
acterization of antimicrobial resis- United States. Emerg. Infect. Dis. 8, (2009). Quantitative PCR monitor- Cantas, L., Midtlyng, P. J., and
tance genes in feces shed from cattle 713716. ing of antibiotic resistance genes Srum, H. (2012c). Impact of
fed different subtherapeutic antibi- Baltz, R. H. (2007). Antimicrobials and bacterial pathogens in three antibiotic treatments on the
otics. BMC Microbiol. 11:19. doi: from actinomycetes: back to the European artificial groundwater expression of the R plasmid tra
10.1186/1471-2180-11-19. future. Microbe 2, 125131. recharge systems. J. Appl. Environ. genes and on the host innate
Allen, H. K., Donato, J., Wang, H. Bannoehr, J., Ben Zakour, N. L., Waller, Microbiol. 75, 154163. immune activity during pRAS1
H., Cloud-Hansen, K. A., Davies, J., A. S., Guardabassi, L., Thoday, K. L., Brown, S., Bantar, C., Young, H. K., and bearing Aeromonas hydrophila
and Handelsman, J. (2010). Call of van den Broek, A. H., et al. (2007). Amyes, S. G. B. (1998). Limitation infection in zebrafish (Danio
the wild: antibiotic resistance genes Population genetic structure of the of Acinetobacter baumannii treat- rerio). BMC Microbiol. 12:37. doi:
in natural environments. Nat. Rev. Staphylococcus intermedius group: ment by plasmid-mediated car- 10.1186/1471-2180-12-37
Microbiol. 8, 251259. insights into agr diversification bapenemase ARI-2. Lancet 351, Cantas, L., Thoresen, I. S., Gjermund,
American Academy of Microbiology. and the emergence of methicillin- 186187. G., Sivertsen, T., Framstad,
(2009). Antibiotic resistance: an resistant strains. J. Bacteriol. 189, Bush, K., Courvalin, P., Dantas, G., T., and Srum, H. (2013).
ecological perspective on an old 86858692. Davies, J., Eisenstein, B., Huovinen, Antibiotikabehandling av
problem, in Report of a colloquium, Baquero, F., Alvarez-Ortega, C., and P., et al. (2011). Tackling antibiotic kolidiar hos spedgris med mini-
12 to 14 October 2008 (Annecy, Martinez, J. L. (2009). Ecology resistance. Nat. Rev. Microbiol. 9, mal antibiotikaresistensutvikling
France). and evolution of antibiotic resis- 894896. en modellstudie (in Norwegian),
Aminov, R., and Mackie, R. I. (2007). tance. Environ. Microbiol. Rep. 1, Cabello, F. C. (2006). Heavy use of pro- in Husdyrforsksmte 2013 - UMB
Evolution and ecology of antibiotic 469476. phylactic antibiotics in aquaculture: (Lillestrm).

Frontiers in Microbiology | Antimicrobials, Resistance and Chemotherapy May 2013 | Volume 4 | Article 96 | 10
Cantas et al. The problem of antimicrobial resistance: a multi-disciplinary review

Caprioli, A., Busani, L., Martel, antibiotic resistome. Science 311, Como-Sabetti, K., et al. (2010). Gustafson, R. H., and Bowen, R. E.
J. L., and Helmuth, R. (2000). 374377. Excess costs and utilization asso- (1997). Antibiotic use in animal
Monitoring of antibiotic resistance Decousser, J. W., Poirel, L., ciated with methicillin resistance agriculture. J. Appl. Microbiol. 83,
in bacteria of animal origin: epi- and Nordmann, P. (2001). for patients with Staphylococcus 531541.
demiological and microbiological Characterization of a chromoso- aureus infection. Infect. Control Halverson, M. (2000). The Price We Pay
methodologies. Int. J. Antimicrob. mally encoded extended-spectrum Hosp. Epidemiol. 31, 365373. for Corporate Hogs. Minneapolis,
Agents 14, 295301. class A -lactamase from Kluyvera Fischer, J., Rodriguez, I., Schmoger, MN: Institute for Agriculture and
Casewell, M., Friis, C., Marco, E., cryocrescens. Antimicrob. Agents S., Friese, A., Roesler, U., Helmuth, Trade policy, 32.
McMullin, P., and Phillips, I. Chemother. 45, 35953598. R., et al. (2012). Escherichia coli Hammerum, A. M., Heuer, O. E.,
(2003). The European ban on Defoirdt, T., Sorgeloos, P., and Bossier, producing VIM-1 carbapenemase Emborg, H. D., Bagger-Skjot, L.,
growth-promoting antibiotics and P. (2011). Alternatives to antibiotics isolated on a pig farm. J. Antimicrob. Jensen, V. F., Rogues, A. M., et al.
emerging consequences for human for the control of bacterial disease in Chemother. 67, 17931795. (2007). Danish integrated antimi-
and animal health. J. Antimicrob. aquaculture. Curr. Opin. Microbiol. Forsberg, K. J., Reyes, A., Wang, B., crobial in resistance monitoring and
Chemother. 52, 159161. 14, 251258. Selleck, E. M., Sommer, M. O. A., research program. Emerg. Infect.
Cattoir, V., Poirel, L., Mazel, D., Soussy, Dodd, M. C. (2012). Potential impacts and Dantas, G. (2012). The shared Dis. 13, 16321639.
C. J., and Nordmann, P. (2007). of disinfection processes on antibiotic resistome of soil bacteria Hektoen, H., Berge, J. A., Hormazabal,
Vibrio splendidus as the source elimination and deactivation of and human pathogens. Science 337, V., and Yndestad, M. (1995).
of plasmid-mediated qnrS-Like antibiotic resistance genes during 11071111. Persistence of antibacterial agents in
quinolone resistance determinants. water and wastewater treatment. Gigure, S., Prescott, J. F., Baggot, J. marine sediments. Aquaculture 133,
Antimicrob. Agents Chemother. 51, J. Environ. Monit. 14, 17541771. D., Walker, R. D., and Dowling, P. 175184.
26502651. Derewacz, D. K., Goodwin, C. M. (2007). Antimicrobial Therapy in Heuer, O. E., Kruse, H., Grave, K.,
Cheng, A. C., Turnidge, J., Collignon, R., McNees, C. R., McLean, Veterinary Medicine. Ames; Oxford: Collignon, P., Karunasagar, I., and
P., Looke, D., Barton, M., and J. A., and Bachmann, B. O. Iowa State University Press. Angulo, F. J. (2009). Human health
Gottlieb, T. (2012). Control of fluo- (2013). Antimicrobial drug resis- Glad, T.,Bernhardsen, P.,Nielsen, K. consequences of use of antimicro-
roquinolone resistance through suc- tance affects broad changes in M., Brusetti, L., Andersen, M., Aars, bial agents in aquaculture. Clin.
cessful regulation, Australia. Emerg. metabolomic phenotype in addi- J., et al. (2010). Bacterial diversity Infect. Dis. 49, 12481253.
Infect. Dis. 18, 14531460. tion to secondary metabolism. in faeces from polar bear (Ursus Hoa, P. T. P., Managaki, S., Nakada, N.,
Colquhoun, D. J., Aarflot, L., and Proc. Natl. Acad. Sci. U.S.A. 110, maritimus) in Arctic Svalbard. Takada, H., Shimizu, A., Anh, D. H.,
Melvold, C. F. (2007). gyrA and 23362341. BMC Microbiol. 10:10. doi: 10.1186/ et al. (2011). Antibiotic contamina-
parC mutations and associated FAAIR Scientific. (2002). Select find- 1471-2180-10-10 tion and occurrence of antibiotic-
quinolone resistance in Vibrio ings and conclusions. Clin. Infect. Goi-Urriza, M., Capdepuy, M., Arpin, resistant bacteria in aquatic envi-
anguillarum serotype O2b strains Dis. 34, S73S75. C., Raymond, N., Caumette, P., and ronments of northern Vietnam. Sci.
isolated from farmed Atlantic Falagas, M. E., and Bliziotis, I. A. Quentin, C. (2000). Impact of an Total Environ. 409, 28942901.
cod (Gadus morhua) in Norway. (2007). Pandrug-resistant Gram- urban effluent on antibiotic resis- Holmberg, S. D., Solomon, S. L., and
Antimicrob. Agents Chemother. 51, negative bacteria: the dawn of tance of riverine Enterobacteriaceae Blake, P. A. (1987). Health and
25972599. the post-antibiotic era? Int. J. and Aeromonas spp. J. Appl. Environ. economic impacts of antimicro-
Corpet, D. E. (1988). Antibiotic resis- Antimicrob. Agents 29, 630636. Microb. 66, 125132. bial resistance. Rev. Infect. Dis. 9,
tance from food. N. Engl. J. Med. Falcone-Dias, M. F., Vaz-Moreira, I., Gtz, A., Pukall, R., Smit, E., Tietze, 10651078.
318, 12061207. and Manaia, C. M. (2012). Bottled E., Prager, R., Tschpe, H., et al. Holmstrm, K., Grslund, S.,
Crofton, J., and Mitchison, D. A. mineral water as a potential source (1996). Detection and characteri- Wahlstrm, A., Poungshompoo, S.,
(1948). Streptomycin resistance in of antibiotic resistant bacteria. zation of broad-host range plas- Bengtsson, B. E., and Kautsky, N.
pulmonary tuberculosis. Br. Med. J. Water Res. 46, 36123622. mids in environmental bacteria by (2003). Antibiotic use in shrimp
2, 10091015. FAO. (2010). The State of the PCR. Appl. Environ. Microbiol. 62, farming and implications for envi-
Cunha, B. A. (2002). Strategies to World Fisheries and Aquaculture. 26212628. ronmental impacts and human
control antibiotic resistance. Semin. Rome: United Nations Food and Graham, D. W., Olivares-Rieumont, S., health. Int. J. Food Sci. Technol. 38,
Respir. Infect. 17, 250258. Agriculture Organization. Knapp, C. W., Lima, L., Werner, D., 255266.
Cuny, C., Friedrich, A., Kozytska, Farmed Fish Health Report. (2010). and Bowen, E. (2011). Antibiotic Horton, R. A., Randall, L. P., Snary, E.
S., Layer, F., Nubel, U., Ohlsen, Norwegian Veterinary Institute, in resistance gene abundances asso- L., Cockrem, H., Lotz, S., Wearing,
K., et al. (2010). Emergence of The Health Situation in Norwegian ciated with waste discharges to H., et al. (2011). Fecal carriage
methicillin-resistant Staphylococcus Aquaculture 2010, eds G. Born the Almendares River near Havana, and shedding density of CTX-
aureus (MRSA) in different animal and C. Sviland (Oslo: Norwegian Cuba. Environ. Sci. Technol. 45, M extended-spectrum -lactamase-
species. Int. J. Med. Microbiol. 300, Veterinary Institute). 418424. producing Escherichia coli in cat-
109117. Ferreira da Silva, M., Tiago, I., Grslund, S., Holmstrm, K., and tle, chickens, and pigs: implications
Czekalski, N., Berthold, T., Caucci, Verissimo, A., Boaventura, R. A. Wahlstrm, A. (2003). A field survey for environmental contamination
S., Egli, A., and Burgmann, H. R., Nunes, O. C., and Manaia, C. of chemicals and biological prod- and food production. Appl. Environ.
(2012). Increased levels of multire- M. (2006). Antibiotic resistance of ucts used in shrimp farming. Mar. Microbiol. 77, 37153719.
sistant bacteria and resistance genes enterococci and related bacteria Pollut. Bull. 46, 8190. Jean-Louis, M., Tardy, F., Brisabois, A.,
after wastewater treatment and their in an urban wastewater treatment Grave, K., Torren-Edo, J., and Mackay, Lailler, R., Coudert, M., Chaslus-
dissemination into Lake Geneva, plant. FEMS Microbiol. Ecol. 55, D. (2010). Comparison of the sales Dancla, E. (2000). The French
Switzerland. Front. Microbiol. 3:106. 322329. of veterinary antibacterial agents antibiotic resistance monitoring
doi: 10.3389/fmicb.2012.00106 Ferreira da Silva, M., Vaz-Moreira, I., between 10 European countries. programs. Int. J. Antimicrob. Agents
DCosta, V. M., King, C. E., Kalan, Gonzalez-Pajuelo, M., Nunes, O. J. Antimicrob. Chemother. 65, 14, 275283.
L., Morar, M., Sung, W. W. L., C., and Manaia, C. M. (2007). 20372040. Klugman, K. P. (2002). Bacteriological
Schwarz, C., et al. (2011). Antibiotic Antimicrobial resistance patterns in Gullberg, E., Cao, S., Berg, O. G., Ilback, evidence of antibiotic failure in
resistance is ancient. Nature 477, Enterobacteriaceae isolated from an C., Sandegren, L., Hughes, D., et al. pneumococcal lower respiratory
457461. urban wastewater treatment plant. (2011). Selection of resistant bacte- tract infections. Eur. Respir. J. 20,
DCosta, V. M., McGrann, K. M., FEMS Microbiol. Ecol. 60, 166176. ria at very low antibiotic concentra- 3S8S.
Hughes, D. W., and Wright, Filice, G. A., Nyman, J. A., Lexau, tions. PLoS Pathog. 7:e1002158. doi: Kluytmans, J. A. J. W. (2010).
G. D. (2006). Sampling the C., Lees, C. H., Bockstedt, L. A., 10.1371/journal.ppat.1002158 Methicillin-resistant Staphylococcus May 2013 | Volume 4 | Article 96 | 11

Cantas et al. The problem of antimicrobial resistance: a multi-disciplinary review

aureus in food products: cause for Lie, . (2008). Improving Farmed Fish Norwegian aquaculture. Aquac. Res. Appl. Microbiol. Biotechnol. 87,
concern or case for complacency? Quality and Safety. Woodhead, 42, 2834. 11571166.
Clin. Microbiol. Infect. 16, 1115. Publishing Series in Food Science, Moura, A., Henriques, I., Smalla, K., Oberl, K., Capdeville, M., Berthe,
Knapp, C. W., Dolfing, J., Ehlert, P. Technology and Nutrition No. 162. and Correia, A. (2010). Wastewater T., and Petit, F. (2012). Evidence
A., and Graham, D. W. (2010). E-ISBN: 978-1-84569-492-0. bacterial communities bring for a complex relationship between
Evidence of increasing antibiotic Linton, K. B., Lee, P. A., Rowland, together broad-host range plas- antibiotics and antibiotic-resistant
resistance gene abundances in A. J., Baker, V. N., Gillespi, W. mids, integrons and a wide diversity Escherichia coli: from medical cen-
archived soils since 1940. Environ. A., and Richmond, M. H. (1972). of uncharacterized gene cassettes. ter patients to a receiving envi-
Sci. Technol. 44, 580587. Antibiotic resistance and transmis- Res. Microbiol. 161, 5866. ronment. Environ. Sci. Technol. 46,
Knapp, C. W., Engemann, C. A., sible R-factors in intestinal Coliform Muto, C. A., Jernigan, J. A., Ostrowsky, 18591868.
Hanson, M. L., Keen, P. L., flora of healthy adults and chil- B. E., Richet, H. M., Jarvis, W. R., Olarte, J. (1983). Antibiotic resistance
Hall, K. J., and Graham, D. W. dren in an urban and a rural Boyce, J. M., et al. (2003). SHEA in Mexico. APUA Newslett. 1, 3.
(2008). Indirect evidence of community. J. Hyg. (Lond.) 70, guideline for preventing nosocomial Olliver, A., Vall, M., Chaslus-Dancla,
transposon-mediated selection 99104. transmission of multidrug- E., and Cloeckaert, A. (2005).
of antibiotic resistance genes in Literak, I., Petro, R., Dolejska, M., resistant strains of Staphylococcus Overexpression of the multidrug
aquatic systems at low-level oxyte- Gruberova, E., Dobiasova, H., Petr, aureus and Enterococcus. Infect. efflux operon acrEF by insertional
tracycline exposures. Environ. Sci. J., et al. (2011). Antimicrobial resis- Control Hosp. Epidemiol. 24, activation with IS1 or IS10 elements
Technol. 42, 53485353. tance in fecal Escherichia coli iso- 362386. in Salmonella enterica Serovar
Kohanski, M. A., DePristo, M. A., lates from healthy urban children Ndi, O., and Barton, M. (2012). Typhimurium DT204 acrB mutants
and Collins, J. J. (2010). Sublethal of two age groups in relation to Antibiotic resistance in animals selected with fluoroquinolones.
antibiotic treatment leads to their antibiotic therapy. Antimicrob. The Australian perspective, in Antimicrob. Agents Chemother. 49,
multidrug resistance via radical- Agents Chemother. 55, 30053007. Antimicrobial Resistance in the 289301.
induced mutagenesis. Mol. Cell 37, Ma, J., Liu, J. H., Lv, L., Zong, Z., Environment, eds P. L. Keen and M. Otter, J. A., and French, G. L.
311320. Sun, Y., Zheng, H., et al. (2012). H. H. M. Montforts (New Jersey, (2010). Molecular epidemiol-
Korczak, D., and Schffmann, C. Characterization of extended- NJ: Wiley-Blackwell), 265290. ogy of community-associated
(2010). Medical and health eco- spectrum -lactamase genes among Nkogwe, C., Raletobana, J., Stewart- meticillin-resistant Staphylococcus
nomic evaluation of prevention- Escherichia coli isolates from duck Johnson, A., Suepaul, S., and aureus in Europe. Lancet Infect. Dis.
and control measures related to and environment samples in a duck Adesiyun, A. (2011). Frequency 10, 227239.
MRSA infections or -colonisations farm. Appl. Environ. Microbiol. 78, of detection of Escherichia Pallett, A., and Hand, K. (2010).
at hospitals. GMS Health Technol. 36683673. coli, Salmonella spp., and Complicated urinary tract infec-
Assess. 6, 19. Markestad, A., and Grave, K. (1997). Campylobacter spp. in the fae- tions: practical solutions for the
Kumarasamy, K. K., Toleman, M. A., Reduction of antibacterial drug use ces of wild rats (Rattus spp.) in treatment of multiresistant Gram-
Walsh, T. R., Bagaria, J., Butt, F., in Norwegian fish farming due to Trinidad and Tobago. Vet. Med. negative bacteria. J. Antimicrob.
Balakrishnan, R., et al. (2010). vaccination. Dev. Biol. Stand. 90, Int. 2011:686923. doi: 10.4061/ Chemother. 65, 2533.
Emergence of a new antibiotic 365369. 2011/686923 Patra, S., Das, T. K., Avila, C., Cabello,
resistance mechanism in India, Marshall, B., Petrowski, D., and Levy, Nordmann, P., Dortet, L., and Poirel, V., Castillio, F., Sarkar, D., et al.
Pakistan, and UK: a molecular, S. B. (1990). Inter- and intraspecies L. (2012). Carbapenem resistance (2012). Cadmium tolerance and
biological, and epidemiologi- spread of Escherichia coli in a in Enterobacteriaceae: here is antibiotic resistance in Escherichia
cal study. Lancet Infect. Dis. 10, farm environment in the absence of the storm! Trends Mol. Med. 18, coli isolated from waste stabiliza-
597602. antibiotic usage. Proc. Natl. Acad. 263272. tion ponds. Indian J. Exp. Biol. 50,
Lang, K. S., Anderson, J. M., Schwarz, Sci. U.S.A. 87, 66096613. Nordmann, P., Poirel, L., Toleman, M. 300307.
S., Williamson, L., Handelsman, J., Marshall, B. M., and Levy, S. B. (2011). A., and Walsh, T. R. (2011). Does Petersen, A., Andersen, J. S., Kaewmak,
and Singer, R. S. (2010). Novel flor- Food animals and antimicrobials: broad-spectrum -lactam resistance T., Somsiri, T., and Dalsgaard,
fenicol and chloramphenicol resis- impacts on human health. Clin. due to NDM-1 herald the end of A. (2002). Impact of integrated
tance gene discovered in Alaskan Microbiol. Rev. 24, 718733. the antibiotic era for treatment of fish farming on antimicrobial
soil by using functional metage- Martinez, J. L. (2009). Environmental infections caused by Gram-negative resistance in a pond environ-
nomics. Appl. Environ. Microbiol. pollution by antibiotics and by bacteria? J. Antimicrob. Chemother. ment. Appl. Environ. Microbiol. 68,
76, 53215326. antibiotic resistance determinants. 66, 689692. 60366042.
Levy, S. B. (1984). Antibiotic resis- Environ. Pollut. 157, 28932902. NORM/NORM-VET. (2011). Usage of Picao, R. C., Poirel, L., Demarta, A.,
tant bacteria in food of man and McEwen, S. A. (2006). Antibiotic use Antimicrobial Agents and Occurrence Silva, C. S. F., Corvaglia, A. R.,
animals, in Antimicrobials Ans in animal agriculture: what have we of Antimicrobial Resistance in Petrini, O., et al. (2008). Plasmid-
Agriculture, ed M. Woodbine learned and where are we going? Norway. Troms/Oslo 2012. mediated quinolone resistance in
(London: Butterworths), 525531. Anim. Biotechnol. 17, 239250. ISSN:1502-2307 (print)/1890- Aeromonas allosaccharophila recov-
Levy, S. B. (1998). The challange of McManus, P. S., Stockwell, V. O., 9965 (electronic). (Troms/Oslo: ered from a Swiss lake. J. Antimicrob.
antibiotic resistance. Sci. Am. 278, Sundin, G. W., and Jones, A. L. Norwegian Veterinary Institute). Chemother. 62, 948950.
4653. (2002). Antibiotic use in plant Available online at: http://www. Poirel, L., Liard, A., Rodriguez-
Levy, S. B. (2001). Antibiotic resis- agriculture. Annu. Rev. Phytopathol. Martinez, J. M., and Nordmann, P.
tance: consequences of inaction. 40, 443465. Norm-Vet-Report/Norm-Norm-Vet- (2005). Vibrionaceae as a possible
Clin. Infect. Dis. 33, 124129. Michael, I., Rizzo, L., McArdell, C. S., rapporten-2010 source of Qnr-like quinolone resis-
Levy, S. B., FitzGerald, G. B., and Manaia, C. M., Merlin, C., Schwartz, Novo, A., Andr, S., Viana, P., Nunes, tance determinants. J. Antimicrob.
Macone, A. B. (1976). Changes in T., et al. (2013). Urban wastewa- O. C., and Manaia, C. M. (2013). Chemother. 56, 11181121.
intestinal flora of farm personnel ter treatment plants as hotspots for Antibiotic resistance, antimicrobial Popowska, M., and Krawczyk-Balska,
after introduction of a tetracycline- the release of antibiotics in the envi- residues and bacterial community A. (2013). Broad-Host-Range IncP-
supplemented feed on a farm. N. ronment: a review. Water Res. 47, composition in urban wastewater. 1 plasmids and their resistance
Engl. J. Med. 295, 583588. 957995. Water Res. 47, 18751887. potential. Front. Microbiol. 4:44. doi:
Levy, S. B., and Marshall, B. (2004). Midtlyng, P. J., Grave, K., and Horsberg, Novo, A., and Manaia, C. M. (2010). 10.3389/fmicb.2013.00044
Antibacterial resistance worldwide: T. E. (2011). What has been done Factors influencing antibiotic Popowska, M., Miernik, A., Rzeczycka,
causes, challenges and responses. to minimize the use of antibac- resistance burden in municipal M., and Lopaciuk, A. (2010).
Nat. Med. 10, 122129. terial and antiparasitic drugs in wastewater treatment plants. The impact of environmental

Frontiers in Microbiology | Antimicrobials, Resistance and Chemotherapy May 2013 | Volume 4 | Article 96 | 12
Cantas et al. The problem of antimicrobial resistance: a multi-disciplinary review

contamination with antibiotics for antibiotic resistant bacteria and in FAO Fisheries technical paper 469 Srum, H. (2008). Antibiotic resis-
on levels of resistance in soil genes spread into the environment: (Rome; United Nations), 89. tance associated with veterinary
bacteria. J. Environ. Qual. 39, a review. Sci. Total Environ. 447, Available online at: drug use in fish farms, in Improving
16791687. 345360. docrep/fao/009/a0282e/a0282e00. Farmed Fish Quality and Safety,
Popowska, M., Rzeczycka, M., Miernik, Roberts, R. R., Hota, B., Ahmad, I., pdf ed . Lie (Cambridge: WoodHead
A., Krawczyk-balska, A., Walsh, Scott, R. D., Foster, S. D., Abbasi, Shah, S. Q. A., Karatas, S., Nilsen, Publishing Limit), 157182.
F., and Duffy, B. (2012). Influence F., et al. (2009). Hospital and soci- H., Steinum, T. M., Colquhoun, Stockwell, V. O., and Duffy, B.
of soil use on prevalence of etal costs of antimicrobial-resistant D. J., and Srum, H. (2012a). (2012). Use of antibiotics in
tetracycline, streptomycin, and ery- infections in a Chicago teaching Characterization and expression of plant agriculture. Rev. Sci. Tech. 31,
thromycin resistance and associated hospital: implications for antibiotic the gyrA gene from quinolone resis- 199210.
resistance genes. Antimicrob. Agents stewardship. Clin. Infect. Dis. 49, tant Yersinia ruckeri strains iso- Stokes, H. W., and Gillings, M. R.
Chemother. 56, 14341443. 11751184. lated from Atlantic salmon (Salmo (2011). Gene flow, mobile genetic
Potter, A., Gerdts, V., and Littel-Van Rodriguez, M. M., Power, P., Radice, salar L.) in Norway. Aquaculture elements and the recruitment of
den Hurk, S. V. (2008). Veterinary M., Vay, C., Famiglietti, A., Galleni, 350353, 3741. antibiotic resistance genes into
vaccines: alternatives to antibiotics? M., et al. (2004). Chromosome- Shah, S. Q. A., Colquhoun, D. J., Gram negative pathogens. FEMS
Anim. Health Res. Rev. 9, 187199. encoded CTX-M-3 from Kluyvera Nikuli, H. L., and Srum, H. Microbiol. Rev. 35, 790819.
Pouillard, J. (2002). A forgotten dis- ascorbata: a possible origin of (2012b). Prevalence of antibiotic Strahilevitz, J., Jacoby, G., Hooper,
covery: doctor of medicine Ernest plasmid-borne CTX-M-1-derived resistance genes in the bacterial D. C., and Robicsek, A. (2009).
Duchesne, s thesis (1874-1912) cefotaximases. Antimicrob. Agents flora of integrated fish farming Plasmid-mediated quinolone resis-
[Article in French]. Hist. Sci. Med. Chemother. 48, 48954897. environments of Pakistan and tance: a multifaceted threat. Clin.
36, 1120. Roe, M. T., and Pillai, S. D. (2003). Tanzania. Environ. Sci. Technol. 46, Microbiol. Rev. 22, 664689.
Pratt, R. (2010). Preparation for a post Monitoring and identifying antibi- 86728679. Sundin, G. W., Monks, D. E., and
antibiotic era must start now. Nurs. otic resistance mechanisms in bac- Sharma, R., Munns, K., Alexander, Bender, C. L. (1995). Distribution
Times 106, 26. teria. Poult. Sci. 82, 622626. T., Entz, T., Mirzaagha, P., Yanke, of the streptomycin-resistance
Primavera, J. H. (2006). Overcoming Roura, E., Homedes, J., and Klasing, K. L. J., et al. (2008). Diversity and transposon Tn5393 among
the impacts of aquaculture on the C. (1992). Prevention of immuno- distribution of commensal fecal phylloplane and soil bacte-
coastal zone. Ocean Coast. Manage. logic stress contributes to the Escherichia coli bacteria in beef cat- ria from managed agricultural
49, 531545. growth-permitting ability of dietary tle administered selected subthera- habitats. Can. J. Microbiol. 41,
Pruden, A., Arabi, M., and Storteboom, antibiotics in chicks. J. Nutr. 122, peutic antimicrobials in a feedlot 792799.
H. N. (2012). Correlation between 23832390. setting. Appl. Environ. Microbiol. 74, Swann, M. M. (1969). Use of Antibiotics
upstream human activities and Sato, K., Bartlett, P. C., and Saeed, 61786186. in Animal Husbandry and Veterinary
riverine antibiotic resistance M. A. (2005). Antimicrobial sus- Shtienberg, D., Zilberstaine, M., Medicine (Swann Report). London:
genes. Environ. Sci. Technol. 46, ceptibility of Escherichia coli isolates Oppenheim, D., Herzog, Z., HMSO.
11541-11549. from dairy farms using organic ver- Manulis, S., Shwartz, H., et al. Swartz, M. N. (2002). Human diseases
Rassow, D., and Schaper, H. (1996). sus conventional production meth- (2001). Efficacy of oxolinic acid caused by foodborne pathogens of
The use of feed medications in ods. J. Am. Vet. Med. Assoc. 226, and other bactericides in suppres- animal origin. Clin. Infect. Dis. 34,
swine and poultry facilities in 589594. sion of Erwinia amylovora in pear S111S122.
the Weser-Ems region [Article Schwartz, T., Volkmann, H., Kirchen, orchards in Israel. Phytoparasitica Szczepanowski, R. H., Carpenter,
in German]. Dtsch. Tierarztl. S., Kohnen, W., Schn-Hlz, K., 29, 143154. M. A., Czapinska, H., Zaremba,
Wochenschr. 103, 244249. Jansen, B., et al. (2006). Real- Smith, P. R., Le Breton, A., Horsberg, M., Tamulaitis, G., Siksnys, V.,
Reinthaler, F. F., Posch, J., Feierl, G., time PCR detection of Pseudomonas T. E., and Corsin, F. (2009). et al. (2008). Central base pair
Wst, G., Haas, D., Ruckenbauer, aeruginosa in clinical and munic- Guidelines for antimicrobial flipping and discrimination by
G., et al. (2003). Antibiotic resis- ipal wastewater and genotyping use in aquaculture, in Guide to PspGI. Nucleic Acids Res. 36,
tance of E. coli in sewage and sludge. of the ciprofloxacin-resistant iso- Antimicrobial Use in Animals, 61096117.
Water Res. 37, 16851690. lates. FEMS Microbiol. Ecol. 57, eds L. Guardabassi, L. B. Jensen, Szczepanowski, R., Linke, B., Krahn,
Rhodes, G., Huys, G., Swings, J., 158167. and H. Kruse (Oxford: Blackwell I., Gartemann, K.-H., Gutzkow,
McGann, P., Hiney, M., Smith, Segura, P. A., Francois, M., Gagnon, Publishing Ltd.), 207218. T., Eichler, W., et al. (2009).
P., et al. (2000). Distribution of C., and Sauve, S. (2009). Review Soonthornchaikul, N., Garelick, H., Detection of 140 clinically relevant
oxytetracycline resistance plasmids of the occurrence of anti-infectives Jones, H., Jacobs, J., Ball, D., and antibiotic- resistance genes in the
between Aeromonads in hospital in contaminated wastewaters Choudhury, M. (2006). Resistance plasmid metagenome of wastewater
and aquaculture environments: and natural and drinking waters. to three antimicrobial agents of treatment plant bacteria showing
implication of Tn1721 in dissemi- Environ. Health Perspect. 117, Campylobacter isolated from inten- reduced susceptibility to selected
nation of the tetracycline resistance 675684. sively and organically reared chick- antibiotics. Microbiology 155,
determinant Tet, A. Appl. Environ. Seiler, C., and Berendonk, T. U. ens purchased from retail out- 23062319.
Microbiol. 66, 38833890. (2012). Heavy metal driven lets. Int. J. Antimicrob. Agents 27, Tablan, O. C., Anderson, L. J., Besser,
Riesenfeld, C. S., Goodman, R. M., and co-selection of antibiotic resis- 125130. R., Bridges, C., and Hajjeh, R.
Handelsman, J. (2004a). Uncultured tance in soil and water bodies Soonthornchaikul, N., and Garelick, (2004). Guidelines for preventing
soil bacteria are a reservoir of new impacted by agriculture and aqua- H. (2009). Antimicrobial resistance health-care-associated pneumonia,
antibiotic resistance genes. Environ. culture. Front. Microbiol. doi: of Campylobacter species isolated 2003: recommendations of CDC
Microbiol. 6, 981989. 10.3389/fmicb.2012.00399 from edible bivalve molluscs pur- and the Healthcare Infection
Riesenfeld, C. S., Schloss, P. D., Sen, D., Van Der Auwera, G., Rogers, chased from Bangkok markets, Control Practices Advisory
and Handelsman, J. (2004b). L., Thomas, C. M., Brown, C. J., Thailand. Foodborne Pathog. Dis. 6, Committee. MMWR Recomm.
Metagenomics: genomic analysis of and Top, E. M. (2011). Broad- 947951. Rep. 53, 136.
microbial communities. Annu. Rev. host-range plasmids from agricul- Srum, H. (2006). Antimicrobial drug Tennstedt, T., Szczepanowski, R.,
Genet. 38, 525552. tural soils have IncP-1 backbones resistance in fish pathogens, in Braun, S., Puhler, A., and Schluter,
Rizzo, L., Manaia, C. M., Merlin, C., with diverse accessory genes. Appl. Antimicrobial Resistance in Bacteria A. (2003). Occurrence of integron-
Schwartz, T., Dagot, D., Ploy, M. Environ. Microbiol. 77, 79757983. of Animal Origin, ed F. M. Aarestrup associated resistance gene cassettes
C., et al. (2013). Urban wastew- Serrano, P. H. (2005). Responsible (Washington, DC: ASM Press), located on antibiotic resistance
ater treatment plants as hotspots use of antibiotics in aquaculture, 213238. plasmids isolated from a wastewater May 2013 | Volume 4 | Article 96 | 13

Cantas et al. The problem of antimicrobial resistance: a multi-disciplinary review

treatment plant. FEMS Microbiol. municipal wastewater using real- zoonotic pathogens in clinical Q. Q., et al. (2009). Phenotypic
Ecol. 45, 239252. time PCR (TaqMan). J. Microbiol. samples. Int. J. Med. Microbiol. 301, and genotypic characterisation of
Thaker, M., Spanogiannopoulos, P., Methods 56, 277286. 635641. antimicrobial resistance in faecal
and Wright, G. D. (2010). The tetra- Walsh, T. R., Weeks, J., Livermore, D. Wilke, M. H. (2010). Multiresistant bacteria from 30 Giant pandas.
cycline resistome. Cell. Mol. Life Sci. M., and Toleman, M. A. (2011). bacteria and current therapythe Int. J. Antimicrob. Agents 33,
67, 419431. Dissemination of NDM-1 positive economical side of the story. Eur. J. 456460.
Thiele-Bruhn, S. (2003). Pharma- bacteria in the New Delhi envi- Med. Res. 15, 571576.
ceutical antibiotic compounds in ronment and its implications for Yang, C., Zhang, W., Liu, R., Li, Q., Conflict of Interest Statement: The
soilsa review. J. Plant Nutr. Soil human health: an environmental Li, B., Wang, S., et al. (2011). authors declare that the research
Sci. 166, 145167. point prevalence study. Lancet Phylogenetic diversity and was conducted in the absence of any
Torres-Corts, G., Millan, V., Ramirez- Infect. Dis. 11, 355362. metabolic potential of activated commercial or financial relationships
Saad, H.C., Nisa-Martinez, R., Toro, Watanabe, T. (1963). Infective hered- sludge microbial communities in that could be construed as a potential
N., and Martinez-Abarca, F. (2011). ity of multiple drug resistance in full-scale wastewater treatment conflict of interest.
Characterization of novel antibi- bacteria. Bacteriol. Rev. 27, 87115. plants. Environ. Sci. Technol. 45,
otic resistance genes identified by Watkinson, A. J., Micalizzi, G. R., 74087415. Received: 13 December 2012; paper
functional metagenomics on soil Bates, J. R., and Costanzo, S. D. Ye, L., and Zhang, T. (2011). Pathogenic pending published: 04 January 2013;
samples. Environ. Microbiol. 13, (2007). Novel method for rapid bacteria in sewage treatment plants accepted: 04 April 2013; published
11011114. assessment of antibiotic resistance as revealed by 454 pyrosequenc- online: 14 May 2013.
Vaz-Moreira, I., Nunes, O. C., and in Escherichia coli isolates from ing. Environ. Sci. Technol. 45, Citation: Cantas L, Shah SQA, Cavaco
Manaia, C. M. (2011). Diversity environmental waters by use of a 71737179. LM, Manaia CM, Walsh F, Popowska
and antibiotic resistance pat- modified chromogenic agar. Appl. Ye, L., and Zhang, T. (2013). Bacterial M, Garelick H, Brgmann H and Srum
terns of Sphingomonadaceae Environ. Microbiol. 73, 22242229. communities in different sections of H (2013) A brief multi-disciplinary
isolated from drinking water. Weese, J. S. (2010). Methicillin-resistant a municipal wastewater treatment review on antimicrobial resistance in
Appl. Environ. Microbiol. 77, Staphylococcus aureus in animals. plant revealed by 16S rDNA 454 medicine and its linkage to the global
56975706. ILAR J. 51, 233244. pyrosequencing. Appl. Microbiol. environmental microbiota. Front.
Vazquez-Moreno, L., Bermudez, A., Welch, T. J., Fricke, W. F., McDermott, Biotechnol. 97, 26812690. Microbiol. 4:96. doi: 10.3389/fmicb.
Langure, A., Higuera-Ciapara, I., P. F., White, D. G., Rosso, M. Yoon, J. W., Lee, K. J., Lee, S. Y., Chae, 2013.00096
Diaz De Aguayo, M., and lores, L., Rasko, D. A., et al. (2007). M. J., Park, J. K., Yoo, J. H., et al. This article was submitted to Frontiers
E. (1990). Antibiotic residues and Multiple antimicrobial resistance (2010). Antibiotic resistance profiles in Antimicrobials, Resistance and
drug resistant bacteria in beef, and in plague: an emerging public of Staphylococcus pseudintermedius Chemotherapy, a specialty of Frontiers in
chicken tissues. J. Food Sci. 55, health risk. PLoS ONE 2:e309. doi: isolates from Canine patients in Microbiology.
632634. 10.1371/journal.pone.0000309 Korea. J. Microbiol. Biotechnol. 20, Copyright 2013 Cantas, Shah,
Verschuere, L., Rombaut, G., Sorgeloos, Wieler, L. H., Ewers, C., Guenther, 17641768. Cavaco, Manaia, Walsh, Popowska,
P., and Verstraete, W. (2000). S., Walther, B., and Lbke-Becker, Zhang, T., Zhang, X.-X., and Ye, Garelick, Brgmann and Srum. This is
Probiotic bacteria as biological A. (2011). Methicillin-resistant L. (2011). Plasmid metagenome an open-access article distributed under
control agents in aquaculture. staphylococci (MRS) and reveals high levels of antibiotic the terms of the Creative Commons
Microbiol. Mol. Biol. Rev. 64, extended-spectrum beta- resistance genes and mobile genetic Attribution License, which permits use,
655671. lactamases (ESBL)-producing elements in activated sludge. PLoS distribution and reproduction in other
Volkmann, H., Schwartz, T., Bischoff, Enterobacteriaceae in companion ONE 6:e26041. doi: 10.1371/ forums, provided the original authors
P., Kirchen, S., and Obst, U. (2004). animals: nosocomial infections journal.pone.0026041 and source are credited and subject to
Detection of clinically relevant as one reason for the rising Zhang, A. Y., Wang, H. N., Tian, any copyright notices concerning any
antibiotic-resistance genes in prevalence of these potential G. B., Zhang, Y., Yang, X., Xia, third-party graphics etc.

Frontiers in Microbiology | Antimicrobials, Resistance and Chemotherapy May 2013 | Volume 4 | Article 96 | 14