The class of beta-lactam antibiotics is among the most important groups of antimicrobial agents in human and veterinary medicine. The chemical substances are in principal identical in both fields of clinical use. Besides the first widely used antimicrobial substance penicillin, other members of this family have gained a similar importance over the last decades, namely the first- to fourth-generation cephalosporins and the beta-lactamase-inhibitors. In the veterinary context the few studies that exist confirm that beta-lactam antimicrobials are the most commonly prescribed antimicrobials in small animals (DANMAP, 2007; SVARM, 2008). In livestock, a decrease in the use of beta-lactam antimicrobials could be observed over the last years (NORM/NORM-VET, 2010), basically due to restrictions in prescription. All beta-lactams interfere with the final stage of peptidoglycan synthesis through acting on penicillin-binding proteins, thereby preventing the bacterial cell wall from forming. The peptidoglycan constitutes a layer between the outer membrane and the cytoplasmic membrane which maintains the cell shape and protects the bacterium against osmotic forces. The most common resistance mechanism of Enterobacteriaceae spp. against beta-lactams is the inactivation of the drug by hydrolytic cleavage of the beta-lactam ring system (Greenwood, 2000).

More than 400 different beta-lactamase enzymes are currently known, sharing the same resistance mechanism but differing in their range of substrates and susceptibility against inhibitory substances². Extended-spectrum beta-lactamases display an extended substrate spectrum, and this has directly influenced a global change in the epidemiology of beta-lactamases since the early 1990s in human medicine and since 2000 in veterinary medicine (Kong et al., 2010; Pitout, 2010; Smet et al., 2010b). The term extended-spectrum determines the ability of ESBLs to hydrolyze a broader spectrum of beta-lactam antimicrobials than the parent beta-lactamases they were originally derived from. While they are capable of inactivating beta-lactam antimicrobials containing an oxyimino-group such as oxyimino-cephalosporins (e.g., ceftazidime, cefotaxime) as well as oxyimino-monobactam (aztreonam), ESBLs are not active against cephamycins and carbapenems. They are usually inhibited by beta-lactamase-inhibitors like clavulanic acid and tazobactam, which marks a difference between ESBL- and AmpC–beta-lactamases producing bacteria (Bradford, 2001). Several different classification schemes for bacterial beta-lactamases have been described, including the system devised by Bush et al. (1995) which is based on the activity of the beta-lactamases against different beta-lactam antimicrobials, and the currently most widely used Ambler system, which divides beta-lactamases into four classes (A, B, C, and D), based on their amino acid sequences (Ambler, 1980). The majority of ESBLs belong to Ambler class A and to the Bush group 2be. ESBLs have been found in a wide range of Gram-negative bacteria, but the vast majority of bacterial hosts belong to the family of Enterobacteriaceae, including Klebsiella spp., E. coli, Salmonella enterica, Citrobacter spp., and Enterobacter spp. (Bradford, 2001). Four enzyme families, namely TEM (Temoneira) -type beta-lactamases, SHV (Sulfhydryl variable) -type beta-lactamases, CTX (cefotaximase) -M-type beta-lactamases, and OXA (oxacillinase) -type beta-lactamases are currently regarded the most common ESBLs among Enterobacteriaceae spp. TEM-type beta-lactamases are derivatives of TEM-1, which was first demonstrated in 1965 in an E. coli isolate from a patient in Athens, Greece, named Temoneira, and of TEM-2 and consist of more than 150 different enzymes. While the majority of TEM beta-lactamases are ESBLs, TEM-1, TEM-2, and TEM-13 are only able to hydrolyse penicillin derivates and thus are not regarded as ESBLs (Livermore, 1995).

Similar to TEM-type enzymes the majority of SHV enzymes are ESBLs. All currently recognized SHV enzymes are derivatives of SHV-1 and SHV-2. Whereas SHV-1 merely confers resistance to broad-spectrum penicillins, SHV-2, which was first described in 1983 in a Klebsiella ozaenae strain isolated in Germany, is able to hydrolyse cefotaxime (Gupta, 2007). In contrast to TEM- and SHV-type beta-lactamases, most of the members of the OXA-type beta-lactamase family are not regarded as ESBLs because they do not hydrolyze third generation cephalosporins with the exception of OXA-10, OXA-2, and their derivatives³. However, distinct OXA-types (OXA-carbapenemases) play an important role in antimicrobial resistance, e.g., of Acinetobacter baumannii (Pfeifer et al., 2010).

Currently regarded as the most important ESBL enzyme family are the CTX-M-type beta-lactamases, named after their ability to hydrolyze cefotaxime. They are supposed to originate from beta-lactamases from Kluyvera spp. and currently comprise of more than 70 different CTX-M enzymes divided into five groups depending on their amino acid sequence (CTX-M-1, CTX-M-2, CTX-M-8, CTX-M-9, and CTX-M-25; Hawkey and Jones, 2009; Pitout, 2010; Naseer and Sundsfjord, 2011). AmpC–beta-lactamases confer resistance to most of the beta-lactam antimicrobials with the exception of methoxy-imino-cephalosporins (cefepime) and carbapenems, while they are not inactivated by beta-lactamase-inhibitors like clavulanic acid.

Within the last years the emergence of carbapenem-hydrolyzing beta-lactamases like NDM-1, KPC, and OXA has threatened the clinical utility of this antibiotic class (Pfeifer et al., 2010, 2011; Poirel et al., 2010; Walsh, 2010). Carbapenemases are beta-lactamases that are active not only against the oxyimino-cephalosporins and cephamycins but also capable of hydrolyzing carbapenems like imipenem or meropenem. These substances often display the “last line of defense” in the treatment of infections with multiresistant Gram-negative pathogens. This group of beta-lactamases is very diverse and can be found in three different β-lactamase classes (class A, B, and D). Detailed information on these enzymes is given in some excellent reviews (Walsh, 2010; Patel and Bonomo, 2011).

The first nosocomial outbreak of CTX-M-1 type ESBLs was recorded in an intensive care unit in a hospital in Paris, France (Kitzis et al., 1988). Shortly after that, Bauernfeind et al. (1989) reported on a clinical cefotaxime-resistant E. coli strain in Germany which produced a CTX-M-1 type beta-lactamase. In the following 10 years several studies reported about an explosive dissemination of ESBLs in human clinical settings worldwide (Bernard et al., 1992; Gniadkowski et al., 1998; Radice et al., 2002; Canton and Coque, 2006). Several review articles provide detailed insight into the occurrence and molecular epidemiology of ESBL producing Enterobacteriaceae in humans and animals (Bradford, 2001; Bonnet, 2004; Canton and Coque, 2006; Livermore et al., 2007; Cantón et al., 2008; Oteo et al., 2010; Pfeifer et al., 2010; Pitout, 2010; Wieler et al., 2011).

Since about 2000, the CTX-M enzymes have formed a rapidly growing family of ESBLs in human clinical and community settings (Bonnet, 2004; Pitout and Laupland, 2008; Mshana et al., 2009), whereas the prevalence of classical ESBL enzymes like TEM or SHV is decreasing (Livermore et al., 2007). With the beginning of the twenty-first century E. coli producing CTX-M-15 have emerged and disseminated worldwide as an important cause of both nosocomial and community-onset urinary tract and bloodstream infections in humans (Coque et al., 2008; Hunter et al., 2010; Oteo et al., 2010; Pitout, 2010). A number of molecular epidemiological studies revealed that the sudden worldwide increase of CTX-M-15-producing E. coli has been largely influenced by the spread of one single clonal group of strains, namely B2:O25b:H4-ST131-CTX-M-15, across different continents (Nicolas-Chanoine et al., 2008; Rogers et al., 2011). The recent emergence of yet another clonal group, ABD-O1:H6-ST648-CTX-M-15, envisions the potential of just a limited number of clones to spread globally (Doi et al., 2010; Zong and Yu, 2010; Van Der Bij et al., 2011; Wieler et al., 2011). Unraveling the microevolution of strains of these clones in habitats and ecological niches others than human and veterinary clinics offers the chance to understand what leads to persistence of ESBL-E. coli in surroundings lacking selective antibiotic pressure.

In the field of veterinary medicine an SHV-12-type beta-lactamase producing E. coli was the first clinical ESBL producing bacteria isolated from a dog with recurrent urinary tract infection in Spain in 1998 (Teshager et al., 2000). This was followed by the detection of ESBL producing E. coli (mostly TEM and SHV) in dogs from Italy, and Portugal (Feria et al., 2002; Carattoli et al., 2005).Very recently several studies also reported companion animals as hosts for ESBL-E. coli harboring CTX-M enzymes, leading to the assumption that CTX-M-type enzymes will dominate the situation in veterinary medicine in the future as well (Vo et al., 2007; Carattoli, 2008; O’Keefe et al., 2010; Smet et al., 2010b). This is exemplified by the emergence of the clonally related group of E. coli B2-O25b:H4-ST131-CTX-M-15 in the field of companion animals, as well (Pomba et al., 2009; Ewers et al., 2010, 2011; Biohaz, 2011; Wieler et al., 2011).

Extended-Spectrum beta-lactamases mostly of the TEM, CTX-M, and SHV-type have been frequently demonstrated in the microbiota of food-producing animals which has nicely been reviewed by Smet et al. (2010b). Within the last decade, the number of publications reporting ESBL-E. coli isolated from food-producing animals has increased drastically. Noticeably, most ESBL enzymes identified in E. coli from livestock are likewise present in bacteria from humans (Smet et al., 2010b).

The first reports on the presence of resistance determinants in E. coli from human and animal populations lacking selective antimicrobial pressure date back to the 1960s (Mare, 1968). Antimicrobial resistant E. coli isolates originating from wildlife species were reported for the first time at the beginning of the 1980s from Japanese wild birds (Sato et al., 1978; Kanai et al., 1981; Tsubokura et al., 1995) and 5 years later in South African baboons feeding on human refuse (Rolland et al., 1985; Routman et al., 1985). With the new millenium the number of studies describing the occurrence of antimicrobial resistant E. coli in wildlife increased significantly (Gilliver et al., 1999; Souza et al., 1999; Sherley et al., 2000; Fallacara et al., 2001; Livermore et al., 2001; Osterblad et al., 2001; Swiecicka et al., 2003; Cole et al., 2005; Lillehaug et al., 2005; Middleton and Ambrose, 2005; Sayah et al., 2005; Skurnik et al., 2006; Dolejska et al., 2007; Literak et al., 2007; Carattoli, 2008; Gionechetti et al., 2008; Ewers et al., 2009; Guenther et al., 2010c).

However, the detection of ESBL-E. coli of wildlife origin dates back to 2006 only (Costa et al., 2006). Since then several reports followed (Costa et al., 2008; Poeta et al., 2008, 2009; Bonnedahl et al., 2009, 2010; Dolejska et al., 2009; Literak et al., 2009a,b, 2010; Guenther et al., 2010a,b; Hernandez et al., 2010; Pinto et al., 2010; Radhouani et al., 2010; Simoes et al., 2010; Smet et al., 2010b; Garmyn et al., 2011; Ho et al., 2011; Silva et al., 2011; Sousa et al., 2011; Wallensten et al., 2011).

Although ESBL-E. coli isolates of wildlife origin have only been reported from Europe (Costa et al., 2008; Poeta et al., 2008, 2009; Bonnedahl et al., 2009, 2010; Dolejska et al., 2009; Literak et al., 2009b, 2010; Guenther et al., 2010a,b; Pinto et al., 2010; Radhouani et al., 2010; Simoes et al., 2010; Garmyn et al., 2011; Silva et al., 2011; Sousa et al., 2011; Wallensten et al., 2011), Africa (Literak et al., 2009a), and Asia (Hernandez et al., 2010; Ho et al., 2011) so far, their absence in the Americas, Antarctica, and Australia might simply reflect the different number of studies performed in these continents. As multiresistant E. coli have already been reported from the latter continents (Souza et al., 1999; Sherley et al., 2000; Fallacara et al., 2001; Cole et al., 2005; Middleton and Ambrose, 2005; Sayah et al., 2005; Kozak et al., 2009; Silva et al., 2009) one could anticipate ESBL-E. coli of wildlife origin to be present as well. Nevertheless data from one continent or region may not act as a suitable baseline for another, and may not correlate with the level of antibiotic use in the regions involved. Besides simple geographical effects like the continent of origin it seems more appropriate to reconsider the type of region where the isolates originate from. Parameters which have been assumed as important criteria include the natural preservation state, livestock, and human density or the remoteness of an area (Allen et al., 2010). The level of resistant bacteria observed in wild animals seems to correlate well with the degree of association with human activity (Skurnik et al., 2006; Allen et al., 2010). Nevertheless, several studies report the occurrence of ESBL-E. coli in remote places or preservation areas as well (Hernandez et al., 2010; Pinto et al., 2010) underlining the complexity of the spread of antimicrobial resistance in wild animals. These findings suggest on the one hand an influence of migratory behavior of wild birds for instance into remote areas or on the other hand the omnipresence of human influence in various ecological niches of the planet basically via human feces. Most studies on ESBL-E. coli in wildlife originate from Central Europe, an area with high livestock and human density and an assumable frequent interaction of wildlife with human influenced habitats of any kind like livestock farms, landfills, sewage systems, or wastewater treatment facilities, resulting in a higher risk for wildlife acquiring antibiotic-resistant bacteria (Allen et al., 2010). It has previously been shown that gulls shared strains of E. coli with isolates cultured from landfills and wastewater treatment plants (Nelson et al., 2008). This underlines the possibility of bacterial exchange between human sewage and birds.

As summarized in Table 1 the detection rates of ESBL-E. coli in different geographical areas ranged from 0.5% in birds of the remote Azores islands in the Atlantic Ocean (Silva et al., 2011) to 32% for birds of the Iberean peninsula (Simoes et al., 2010). However, one should certainly keep in mind differences with regards to host species, sampling schemes, and geographic regions and the limitations that arise from this when interpreting these data. Nevertheless, for Central Europe the number of studies performed is relatively high, and there does not seem to be a difference in the detection rates between agriculturally used lands or urban environments compared to natural preserve areas, since in both types of areas detection rates higher than 20% have been observed (Table 1). Only in remote areas like the Azores or the Kamchatka peninsula the rates seem to be lower with approximately 1% ESBL-E. coli (Hernandez et al., 2010; Silva et al., 2011), suggesting a possible dilution effect of the pollution of wild animals with ESBL-E. coli. Nevertheless our own data from birds of prey from the Mongolian Gobi-Desert, an area among the ones with the lowest human density, revealed ESBL rates which were comparable with the situation in Central Europe (Guenther et al., 2010c).

General information about the microbiota of wild living birds and rodents is scarce and restricted to single species as hosts of certain pathogens. E. coli is a common gastrointestinal but very versatile bacterium, and can be grouped into non-pathogenic (commensal) and pathogenic strains; the latter cause intestinal or extraintestinal diseases in humans and animals (Johnson and Russo, 2002; Wirth et al., 2006). The ubiquitous occurrence of E. coli is based on its asymptomatical colonization of the gut of birds and mammals and in turn the resulting spread into the environment (Rwego et al., 2008; Schierack et al., 2008a). The degree of colonization varies a lot between different bird species (Gordon and Cowling, 2003) and the same has been shown for rodents and small mammals (Swiecicka et al., 2003; Guenther et al., 2010c). E. coli is most likely to be isolated from omnivore birds and mammals (Gordon and Cowling, 2003). More than 30 wild animal species have been found shedding ESBL-E. coli and most of them were birds or rodents (Table 1). The occurrence of ESBL-E. coli is therefore clearly influenced by the host spectrum of E. coli and furthermore by the degree of synanthropic behavior shown by the host animal species. In other words, animals living in urbanized areas are more likely to carry E. coli than animals living in remote areas (Allen et al., 2010; Bonnedahl, 2011).

Other basic questions concerning the occurrence of ESBL-E. coli in fecal samples are still unsolved. Future studies should therefore address the nature of the abundance of these multiresistant strains in feces to clarify if they are just shedded in short terms, present transient, or long term colonizations of the gut of the animals asymptomatically or even are persistent infections.

When reviewing the current literature it appears that wild birds could be the main wildlife hosts for ESBL-E. coli. This impression is created because most of the studies were carried out on wild birds; however, taking into account studies involving other wildlife animals such as deer, small ruminants, small and large predators, lagomorphs, reptiles, and amphibians (Costa et al., 2006; Literak et al., 2009b) an insignificant number of ESBL-E. coli was observed.

Due to their diversity in ecological niches, and their ease in picking up human and environmental bacteria, wild birds might act as mirrors of human activities. Within the heterogeneous class of birds two groups seem to be in the focus of ESBL carriage in wildlife: waterfowl/water related species (Poeta et al., 2008; Bonnedahl et al., 2009, 2010; Dolejska et al., 2009; Guenther et al., 2010b; Hernandez et al., 2010; Literak et al., 2010; Simoes et al., 2010; Garmyn et al., 2011; Wallensten et al., 2011) and birds of prey (Costa et al., 2006; Pinto et al., 2010; Radhouani et al., 2010; detailed species information is given in Table 1). Other groups of birds like passerines (Guenther et al., 2010a; Silva et al., 2011) seem to carry ESBL-E. coli less often or sometimes not at all (Silva et al., 2010). This finding might be influenced by differences in the composition of the microbiota and the harboring of E. coli within these diverse avian species. In a recent study we were able to show that if E. coli could be isolated from different bird species, multiresistant E. coli clones originated from birds of prey or waterfowl (Guenther et al., 2010d). Other avian hosts reported were Owls (Costa et al., 2006; Pinto et al., 2010) and Ravens (Pinto et al., 2010), birds which display a feeding behavior comparable to birds of prey.

While the dominance of waterfowl within the avian host spectrum of ESBL-E. coli can be explained by fecal pollution of water by human or livestock sources, the transmission scenarios for the other main group – birds of prey – seem to be more complex. As birds of prey are on top of the food chain they could accumulate ESBL-E. coli from their typical prey, like mice and shrews. Due to their synantropic behavior, they are presumably more often in contact with humans or livestock. Indeed for mice it has been shown that proximity to livestock farming increases the carriage rates of multiresistant E. coli (Kozak et al., 2009). Although rodents have earlier been in the focus of research on ESBL in wildlife (Gilliver et al., 1999; Kozak et al., 2009; Literak et al., 2009b; Guenther et al., 2010c), to the best of our knowledge ESBL-E. coli have not yet been detected in rodents with the exception of urban rats (Guenther et al., 2010b; Ho et al., 2011).

Our own data from Germany revealed a very low abundance for multiresistant E. coli in rodent and shrews, indicating that other groups of prey and transmission routes between the human influenced ecosphere and birds of prey might be possible (Guenther et al., 2010c). Furthermore, many of the bird species which have been tested positive for ESBL-E. coli carriage display migration behavior which provides a possible mechanism for the establishment of new endemic foci over great distances from where a multiresistant microorganism was first acquired (Bonnedahl, 2011).

As mentioned above another important host of ESBL-E. coli seems to be a group of rodents namely Norway rats and Black rats with reports on ESBL producing isolates from different continents (Literak et al., 2009a; Guenther et al., 2010b; Ho et al., 2011). This synantropic species can easily pick up human waste and often interacts with human feces in the sewage system in urban environments and can therefore easily acquire multiresistant bacteria. Interestingly wild boars have also been reported as host s of ESBL-E. coli in Central Europe, which might reflect their omnivorous feeding behavior (Literak et al., 2009b; Poeta et al., 2009). Other mammals found to be positive hosts of ESBL producing bacteria were deer and foxes (Costa et al., 2006). Very recently there has been a report on a marine fish, the Gilthead Sea bream (Sousa et al., 2011) as a carrier of ESBL-E. coli, indicating a dissemination of ESBL-E. coli into the Atlantic ocean.

In parallel to the current situation in human and veterinary medicine the type of extended-spectrum beta-lactamases found in wild animals are clearly dominated by the bla_CTX-M gene-family. With the exception of one study (Sousa et al., 2011) all wildlife studies identified the bla_CTX-M genes as the main ESBL enzyme. In 35% of the studies different SHV enzymes were additionally detected. As shown in Table 1, most of the studies reported bla_CTX-M-1, followed by bla_CTX-M-15, bla_CTX-M-14, bla_CTX-M-32, and bla_CTX-M-9. Only occasionally bla_CTX-M-2, bla_CTX-M-13, bla_CTX-M-55, and bla_CTX-M-65 were detected (Table 1). Besides the bla_CTX-M-type family only bla_SHV-12 and bla_TEM-52 were also often detected. Other less prevalent ESBL genes were bla_OXA-1, bla_SHV-5, and bla_TEM-20. The spectrum of the different enzyme types found in wild animals is very narrow compared to clinical isolates of human and veterinary origin (Pitout, 2010; Smet et al., 2010b). While the reason for this is unknown, we offer the following hypotheses: these findings might simply reflect the small number of studies performed on wildlife so far, or they could indicate that certain types of beta-lactamases are more successful in the environment, for example due to co-selection of other non-resistance genes accompanied by these beta-lactamases. Another explanation could be that the types of ESBLs found in wild animals simply reflect the ones that are most prevalent in human and veterinary clinics and in livestock farming, such as bla_CTX-M-1 or bla_CTX-M-15 (Pitout, 2010; Smet et al., 2010b). This could lead to the assumption that the situation we are observing in wild animals is just presenting spill-over effects from clinics and livestock farming. If this was true, future studies presumably should find a rise in those pandemic CTX-M-15 types, exemplified by the clonal E. coli lineages of ST131 and ST648. Several studies observed a similarity in the overall resistance profiles of wild animal isolates with human or veterinarian clinical isolates which supports this hypothesis (Costa et al., 2008; Literak et al., 2009b; Guenther et al., 2010d). The most prevalent non-ESBL resistant phenotype in wildlife E. coli is resistance to streptomycin, ampicillin, and tetracycline. This pattern is also very common in human and livestock populations in Europe (Van Den Bogaard et al., 2000; Guerra et al., 2003). As mentioned above the types of ESBL genes are basically the same in human, livestock, and wildlife, which strengthens the hypothesis that wildlife isolates resemble those found in animal and human patients. However, as the dissemination of ESBL genes is highly driven by horizontal gene transfer through plasmids, the occurrence of identical ESBL genes could also be based on the spread of ESBL-plasmids which are randomly distributed in the environment. In summary, unraveling the basis of the ESBL-E. coli spill-over into wildlife needs to include both a characterization of the clonal nature of bacterial strains isolated from different hosts as well as an accurate identification of the ESBL genes and their episomal or chromosomal localization.

Regarding the basic question of the zoonotic potential of E. coli it is useful to address the population genetics of this bacterial species. Besides comparative whole genome analysis of bacteria, this can also be done by other approaches like Multi-locus sequence typing (MLST)⁴. Although it is based on a small set of marker genes only, this method seems to reflect the microevolution of the E. coli core genome. In general, MLST analysis revealed the existence of strains belonging to identical sequence types (STs) and being isolated from different hosts rather being the rule than the exception. This indicates a common phylogeny and therefore a zoonotic potential for most strains analyzed so far (Wirth et al., 2006). Indeed, several research groups found clusters of E. coli causing systemic infections in birds, and urinary tract infection and neonatal meningitis in humans, which are genetically so similar, that a zoonotic potential is foreseen (Johnson and Russo, 2002; Ewers et al., 2007; Moulin-Schouleur et al., 2007). So far the number of ESBL-E. coli from wildlife in that global data base is rather limited. However, if the same clusters of E. coli can cause disease in humans and domesticated birds, their transmission scenarios become important and such routes of transfer indeed are a plausible transfer mechanism of ESBL-E. coli from humans to wild birds and vice versa.

To answer the question about the similarity of human clinical, livestock, companion animal, and wildlife ESBL-E. coli isolates we need to gain insight into the clonal relatedness of isolates from all these groups. Initial MLST paired with pulsed field gel electrophoresis (PFGE) is an ideal tool to reveal clonal relatedness or even clonal identity of epidemiologically unrelated isolates. This attempt has been put forward by a small number of studies on wild birds, all clearly pointing out that similar STs or clonal groups are present in humans, domestic animals, and wild birds (Bonnedahl et al., 2009, 2010; Guenther et al., 2010a; Hernandez et al., 2010; Simoes et al., 2010). Overall up to 35 different STs have been detected in wild avian ESBL-E. coli (Table 1; Figure 1). Although some of the “avian” STs appeared twice in different wildlife studies like ST746 (Bonnedahl et al., 2009; Hernandez et al., 2010) and have not been detected in human clinical samples yet, the majority of the STs found in avian ESBL-E. coli, such as ST131, ST10, ST90, ST648, or ST69, are also present in human clinical isolates.

Figure 1 shows a minimum spanning tree (MSTree) displaying human, domestic animal, and wildlife ESBL–STs based on data of the MLST database⁵ as of October 2011 and the current literature on human and animal ESBL-E. coli isolates providing MLST data (Minarini et al., 2007; Yumuk et al., 2008; Blanco et al., 2009; Hrabak et al., 2009; Naseer et al., 2009; Oteo et al., 2009; Sidjabat et al., 2009; Suzuki et al., 2009; Valverde et al., 2009; Coelho et al., 2010; Doi et al., 2010; Peirano et al., 2010; Smet et al., 2010a; Zong and Yu, 2010; Ben Slama et al., 2011; Djamdjian et al., 2011; Leverstein-Van Hall et al., 2011; Mshana et al., 2011; Van Der Bij et al., 2011; Woerther et al., 2011). In the MSTree each circle represents a ST and the size of the circle is proportional to the number of ESBL-E. coli isolates belonging to this ST. Here is becomes remarkably clear that ESBL-E. coli of wildlife, domestic animal, and human origin share identical STs suggesting an interspecies transmission of phylogenetically related multiresistant strains. This hypothesis is further strengthened by the detection of the worldwide emerging clonal group of E. coli specified as B2-O25b:H4-ST131 in human (Nicolas-Chanoine et al., 2008), veterinary clinical settings (Ewers et al., 2010), and in a Glaucous winged gull in Kamchatka (Hernandez et al., 2010).

In another study (Bonnedahl et al., 2010) in south Sweden ESBL-E. coli of several new STs were detected, including ST1646 which is closely related to ST648 previously also found in wild birds in Germany (Guenther et al., 2010a) and in humans in Africa, Asia, and the United States (Doi et al., 2010; Zong and Yu, 2010). Interestingly, ST648 has been detected as one of the STs associated with the carriage of the newly emerging carbapenemase NDM-1 which underlines unforeseeable consequences of the entry of certain multiresistant clones into wild bird populations (Mushtaq et al., 2011).

As mentioned above there are currently three studies that provide evidence for the frequent occurrence of ESBL-E. coli in rats (Literak et al., 2009a; Guenther et al., 2010b; Ho et al., 2011). However, comparative data on the clonal relatedness of these isolates and those of human or domestic animals as assessed by MLST or PFGE is limited to a single study only (Guenther et al., 2010b). Here an ESBL-E. coli from a rat belonging to the pandemic clone B2-O25b:H4-ST131 was detected, which might point toward a direct transmission from human feces to the rat in an urban sewage system.