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Article

Resistance Profiling and Molecular Characterization of Extended-Spectrum/Plasmid-Mediated AmpC β-Lactamase-Producing Escherichia coli Isolated from Healthy Broiler Chickens in South Korea

by
Hyun-Ju Song
,
Dong Chan Moon
,
Abraham Fikru Mechesso
,
Hee Young Kang
,
Mi Hyun Kim
,
Ji-Hyun Choi
,
Su-Jeong Kim
,
Soon-Seek Yoon
and
Suk-Kyung Lim
*
Bacterial Disease Division, Animal and Plant Quarantine Agency, 177 Hyeksin 8-ro, Gimcheon-si, Gyeongsangbuk-do 39660, Korea
*
Author to whom correspondence should be addressed.
Microorganisms 2020, 8(9), 1434; https://0-doi-org.brum.beds.ac.uk/10.3390/microorganisms8091434
Submission received: 1 September 2020 / Revised: 16 September 2020 / Accepted: 17 September 2020 / Published: 18 September 2020
(This article belongs to the Special Issue Antimicrobial Resistance and Molecular Tracing of Foodborne Pathogens)
Review Reports Versions Notes

Abstract

:
We aimed to identify and characterize extended-spectrum β-lactamase (ESBL)-and/or plasmid-mediated AmpC β-lactamase (pAmpC)-producing Escherichia coli isolated from healthy broiler chickens slaughtered for human consumption in Korea. A total of 332 E. coli isolates were identified from 339 cloacal swabs in 2019. More than 90% of the isolates were resistant to multiple antimicrobials. ESBL/pAmpC-production was noted in 14% (46/332) of the isolates. Six of the CTX-M-β-lactamase-producing isolates were found to co-harbor at least one plasmid-mediated quinolone resistance gene. We observed the co-existence of blaCMY-2 and mcr-1 genes in the same isolate for the first time in Korea. Phylogenetic analysis demonstrated that the majority of blaCMY-2-carrying isolates belonged to subgroup D. Conjugation confirmed the transferability of blaCTX-M and blaCMY-2 genes, as well as non-β-lactam resistance traits from 60.9% (28/46) of the ESBL/pAmpC-producing isolates to a recipient E. coli J53. The ISECP, IS903, and orf477 elements were detected in the upstream or downstream regions. The blaCTX-M and blaCMY-2 genes mainly belonged to the IncI1, IncHI2, and/or IncFII plasmids. Additionally, the majority of ESBL/pAmpC-producing isolates exhibited heterogeneous PFGE profiles. This study showed that healthy chickens act as reservoirs of ESBL/pAmpC-producing E. coli that can potentially be transmitted to humans.

1. Introduction

Escherichia coli is a commensal bacterium of the intestinal tract of humans and animals. It constitutes a reservoir of resistance genes for a wide range of pathogenic bacteria. The level of resistance in this bacterium is a good indicator of the selection pressure exerted by antimicrobial use and for the resistance problem to be expected in related pathogenic bacteria [1]. Therefore, investigation of the antimicrobial resistance profiles of indicator bacteria, such as E. coli, is essential to detect the spread of resistant bacteria between animals and humans [2].
Healthy food animals are frequently reported as reservoirs of extended-spectrum β-lactamase (ESBL) and plasmid-mediated AmpC β-lactamase (pAmpC)-producing E. coli, and have caught considerable attention worldwide [3,4]. The ESBL/pAmpC enzymes are known to hydrolyze the β-lactam ring of β-lactam antibiotics and cause the emergence of resistance to a considerable number of β-lactam antibiotics, including extended-spectrum cephalosporins [5]. Besides, ESBL/pAmpC-producing bacteria carry MDR genes, leaving only limited therapeutic options [6]. Human infections presumably occur following the ingestion of contaminated food of animal origin or via close contact with infected animals [7].
CTX-M-14 was the first CTX-M-type ESBL to be detected from isolates originated from food animals—i.e., E. coli isolated from chickens [8]. Since then, various types of CTX-M β-lactamases have been identified in E. coli recovered from food animals worldwide [9,10,11,12,13]. The distribution of CTX-M-type ESBLs varies depending upon geographical location. In the Republic of Korea (Korea), CTX-M-1, CTX-M-14, and CTX-M-15 are the most frequently detected ESBL types in isolates from food animals [14,15,16]. Recently, CTX-M-55 and CTX-M-65 ESBL types were noted in E. coli isolated from food animals and farm workers [16,17]. The observation implies that continuous surveillance of the phenotypic and molecular characteristics of ESBL/pAmpC-producing E. coli in food animals is vital to identify the prevalent ESBL/pAmpC phenotypes and to prevent the dissemination of β-lactam antibiotic resistance. Consequently, we undertook this study to provide new knowledge on the diversity of ESBL/pAmpC-producing E. coli isolated from healthy broiler chickens in Korea. Further investigations were also conducted to determine the mechanism(s) of the transfer of β-lactamases.

2. Materials and Methods

2.1. Collection of Samples and Isolation of E. coli

Fecal samples were collected from chickens originated from 34 broiler chicken farms located in six provinces of Korea in 2019. All broiler farms were conventional farms, with capacities of <50,000 (five farms), 50,000–100,000 (21 farms), 100,000–150,000 (six farms), and >150,000 (two farms) broilers. Cloacal swabs or fecal samples (8–12 samples per farm) were collected from six slaughterhouses using disposable sterile swabs. Samples were kept in an icebox and immediately transported to the Animal and Plant Quarantine Agency for further processing. The isolation and identification of E. coli were performed as described previously [18], using eosin methylene blue agar (EMB, Becton Dickinson, Sparks, MD, USA) and MacConkey agar plates (MAC, BD, Spark, MD, USA). Isolates were then confirmed by matrix-assisted laser desorption and ionization-time-of-flight mass spectrometry (MALDI-TOF, Biomerieux, Marcy L’Etoile, France). Only a single isolate per sample was considered for further assay.

2.2. Antimicrobial Susceptibility Testing

Antimicrobial resistance profiles of the isolates were determined by the broth microdilution method, according to the Clinical and Laboratory Standards Institute guideline (CLSI) [19], using commercially available Sensititre plates KRVP5F (Thermo Trek Diagnostics, Waltham, MA, USA). Sixteen antimicrobials were tested: amoxicillin/clavulanic acid, ampicillin, cefepime, cefoxitin, ceftazidime, ceftiofur, chloramphenicol, ciprofloxacin, colistin, gentamicin, meropenem, nalidixic acid, streptomycin, sulfisoxazole, tetracycline, and trimethoprim-/sulfamethoxazole. E. coli ATCC 25,922 and E. coli ATCC 35,218 were used as quality control strains. The interpretation of the results was according to the CLSI guidelines [19], the National Antimicrobial Resistance Monitoring System [20], and the European Committee on Antimicrobial Susceptibility Testing [21] guidelines. The MIC50 and MIC90 were calculated as the MIC that inhibited 50% and 90% of the isolates, respectively. Multi-drug resistance (MDR) was defined as resistance to at least three antimicrobial subclasses.
In addition, a double-disc synergy test was conducted to identify ESBL-producing isolates among ceftiofur-resistant E. coli using cefotaxime–cefotaxime/clavulanic acid and ceftazidime–ceftazidime/clavulanic acid discs (BD, Sparks, MD, USA), according to CLSI guidelines [19].

2.3. Detection of Resistance Genes

Polymerase chain reaction (PCR) assay was performed to detect the presence of blaCTX-M genes using group-specific primers for CTX-M-1 and CTX-M-9. The complete blaCTX-M was amplified and sequenced using previously-described primers. Additionally, a multiplex PCR assay was conducted to detect genes encoding for six AmpC families and positive isolates were amplified using specific primers. The blaCTX-M and AmpC-positive strains were further screened for plasmid-mediated quinolone resistance (PMQR) genes: qnrA, qnrB, qnrC, qnrD, qnrS1, qnrV, qepA, and aac (6′) Ib-cr genes. Sequence analysis was performed using ABI3730XL DNA sequence analyzer (SolGent, Daejeon, Korea) and comparison with known sequences was performed with the Basic Local Alignment Search Tool (BLAST) programs at the National Center for Biotechnology Information website (www.ncbi.nlm.nih.gov/BLAST). The primers and their PCR conditions used for the detection of resistance genes are listed in Table S1.

2.4. Conjugation Experiment

The broth-mating experiment was performed to determine the transferability of blaCTX-M genes to sodium azide-resistant E. coli J53 [22]. Transconjugants were selected on Muller–Hinton agar, supplemented with sodium azide (150 μg/mL) and cefotaxime (2 μg/mL). The antimicrobial susceptibility profiles and β-lactamase gene carriage of the transconjugants were also determined, as described above.

2.5. Molecular Characterization of ESBL/pAmpC-Producing E. coli

A PCR-based replicon typing kit (DIATHEVA, Fano, Italy) was used to determine the replicon types of the transconjugants following the manufacturer’s protocol. The genetic environment of the blaCTX-M/CMY-2 genes was investigated using PCR and Sanger sequencing, as described previously [23,24]. A combination of IS26 or ISEcp1 forward primers, and a CTX-M reverse consensus primer (MA2) were used to investigate regions upstream of the bla genes. A MA1 primer and reverse primers of IS903 or orf477 were used to characterize downstream regions of the bla genes. The primers and their PCR conditions used for the detection of the blaCTX-M and blaCMY-2 genetic environments are listed in Table S1. Additionally, pulsed-field gel electrophoresis (PFGE) analysis of ESBL/pAmpC-producing E. coli strains was also performed following XbaI digestion of chromosomal DNA (Takara Bio Inc., Shiga, Japan), as described previously [25]. Then, PFGE bands were analyzed using Bionumerics software (UPGMA) and relatedness of the isolates was calculated using the unweighted pair group method with the arithmetic average algorithm based on the Dice similarity index. Further, a multiplex PCR assay targeting chuA, yjaA, and the DNA fragment TspE4.C2 was used to determine the phylogenetic characteristics of the ESBL/pAmpC-producing strains [26].

3. Results

3.1. Antimicrobial Resistance of Indicator E. coli

We identified 332 E. coli isolates from 339 fecal samples obtained from 34 different broiler farms. Resistance to nalidixic acid (92.5%) was the highest, followed by resistance to ampicillin (86.4%), ciprofloxacin (78.3%), and tetracycline (71.7%) (Table 1). Resistance to amoxicillin/clavulanic acid, cefepime, cefoxitin, ceftazidime, and colistin was low (0.6–3.6%). We observed ceftiofur resistance in 13.9% (46/332) of the isolates. However, resistance to meropenem was not detected. All isolates were resistant to at least one antimicrobial agent, and MDR was noted in 94.3% of the isolates (Table 2). Besides, about 34% of the isolates exhibited resistance to at least eight antimicrobials. Among 103 different resistance patterns observed in this study, resistance to ampicillin, chloramphenicol, ciprofloxacin, nalidixic acid, streptomycin, sulfisoxazole, tetracycline, and trimethoprim/sulfamethoxazole (12.5%) was the most frequent MDR pattern.

3.2. Distribution of ESBL/pAmpC-Producing E. coli

We identified 46 (13.9%) ESBL/pAmpC-producing E. coli strains from 22 (64.7%) different broiler farms (Table 3). We observed four different types of ESBLs, namely CTX-M-55 (n = 18, 39.1%), CTX-M-14 (n = 12, 26.1%), CTX-M-1 (n = 4, 8.7%), and CTX-M-65 (n = 2, 4.3%). CMY-2 is the only pAmpC detected in eight (17.4%) E. coli strains, and two (4.3%) strains were positive for both CTX-M-55 and CMY-2 β-lactamases. The prevalence of ESBL/pAmpC-producing E. coli strains among farms ranged between 9.1% and 50%. Most farms carried one (59.1%) or two (36.4%) ESBL/pAmpC-types, while we noted three different ESBL/pAmpC-types from a farm in Jeonnam province.

3.3. Molecular Characteristics of ESBL/pAmpC-Producing E. coli

The ESBL/pAmpC-producing isolates exhibited resistance to several antimicrobial classes, such as aminoglycoside, tetracycline, quinolones, and folate pathway inhibitors (Table 4). Six of the CTX-M β lactamase-producing isolates were found to co-harbor at least one PMQR gene, with qnrS1, qnrS2, and aac (6′)-Ib-cr being detected alone or in combination. Notably, the blaCTX-M-65, qnrS2, and aac (6′)-Ib-cr genes were found to be carried together in one isolate. Additionally, one isolate from farm E co-carried blaCMY-2 and mcr-1 genes.
The blaCTX-M and blaCMY-2 genes were transferred to recipient E. coli J53 from 55.3% (21/38) of blaCTX-M-positive (three blaCTX-M-1, five blaCTX-M-14, and 13 blaCTX-M-55) and 70% (7/10) of blaCMY-2-positive E. coli strains (Table 4). In addition, we observed the co-transfer of non-β-lactam antibiotic resistance, such as resistance to chloramphenicol, sulfisoxazole, tetracycline, and aminoglycosides along with blaCTX-M and blaCMY-2 genes.
We identified various plasmid replicon types including IncI1α, IncFIB, IncFII, and IncHI2. IncFII (60.7%, 17/28) and IncI1α (35.7%, 10/28) were the most frequent plasmid replicon types (Table 4 and Table 5). Multiple replicon types were observed in 39.3% (11/28) of the transconjugants. Plasmids harboring blaCTX-M-1 and blaCMY-2 genes mainly belonged to IncI1α replicon type. Whereas, plasmids harboring blaCTX-M-14 and blaCTX-M-55 genes were predominantly associated with IncHI2 and IncFII replicon types, respectively.
The transconjugants carrying the blaCTX-M-55 gene presented distinct types of genetic environments, namely blaCTX-M-55-orf477 (n = 9) and ISEcp1-blaCTX-M-55-orf477 (n = 4) elements (Table 5). ISEcp1-blaCTX-M-1-orf477 and blaCTX-M-14-IS903 elements were identified in three and five transconjugants, respectively. The blaCMY-2 and blaCTX-M-55+CMY-2 gene expression was driven by the ISEcp1 insertion sequence, but IS903 and orf477 elements were not detected downstream of blaCMY-2 and blaCTX-M-55+CMY-2 genes.
PFGE analysis of 46 E. coli strains carrying blaCTX-M and blaCMY-2 genes from 21 different farms demonstrated 34 arbitrary pulsotypes (Figure S1). In general, most of the isolates were heterogeneous. We observed identical PFGE profiles in blaCTX-M-14, blaCTX-M-55, and blaCTX-M-65-carrying strains from farms AC, AE, AG, and I. Similarly, the two blaCTX-M-14-carrying isolates from farms AC and AE exhibited identical PFGE profiles. However, DNA from five strains was constantly auto-digested. Consequently, a cluster formed by these strains was excluded from the analysis.
Phylogenetic analysis of ESBL/pAmpC-producing strains showed that subgroup B1 was predominant (20/46, 43.5%), followed by A (20/46, 39.1%) and D (8/46, 17.4%). Notably, most blaCMY-2 carrying isolates (6/8, 75%) belonged to subgroup D.

4. Discussion

Our observations revealed that most of E. coli isolated from healthy broilers were resistant to multiple antimicrobials and possessed diverse ESBL-encoding genes that could be readily spread to humans. Although CTX-M-15 is considered the predominant ESBL type in the Korean poultry industry [27], we observed CTX-M-14 and CTX-M-55 type ESBLs in most of the isolates.
Consistent with previous findings in Korea [28,29] and other countries [30,31,32,33], E. coli isolates exhibited high rates of resistance to ampicillin, nalidixic acid, tetracycline, and sulfisoxazole. However, it was lower than those described in recent reports in Asia and Africa [34,35,36]. Additionally, the proportion of MDR isolates in this study corresponded with previous reports [28,33]. The isolates exhibited more than 100 different resistance patterns and most of these patterns were associated with quinolones, penicillins, and tetracyclines. High antimicrobial resistance rates and diverse resistance patterns observed in this study coincide with the marked increase in the use of antimicrobials, including penicillins, fluoroquinolones, phenicols, and tetracyclines in the Korean poultry industry [37]. The variations in antimicrobial resistance among countries might be because of differences in geographical region, locally approved antimicrobials, and farm management systems.
Fluoroquinolones are considered critically important antimicrobials for both humans and animals [38]. About 80% of the isolates were resistant to ciprofloxacin, a finding which is consistent with previous reports in Poland [32], Korea [39], and Vietnam [40]. However, it was higher than those reported in several Asian countries [31,35,41,42,43]. Although ciprofloxacin is not approved for animal uses, the continuous utilization of enrofloxacin in food animals, especially chickens in Korea, could be contributing to the increase in ciprofloxacin resistance [37].
Third-generation cephalosporin-resistant isolates are often resistant to multiple antimicrobials and are considered a potential threat to animal and human health [44]. The ceftiofur resistant rate in this study was slightly higher than previous reports in Korea (12%) [45] and the US (7%) [46]. Nevertheless, it was lower than Lee et al. (22%) [47] and Zhang et al. (47%) [33] in Korea and China, respectively. Various authors reported the relationship between ceftiofur use and resistance to third-generation cephalosporins in poultry production [48,49,50]. Therefore, although information on the use of this antimicrobial in farms was not available, the frequent application of ceftiofur in food animals could lead to the emergence of ceftiofur-resistant E. coli isolates.
A variety of ESBL/pAmpC genes have been identified in bacteria isolated from food animals worldwide. Most noteworthy of these are the blaCTX-M-14, blaCTX-M-15, blaCTX-M-27, and blaCTX-M-55 variants, which have been associated with the global spread of β-lactam antibiotic resistance in humans and food animals [51,52]. In Korea, β-lactam antibiotics resistance in chicken [14,16,28] and human [53,54,55] isolates is commonly associated with blaCTX-M-1, blaCTX-M-14, and blaCTX-M-15. However, blaCTX-M-55 was the most frequent ESBL gene observed in this study. Our finding concurred with a recent report in E. coli strains from retail chicken meat in Korea [17]. CTX-M-55 is a CTX-M-15 variant that possesses enhanced β-lactamase-hydrolyzing activity and structural stability [56]. Since its first detection in ESBL-producing E. coli in 2004 and 2005 in Thailand, it has been widely reported in E. coli isolated from food animals and humans in many countries [17,48,57,58,59,60]. The observation suggests that CTX-M-55 may be supplanting CTX-M-15.
E. coli harboring blaCTX-M-14 has been frequently detected in food animals in Korea [14,16,22] and other countries [57,60]. In this study, blaCTX-M-14 (26.1%) was the second most frequent ESBL gene. Similarly, Park et al. [17] and Seo et al. [28] detected blaCTX-M-14 in 22% and 14% of ESBL-producing broiler chicken E. coli isolates in Korea, respectively. Additional studies have also observed blaCTX-M-14-carrying E. coli isolates in food and companion animals, as well as in humans in several Asian countries [52,53,54,61,62], indicating its widespread distribution and the potential threat to public health.
In this study, only a few isolates were positive for blaCTX-M-1 and blaCTX-M-65. blaCTX-M-65 was frequently detected in ESBL-producing E. coli isolated from chicken in Korea [16,17] and China [52]. Although blaCTX-M-1 was detected in ESBL-producing strains recovered from chickens and farm environments in Korea [14,22,28], it is among the most frequent ESBL-encoding gene reported in Europe [61,63,64]. blaCTX-M is known to spread between animals and humans through the food chain and isolates of humans and foods of animal origin commonly shared dominant CTX-M genotypes. Thus, broiler chickens may serve as an important reservoir and source of human infection [51].
pAmpC β-lactamase enzymes such as CMY-2 are less frequent in ceftiofur-resistant Enterobacteriaceae compared to the ESBLs [65]. We detected the blaCMY-2 gene in 21.3% of the ceftiofur-resistant isolates. Agreeing with this study, blaCMY-2 was the most common pAmpC β-lactamase-encoding gene in E. coli recovered from broiler chickens and humans worldwide [15,66,67,68,69,70,71]. The distribution of blaCMY-2 in several countries appears to be related to the efficient horizontal transmission of its encoding plasmids [72].
PMQR genes were commonly associated with low-level fluoroquinolone resistance and promoted the selection of high-level resistant strains [73]. In this study, the PMQR genes were identified in association with blaCTX-M-1, blaCTX-M-55, and blaCTX-M-65 genes. Most of the PMQR genes were associated with blaCTX-M-55. The blaCTX-M-55 genes commonly co-localize with other resistance genes, such as PMQR genes and genes encoding 16S rRNA methyltransferases [74,75]. The co-existence of PMQR and ESBL genes in Enterobacteriaceae have been reported in many countries, including Korea [73,76,77,78]. The widespread use of quinolones and third-generation cephalosporins in food animals has led to the emergence of PMQR and ESBL-producing E. coli. The co-occurrence of these genes in chicken isolates constitutes a public health concern.
The co-existence of ESBL and mcr-1 genes in Enterobacteriaceae poses a serious public health threat. Despite several reports on the co-existence of mcr-1 and ESBL genes in E. coli strains isolated from humans, food animals, and fresh vegetables in various countries [52,79,80,81,82,83], only a few reports are available on the co-existence of mcr-1 and blaCMY-2 in E. coli [84,85,86]. Notably, this is the first report on the co-existence of mcr-1 and blaCMY-2 in E. coli in Korea. Colistin is the last-resort antibiotic against multidrug-resistant E. coli, hence the co-existence of mcr-1 and blaCMY-2 poses a serious challenge to the application of antimicrobials in humans and animals.
Various plasmid replicon types, either alone or in combination, were identified in E. coli transconjugants. Several studies have reported the association between blaCTX-M-14 gene and different plasmid types, including IncF family plasmids, IncK, and IncI1-Iγ [12,87,88]. However, this study identified the blaCTX-M-14 gene predominantly on the IncHI2 plasmid. The blaCTX-M-55 gene was efficiently transferred to recipient E. coli from 72% of blaCTX-M-55-carrying strains. This is presumably due to its frequent association with the IncF family of plasmids [27]. The IncF plasmid family is implicated in the dissemination of ESBLs because it is stably maintained in commensal E. coli [51]. In addition, the blaCTX-M-1 and blaCMY-2 genes predominantly belonged to IncI1α plasmid, a finding which concurred with Bevan et al. [51] and Carattoli, [7]. Further, the observation of diverse plasmid backbones in this study may reflect the co-occurrence of antimicrobial-resistant genes [27] and the dissemination of co-resistant bacteria [89].
ESBL-genes are often associated with insertion sequences (ISs), which are the smallest transposable elements capable of independent transposition in an organism [90]. The co-existence of ISEcp1 and ESBL/pAmpC genes in E. coli isolates is well documented [90,91,92]. Agreeing with this study, ISEcp1 is frequently found in the upstream regions of ESBL/pAmpC genes and plays an important role in the efficient capture, expression, and mobilization of blaCTX-M and blaCMY-2 genes [24,90]. Agreeing with previous reports [10,23,93], the orf477 element was found downstream of blaCTX-M-1 and blaCTX-M-55 genes, while IS903 was located downstream of blaCTX-M-55.
PFGE analysis demonstrated that the majority of the blaCTX-M-carrying isolates were highly diverse, except for specific clonal strains from the same or different farms, whereas all blaCMY-2-positive isolates showed different PFGE patterns. Therefore, clonal expansion and horizontal transmission within and between farms might contribute to the spread of ESBL/pAmpC-producing E. coli isolates. The proportion of subgroup D, which is considered pathogenic or an extraintestinal virulence-associated strain in our study (17.4%) was lower than Song et al. [27] (31%). The majority (82.6%) of ESBL/pAmpC-producing isolates in the current study mainly belonged to the commensal subgroups A or B1, which coincides with previous reports in Korea [27] and China [60]. Most of the pathogenic strains predominantly carried blaCMY-2, suggesting the emergence of pathogenic strains of E. coli carrying quinolone resistance genes in the Korean poultry industry.
In conclusion, our study showed that healthy broiler chickens were a major reservoir of E. coli that are resistant to multiple antimicrobials, including those ranked as medically important. This study identified ESBL/pAmpC-producing E. coli strains carrying predominantly blaCTX-M-14, blaCTX-M-55, and blaCMY-2 genes. Notably, the majority of blaCMY-2-carrying strains were pathogenic. This is the first report on the co-existence of mcr-1 and blaCMY-2 in pathogenic E. coli in Korea. Both horizontal and clonal spread could be implicated in the dissemination of ESBL/pAmpC-producing E. coli. However, the multilocus sequence types of the isolates remained unclear. Altogether, the results suggest that healthy chickens are a matter of concern in terms of transmission of ESBL/pAmpC-producing E. coli to humans through the food chain. Therefore, the prudent use of antimicrobials in food animals is needed to prevent the introduction of ESBL/pAmpC-producing isolates into the food chain. Additionally, long-term surveillance is needed to trace the evolution and dissemination of ESBL/pAmpC-producing E. coli in food animals and its possible association with human isolates.

Supplementary Materials

The following are available online at https://0-www-mdpi-com.brum.beds.ac.uk/2076-2607/8/9/1434/s1, Table S1: Lists of primer sequences and PCR conditions. Figure S1: Xbal-digested pulsed-field gel electrophoresis patterns of blaCTX-M and blaCMY-2 carrying E. coli strains isolated from healthy broiler chickens in Korea. Xbal macrorestriction analysis yielded no DNA banding patterns in five E. coli strain due to constant autodigestion of the genomic DNA during agarose plug preparation, and thus clusters formed by these strains were excluded (ND, not determined).

Author Contributions

Conceptualization, S.-K.L. and D.C.M.; Methodology, H.Y.K., H.-J.S., and S.-K.L., and D.C.M.; Software, H.Y.K., J.-H.C., and S.-J.K.; Validation, A.F.M. and M.H.K.; Formal analysis, H.-J.S., and M.H.K.; Investigation, A.F.M., H.Y.K., H.-J.S., M.H.K., J.-H.C., and S.-J.K.; Data Curation, D.C.M., H.-J.S., and M.H.K.; Writing—Original Draft Preparation, A.F.M. and H.-J.S.; Writing—Review and Editing, S.-S.Y., S.-K.L., and D.C.M.; Supervision, S.-S.Y., S.-K.L., and D.C.M.; Project Administration, D.C.M. and H.Y.K.; Funding Acquisition; S.-K.L. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded from the Animal and Plant Quarantine Agency, Ministry of Agriculture, Food, and Rural affairs, Korea, grant number N-1543081-2017-24-1 and the Korean Center for Disease Control and Prevention, grant number 2017N-ER5407-00.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

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Table
Table 1. Antimicrobial resistance profiles and MIC distribution of Escherichia coli isolated from healthy broiler chickens in Korea.
Table 1. Antimicrobial resistance profiles and MIC distribution of Escherichia coli isolated from healthy broiler chickens in Korea.
AntimicrobialsDistribution (%) of MICs (µg/mL)MIC50MIC90MIC Resistance
≤0.120.250.51248163264128256≥512Range(%)
Amoxicillin/clavulanic acid 3.610.869.912.33.3 8162–323.3
Ampicillin 4.88.10.6 86.4 64642–6486.4
Cefepime 87.31.82.40.633.61.2 0.2510.25–161.2
Cefoxitin 7.248.235.25.73.6 141–323.6
Ceftazidime 89.51.52.433.6 121–323.6
Ceftiofur 7510.5 0.314.2 0.580.5–813.9
Chloramphenicol 0.312.718.41.52.165.1 64642–6467.2
Ciprofloxacin1.811.74.81.51.82.743.731.9 8160.12–1678.3
Colistin 99.4 0.6 222–80.6
Gentamicin 70.23.9 0.32.4320.2 1641–6425.6
Meropenem 100 0.250.250.25–0.250
Nalidixic Acid 2.11.82.11.50.61.590.4 1281282–12892.5
Streptomycin 38.35.47.548.8 6412816–12861.7
Sulfisoxazole 29.82.1 68.151251216–51268.1
Tetracycline 28.3 14.822.634.3 641282–12871.7
Trimethoprim/33.49.34.82.40.349.7 140.12–449.7
sulfamethoxazole
The dilution ranges tested are those contained in the white area. The breakpoints of tested antimicrobial agents are indicated by vertical lines. MIC50 and MIC90 are the concentrations at which 50% and 90% of the isolates were inhibited, respectively.
Table
Table 2. Frequent antimicrobial resistance patterns of Escherichia coli isolated from healthy broiler chickens in Korea.
Table 2. Frequent antimicrobial resistance patterns of Escherichia coli isolated from healthy broiler chickens in Korea.
No. of Antimicrobials Total No. of Isolates (%)Frequent Resistance Pattern (No. of Isolates)
00 (0)
11 (0.3)NAL (n = 1)
218 (5.4)AMP TET (n = 8)
330 (9)AMP CIP NAL (n = 8)
426 (7.8)AMP CIP NAL TET (n = 9)
553 (16)AMP CHL CIP NAL TET (n = 16)
634 (10.2)AMP CIP GEN NAL STR TET (n = 4)
758 (17.5)AMP CHL CIP NAL STR FIS TET (n = 13)
855 (16.6)AMP CHL CIP NAL STR FIS TET SXT (n = 39)
945 (13.6)AMP CHL CIP GEN NAL STR FIS TET SXT (n = 35)
106 (1.8)AMP XNL CHL CIP GEN NAL STR FIS TET SXT (n = 3)
112 (0.6)AMC AMP FOX CAZ XNL CHL CIP NAL STR FIS TET (n = 1)
121 (0.3)AMC AMP FOX CAZ XNL CHL CIP NAL STR FIS TET SXT (n = 1)
133 (0.9)AMC AMP FOX CAZ XNL CHL CIP COL NAL STR FIS TET SXT (n = 1)
MDR (≥3 subclass)313 (94.3)
AMC, Amoxicillin/clavulanic acid; AMP, ampicillin; FOX, cefoxitin; CAZ, ceftazidime; XNL, ceftiofur; CHL, chloramphenicol; CIP, ciprofloxacin; COL, colistin; GEN, gentamicin; NAL, nalidixic acid; STR, streptomycin, FIS, sulfisoxazole; TET, tetracycline; SXT, Trimethoprim/Sulfamethoxazole. MDR; Multi drug resistant (resistance to 3 or more antimicrobial subclasses).
Table
Table 3. Distribution of blaCTX-M and blaCMY-2-carrying Escherichia coli isolates in broiler chicken farms in Korea.
Table 3. Distribution of blaCTX-M and blaCMY-2-carrying Escherichia coli isolates in broiler chicken farms in Korea.
Farm IDProvincePrevalence (%)
(No. of bla-Positive Isolates/
Total No. of Isolates per Farm)		CTX-M-1CTX-M-14CTX-M-55CTX-M-65CMY-2CTX-M-55+CMY-2
2019-P-AChungbuk12.5 (1/8) 1
2019-P-CGyeongbuk25 (2/8)1 1
2019-P-EGyeongbuk27.3 (3/11) 1 2
2019-P-GJeonbuk10 (1/10) 1
2019-P-IJeonbuk50 (5/10) 41
2019-P-KJeonbuk20 (2/10) 2
2019-P-MJeonnam10 (1/10) 1
2019-P-NChungbuk10 (1/10) 1
2019-P-OGyeongbuk10 (1/10)1
2019-P-PGyeongbuk20 (2/10) 11
2019-P-TChungnam9.1 (1/11)1
2019-P-VJeonnam10 (1/10) 1
2019-P-WJeonbuk30 (3/10) 2 1
2019-P-YJeonbuk10 (1/10) 1
2019-P-ZChungnam20 (2/10)1 1
2019-P-AAChungnam9.1 (1/11) 1
2019-P-ABJeonnam10 (1/10) 1
2019-P-ACJeonbuk40 (4/10) 13
2019-P-ADGyeonggi30 (3/10) 21
2019-P-AEJeonnam40 (4/10) 1 21
2019-P-AFJeonbuk20 (2/10) 2
2019-P-AGJeonbuk40 (4/10) 4
Total 22.4 (46/219)41218282
The numbers in columns 4–9 represent the number of isolates that carried blaCTX-M and/or blaCMY-2 genes.
Table
Table 4. Characteristics of ESBL/pAmpC-producing Escherichia coli isolated from healthy broiler chickens in Korea.
Table 4. Characteristics of ESBL/pAmpC-producing Escherichia coli isolated from healthy broiler chickens in Korea.
Isolates Farm IDProvincesMICs (µg/mL)bla GenePMQR GeneNon-β Lactam Antibiotic Resistance Transfer-
Ability 		Plasmid TypePhylogenetic GroupPulsotype
XNLFOXCAZ
A-CF-6AChungbuk>844CTX-M-55-CIP NAL+FⅡAP22
C-CF-6CGyeongbuk>882CTX-M-1qnrS1CHL GEN STR FIS TET SXT+I1α, FIB, FⅡAP9
C-CF-8CGyeongbuk>884CTX-M-55qnrS1CHL FIS+I1α, FⅡDP6
E-CF-2EGyeongbuk>83216CMY-2-AMC STR FIS TET SXT--DP31
E-CF-M-5EGyeongbuk>8>3216CMY-2mcr-1CHL CIP COL NAL STR FIS TET SXT+I1α, FⅡDP32
E-CF-8EGyeongbuk88≤1CTX-M-14-CHL CIP NAL FIS+HI2, Iγ, FⅡAP26
G-CF-M-6GJeonbuk>8>32>16CMY-2-CHL CIP NAL STR FIS TET SXT+I1αAP34
I-CF-1IJeonbuk>824CTX-M-55qnrS1TET+FⅡB1P7
I-CF-M-2IJeonbuk>84≤1CTX-M-14-CIP GEN NAL--AP2
I-CF-5IJeonbuk>84≤1CTX-M-14-CIP GEN NAL--AP1
I-CF-M-7IJeonbuk>84≤1CTX-M-14-CIP GEN NAL--AP2
I-CF-M-8IJeonbuk>82≤1CTX-M-14-CIP GEN NAL--AP1
K-CF-M-1KJeonbuk>8>32>16CMY-2-CHL CIP NAL TET+I1α, FIB, FⅡDND
K-CF-7KJeonbuk>83216CMY-2-CIP NAL--DND
M-CF-M-3MJeonnam>888CTX-M-55-CIP NAL--B1ND
N-CF-5NChungbuk>8>3216CTX-M-55, CMY-2-CHL CIP NAL STR FIS+K, X4DP27
O-CF-4OGyeongbuk>842CTX-M-1-NAL FIS TET+I1αAP10
P-CF-M-2PGyeongbuk>884CTX-M-55-CIP NAL+FⅡAP20
P-CF-9PGyeongbuk>82≤1CTX-M-14-CIP GEN NAL TET--AP4
T-CF-M-3TChungbuk>842CTX-M-1-CHL CIP NAL FIS TET+I1αB1P21
V-CF-M-2VJeonnam>848CTX-M-55-CHL CIP NAL STR FIS TET- B1P11
W-CF-M-5WJeonbuk>848CTX-M-55-CIP GEN NAL TET+I1-α, FIB, FⅡDP24
W-CF-6WJeonbuk>888CTX-M-55-CHL CIP NAL TET+FⅡB1P14
W-CF-M-10WJeonbuk>832>16CTX-M-55, CMY-2-CHL CIP NAL STR FIS TET SXT- B1P25
Y-CF-4YJeonbuk>848CTX-M-55qnrS1TET+FⅡB1P5
Z-CF-M-1ZChungnam8>328CMY-2-CHL CIP NAL STR FIS TET+KB1P29
Z-CF-7ZChungnam>842CTX-M-1-CIP NAL TET- B1P28
AA-CF-M-2AAChungnam>844CTX-M-55-CIP NAL+FIB, FⅡB1P23
AB-CF-M-1ABJeonbuk>8>3216CMY-2-CHL CIP NALSTR FIS TET+I1αDP33
AC-CF-2ACJeonbuk>832>16CTX-M-55-CHL CIP NAL FIS TET- B1P13
AC-CF-M-3ACJeonbuk>844CTX-M-55-CHL CIP NAL STR FIS SXT+FⅡAP15
AC-CF-M-5ACJeonbuk>8816CTX-M-55-CHL CIP NAL FIS TET- B1P13
AC-CF-10ACJeonbuk>82≤1CTX-M-14-CIP GEN NAL- AP3
AD-CF-M-2ADGyeonggi88≤1CTX-M-14-CHL CIP GEN NAL FIS TET SXT+HI2, I1αB1P18
AD-CF-8ADGyeonggi816≤1CTX-M-14-CHL CIP GEN NAL STR FIS TET+HI2B1P16
AD-CF-M-10ADGyeonggi>848CTX-M-55-CHL CIP NAL STR FIS TET SXT- AP8
AE-CF-M-1AEJeonnam>8>3216CMY-2-CHL CIP GEN NAL STR FIS TET SXT+I1αB1P30
AE-CF-4AEJeonnam>82≤1CTX-M-14-CIP GEN NAL- AP3
AE-CF-M-9AEJeonnam>88≤1CTX-M-65qnrS2, aac(6′)-Ib-crCHL CIP GEN NAL STR FIS TET SXT- B1P12
AE-CF-M-10AEJeonnam>882CTX-M-65aac(6′)-Ib-crCHL CIP GEN NAL STR FIS TET SXT- B1P12
AF-CF-M-1AFJeonbuk84≤1CTX-M-14-CHL CIP GEN NAL FIS TET SXT+HI2B1ND
AF-CF-M-4AFJeonbuk>84≤1CTX-M-14-CHL CIP GEN NAL FIS TET+HI2B1ND
AG-CF-M-4AGJeonbuk>888CTX-M-55-CHL CIP NAL STR FIS TET SXT+FⅡAP19
AG-CF-6AGJeonbuk>848CTX-M-55-CHL CIP NAL STR FIS TET SXT+FⅡAP19
AG-CF-M-9AGJeonbuk>888CTX-M-55-CHL CIP NAL STR FIS TET SXT+FⅡAP19
AG-CF-M-10AGJeonbuk>844CTX-M-55-CHL STR FIS TET+I1α, FⅡB1P17
AMC, Amoxicillin/clavulanic acid; CAZ, Ceftazidime; CHL, chloramphenicol; CIP, ciprofloxacin; COL, colistin; FOX, cefoxitin; GEN, gentamicin; NAL, nalidixic acid; STR, streptomycin; FIS, sulfisoxazole; TET, tetracycline; SXT, Trimethoprim/sulfamethoxazole; XNL, ceftiofur. PMQR, plasmid-mediated quinolone resistance. Xbal macrorestriction analysis yielded no DNA banding patterns in five E. coli isolates due to constant autodigestion of the genomic DNA, and thus, a cluster formed by this strain is excluded (ND, not determined). The underlined resistance markers were transferred to the recipient E. coli J53 strain by conjugation.
Table
Table 5. Plasmid replicon types and genetic environments of ESBL/pAmpC gene-carrying E. coli transconjugants.
Table 5. Plasmid replicon types and genetic environments of ESBL/pAmpC gene-carrying E. coli transconjugants.
Type of bla GeneNo. of IsolatesSelf-TransferNo. of Replicon Type Genetic Environment
I1αI1α+ FⅡI1α + FⅡ + FIBFⅡFⅡ + FIBHI2HI2 + I1αHI2 +
FⅡ + Iγ		KB/O +K + X4UpstreamDownstream
ISEcp1IS26IS903orf477
CTX-M-1432-1-------3--3
CTX-M-14125-----311----5-
CTX-M-55 a119-1-8---------9
CTX-M-55 b74-1111-----4--4
CTX-M-6520--------------
CMY-286311-----1-6---
CTX-M-55+CMY-221---------11---
Total46285339131111140516
ablaCTX-M-55-orf477; bISEcp1-blaCTX-M-55-orf477.

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Song, H.-J.; Moon, D.C.; Mechesso, A.F.; Kang, H.Y.; Kim, M.H.; Choi, J.-H.; Kim, S.-J.; Yoon, S.-S.; Lim, S.-K. Resistance Profiling and Molecular Characterization of Extended-Spectrum/Plasmid-Mediated AmpC β-Lactamase-Producing Escherichia coli Isolated from Healthy Broiler Chickens in South Korea. Microorganisms 2020, 8, 1434. https://0-doi-org.brum.beds.ac.uk/10.3390/microorganisms8091434

AMA Style

Song H-J, Moon DC, Mechesso AF, Kang HY, Kim MH, Choi J-H, Kim S-J, Yoon S-S, Lim S-K. Resistance Profiling and Molecular Characterization of Extended-Spectrum/Plasmid-Mediated AmpC β-Lactamase-Producing Escherichia coli Isolated from Healthy Broiler Chickens in South Korea. Microorganisms. 2020; 8(9):1434. https://0-doi-org.brum.beds.ac.uk/10.3390/microorganisms8091434

Chicago/Turabian Style

Song, Hyun-Ju, Dong Chan Moon, Abraham Fikru Mechesso, Hee Young Kang, Mi Hyun Kim, Ji-Hyun Choi, Su-Jeong Kim, Soon-Seek Yoon, and Suk-Kyung Lim. 2020. "Resistance Profiling and Molecular Characterization of Extended-Spectrum/Plasmid-Mediated AmpC β-Lactamase-Producing Escherichia coli Isolated from Healthy Broiler Chickens in South Korea" Microorganisms 8, no. 9: 1434. https://0-doi-org.brum.beds.ac.uk/10.3390/microorganisms8091434

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