First Isolation and Molecular Characterization of bla_CTX-M-121-Producing Escherichia coli O157:H7 From Cattle in Xinjiang, China

Introduction

Escherichia coli O157:H7 is a major foodborne pathogen that causes severe bloody diarrhea, hemorrhagic colitis (HC), and hemolytic uremic syndrome (HUS) in humans (1). E. coli O157:H7 was first recognized as a pathogen contributing to an outbreak of HC associated with hamburger consumption in 1982 (2). Since then, E. coli O157:H7 outbreaks have been reported in the United States, Canada, Japan, and China (3–6). E. coli O157:H7 has been reportedly detected in healthy cattle worldwide (7). The infected, asymptomatic cattle irregularly excrete E. coli O157:H7, resulting in contaminating food and water in the environment, as well as infecting humans and other animals (8). Cattle are recognized major reservoir and source of E. coli O157:H7.

Pathogenic virulence of E. coli O157:H7 is attributable to genes coding for Shiga toxin (Stx), the intestinal cell shedding site [locus of entericyte effacement (LEE)] virulence island, and the large plasmid pO157 (9). Stx, comprising Stx1 and Stx2, is able to induce cell necrosis and tissue lesions, and Stx2 is more potent than Stx1 (10, 11). The LEE region encodes a type III secretion system, and the secreted proteins E. coli secreted proteins (Esp) and translocated intimin receptor (Tir). Both Esp and Tir are required for intimate attachment and A/E lesion formation (12). The LEE region also encodes intimin, an outer membrane protein adhesin (Eae) that mediates the intimate attachment of bacteria to the host epithelial cell surface (13). In addition, Tir cytoskeleton-coupling protein (TccP) stimulates actin polymerization during the formation of A/E lesion (14). The large plasmid pO157 carries genes coding for type II secretion systems, such as hemolysin (Hly) and ToxB. All these virulence factors of E. coli O157:H7 reportedly regulate the adhesion of pathogenic bacteria to intestinal epithelial cells, causing the shedding of intestinal cells. These virulence genes have been used to identify bacterial strains isolated from various sources in epidemiological studies (6, 15, 16).

Antimicrobials have been the mainstay for the prevention and treatment of bacterial diseases in animals. However, their use is getting limited due to rising antibiotic resistance, which has become a serious problem worldwide, especially in developing countries where the quality, distribution, and use of antibiotics in human and veterinary medicine is not strictly regulated (15, 17). Extended-spectrum cephalosporins (ESCs), especially the third- and fourth-generation cephalosporins, are classified by the World Health Organization (WHO) to treat infections of multidrug-resistant Gram-negative bacteria (18). However, acquisition of genes encoding extended spectrum β-lactamases (ESBLs), especially CTX-M enzymes, by E. coli plays an important role in the resistance to ESCs (19). The genes encoding these enzymes, i.e., bla_CTX−M genes, are usually located on transferable plasmids, which also carry resistance genes for other types of antimicrobials (i.e., fluoroquinolones, aminoglycosides). These plasmids mediate the spread of drug resistance between bacteria via conjugation (20). E. coli O157:H7 isolates collected from humans and animals have shown resistance to a variety of antibiotics; therefore, the emergence of multidrug resistant (MDR) E. coli O157:H7 has become a public health issue (21, 22).

The sustainability of cattle industry and food safety depend upon the effective prevention and control of bovine pathogenic microorganisms. Xinjiang is one of largest cattle-raising regions in China. To further assess the potential public health impact of E. coli O157:H7 in Xinjiang, we investigated the pathogenicity and antibiotic resistance of isolates collected from farms and slaughterhouses. We examined the intrinsic relationship among different isolates and assessed the potential dissemination of MDR profiles in vitro.

Materials and Methods

Sample Collection

Total samples (n = 2,439) included 1,155 fresh feces, 1,236 rectal swabs, and 48 carcass swabs that were collected from 18 beef cattle and dairy farms (industrial, semi-industrial, and traditional farms, with a herd size of 200–8,000 cattle) and one slaughterhouse in the region of Akesu, Bole, Changji, Tacheng, Urumqi, Wujiaqu, and Yili in Xinjiang, China between October 2012 and March 2017. Samples were collected from Xinjiang brown cattle, Holstein cattle, Simmental cattle, and Angus cattle (1–7 years old, 400–800 kg body weight). Approximately 25 g of fecal samples were collected from each animal by rectal palpation or during defecation using disposable sleeve gloves and then placed in sterile Whirl-Pak bags (Nasco, Fort Atkinson, WI, USA). Rectal swabs were collected when rectal palpation is not applicable or no bowel movement is observed. Sterile cotton swabs (length, 150 mm; Copan Italia SpA) were used to collect mucus samples from the rectal anal junction. Sterile cotton swabs were also used to swab ~10 cm² of carcass surface. All samples were transported in icebox to the laboratory and stored at 4°C until processed within 2 h.

Escherichia coli O157:H7 Isolation

Selective enrichment was carried out according to the method reported by Mersha et al. (23) with minor modifications. One gram of each feces was aseptically added to 9 ml of modified tryptone soya broth containing 20 mg/L novobiocin (mTSB + n) (Hopebio, Qingdao, China) and incubated at 37°C for 16 h. To all the swab samples, 90 ml of mTSB + n was added and homogenized using a vortex mixer. After incubation for 16 h, all the samples were processed for immunomagnetic separation (IMS) using anti-E. coli O157 Dynabeads (Dynal, Invitrogen, USA) as follows. One microliters of the enriched broth culture was put in a sterile screw cupped Eppendorf tubes to which 20 μl of anti-O157:H7 immunomagnetic beads was added, followed by shaking at ambient temperature for 30 min. The tubes were then kept inside the manual magnetic particle concentrator. The beads were washed thrice using 300 μl phosphate-buffered saline (PBS) buffer for each wash. Finally, 100 μl of PBS was added in each tube and mixed gently (24). Fifty microliters of the mixture was streaked onto Sorbitol MacConkey agar containing 0.05 mg/L cefixime and 2.5 mg/L potassium tellurite (CT-SMAC) (Hopebio, Qingdao, China) and incubated at 37°C for 20–24 h to develop colonies. Pale-colored colonies were purified by repeated streak plating until a uniform colony morphology was obtained (25). One or more of the colonies were individually selected as presumptive E. coli O157 per sample. E. coli CICC 21530 (O157:H7, stx1 + stx2 + eae + hly + tccp) (26, 27) and ATCC 25922 strains were used as positive and negative controls, respectively. Two genes (rfbEO157 and fliCH7) were used to identify E. coli O157:H7 (28). Pink colonies (suspected the general E. coli) were purified by restreaking on McConkey agar and confirmed by PCR method as described by Teichmann et al. (29) (Table 1). The PCR amplicons (10 μl) were subjected to electrophoresis on a 1.2% agarose gel in 1× Tris–acetate–EDTA (TAE) buffer at 115 V for 30 min and stained with SYBR Green (Fermentas, Germany). The positive isolates were each inoculated in separate TSB and incubated overnight at 37°C, from which glycerol stocks were made and then stored at −80°C for further analysis.

Table 1. Primers used in PCR to detect targeted genes.

Analysis of Virulence Genes

Genomic DNA contents were extracted from 21 E. coli O157:H7 isolates as confirmed by PCR serotyping. In brief, 3–5 colonies were individually suspended in 200 μl of sterile distilled water. Bacterial suspensions were then heated at 95°C for 10 min centrifugation at 13,400 × g for 10 min to obtain the supernatant containing the template DNA and were transferred into 1.5-ml Eppendorf tubes without nuclease and stored at −20°C.

A multiplex PCR procedure was used to detect the stx1 and stx2 genes (30), and a single PCR procedure was used to detect the eae (31), hly (32), and tccp (14) genes. The primers, conditions, and references cited are listed in Table 1. E. coli CICC 21530 was used as a positive control for all the five virulence genes, while ATCC 25922 was used as a negative control. Amplification of the targeted gene was carried out using EX Taq (TaKaRa, Dalian, China) with the following PCR program: 94°C for 4 min, 30 cycles of denaturation at 94°C for 30 s, annealing at 54°C for 30 s, and extension at 72°C for 30 s, with a final extension at 72°C for 10 min. The annealing temperature was adjusted according to the primer Tm value (Table 1).

Antimicrobial Susceptibility Tests

Antibiotic susceptibility was tested using the Kirby–Bauer disk diffusion technique. Antibiotic disks of 6 mm in diameter obtained from OXOID, UK, containing ampicillin (AMP, 10 μg/disk), piperacillin (PIP, 100 μg/disk), cefotaxime (CTX, 30 μg/disk), ceftazidime (CAZ, 30 μg/disk), cefepime (FEP, 30 μg/disk), aztreonam (ATM, 30 μg/disk), ampicillin-sulbactam (SAM, 10/10 μg/disk), piperacillin-tazobactam (TZP, 100/10 μg/disk), amoxicillin-clavulanic acid (AMC, 20/10 μg/disk), gentamicin (GEN, 10 μg/disk), amikacin (AMI, 30 μg/disk), streptomycin (STR, 10 μg/disk), cotrimoxazole (SXT, 25 μg/disk), chloramphenicol (CHL, 30 μg/disk), levofloxacin (LEV, 5 μg/disk), ciprofloxacin (CIP, 5 μg/disk), tetracycline (TET, 30 μg/disk), and polymyxin B (PB, 300 U/disk) (20). E. coli ATCC25922, purchased from China Center of Industrial Culture Collection (CICC), was used as a quality control strain in the susceptibility tests. The ESBL-producing isolates were determined by double-disk synergy tests according to CLSI (33). Isolates shown to be resistant to at least three different classes of antimicrobial agents were determined to be multidrug resistant (MDR) (34).

Detection of Antibiotic Resistance Genes

The following resistance determinants were investigated by PCR: bla_CTX−M [the CTX-M-type genes were detected using universal primers bla_CTX−M−U (35), and the entire CTX-M-type genes were amplified using the primers bla_CTX−M−1G (35), bla_CTX−M−2G (36), or bla_CTX−M−9G (37)], bla_TEM (38), and bla_SHV (39), which encode β-lactamases, chloramphenicol efflux pumps [cmlA1(39)], sulfonamide resistance gene [sul1 (40)], and the tetA (41), tetE (41), and tetG (41) tetracycline efflux pumps. bla_TEM and bla_SHV genes were amplified by double PCR; tetA, tetE, and tetG genes were amplified by triplex PCR, while other resistant genes were amplified by single PCR. Primers used for the different genes are listed in (Table 1). The PCR products were sent to Sangon Biotech Co., Ltd. (Shanghai, China) for sequence determination. The DNA sequences and deduced amino acid sequences were compared with sequences reported in GenBank to confirm the subtypes of the β-lactamase gene.

Conjugation Experiments and Plasmid Analysis

Sodium azide-resistant E. coli J53 was used as a recipient and conjugated to a bla_CTX-_M-producing isolate by filtration. Transconjugants were selected on Mac Conkey agar containing cefotaxime or ceftazidime (4 μg/ml) and sodium azide (200 μg/ml). ESBL and antibiotic susceptibility was also tested in selected transconjugants, and the presence of bla genes was determined using PCR as described above. The resistance plasmids carried by transconjugants were typed using PCR-based replicon typing (42).

Epidemiological Typing

All the 21 E. coli O157:H7 isolates were characterized by pulsed field gel electrophoresis (PFGE) using the CHEF-MAP-PER System (Bio-Rad Laboratories, Hercules, CA, USA) as described by Gautom (43). Briefly, chromosomal DNA of E. coli O157:H7 isolates was isolated, and the inserts were digested with XbaI (TaKaRa Dalian, China) for 16 h at 37°C. The electrophoresis was performed at 6.0 V/cm for 18.5 h with an angle of 120 at 14°C. The pulse time was increased from 0.5 to 60 s. The Salmonella serotype Braenderup H9812 (ATCC BAA-664) was chosen as the molecular weight marker. Gels were then stained in ethidium bromide (1.0 mg/L). Isolates were considered to belong to the same PFGE cluster when the similarity index was >80% (44).

Results

Isolation and Presence of Virulence Genes

To investigate the virulence and antibiotic resistance of E. coli O157:H7, we collected 2,439 samples from farms and slaughterhouses in Xinjiang regions (Table 2). We successfully isolated E. coli clones from all the feces (100%), rectal swabs (100%), and carcass swabs (100%). Studying these E. coli isolates, we detected that 21 isolates were the E. coli O157:H7 strain (19 isolates collected from cattle farms and 2 isolates obtained from one slaughterhouse). As shown in Table 2, the isolation rates of E. coli O157:H7 in feces, rectal swabs, and carcass swabs were 0.7% (8/1155), 1% (11/1236), and 4% (2/48), respectively.

Table 2. Sample collection and isolation of E. coli.

Of the 21 E. coli O157:H7 isolates, 18 (86%) carried at least one virulence gene and 3 (14%) did not carry any (Table 3). Using PCR technique, we detected that seven (33%) possessed only stx2, seven (33%) isolates were positive for stx1 and stx2, and only one (5%) isolate had just stx1 gene. The eae gene and hly gene were detected in 16 (76%) and 14 (67%) E. coli O157:H7 isolates, respectively. Tccp in combination with hly and eae was found in 12 (57%) isolates. In total, six diverse virulence profiles were determined, including stx1/stx2/eae/hly/tccp (seven isolates), stx2/eae/hly/tccp (five isolates), stx2 (two isolates), eae (two isolates), stx1/eae/hly (one isolate), and eae/hly (one isolate) (Table 3).

Table 3. Typing antibiotic resistance and virulence genes in E. coli O157:H7 isolates.

Antibiotic Resistance Spectrum and Distribution of Antibiotic Resistance Genes

Studying the resistance of isolated E. coli O157:H7 to antibiotics, we detected that one isolate (Y4-A103) was resistant to tetracycline and carried the tetA gene, which encodes a tetracycline efflux pump. Y4-A109 and Y4-C21-1 were MDR isolates with the resistant patterns: AMP/CAZ/CHL/CIP/CTX/LEV/PIP/SXT/TET (Y4-A109) and AMP/CHL/CIP/CTX/LEV/PIP/SXT/TET (Y4-C21-1). In particular, the Y4-A109 was an ESBL-producing isolate carrying the bla_{CTX−M−121} gene (Table 3). Although both Y4-A109 and Y4-C21-1 isolates were resistant to chloramphenicol and sulfonamides, the cmlAI and sulI genes were not detectable in these isolates, indicating other genes involved in the resistance to chloramphenicol and sulfonamides. In addition, those two MDR isolates (Y4-A109 and Y4-C21-1) simultaneously harbored five virulence genes (stx1/stx2/eae/hly/tccp).

Transferability of bla_CTX-M Genes and Plasmid Replicon Typing

Studying transferability, we detected that the bla_{CTX−M−121} gene of the E. coli O157:H7 Y4-A109 isolate was transferable to the recipient strain azide-resistant E. coli J53 by conjugation at a frequency of approximately 10⁻⁶ per donor cell after coincubation of bacteria. We also determined that the resistance of Y4-A109 to ampicillin, cefotaxime, ceftazidime, cotrimoxazole, and tetracycline was also transferable to the recipient. However, plasmid replicon carrying these resistance genes in Y4-A109 remained to be determined.

Epidemiological Typing

Overall, the genetic relatedness ranged from 66 to 100% among the 21 isolates (Figure 1). Furthermore, the studied isolates shared ≤80% genetic similarity to the reference strain 21530. Seventeen of the 21 isolates were grouped into two clusters using >80% similarity of the Dice coefficient. Isolates Y4-A20-1 and Y4-A41-2 (cluster II) were simultaneously isolated from different cattle at Yili in 2015 but shared identical pattern of PFGE, virulence genes, and antibiotic susceptibility (Figure 1). This suggests that potential pathogen transmission might occur from animals to animals within the farm. In addition, three drug-resistant isolates were all identified from Yili. However, they were genetically distantly related (<71% similarity of the Dice coefficient). Noticeably, the PFGE profiles of two isolates from the slaughterhouse were identical to those from the farms. However, Y4-C21-2 carried stx1 gene, which was absent from its identical farm isolate, whereas Y4-C21-1 appeared to be resistant to eight drugs tested, which were not observed in its identical counterparts (Figure 1).

Figure 1. Dendrogram of Xbal pulsed-field gel electrophoresis profiles of E. coli O157:H7 isolates. The box indicates that the strains isolated from slaughterhouse. The asterisk represents the resistant strains.

Discussion

In this communication, we reported, for the first time, that the bla_{CTX−M−121} gene was detected in E. coli O157:H7 isolated from cattle in Xinjiang. The bla_{CTX−M−121} gene belongs to the bla_CTX−M−9 group. Rao et al. (45) reported the bla_{CTX−M−121} gene detected in two E. coli isolates collected from farm ducks in China. Zhou et al. (46) identified the bla_{CTX−M−121} gene in one E. coli isolated from healthy people in Guangdong Province. Jin (47) reported the bla_{CTX−M−121} gene in chicken E. coli isolated from Guangdong Province. The cephalosporins are used to treat infectious disease such as bovine respiratory infection and mastitis, which may promote production and dissemination of β-lactamase genes (48).

Besides the transferable bla_{CTX−M−121} gene between the bacterial strains via plasmid transmission, we also detected a wide spectrum of virulence genes, including the stx1, stx2, eae, hly, and tccp genes in E. coli O157:H7 isolates, which were consistent with the virulence gene types of E. coli O157:H7 from bovine in Jiangsu Province (49). We also detected three isolates of E. coli O157:H7 lacking any of these virulence genes, which was similar to the bovine E. coli O157:H7 isolates reported by Akomoneh et al. (50). E. coli O157:H7 isolates possessing only eae or stx2 gene were similar to the isolates obtained from cattle in USA and milk in Nigeria, respectively (51, 52). The attendance of the eae gene in O157:H7 STEC (Shiga toxin-producing E. coli) isolates resulted in the formation of a highly virulent subpathotype, Enterohemorrhage E. coli (EHEC) (53), which was observed in two MDR isolates in the present survey.

In addition, the tet resistance gene has been increasingly detected in bovine O157 and non-O157 STEC isolates worldwide (54–56). Our studies also revealed, for the first time, the presence of the tetA gene detected in bovine E. coli O157:H7 in Xinjiang. Horizontal gene transfer plays a key role in bacterial evolution and transmission of antibiotic resistance genes (57). Resistance traits located in genetic mobile elements, such as plasmids, transposons, and integrons, can be transferred to different strains or bacterial species (58, 59). It is conceivable that virulence gene and drug-resistance gene are carried by the same genetic element; cotransfer may occur under the selection of antibiotics to result in stable virulence clones, thereby leading to production of drug-resistant pathogenic bacteria and persistent bacterial infection in humans and food animals.

We found that the isolates obtained in the same geographical location at the same time had similar PFGE patterns and vice versa, indicating that clonal propagation in cattle population and cross-regional transmission. E. coli O157:H7 with identical PFGE pattern (100% similarity) carry different virulence genes and different drug resistance phenotypes, suggesting that the virulence and drug resistance carried by E. coli O157:H7 may be acquired or lost during the evolution and transfer of the same cluster of strains. The β-lactam-resistant E. coli O157:H7 may give β-lactam resistance to other pathogenic enterobacteria via plasmid-mediated conjugation, thereby posing potential challenges in the management of their associated infectious disease in cattle (60).

E. coli O157:H7 was prevalent in 2–15% population of cattle and other animals in China (47). Our results revealed that the overall isolation rate at ~0.9% (21 of 2,439 samples) of E. coli O157:H7 and the bla_CTX−M gene detected in 1 of 21 isolates indicated that the transmission of the bla_CTX−M gene in E. coli O157:H7 population was at an early stage in Xinjiang. Thus, it is important to not only continuously monitor but also identify methods to intervene in the transmission of bla_CTX−M genotypes to E. coli and other bacterial strains, thereby minimizing potential dissemination of β-lactam resistance from the cattle production to their surrounding environment.

Data Availability Statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.

Ethics Statement

The animal study was reviewed and approved by the Animal Care and Use Committee of Xinjiang Agricultural University. Written informed consent was obtained from the owners for the participation of their animals in this study.

Author Contributions

ZS and PT conceived and designed the experiments. LZ, MZ, DW, and KM performed the experiments. YZ and YL analyzed the date. PT, LX, and JX contributed to the writing of the manuscript. All authors read and approved the article.

Funding

The project was funded by the National Natural Science Foundation of China (31960695 and 31560485), Natural Science Foundation of Xinjiang Province (2019D01A51), Prior Period Project of Xinjiang Agricultural University (XJAU201703), and by Postdoctoral Science Foundation of Xinjiang Agricultural University and Xinjiang Uygur Autonomous Region High-Level Talent Introduction.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

The PFGE analysis was supported by State Key Laboratory for Infectious Disease Prevention and Control National Institute for Communicable Disease Control and Prevention, China CDC for her support. We also thank professor Hwa-Chain R. Wang for his instructive suggestions in manuscript preparation. This manuscript has been released as a pre-print at (61).

References