Next Article in Journal
Prevalence and Characterization of Coagulase Positive Staphylococci from Food Products and Human Specimens in Egypt
Previous Article in Journal
Defining the Scope of Antimicrobial Stewardship Interventions on the Prescription Quality of Antibiotics for Surgical Intra-Abdominal Infections
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Antibiotics
Volume 10
Issue 1
10.3390/antibiotics10010074
antibiotics-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Antimicrobial Resistance of Non-O157 Shiga Toxin-Producing Escherichia coli Isolated from Humans and Domestic Animals

by
Yanyu Pan
1,†,
Bin Hu
2,†,
Xiangning Bai
1,3,
Xi Yang
1,
Lijiao Cao
1,
Qian Liu
1,
Hui Sun
1,
Juan Li
1,
Ji Zhang
4,
Dong Jin
1,* and
Yanwen Xiong
1,*
1
State Key Laboratory of Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China
2
Shandong Center for Disease Control and Prevention, Jinan 250014, China
3
Division of Infectious Diseases, Department of Medicine Huddinge, Karolinska Institutet, 14186 Stockholm, Sweden
4
mEpiLab, New Zealand Food Safety Science & Research Center, Institute of Veterinary, Animal and Biomedical Sciences, Massey University, 4442 Palmerston North, New Zealand
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to the work.
Antibiotics 2021, 10(1), 74; https://doi.org/10.3390/antibiotics10010074
Submission received: 7 December 2020 / Revised: 8 January 2021 / Accepted: 12 January 2021 / Published: 14 January 2021
(This article belongs to the Section Antibiotics Use and Antimicrobial Stewardship)
Browse Figures
Review Reports Versions Notes

Abstract

:
Non-O157 Shiga toxin-producing Escherichia coli (STEC) is an important pathogen that can cause zoonotic diseases. To investigate the antimicrobial resistance of STEC in China, non-O157 STEC isolates, recovered from domestic animals and humans from 12 provinces, were analyzed using antimicrobial susceptibility testing and whole genome characterization. Out of the 298 isolates tested, 115 strains showed resistance to at least one antimicrobial and 85 strains showed multidrug resistance. The highest resistance rate was to tetracycline (32.6%), followed by nalidixic acid (25.2%) and chloramphenicol and azithromycin (both 18.8%). However, imipenem and meropenem were effective against all isolates. Antimicrobial resistance patterns varied among strains from different sources. Strains from pig, sheep, humans, and cattle showed resistance rates of 100.0%, 46.9%, 30.3%, and 6.3% to one or more antimicrobials, respectively. Forty-three genes related to 11 antimicrobial classes were identified among these strains. The colistin-resistance gene mcr was only carried by strains from pigs. A new fosfomycin-resistant gene, fosA7, was detected in strains from humans, cattle, and sheep. Whole genome phylogenetic analysis showed that strains from the four sources were genetically diverse and scattered throughout the phylogenetic tree; however, some strains from the same source had a tendency to cluster closely. These results provide a reference to monitor the emergence and spread of multidrug resistant STEC strains among animals and humans. Furthermore, with a better understanding of antimicrobial genotypes and phenotypes among the diverse STEC strains obtained, this study could guide the administration of antimicrobial drugs in STEC infections when necessary.

1. Introduction

Shiga toxin-producing Escherichia coli (STEC) is an important zoonotic foodborne pathogen, which can cause watery diarrhea, hemorrhagic colitis (HC), and even life-threatening hemolytic uremic syndrome (HUS) [1,2]. STEC O157:H7 was first recognized as a cause of a foodborne outbreak in the USA in 1982, and remains the most predominant and virulent serotype associated with outbreaks and severe human illnesses worldwide [3]. However, in recent years, non-O157 STEC strains have emerged as a major public health concern [4,5]. Sporadic cases or outbreaks caused by non-O157 STEC strains have been reported increasingly, especially strains of several serogroups (O26, O45, O103, O111, O121, and O145, termed as the “top six”) that were the most prevalent during STEC outbreaks [6,7,8].
Shiga toxin (Stx) comprises two immunologically distinct types, Stx1 and Stx2, each of which includes several genetic subtypes. Stx is the essential virulence factor contributing to the development of HUS [9]. Stx acts as ribotoxin that inhibits protein synthesis within sensitive eukaryotic cells and induces apoptosis [10]. To date, the treatment of STEC infections is mainly supportive, including rehydration therapy and dialysis where necessary [11]. The use of antimicrobials to treat STEC infections remains highly controversial and challenging, because some antimicrobial agents can induce Stx production, thus promoting the development of HUS [12,13]. However, other studies have suggested that certain antimicrobials, such as rifaximine, tetracycline, azithromycin, gentamicin, or ampicillin, can block the SOS response (DNA damage response pathway) and Stx production, thus preventing the development of HUS, especially if administered during the early course of the disease [14,15].
STECs have been isolated from a wide variety of domestic and wild animals, while ruminants are recognized as the most important reservoirs of STECs. Human infections are mainly caused by direct contact with infected animals or the consumption of contaminated foods and water [16,17]. As the natural hosts of STECs, cattle, sheep, and pigs are also important repositories for antibiotic resistance genes that potentially impact food and the environment [16,18]. For example, the novel plasmid-mediated polymyxin resistance gene, mcr-1, in zoonotic E. coli was firstly identified in China in November 2015, and was then detected extensively in various Gram-negative bacterial species from domestic animal hosts, as well as animal-originated food around the world [19,20,21].
Due to the extensive use of antimicrobial agents in farm animals, antimicrobial-resistant bacteria have become a serious issue. A comprehensive understanding of the prevalence of antibiotic-resistant STECs and the mechanisms underlying various resistance patterns could help possible therapeutic options for human infections [11]. However, limited information on antimicrobial resistance (AMR)-STECs is available in China. In this study, we investigated AMR in a diverse collection of non-O157 STEC isolates recovered from cattle, sheep, pigs, and human patients with diarrhea in China. We also screened for resistance genes using whole genome sequencing (WGS) to understand the potential risk of transmission of AMR-STECs from animals to humans. With an advanced understanding of antimicrobial genotypes and phenotypes among diverse STEC strains, the results of our study could guide the administration of antimicrobial drugs in STEC infections when necessary.

2. Results

2.1. The Distribution of O:H Serotypes and Stx Subtypes

Among 298 non-O157 STEC strains, 271 had draft genomes determined using the Illumina platform, and the remaining 27 had complete genomes sequenced using the PacBio platform. Using the genome sequences, 63 O-serogroups and 26 H-types were identified among the 298 STEC strains, constituting 92 different O:H serotypes. O21:H45 was the most predominant (15.1%, 45/298), followed by O22:H16 and O155:H21 (5.7%, 17/298). The most predominant O-serogroup was O21 (15.1%), followed by O22 (8.7%), O8 (5.7%), O155 (5.7%), and O171 (3.4%). The most predominant O-serogroups from cattle and sheep isolates were O8 (13.8%) and O21 (27.5%), respectively. Non-O157 STEC strains from diarrheal patients belonged to 19 O-serogroups, among which O130 was the most predominant (18.2%), followed by O26 (12.1%) and O117 (9.1%). Although 12 out of 19 O-serogroups were also detected in one or more animal-derived strains, only O8 was identified from all sources (Table S1).
Two stx1 and eight stx2 subtypes were found among the 298 non-O157 STEC strains, respectively, resulting in 14 different stx1 and/or stx2 subtype combinations. The most predominant stx subtype was stx1a (90/298, 30.2%), followed by stx1c (58/298, 19.5%) and stx2b (34/298, 11.4%). The most predominant stx subtype in cattle-origin strains was stx1a (20/80), followed by stx1a + stx2d (13/80) and stx2a (11/80). Among strains from sheep, stx1a (57/160) was the most predominant, followed by stx1c (43/160) and stx2b (28/160). All 25 strains from pigs carried the stx2e subtype. Six stx subtypes or combinations were identified among the human strains, including stx1c (15/33), stx1a (13/33), stx2e (2/33), stx1a + stx2b (1/33), stx2d (1/33), and stx2k (1/33). The stx subtypes identified in this study are shown in Table S1.

2.2. Antimicrobial Susceptibility

Among the 19 antibiotics tested in this study, the resistance rate toward tetracycline was the highest, with 32.6% (97/298) having resistant strains, followed by nalidixic acid (25.2%), chloramphenicol and azithromycin (18.8%), ampicillin (18.5%), and trimethoprim-sulfamethoxazole (14.1%). All isolates were susceptible to three antibiotics, i.e., ceftazidime-avibactam, imipenem, and meropenem (Figure 1).
Out of 298 non-O157 STEC isolates, 115 were resistant to one or more antibiotics, and isolates from different sources showed different antimicrobial resistance patterns. All 25 isolates from pigs were resistant to one or more antibiotics, among which 96.0% were resistant to tetracycline, 76.0% to trimethoprim-sulfamethoxazole, 72.0% to nalidixic acid, and 32.0% to chloramphenicol. All eight colistin-resistant isolates identified in this study were recovered from pigs. Among the 160 isolates from sheep, 46.9% showed resistance to at least one antibiotic. The resistance rate was highest for tetracycline (36.9%), followed by nalidixic acid and azithromycin (30.0%) and ampicillin (28.1%). Most cattle strains were antimicrobial susceptible, with five strains being resistant to one or more antimicrobials. Among 33 human STEC isolates, 30.3% showed resistance to at least one antibiotic. The resistance rate was highest for tetracycline (30.3%), followed by nalidixic acid (18.2%), azithromycin (12.1%), and trimethoprim-sulfamethoxazole and ampicillin (9.1%) (Table 1 and Table S1). Isolates resistant to ampicillin, azithromycin, aztreonam, cefotaxime, chloramphenicol, nalidixic acid, tetracycline, and trimethoprim-sulfamethoxazole were found in all sources.
Multidrug resistance (MDR) was identified in 85 isolates (28.5%). The MDR rate was highest among isolates from pigs (21/25, 84.0%,), followed by those from sheep (56/160, 35.0%), humans (5/33, 15.2%), and cattle (3/80, 3.8%). The MDR frequency was statistically different among strains from different sources (χ 2 = 68.008, p < 0.001), especially in the pig-origin strains (Table 1).

2.3. Antimicrobial Resistance Genes

In this study, 43 genes associated with resistance to 11 antimicrobial classes were identified (Table 2). The prevalence of resistance genes was highest in the sheep-derived isolates, with 32 AMR-related genes, followed by pig-derived isolates with 29 AMR-related genes. Cattle-derived isolates harbored 23 AMR-related genes, and 17 AMR-related genes were identified in human-derived isolates. The genes related to resistance to four classes of antibiotics (aminoglycosides: aac(3)-IV, aadA16, aph(4)-Ia, aadA22; chloramphenicol: catA2; quinolones: qnrB17; rifampin: arr-3) were only found in sheep-derived strains. Four genes involved in two classes of antibiotic resistance (macrolides: ermB, mefB; colistin: mcr-1, mcr-3.1) only existed in pig-derived strains. Genes related to chloramphenicol resistance (catB3), macrolides resistance (ermB) and extended-spectrum β-lactamase (ESBL) resistance (blaCTX-M-15) were only identified in human-derived strains. Genes implicated in aminoglycoside resistance (rmtB) and fosfomycin resistance (fosA3) were only found in cattle-derived strains. Twelve genes related to seven antimicrobial resistances were identified in strains from all sources, including aminoglycosides (aac(3)-IIa, aadA5, aph(3″)-Ib, aph(6)-Id, and aadA), trimethoprim (dfrA17), macrolides (mphA), quinolones (qnrS1), sulfonamides (sul1, sul2), tetracyclines (tetA), and class A β-lactamase (blaTEM-1).
The aminoglycoside resistance genes were highly diverse, with 18 different combinations being identified in these strains. In cattle isolates, there were three combinations: aac(3)-IIa + aph(3″)-Ib + aph(6)-Id + ant(3″)-Ia, ant(3″)-Ia, and aph(3″)-Ib + aph(6)-Id + ant(3″)-Ia + rmtB. In sheep, pig, and human isolates, there were 10, 13, and 4 different combinations, respectively (Table 2 and Table S2).
The antibiotic resistance phenotypes corresponded well to the presence of specific antibiotic resistance-related genes. The 50 STEC isolates carrying chloramphenicol resistance-related genes were all resistant to chloramphenicol. Fifty out of 53 STEC isolates carrying macrolide resistance genes were resistant to azithromycin. Eight-nine out of 90 STEC isolates carrying tetracycline resistance genes were resistant to tetracycline (Table 3).

2.4. Phylogenetic Analysis

Although non-O157 STEC isolates from the four sources were scattered throughout the phylogenetic tree, they had a tendency to cluster closely. Cluster I only contained sheep-derived isolates, which all belonged to the O21:H25 serotype, carried the stx1a subtype, and demonstrated an MDR phenotype. The antibiotic resistance pattern of 89.3% (25/28) isolates in cluster I was AMP-AZM-CHL-NA-TET. These isolates were all from Sichuan province, and they all carried blaTEM-1. Some other sheep-derived isolates were grouped into cluster IV with the variable presence of AMR genes. Cluster II contained isolates from all four sources, and most of the pig-derived isolates were grouped into this cluster. Six out of eight mcr genes were clustered in cluster II and were specific to pig-derived isolates. However, the tetA gene was predominant (67.3%) and was shared by isolates from all sources in cluster II. Most of the human-derived isolates were grouped into cluster III, which also contained sheep-derived isolates. Compared with the other clusters, cluster III carried fewer antibiotic resistance genes (Figure 2 and Table S3).
Strains harboring multiple AMR-related genes were concentrated in clusters I, II, and IV, and strains carrying one or fewer AMR-related genes were concentrated in cluster III or other unnamed clusters. The MDR-strains in cluster I also showed a high frequency of AMR gene combinations (qnrS1, blaTEM-1, dfrA14, floR, mphA, and tetA) (Tables S1 and S3).

3. Discussion

Animals, especially cattle, are important natural reservoirs of STECs. The prevalence and diversity of non-O157 STEC in healthy pigs and cattle in China were reported in previous studies [22,23]. The present study provided an overview of antibiotic resistance of non-O157 STECs from cattle, sheep, pig, and humans in China. These strains are highly diverse, based on serotype, stx subtype, and genome analysis. Our results showed that 115 out of 298 strains were resistant to one or more antimicrobials, and MDR was identified in 85 strains. The pig-derived strains showed the highest antibiotic resistance, followed by sheep, human, and cattle strains, which contrasted with other reports from Spain [24] and Mexico [15].
Polymyxin E is considered as the last resort treatment for carbapenem-resistant Enterobacteriaceae infection [19]. A recent report showed that the resistance rate toward colistin in pig-derived E. coli was about 33.95% [25]. In the present study, colistin-resistant and mcr-positive strains were only identified in pig-derived strains. These mcr-positive strains were isolated from different regions, including Beijing, Chongqing, and Heilongjiang, demonstrating the wide spread of the mcr gene in China.
A new fosfomycin-resistant gene, fosA7, was identified in non-O157 STEC isolates from multiple sources (three from clinical patients, three from cattle, and one from sheep) in the present study. This gene was firstly identified in Salmonella in 2017, and was considered to reside on the chromosome, which was different from the plasmid-mediated fosfomycin resistance genes (such as fosA3) in E. coli and other bacteria [26]. We further determined the location of fosA7 on the STEC chromosome and found that the fosA7 5’ end contained a transposase gene (two types, 1254 bp or 1284 bp), which was different from those detected in Salmonella (Accession Number: LAOS01000001.1). By BLAST searching against the E. coli genome sequences (102,256 genomes in total available from the NCBI nucleotide collection (nr/nt) on 29 June 2020), the fosA7 gene was also found in 14 other E. coli genomes, and 3 out of 14 were from China (Table S4). This indicated that the fosfomycin resistance gene fosA7 might spread to E. coli in China. In this study, fosA7-positive isolates were scattered throughout the phylogenetic tree, indicating the gene might have the potential to transfer between different genetic strains. Fosfomycin could be included in antibiotic sensitivity testing in the future. Notably, the tetA gene was predominant and shared by isolates from all sources in phylogenetic cluster II, implying that this cluster might have higher capacity of transfer between different hosts.
Extended-Spectrum β-Lactamases (ESBLs) are one of the main causes of MDR in Enterobacteriaceae bacteria [27]. In this study, seven isolates from four provinces in China carried ESBL genes, and all strains showed MDR (Table S3). Among the class A β-lactamase genes, blaTEM-1 was the predominant gene (90.4%; 47/52). Notably, most of the blaTEM-1-positive strains were concentrated in cluster I and cluster III, and most of these strains were isolated in Sichuan province. The co-existence of two AMR genes, blaCTX-M-65 + blaTEM-1 and blaCTX-M-15 + blaTEM-1, were found. TEM, SHV, and CTX-M are considered as the three main genetic types of ESBLs [28]. CTX-M is the main type in many countries, such as CTX-M-14 in Japan [29] and CTX-M-2 in South America [30]. However, studies have shown wide geographical differences in their distribution [30,31]. We found that the TEM type seems to be dominant in Chinese STECs, which was supported by the results of an early study [32], in which 51 ESBL-producing E. coli isolates were found from 912 E. coli strains in China. Among them, the TEM type was the second most prevalent type. Notably, our previous study [33] showed that 47 ESBL-producing atypical enteropathogenic E. coli (aEPEC) strains were mainly the CTX-M type, and no TEM or SHV types were detected. The reason for this difference requires further analysis.
Some studies have indicated that quinolones, β-lactams, trimethoprim, trimethoprim-sulfamethoxazole, and others can cause bacterial SOS reactions and the massive release of Shiga toxins. However, the influences of different antibiotic classes on Shiga toxin production in vitro differ [34]. Some antibiotics, such as azithromycin, tetracycline, chloramphenicol, and fosfomycin, not only inhibit Shiga toxin release, but also affect the intestinal adhesion of pathogens and have other functions, such that they have been used to treat STEC infection to prevent HUS [15,24,35,36]. We found that the human STEC isolates in this study comprised a high percentage of strains that were susceptible to β-lactams, trimethoprim, and quinolones drugs. It has been reported that when STECs were exposed to inhibitory or sub-inhibitory concentrations of these antibiotics, the SOS reaction would occur [14]. Hence, it is not recommended to use these antibiotics to treat patients with STEC infections. Among these potential antibiotic classes, i.e., tetracycline, chloramphenicol, and azithromycin, high resistance rates were observed. However, all isolates were susceptible to imipenem and meropenem, which might be considered for the treatment of STEC infections when necessary.

4. Materials and Methods

4.1. Bacterial Strains

A total of 298 non-O157 STEC strains collected during 2009–2019 were used in this study. Strains were isolated from fecal samples from sheep (160), cattle (80), pigs (25), and human diarrheal patients (33) in 12 geographical regions in China (Table S1). All STEC strains were confirmed by screening for the presence of stx1 and/or stx2 genes and biochemical tests as previously described [37].

4.2. Antimicrobial Susceptibility Testing

The minimal inhibitory concentrations (MICs) of all isolates were determined by broth microdilution method using the BD PhoenixTM M50 Automated Microbiology System (BD, San Jose, CA, USA). Nineteen antimicrobial agents were tested in this study, including colistin (PB, 0.25–8 μg/mL), chloramphenicol (CHL, 4–32 μg/mL), tetracycline (TET, 1–16 μg/mL), ampicillin (AMP, 2–32 μg/mL), cefoxitin (FOX, 2–64 μg/mL), nalidixic acid (NA, 4–32 μg/mL), ciprofloxacin (CIP, 0.015–2 μg/mL), amikacin (AMK, 4–64 μg/mL), nitrofurantoin (F, 32–256 μg/mL), ampicillin-sulbactam (SAM, 1–32 μg/mL), ceftazidime-avibactam (CZA, 0.25/4–8/4 μg/mL), azithromycin (AZM, 2–64 μg/mL), aztreonam (ATM, 0.25–16 μg/mL), cefotaxime (CTX, 0.25–16 μg/mL), ceftazidime (CAZ, 0.25–16 μg/mL), imipenem (IPM, 0.25–8 μg/mL), meropenem (MEM, 0.125–8 μg/mL), ertapenem (ETP, 0.25–8 μg/mL), and trimethoprim-sulfamethoxazole (SXT, 0.5–8 μg/mL). The qualitative interpretations of susceptible (S), intermediate (I), or resistant (S) strains were determined according to the standard of the Clinical Laboratory Standards Institute guidelines (CLSI 2020). Multidrug resistance (MDR) was defined as resistance to at least one agent in three or more antimicrobial classes [38].

4.3. Whole Genome Sequencing (WGS)

Bacterial DNA was extracted using a Wizard Genomic DNA Purification Kit (Promega, Madison, WI, USA) according to the manufacturer’s instructions. Two sequencing libraries were prepared. One was used for sequencing on the Illumina NovaSeq platform with paired-end reads (2 × 350 bp) to obtain the draft genomes (Illumina, San Diego, CA, USA). The adapter and low-quality reads (a quality score below Q20) were removed using fastp 0.20.1, the filtered reads were assembled de novo using SKESA v.2.3.0 [39], and low quality contigs with <500 bp were filtered with Seqkit 0.11.0 [40]. The other library was for sequencing on the PacBio Sequel platform (Pacific Biosciences, Menlo Park, CA, USA). The raw sequencing reads were processed using SMRT Link v5.0.1 (www.pacb.com/support/software-downloads). Briefly, raw reads were trimmed by a “RUN QC” step, and then assembled de novo using a hierarchical genome-assembly process (HGAP), which belongs to a non-hybrid approach and included three steps: Preassembly-Assembly-Consensus polishing [41].

4.4. In Silico O:H Serotyping, Stx Subtyping and AMR Gene Screening

The genome sequences were compared to the data at SerotypeFinder (https://cge.cbs.dtu.dk/services/SerotypeFinder/) to determine the O:H serotypes [42]. NCBI AMRFinderPlus [43] and CARD [44] databases were used to screen the antimicrobial resistance genes, using ABRicate version 0.8.10 (https://github.com/tseemann/abricate). A relative coverage threshold of >97%, which was defined as the coverage percentage multiplied by the similarity percentage, was used to define the presence of AMR genes [45]. To determine stx subtypes, an in-house stx subtyping database was first created using ABRicate by including representative nucleotide sequences of all identified stx1 and stx2 subtypes, and then the genome sequences were used to search against the created stx subtyping database.

4.5. SNP-Based Phylogenetic Analyses

To obtain a high-resolution phylogeny, we adopted a phylogenetic analysis based on single nucleotide polymorphisms (SNPs) [46]. First, the fasta files of the 298 STEC isolates were used to map the sequences to the reference genome Sakai.gbk using Snippy version 4.3.6 (https://github.com/tseemann/snippy) with default parameters. The core alignment file of the SNPs, including invariant sites, was generated, followed by the removal of recombination using Gubbins version 2.3.4 [47]. The non-SNP regions were then removed using SNP-sites [48]. Finally, IQ-TREE version 1.6.8 [49] was used to build the Maximum-Likelihood phylogenetic tree using clean.core.aln (fasta format) as the input file; the branch bootstrap value was estimated 1000 times using the Ultrafast bootstrap algorithm [50].

4.6. Statistical Analysis

The distributions of antibiotic resistance in different sources were assessed using the χ2 and Fisher’s exact tests, using SPSS version 20.0 (IBM Corp., Armonk, NY, USA). p < 0.05 was considered statistically significant.

4.7. Data Availability

The genome sequences of the 298 non-O157 STEC strains used in this study have been submitted to GenBank. The accession numbers are shown in Table S1.

5. Conclusions

The present study revealed an overview of antimicrobial resistance phenotypes and genotypes among non-O157 STEC strains from diverse sources in China. We identified mcr-1 and mcr-3 in pig-derived non-O157 STEC strains, and the existence of the fosA7 gene in non-O157 STECs from different sources in China. These results suggest that the emergence and spread of multi-drug resistant STECs among diverse animal and human sources should be continuously monitored. In addition, given the challenges associated with the treatment of STEC infections, our study might provide guidance for antimicrobial selection in the clinical treatment of STEC infections.

Supplementary Materials

The following are available online at https://www.mdpi.com/2079-6382/10/1/74/s1, Table S1: Details of the 298 non-O157 STEC isolates used in this study, Table S2: Eighteen different combinations of aminoglycoside-resistance genes in 58 genome-sequenced isolates, Table S3: Distribution of antibiotic resistance genes and phylogenetic cluster of 298 non-O157 STEC isolates, Table S4: BLAST search results of the fosA7 gene in NCBI nr/nt database.

Author Contributions

Conceptualization, Y.X. and D.J.; methodology, J.L., L.C., H.S. and X.Y.; data analysis, Y.P., Q.L., B.H., J.Z. and X.B.; resources, B.H., Y.X. and J.L.; writing—original draft preparation, Y.P.; writing—review and editing, X.B., D.J. and Y.X. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by grants from the National Natural Science Foundation of China (81772152, 81701977), and the National Science and Technology Major Project (2018ZX10201001-006, 2018ZX10301407-002). The funders had no role in the study design, data collection and interpretation, or the decision to submit the work for publication.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Ethics Committee of National Institute for Communicable Disease Control and Prevention, China CDC (No. ICDC2017-003)”.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data presented in this study are openly available in GenBank and in supplementary material here.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Newell, D.G.; La Ragione, R.M. Enterohaemorrhagic and other Shiga toxin-producing Escherichia coli (STEC): Where are we now regarding diagnostics and control strategies? Transbound. Emerg. Dis. 2018, 65 (Suppl. 1), 49–71. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Mughini-Gras, L.; van Pelt, W.; van der Voort, M.; Heck, M.; Friesema, I.; Franz, E. Attribution of human infections with Shiga toxin-producing Escherichia coli (STEC) to livestock sources and identification of source-specific risk factors, The Netherlands (2010–2014). Zoonoses Public Health 2018, 65. [Google Scholar] [CrossRef] [PubMed]
  3. Heiman, K.E.; Mody, R.K.; Johnson, S.D.; Griffin, P.M.; Gould, L.H. Escherichia coli O157 outbreaks in the United States, 2003–2012. Emerg. Infect. Dis. 2015, 21, 1293–1301. [Google Scholar] [CrossRef] [PubMed]
  4. Valilis, E.; Ramsey, A.; Sidiq, S.; DuPont, H.L. Non-O157 Shiga toxin-producing Escherichia coli—A poorly appreciated enteric pathogen: Systematic review. Int. J. Infect. Dis. 2018, 76, 82–87. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Joseph, A.; Cointe, A.; Kurkdjian, P.M.; Rafat, C.; Hertig, A. Shiga toxin-associated hemolytic uremic syndrome: A narrative review. Toxins 2020, 12, 67. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Kinnula, S.; Hemminki, K.; Kotilainen, H.; Ruotsalainen, E.; Tarkka, E.; Salmenlinna, S.; Hallanvuo, S.; Leinonen, E.; Jukka, O.; Rimhanen-Finne, R. Outbreak of multiple strains of non-O157 Shiga toxin-producing and enteropathogenic associated with rocket salad, Finland, autumn 2016. Euro Surveill. 2018, 23. [Google Scholar] [CrossRef] [Green Version]
  7. Baker, K.S.; Dallman, T.J.; Thomson, N.R.; Jenkins, C. An outbreak of a rare Shiga-toxin-producing Escherichia coli serotype (O117:H7) among men who have sex with men. Microb. Genom. 2018, 4. [Google Scholar] [CrossRef]
  8. Crowe, S.J.; Bottichio, L.; Shade, L.N.; Whitney, B.M.; Corral, N.; Melius, B.; Arends, K.D.; Donovan, D.; Stone, J.; Allen, K.; et al. Shiga toxin-producing E. coli infections associated with flour. N. Engl. J. Med. 2017, 377, 2036–2043. [Google Scholar] [CrossRef]
  9. Kakoullis, L.; Papachristodoulou, E.; Chra, P.; Panos, G. Shiga toxin-induced haemolytic uraemic syndrome and the role of antibiotics: A global overview. J. Infect. 2019, 79, 75–94. [Google Scholar] [CrossRef]
  10. Melton-Celsa, A.R. Shiga toxin (Stx) classification, structure, and function. Microbiol. Spectr. 2014, 2, EHEC-0024-2013. [Google Scholar] [CrossRef] [Green Version]
  11. Muhlen, S.; Dersch, P. Treatment strategies for infections with Shiga toxin-producing Escherichia coli. Front. Cell. Infect. Microbiol. 2020, 10, 169. [Google Scholar] [CrossRef] [PubMed]
  12. Brigotti, M.; He, X.; Carnicelli, D.; Arfilli, V.; Porcellini, E.; Galassi, E.; Tazzari, P.L.; Ricci, F.; Patfield, S.A.; Testa, S.; et al. Particulate Shiga toxin 2 in blood is associated to the development of hemolytic uremic syndrome in children. Thromb. Haemost. 2020, 120, 107–120. [Google Scholar] [CrossRef] [PubMed]
  13. Puño-Sarmiento, J.; Anderson, E.M.; Park, A.J.; Khursigara, C.M.; Foster, D.B. Potentiation of antibiotics by a novel antimicrobial peptide against Shiga toxin producing E. coli O157:H7. Sci. Rep. 2020, 10, 10029. [Google Scholar] [CrossRef] [PubMed]
  14. Berger, M.; Aijaz, I.; Berger, P.; Dobrindt, U.; Koudelka, G. Transcriptional and translational inhibitors block SOS response and Shiga toxin expression in enterohemorrhagic Escherichia coli. Sci. Rep. 2019, 9, 18777. [Google Scholar] [CrossRef] [PubMed]
  15. Oporto, B.; Ocejo, M.; Alkorta, M.; Marimón, J.M.; Montes, M.; Hurtado, A. Zoonotic approach to Shiga toxin-producing Escherichia coli: Integrated analysis of virulence and antimicrobial resistance in ruminants and humans. Epidemiol. Infect. 2019, 147, e164. [Google Scholar] [CrossRef] [Green Version]
  16. Kim, J.S.; Lee, M.S.; Kim, J.H. Recent updates on outbreaks of Shiga toxin-producing Escherichia coli and its potential reservoirs. Front. Cell. Infect. Microbiol. 2020, 10, 273. [Google Scholar] [CrossRef]
  17. de Assis, D.C.S.; da Silva, T.M.L.; Brito, R.F.; da Silva, L.C.G.; Lima, W.G.; Brito, J.C.M. Shiga toxin-producing Escherichia coli (STEC) in bovine meat and meat products over the last 15 years in Brazil: A systematic review and meta-analysis. Meat Sci. 2020, 173, 108394. [Google Scholar] [CrossRef]
  18. Gonzalez, A.G.M.; Cerqueira, A.M.F. Shiga toxin-producing Escherichia coli in the animal reservoir and food in Brazil. J. Appl. Microbiol. 2020, 128, 1568–1582. [Google Scholar] [CrossRef] [Green Version]
  19. Liu, Y.-Y.; Wang, Y.; Walsh, T.R.; Yi, L.-X.; Zhang, R.; Spencer, J.; Doi, Y.; Tian, G.; Dong, B.; Huang, X.; et al. Emergence of plasmid-mediated colistin resistance mechanism MCR-1 in animals and human beings in China: A microbiological and molecular biological study. Lancet Infect. Dis. 2016, 16, 161–168. [Google Scholar] [CrossRef]
  20. Liu, J.-Y.; Liao, T.-L.; Huang, W.-C.; Liu, Y.-M.; Wu, K.-M.; Lauderdale, T.-L.; Tsai, S.-F.; Kuo, S.-C.; Kuo, H.-C. Increased mcr-1 in pathogenic Escherichia coli from diseased swine, Taiwan. J. Microbiol. Immunol. Infect. 2020, 53, 751–756. [Google Scholar] [CrossRef]
  21. Mariani, B.; Corbella, M.; Merla, C.; Tallarita, M.; Piralla, A.; Girello, A.; Castelli, M.; Bracchi, C.; Marone, P.; Cambieri, P. Bloodstream infections caused by Escherichia coli carrying mcr-1 gene in hospitalized patients in northern Italy from 2012 to 2018. Infection 2020, 48, 223–230. [Google Scholar] [CrossRef]
  22. Fan, R.; Shao, K.; Yang, X.; Bai, X.; Fu, S.; Sun, H.; Xu, Y.; Wang, H.; Li, Q.; Hu, B.; et al. High prevalence of non-O157 Shiga toxin-producing Escherichia coli in beef cattle detected by combining four selective agars. BMC Microbiol. 2019, 19, 213. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Meng, Q.; Bai, X.; Zhao, A.; Lan, R.; Du, H.; Wang, T.; Shi, C.; Yuan, X.; Bai, X.; Ji, S.; et al. Characterization of Shiga toxin-producing Escherichia coli isolated from healthy pigs in China. BMC Microbiol. 2014, 14, 5. [Google Scholar] [CrossRef] [Green Version]
  24. Mora, A.; Blanco, J.E.; Blanco, M.; Alonso, M.P.; Dhabi, G.; Echeita, A.; González, E.A.; Bernárdez, M.I.; Blanco, J. Antimicrobial resistance of Shiga toxin (verotoxin)-producing Escherichia coli O157:H7 and non-O157 strains isolated from humans, cattle, sheep and food in Spain. Res. Microbiol. 2005, 156, 793–806. [Google Scholar] [CrossRef] [PubMed]
  25. Wang, Y.; Xu, C.; Zhang, R.; Chen, Y.; Shen, Y.; Hu, F.; Liu, D.; Lu, J.; Guo, Y.; Xia, X.; et al. Changes in colistin resistance and mcr-1 abundance in Escherichia coli of animal and human origins following the ban of colistin-positive additives in China: An epidemiological comparative study. Lancet Infect. Dis. 2020, 20, 1161–1171. [Google Scholar] [CrossRef]
  26. Rehman, M.A.; Yin, X.; Persaud-Lachhman, M.G.; Diarra, M.S. First detection of a fosfomycin resistance gene, fosA7, in Salmonella enterica serovar Heidelberg isolated from broiler chickens. Antimicrob. Agents Chemother. 2017, 61. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Poirel, L.; Bonnin, R.A.; Nordmann, P. Genetic support and diversity of acquired extended-spectrum β-lactamases in Gram-negative rods. Infect. Genet. Evol. 2012, 12, 883–893. [Google Scholar] [CrossRef] [PubMed]
  28. Chong, Y.; Ito, Y.; Kamimura, T. Genetic evolution and clinical impact in extended-spectrum β-lactamase-producing Escherichia coli and Klebsiella pneumoniae. Infect. Genet. Evol. 2011, 11, 1499–1504. [Google Scholar] [CrossRef]
  29. Hayashi, W.; Ohsaki, Y.; Taniguchi, Y.; Koide, S.; Kawamura, K.; Suzuki, M.; Kimura, K.; Wachino, J.-I.; Nagano, Y.; Arakawa, Y.; et al. High prevalence of bla among genetically diverse Escherichia coli recovered from retail raw chicken meat portions in Japan. Int. J. Food Microbiol. 2018, 284. [Google Scholar] [CrossRef]
  30. Bevan, E.R.; Jones, A.M.; Hawkey, P.M. Global epidemiology of CTX-M β-lactamases: Temporal and geographical shifts in genotype. J. Antimicrob. Chemother. 2017, 72, 2145–2155. [Google Scholar] [CrossRef] [Green Version]
  31. Gatica, J.; Jurkevitch, E.; Cytryn, E. Comparative metagenomics and network analyses provide novel insights into the scope and distribution of β-lactamase homologs in the environment. Front. Microbiol. 2019, 10, 146. [Google Scholar] [CrossRef] [Green Version]
  32. Bai, L.; Wang, L.; Yang, X.; Wang, J.; Gan, X.; Wang, W.; Xu, J.; Chen, Q.; Lan, R.; Fanning, S.; et al. Prevalence and molecular characteristics of extended-spectrum β-lactamase genes in isolated from diarrheic patients in China. Front. Microbiol. 2017, 8, 144. [Google Scholar] [CrossRef] [Green Version]
  33. Xu, Y.; Sun, H.; Bai, X.; Fu, S.; Fan, R.; Xiong, Y. Occurrence of multidrug-resistant and ESBL-producing atypical enteropathogenic in China. Gut Pathog. 2018, 10, 8. [Google Scholar] [CrossRef] [Green Version]
  34. Bielaszewska, M.; Idelevich, E.A.; Zhang, W.; Bauwens, A.; Schaumburg, F.; Mellmann, A.; Peters, G.; Karch, H. Effects of antibiotics on Shiga toxin 2 production and bacteriophage induction by epidemic Escherichia coli O104:H4 strain. Antimicrob. Agents Chemother. 2012, 56, 3277–3282. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Mir, R.A.; Kudva, I.T. Antibiotic-resistant Shiga toxin-producing Escherichia coli: An overview of prevalence and intervention strategies. Zoonoses Public Health 2019, 66. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Gibbons, J.F.; Boland, F.; Egan, J.; Fanning, S.; Markey, B.K.; Leonard, F.C. Antimicrobial resistance of faecal Escherichia coli isolates from pig farms with different durations of in-feed antimicrobial use. Zoonoses Public Health 2016, 63, 241–250. [Google Scholar] [CrossRef] [PubMed]
  37. Bai, X.; Wang, H.; Xin, Y.; Wei, R.; Tang, X.; Zhao, A.; Sun, H.; Zhang, W.; Wang, Y.; Xu, Y.; et al. Prevalence and characteristics of Shiga toxin-producing Escherichia coli isolated from retail raw meats in China. Int. J. Food Microbiol. 2015, 200, 31–38. [Google Scholar] [CrossRef] [PubMed]
  38. Magiorakos, A.P.; Srinivasan, A.; Carey, R.B.; Carmeli, Y.; Falagas, M.E.; Giske, C.G.; Harbarth, S.; Hindler, J.F.; Kahlmeter, G.; Olsson-Liljequist, B.; et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: An international expert proposal for interim standard definitions for acquired resistance. Clin. Microbiol. Infect. 2012, 18, 268–281. [Google Scholar] [CrossRef] [Green Version]
  39. Souvorov, A.; Agarwala, R.; Lipman, D.J. SKESA: Strategic k-mer extension for scrupulous assemblies. Genome Biol. 2018, 19, 153. [Google Scholar] [CrossRef] [Green Version]
  40. Shen, W.; Le, S.; Li, Y.; Hu, F. SeqKit: A cross-platform and ultrafast toolkit for FASTA/Q file manipulation. PLoS ONE 2016, 11, e0163962. [Google Scholar] [CrossRef]
  41. Chin, C.-S.; Alexander, D.H.; Marks, P.; Klammer, A.A.; Drake, J.; Heiner, C.; Clum, A.; Copeland, A.; Huddleston, J.; Eichler, E.E.; et al. Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data. Nat. Methods 2013, 10, 563–569. [Google Scholar] [CrossRef]
  42. Joensen, K.G.; Tetzschner, A.M.; Iguchi, A.; Aarestrup, F.M.; Scheutz, F. Rapid and easy in silico serotyping of Escherichia coli isolates by use of whole-genome sequencing data. J. Clin. Microbiol. 2015, 53, 2410–2426. [Google Scholar] [CrossRef] [Green Version]
  43. Feldgarden, M.; Brover, V.; Haft, D.H.; Prasad, A.B.; Slotta, D.J.; Tolstoy, I.; Tyson, G.H.; Zhao, S.; Hsu, C.-H.; McDermott, P.F.; et al. Validating the AMRFinder tool and resistance gene database by using antimicrobial resistance genotype-phenotype correlations in a collection of isolates. Antimicrob. Agents Chemother. 2019, 63. [Google Scholar] [CrossRef] [Green Version]
  44. Jia, B.; Raphenya, A.R.; Alcock, B.; Waglechner, N.; Guo, P.; Tsang, K.K.; Lago, B.A.; Dave, B.M.; Pereira, S.; Sharma, A.N.; et al. CARD 2017: Expansion and model-centric curation of the comprehensive antibiotic resistance database. Nucleic Acids Res. 2017, 45, D566–D573. [Google Scholar] [CrossRef]
  45. Gordon, N.C.; Price, J.R.; Cole, K.; Everitt, R.; Morgan, M.; Finney, J.; Kearns, A.M.; Pichon, B.; Young, B.; Wilson, D.J.; et al. Prediction of Staphylococcus aureus antimicrobial resistance by whole-genome sequencing. J. Clin. Microbiol. 2014, 52, 1182–1191. [Google Scholar] [CrossRef] [Green Version]
  46. Leaché, A.D.; Banbury, B.L.; Felsenstein, J.; de Oca, A.N.-M.; Stamatakis, A. Short tree, long tree, right tree, wrong tree: New acquisition bias corrections for inferring SNP phylogenies. Syst. Biol. 2015, 64, 1032–1047. [Google Scholar] [CrossRef] [Green Version]
  47. Croucher, N.J.; Page, A.J.; Connor, T.R.; Delaney, A.J.; Keane, J.A.; Bentley, S.D.; Parkhill, J.; Harris, S.R. Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins. Nucleic Acids Res. 2015, 43, e15. [Google Scholar] [CrossRef] [Green Version]
  48. Page, A.J.; Taylor, B.; Delaney, A.J.; Soares, J.; Seemann, T.; Keane, J.A.; Harris, S.R. Rapid efficient extraction of SNPs from multi-FASTA alignments. Microb. Genom. 2016, 2, e000056. [Google Scholar] [CrossRef] [Green Version]
  49. Nguyen, L.-T.; Schmidt, H.A.; von Haeseler, A.; Minh, B.Q. IQ-TREE: A fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol. Biol. Evol. 2015, 32, 268–274. [Google Scholar] [CrossRef]
  50. Zhou, X.; Shen, X.-X.; Hittinger, C.T.; Rokas, A. Evaluating fast Maximum Likelihood-based phylogenetic programs using empirical phylogenomic data sets. Mol. Biol. Evol. 2018, 35, 486–503. [Google Scholar] [CrossRef] [Green Version]
Antibiotics 10 00074 g001 550
Figure 1. Distribution of minimum inhibitory concentration (MIC) values of 19 antimicrobials among the 298 non-O157 STEC isolates tested in this study.
Figure 1. Distribution of minimum inhibitory concentration (MIC) values of 19 antimicrobials among the 298 non-O157 STEC isolates tested in this study.
Antibiotics 10 00074 g001
Antibiotics 10 00074 g002 550
Figure 2. Phylogenetic (cladogram) tree based on core-genome single nucleotide polymorphisms (SNPs) using the Maximum-Likelihood method. The Maximum-Likelihood tree was based on core-genome SNPs of the 298 non-O157 STEC strains from different sources used in this study with strain Sakai (BioSample: SAMN01911278) as a reference. After the removal of recombined regions, a phylogenetic tree was built using 1662 SNP sites by IQ-TREE, which was then visualized and annotated by iTOL. The blue circle on the branch indicates the bootstraps (≥ 60%) of the node. The outer circle indicates the AMR phenotype, with a white background indicating antimicrobial susceptible strains and red indicating MDR. The inner circles (A–K) show the heat map of the AMR genes, red in the white background means the presence of a specific AMR gene. The outermost text indicates the isolate name. Isolates from different sources are indicated using different colors (yellow, sheep; blue, cattle; green, pig; and red, human).
Figure 2. Phylogenetic (cladogram) tree based on core-genome single nucleotide polymorphisms (SNPs) using the Maximum-Likelihood method. The Maximum-Likelihood tree was based on core-genome SNPs of the 298 non-O157 STEC strains from different sources used in this study with strain Sakai (BioSample: SAMN01911278) as a reference. After the removal of recombined regions, a phylogenetic tree was built using 1662 SNP sites by IQ-TREE, which was then visualized and annotated by iTOL. The blue circle on the branch indicates the bootstraps (≥ 60%) of the node. The outer circle indicates the AMR phenotype, with a white background indicating antimicrobial susceptible strains and red indicating MDR. The inner circles (A–K) show the heat map of the AMR genes, red in the white background means the presence of a specific AMR gene. The outermost text indicates the isolate name. Isolates from different sources are indicated using different colors (yellow, sheep; blue, cattle; green, pig; and red, human).
Antibiotics 10 00074 g002
Table
Table 1. The distribution of multidrug resistance (MDR) among the 298 non-O157 STEC isolates.
Table 1. The distribution of multidrug resistance (MDR) among the 298 non-O157 STEC isolates.
No. of Antimicrobial GroupsNo. of Resistant Isolates from Different Sources (%)Total
CattleSheepPigHuman
075 (93.8)85 (53)0 (0.0)23 (69.7)183 (61.4)
11 (1.3)14 (8.8)3 (12.0)2 (6.1)20 (6.7)
21 (1.3)5 (3)1 (4.0)3 (9.1)10 (3.4)
≥33 (3.8) a56 b (35.0)21 (84.0) c5 (15.2) a,b85 (28.5)
Note: The same superscript letter (a, b, c) means no significant difference between the two sources.
Table
Table 2. Antibiotic resistance-related genes among the 298 genome-sequenced non-O157 STEC isolates.
Table 2. Antibiotic resistance-related genes among the 298 genome-sequenced non-O157 STEC isolates.
Antibiotic ClassNo. of Isolates (%)
(No. of Isolates)Resistance GenesCattleSheepPigHuman
ChloramphenicolscmlA51 (50.0)---
50cmlA61 (50.0)-4 (66.6)-
floR-37 (90.2)--
cmlA5 + floR-3 (7.3)--
cmlA6 + floR--2 (33.3)-
catB3 + catA1---1 (100)
TrimethoprimdfrA121 (33.3)1 (2.3)6 (37.5)-
50dfrA141 (33.3)36 (83.7)1 (6.2)-
dfrA171 (33.3)1 (2.3)6 (37.5)2 (66.6)
dfrA15-5 (11.6)2 (12.5)1 (33.3)
dfrA12 + dfrA14--1 (6.2)-
MacrolidesmphA2 (100)45 (100)-3 (100)
53mefB--2 (66.6)-
ermB + mphA--1 (33.3)-
QuinolonesqnrS11 (100)48 (87.2)-1 (100.0)
66qnrB17-5 (9.0)--
oqxAB-1 (1.8)5 (55.5)-
qnrS1 + oqxAB-1 (1.8)4 (44.4)-
Sulfonamidessul11 (33.3)8 (28.5)4 (21.0)2 (28.5)
57sul21 (33.3)11 (39.2)2 (10.5)3 (42.8)
sul31 (33.3)5 (17.89)5 (26.3)-
sul1 + sul2-3 (10.7)4 (21.0)2 (28.5)
sul1 + sul3--3 (15.7)-
sul2 + sul3-1 (3.5)--
sul1 + sul2 + sul3--1(5.2)-
TetracyclinestetA3 (100.0)21 (84.0)21 (84.0)7 (77.7)
90tetA + tetD-4 (16.0)4 (16.0)2 (22.2)
FosfomycinsfosA31 (25.0)---
8fosA73 (75.0)1 (100)-3 (100)
class A β-lactamaseblaTEM-11 (50.0)39 (92.8)4 (66.6)1 (50.0)
52blaCTX-M-551 (50.0)1 (2.3)1 (16.6)-
blaCTX-M-65-2 (4.7)--
blaCTX-M-65--1 (16.6)-
+blaTEM-1
blaCTX-M-15---1 (50.0)
+blaTEM-1
Colistinmcr-1--7 (87.5)-
8mcr-3--1 (12.5)-
Rifampinarr-21 (100)7 (58.3)--
13arr-3-5 (41.6)--
Aminoglycosidesant(3″)-Ia1 (33.3)7 (23.3)4 (21.1)1 (16.7)
58aac(3)-IIa + aph(3″)-Ib + aph(6)-Id-10 (33.3)-1 (16.7)
aph(3″)-Ib + aph(6)-Id-4 (13.3)-2 (33.3)
aph(3″)-Ib + aph(3′)-Ia+ aph(6)-Id + ant(3″)-Ia--6 (31.6)-
aph(3″)-Ib + aph(6)-Id + ant(3″)-Ia-1 (3.3)1 (5.3)2 (33.3)
aac(3)-IV + aph(3″)-Ib + aph(3′)-Ia + aph(4)-Ia + aph(6)-Id + ant(3″)-Ia-4 (13.3)--
others2 (66.6)4 (13.3)8 (42.1)-
Table
Table 3. Correspondence between drug-resistant phenotypes and genotypes of genes associated with resistance to seven classes of antimicrobials.
Table 3. Correspondence between drug-resistant phenotypes and genotypes of genes associated with resistance to seven classes of antimicrobials.
Antimicrobial AgentNo. of Phenotypic Resistant IsolatesNo. of Phenotypic Susceptible IsolatesSensitivity (%)Specificity (%)
Susceptible by GenotypeResistant by GenotypeSusceptible by GenotypeResistant by Genotype
Chloramphenicol650242089100
Quinolone *3738195285187
Aminoglycoside11239575081
Macrolide65023938999
Tetracycline889200192100
Trimethoprim-Sulfamethoxazole933255179100
Colistin26289175100
* Quinolone results were based on nalidixic acid.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Pan, Y.; Hu, B.; Bai, X.; Yang, X.; Cao, L.; Liu, Q.; Sun, H.; Li, J.; Zhang, J.; Jin, D.; et al. Antimicrobial Resistance of Non-O157 Shiga Toxin-Producing Escherichia coli Isolated from Humans and Domestic Animals. Antibiotics 2021, 10, 74. https://doi.org/10.3390/antibiotics10010074

AMA Style

Pan Y, Hu B, Bai X, Yang X, Cao L, Liu Q, Sun H, Li J, Zhang J, Jin D, et al. Antimicrobial Resistance of Non-O157 Shiga Toxin-Producing Escherichia coli Isolated from Humans and Domestic Animals. Antibiotics. 2021; 10(1):74. https://doi.org/10.3390/antibiotics10010074

Chicago/Turabian Style

Pan, Yanyu, Bin Hu, Xiangning Bai, Xi Yang, Lijiao Cao, Qian Liu, Hui Sun, Juan Li, Ji Zhang, Dong Jin, and et al. 2021. "Antimicrobial Resistance of Non-O157 Shiga Toxin-Producing Escherichia coli Isolated from Humans and Domestic Animals" Antibiotics 10, no. 1: 74. https://doi.org/10.3390/antibiotics10010074

APA Style

Pan, Y., Hu, B., Bai, X., Yang, X., Cao, L., Liu, Q., Sun, H., Li, J., Zhang, J., Jin, D., & Xiong, Y. (2021). Antimicrobial Resistance of Non-O157 Shiga Toxin-Producing Escherichia coli Isolated from Humans and Domestic Animals. Antibiotics, 10(1), 74. https://doi.org/10.3390/antibiotics10010074

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop