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Article

F18:A-:B1 Plasmids Carrying blaCTX-M-55 Are Prevalent among Escherichia coli Isolated from Duck–Fish Polyculture Farms

by
Li-Juan Zhang
1,2,3,
Jin-Tao Yang
2,4,
Hai-Xin Chen
2,4,
Wen-Zi Liu
4,
Yi-Li Ding
3,
Rui-Ai Chen
1,4,
Rong-Min Zhang
2,4,* and
Hong-Xia Jiang
2,4,*
1
Zhaoqing Branch Center of Guangdong Laboratory for Lingnan Modern Agricultural Science and Technology, Zhaoqing 526000, China
2
Guangdong Key Laboratory for Veterinary Pharmaceutics Development and Safety Evaluation, College of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, China
3
Life Science Department, Foshan University, Foshan 528000, China
4
Guangdong Laboratory for Lingnan Modern Agriculture, Guangzhou 510642, China
*
Authors to whom correspondence should be addressed.
Antibiotics 2023, 12(6), 961; https://doi.org/10.3390/antibiotics12060961
Submission received: 5 May 2023 / Revised: 22 May 2023 / Accepted: 22 May 2023 / Published: 25 May 2023
(This article belongs to the Special Issue Molecular Characterization of Gram-Negative Bacteria: Antimicrobial Resistance, Virulence and Epidemiology)
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Abstract

:
We determined the prevalence and molecular characteristics of blaCTX-M-55-positive Escherichia coli (E. coli) isolated from duck–fish polyculture farms in Guangzhou, China. A total of 914 E. coli strains were isolated from 2008 duck and environmental samples (water, soil and plants) collected from four duck fish polyculture farms between 2017 and 2019. Among them, 196 strains were CTX-M-1G-positive strains by PCR, and 177 (90%) blaCTX-M-1G-producing strains were blaCTX-M-55-positive. MIC results showed that the 177 blaCTX-M-55-positive strains were highly resistant to ciprofloxacin, ceftiofur and florfenicol, with antibiotic resistance rates above 95%. Among the 177 strains, 37 strains carrying the F18:A-:B1 plasmid and 10 strains carrying the F33:A-:B- plasmid were selected for further study. Pulse field gel electrophoresis (PFGE) combined with S1-PFGE, Southern hybridization and whole-genome sequencing (WGS) analysis showed that both horizontal transfer and clonal spread contributed to dissemination of the blaCTX-M-55 gene among the E. coli. blaCTX-M-55 was located on different F18:A-:B1 plasmids with sizes between ~76 and ~173 kb. In addition, the presence of blaCTX-M-55 with other resistance genes (e.g., tetA, floR, fosA3, blaTEM, aadA5 CmlA and InuF) on the same F18:A-:B1 plasmid may result in co-selection of resistance determinants and accelerate the dissemination of blaCTX-M-55 in E. coli. In summary, the F18:A-:B1 plasmid may play an important role in the transmission of blaCTX-M-55 in E. coli, and the continuous monitoring of the prevalence and transmission mechanism of blaCTX-M-55 in duck–fish polyculture farms remains important.

1. Introduction

Antimicrobial resistance is a serious global public health problem associated with significant clinical, economic and social impacts. Escherichia coli exists as part of the commensal microbiota in the mammalian digestive tract, as a zoonotic pathogen responsible for intestinal and extraintestinal infections in both humans and animals [1,2]. Globally, the emergence of multidrug-resistant (MDR) E. coli producing extended-spectrum β-lactamase (ESBL) enzymes has led to empirical therapy failure, leading to high morbidity and mortality, which has raised great public concern [1,2].
Currently, CTX-M-bearing E. coli is the most common species related to ESBLs and more than 220 CTX-M family members have been identified. These variants were divided into five major groups (groups 1, 2, 8, 9 and 25) based on their amino acid homology. Among these groups, 1 and 9 were the most common globally [2,3,4]. Over the past decade, CTX-M-55, as a variant of CTX-M-15, from animal-origin E. coli, which was first discovered in Thailand in 2006, has spread rapidly in dozens of countries around the world, especially in China [4,5,6]. The dissemination of blaCTX-M-55 was mainly caused by plasmid-mediated gene horizontal transfer, and epidemic self-mobilizable F33:A-:B, IncI1, IncI2 and IncHI2 plasmids played an important role in the transmission of blaCTX-M-55 [6,7,8]. In addition to animals, blaCTX-M-55 is also distributed in food products and humans, and frequently co-localized with other resistance genes, such as fosA3, rmtB, mcr-1, blaTEM, tet(A) and floR [7,8,9,10]. The wide distribution of blaCTX-M-55 and the co-transfer of blaCTX-M-55 with different resistance genes worldwide represent a growing threat to public health.
As the largest producer and consumer of cultivated duck in the world, duck production plays a major role in the agricultural economy of China [11]. Duck farming in China is practiced on a large and diverse scale, and the integrated culture of fish–duck farming using untreated duck manure as fish feed, is the typical farming method throughout coastal areas of China, particularly in Guangdong Province. Previous studies have shown that fish–duck integrated farming systems have become a hotspot environment for the occurrence and proliferation of antibiotic resistance genes (ARGs) and antibiotic-resistant bacteria (ARB), which can facilitate the spread of resistance genes and have the potential to be the reservoir of novel ARGs [12,13,14]. Owing to the threat of blaCTX-M-55 to public health and the risks of ARG transmission in fish–duck farming, monitoring the prevalence of blaCTX-M-55-positive E. coli isolates from duck–fish polyculture farms should receive more attention.
However, CTX-M-55 has been widely reported in E. coli isolated from food animals, pets and humans in China [6,8,15]. Current data on the prevalence, genetic information and the transmission mechanism of CTX-M-55-producing E. coli from duck–fish polyculture farms are still limited. In this study, we investigated the prevalence of blaCTX-M-55 and illustrated the characteristics of blaCTX-M-55-bearing E. coil and plasmids recovered from ducks and the environment in duck–fish polyculture farms. Our findings emphasize the importance of the surveillance of ESBL-producing E. coli in duck–fish polyculture farms in China and provide knowledge for further One Health studies to control the spread of resistant bacteria from food animals to humans.

2. Results

2.1. Identification of blaCTX-M-55-Positive E. coli Isolates

A total of 196 blaCTX-M-1G-positive E. coli isolates were obtained from 2008 different samples, and the blaCTX-M-1G-producing E. coli-positive rates from duck fecal samples, water, soil and foliage were 14.4% (138/957), 6.25% (31/496), 1.5% (7/476) and 1.3% (1/79), respectively (Table S1). Six different CTX-M-1G subtypes were obtained from the 196 blaCTX-M-1G-positive strains, including CTX-M-55 (177 strains), CTX-M-79 (8 strains), CTX-M-123 (5 strains), CTX-M-3 (3 strains), CTX-M-64 (2 strains) and CTX-M-224 (only 1 strain). Among the 177 CTX-M-55-positive strains, 77.9% (138/177) were isolated from fecal samples, 17.5% (31/177) were isolated from water, 4.0% (7/177) were isolated from soil and only 1 (1/177, 0.6%) isolate was obtained from foliage (Table S1).
The antimicrobial susceptibility results showed that the 177 E. coli isolates were highly resistant to ceftiofur, ciprofloxacin and florfenicol, with resistance rates of 98.3%, 96.7% and 95.4%, respectively. The rates of resistance to colistin, ceftazidime and fosfomycin were 35.0%, 31.7% and 29.9%, respectively. However, these strains were less resistant to tigecycline, meropenem and amikacin, and the resistance rates were less than 10% (Table S2).
To further understand the molecular characteristics of blaCTX-M-55-positive E. coli, the PCR-base replicon typing (PBRT) method was performed on the 177 strains. The results showed that 19.2% (34/177), 6.2% (11/177), 1.7% (3/177) and 1.1% (2/177) of the strains carried the IncT, IncN, IncHI1 and IncP plasmids, respectively, and 10.7% (19/177) and 5.6% (10/177) of the strains carried IncY and IncI1 plasmids, respectively. Notably, 81.4% (144/177) of the strains carried IncF plasmids. We further performed F plasmid replicon sequencing typing (RST) on these 144 IncF-type plasmid-carrying strains. The results showed that F18:A-:B1-plasmid-carrying strains accounted for the largest proportion, with 37 (37/144, 25.7%) strains, followed by F33:A-:B-plasmid-carrying strains, with 10 (10/144, 6.9%) strains carrying this type of plasmid and the remaining 97 strains carrying other types of IncF plasmids.
Based on the above results, we selected the 37 F18:A-:B1-plasmid-carrying strains and 10 F33:A-:B-plasmid-carrying strains for further study of the characteristics and transmission mechanism of plasmids carrying blaCTX-M-55-positive E. coli. Among the 47 isolates, the number of strains from duck fecal samples was the largest, accounting for 81% (38/47), followed by the strains from water samples, accounting for 13% (6/47). The remaining 6.4% (3/47) of strains were isolated from soil samples (Figure 1).

2.2. Molecular Characterization of blaCTX-M-55-Positive E. coli

PFGE was successfully performed for all 47 selected strains, and the PFGE results were divided into 15 different clusters according to similarity >85%, indicating the genetically different backgrounds of strains from different sources. In addition, two clusters of strains with the same PFGE spectrum were derived from the different types of samples from farms B, C and D (TC5, UD5, RD1, B1W1, UD9 and D7), suggesting that there is clonal transmission among different farms (Figure 1).
The conjugation results indicated that 17 of the 47 strains could successfully transfer blaCTX-M-55 from the donor strain to the recipient strain E. coli C600, and the transfer frequency was between 2.6 × 10−5 and 4.65 × 10−1 (Table S3). There were four strains that could transfer blaCTX-M-55 from the donor strain to the recipient strain E. coli J53 with conjugative transfer frequencies between 3.89 × 10−6 and 8.35 × 10−5. The remaining 26 strains showed unsuccessful transfer of blaCTX-M-55 from the donor strain to the recipient strain after multiple attempts (Table S3). To further determine the location of the blaCTX-M-55 gene in the non-conjugatively transferable strains and the genetic environment of the blaCTX-M-55 gene, whole-genome sequencing was performed on all 47 strains. Sequence analysis showed that among the 26 non-conjugable strains, the blaCTX-M-55 gene was located on the chromosome of 11 strains, while the blaCTX-M-55 gene of the remaining 15 strains was located on plasmids.

2.3. Genomic Analysis of blaCTX-M-55-Positive E. coli

Whole-genome sequencing data were generated for the 47 blaCTX-M-55-positive E. coli isolates. The results of WGS demonstrated that these isolates belonged to seventeen distinct strains (STs). Among them, the most dominant ST type was ST602, with a total of nine (9/47, 19%) strains belonging to this ST type; followed by ST155, ST410 and ST2179 (five, 10.6% each); ST48, ST162 and ST354 (three, 6.4% each); and ST165 and ST224 (two, 4.3% each). Of the remaining eight ST types, only one strain belonged to each ST type.
We identified 14 ARGs that mediated resistance to 9 types of antibiotics that coexisted with blaCTX-M-55 in these 47 E. coli isolates. These included genes that mediated resistance to fosfomycin, colistin, tetracycline, aminoglycosides, chloramphenicol, quinolones, macrolides, sulfonamides and lincomycin. Among these, 26% (12/47) and 13% (6/47) of the strains carried the quinolone resistance genes oqxAB and qnrS, respectively. In addition, 38% (18/47) of the strains carried the colistin resistance gene mcr-1, and 26% (12/47) and 21% (10/47) of the strains carried the fosfomycin resistance genes fosA3 and fosA7.5, respectively. Eleven percent (5/47) of the strains carried the chloramphenicol resistance gene floR, and thirteen percent (6/47) of the strains carried the lincomycin resistance gene lnuF. Interestingly, our results showed that all strains belonging to ST602 carried the fosfomycin resistance gene fosA7.5, and fosA7.5 was located on the chromosome. Additionally, all ST410 strains carried the lnuF gene, and the blaCTX-M-55 gene carried by the ST410 strains in the current study could not be transferred by conjugation (Figure 1 and Table S3).
Genetic environment analysis showed that blaCTX-M-55 was present in four genomic contexts, including types I, II, III and IV. The structure of type I was ISEcp1-blaCTX-M-55-orf477, which was the most prevalent, and was isolated in a total of 21 (45%) strains originating from feces, soil and water (Table S3 and Figure S1). The structure of type II was ΔIS26-ΔISEcp1-blaCTX-M-55-orf477-ΔTn2, and there were 12 (26%) strains belonging to this genetic environment. There were 10 (21%) strains belonging to the type III genetic environment, and the structure of type III was ΔIS26-ΔISEcp1-blaCTX-M-55-orf477-ΔTn2-ΔIS26. The type IV genetic environment was more complex, and its structure was ΔTn2-ISEcp1-blaCTX-M-55-orf477-ΔTn2-ΔIS26. Only three isolates belonged to this genetic environment. Notably, among the strains belonging to the type I genetic structure, the blaCTX-M-55 gene of the ten strains was located on the plasmid, and the blaCTX-M-55 gene of the other eleven strains was located on the chromosome. The blaCTX-M-55 gene in the strains belonging to the type II and type III genetic structures were all located on the plasmid. Among the strains with type IV genetic structure, one strain had the blaCTX-M-55 gene located on the chromosome, and blaCTX-M-55 in the other two strains was located on plasmids (Table S3 and Supplementary Figure S1).

2.4. Complete Sequence Analysis of blaCTX-M-55-Carrying F18:A-:B1 Plasmids

To better understand the characteristics of the blaCTX-M-55-bearing F18:A-:B1 plasmid, S1-PFGE and Southern blotting were performed on the 12 conjugants successfully obtained from the F18:A-:B1 plasmid harboring blaCTX-M-55-positive strains. The results showed that blaCTX-M-55 from 12 strains was located on F18:A-:B1 plasmids with sizes between ~76 kb and ~173 kb (Supplementary Figure S2). To further explore the sequence features of the F18:A-:B1 plasmid, four representative strains (PBS4, B1W1, B1S11 and KW21) were subjected to long-read sequencing to obtain the complete sequence of different F18:A-:B1 plasmids. The complete sequences of the F18:A-:B1 plasmids pPBS4, pB1W1, pB1S11 and pKW21 were obtained by long-read combined with short-read sequencing, and detailed information on the four plasmids is shown in Supplementary Table S4.
Sequence analysis revealed that all four plasmids were novel IncF18:A-:B1 plasmids, three (pBS4, pB1W1 and pKW21) of which carried blaCTX-M-55, and the remaining plasmid (pB1S11) did not carry blaCTX-M-55. In strain B1S11, blaCTX-M-55 was located on an IncHI2 plasmid. Linear comparison revealed that the backbone of the four F18:A-:B1 plasmids was similar to that of other typical IncF plasmids containing regions for functions of replication (repA, repB), conjugal transfer (tra, trb), partitioning (parA, parB) and maintenance and stability (pemI, pemK, stbA). Notably, in the plasmid pB1W1, ~29-kb conjugative regions containing the traV, traR, traC, traW, traU, traN, traF, traH, traG, traD, traT, traS, trbD, trbG, trbI, trbB, trbJ and trbF genes were lacking, which may explain the conjugative transfer failure of pB1W1 (Figure 2). Basic Local Alignment Search Tool (BLAST) analysis indicated that the four plasmids (pBS4, pB1W1, pB1S11 and pKW21) had high similarity to the blaCTX-M-55-carrying plasmid pTREC8 of an E. coli strain isolated from wetland sediment in the United States (GenBank accession no. MN158991.1) and shared high identities of 99.9%, 100%, 99.9% and 99.8%, respectively (Figure 2).
Although the F18:A-:B1 plasmid possessed a conserved backbone region, the variable regions, especially multidrug resistance regions, were distinct. The multidrug resistance region of pKW21 was 80,273 bp, which is quite different from the resistance regions of the other three F18:A-:B1 plasmids in this study. The ~80.3 kb MDR region contained 11 ARGs (blaCTX-M-55, aac(3′)-IIa, aph(3′)-Ib, mph(A), aph(6′)-Id, tet(R), tet(A), floR, blaTEM-1B, fosA3 and aadA5) with one or two copies, interspersed with different complete or truncated insertion sequences and transposons (IS26, IS4 family, ΔTn3, ΔTn2, ΔISEcp1, ΔIS1R, IS5075, IS91 and ISCfr1) (Figure 3a). BLAST analysis showed that the ~80.3 kb region shared a high identity (>99.99%) with plasmids collected from humans and pigs that did not bear blaCTX-M-55, such as E. coli plasmid p14406-FII (GenBank accession no. MN823988), p13P484A-2 (GenBank accession no. CP019282) and pTEM-1-GZC065 (GenBank accession no. CP048026). Compared with p14406-FII, p13P484A-2 and pTEM-1-GZC065, the difference was that three regions of pKW21 (IS26-aph(3′)-Ib-IS26-mph(A)-IS26, IS26-hp-hp-hp-IS26-hp-hp-IS26 and IS26-hp-hp-hp-ΔTn2-hp-tet(R)-tet(A)-hp-ΔTn2-IS26-hp-hp-IS26) were inverted. Notably, there was a region of pKW21 (~33 kb) containing blaCTX-M-55 that completely mismatched with the compared plasmids (Figure 3a).
The MDR regions of pB1W1, pB1S11 and pPBS4 were ~46.0 kb, ~26.5 kb and ~38.9 kb, respectively. Even though the resistance genes in the three plasmids were varied, they all contained floR, tet(A) and tet(R) and blaCTX-M-55, except pB1S11. In addition to the mentioned genes, the pB1S1 MDR region also contained the quinolone resistance gene qnrS1, which was highly similar to pGSH8M-2-1 (GenBank accession no. AP019676.1) and shared 99.8% identify with 100% coverage. pGSH8M-2-1 was recovered from the effluent of a wastewater treatment plant in Tokyo Bay, and the only difference in the MDR region between pGSH8M-2-1 and pB1S11 was that an IS26 was inserted between two ΔTn2 in pB1S11 (Figure 3b). Compared with pB1S11, pB1W1 and pPBS4 contained more resistance genes and carried multiple copies of IS26 and transposons. BLAST analysis did not detect plasmids with high homology to the MDR region of pPBS4 and pB1W1, which may suggest that multiple copies of IS26 and transposons formed the distinctive MDR regions of pPBS4 and pB1W1 through multiple complex recombination events. Notably, although pPBS4 and pB1W1 were derived from the same farm (Farm B), the genetic environments of blaCTX-M-55 in pPBS4 and pB1W1 were different, indicating that the blaCTX-M-55 in these two plasmids originated from different sources (Figure 3b). In addition, we also found a truncated class I integron in the plasmid pB1W1 (Figure 3b).

3. Materials and Methods

3.1. Sampling Information, Bacterial Isolation and Identification

From March 2017 to August 2019, a total of 2008 nonduplicate samples including 496 water samples, 476 soil samples, 957 duck fecal samples and 79 foliage samples were collected from four duck–fish polyculture farms in the Panyu District of Guangzhou, China (Figure 1; see also Table S1 in the Supplemental Material). All samples were screened for cefotaxime-resistant E. coli by a selective isolation procedure. In brief, each sample was suspended in 10 mL of buffered peptone water (BPW; BD Difco, Sparks, MD, USA) and incubated at 37 °C for 24 h. Then, subsequent selective cultivation on MacConkey (MC; BD Difco) agar supplemented with 1 mg/L cefotaxime (CTX) was performed. For each sample, only one red colony was selected and identified as E. coli by MALDI-TOF MS AximaTM (Shimadzu-Biotech Corp., Kyoto, Japan) and 16S rRNA sequencing by Sanger sequencing. In all cefotaxime-resistant E.coli, blaCTX-M-1G was detected by PCR using previously reported primers [16] and sequencing (Supplementary Table S1).

3.2. Antimicrobial Susceptibility Testing

Antibiotic susceptibility testing was performed by the agar dilution method and interpreted according to the Clinical and Laboratory Standards Institute guidelines (CLSI M100-S29) for the following antimicrobials: amikacin, meropenem, cefotaxime, ceftazidime, ceftiofur, florfenicol, ciprofloxacin and fosfomycin [17]. Susceptibility to colistin and tigecycline was assessed by broth microdilution as recommended by the European Committee on Antimicrobial Susceptibility Testing (EUCAST Version 9.0) [18]. E. coli ATCC 25922 was used as the quality control strain.

3.3. Molecular Typing

The incompatibility (Inc) groups of all blaCTX-M-55-producing E. coli were assigned by PCR-base replicon typing (PBRT) [19]. To better characterize IncFII plasmid, replicon sequencing typing (RST) was performed, according to protocols described previously [20]. Based on the results of PBRT analysis, a total of 47 strains (37 strains harboring the F18:A-:B1 plasmid and 10 strains harboring the F33:A-:B- plasmid) were selected for further study to explore the transmission characteristics and molecular mechanism of blaCTX-M-55 in these strains.
The genetic typing of the 47 selected blaCTX-M-55-producing E. coli isolates was performed by digestion with restriction endonuclease XbalI and pulsed-field gel electrophoresis (PFGE) according to our previous study [21]. The band patterns were analyzed with BioNumerics software version 5.10 (Applied Maths, Austin, TX, USA).

3.4. Conjugation Assay and Southern Blotting

To investigate the transferability of the resistance genes, a conjugation assay was performed for all selected blaCTX-M-55-positive E.coli isolates with streptomycin-resistant E. coli C600 or sodium-azide-resistant E. coli J53 as the recipient strain. For E. coli C600, donor strains and E. coli C600 were mixed and applied to a 0.22 μm filter in Luria-Bertani (LB) plates for 16~18 h. The mixed culture was then diluted and spread on selective MacConkey agar plates containing both 1 mg/L of cefotaxime and 2 g/L of streptomycin to recover transconjugants. For E. coli J53, donor strains and E. coli J53 were mixed and applied to a 0.22 μm filter in LB plates for 16–18 h. The mixed culture was then diluted and spread on selective MacConkey agar plates supplemented with 0.5 mg/L cefotaxime and 0.2 g/L sodium azide. Transconjugants were confirmed by PCR. S1-PFGE and Southern blotting were performed to determine plasmid size according to previous study, and the Salmonella enterica serotype, Braenderup H9812, was used as the standard size marker [22].

3.5. DNA Extraction and Whole-Genome Sequencing

Total DNA was extracted from 47 blaCTX-M-55-producing E. coli isolates using a Genomic DNA Purification Kit (TIANGEN, Beijing, China) according to the manufacturer’s instructions. WGS was performed with the Illumina HiSeq 2500 System (Novogene Guangzhou, China) using the paired-end 2 × 150-bp sequencing protocol. The draft genome was assembled using the tools available at EnteroBase (https://enterobase.warwick.ac.uk/species/ecoli, accessed on 28 November 2020) with default parameters. All genome assemblies of the 47 sequenced E. coli isolates were deposited in GenBank and are registered with BioProject number PRJNA934699. Then, the sequence types, replicon types and antibiotic resistance genes of all the sequenced isolates were identified by the Center for Genomic Epidemiology (http://www.genomicepidemiology.org/, accessed on 20 March 2021). Four representative strains (PBS4, B1W1, B1S11 and KW21) were further selected for whole-genome sequencing on the PacBio RS II sequencing platform (Biochip Company, Tianjin, China) to obtain the complete sequence of the F18:A-:B1 plasmid. Sequences of those strains were assembled using HGAP version 4.0. to analyze the genetic features. BRIG (Vision 0.95) and Easyfig (Vision 2.2.5) software were used for comparative analysis with other plasmid sequences published in NCBI. The complete sequence of the plasmid was annotated and analyzed using RAST (https://rast.nmpdr.org/rast.cgi, accessed on 12 March 2021), ISfinder (https://www-is.biotoul.fr/, accessed on 20 March 2021), Resfinder (https://cge.cbs.dtu.dk//services/ResFinder/, accessed on 22 March 2021) and BLAST (https://blast.ncbi.nlm.nih.gov/Blast.cgi, accessed on 23 March 2021).

3.6. Nucleotide Sequence Accession Numbers

The complete sequences of the plasmids (pPBS4, pB1W1, pB1S11 and pKW21) have been deposited in GenBank under accession numbers CP117716, CP117722, CP117718 and CP117673.

4. Discussion

Duck–fish polyculture is a common circular farming model in the Pearl River Delta in southern China, specifically in Guangdong Province. In this model, duck manure is discharged directly without treatment, and a large number of ARGs or residual agents can directly contaminate fish ponds, promoting the transmission of ARGs between ducks and fish [14,23,24]. Previous studies have shown that fish–duck integrated farming systems have become a hotspot environment for the occurrence and proliferation of ARGs and ARB, and both ARGs and pathogen-related ARB have been detected in the water and sediment of this culture system [12,13,14]. Moreover, fish–duck integrated aquaculture farms have significantly higher levels of antibiotic resistance compared to monoculture fish farms, suggesting a higher risk of transmission of ARGs and mobile genetic elements (MGEs) to humans or the environment [13]. The Pearl River Delta water system is intricate, which provides a unique opportunity to develop freshwater aquaculture, but there is also the risk of contaminating river or sea areas on a large scale by ARG and ARB dissemination via aquatic water or sediment [24,25]. Based on the “one health” concept, considering the common duck–fish freshwater aquaculture system in the Pearl River Delta in southern China, greater attention should be given to the transfer risk of ARGs in integrated duck–fish farming to promote the healthy development of Chinese aquaculture and the environment.
In this study, the antibiotic susceptibility of 177 blaCTX-M-55-positive strains was tested with 10 antibiotics commonly used in both veterinary and human medicine. The results showed that the blaCTX-M-55-positive strains were highly resistant strains, and almost all strains were multidrug-resistant. In addition to resistance to cephalosporins, they were also highly resistant to ciprofloxacin and florfenicol (with resistance rates at 96.7 and 95.4%, respectively). These strains also had a high resistance rate to ceftazidime (31.7%), colistin (35.0%) and fosfomycin (29.9%), and the resistance rate to tigecycline, meropenem and amikacin was less than 10%. Two recent studies also showed that E. coli strains isolated from ducks and the environment were not only resistant to cephalosporins but also resistant to chloramphenicols, aminoglycosides, quinolones and tetracyclines. Our results were similar to those reported in their study. Notably, the rate of detection of strains carrying the blaCTX-M-55 gene was higher than that of strains without this gene for both the antibiotic resistance spectra and ARGs [10,26].
Previous studies have shown that blaCTX-M-55 is mainly transmitted by the horizontal transfer of epidemical plasmids, and IncI1 and F33:A-:B- plasmids were the most important types of plasmids that mediated the spread of blaCTX-M-55 in human and animal E. coli in China [6,15]. In the present study, we selected 37 blaCTX-M-55-positive strains carrying the F18:A-:B1 plasmid and 10 blaCTX-M-55-positive strains carrying the F33:A-:B- plasmid to explore the transmission mechanism and molecular characteristics of blaCTX-M-55 among these strains. The PFGE results showed that the 47 strains could be divided into 15 different clusters, and the genetic backgrounds were relatively different. However, strains from different farms also had the same PFGE profile. CTX-M-positive E. coli isolates from ducks in Korea also had significant differences in PFGE profiles, but the same PFGE profiles were found in different livestock farms and slaughterhouses, which was consistent with the results of our study [27].
Multilocus sequence typing results indicated that ST602, ST155, ST410 and ST2179 were the prevalent ST types in our study, and the internationally prevalent ST10 and ST131 clones were not detected. ST602 has not been widely reported in previous studies, but a recent epidemiological surveillance of ESBL E. coli from human and food-chain-derived samples from England, Wales and Scotland found that the CTX-M-1G-positive ST602 strain was widely present in chicken samples [28]. Notably, all ST602 strains carried the blaCTX-M-55 gene chromosomally, and co-carried the chromosomal fosfomycin resistance gene fosA7.5. fosA7.5 is a new member of the fosfomycin resistance gene fosA7 gene family recently reported in E. coli isolates in Canadian hospitals. Its distribution is limited to E. coli, and it can be located on both plasmids and chromosomes [29]. Because fosfomycin was effective as a first-line therapy for urinary tract infections, the emergence of fosA7.5 and blaCTX-M-55 co-carrying ST602 clone needs more attention.
ST410 E. coli is an emerging multidrug-resistant pathogen. Two major sublineages are currently circulating in Europe and North America, one is a fluoroquinolone- and extended-spectrum cephalosporin-resistant clade that emerged in the 1980s, and the other is a carbapenem-resistant clone that emerged in 2003. ST410 has been considered a “high-risk” clone similar to ST131 owing to its high transmissibility, its capacity to cause recurrent infections and its ability to persist in the gut [30,31]. This clone has also been found to harbor mcr-1 in isolates recovered from food and human samples worldwide, and tet(X)-carrying ST410 E. coli in China and South Asia has been recently reported [10,31,32,33]. Given the potential of ST 410 E. coli to acquire resistance to last-resort antimicrobials, this clone should arouse regional and global concern.
The genetic contexts of blaCTX-M-55 were divided into four types in the current study. In the genetic context of type III (ΔIS26-ΔISEcp1-blaCTX-M-55-orf477-ΔTn2-ΔIS26) and type IV (ΔTn2-ISEcp1-blaCTX-M-55-orf477-ΔTn2-ΔIS26), ΔTn2 and ΔIS26 were located both downstream and upstream of ΔISEcp1/ISEcp1-blaCTX-M-55-orf477’s structure. This structure was found not only in E. coli but also in Klebsiella, Vibrio parahaemolyticus and Salmonella. This structure, possible formed by a copy of IS26 and an ISEcp1-mediated transposon carrying blaCTX-M-55 and orf477, was inserted into a tnpA gene; this finding stresses the need for further assessment of the mobility of IS26 or its variant [34].
Plasmids play a key role in the horizontal transfer of the ESBL gene among E. coli strains. Our results suggest that the F18:A-:B1 plasmid may play an important role in the transmission of the blaCTX-M-55 gene in E. coli isolated from duck farms and the environment. The F18:A-:B1 plasmid was first reported in avian pathogenic E. coli in 2010. It is characterized by the lack of an iron uptake gene (eitABCD), hemagglutinin and a survival gene. The blaCTX-M-55-bearing F18:A-:B1 plasmid was first reported in E. coli isolated from patients with urinary tract infections in the United States in 2016, and carried the mcr gene [20,33]. Subsequently, the F18:A-:B1-plasmid-carrying blaCTX-M-55 was reported in E. coli isolated from human clinical samples in China [35]. Recently, a study in Southeast Asia reported that the highly pathogenic clone E. coli ST410 isolated from the environment and humans carried the blaCTX-M-55-bearing F18:A-:B1 plasmid with a high prevalence [30]. In addition, studies from Tunisia and China also reported the high prevalence of the F18:A-:B1 subtype in animal-derived E. coli strains, which also contained fosA3, oqxAB, blaCTX-M-14 and other resistance genes [36,37,38]. These studies emphasize the possibility of horizontal transfer of the F18:A-:B1 plasmid between humans and animals.
However, to the best of our knowledge, only one recent study reported blaCTX-M-55, floR and fosA3 carrying the F18:A-:B1 plasmid obtained from ducks [10]. Our study is the first to report the high prevalence of the blaCTX-M-55-carrying F18:A-:B1 plasmid in E. coli isolated from duck–fish polyculture farms. Complete plasmid sequence analysis showed that blaCTX-M-55 was colocalized with tetA, floR, fosA3, blaTEM, aadA5, aph(3′)-Ib, aph(6′)-Id, CmlA, InuF and other ARGs on the F18:A-:B1 plasmid. These ARGs, linked by different kinds of insertion sequences and transposable sequences and multiple copies of IS26, constitute the complex multidrug resistance region of the F18:A-:B1 plasmid. IS26 is commonly associated with ARGs in multidrug-resistant Gram-negative and Gram-positive species, and is most widespread in Gram-negative bacteria. Clusters of ARGs can be generated by directly oriented IS26 interspersed in multiple resistant pathogens [34,39]. As the best-studied member of the IS26 family, IS26 is known to form cointegrates using conservative transposition, homologous recombination and replicative transposition [39,40]. Multiple copies of IS26 with different orientations located on the F18:A-:B1 plasmid are very likely to form cointegrates to promote the transmission of ARGs.

5. Conclusions

We reported the high prevalence of blaCTX-M-55-carrying E. coli isolated from duck–fish polyculture farms. Both horizontal transfer and clonal spread contributed to the dissemination of the blaCTX-M-55 gene among E. coli strains isolated from ducks and their environment, and the F18:A-:B1 plasmid may play an important role in the spread of blaCTX-M-55. Coexistence of blaCTX-M-55 and other resistance genes (eg., tetA, floR, fosA3, blaTEM, aadA5 CmlA, InuF) on the same F18: A-: B1 plasmid may result in the co-selection of these resistance determinants and accelerate the dissemination of blaCTX-M-55 in E. coli. In addition, our study is the first to report the emergence of a fosA7.5 and blaCTX-M-55 co-carrying ST602 clone in E. coli isolated from ducks and soil. These findings emphasize the importance of the ongoing surveillance of blaCTX-M-55-positive E. coli in duck–fish polyculture farms in China.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/antibiotics12060961/s1, Table S1: Sample and isolate information from different sources; Table S2: The MIC results of 177 blaCTX-M-55-positive E. coli strains; Table S3: Bacterial information and antimicrobial resistance profiles; Table S4: Characteristics of sequenced strains and obtained F18:A-:B1 plasmids and Figure S1: Comparison of four types of blaCTX-M-55 genomic contexts in 47 strains. Figure S2: Pulsed field gels of S1 digested genomic DNA and Southern blot in-gel hybridization with blaCTX-M-55 probe. M: H9812, 1-12: blaCTX-M-55-positive transconjugants MA121, D5, KW21, PBS4, KS22, PBS10, BT2, PBS5, PBS13, PBS21, UD1 and A44.

Author Contributions

H.-X.J., R.-M.Z. and L.-J.Z. conceived the research. J.-T.Y., H.-X.C. and L.-J.Z. carried out the experiments. H.-X.J., R.-M.Z., W.-Z.L. and L.-J.Z. collected and analyzed the data. L.-J.Z. drafted the manuscript, and H.-X.J., R.-M.Z., R.-A.C. and Y.-L.D. revised the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by grants from the National Natural Science Foundation of China (NSFC) (31972734), the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2019BT02N054) and the independent project of Zhaoqing Branch Center of Guangdong Laboratory for Lingnan Modern Agricultural Science and Technology (P20211154-0101-09).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The whole genome sequence generated in this study is available from the National Center for Biotechnology Information (Accession No. PRJNA934699).

Conflicts of Interest

The authors declare no conflict of interest.

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Antibiotics 12 00961 g001 550
Figure 1. Pulsed-field gel electrophoresis fingerprinting patterns of XbaI-digested total DNA preparations from 47 strains harboring blaCTX-M-55. In yellow is indicated the PBRT classification, in red are indicated antimicrobial resistance genes.
Figure 1. Pulsed-field gel electrophoresis fingerprinting patterns of XbaI-digested total DNA preparations from 47 strains harboring blaCTX-M-55. In yellow is indicated the PBRT classification, in red are indicated antimicrobial resistance genes.
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Figure 2. Circular sequence alignments of the plasmids pKW21, pB1W1, pB1S11, pPBS4 and pTREC8. Genes depicted in the outer circle belong to plasmid pKW21, which was included as a reference, and the image was generated using BRIG.
Figure 2. Circular sequence alignments of the plasmids pKW21, pB1W1, pB1S11, pPBS4 and pTREC8. Genes depicted in the outer circle belong to plasmid pKW21, which was included as a reference, and the image was generated using BRIG.
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Antibiotics 12 00961 g003a 550Antibiotics 12 00961 g003b 550
Figure 3. Comparison of the multidrug resistance regions of F18:A-:B1 plasmids identified in this study. (a) Comparison of pKW21 with similar plasmids p14406-FII (GenBank accession no. MN823988), p13P484A-2 (GenBank accession no. CP019282) and pTEM-1-GZC065 (GenBank accession no. CP048026). (b) Comparison of pB1S11, pPBS4 and pB1W1 with the similar plasmid pGSH8M-2-1 (GenBank accession no. AP019676.1). Genes are denoted by arrows. Genes, mobile elements and other features are colored based on functional classification. Shaded regions denote shared DNA homology (>95% nucleotide identity).
Figure 3. Comparison of the multidrug resistance regions of F18:A-:B1 plasmids identified in this study. (a) Comparison of pKW21 with similar plasmids p14406-FII (GenBank accession no. MN823988), p13P484A-2 (GenBank accession no. CP019282) and pTEM-1-GZC065 (GenBank accession no. CP048026). (b) Comparison of pB1S11, pPBS4 and pB1W1 with the similar plasmid pGSH8M-2-1 (GenBank accession no. AP019676.1). Genes are denoted by arrows. Genes, mobile elements and other features are colored based on functional classification. Shaded regions denote shared DNA homology (>95% nucleotide identity).
Antibiotics 12 00961 g003aAntibiotics 12 00961 g003b
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Zhang, L.-J.; Yang, J.-T.; Chen, H.-X.; Liu, W.-Z.; Ding, Y.-L.; Chen, R.-A.; Zhang, R.-M.; Jiang, H.-X. F18:A-:B1 Plasmids Carrying blaCTX-M-55 Are Prevalent among Escherichia coli Isolated from Duck–Fish Polyculture Farms. Antibiotics 2023, 12, 961. https://doi.org/10.3390/antibiotics12060961

AMA Style

Zhang L-J, Yang J-T, Chen H-X, Liu W-Z, Ding Y-L, Chen R-A, Zhang R-M, Jiang H-X. F18:A-:B1 Plasmids Carrying blaCTX-M-55 Are Prevalent among Escherichia coli Isolated from Duck–Fish Polyculture Farms. Antibiotics. 2023; 12(6):961. https://doi.org/10.3390/antibiotics12060961

Chicago/Turabian Style

Zhang, Li-Juan, Jin-Tao Yang, Hai-Xin Chen, Wen-Zi Liu, Yi-Li Ding, Rui-Ai Chen, Rong-Min Zhang, and Hong-Xia Jiang. 2023. "F18:A-:B1 Plasmids Carrying blaCTX-M-55 Are Prevalent among Escherichia coli Isolated from Duck–Fish Polyculture Farms" Antibiotics 12, no. 6: 961. https://doi.org/10.3390/antibiotics12060961

APA Style

Zhang, L.-J., Yang, J.-T., Chen, H.-X., Liu, W.-Z., Ding, Y.-L., Chen, R.-A., Zhang, R.-M., & Jiang, H.-X. (2023). F18:A-:B1 Plasmids Carrying blaCTX-M-55 Are Prevalent among Escherichia coli Isolated from Duck–Fish Polyculture Farms. Antibiotics, 12(6), 961. https://doi.org/10.3390/antibiotics12060961

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