ORIGINAL RESEARCH article
Sec. Antimicrobials, Resistance and Chemotherapy
Volume 13 - 2022 | https://doi.org/10.3389/fmicb.2022.918561
Clonal Dissemination of Aeromonas hydrophila With Binary Carriage of blaKPC-2-Bearing Plasmids in a Chinese Hospital
- Clinical Microbiology Laboratory, The Second Affiliated Hospital of Zhejiang University School of Medicine, Zhejiang University, Hangzhou, China
Dissemination of the Klebsiella pneumoniae carbapenemase (KPC)-encoding gene among Enterobacterales is common but relatively rare in Aeromonas spp. In this study, we characterized two KPC-2-producing Aeromonas hydrophila strains (Ah2101 and Ah2111), each isolated from a patient in different intensive care units (ICUs) of a Chinese hospital. Whole-genome sequencing (WGS) revealed simultaneous carriage of the blaKPC−2 and imiH genes, both of which encode high-level carbapenem resistance in these two A. hydrophila isolates. The two isolates were shown to be clonally related and each isolate harbored two distinguishable blaKPC−2-bearing plasmids, only one of which was transferrable to A. hydrophila, but not Escherichia coli EC600 via conjugation. The genetic element that contains blaKPC−2 in these two plasmids, namely ISKpn27-ΔblaTEM−1-blaKPC−2-ISKpn6, was structurally identical, commonly detected in Enterobacterales, and associated with Tn3-based transposons. In addition, more than sixty putative genes that encode various virulence factors were identified in these two A. hydrophila isolates. This is the first study that reports clonal dissemination of carbapenem-resistant A. hydrophila strains carrying structurally different blaKPC−2-bearing plasmids. Further investigation is warranted to monitor the future transmission of blaKPC−2-bearing plasmids in A. hydrophila in clinical settings.
Global dissemination of carbapenemase-producing organisms (CPOs) is an emerging public health issue, with the potential of further compromising the effectiveness of treatment of bacterial infection. Klebsiella pneumoniae carbapenemase (KPC), which is encoded by the plasmid-borne gene blaKPC, possesses a large and shallow active site, allowing such an enzyme to accommodate and hydrolyze a wide range of β-lactam molecules, including cephalosporins, monobactams, and carbapenems (Bush and Bradford, 2020). KPC producers are not only resistant to most β-lactams but also display a multidrug resistance phenotype as they also carry additional resistance genes which confer resistance to many of the currently available first-line therapeutic alternatives (Munoz-Price et al., 2013). Meanwhile, infections caused by KPC-producing organisms are associated with high mortality rates of up to 51%, thus imposing a heavy burden on the healthcare sector (Giacobbe et al., 2015). Since its first description in 1996 (Yigit et al., 2001), genetic elements encoding these types of carbapenemase have spread extensively among Gram-negative bacteria. In China, such an enzyme was identified for the first time in a K. pneumoniae isolate collected in Zhejiang Province in 2004 (Wei et al., 2007). KPC-2 is the most prevalent carbapenemase in China, with K. pneumoniae being the most common host species that produces such an enzyme. The high mobility of genetic elements carrying the blaKPC gene implies that such elements can be readily disseminated to other Gram-negative bacteria including those of the genus Aeromonas (Picao et al., 2013).
Aeromonas spp. are ubiquitous organisms widely distributed in various aquatic environmental niches and may act as opportunistic pathogens that cause a number of self-limiting gastrointestinal infections and extra-intestinal infections, including those of the skin, soft tissue, and wound, as well as pneumonia and bacteremia (Janda and Abbott, 2010; Nolla-Salas et al., 2017). In recent years, multidrug-resistant Aeromonas strains have been isolated from clinical, animal, food, and environmental samples (Tang et al., 2020). In particular, carbapenem-resistant strains exhibit a prevalence rate ranging from 0.5 to 7.7% in different countries. Aeromonas spp. producing KPC-2 carbapenemases have also been successively isolated in the past decades from environmental samples in Brazil (Montezzi et al., 2015), the United States (van Duin and Doi, 2017; Mathys et al., 2019), Japan (Sekizuka et al., 2019), and China (Xu et al., 2018; Hu et al., 2019), indicating that the strains of this genus may serve as a vector for dissemination of the blaKPC−2 gene. Although KPC-2-producing Aeromonas spp. were once isolated from routine perirectal surveillance in hospitalized adult patients in the United States (Hughes et al., 2016), this type of strain was rarely detected in clinical settings. Here, we report the recovery of two structurally different blaKPC−2-bearing plasmids from two clinical isolates of A. hydrophila. Genome analysis based on whole-genome sequencing (WGS) data was performed to reveal the genetic relatedness between these two strains and shed light on the genetic environment of blaKPC−2 genes, as well as the molecular features of plasmids that harbor such genes.
Materials and Methods
The Patients and Bacterial Strains
Two Aeromonas spp. (strains Ah2101 and Ah2111) were isolated from two patients hospitalized in intensive care units (ICUs) of The Second Affiliated Hospital of Zhejiang University School of Medicine in 2021. The species identity of the test strains was determined by MALDI-TOF MS (Bruker Daltonik GmbH, Bremen, Germany). A comparison of genomes between the reference strain (A. hydrophila OnP3.1, GenBank accession no. NZ_CP050851.1) and the two isolates was performed by using the average nucleotide identity (ANI) calculator (http://enve-omics.ce.gatech.edu/ani/index). The result showed that the ANI values between A. hydrophila OnP3.1 and strain Ah2101, and between A. hydrophila OnP3.1 and strain Ah2111 were 96.86% and 96.87%, respectively, confirming that both isolates belonged to A. hydrophila. This study was approved by the Ethics Committee of The Second Affiliated Hospital of Zhejiang University School of Medicine, and consents were given by the patients or their families.
Patient A, a 52-year-old male, was admitted to the emergency ICU due to skull fractures and traumatic intracranial hemorrhage caused by a traffic accident in January 2021. After seven days of empirical therapy with piperacillin/tazobactam (8:1, 4.5 g IV for every 8 h), the patient developed complications that involved severe intracranial infection and the treatment strategy was then changed to the use of meropenem (1 g IV for every 8 h). On the second day of administration, the cerebrospinal fluid culture grew two carbapenem-resistant strains of A. hydrophila (strain Ah2101) and Acinetobacter baumannii. A course of tigecycline treatment (100 mg IV for every 12 h) was then applied according to the antimicrobial susceptibility results, and these two isolates were cleared from the cerebrospinal fluid after 4 days of treatment. Unfortunately, the patient became critically ill without indications of the benefit of another operation upon thorough assessment; only supportive treatment was given and the prognosis was grave. Finally, the patient was discharged at the request of the family.
Patient B, a 75-year-old female with mitral stenosis and cardiac dysfunction, underwent mitral valve replacement and was admitted to the cardiac ICU in September 2021. After hospitalization for 1 month, the patient suffered from abdominal pain and developed a fever. CT examination suggested cholecystitis and peritoneal effusion. Cholecystostomy and abdominal catheterization/drainage were then performed and a course of imipenem (500 mg IV for every 8 h) was started. On the 25th day of treatment, a carbapenem-resistant A. hydrophila strain, Ah2111, was isolated from the drainage sample. Fortunately, the patient's condition gradually improved upon receipt of various supportive treatments and continuous drainage of peritoneal effusion. The second culture of the drainage fluid for 8 days after the initial isolation was negative for A. hydrophila. The drainage volume decreased gradually and the drainage tube was removed 2 weeks later. The patient was ultimately discharged from the hospital.
Antimicrobial Susceptibility Testing (AST)
The minimal inhibitory concentrations (MICs) of 15 antimicrobial agents, including imipenem, meropenem, ertapenem, ceftazidime, cefotaxime, cefepime, piperacillin/tazobactam, cefoperazone/sulbactam, aztreonam, ciprofloxacin, amikacin, chloramphenicol, tetracycline, trimethoprim/sulfamethoxazole, and ceftazidime/avibactam were determined using the broth microdilution method and interpreted according to the Clinical and Laboratory Standards Institute (CLSI) guidelines (Clinical Laboratory Standards Institute, 2015, 2021). Escherichia coli ATCC 25922, E. coli ATCC 35218, and Pseudomonas aeruginosa ATCC 27583 were used as the quality control strains in parallel.
Whole-Genome Sequencing (WGS) and Genome Analysis
The genomic DNA extracted from A. hydrophila Ah2101 and Ah2111 was subjected to WGS by using the Illumina NovaSeq 6000 platform with a paired-end read length of 150 bp (NEBNext Ultra DNA Library Prep Kit) and the sequencing data were de novo assembled into contigs using SPAdes version 3.13.1 (Bankevich et al., 2012). A. hydrophila strain Ah2111 was also subjected to sequencing by the Oxford Nanopore PromethION 48 system; hybrid genome assembly of both short and long reads was carried out by using the Unicycler version 0.4.4 software (Wick et al., 2017). Assembled genomes and blaKPC−2-bearing plasmids were annotated by the RAST server (https://rast.nmpdr.org/) (Overbeek et al., 2014). A pairwise comparison of genomes and variant callings for single-nucleotide polymorphisms (SNPs) was conducted using Snippy version 4.4.5 with default settings (https://github.com/tseemann/snippy). Carriage of the antimicrobial resistance genes and the Inc-type of plasmids for the assembly scaffolds were determined with default settings by ResFinder 3.2 (Zankari et al., 2012) and PlasmidFinder 2.0 (Carattoli et al., 2014), respectively, at the Center for Genomic Epidemiology (https://cge.cbs.dtu.dk/services/). Visualization of genome comparison for blaKPC−2-harboring plasmids was implemented using BRIG (version 0.95) (Alikhan et al., 2011). The virulence factors in A. hydrophila were identified using the VFanalyzer (http://www.mgc.ac.cn/VFs/main.htm).
Transferability of the BlaKPC-2 Gene
Conjugation experiments based on the filter mating method were performed to access the transferability of the plasmid-mediated blaKPC−2 gene; a blaKPC−2-positive K. pneumoniae strain K1 reported in our previous study was used as the positive control strain (Cai et al., 2008). Apart from rifampicin-resistant E. coli EC600, an induced-rifampicin-resistant A. hydrophila (strain AhRF100), which was susceptible to carbapenems (Table 1), was also employed as the recipient strain. The putative transconjugants that grew on the MacConkey agar plates supplemented with 50 mg/L rifampicin and 0.3 mg/L meropenem were identified by MALDI-TOF MS and screened for the acquisition of the blaKPC−2 gene by PCR. The conjugation frequency was calculated as the ratio of the number of transconjugants to the number of donors.
Table 1. Antimicrobial susceptibility of A. hydrophila Ah2101 and Ah2111, the corresponding transconjugants, and plasmid-eliminated strains.
Plasmid elimination assays were performed for both A. hydrophila Ah2101 and Ah2111 with repeated sodium dodecyl sulfate (SDS) treatment in Luria-Bertani (LB) broth. For every passage, 100 μl of the culture was added to a subculture of 5 ml fresh LB broth containing 4% SDS, followed by overnight incubation at 37°C with shaking (200 rpm). The culture (20 μl) was then placed and streaked on LB plates, from which 30 single colonies were selected for assessment of carriage of the blaKPC−2 gene by PCR. The serial transfer and SDS treatment experiment were conducted until the blaKPC−2-bearing plasmids were eliminated from the parent isolates.
Nucleotide Sequence Accession Numbers
The genome of A. hydrophila Ah2101 and the complete genome sequence of A. hydrophila Ah2111 containing one chromosome and seven plasmids have been deposited into the NCBI database under BioProject accession number PRJNA823662 and GenBank accession numbers JALKAG000000000 and CP095280 to CP095287.
Antimicrobial Susceptibility Results
A. hydrophila strains Ah2101 and Ah2111 exhibited similar antimicrobial susceptibility profiles characterized by high-level resistance to β-lactams including carbapenems. MIC values of imipenem, meropenem, ertapenem, ceftazidime, cefotaxime, cefepime, piperacillin/tazobactam, cefoperazone/sulbactam, and aztreonam were above 128 mg/L. Both Aeromonas strains were also resistant to ciprofloxacin and amikacin but remained susceptible to ceftazidime/avibactam, chloramphenicol, tetracycline, and trimethoprim/sulfamethoxazole (Table 1).
Whole-Genome and Phylogenetic Analysis
The genome of the two A. hydrophila strains, both of a size of ~5.2 Mbp, was obtained. Whole-genome analysis revealed carriage of a variety of β-lactamase-encoding genes in both strains, including blaKPC−2, ΔblaTEM−1, blaPER−3, ampH, and imiH. Among these genes, imiH is known to encode a species-specific metallo-β-lactamase (MBL), which is a member of the CphA family that selectively hydrolyzes penems and carbapenems rather than penicillin and cephalosporins (Bush and Bradford, 2020). Multiple antimicrobial resistance determinants were also detected, conferring resistance to quinolone (qnrS2), chloramphenicol (catB3), macrolide [mph(A)], quaternary ammonium compounds (qacE), sulfonamides (sul1), and aminoglycosides [armA, aadA16, aac(6′)-Ib, and rmtB]. These two isolates, which share similar virulence gene profiles, produce various virulence factors, including pili, polar flagella, the type VI secretion system (T6SS), Exe T2SS, aerolysin, hemolysin, the repeat in toxin A (RtxA), and heat-stable cytotonic enterotoxin, which are responsible for adherence, effector delivery, motility, and production of exotoxin during the infection process. In addition, several genes encoding nutritional or metabolic factors which may be associated with bacterial virulence were identified (Supplementary Table S1).
To determine the genetic relatedness of A. hydrophila strains Ah2101 and Ah2111, a genome-based phylogenetic analysis was performed. The result showed that the two isolates differed by only eight SNPs and a deletion of a 33-bp fragment among a total of 5,079 putative genes, indicating that they belonged to the same clone despite the fact that they were recovered from two patients in different wards in the same hospital at dates that were 10 months apart. The eight SNPs were detected in one non-coding region and seven coding sequences (CDS), generating missense mutations in genes encoding the histidine permease YuiF, a methyl-accepting chemotaxis sensor/transducer protein, the MSHA biogenesis protein MshG, the sensory histidine kinase CreC, and a tail-specific protease precursor, as well as synonymous mutations in genes that encode a transcriptional regulator YidZ and an uncharacterized protein YfjI. In contrast, the 33-bp deletion was detected in a CDS that encodes a putative lipoprotein (Table 2).
Molecular Characteristics and Transferability of BlaKPC-2-Bearing Plasmids
To determine the location and genetic context of the blaKPC−2 gene, A. hydrophila Ah2111, which was closely related to strain Ah2101 according to the result of phylogenetic analysis which showed that they exhibited differences of only eight SNPs and one deletion, was subjected to long-read sequencing, and the complete genome of the size of around 5.3 Mbp was obtained. The complete sequence of A. hydrophila Ah2111 comprised a chromosome of 5,035,848 bp in length as well as seven plasmids. Two blaKPC−2-carrying plasmids designated as pAh2111-2-KPC and pAh2111-6-KPC, respectively, were identified and found to differ significantly in size (96,480 vs. 18,193 bp) and plasmid structure. Apart from blaKPC−2, an rmtB gene, which can mediate the expression of high-level resistance to aminoglycosides including amikacin, was also located in the plasmid pAh2111-2-KPC. The qnrS2 gene was another plasmid-borne antimicrobial resistance gene located in a third plasmid, whereas the other resistance genes were chromosomally located. Based on the sequences of pAh2111-2-KPC and pAh2111-6-KPC, two structurally similar blaKPC−2-carrying plasmids were obtained from A. hydrophila Ah2101 by PCR mapping. Further analysis showed that the homology of the backbone for plasmid pAh2111-2-KPC exhibited the highest degree of sequence homology to the plasmid pAsa8-b (GenBank accession no. CP039630) in the Aeromonas caviae strain R25-2, with 97.94% identity (Figure 1A). A cluster of tra genes was conserved in plasmids recovered from Aeromonas spp., suggesting that this plasmid originated from this genus. Another blaKPC−2-carrying plasmid, pAh2111-6-KPC, shared 99.54% similarity in 42% of the sequence with plasmid pCRE3-KPC (GenBank accession no. MH919378), which was from Citrobacter braakii, including the blaKPC−2 gene locus in the length of 3,667 bp (Figure 1B). Sequence alignment of the replication gene rep of this plasmid revealed 95.24% identity to a variety of plasmid-borne rep genes from Aeromonas spp. and the lack of the tra module, suggesting that this plasmid was non-conjugative. Unlike some IncP-6-type blaKPC−2-carrying plasmid in Aeromonas spp. (Hu et al., 2019; Sekizuka et al., 2019), the two plasmids tested in this study were found to belong to an unknown Inc-type.
Figure 1. Comparison of two blaKPC−2-carrying plasmids pAh2111-2-KPC (A) and pAh2111-6-KPC (B) with the reference plasmids. The five circles from inside to outside displayed the scale in kilobase pairs, the GC skew, the GC content, level similarity to the reference plasmids, and annotation of the plasmids tested in this study, respectively.
Transferability and Elimination of BlaKPC-2-Bearing Plasmids
Conjugation experiments were conducted to evaluate the intra- and inter-species transferability of two blaKPC−2-bearing plasmids. Both A. hydrophila Ah2101 and Ah2111 were capable of transferring the blaKPC−2 gene to A. hydrophila AhRF100, with a conjugation efficiency of 2.9 × 10−4 and 7.7 × 10−4, respectively. The functionality of blaKPC−2 genes in A. hydrophila transconjugants (A. hydrophila AhRF100-2101-TC and AhRF100-2111-TC) was further verified by antimicrobial susceptibility tests, with results showing that both transconjugant strains exhibited elevated MICs of carbapenems (ranging from 16 to 128 mg/L) when compared with the recipient strain (Table 1). To distinguish between the two blaKPC−2-bearing plasmids, PCR amplification using two pairs of primers that target the rep genes of plasmids pAh2111-2-KPC and pAh2111-6-KPC, respectively, was performed. Both A. hydrophila transconjugants of A. hydrophila Ah2101 and Ah2111 were only positive for the rep gene of plasmid pAh2111-2-KPC. This finding, which was consistent with the high-level amikacin resistance phenotype observed in transconjugants, confirmed the horizontal transferability of pAh2111-2-KPC between two different A. hydrophila strains. However, conjugative transfer of carbapenem resistance to E. coli EC600 was unsuccessful.
Both blaKPC−2-carrying plasmids in A. hydrophila Ah2101 and Ah2111 were eliminated, followed by the SDS treatment in three passages. The MICs of imipenem and meropenem of filial strains for A. hydrophila Ah2111 and Ah2101 (A. hydrophila Ah2101-PE and Ah2111-PE) decreased by more than 8-fold when compared to parent strains. In addition, susceptibility of the two plasmid-eliminated strains to piperacillin/tazobactam, cefoperazone/sulbactam, and amikacin was restored (Table 1).
Genetic Context of the BlaKPC-2 Genes
Analysis of the genetic environment surrounding the blaKPC−2 genes that suggested a highly similar genetic structure of “ISKpn27-ΔblaTEM−1-blaKPC−2-ISKpn6” was shared by plasmid pAh2111-2-KPC and pAh2111-6-KPC of 3,984 bp and 3,667 bp, respectively. In plasmid pAh2111-2-KPC, an integration structure of Tn3-based transposon was found located upstream of ISKpn27 and formed the transposable unit “ΔTn3-ISKpn27-ΔblaTEM−1-blaKPC−2-ISKpn6,” which was common in blaKPC-bearing plasmids in Enterobacterales. An example is K. pneumoniae strain WCHKP13F2 isolated from Chengdu, China (GenBank accession no. CP028389.3). A previous study demonstrated that Tn3-based transposons might mediate the dissemination of the blaKPC−2 gene between different Enterobacterales in China (Shen et al., 2009). As this Tn3-based transposon cannot be conjugated to E. coli EC600, it is conceivable that this Enterobacterales-bearing genetic element plays a role in mediating mobilization and further dissemination of the blaKPC−2 gene to plasmids in Aeromonas spp.
Aeromonas spp. thrive in aquatic environments and are regarded as enteric pathogens of limited pathogenicity (Janda and Abbott, 2010). In the past few decades, isolation of KPC-producing Aeromonas spp. from environmental samples is uncommon; similarly, nosocomial infections due to Aeromonas spp. are rare. In this study, we reported the clonal spread of two blaKPC−2-carrying A. hydrophila strains recovered from clinical samples of patients in ICUs with prior carbapenem exposure. The emergence and dissemination of these isolates were possibly associated with antibiotic therapy. Previous reports on blaKPC−2-carrying Aeromonas spp. in clinical settings have only involved sporadic isolation of a single clinical strain (Tang et al., 2020). Our study showed that there is a risk for clonal dissemination of such strains, presumably due to the selective pressure of β-lactams. Furthermore, a 10-month interval between the isolation of A. hydrophila strains Ah2101 and Ah2111 indicated that these strains may act as blaKPC−2 gene reservoirs that persist for a long period of time in the hospital environment, potentially causing life-threaten infectious diseases, especially among ICU patients who have weakened immunity and often require antimicrobial treatment.
Two blaKPC−2-carrying plasmids of different sizes harbored by A. hydrophila Ah2101 and Ah2111 were also characterized and a similar genetic structure of “ISKpn27-ΔblaTEM−1-blaKPC−2-ISKpn6” was identified. This structure was frequently detected in Enterobacterales and commonly associated with a Tn3-based transposon, which had been reported in a variety of IncP-6 plasmids of Aeromonas strains recovered from both environmental and clinical samples (Hu et al., 2019; Sekizuka et al., 2019). Most of these types of plasmids were detected in China; however, both blaKPC−2-carrying plasmids in this study belonged to an unknown Inc-type. Furthermore, conjugation experiments with E. coli EC600 and A. hydrophila AhRF100 as the recipient strains yielded the opposite results, suggesting that horizontal transfer of the plasmid pAh2111-2-KPC was restricted to the same species or genus. Given the high degree of sequence homology between the backbone of pAh2111-2-KPC and that of plasmids from Aeromonas spp., it is assumed that the spread of the blaKPC−2 gene to Aeromonas spp. might not be mediated by the transmission of the blaKPC−2-carrying plasmids from Enterobacterales.
The structural plasticity of Tn3-based transposons was also demonstrated previously through the identification of various truncated blaTEM−1 genes which typically constitute the Tn3 transposons, with or without carriage of Tn3-transposase and resolvase-encoding variant genes (Shen et al., 2009; Yang et al., 2013). The diversity of this genetic structure explains the difference between the genetic environments of these two blaKPC−2-carrying plasmids and why they appeared to form through different mechanisms. We therefore reasonably speculate that the transposition event mediated by Tn3-based transposon from Enterobacterales results in integration of the blaKPC−2-containing fragment into the backbones of inherent plasmids of Aeromonas spp., thereby generating the blaKPC−2-carrying plasmids like pAh2111-2-KPC. The establishment of another plasmid in our study was presumably due to horizontal transfer facilitated by insertion sequences flanking the blaKPC−2 gene without the Tn3-based transposons; alternatively, it is possible that genes encoding Tn3-transposase and its resolvase were lost upon transposition during the process of dissemination of this plasmid. Moreover, the genus Aeromonas is naturally transformable under optimal conditions, and most Aeromonas spp. prefer to acquire DNA from close relatives (Huddleston et al., 2013); therefore, the horizontal transferability between the Aeromonas spp. for these blaKPC−2-bearing plasmids is a concern if we need to prevent and control the dissemination of resistance elements in this genus.
This study reported the identification of the blaKPC−2 gene located in a conserved genetic structure in two closed-related clinical isolates of A. hydrophila which shared a similar virulence gene profile. Such structure was most likely derived from Enterobacterales. Both Aeromonas isolates displayed high-level resistance to carbapenems encoded by both the chromosomal MBL gene imiH and two blaKPC−2 genes located in two distinct plasmids, one of which can undergo horizontal transfer between Aeromonas spp. To the best of our knowledge, this is the first report of clonal spread of KPC-producing A. hydrophila which carries two blaKPC−2-bearing plasmids in clinical settings. Hence, nosocomial surveillance for blaKPC−2 reservoirs should not be limited to Enterobacterales, but also other Gram-negative bacteria with standard workup established under the conception of “One Health.”
Data Availability Statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
JC and RZ conceived and designed the study. JC collected the A. hydrophila isolates. ZX and WS performed the experiments, analyzed the data, and drafted the manuscript. All authors revised the manuscript and approved the final version.
This study was supported by the Zhejiang Provincial Natural Science Foundation of China (LY22H200001).
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.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
The authors thank Prof. Sheng Chen (City University of Hong Kong, Hong Kong, China) for proofreading the manuscript and Associate Professor Ning Dong (Soochow University, Suzhou, China) for assistance in bioinformatics analysis.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2022.918561/full#supplementary-material
Supplementary Table S1. Virulence factors detectable in the two KPC-2-producing A. hydrophila isolates.
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Keywords: Aeromonas hydrophila, blaKPC−2, clonal spread, clinical setting, genetic environment
Citation: Xu Z, Shen W, Zhang R and Cai J (2022) Clonal Dissemination of Aeromonas hydrophila With Binary Carriage of blaKPC-2-Bearing Plasmids in a Chinese Hospital. Front. Microbiol. 13:918561. doi: 10.3389/fmicb.2022.918561
Received: 12 April 2022; Accepted: 15 June 2022;
Published: 08 July 2022.
Edited by:Masato Suzuki, National Institute of Infectious Diseases (NIID), Japan
Reviewed by:Abigail Perez-Valdespino, Instituto Politécnico Nacional (IPN), Mexico
Costas C. Papagiannitsis, University of Thessaly, Greece
Hazem Ramadan, US National Poultry Research Centre (USDA-ARS), United States
Copyright © 2022 Xu, Shen, Zhang and Cai. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jiachang Cai, firstname.lastname@example.org
†These authors have contributed equally to this work