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Comparative genomic characterization of multidrug-resistant Citrobacter spp. strains in Fennec fox imported to China
Gut Pathogens volume 13, Article number: 59 (2021)
To investigate the antimicrobial profiles and genomic characteristics of MDR-Citrobacter spp. strains isolated from Fennec fox imported from Sudan to China.
Four Citrobacter spp. strains were isolated from stool samples. Individual fresh stool samples were collected and subsequently diluted in phosphate buffered saline as described previously. The diluted fecal samples were plated on MacConkey agar supplemented with 1 mg/l cefotaxime and incubated for 20 h at 37 °C. Matrix-assisted laser desorption/ionization–time of flight mass spectrometry (MALDI–TOF–MS) was used for identification. Antimicrobial susceptibility testing was performed using the broth microdilution method. Whole-genome sequencing was performed on an Illumina Novaseq-6000 platform. Acquired antimicrobial resistance genes and plasmid replicons were detected using ResFinder 4.1 and PlasmidFinder 1.3, respectively. Comparative genomic analysis of 277 Citrobacter genomes was also performed.
Isolate FF141 was identified as Citrobacter cronae while isolate FF371, isolate FF414, and isolate FF423 were identified as Citrobacter braakii. Of these, three C. braakii isolates were further confirmed to be extended-spectrum β-lactamases (ESBL)-producer. All isolates are all multidrug resistance (MDR) with resistance to multiple antimicrobials. Plasmid of pKPC-CAV1321 belong to incompatibility (Inc) group. Comparative genomics analysis of Citrobacter isolates generated a large core-genome. Genetic diversity was observed in our bacterial collection, which clustered into five main clades. Human, environmental and animal Citrobacter isolates were distributed into five clusters.
To our knowledge, this is the first investigation of MDR-Citrobacter from Fennec Fox. Our phenotypic and genomic data further underscore the threat of increased ESBL prevalence in wildlife and emphasize that increased effort should be committed to monitoring the potentially rapid dissemination of ESBL-producers with one health perspective.
The worldwide increase and spread of infections caused by multidrug-resistant (MDR) Gram-negative bacteria of human and animal origin is a significant global public health burden in recent decades [1, 2]. Enterobacteriaceae are common bacteria and usually associated with different types of community- and hospital-acquired infections and sometimes even animal infections [3,4,5,6]. Thus, antimicrobial resistance (AMR) in these bacteria has significantly potential impacts on the control of AMR from the perspective of the One Health concept [7, 8]. Among these organisms, extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae are recognized as the most prevalent group of pathogens due to their mobility [9, 10]. Treatment of infections caused by ESBL- and AmpC-producing Enterobacteriaceae strains is challenging, due to the emergence and spread of carbapenem resistance in ESBL-producing Enterobacteriaceae isolates, which is of particular clinical relevance [11, 12].
The ESBLs are usually carried by mobile genetic elements, such as a variety of self-transferring plasmids, which can be transferred to other bacteria [13,14,15]. Thus far, several ESBL types have been identified in Enterobacteriaceae isolates of which the CTX-M, TEM, and SHV β-lactamases are the most prevalent groups [16, 17]. It is noteworthy that ESBL- and carbapenemase-producing Enterobacteriaceae occurring in animals has become a public-health issue in recent years [4, 17]. Zoonotic pathogens contributed to the cross-transmissions of ESBL-producing Enterobacteriaceae . Previously, we also reported the detection of the transmission of AMR across human, animals and environmental compartments in China [8, 19, 20].
Citrobacter spp. are common Gram-negative bacilli and widely found in water, food, soil, and intestines of animals and humans . AMR encoding genes are frequently reported in Citrobacter freundii, and it became a reservoir of antibiotic resistance genes in recent years [22, 23]. In addition, MDR C. freundii has been reported in numerous hosts including but are not limited to humans [24,25,26]. In this work, we identified four MDR Citrobacter isolates in Fennec fox imported from Sudan to China. Antimicrobial susceptibility tests, conjugation experiments, whole-genome sequencing, and comparative genomic analysis were performed to study the molecular characteristics of these MDR strains.
Isolation and identification
In this work, four Citrobacter spp. isolates resistant to cephalosporins were cultivated by selective medium plates. Among these strains, isolate FF141 was identified as Citrobacter cronae while isolate FF371, isolate FF414, and isolate FF423 were identified as Citrobacter braakii (Additional file 1: Figure S1). Of these, three C. braakii isolates were further confirmed to be ESBL-producer (Table 1).
Assessment of antibiotic susceptibility and MLST analysis
Four Citrobacter isolates are all MDR with resistance to multiple antimicrobials (Table 1). The total resistance rate was observed for cefotaxime, ceftazidime, aztreonam, and chloramphenicol (100%). All the isolates were susceptible to imipenem, meropenem, amikacin, tigecycline, and colistin. Interestingly, only FF371 was resistant to piperacillin-tazobactam. Among these Citrobacter isolates, we found two sequence types (STs), which were ST350 (FF371, FF414, and FF423) and ST370 (FF141).
Resistant and virulence determinants of Citrobacter isolates
The acquired resistance genes detected in four Citrobacter isolates are summarized in Fig. 1A. The following genes were identified in three C. braakii isolates: the phenicol resistance gene floR; the trimethoprim resistance gene dfrA17; the tetracycline resistance gene tet(A); the disinfectant resistance gene qaeE; the quinolone resistance gene qnrS1; the fluoroquinolone and aminoglycoside resistance gene aac(6ʹ)-Ib-cr, the aminoglycoside resistance genes aph(6)-Id, aac(6')-Ib3, aph(3ʺ)-Ib, aac(3)-IId, and aadA5; the macrolide resistance gene mph(A); the β-lactam resistance genes blaCTX-M-55, blaCMY-82, and blaOXA-1; the rifampicin resistance gene ARR-3; sulphonamide resistance genes sul1, and sul2. Of note, C. braakii FF414 and FF423 encoded the fosfomycin resistance gene fosA3, while C. cronae FF141 and C. braakii FF371 were negative. Among four isolates, FF141 encoded fewer resistance genes than other isolates, which carried blaCMY-98, qnrB34, tet(A), dfrA12, and aadA2. Plasmids of incompatibility (Inc) group pKPC-CAV1321, was identified in FF141, and IncR was detected in other Citrobacter braakii isolates (Additional file 2: Table S1). The antimicrobial genes dfrA12, tet(A), and aadA2 genes were co-harbored by IncR plasmid in three C. braakii isolates.
Virulence gene analysis showed that the presence of genes encoding efflux pump protein (arcB), the transport of siderophores (fepC), enterobactin (entB and entE), outer membrane protein A (ompA), extracellular nucleation factors (csgB, csgD, csgE, and csgF), and type VI secretion system-related proteins (hcp/tssD) in all isolates (Fig. 1B). Moreover, three C. braakii isolates also carried genes that involved polymer synthesis (tviB–tviE), and cell surface localization of the CPS (vexA–vexE).
Comparative genomics analysis of Citrobacter isolates
Roary matrix-based gene sequence analysis generated 60,923 total genes and a large core-genome of 1578 gene clusters of 277 whole genomes. The whole-genome phylogeny (Fig. 2) revealed a population structure. Genetic diversity was observed in our bacterial collection, which clustered into five main clades. Interestingly, C. braakii isolates have close relatedness with a clinical isolate (SAMD00112928, C. freundii) from Vietnam and an environmental strain (SAMN11928073, C. freundii), while C. cronae FF141 showed a high similarity with a clinical isolate from Nigeria (SAMN13830004, C. freundii) and a clinical isolate from India (SAMN06660612, C. freundii) (Fig. 2, Additional file 3: Table S2).
The wide dissemination of MDR Enterobacteriaceae is a global concern with one health perspective . In clinical settings, Citrobacter spp. isolates represent up to 6% of all isolated Enterobacteriaceae from clinical specimens . Members of the genus Citrobacter are reported to associate with nosocomial infections for a high mortality rate . The Citrobacter genus is most closely related to Escherichia coli and Salmonella, and is divided into 11 different genomospecies . There is some information indicating a high prevalence of MDR Enterobacteriaceae in wild animals [31, 32]. Although previous studies suggest that fur animals are potential reservoirs of AMR [5, 33], little is known about the antimicrobial patterns, and genomic characteristics of MDR Citrobacter isolates from wildlife. In the present study, we first described the isolation of MDR-Citrobacter strains from Fennec fox. We subsequently obtained the antimicrobial resistance profiles and genomic information by AST and WGS. We also identified antimicrobial resistance and virulence-associated genes.
Citrobacter spp. isolates can have chromosomal AmpC β-lactamases, as well as plasmid encoded carbapenemases, which results in ineffective of many antimicrobial agents for treatment [20, 22, 34, 35]. C. cronae was identified as a new Citrobacter species from human stool samples very recently , the antimicrobial profiles of C. cronae are largely unknow. In this study, we first identified an AmpC β-lactamase encoding gene (blaCMY-98) in C. cronae, which provides a glimpse of antimicrobial insight into this species. Occurrence of ESBL-producing C. braakii isolated from animals and food product are occasionally reported . Our detection of three ESBL-producing C. braakii isolates from Fennec fox further suggests the risk of zoonotic potential MDR C. braakii from animals and animal products deservedly garners considerable attention.
Previous investigations found that CTX-M-55 became one of the prevalent ESBL type detected among clinical, animals, and environment in some countries [13, 14, 37, 38]. Very recently, the occurrences of CTX-M-55-producing Escherichia coli were also increasingly reported in environment and diverse animal species in Europe [39, 40]. Our previous work confirmed that CTX-M-55-producing Escherichia coli was the most prevalent ESBL-producer from Fennec fox . These findings further strengthened that wildlife may act as potential reservoirs and vectors of CTX-M-55, although some of these isolates carried blaCTX-M-55 genes on the chromosome.
Interestingly, the diverging clonality of the human, environmental and animal Citrobacter isolates was confirmed by the fact that strains originating in these three sources distributed into five clusters. It is still not sure whether the ecological and animal strains are highly related to the human strains in terms of genetic phylogeny. The previous investigation highlighted the challenges associated with species designation of Citrobacter by core genome analysis, particularly in regards to Citrobacter freundii, which did not constitute a discrete phylogenetic group . As we noted in our data, C. cronae and C. braakii strains were clustered into the same clade, which suggests further accurate taxonomic inquiry is needed to clarify the lineage of Citrobacter members.
In summary, this investigation involved the first survey of MDR Citrobacter isolates in Fennec fox. We characterized the phenotypic characteristics and genomic basis of MDR Citrobacter strains. Fennec fox may serve as a common vector for the rapid dissemination of ESBL-encoding genes via animal contact and thereby threaten public health. Our findings further underscore the threat of increased ESBL prevalence in Enterobacteriaceae, and improved multisectoral surveillance for ESBL-producing Citrobacter is warranted.
Methods and materials
Bacterial identification and isolation of Citrobacter strains
We collected 168 stool samples of wild Fennec fox imported from North Africa to China . Stool samples were cultured by MacConkey agar supplemented with 1 mg/l cefotaxime as described previously . Bacterial identification was conducted by MALDI–TOF MS (Bruker, Bremen, Germany) as described . Confirmation of ESBL-producing isolations was further performed by a standard double-disk diffusion method as defined by the Clinical and Laboratory Standards Institute (CLSI) (https://clsi.org/).
Antimicrobial susceptibility testing (AST)
Susceptibility to 16 antibiotics (amikacin, aztreonam, cefpirome, cefotaxime, ceftazidime, chloramphenicol, ciprofloxacin, florfenicol, fosfomycin, gentamicin, imipenem, meropenem, piperacillin–tazobactam, polymyxin E, tigecycline, tobramycin, and trimethoprim–sulfamethoxazole) for four MDR Citrobacter isolates were evaluated. The MICs were determined via an agar dilution method for all antibiotics except for colistin and tigecycline, for which a broth microdilution method was used according to the CLSI standards. E. coli ATCC 25922 was used as control.
Whole-genome sequencing (WGS) and bioinformatics analysis
Genomic DNA was extracted from four MDR Citrobacter isolates using the Qiagen Blood/Tissue kit (Qiagen, Hilden, Germany) . The sequencing library was prepared by using Illumina Nextera XT kit (Illumina, San Diego, CA, USA) and sequenced using the Illumina NovaSeq 6000-PE150 platform (Illumina). Paired reads were then assembled into scaffolds using Velvet version 1.2.10 . Acquired antimicrobial resistance genes and plasmid replicons were performed using the CGE server (http://www.genomicepidemiology.org). Antibiotics Resistance Genes (ARGs) were identified using the ResFinder 4.1 database . Genotyping was performed to query the seven domesticated genes (aspC, clpX, fadD, mdh, arcA, dnaG, and lysP) via the MLST database (https://pubmlst.org/organisms/citrobacter-spp). We further created a core genome-based phylogenetic tree using 4 Citrobacter genomes sequenced in this study and 272 randomly selected publicly available Citrobacter genomes (Additional file 1: Table S1). The isolate collection includes strains from clinical (n = 159) and the environment (n = 133) sources that were widely distributed over time and geographical locations. Citrobacter genomes were annotated using Prokka  and RAST tool . The core genes were identified using Prokka  and maximum likelihood-based phylogenetic reconstruction was performed with Roary . Phylogenetic tree visualizations were generated by using iTOL (https://itol.embl.de/).
The transferability of plasmids carrying MDR encoding genes was determined by filter mating as described previously . Animal isolates and Escherichia coli J53 were used as donors and acceptors, respectively. The animal isolates and J53 strains were mixed in (LB) broth at a ratio of 1:3 and incubated at 37 °C for 18 h. Transduction and binding were selected on MacConkey agar plates containing cefotaxime (2 μg/ml) and sodium azide (150 μg/ml) for 12 h. Susceptibility test was performed to determine the horizontal transferability of drug resistance, and the corresponding transduction conjugate was confirmed by PCR amplification and pulsed field gel electrophoresis (PFGE) (Additional file 2: Table S2).
The whole-genome sequences of four Citrobacter spp. isolates have been deposited in the GenBank under the BioProject number PRJNA656097.
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This work was supported by the National Key Research and Development Program of China (No. 2016YFD0501105) and the National Natural Science Foundation of China (No. 82072314).
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Additional file 1: Figure S1.
MS fingerprinting spectrum for each of the four identified Citrobacter strains result of Matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF-MS).
Additional file 2: Table S1.
List of information for the four genomes that were sequenced in this study.
Additional file 3: Table S2.
List of strains and genome sequences that were used in this study.
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Qin, J., Zhao, Y., Wang, A. et al. Comparative genomic characterization of multidrug-resistant Citrobacter spp. strains in Fennec fox imported to China. Gut Pathog 13, 59 (2021). https://doi.org/10.1186/s13099-021-00458-w
- Citrobacter freundii
- Fennec fox
- Comparative genomic analysis
- Bla CTX-M-13