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. 2017 Jan 19;12(1):e0169324.
doi: 10.1371/journal.pone.0169324. eCollection 2017.

Characterization and Genetic Variation of Vibrio cholerae Isolated from Clinical and Environmental Sources in Thailand

Affiliations

Characterization and Genetic Variation of Vibrio cholerae Isolated from Clinical and Environmental Sources in Thailand

Achiraya Siriphap et al. PLoS One. .

Abstract

Cholera is still an important public health problem in several countries, including Thailand. In this study, a collection of clinical and environmental V. cholerae serogroup O1, O139, and non-O1/non-O139 strains originating from Thailand (1983 to 2013) was characterized to determine phenotypic and genotypic traits and to investigate the genetic relatedness. Using a combination of conventional methods and whole genome sequencing (WGS), 78 V. cholerae strains were identified. WGS was used to determine the serogroup, biotype, virulence, mobile genetic elements, and antimicrobial resistance genes using online bioinformatics tools. In addition, phenotypic antimicrobial resistance was determined by the minimal inhibitory concentration (MIC) test. The 78 V. cholerae strains belonged to the following serogroups O1: (n = 44), O139 (n = 16) and non-O1/non-O139 (n = 18). Interestingly, we found that the typical El Tor O1 strains were the major cause of clinical cholera during 1983-2000 with two Classical O1 strains detected in 2000. In 2004-2010, the El Tor variant strains revealed genotypes of the Classical biotype possessing either only ctxB or both ctxB and rstR while they harbored tcpA of the El Tor biotype. Thirty O1 and eleven O139 clinical strains carried CTXφ (Cholera toxin) and tcpA as well four different pathogenic islands (PAIs). Beside non-O1/non-O139, the O1 environmental strains also presented chxA and Type Three Secretion System (TTSS). The in silico MultiLocus Sequence Typing (MLST) discriminated the O1 and O139 clinical strains from other serogroups and environmental strains. ST69 was dominant in the clinical strains belonging to the 7th pandemic clone. Non-O1/non-O139 and environmental strains showed various novel STs indicating genetic variation. Multidrug-resistant (MDR) strains were observed and conferred resistance to ampicillin, azithromycin, nalidixic acid, sulfamethoxazole, tetracycline, and trimethoprim and harboured variants of the SXT elements. For the first time since 1986, the presence of V. cholerae O1 Classical was reported causing cholera outbreaks in Thailand. In addition, we found that V. cholerae O1 El Tor variant and O139 were pre-dominating the pathogenic strains in Thailand. Using WGS and bioinformatic tools to analyze both historical and contemporary V. cholerae circulating in Thailand provided a more detailed understanding of the V. cholerae epidemiology, which ultimately could be applied for control measures and management of cholera in Thailand.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. In silico MLST tree of Vibrio cholerae strains related with virulence gene profiles.
The V. cholerae clinical (*) and environmental (•) strains in Thailand were related to pandemic and epidemic strains. Seven housekeeping genes were extracted from V. cholerae genomes. The phylogenetic tree was generated by FigTree.
Fig 2
Fig 2. Genomic variation of representative Vibrio cholerae strains in Thailand.
BLAST atlas with chromosome I (A) and II (B) of V. cholerae N16961 as reference strain (black) followed by the nine representative strains of serogroup O1, O139, and non-O1/non-O139 composed of serogroup O1 (blue) (clinical strains: 510/77, typical El Tor; VCO1-8, classical; 22116 and P25, El Tor variant; environmental strain: MK14, hybrid El Tor), O139 (green) (clinical strains: 22136, environmental strain: DT8), and non-O1/non-O139 (red) (clinical strains: IPD22I/8 44B, environmental strain: VCR12).
Fig 3
Fig 3. Genetic variation of SXT element in Vibrio cholerae.
The SXT structures of among 43 V. cholerae strains from Thailand were compared. Reads were mapped to genes of ICEVcHai1 (accession no. JN648379) and dfrA18 gene in SXTMO10 element (accession no. AY034138).

References

    1. Bhattacharya SK, Bhattacharya MK, Nair GB, Dutta D, Deb A, Ramamurthy T, et al. Clinical profile of acute diarrhoea cases infected with the new epidemic strain of Vibrio cholerae O139: designation of the disease as cholera. J Infect. 1993;27(1):11–5. - PubMed
    1. Kaper JB, Morris JG Jr., Levine MM. Cholera. Clin Microbiol Rev. 1995;8(1):48–86. - PMC - PubMed
    1. Moore S, Thomson N, Mutreja A, Piarroux R. Widespread epidemic cholera caused by a restricted subset of Vibrio cholerae clones. Clin Microbiol Infect. 2014;20(5):373–9. 10.1111/1469-0691.12610 - DOI - PubMed
    1. Yamai S, Okitsu T, Shimada T, Katsube Y. [Distribution of serogroups of Vibrio cholerae non-O1 non-O139 with specific reference to their ability to produce cholera toxin, and addition of novel serogroups]. Kansenshogaku Zasshi. 1997;71(10):1037–45. - PubMed
    1. Dalsgaard A, Forslund A, Bodhidatta L, Serichantalergs O, Pitarangsi C, Pang L, et al. A high proportion of Vibrio cholerae strains isolated from children with diarrhoea in Bangkok, Thailand are multiple antibiotic resistant and belong to heterogenous non-O1, non-O139 O-serotypes. Epidemiol Infect. 1999;122(2):217–26. - PMC - PubMed

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