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. 2017 May 18:7:188.
doi: 10.3389/fcimb.2017.00188. eCollection 2017.

Spreading of Pandemic Vibrio parahaemolyticus O3:K6 and Its Serovariants: A Re-analysis of Strains Isolated from Multiple Studies

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Spreading of Pandemic Vibrio parahaemolyticus O3:K6 and Its Serovariants: A Re-analysis of Strains Isolated from Multiple Studies

Dongsheng Han et al. Front Cell Infect Microbiol. .

Abstract

In China, V. parahaemolyticus has been a leading cause of foodborne outbreaks and bacterial infectious diarrhea since the 1990s, and most infections have been associated with the pandemic V. parahaemolyticus O3:K6 and its serovariants. However, a comprehensive overview of the sero-prevalence and genetic diversity of the pandemic V. parahaemolyticus clone in China is lacking. To compensate for this deficiency, pandemic isolates in both clinical and environmental Chinese samples collected from multiple studies were analyzed in this study. Surprisingly, as many as 27 clinical pandemic serovariants were identified and were widely distributed across nine coastal provinces and two inland provinces (Beijing and Sichuan). O3:K6, O4:K68, and O1:KUT represented the predominant clinical serovars. Only four environmental pandemic serovariants had previously been reported, and they were spread throughout Shanghai (O1:KUT, O3:K6), Jiangsu (O3:K6, O4:K48), Zhejiang (O3:K6), and Guangdong (O4:K9). Notably, 24 pandemic serovariants were detected within a short time frame (from 2006 to 2012). The pandemic isolates were divided into 15 sequence types (STs), 10 of which fell within clonal complex (CC) 3. Only three STs (ST3, ST192, and ST305) were identified in environmental isolates. Substantial serotypic diversity was mainly observed among isolates within pandemic ST3, which comprised 21 combinations of O/K antigens. The pandemic O3:K6 serotype showed a high level of sequence diversity, which was shared by eight different STs (ST3, ST227, ST431, ST435, ST487, ST489, ST526, and ST672). Antimicrobial susceptibility testing revealed that most isolates shared similar antibiotic susceptibility profiles. They were resistant to ampicillin but sensitive to most other drugs that were tested. In conclusion, the high levels of serotypic and genetic diversity of the pandemic clone suggest that the involved regions are becoming important reservoirs for the emergence of novel pandemic strains. We underscore the need for routine monitoring to prevent pandemic V. parahaemolyticus infection, which includes monitoring antimicrobial responses to avoid excessive misuse of antibiotics. Further investigations are also needed to delineate the specific mechanisms underlying the possible seroconversion of pandemic isolates.

Keywords: Vibrio parahaemolyticus; gastroenteritis; genetic diversity; multilocus sequence typing; pandemic clone.

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Figures

Figure 1
Figure 1
The grouping of the collected isolates and the main points of re-analysis in this study.
Figure 2
Figure 2
Map showing the sero-prevalence and sequence diversity of clinical and environmental pandemic O3:K6 and its serovariants of V. parahaemolyticus found in Chinese samples.
Figure 3
Figure 3
goeBURST full MST of the STs shows the clonal diversity of Chinese clinical and environmental pandemic V. parahaemolyticus isolates: clinical (red) and environmental (blue). The pandemic STs in China are denoted by pink dotted circles. Other STs were selected from the public MLST database (https://pubmlst.org/vparahaemolyticus/) to help us analyze the cluster relationship of pandemic STs in this study. The number of different alleles is presented between STs connected via a line. The circle size varies according to the frequency of STs. Each shaded area represents a unique clone complex.
Figure 4
Figure 4
The antimicrobial profiles within different STs (pandemic: ST3 and ST88, non-pandemic: other STs).

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