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A Novel Molecular Method for Simultaneous Identification of Vibrio parahaemolyticus 57 K-Serogroups Using Probe Melting Curve Analysis.
Lu, Linying; Li, Minxu; Li, Yinghui; Jiang, Min; Jiang, Yixiang; Shi, Xiaolu; Zuo, Le; Wang, Lei; Bian, Shengzhe; Qiu, Yaqun; Cai, Rui; Liao, Yiqun; Li, Qingge; Li, Liqiang; Hu, Qinghua.
Afiliação
  • Lu L; School of Public Health, University of South China, Hengyang, China.
  • Li M; Shenzhen Center for Disease Control and Prevention, Shenzhen, China.
  • Li Y; Shenzhen Center for Disease Control and Prevention, Shenzhen, China.
  • Jiang M; Shenzhen Center for Disease Control and Prevention, Shenzhen, China.
  • Jiang Y; Shenzhen Center for Disease Control and Prevention, Shenzhen, China.
  • Shi X; Shenzhen Center for Disease Control and Prevention, Shenzhen, China.
  • Zuo L; Shenzhen Center for Disease Control and Prevention, Shenzhen, China.
  • Wang L; Shenzhen Center for Disease Control and Prevention, Shenzhen, China.
  • Bian S; School of Public Health (Shenzhen), Sun Yat-sen University, Guangzhou, China.
  • Qiu Y; Shenzhen Key Laboratory of Unknown Pathogen Identification, BGI-Shenzhen, Shenzhen, China.
  • Cai R; Shenzhen Center for Disease Control and Prevention, Shenzhen, China.
  • Liao Y; Shenzhen Center for Disease Control and Prevention, Shenzhen, China.
  • Li Q; School of Life Sciences, Xiamen University, Xiamen, China.
  • Li L; School of Life Sciences, Xiamen University, Xiamen, China.
  • Hu Q; Shenzhen Key Laboratory of Unknown Pathogen Identification, BGI-Shenzhen, Shenzhen, China.
Front Cell Infect Microbiol ; 11: 594808, 2021.
Article em En | MEDLINE | ID: mdl-33718262
ABSTRACT
The serotyping of Vibrio parahaemolyticus, which is crucial to the surveillance and detection of outbreaks of vibriosis infection, has been widely used in many countries. In this study, we developed a molecular assay, named multiplex ligation reaction based on probe melting curve analysis (MLMA), for simultaneous identification of V. parahaemolyticus 57 K-serogroups. Based on the previous genomes of 418 strains including 39 K-serogroups and the 18 K-serogroups sequences from public databases, we obtained 57 K-serogroups specific gene sequences for designing primers and probes. The developed MLMA assay for identifying the V. parahaemolyticus 57 K-serogroups showed high reproducibility, with the intra- and inter-assay standard deviations and coefficients of variation of no more than 1°C and 1%, respectively. The limit of detection for all gene targets ranged from 0.1 to 1.0 ng/µl. We validated the MLMA assay with a double-blind test identifying 595 V. parahaemolyticus isolates using conventional serotyping methods for comparison. The results showed the kappa value between the MLMA assay and the traditional serological method was 0.936 and that there was a 96.97% consistency rate with conventional serotyping methods for all detected isolates. Additionally, five rare K-serogroups were identified using the MLMA assay, as well as 18 strains that could not be identified using the traditional serotyping method. Thus, the MLMA assay provides a rapid, robust, and promising tool for the molecular serotyping of V. parahaemolyticus K-serogroups and has the potential application to the detection of outbreaks and surveillance of V. parahaemolyticus infection.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vibrioses / Vibrio parahaemolyticus Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vibrioses / Vibrio parahaemolyticus Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article