Development of a Multiplex PCR Assay Targeting O-Antigen Modification Genes for Molecular Serotyping of Shigella flexneri

被引:44
作者
Sun, Qiangzheng [1 ]
Lan, Ruiting [2 ]
Wang, Yiting [1 ]
Zhao, Ailan [1 ]
Zhang, Shaomin [1 ]
Wang, Jianping [1 ]
Wang, Yan [1 ]
Xia, Shengli [3 ]
Jin, Dong [1 ]
Cui, Zhigang [1 ]
Zhao, Hongqing [1 ]
Li, Zhenjun [1 ]
Ye, Changyun [1 ]
Zhang, Shuxia [1 ]
Jing, Huaiqi [1 ]
Xu, Jianguo [1 ]
机构
[1] China CDC, State Key Lab Infect Dis Prevent & Control, Natl Inst Communicable Dis Control & Prevent, Beijing, Peoples R China
[2] Univ New S Wales, Sch Biotechnol & Biomol Sci, Sydney, NSW 2052, Australia
[3] Henan Ctr Dis Control & Prevent, Branch Enter Dis Control & Prevent, Inst Infect Dis Control & Prevent, Zhengzhou, Peoples R China
关键词
CONVERSION; STRAINS; BURDEN; GENOME; 1A;
D O I
10.1128/JCM.01259-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Shigella flexneri is the major Shigella species that causes diarrheal disease in developing countries. It is further subdivided into 15 serotypes based on O-antigen structure. Serotyping of S. flexneri is important for epidemiological purposes. In this study, we developed a multiplex PCR assay targeting the O-antigen synthesis gene wzx and the O-antigen modification genes gtrI, gtrIC, gtrII, oac, gtrIV, gtrV, and gtrX for molecular serotyping of S. flexneri. The multiplex PCR assay contained eight sets of specific PCRs in a single tube and can identify 14 of the 15 serotypes (the exception being serotype Xv) of S. flexneri recognized thus far. A nearly perfect concordance (97.8%) between multiplex PCR assay and slide agglutination was observed when 358 S. flexneri strains of various serotypes were analyzed, except that 8 strains were carrying additional cryptic and/or defective serotype-specific genes. The multiplex PCR assay provides a rapid and specific method for the serotype identification of S. flexneri.
引用
收藏
页码:3766 / 3770
页数:5
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