Real-time PCR assays to detect 10 Shiga toxin subtype (Stx1a, Stx1c, Stx1d, Stx2a, Stx2b, Stx2c, Stx2d, Stx2e, Stx2f, and Stx2g) genes

被引:5
作者
Harada, Tetsuya [1 ]
Wakabayashi, Yuki [1 ]
Seto, Kazuko [2 ]
Lee, Kenichi [2 ]
Iyoda, Sunao [2 ]
Kawatsu, Kentaro [1 ]
机构
[1] Osaka Inst Publ Hlth, Div Microbiol, Osaka, Japan
[2] Natl Inst Infect Dis, Dept Bacteriol 1, Tokyo, Japan
关键词
STEC; Stx subtype genes; real-time PCR; ESCHERICHIA-COLI; SPECIFICITY; STRAINS; O26;
D O I
10.1016/j.diagmicrobio.2022.115874
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
To develop subtyping methods for Shiga toxin (Stx)1a, Stx1c, Stx1d, Stx2a, Stx2b, Stx2c, Stx2d, Stx2e, Stx2f, and Stx2g genes for epidemiological analyses of Shiga toxin-producing Escherichia coli (STEC), we developed 10 simplex real-time polymerase chain reaction (PCR) assays with reference to 284 valid stx sequences and evaluated their specificity and quantitative accuracy using STEC and non-STEC isolates and recombinant plasmids, respectively. Three stx1 and 5 stx2 subtype genes, except for stx2c and stx2d, were detected with high specificity using STEC isolates. However, some stx2a sequences potentially being close to both Stx2a and Stx2d cluster in neighbor-joining cluster analysis were positive for stx2a and stx2d by real-time PCR. For the stx2c assay, the number of real-time PCR cycles was reduced to avoid unnecessary false-positive results. Based on these considerations, the real-time PCR assays developed here might aid epidemiological investigations of infections or outbreaks caused by STEC harboring any of the stx subtype genes. (c) 2022 Elsevier Inc. All rights reserved.
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页数:7
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