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

Authors :
Harada T
Wakabayashi Y
Seto K
Lee K
Iyoda S
Kawatsu K
Source :
Diagnostic microbiology and infectious disease [Diagn Microbiol Infect Dis] 2023 Mar; Vol. 105 (3), pp. 115874. Date of Electronic Publication: 2022 Dec 01.
Publication Year :
2023

Abstract

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 stx <subscript>1</subscript> and 5 stx <subscript>2</subscript> subtype genes, except for stx <subscript>2c</subscript> and stx <subscript>2d</subscript> , were detected with high specificity using STEC isolates. However, some stx <subscript>2a</subscript> sequences potentially being close to both Stx2a and Stx2d cluster in neighbor-joining cluster analysis were positive for stx <subscript>2a</subscript> and stx <subscript>2d</subscript> by real-time PCR. For the stx <subscript>2c</subscript> 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.<br />Competing Interests: Declaration of competing interest The authors report no conflicts of interest relevant to this article.<br /> (Copyright © 2022 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1879-0070
Volume :
105
Issue :
3
Database :
MEDLINE
Journal :
Diagnostic microbiology and infectious disease
Publication Type :
Academic Journal
Accession number :
36529020
Full Text :
https://doi.org/10.1016/j.diagmicrobio.2022.115874