| Literature DB >> 8416815 |
P Varela1, M Rivas, N Binsztein, M L Cremona, P Herrmann, O Burrone, R A Ugalde, A C Frasch.
Abstract
A polymerase chain reaction (PCR) to detect a region of the A1 cholera toxin gene was applied to the identification of 43 Vibrio cholerae strains isolated from the recent outbreak in Argentina. A good correlation was observed between the GM1-enzyme-linked immunosorbent assay (GM1-ELISA) to detect the B subunit of the enterotoxin and PCR. However, a V. cholerae non-01 strain that was negative by the ELISA test, was positive by the PCR assay for the A1 region. A second PCR test to detect the A2-B coding region was developed to solve this case. We propose that routine detection of toxigenic V. cholerae by PCR should include analysis of A2-B coding region or the whole cholera toxin operon.Entities:
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Year: 1993 PMID: 8416815 DOI: 10.1016/0014-5793(93)81136-n
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124