Amplification by the polymerase chain reaction of a specific target sequence in the gene coding for Escherichia coli verotoxin (VTe variant).

Abstract:

:Synthetic oligonucleotide primers were used in a polymerase chain reaction (PCR) protocol to target a specific sequence in the gene coding for the A subunit of Escherichia coli verotoxin (VTe-variant, VTev). This PCR protocol permits the VTe-variant target sequence to be distinguished from closely related sequences in the same coding regions for type 1, type 2, and type 2 variant E. coli verotoxins. This procedure will be a valuable adjunct to other DNA amplification techniques currently being used for molecular epidemiological studies of verotoxigenic E. coli.

journal_name

FEMS Microbiol Lett

authors

Johnson WM,Tyler SD,Wang G,Lior H

doi

10.1016/0378-1097(91)90131-s

subject

Has Abstract

pub_date

1991-11-15 00:00:00

pages

227-30

issue

2

eissn

0378-1097

issn

1574-6968

journal_volume

68

pub_type

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