Typing of verotoxins by DNA colony hybridization with poly- and oligonucleotide probes, a bead-enzyme-linked immunosorbent assay, and polymerase chain reaction

76Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

To identify the type of Vetotoxins (VT) produced by Verocytotoxin- producing Escherichia coil (VTEC), a sensitive bead-enzyme-linked immunosorbent assay and polymerase chain reaction with common and specific primers to various VTs (VT1, VT2, VT2vha, VT2vhb, and VT2vp1) were developed. Together with colony hybridization tests with oligo- and polynucleotide probes, these methods were applied to VTEC isolates to type the VT produced. The toxin types of 26 of 37 strains were identified, but the reaction profiles in assays of the remaining 11 strains suggested the existence of new VT2 variants. The application of these identification procedures may be useful as a tool for clinical and epidemiological studies of VTEC infection.

Cite

CITATION STYLE

APA

Yamasaki, S., Lin, Z., Shirai, H., Terai, A., Oku, Y., Ito, H., … Takeda, Y. (1996). Typing of verotoxins by DNA colony hybridization with poly- and oligonucleotide probes, a bead-enzyme-linked immunosorbent assay, and polymerase chain reaction. Microbiology and Immunology, 40(5), 345–352. https://doi.org/10.1111/j.1348-0421.1996.tb01078.x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free