Expanding allelic diversity of Helicobacter pylori vacA

• Type: Article in International Scientific Journal
• Date: 1998

Authors

van Doorn, LJ (Author) Other; Figueiredo C (Author) Other; Sanna, R (Author) Other; Pena, S (Author) Other; Midolo, P (Author) Other; Ng, EKW (Author) Other; Atherton, JC (Author) Other; Blaser, MJ (Author) Other; Quint, WGV (Author) Other

Journal

Title: Journal of Clinical Microbiology

Vol. 36

Pages: 2597-2603

ISSN: 0095-1137

Publisher: American Society for Microbiology

Indexing

ISI Web of Knowledge - 228 Citations

Scopus - 257 Citations

Other information

Authenticus ID: P-001-76Z

Abstract (EN): The diversity of the gene encoding the vacuolating cytotoxin (vacA) of Helicobacter pylori was analyzed in 98 isolates obtained from different geographic locations. The studies focused on variation in the previously defined s and m regions of vacA, as determined bg PCR and direct sequencing. Phylogenetic analysis revealed the existence of four distinct types of s-region alleles: aside from the previously described sla, s1b, and s2 allelic types, a novel subtype, designated sie, was found. Subtype sie was observed exclusively in isolates from East Asia and appears to be the major sl allele in that part of the world. Three different allelic forms (m1, m2a, and m2b) were detected in the m region. On the basis of sequence alignments, universal PCR primers that allow effective amplification of the s and m regions from H. pylori isolates from all over the world were defined. Amplimers were subsequently analyzed by reverse hybridization onto a line probe assay (LiPA) that allows the simultaneous and highly specific hybridization of the different vacA s- and m-region alleles and tests for the presence of the cytotoxin-associated gene (cagA). This PCR-LiPA method permits rapid analysis of the vacA and cagA status of H. pylori strains for clinical and epidemiological studies and will facilitate identification of any further variations.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 7