Brief Reports
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World J Gastroenterol. Oct 28, 2005; 11(40): 6366-6372
Published online Oct 28, 2005. doi: 10.3748/wjg.v11.i40.6366
Helicobacter pylori vacA s1a and s1b alleles from clinical isolates from different regions of Chile show a distinct geographic distribution
MI Díaz, A Valdivia, P Martínez, JL Palacios, P Harris, J Novales, E Garrido, D Valderrama, C Shilling, A Kirberg, E Hebel, J Fierro, R Bravo, F Siegel, G Leon, G Klapp, A Venegas
MI Díaz, A Valdivia, P Martínez, JL Palacios, A Venegas, Departamento de Genética Molecular y Microbiología. Pontificia Universidad Católica de Chile. Santiago, Chile
P Harris, Departamento de Pediatría, Unidad de Gastroenterología, Facultad de Medicina, Pontificia Universidad Católica de Chile. Santiago Chile
J Novales, E Garrido, Centro de Diagnóstico Terapéutico Los Angeles, Servicio Salud Bio-Bio. Los Angeles, Chile
D Valderrama, Unidad de Gastroenterología, Hospital Valparaíso, Valparaíso, Chile
C Shilling, Anatomía Patológica, Hospital San Martín de Quillota, Quillota, Chile
A Kirberg, Centro de Endoscopía Quirúrgica, Hospital de Iquique. Iquique, Chile
E Hebel, J Fierro, Departamento de Pediatría, Universidad de La Frontera, Temuco, Chile
R Bravo, Hospital Base de Linares, Linares, Chile
F Siegel, Hospital Regional de Valdivia, Valdivia Chile
G Leon, Instituto de Bioquímica, Universidad Austral de Chile, Valdivia, Chile
G Klapp, Hospital Regional de Punta Arenas, Chile
Author contributions: All authors contributed equally to the work.
Supported by FONDECYT, Comisión Nacional Científica y Tecnológica, Chile No.1000730 No.1030894 and No. 1000734 from and NIH No.DK54495
Correspondence to: Venegas A, Departamento de Genética Molecular y Microbiología. Pontificia Universidad Católica de Chile. Alameda 340, Santiago Chile. avenegas@genes.bio.puc.cl
Telephone: +56-2-686-2661 Fax: +56-2-222-2810
Received: April 1, 2005
Revised: April 6, 2005
Accepted: April 9, 2005
Published online: October 28, 2005
Abstract

AIM: To establish the most common vacA alleles in Helicobacter pylori (H pylori) strains isolated from Chilean patients and its relationship with gastritis and gastroduodenal ulcers.

METHODS: Two hundred and forty five H pylori clinical isolates were obtained from 79 biopsies from Chilean infected patients suffering from gastrointestinal diseases. An average of 2-3 strains per patient was isolated and the vacA genotype was analyzed by PCR and 3% agarose electrophoresis. Some genotypes were checked by DNA sequencing.

RESULTS: The most prevalent vacA genotype in Chilean patients was s1b m1 (76%), followed by s1a m1 (21%). In contrast, the s2 m2 genotype was scarcely represented (3%). The s1b m1 genotype was found most frequently linked to gastropathies (P<0.05) rather than ulcers. Ulcers were found more commonly in male and older patients. Curiously, patients living in cities located North and far South of Santiago, the capital and largest Chilean city, carried almost exclusively strains with the s1b m1 genotype. In contrast, patients from Santiago and cities located South of Santiago carried strains with either one or both s1a m1 and s1b m1 genotypes. Regarding the s2 m2 genotype, comparison with GenBank sequences revealed that Chilean s2 sequence was identical to those of Australian, American, and Colombian strains but quite different from those of Alaska and India.

CONCLUSION: Differences in geographic distribution of the s and m vacA alleles in Chile and a relationship of s1b m1 genotype with gastritis were found. Sequence data in part support a hispanic origin for the vacA genotype. Asymmetric distribution of genotypes s1b m1 and s2 m2 recedes H Pylori strain distribution in Spain and Portugal.

Keywords: H pylori, vacA alleles, Chilean isolates, s1, s2, m1 and m2 sequences