Prevalence of vacA, cagA and babA2 genes in Cuban Helicobacter pylori isolates  被引量:4

Prevalence of vacA, cagA and babA2 genes in Cuban Helicobacter pylori isolates

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作  者:Lino E Torres Karelia Melián Arlenis Moreno Jordis Alonso Carlos A Sabatier Mayrín Hernández Ludisleydis Bermúdez Boris L Rodríguez 

机构地区:[1]Department of Microbiology and Immunology, Biotechnology Division, National Centre for Scientif ic Research, Ciudad de La Habana, Cuba [2]Department of Gastroenterology, Medical and Chirurgic Research Centre (CIMEQ), Ciudad de La Habana, Cuba [3]Anatomopathology Department, Medical and Chirurgic Research Centre (CIMEQ), Ciudad de La Habana, Cuba

出  处:《World Journal of Gastroenterology》2009年第2期204-210,共7页世界胃肠病学杂志(英文版)

基  金:Supported by The National Centre for Scientific Research of Cuba, No. 220207

摘  要:AIM: To investigate the prevalence of vacuolating cytotoxin (vacA), cytotoxin associated gene A (cagA) and blood adhesion binding antigen (babA2) genotypes of Helicobacter pylori (H pylori) isolates from Cuban dyspeptic patients. METHODS: DNA was extracted from Hpylori-positive cultures taken from 130 dyspeptic patients. Genotyping was performed by PCR, using specific primers for vacA (s1, s2, m1, m2), cagA and babA2 genes. Endoscopic observations and histological examinations were used to determine patient pathologies. RESULTS: vacA alleles s1, s2, m1 and m2 were detected in 96 (73.8%), 34 (26.2%), 75 (57.7%) and 52 isolates (40%), respectively, while the cagA gene was detected in 95 isolates (73.2%). One hundred and seven isolates (82.3%) were babA2-positive. A significant correlation was observed between vacAs1m1 and cagA and between vacAs1ml and babA2 genotypes (P 〈 0.001 and P 〈 0.05, respectively) and between babA2 genotype and cagA status (P 〈 0.05); but, no correlation was observed between vacAsl and babA2 genotypes. Eighty five (65.4%) and 73 (56.2%) strains were type 1 (vacAsl-cagA-positive) and "triplepositive" (vacAs1-cagA-babA2-positive), respectively, and their presence was significantly associated with duodenal ulcer (P 〈 0.01 and P 〈 0.001, respectively). CONCLUSION: The distribution of the main virulence factors in the Cuban strains in this study resembled that of the Western-type strains, and the more virulent H pylori isolates were significantly associated with duodenal ulcer, ulcer disease being the worst pathology observed in the group studied.AIM: To investigate the prevalence of vacuolating cytotoxin (vacA), cytotoxin associated gene A (cagA) and blood adhesion binding antigen (babA2) genotypes of Helicobacter pylori (H pylori) isolates from Cuban dyspeptic patients. METHODS: DNA was extracted from H pylori-positive cultures taken from 130 dyspeptic patients. Genotyping was performed by PCR, using specifi c primers for vacA (s1, s2, m1, m2), cagA and babA2 genes. Endoscopic observations and histological examinations were used to determine patient pathologies. RESULTS: vacA alleles s1 , s2 , m1 and m2 were detected in 96 (73.8%), 34 (26.2%), 75 (57.7%) and 52 isolates (40%), respectively, while the cagA gene was detected in 95 isolates (73.2%). One hundred and seven isolates (82.3%) were babA2-positive. A signif icant correlation was observed between vacAs1m1 and cagA and between vacAs1m1 and babA2 genotypes (P < 0.001 and P < 0.05, respectively) and between babA2 genotype and cagA status (P < 0.05); but, no correlation was observed between vacAs1 and babA2 genotypes. Eighty fi ve (65.4%) and 73 (56.2%) strains were type 1 (vacAs1-cagA-positive) and "triple- positive" (vacAs1-cagA-babA2-positive), respectively, and their presence was significantly associated with duodenal ulcer (P < 0.01 and P < 0.001, respectively). CONCLUSION: The distribution of the main virulence factors in the Cuban strains in this study resembled that of the Western-type strains, and the more virulent H pylori isolates were signifi cantly associated with duodenal ulcer, ulcer disease being the worst pathology observed in the group studied.

关 键 词:Cuban dyspeptic patients He/icobacterpylori vacA  cagA and babA 

分 类 号:R573[医药卫生—消化系统]

 

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