Abstract
Studies of Helicobacter pylori from the West have linked production of vacuolating cytotoxin and a particular signal sequence (s1a) allele of the underlying vacA gene to peptic ulcer disease (PUD). Among Chinese H. pylori, most isolates from PUD and gastritis patients were toxigenic (35/46 and 29/35, respectively). Polymerase chain reaction and DNA sequencing showed that 95 of 96 isolates carried vacA s1a alleles. In the mid-region, 78 of 96 isolates carried m2; 14 were m1-like but only 87% identical (DNA-level) to classical m1 and were designated m1b; the other 4 were unusual hybrids (m1b- type proximal, m2-type distal). Isolates with m1b and m1b-m2 alleles produced higher levels of vacuolating activity than did isolates with m2 alleles (P < .01). There was no association between any vacA allele and disease. These results suggest that the composition of H. pylori gene pools varies geographically and that other as-yet-unknown polymorphic H. pylori genes are important in PUD.
Original language | English |
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Pages (from-to) | 220-226 |
Number of pages | 7 |
Journal | Journal of Infectious Diseases |
Volume | 178 |
Issue number | 1 |
DOIs | |
Publication status | Published - 1998 |
Bibliographical note
Funding Information:Financial support: Dutch Ministry of Education and Science and the Royal Dutch Academy of Science; US NIH (DK-48029, AI-38166, HG-00820) and American Cancer Society (VM-121 to D.E.B.); Chinese Ministry of Public Health (1994).
ASJC Scopus Subject Areas
- Immunology and Allergy
- Infectious Diseases
PubMed: MeSH publication types
- Journal Article
- Research Support, Non-U.S. Gov't
- Research Support, U.S. Gov't, P.H.S.