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Molecular typing of Helicobacter pylori isolates from asymptomatic, ulcer and gastritis patients by urease gene polymorphism

Published online by Cambridge University Press:  15 May 2009

M. Desai
Affiliation:
National Collection of Type Cultures, Central Public Health Laboratory, 61 Colindale Avenue, London NW9 5HT
D. Linton
Affiliation:
National Collection of Type Cultures, Central Public Health Laboratory, 61 Colindale Avenue, London NW9 5HT
R. J. Owen
Affiliation:
National Collection of Type Cultures, Central Public Health Laboratory, 61 Colindale Avenue, London NW9 5HT
J. Stanley*
Affiliation:
National Collection of Type Cultures, Central Public Health Laboratory, 61 Colindale Avenue, London NW9 5HT
*
*Corresponding author
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The gastric-adapted bacterium Helicobacter pylori plays an important role in gastritis and ulcer disease, but no phenotypic typing scheme presently exists for this organism. With a view to the development of genotypic typing, we have compared isolates of H. pylori from gastritis or ulcer patients with those from subjects exhibiting no disease. Variation was analysed at the urease genes, ureA and ureCD, by employing PCR-generated probes in genomic Southern blot hybridizations. Whilst ureA restriction fragments provided a fourfold subgrouping of strains, ureCD fragments were considerably more discriminatory. Twenty-four combined ureACD profiles were generated with Hind III, subdividing the 64 strains into 11 types and 13 single profiles. The most prevalent profile (UI) was found in 33% of strains, almost all from gastritis or ulcer patients. On the other hand strains isolated from asymptomatic individuals had the most diverse ureACD profiles. A key finding from this set of isolates was that strains of H. pylori associated with general gastroduodenal disease were genetically more homogeneous than strains carried by people without disease symptoms.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1994

References

REFERENCES

Warren, RJ, Marshall, B. Unidentified curved bacilli on gastric epithelium in active chronic gastritis. Lancet 1983; i: 1273–5.Google Scholar
Blaser, MJ. Epidemiology and pathophysiology of Campylobacter pylori infections. Rev Infect Dis 1990; 12: S99–S106.Google Scholar
Dooley, CP, Fitzgibbons, P, Cohen, H, Appleman, MD, Perez-Perez, G.Blaser, MJ. Prevalence and distribution of Campylobacter pylori in an asymptomatic population. Gastroenterology 1988; 94: A102.Google Scholar
Marshall, BJ. Campylobacter pylori: Its link to gastritis and peptic ulcer disease. Rev Infect Dis 1990; 12: S87–S93.Google Scholar
Correa, P, Fox, J, Fontham, E. et al. , Helicobacter pylori and gastric carcinoma. Serum antibody prevalence in populations with contrasting cancer risks. Cancer 1990: 66: 2569–74.3.0.CO;2-I>CrossRefGoogle ScholarPubMed
Loffield, RJLF, Willens, I, Flendrig, JA, Arends, JW. Helicobacter pylori and gastric carcinoma. Histopathology 1990; 17: 537–41.CrossRefGoogle Scholar
Alper, J. Bacterial infections can cause ulcers. ASM News 1993: 59: 114–5.Google Scholar
Ferrero, RL, Lee, A. The importance of urease in acid protection for the gastric-colonising bacteria Helicobacter pylori and Helicobacter felis sp. Nov. Microb Ecol Hlth Dis 1991; 4: 121–34.Google Scholar
Segal, ED, Shon, J, Tompkins, LS. Characterization of Helicobacter pylori urease mutants. Infect Immun 1992; 60: 1883–9.CrossRefGoogle ScholarPubMed
Clayton, CL, Pallen, MJ, Kleanthous, H, Wren, W.Tabaqchali, S. Nucleotide sequence of two genes from Helicobacter pylori encoding for urease subunits. Nucleic Acids Res 1990; 18: 362.CrossRefGoogle ScholarPubMed
Labigne, A, Cussac, V, Courcoux, P. Shuttle cloning and nucleotide sequences of Helicobacter pylori genes responsible for urease activity. J Bact 1991: 173: 1920–31.Google Scholar
Wilson, K. Preparation of genomic DNA from bacteria. Current protocols in molecular biology. New York: Wiley, 1987.Google Scholar
Clayton, CL, Kleanthous, H, Coates, PJ, Morgan, DD, Tabaqchali, S. Sensitive detection of Helicobacter pylori by using polymerase chain reaction. J Clin Microbiol 1991; 30: 192200.CrossRefGoogle Scholar
Akopyanz, N, Bukanov, NO, Westblom, TU, Berg, DE. PCR-based RFLP analysis of DNA sequence diversity in the gastric pathogen Helicobacter pylori. Nucleic Acids Res 1992; 20: 6221–5.CrossRefGoogle ScholarPubMed
Sambrook, J, Fritsch, EF, Maniatis, T. Molecular cloning: a laboratory manual. 2nd ed.New York: Cold Spring Harbor Laboratory Press, 1989.Google Scholar
Linton, D, Moreno, M, Owen, RJ, Stanley, J. 16S rrn gene copy number in Helicobacter pylori and its application to molecular typing. J Appl Bacteriol 1992; 73: 501–6.CrossRefGoogle ScholarPubMed
Sneath, PHA, Sokal, RR. Numerical taxonomy. San Francisco: W.H. Freeman Co. 1973.Google Scholar
Costas, M. Numerical analysis of sodium dodecylsulphate-polyacrylamide gel electrophoretic protein patterns for the classification, identification and typing of medically important bacteria. Electrophoresis 1990; 11: 382–91.CrossRefGoogle Scholar
Owen, RJ, Bickley, J, Costas, M, Morgan, DR. Genomic variation in Helicobacter pylori: application to identification of strains. Scand J Gastroenterol 1991: 26 (S181): 4350.Google Scholar
Lee, A. Peptic ulceration. H. pylori-initiated ulcerogenesis: look to the host. Lancet 1993; 341: 280–1.Google Scholar