Helicobacter pylori and gastroduodenal pathology: New threats of the old friend

被引:32
作者
Ahmed N. [1 ]
Sechi L.A. [2 ]
机构
[1] Pathogen Evolution Group, Centre for DNA Fingerprinting and Diagnostics, Hyderabad
[2] Department of Biomedical Sciences, University of Sassari, Sassari
关键词
Pylorus Infection; Pylorus Strain; cagA Gene; cagA Protein; Pylorus Isolate;
D O I
10.1186/1476-0711-4-1
中图分类号
学科分类号
摘要
The human gastric pathogen Helicobacter pylori causes chronic gastritis, peptic ulcer disease, gastric carcinoma, and mucosa-associated lymphoid tissue (MALT) lymphoma. It infects over 50% of the worlds' population, however, only a small subset of infected people experience H. pylori-associated illnesses. Associations with disease-specific factors remain enigmatic years after the genome sequences were deciphered. Infection with strains of Helicobacter pylori that carry the cytotoxin-associated antigen A (cagA) gene is associated with gastric carcinoma. Recent studies revealed mechanisms through which the cagA protein triggers oncopathogenic activities. Other candidate genes such as some members of the so-called plasticity region cluster are also implicated to be associated with carcinoma of stomach. Study of the evolution of polymorphisms and sequence variation in H. pylori populations on a global basis has provided a window into the history of human population migration and co-evolution of this pathogen with its host. Possible symbiotic relationships were debated since the discovery of this pathogen. The debate has been further intensified as some studies have posed the possibility that H. pylori infection may be beneficial in some humans. This assumption is based on increased incidence of gastro-oesophageal reflux disease (GERD), Barrett's oesophagus and adenocarcinoma of the oesophagus following H. pylori eradication in some countries. The contribution of comparative genomics to our understanding of the genome organisation and diversity of H. pylori and its pathophysiological importance to human healthcare is exemplified in this review. © 2005 Ahmed and Sechi; licensee Biomed Central Ltd.
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页数:10
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共 86 条
[1]  
Dunn B.E., Cohen H., Blaser M.J., Helicobacter pylori, Clin. Microbiol. Rev., 10, pp. 720-741, (1997)
[2]  
Colding H., Hartzen S.H., Roshanisefat H., Andersen L.P., Krogfelt K.A., Molecular methods for typing of Helicobacterpytori and their applications, FEMS Immunol. Med. Microbiol., 24, pp. 193-199, (1999)
[3]  
Ahmad A., Govil Y., Frank B.B., Gastric mucosa-associated lymphoid tissue lymphoma, Am. J. Gastroenterol., 98, pp. 975-986, (2003)
[4]  
van Belkum A., High-throughput epidemiologic typing in clinical microbiology, Clin. Microbiol. Infect., 9, pp. 86-100, (2003)
[5]  
Akopyanz N., Bukanov N.O., Westblom T.U., Kresovich S., Berg D.E., DNA diversity among clinical isolates of Helicobacter pylori detected by PCR-based RAPD fingerprinting, Nucleic Acids Res., 20, pp. 5137-5142, (1992)
[6]  
Wang J.T., Sheu J.C., Lin J.T., Wang T.H., Wu M.S., Direct DNA amplification and restriction pattern analysis of Helicobacter pylori in patients with duodenal ulcer and their families, J. Infect. Dis., 168, pp. 1544-1548, (1993)
[7]  
Marshall D.G., Chua A., Keeling P.W., Sullivan D.J., Coleman D.C., Smyth C.J., Molecular analysis of Helicobacter pylori populations in antral biopsies from individual patients using randomly amplified polymorphic DNA (RAPD) fingerprinting, FEMS Immunol. Med. Microbiol., 10, pp. 317-323, (1995)
[8]  
Marshall D.G., Coleman D.C., Sullivan D.J., Xia H., O'Morain C.A., Smyth C.J., Genomic DNA fingerprinting of clinical isolates of Helicobacter pylori using short oligonucleotide probes containing repetitive sequences, J. Appl. Bacteriol., 81, pp. 509-517, (1996)
[9]  
Achtman M., Azuma T., Berg D.E., Ito Y., Morelli G., Pan Z.J., Suerbaum S., Thompson S.A., van der Ende A., van Doorn L.J., Recombination and clonal groupings within Helicobacter pylori from different geographical regions, Mol. Microbiol., 32, pp. 459-470, (1999)
[10]  
Owen R.J., Xerry J., Tracing clonality of Helicobacter pylori infecting family members from analysis of DNA sequences of three housekeeping genes (urel, atpA and ahpC), deduced amino acid sequences, and pathogenicity-associated markers (cagA and vacA), J. Med. Microbiol., 52, pp. 515-524, (2003)