A variety of Helicobacter pylori strains colonize the stomach of non-bleeding Egyptian patients with upper gastrointestinal disorders
Background Chronic infection with Helicobacter pylori is associated with protean manifestations, which vary from no symptoms to multiple gastric diseases. Other H. pylori infections could provide protection against reflux esophagitis, and lower esophageal cancer. The current study aims to scan H. py...
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Veröffentlicht in: | Bulletin of the National Research Centre 2019-12, Vol.43 (1), p.1-8, Article 183 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background
Chronic infection with
Helicobacter pylori
is associated with protean manifestations, which vary from no symptoms to multiple gastric diseases. Other
H. pylori
infections could provide protection against reflux esophagitis, and lower esophageal cancer. The current study aims to scan
H. pylori
strains that colonize the stomach of Egyptian patients with upper gastrointestinal disorders and its association with the endoscopic outcomes. Identification of
H. pylori
strains was done by PCR amplification of the 16s rRNA gene from gastric biopsies, proved to be positive for
H. pylori
by both Giemsa stain and histopathology. PCR products were purified, sequenced, and aligned to GenBank.
Results
BLAST results of
H. pylori
16s rRNA gene sequences showed identity between Egyptian
H. pylori
isolates and four H.
pylori
strain subpopulations: hspSAfrica, hspEAsia, hpEurope, hspWAfrica. The frequency of
H. pylori
isolates that showed identity to hspEAsia subpopulation was significantly higher in Ulcerative lesions.
H. pylori
isolates from ulcerative and neoplasm specimens illustrate base substitutions in 16s rRNA gene variable 9 region compared to the consensus sequence of
H. pylori
43504 16s rRNA.
Conclusion
Different
H. pylori
strains may be associated with differences in the clinical manifestations and could be used as a prognostic marker to predict the outcome of the
H. pylori-
associated diseases
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ISSN: | 2522-8307 2522-8307 |
DOI: | 10.1186/s42269-019-0224-5 |