Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015:2015:753710.
doi: 10.1155/2015/753710. Epub 2015 Apr 6.

Prevalence of Helicobacter pylori vacA, cagA, and iceA Genotypes in Cuban Patients with Upper Gastrointestinal Diseases

Affiliations

Prevalence of Helicobacter pylori vacA, cagA, and iceA Genotypes in Cuban Patients with Upper Gastrointestinal Diseases

Onelkis Feliciano et al. Biomed Res Int. 2015.

Abstract

Virulence factors of Helicobacter pylori can predict the development of different gastroduodenal diseases. There are scarce reports in Cuba about H. pylori isolates genotyping. The aim of the present investigation was to identify allelic variation of the virulence genes vacA, cagA, and iceA in sixty-eight patients diagnosed as H. pylori positive by culture. In seven out of 68 patients, strains from both gastric regions were obtained and considered independent. DNA was extracted from all the H. pylori strains and evaluated by PCR-genotyping. The vacA s1 allele, cagA gene, and iceA2 allele were the most prevalent (72.0%, 56.0%, and 57.3%, respectively). Alleles from m-region showed a similar frequency as s1a and s1b subtypes. The presence of multiple H. pylori genotypes in a single biopsy and two gastric region specimens were found. Significant statistical association was observed between iceA2 allele and patients with non-peptic ulcer dyspepsia (NUD) (P = 0.037) as well as virulence genotypes (s1, s1m2) and patients over 40 years old (P < 0.05). In conclusion, the results demonstrated a high prevalence of H. pylori virulent genotypes in Cuban patients over 40 years old while iceA2 alleles demonstrated a good specificity in patients with NUD.

PubMed Disclaimer

References

    1. Kusters J. G., van Vliet A. H. M., Kuipers E. J. Pathogenesis of Helicobacter pylori infection. Clinical Microbiology Reviews. 2006;19(3):449–490. doi: 10.1128/cmr.00054-05. - DOI - PMC - PubMed
    1. Yamaoka Y. Mechanisms of disease: Helicobacter pylori virulence factors. Nature Reviews Gastroenterology and Hepatology. 2010;7(11):629–641. doi: 10.1038/nrgastro.2010.154. - DOI - PMC - PubMed
    1. Suzuki R., Shiota S., Yamaoka Y. Molecular epidemiology, population genetics, and pathogenic role of Helicobacter pylori . Infection, Genetics and Evolution. 2012;12(2):203–213. doi: 10.1016/j.meegid.2011.12.002. - DOI - PMC - PubMed
    1. Cover T. L., Blanke S. R. Helicobacter pylori VacA, a paradigm for toxin multifunctionality. Nature Reviews Microbiology. 2005;3(4):320–332. doi: 10.1038/nrmicro1095. - DOI - PubMed
    1. Atherton J. C., Cao P., Peek R. M., Jr., Tummuru M. K. R., Blaser M. J., Cover T. L. Mosaicism in vacuolating cytotoxin alleles of Helicobacter pylori. Association of specific vacA types with cytotoxin production and peptic ulceration. The Journal of Biological Chemistry. 1995;270(30):17771–17777. doi: 10.1074/jbc.270.30.17771. - DOI - PubMed

MeSH terms

Substances

LinkOut - more resources