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Molecular Epidemiology of Helicobacter pylori Infection in Nepal: Specific Ancestor Root

Prevalence of Helicobacter pylori infection in Nepal, a low-risk country for gastric cancer, is debatable. To our knowledge, no studies have examined H. pylori virulence factors in Nepal. We determined the prevalence of H. pylori infection by using three different tests, and the genotypes of virulen...

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Autores principales: Miftahussurur, Muhammad, Sharma, Rabi Prakash, Shrestha, Pradeep Krishna, Suzuki, Rumiko, Uchida, Tomohisa, Yamaoka, Yoshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4520618/
https://www.ncbi.nlm.nih.gov/pubmed/26226153
http://dx.doi.org/10.1371/journal.pone.0134216
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author Miftahussurur, Muhammad
Sharma, Rabi Prakash
Shrestha, Pradeep Krishna
Suzuki, Rumiko
Uchida, Tomohisa
Yamaoka, Yoshio
author_facet Miftahussurur, Muhammad
Sharma, Rabi Prakash
Shrestha, Pradeep Krishna
Suzuki, Rumiko
Uchida, Tomohisa
Yamaoka, Yoshio
author_sort Miftahussurur, Muhammad
collection PubMed
description Prevalence of Helicobacter pylori infection in Nepal, a low-risk country for gastric cancer, is debatable. To our knowledge, no studies have examined H. pylori virulence factors in Nepal. We determined the prevalence of H. pylori infection by using three different tests, and the genotypes of virulence factors were determined by PCR followed by sequencing. Multilocus sequence typing was used to analyze the population structure of the Nepalese strains. The prevalence of H. pylori infection in dyspeptic patients was 38.4% (56/146), and was significantly related with source of drinking water. In total, 51 strains were isolated and all were cagA-positive. Western-type-cagA (94.1%), cagA pre-EPIYA type with no deletion (92.2%), vacA s1a (74.5%), and m1c (54.9%) were the predominant genotypes. Antral mucosal atrophy levels were significantly higher in patients infected with vacA s1 than in those infected with s2 genotypes (P = 0.03). Several Nepalese strains were H. pylori recombinants with genetic features of South Asian and East Asian genotypes. These included all East-Asian-type-cagA strains, with significantly lesser activity and inflammation in the corpus than the strains of the specific South Asian genotype (P = 0.03 and P = 0.005, respectively). Although the population structure confirmed that most Nepalese strains belonged to the hpAsia2 population, some strains shared hpEurope- and Nepalese-specific components. Nepalese patients infected with strains belonging to hpEurope showed higher inflammation in the antrum than strains from the Nepalese specific population (P = 0.05). These results support that ancestor roots of Kathmandu`s people not only connected with India alone.
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spelling pubmed-45206182015-08-06 Molecular Epidemiology of Helicobacter pylori Infection in Nepal: Specific Ancestor Root Miftahussurur, Muhammad Sharma, Rabi Prakash Shrestha, Pradeep Krishna Suzuki, Rumiko Uchida, Tomohisa Yamaoka, Yoshio PLoS One Research Article Prevalence of Helicobacter pylori infection in Nepal, a low-risk country for gastric cancer, is debatable. To our knowledge, no studies have examined H. pylori virulence factors in Nepal. We determined the prevalence of H. pylori infection by using three different tests, and the genotypes of virulence factors were determined by PCR followed by sequencing. Multilocus sequence typing was used to analyze the population structure of the Nepalese strains. The prevalence of H. pylori infection in dyspeptic patients was 38.4% (56/146), and was significantly related with source of drinking water. In total, 51 strains were isolated and all were cagA-positive. Western-type-cagA (94.1%), cagA pre-EPIYA type with no deletion (92.2%), vacA s1a (74.5%), and m1c (54.9%) were the predominant genotypes. Antral mucosal atrophy levels were significantly higher in patients infected with vacA s1 than in those infected with s2 genotypes (P = 0.03). Several Nepalese strains were H. pylori recombinants with genetic features of South Asian and East Asian genotypes. These included all East-Asian-type-cagA strains, with significantly lesser activity and inflammation in the corpus than the strains of the specific South Asian genotype (P = 0.03 and P = 0.005, respectively). Although the population structure confirmed that most Nepalese strains belonged to the hpAsia2 population, some strains shared hpEurope- and Nepalese-specific components. Nepalese patients infected with strains belonging to hpEurope showed higher inflammation in the antrum than strains from the Nepalese specific population (P = 0.05). These results support that ancestor roots of Kathmandu`s people not only connected with India alone. Public Library of Science 2015-07-30 /pmc/articles/PMC4520618/ /pubmed/26226153 http://dx.doi.org/10.1371/journal.pone.0134216 Text en © 2015 Miftahussurur et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Miftahussurur, Muhammad
Sharma, Rabi Prakash
Shrestha, Pradeep Krishna
Suzuki, Rumiko
Uchida, Tomohisa
Yamaoka, Yoshio
Molecular Epidemiology of Helicobacter pylori Infection in Nepal: Specific Ancestor Root
title Molecular Epidemiology of Helicobacter pylori Infection in Nepal: Specific Ancestor Root
title_full Molecular Epidemiology of Helicobacter pylori Infection in Nepal: Specific Ancestor Root
title_fullStr Molecular Epidemiology of Helicobacter pylori Infection in Nepal: Specific Ancestor Root
title_full_unstemmed Molecular Epidemiology of Helicobacter pylori Infection in Nepal: Specific Ancestor Root
title_short Molecular Epidemiology of Helicobacter pylori Infection in Nepal: Specific Ancestor Root
title_sort molecular epidemiology of helicobacter pylori infection in nepal: specific ancestor root
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4520618/
https://www.ncbi.nlm.nih.gov/pubmed/26226153
http://dx.doi.org/10.1371/journal.pone.0134216
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