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Helicobacter pylori strains harboring babA2 from Indian sub population are associated with increased virulence in ex vivo study
BACKGROUND: The babA2 gene along with the cagA and vacA of Helicobacter pylori has been considered as a risk factor for the disease outcome in certain populations. This study was aimed to understand the role of babA2 of H. pylori with the background of cagA and vacA in disease manifestations in Indi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709984/ https://www.ncbi.nlm.nih.gov/pubmed/26759607 http://dx.doi.org/10.1186/s13099-015-0083-z |
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author | Ghosh, Prachetash Sarkar, Avijit Ganguly, Mou Raghwan Alam, Jawed De, Ronita Mukhopadhyay, Asish K. |
author_facet | Ghosh, Prachetash Sarkar, Avijit Ganguly, Mou Raghwan Alam, Jawed De, Ronita Mukhopadhyay, Asish K. |
author_sort | Ghosh, Prachetash |
collection | PubMed |
description | BACKGROUND: The babA2 gene along with the cagA and vacA of Helicobacter pylori has been considered as a risk factor for the disease outcome in certain populations. This study was aimed to understand the role of babA2 of H. pylori with the background of cagA and vacA in disease manifestations in Indian sub population. METHODS: A total of 114 H. pylori strains isolated from duodenal ulcer (DU) (n = 53) and non-ulcer dyspepsia (NUD) patients (n = 61) were screened for the prevalence of these virulence markers by PCR. The comparative study of IL-8 production and apoptosis were done by co-culturing the AGS cell line with H. pylori strains with different genotypes. Adherence assay was performed with babA2 positive and negative strains. Two isogenic mutants of babA2 were constructed and the aforesaid comparative studies were carried out. RESULTS: PCR results indicated that 90.6 % (48/53), 82 % (50/61) and 73.6 % (39/53) strains from DU patients were positive for cagA, vacA, and babA2, respectively. Whereas the prevalence of these genes in NUD subjects were 70.5 % (43/61); 69.8 % (37/53), and 65.6 % (39/61), respectively. Although adherence to AGS cells was comparable among strains with babA2 positive and negative genotypes, but the triple positive strains could induce highest degree of IL-8 production and apoptosis, followed by the cagA(−)/vacA(−)/babA2(+) strains and triple negative strains, respectively. The wild type strains showed significantly higher IL-8 induction as well as apoptosis in ex vivo than its isogenic mutant of babA2. CONCLUSION: PCR study demonstrated that there was no significant association between the distribution of babA2 genotype or of triple positive strains and disease outcome in this sub population. The adherence assay showed that there was no significant difference in the extent of adherence to AGS cells among babA2 positive and negative strains. But the ex vivo study indicated that the triple positive or even the babA2 only positive strains are involved in increased virulence. The wild type strains also exhibited increased virulence compared to the babA2 mutant strains. This inconsistency demonstrated that bacterial genotype along with host genetic polymorphisms or other factors play important role in determining the clinical manifestation of H. pylori infections. |
format | Online Article Text |
id | pubmed-4709984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47099842016-01-13 Helicobacter pylori strains harboring babA2 from Indian sub population are associated with increased virulence in ex vivo study Ghosh, Prachetash Sarkar, Avijit Ganguly, Mou Raghwan Alam, Jawed De, Ronita Mukhopadhyay, Asish K. Gut Pathog Research BACKGROUND: The babA2 gene along with the cagA and vacA of Helicobacter pylori has been considered as a risk factor for the disease outcome in certain populations. This study was aimed to understand the role of babA2 of H. pylori with the background of cagA and vacA in disease manifestations in Indian sub population. METHODS: A total of 114 H. pylori strains isolated from duodenal ulcer (DU) (n = 53) and non-ulcer dyspepsia (NUD) patients (n = 61) were screened for the prevalence of these virulence markers by PCR. The comparative study of IL-8 production and apoptosis were done by co-culturing the AGS cell line with H. pylori strains with different genotypes. Adherence assay was performed with babA2 positive and negative strains. Two isogenic mutants of babA2 were constructed and the aforesaid comparative studies were carried out. RESULTS: PCR results indicated that 90.6 % (48/53), 82 % (50/61) and 73.6 % (39/53) strains from DU patients were positive for cagA, vacA, and babA2, respectively. Whereas the prevalence of these genes in NUD subjects were 70.5 % (43/61); 69.8 % (37/53), and 65.6 % (39/61), respectively. Although adherence to AGS cells was comparable among strains with babA2 positive and negative genotypes, but the triple positive strains could induce highest degree of IL-8 production and apoptosis, followed by the cagA(−)/vacA(−)/babA2(+) strains and triple negative strains, respectively. The wild type strains showed significantly higher IL-8 induction as well as apoptosis in ex vivo than its isogenic mutant of babA2. CONCLUSION: PCR study demonstrated that there was no significant association between the distribution of babA2 genotype or of triple positive strains and disease outcome in this sub population. The adherence assay showed that there was no significant difference in the extent of adherence to AGS cells among babA2 positive and negative strains. But the ex vivo study indicated that the triple positive or even the babA2 only positive strains are involved in increased virulence. The wild type strains also exhibited increased virulence compared to the babA2 mutant strains. This inconsistency demonstrated that bacterial genotype along with host genetic polymorphisms or other factors play important role in determining the clinical manifestation of H. pylori infections. BioMed Central 2016-01-12 /pmc/articles/PMC4709984/ /pubmed/26759607 http://dx.doi.org/10.1186/s13099-015-0083-z Text en © Ghosh et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ghosh, Prachetash Sarkar, Avijit Ganguly, Mou Raghwan Alam, Jawed De, Ronita Mukhopadhyay, Asish K. Helicobacter pylori strains harboring babA2 from Indian sub population are associated with increased virulence in ex vivo study |
title | Helicobacter pylori strains harboring babA2 from Indian sub population are associated with increased virulence in ex vivo study |
title_full | Helicobacter pylori strains harboring babA2 from Indian sub population are associated with increased virulence in ex vivo study |
title_fullStr | Helicobacter pylori strains harboring babA2 from Indian sub population are associated with increased virulence in ex vivo study |
title_full_unstemmed | Helicobacter pylori strains harboring babA2 from Indian sub population are associated with increased virulence in ex vivo study |
title_short | Helicobacter pylori strains harboring babA2 from Indian sub population are associated with increased virulence in ex vivo study |
title_sort | helicobacter pylori strains harboring baba2 from indian sub population are associated with increased virulence in ex vivo study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4709984/ https://www.ncbi.nlm.nih.gov/pubmed/26759607 http://dx.doi.org/10.1186/s13099-015-0083-z |
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