Molecular Detection and Clinical Impact of Helicobacter pylori Virulence Genes in Gastric Diseases: A Study in Arequipa, Peru

<b>Background:</b><i>Helicobacter pylori</i> is a globally prevalent pathogen and a major contributor to gastric diseases, including chronic gastritis, peptic ulcer disease, and gastric cancer. This study investigates the prevalence, distribution, and clinical relevance of its key virulence genes, <i>vacA</i> and <i>cagA</i>, in a Peruvian patient cohort. <b>Materials and Methods</b>: Fifty-one gastric biopsies were collected from patients with a presumptive diagnosis of <i>H. pylori</i>-induced gastritis at Hospital Carlos Alberto Seguín Escobedo in Arequipa, Peru, in March 2024. Two biopsies per patient-one from the antrum and one from the gastric body-were obtained during endoscopy. DNA extraction was performed using the Quick-DNA Fungal/Bacterial Kit (Zymo Research, USA). Molecular identification of <i>H. pylori</i> was conducted via PCR targeting the <i>glmM</i> gene, while the <i>vacA</i> and <i>cagA</i> virulence genes were detected using specific primers. Statistical analyses, including Pearson's chi-square and Mann-Whitney tests, were applied to assess associations between virulence gene presence and clinical or histopathological variables. <b>Results</b>: Among the gastric biopsies, the <i>vacA</i> gene was detected in 37.3% of samples, while <i>cagA</i> was present in 17.6%. Statistical analysis revealed significant associations between <i>vacA</i> and specific clinical and endoscopic features, including erythematous gastropathy, nodular gastritis, and emetic syndrome, suggesting its localized role in disease pathogenesis. Additionally, the presence of <i>cagA</i> was significantly linked to moderate inflammatory intensity in gastric body biopsies, indicating its association with more severe histopathological outcomes. Chronic gastritis was the most common histopathological finding, with moderate intensity correlating strongly with the presence of virulence genes. <b>Conclusions</b>: These findings highlight substantial regional variability in the distribution and pathogenicity of <i>H. pylori</i> genotypes. This study underscores the importance of incorporating molecular diagnostics into routine clinical practice to improve diagnostic accuracy and inform region-specific therapeutic strategies. This is particularly crucial in endemic regions like Peru, where unique environmental and genetic factors may influence infection dynamics and disease outcomes.

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Journal
Biomedicines
Published
2025-04-09
DOI
https://doi.org/10.3390/biomedicines13040914
Citations
1
Primary Topic
Helicobacter pylori-related gastroenterology studies
Type
article
Field-Weighted Citation Impact
2.01
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article

Molecular Detection and Clinical Impact of Helicobacter pylori Virulence Genes in Gastric Diseases: A Study in Arequipa, Peru

Alexis Germán Murillo Carrasco, Cecilia Manrique-Sam, Yuma Ita-Balta, André Luíz de Carvalho Braule Pinto et al.
1 citations
Biomedicines
Helicobacter pylori-related gastroenterology studies
2.01
article

Molecular Detection and Clinical Impact of Helicobacter pylori Virulence Genes in Gastric Diseases: A Study in Arequipa, Peru

Alexis Germán Murillo Carrasco, Cecilia Manrique-Sam, Yuma Ita-Balta, André Luíz de Carvalho Braule Pinto, Alice Zegarra-Adanaqué, Johany Sanchez-Guillen, Miguel Farfán-Delgado, Carlos Ortiz-Castro
article en
1 citations

Abstract

<b>Background:</b><i>Helicobacter pylori</i> is a globally prevalent pathogen and a major contributor to gastric diseases, including chronic gastritis, peptic ulcer disease, and gastric cancer. This study investigates the prevalence, distribution, and clinical relevance of its key virulence genes, <i>vacA</i> and <i>cagA</i>, in a Peruvian patient cohort. <b>Materials and Methods</b>: Fifty-one gastric biopsies were collected from patients with a presumptive diagnosis of <i>H. pylori</i>-induced gastritis at Hospital Carlos Alberto Seguín Escobedo in Arequipa, Peru, in March 2024. Two biopsies per patient-one from the antrum and one from the gastric body-were obtained during endoscopy. DNA extraction was performed using the Quick-DNA Fungal/Bacterial Kit (Zymo Research, USA). Molecular identification of <i>H. pylori</i> was conducted via PCR targeting the <i>glmM</i> gene, while the <i>vacA</i> and <i>cagA</i> virulence genes were detected using specific primers. Statistical analyses, including Pearson's chi-square and Mann-Whitney tests, were applied to assess associations between virulence gene presence and clinical or histopathological variables. <b>Results</b>: Among the gastric biopsies, the <i>vacA</i> gene was detected in 37.3% of samples, while <i>cagA</i> was present in 17.6%. Statistical analysis revealed significant associations between <i>vacA</i> and specific clinical and endoscopic features, including erythematous gastropathy, nodular gastritis, and emetic syndrome, suggesting its localized role in disease pathogenesis. Additionally, the presence of <i>cagA</i> was significantly linked to moderate inflammatory intensity in gastric body biopsies, indicating its association with more severe histopathological outcomes. Chronic gastritis was the most common histopathological finding, with moderate intensity correlating strongly with the presence of virulence genes. <b>Conclusions</b>: These findings highlight substantial regional variability in the distribution and pathogenicity of <i>H. pylori</i> genotypes. This study underscores the importance of incorporating molecular diagnostics into routine clinical practice to improve diagnostic accuracy and inform region-specific therapeutic strategies. This is particularly crucial in endemic regions like Peru, where unique environmental and genetic factors may influence infection dynamics and disease outcomes.

BiomedicinesVol. 13(4)
Catholic University of Santa María (PE)
Good health and well-being
Openalex Percentile: Top 17%
Helicobacter pylori-related gastroenterology studies
2.01
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