Abstract

The aim of this work was to determine current cagA gene EPIYA motifs present in Colombian Helicobacter pylori isolates using a fast and reliable molecular test. DNA from eighty-five Helicobacter pylori-cagA positive strains were analyzed. Strains were obtained from patients diagnosed with functional dyspepsia at Clínica Fundadores in Bogotá. The 3' region of the cagA gene was amplified through conventional Polymerase Chain Reaction (PCR). Obtained amplicons were sequenced using the Sanger method and analyzed with bioinformatics tools. Additionally, a significant Spearman correlation coefficient was determined between the patients' age and the number of EPIYA-C repeats; with p values < 0.05 considered significant. Estimates were obtained using a 95% CI. The 3´ variable region of the cagA gene was amplified and PCR products of the following sizes corresponded to the following EPIYA motifs: 400 bp: EPIYA AB, 500 bp: EPIYA ABC, 600 bp: EPIYA ABCC and 700 bp: ABCCC. A single PCR band was observed for 58 out of 85 Helicobacter pylori isolates, with an EPIYA distribution motif as follows: 7/85 AB (8.2%), 34/85 ABC (40%), 26/85 ABCC (30.6%) and 18/85 ABCCC (21.2%). However, in 27 out of 85 Helicobacter pylori isolates, two or more bands were observed, where the most predominant cagA genotype were ABC-ABCC (26%, 7/27) and ABCC-ABCCC (22.2%, 6/27). A direct proportionality between the number of EPIYA-C repeats and an increase in the patients’ age was observed, finding a greater number of EPIYA ABCC and ABCCC repeats in the population over 50 years old. All isolates were of the Western cagA type and 51.8% of them were found to have multiple EPIYA-C repeats. These standardized molecular test allowed to identify the number of EPIYA C motifs based on band size.

Highlights

  • Helicobacter pylori (H. pylori) bacteria infecting human gastric mucosa has been associated with development of gastroduodenal diseases, such as chronic gastritis, peptic and duodenal ulcer, MALT lymphoma and gastric cancer

  • Current publications have focused on this diversity only in patients with gastric cancer. This information does not reflect the existing circulating diversity, which allows development of additional studies to assess the impact of cagA gene diversity on gastroduodenal diseases. To contribute with this understanding, this study aimed to determine current cagA gene EPIYA motifs circulation in Colombian H. pylori isolates through a rapid molecular test

  • It was identified that all Colombian H. pylori isolates contained the Western cagA gene type, with a predominant EPIYA-ABC and multiple EPIYA-C repeats

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Summary

Introduction

Helicobacter pylori (H. pylori) bacteria infecting human gastric mucosa has been associated with development of gastroduodenal diseases, such as chronic gastritis, peptic and duodenal ulcer, MALT lymphoma and gastric cancer. Some populations displaying high infection prevalence, present a high incidence of gastric cancer (East Asia). This same relationship does not apply to Africa and South Asia. A plausible explanation for these differences might be due to H. pylori genetic plasticity, suggesting geographical differences in virulence genes [1]. Gastric cancer is a multifactorial disease, where genetic and environmental factors, as well as H. pylori infection are involved. Some of the characteristics attributed to this microorganism are virulence factors, where the most studied and important is the CagA protein [2]

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