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Updated: Aug 18, 2026

Gastric Mucosa Quantitative Polymerase Chain Reaction Analysis for Detecting Helicobacter pylori and Antibiotic Resistance
Published on: March 7, 2025
[Helicobacter pylori: cagA analysis and vacA genotyping in Chile. Detection of a s2/m1 strain]
A Martínez1, C González, F Kawaguchi
1Facultad de Ciencias Biológicas y Facultad de Medicina, Universidad de Concepción, Sección de Gastroenterología, Hospital Asociación Chilena de Seguridad, Concepción, Hospital San Borja Arriarán, Santiago, Chile. h.pylori@usa.net
Background:
The genes cagA and vacA encode H pylori virulence factors.
Aim:
To genotype these genes in H pylori strains isolated from patients with upper gastrointestinal symptoms.
Material And Methods:
We studied 50 patients who underwent an upper gastrointestinal endoscopy, with positive culture for H pylori. Detection of cagA and vacA genotyping was done using polymerase chain reactions.
Results:
The gene cagA was detected in 19 samples (38%). Signal sequences s1 and s2 of vacA gene were detected in 16 samples each (32%). There was simultaneous amplification of s1 and s2 in 6 samples and they were not detected in 9 samples. The middle region of vacA was m1 in 9 samples, m2 in 29 samples and there was simultaneous amplification of m1 and m2 in 12 samples. In 16 samples (32%), more than one type of signal sequence or medial region was detected. Of those patients in whom vacA was the only genotype detected, 15 were s2/m2, 7 were s1/m1, 4 were s1/m2 and 1 was s2/m1.
Conclusions:
In these patients, the infection with cagA- H pylori strains, predominates, the prevalence of infection with s1 or s2 strains is similar and the predominant medial region is m2.
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