# Prevalence and Variability of Helicobacter pylori Clarithromycin Resistance Mutations in Pediatric Patients in Poland: A Genotypic Analysis Using the Bosphore Genotyping Kit

**Authors:** Tomasz Bogiel, Anna Szaflarska-Popławska, Agnieszka Krawczyk

PMC · DOI: 10.3390/antibiotics14040352 · Antibiotics · 2025-03-31

## TL;DR

This study analyzed clarithromycin resistance mutations in Helicobacter pylori from Polish children and found that A2143G is the most common mutation, with some cases showing mixed infections.

## Contribution

The study provides new insights into the prevalence of specific clarithromycin resistance mutations in pediatric H. pylori infections in Poland.

## Key findings

- A2143G was the most common clarithromycin resistance mutation (58.3%) in the studied pediatric population.
- One sample showed a mix of wild-type and mutant strains, indicating possible co-infections.
- A2142C mutation was not detected in any of the samples.

## Abstract

Background: Helicobacter pylori is a Gram-negative bacterium responsible for various gastrointestinal diseases, including peptic ulcers and gastric cancer. Despite available antibiotic therapies, increasing resistance to clarithromycin—a key antibiotic in eradication regimens—poses a significant challenge. This resistance is primarily linked to point mutations in the 23S rRNA gene, particularly A2143G, A2142G, and A2142C, which hinder clarithromycin binding, reducing its bacteriostatic efficacy. This study aimed to assess the prevalence and variability of clarithromycin resistance mutations in pediatric patients from Bydgoszcz, Poland. Methods: A total of 45 gastric biopsy samples from pediatric patients were analyzed using the Bosphore® Helicobacter pylori Genotyping Kit v1 to detect clarithromycin resistance-associated mutations. Results: Among the 45 tested samples, 30 were classified as wild-type, while 12 contained resistance-associated mutations. The most frequently detected mutation was A2143G (58.3%), followed by A2142G (33.3%). One sample exhibited both A2142G and A2143G mutations, and another contained a mixture of wild-type and mutant strains. The A2142C mutation was not detected in any sample. Conclusions: Our findings confirm the predominance of A2143G among clarithromycin-resistant H. pylori strains, consistent with global trends. The detection of both mutant and wild-type strains in a single patient highlights potential co-infections or subpopulations with varying resistance profiles. Continuous surveillance and improved diagnostic tools are crucial for optimizing treatment strategies. Tailored eradication protocols based on resistance profiling are necessary to enhance treatment efficacy and mitigate the spread of resistant strains. Further research is needed to understand the clinical implications of mixed infections and double mutations in H. pylori resistance development.

## Linked entities

- **Genes:** 23S rRNA (23S ribosomal RNA) [NCBI Gene 2597968]
- **Chemicals:** clarithromycin (PubChem CID 84029)
- **Diseases:** gastric cancer (MONDO:0001056)
- **Species:** Helicobacter pylori (taxon 210)

## Full-text entities

- **Diseases:** gastrointestinal diseases (MESH:D005767), gastric cancer (MESH:D013274), peptic ulcers (MESH:D010437)
- **Chemicals:** Clarithromycin (MESH:D017291)
- **Species:** Homo sapiens (human, species) [taxon 9606], Helicobacter pylori (species) [taxon 210]
- **Mutations:** A2143G, A2142C, A2142G

## Full text

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## Figures

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## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12024284/full.md

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Source: https://tomesphere.com/paper/PMC12024284