Evidence map›Paper›PMID 42108439›Full record

ArticleBMC microbiology2026

Genomic characterization of clinical Helicobacter pylori strains from Korea: insights into phylogeny, pan-genome structure, and virulence factors.

Hi Eun Jung, Chang Seol Bang, Ji Yong Ahn, Hwoon-Yong Jung, Sun Mi Lee, So Won Kim, Dong Woo Chae, Eun Jeong Gong

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Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Hi Eun Jung *Department of Pharmacology, University of Ulsan College of Medicine, Seoul, Korea.
Chang Seol Bang *Department of Internal Medicine, Hallym University College of Medicine, 77 Sakju-ro, Chuncheon, Gangwon-do, 24253, South Korea.
Ji Yong AhnDepartment of Gastroenterology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Hwoon-Yong JungDepartment of Gastroenterology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Sun Mi LeeAsan Institute for Life Sciences, Asan Medical Center, Seoul, Korea.
So Won KimDepartment of Pharmacology, University of Ulsan College of Medicine, Seoul, Korea.
Dong Woo Chae *Department of Pharmacology, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seoul, 03722, Korea. DONGY@yuhs.ac.
Eun Jeong Gong *Department of Internal Medicine, Hallym University College of Medicine, 77 Sakju-ro, Chuncheon, Gangwon-do, 24253, South Korea. gong-eun@hanmail.net.

Funding

a National Research Foundation (NRF) grant funded by the Korean government (MIST) NRF-2021R1C1C1010631Basic Science Research Program through the NRF of Korea funded by the Ministry of Education RS-2022-NR075350Bio & Medical Technology Development Program of the National Research Foundation (NRF) funded by the Korean government (MSIT) RS-2023-00223501
6 · The paper itself

Abstract

backgroundHelicobacter pylori (H. pylori) is a globally prevalent gastric pathogen whose genetic diversity and virulence contribute to the varied clinical outcomes. Whole-genome sequencing has revolutionized microbial genomics by allowing high-resolution analyses to obtain insights into the evolution of pathogenic organisms; however, few studies have specifically focused on strains from Korea, where H. pylori infection and gastric cancer are highly prevalent. This study aimed to investigate the phylogenetic characteristics and virulence factor profiles of Korean H. pylori strains using whole-genome sequencing.

methodsTwelve H. pylori strains from Korean patients with chronic gastritis or early gastric cancer were subjected to whole-genome sequencing. Draft genomes were assembled de novo, and multi-locus sequence typing was conducted to determine the population structure. Pan-genome analysis and virulence factor profiling were also performed.

resultsAll strains were clustered within the East Asian (hspEAsia) population in the phylogenetic tree. The pan-genome analysis identified 2574 gene clusters, with 1161 core genes (45.1%), 519 shell genes (20.2%), and 894 cloud genes (34.7%). The cytotoxin-associated gene pathogenicity island (cagPAI) was intact in 11/12 strains, and all strains harbored East Asian-type ABD Glu-Pro-Ile-Tyr-Ala (EPIYA) motifs. Notably, cag2 was not detected in all strains and cagY exhibited significant sequence variation. Vacuolating cytotoxin A (vacA) genotyping identified s1c/i1/m1 as the predominant type (66.7%), followed by s1a/i1/m1 (25.0%) and s1c/i1/m2 (8.3%).

conclusionThe Korean H. pylori strains demonstrated typical East Asian characteristics, and intact cagPAI and virulent vacA genotypes were highly prevalent, providing essential genomic insights into H. pylori pathogenesis in the Korean populations.

Indexed as

Genome, BacterialHelicobacter InfectionsHelicobacter pyloriPhylogenyVirulence FactorsBacterial ProteinsGastritisGenetic VariationGenomic IslandsGenomicsHumansMultilocus Sequence TypingRepublic of KoreaStomach NeoplasmsWhole Genome SequencingBacterial ProteinsVirulence FactorsGenomeHelicobacter pyloriVirulence factorsWhole genome sequencing

Identifiers

PMID42108439
PMCPMC13330472

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