Rapid Characterization of Virulence Determinants in Helicobacter pylori Isolated from Non-Atrophic Gastritis Patients by Next-Generation Sequencing

被引:16
作者
Imkamp, Frank [1 ]
Lauener, Francis N. [1 ]
Pohl, Daniel [2 ]
Lehours, Philippe [3 ,4 ]
Vale, Filipa F. [5 ]
Jehanne, Quentin [4 ]
Zbinden, Reinhard [1 ]
Keller, Peter M. [1 ,6 ]
Wagner, Karoline [1 ,7 ]
机构
[1] Univ Zurich, Inst Med Microbiol, CH-8006 Zurich, Switzerland
[2] Univ Hosp Zurich, Gastroenterol Div, CH-8006 Zurich, Switzerland
[3] Univ Bordeaux, BaRITOn, Bordeaux Res Translat Oncol, INSERM UMR1053, F-33076 Bordeaux, France
[4] Bordeaux Hosp, French Natl Reference Ctr Campylobacter & Helicob, F-33076 Bordeaux, France
[5] Univ Lisbon, Fac Farm, Res Inst Med iMed ULisboa, Host Pathogen Interact Unit, P-1649003 Lisbon, Portugal
[6] Univ Bern, Inst Infect Dis, CH-3001 Bern, Switzerland
[7] Univ Hosp Basel, Petersgraben 4, CH-4031 Basel, Switzerland
关键词
Helicobacter pylori; next generation sequencing; virulence; gastritis; cagA; vacA; iceA; dupA; babA; babB; sabA; sabB; hopZ; hopQ; oipA; OUTER-MEMBRANE PROTEIN; ULCER-PROMOTING GENE; CLINICAL-RELEVANCE; HIGH PREVALENCE; VACA GENOTYPES; CYTOTOXIN PRODUCTION; POSITIVE STRAINS; DUODENAL-ULCER; CAGA STATUS; ASSOCIATION;
D O I
10.3390/jcm8071030
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Helicobacter pylori is a major human pathogen that causes a wide range of gastrointestinal pathology. Progression of H. pylori induced gastritis to more severe disease has been found to highly correlate with the array of virulence factors expressed by the pathogen. The objective of this study was twofold: first, to characterize the genetic diversity of H. pylori strains isolated from 41 non-atrophic gastritis patients in Switzerland, an issue that has not been investigated to date. And second, to assess the prevalence and sequence variation of H. pylori virulence factors (cagA, vacA, iceA and dupA) and genes encoding outer membrane proteins (OMPs; babA, babB, sabA, sabB, hopZ, hopQ and oipA) by whole genome sequencing (WGS) using an Illumina MiSeq platform. WGS identified high genetic diversity in the analyzed H. pylori strains. Most H. pylori isolates were assigned to hpEurope (95.0%, 39/41), and the remaining ones (5.0%, 2/41) to hpEastAsia, subpopulation hspEAsia. Analysis of virulence factors revealed that 43.9% of the strains were cagA-positive, and the vacA s1 allele was detected in 56.0% of the isolates. The presence of cagA was found to be significantly associated (P < 0.001) with the presence of vacA s1, babA2 and hopQ allele 1 as well as expression of oipA. Moreover, we found an association between the grade of gastritis and H. pylori abundance in the gastric mucosa, respectively and the presence of cagA, vacA s1 and hopQ allele 1. Among our 41 gastritis patients, we identified seven patients infected with H. pylori strains that carried a specific combination of virulence factors (i.e., cagA, vacA s1 allele and babA2 allele), recently implicated in the development of more severe gastrointestinal pathology, like peptic ulcer disease and even gastric cancer. To this end, WGS can be employed for rapid and detailed characterization of virulence determinants in H. pylori, providing valuable insights into the pathogenic capacity of the bacterium. This could ultimately lead to a higher level of personalized treatment and management of patients suffering from H. pylori associated infections.
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页数:16
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