Helicobacter pylori Strains 26695 Vs Strain  J99 Vs Strain P12 Vs Strain PMSS1

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CriteriaStrain 26695Strain J99Strain P12Strain PMSS1Remarks
Geographic OriginUK patient with gastritisUS patient with duodenal ulcerGerman patient with gastric adenocarcinomaUS patient with duodenal ulcerReflects strain-specific geographic and clinical diversity
Clinical SourceGastritisDuodenal ulcerGastric adenocarcinomaDuodenal ulcerAssociated with different stages and outcomes of gastric disease
Genome Size~1.67 Mb~1.64 Mb~1.65 Mb~1.67 MbComparable genome sizes with differences in plasticity zones
Cag Pathogenicity IslandIntact and functionalIntact and functionalIntact, well-characterizedIntact and highly activeAll strains are cagA-positive and used in CagA function studies
CagA EPIYA MotifsWestern-type (EPIYA-ABC)Western-type, fewer repeatsWestern-type, often studied for delivery and phosphorylationWestern-type with strong phosphorylation potentialImportant for SHP2 binding and phosphorylation-dependent signaling
VacA Genotypes1/m1 (highly cytotoxic)s1/m2 (less toxic)s1/m1s1/m126695, P12, and PMSS1 show stronger vacuolating toxin activity
Genetic Tools AvailabilityExtensive (first genome sequenced)Second sequenced, widely usedUsed in host-pathogen interaction studiesGold standard for murine infection modelsPMSS1 is highly transformable and mouse-colonization competent
Mouse ColonizationPoorPoorNot well-characterizedStrong colonizer in C57BL/6 micePMSS1 is ideal for in vivo infection and chronic disease modeling
Natural CompetenceModerateHighModerateHighUseful for transformation and genetic manipulation
Plasticity ZonesPresentFewer than 26695Contain diverse virulence-related genesPresentReflects horizontal gene transfer and genomic plasticity
Use in ResearchFunctional genomics, virulence studiesEvolutionary genomicsHost-pathogen interaction, CagA deliveryIn vivo infection, inflammation, and CagA studiesEach strain provides unique advantages depending on research focus
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