ArticleInfection and immunity1998
The number of direct repeats in hagA is variable among Porphyromonas gingivalis strains.
Article in Infection and immunity, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed.
- Virulence diversity amongJournal of oral microbiology · 2026Review
- Surface Proteins on Gram-Positive Bacteria.Microbiology spectrum · 2019Review
- Article
- Article
- Invasion of Porphyromonas gingivalis strains into vascular cells and tissue.Journal of oral microbiology · 2015Article
- Disruption of gingipain oligomerization into non-covalent cell-surface attached complexes.Biological chemistry · 2012Article
- Genomic comparison of invasive and rare non-invasive strains reveals Porphyromonas gingivalis genetic polymorphisms.Journal of oral microbiology · 2011Article
- Binding of complement inhibitor C4b-binding protein contributes to serum resistance of Porphyromonas gingivalis.Journal of immunology (Baltimore, Md. : 1950) · 2008Article
- Article
- Porphyromonas gingivalis gingipains and adhesion to epithelial cells.Infection and immunity · 2001Article
- Expression and immunogenicity of hemagglutinin A from Porphyromonas gingivalis in an avirulent Salmonella enterica serovar typhimurium vaccine strain.Infection and immunity · 2000Article
- Molecular mechanism for the spontaneous generation of pigmentless Porphyromonas gingivalis mutants.Infection and immunity · 1999Article
- Localization of HArep-containing genes on the chromosome of Porphyromonas gingivalis W83.Infection and immunity · 1999Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
The coding sequence for the surface protein hemagglutinin A (HagA) of Porphyromonas gingivalis 381 has previously been shown to contain four direct 1.35-kb repeats, designated repHA. This study was performed to determine if the number of repHA units in hagA is consistently 4 or if allelic polymorphism exists among strains and/or upon multiple passage of P. gingivalis. To this end, primers which were homologous to the regions directly 5' and 3' of the repeat domain in hagA were synthesized. PCR conditions which allowed amplification of the 8.4-kb repeat region between the primers in P. gingivalis 381 were established. Genomic DNA templates from 13 other P. gingivalis strains and 9 fresh clinical isolates from patients were analyzed under the same conditions as used above. Analysis of these PCR products demonstrated that the strains tested had different numbers (two to four) of repHA units in the respective hagA genes. The PCR products of 8.4, 7.0, and 5.7 kb represent four, three, and two repeats, respectively. One strain from each group (381, four repeats; W83, three repeats; and AJW4, two repeats) was also tested to determine if the number of repeats remained invariant upon passaging onto solid medium. No variability in the number of repeats in hagA within a strain was detected after 18 passages. P. gingivalis 381 was chosen for further testing in a mouse abscess model to determine if conditions of in vivo growth would select for deletions or duplications of the repeated sequences. Five days after infection, no change in the number of repeats was detected in cells recovered from either nonimmunized or preimmunized mice. This data indicates an interstrain variability of the number of repeat units and hence a size variability of the HagA protein of P. gingivalis, but unlike some surface antigens of other pathogenic species, the number of repeats remains relatively stable given the conditions of growth tested here.
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