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Diversity analysis of genes encoding Mfa1 fimbrial components in Porphyromonas gingivalis strains

Porphyromonas gingivalis, a gram-negative anaerobic bacterium, is associated with the development of periodontal disease. The genetic diversity in virulence factors, such as adhesive fimbriae, among its strains affects the bacterial pathogenicity. P. gingivalis generally expresses two distinct types...

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Autores principales: Sakae, Kotaro, Nagano, Keiji, Furuhashi, Miyuna, Hasegawa, Yoshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313007/
https://www.ncbi.nlm.nih.gov/pubmed/34310632
http://dx.doi.org/10.1371/journal.pone.0255111
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author Sakae, Kotaro
Nagano, Keiji
Furuhashi, Miyuna
Hasegawa, Yoshiaki
author_facet Sakae, Kotaro
Nagano, Keiji
Furuhashi, Miyuna
Hasegawa, Yoshiaki
author_sort Sakae, Kotaro
collection PubMed
description Porphyromonas gingivalis, a gram-negative anaerobic bacterium, is associated with the development of periodontal disease. The genetic diversity in virulence factors, such as adhesive fimbriae, among its strains affects the bacterial pathogenicity. P. gingivalis generally expresses two distinct types of fimbriae, FimA and Mfa1. Although the genetic diversity of fimA, encoding the major FimA fimbrilin protein, has been characterized, the genes encoding the Mfa1 fimbrial components, including the Mfa1 to Mfa5 proteins, have not been fully studied. We, therefore, analyzed their genotypes in 12 uncharacterized and 62 known strains of P. gingivalis (74 strains in total). The mfa1 genotype was primarily classified into two genotypes, 53 and 70. Additionally, we found that genotype 70 could be further divided into two subtypes (70A and 70B). The diversity of mfa2 to mfa4 was consistent with the mfa1 genotype, although no subtype in genotype 70 was observed. Protein structure modeling showed high homology between the genotypes in Mfa1 to Mfa4. The mfa5 gene was classified into five genotypes (A to E) independent of other genotypes. Moreover, genotype A was further divided into two subtypes (A1 and A2). Surprisingly, some strains had two mfa5 genes, and the 2(nd) mfa5 exclusively occurred in genotype E. The Mfa5 protein in all genotypes showed a homologous C-terminal half, including the conserved C-terminal domain recognized by the type IX secretion system. Furthermore, the von Willebrand factor domain at the N-terminal was detected only in genotypes A to C. The mfa1 genotypes partially correlated with the ragA and ragB genotypes (located immediately downstream of the mfa gene cluster) but not with the fimA genotypes.
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spelling pubmed-83130072021-07-31 Diversity analysis of genes encoding Mfa1 fimbrial components in Porphyromonas gingivalis strains Sakae, Kotaro Nagano, Keiji Furuhashi, Miyuna Hasegawa, Yoshiaki PLoS One Research Article Porphyromonas gingivalis, a gram-negative anaerobic bacterium, is associated with the development of periodontal disease. The genetic diversity in virulence factors, such as adhesive fimbriae, among its strains affects the bacterial pathogenicity. P. gingivalis generally expresses two distinct types of fimbriae, FimA and Mfa1. Although the genetic diversity of fimA, encoding the major FimA fimbrilin protein, has been characterized, the genes encoding the Mfa1 fimbrial components, including the Mfa1 to Mfa5 proteins, have not been fully studied. We, therefore, analyzed their genotypes in 12 uncharacterized and 62 known strains of P. gingivalis (74 strains in total). The mfa1 genotype was primarily classified into two genotypes, 53 and 70. Additionally, we found that genotype 70 could be further divided into two subtypes (70A and 70B). The diversity of mfa2 to mfa4 was consistent with the mfa1 genotype, although no subtype in genotype 70 was observed. Protein structure modeling showed high homology between the genotypes in Mfa1 to Mfa4. The mfa5 gene was classified into five genotypes (A to E) independent of other genotypes. Moreover, genotype A was further divided into two subtypes (A1 and A2). Surprisingly, some strains had two mfa5 genes, and the 2(nd) mfa5 exclusively occurred in genotype E. The Mfa5 protein in all genotypes showed a homologous C-terminal half, including the conserved C-terminal domain recognized by the type IX secretion system. Furthermore, the von Willebrand factor domain at the N-terminal was detected only in genotypes A to C. The mfa1 genotypes partially correlated with the ragA and ragB genotypes (located immediately downstream of the mfa gene cluster) but not with the fimA genotypes. Public Library of Science 2021-07-26 /pmc/articles/PMC8313007/ /pubmed/34310632 http://dx.doi.org/10.1371/journal.pone.0255111 Text en © 2021 Sakae et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sakae, Kotaro
Nagano, Keiji
Furuhashi, Miyuna
Hasegawa, Yoshiaki
Diversity analysis of genes encoding Mfa1 fimbrial components in Porphyromonas gingivalis strains
title Diversity analysis of genes encoding Mfa1 fimbrial components in Porphyromonas gingivalis strains
title_full Diversity analysis of genes encoding Mfa1 fimbrial components in Porphyromonas gingivalis strains
title_fullStr Diversity analysis of genes encoding Mfa1 fimbrial components in Porphyromonas gingivalis strains
title_full_unstemmed Diversity analysis of genes encoding Mfa1 fimbrial components in Porphyromonas gingivalis strains
title_short Diversity analysis of genes encoding Mfa1 fimbrial components in Porphyromonas gingivalis strains
title_sort diversity analysis of genes encoding mfa1 fimbrial components in porphyromonas gingivalis strains
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313007/
https://www.ncbi.nlm.nih.gov/pubmed/34310632
http://dx.doi.org/10.1371/journal.pone.0255111
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