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Mfa4, an Accessory Protein of Mfa1 Fimbriae, Modulates Fimbrial Biogenesis, Cell Auto-Aggregation, and Biofilm Formation in Porphyromonas gingivalis

Porphyromonas gingivalis, a gram-negative obligate anaerobic bacterium, is considered to be a key pathogen in periodontal disease. The bacterium expresses Mfa1 fimbriae, which are composed of polymers of Mfa1. The minor accessory components Mfa3, Mfa4, and Mfa5 are incorporated into these fimbriae....

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Autores principales: Ikai, Ryota, Hasegawa, Yoshiaki, Izumigawa, Masashi, Nagano, Keiji, Yoshida, Yasuo, Kitai, Noriyuki, Lamont, Richard J., Yoshimura, Fuminobu, Murakami, Yukitaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593637/
https://www.ncbi.nlm.nih.gov/pubmed/26437277
http://dx.doi.org/10.1371/journal.pone.0139454
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author Ikai, Ryota
Hasegawa, Yoshiaki
Izumigawa, Masashi
Nagano, Keiji
Yoshida, Yasuo
Kitai, Noriyuki
Lamont, Richard J.
Yoshimura, Fuminobu
Murakami, Yukitaka
author_facet Ikai, Ryota
Hasegawa, Yoshiaki
Izumigawa, Masashi
Nagano, Keiji
Yoshida, Yasuo
Kitai, Noriyuki
Lamont, Richard J.
Yoshimura, Fuminobu
Murakami, Yukitaka
author_sort Ikai, Ryota
collection PubMed
description Porphyromonas gingivalis, a gram-negative obligate anaerobic bacterium, is considered to be a key pathogen in periodontal disease. The bacterium expresses Mfa1 fimbriae, which are composed of polymers of Mfa1. The minor accessory components Mfa3, Mfa4, and Mfa5 are incorporated into these fimbriae. In this study, we characterized Mfa4 using genetically modified strains. Deficiency in the mfa4 gene decreased, but did not eliminate, expression of Mfa1 fimbriae. However, Mfa3 and Mfa5 were not incorporated because of defects in posttranslational processing and leakage into the culture supernatant, respectively. Furthermore, the mfa4-deficient mutant had an increased tendency to auto-aggregate and form biofilms, reminiscent of a mutant completely lacking Mfa1. Notably, complementation of mfa4 restored expression of structurally intact and functional Mfa1 fimbriae. Taken together, these results indicate that the accessory proteins Mfa3, Mfa4, and Mfa5 are necessary for assembly of Mfa1 fimbriae and regulation of auto-aggregation and biofilm formation of P. gingivalis. In addition, we found that Mfa3 and Mfa4 are processed to maturity by the same RgpA/B protease that processes Mfa1 subunits prior to polymerization.
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spelling pubmed-45936372015-10-14 Mfa4, an Accessory Protein of Mfa1 Fimbriae, Modulates Fimbrial Biogenesis, Cell Auto-Aggregation, and Biofilm Formation in Porphyromonas gingivalis Ikai, Ryota Hasegawa, Yoshiaki Izumigawa, Masashi Nagano, Keiji Yoshida, Yasuo Kitai, Noriyuki Lamont, Richard J. Yoshimura, Fuminobu Murakami, Yukitaka PLoS One Research Article Porphyromonas gingivalis, a gram-negative obligate anaerobic bacterium, is considered to be a key pathogen in periodontal disease. The bacterium expresses Mfa1 fimbriae, which are composed of polymers of Mfa1. The minor accessory components Mfa3, Mfa4, and Mfa5 are incorporated into these fimbriae. In this study, we characterized Mfa4 using genetically modified strains. Deficiency in the mfa4 gene decreased, but did not eliminate, expression of Mfa1 fimbriae. However, Mfa3 and Mfa5 were not incorporated because of defects in posttranslational processing and leakage into the culture supernatant, respectively. Furthermore, the mfa4-deficient mutant had an increased tendency to auto-aggregate and form biofilms, reminiscent of a mutant completely lacking Mfa1. Notably, complementation of mfa4 restored expression of structurally intact and functional Mfa1 fimbriae. Taken together, these results indicate that the accessory proteins Mfa3, Mfa4, and Mfa5 are necessary for assembly of Mfa1 fimbriae and regulation of auto-aggregation and biofilm formation of P. gingivalis. In addition, we found that Mfa3 and Mfa4 are processed to maturity by the same RgpA/B protease that processes Mfa1 subunits prior to polymerization. Public Library of Science 2015-10-05 /pmc/articles/PMC4593637/ /pubmed/26437277 http://dx.doi.org/10.1371/journal.pone.0139454 Text en © 2015 Ikai et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ikai, Ryota
Hasegawa, Yoshiaki
Izumigawa, Masashi
Nagano, Keiji
Yoshida, Yasuo
Kitai, Noriyuki
Lamont, Richard J.
Yoshimura, Fuminobu
Murakami, Yukitaka
Mfa4, an Accessory Protein of Mfa1 Fimbriae, Modulates Fimbrial Biogenesis, Cell Auto-Aggregation, and Biofilm Formation in Porphyromonas gingivalis
title Mfa4, an Accessory Protein of Mfa1 Fimbriae, Modulates Fimbrial Biogenesis, Cell Auto-Aggregation, and Biofilm Formation in Porphyromonas gingivalis
title_full Mfa4, an Accessory Protein of Mfa1 Fimbriae, Modulates Fimbrial Biogenesis, Cell Auto-Aggregation, and Biofilm Formation in Porphyromonas gingivalis
title_fullStr Mfa4, an Accessory Protein of Mfa1 Fimbriae, Modulates Fimbrial Biogenesis, Cell Auto-Aggregation, and Biofilm Formation in Porphyromonas gingivalis
title_full_unstemmed Mfa4, an Accessory Protein of Mfa1 Fimbriae, Modulates Fimbrial Biogenesis, Cell Auto-Aggregation, and Biofilm Formation in Porphyromonas gingivalis
title_short Mfa4, an Accessory Protein of Mfa1 Fimbriae, Modulates Fimbrial Biogenesis, Cell Auto-Aggregation, and Biofilm Formation in Porphyromonas gingivalis
title_sort mfa4, an accessory protein of mfa1 fimbriae, modulates fimbrial biogenesis, cell auto-aggregation, and biofilm formation in porphyromonas gingivalis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593637/
https://www.ncbi.nlm.nih.gov/pubmed/26437277
http://dx.doi.org/10.1371/journal.pone.0139454
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