Cargando…
Role of FAD-I in Fusobacterial Interspecies Interaction and Biofilm Formation
RadD, a major adhesin of oral fusobacteria, is part of a four-gene operon encoding the small lipoprotein FAD-I and two currently uncharacterized small proteins encoded by the rapA and rapB genes. Previously, we described a role for FAD-I in the induction of human B-defensin 2 (hBD2) upon contact wit...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023056/ https://www.ncbi.nlm.nih.gov/pubmed/31906541 http://dx.doi.org/10.3390/microorganisms8010070 |
_version_ | 1783498160640884736 |
---|---|
author | Shokeen, Bhumika Park, Jane Duong, Emily Rambhia, Sonam Paul, Manash Weinberg, Aaron Shi, Wenyuan Lux, Renate |
author_facet | Shokeen, Bhumika Park, Jane Duong, Emily Rambhia, Sonam Paul, Manash Weinberg, Aaron Shi, Wenyuan Lux, Renate |
author_sort | Shokeen, Bhumika |
collection | PubMed |
description | RadD, a major adhesin of oral fusobacteria, is part of a four-gene operon encoding the small lipoprotein FAD-I and two currently uncharacterized small proteins encoded by the rapA and rapB genes. Previously, we described a role for FAD-I in the induction of human B-defensin 2 (hBD2) upon contact with oral epithelial cells. Here, we investigated potential roles for fad-I, rapA, and rapB in interspecies interaction and biofilm formation. Gene inactivation mutants were generated for each of these genes in the nucleatum and polymorphum subspecies of Fusobacterium nucleatum and characterized for their adherence to partner species, biofilm formation, and operon transcription. Binding to Streptococcus gordonii was increased in all mutant strains with Δfad-I having the most significant effect. This increased adherence was directly proportional to elevated radD transcript levels and resulted in significantly different architecture and height of the biofilms formed by Δfad-I and S. gordonii compared to the wild-type parent. In conclusion, FAD-I is important for fusobacterial interspecies interaction as its lack leads to increased production of the RadD adhesin suggesting a role of FAD-I in its regulation. This regulatory effect does not require the presence of functional RadD. |
format | Online Article Text |
id | pubmed-7023056 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70230562020-03-12 Role of FAD-I in Fusobacterial Interspecies Interaction and Biofilm Formation Shokeen, Bhumika Park, Jane Duong, Emily Rambhia, Sonam Paul, Manash Weinberg, Aaron Shi, Wenyuan Lux, Renate Microorganisms Article RadD, a major adhesin of oral fusobacteria, is part of a four-gene operon encoding the small lipoprotein FAD-I and two currently uncharacterized small proteins encoded by the rapA and rapB genes. Previously, we described a role for FAD-I in the induction of human B-defensin 2 (hBD2) upon contact with oral epithelial cells. Here, we investigated potential roles for fad-I, rapA, and rapB in interspecies interaction and biofilm formation. Gene inactivation mutants were generated for each of these genes in the nucleatum and polymorphum subspecies of Fusobacterium nucleatum and characterized for their adherence to partner species, biofilm formation, and operon transcription. Binding to Streptococcus gordonii was increased in all mutant strains with Δfad-I having the most significant effect. This increased adherence was directly proportional to elevated radD transcript levels and resulted in significantly different architecture and height of the biofilms formed by Δfad-I and S. gordonii compared to the wild-type parent. In conclusion, FAD-I is important for fusobacterial interspecies interaction as its lack leads to increased production of the RadD adhesin suggesting a role of FAD-I in its regulation. This regulatory effect does not require the presence of functional RadD. MDPI 2020-01-02 /pmc/articles/PMC7023056/ /pubmed/31906541 http://dx.doi.org/10.3390/microorganisms8010070 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shokeen, Bhumika Park, Jane Duong, Emily Rambhia, Sonam Paul, Manash Weinberg, Aaron Shi, Wenyuan Lux, Renate Role of FAD-I in Fusobacterial Interspecies Interaction and Biofilm Formation |
title | Role of FAD-I in Fusobacterial Interspecies Interaction and Biofilm Formation |
title_full | Role of FAD-I in Fusobacterial Interspecies Interaction and Biofilm Formation |
title_fullStr | Role of FAD-I in Fusobacterial Interspecies Interaction and Biofilm Formation |
title_full_unstemmed | Role of FAD-I in Fusobacterial Interspecies Interaction and Biofilm Formation |
title_short | Role of FAD-I in Fusobacterial Interspecies Interaction and Biofilm Formation |
title_sort | role of fad-i in fusobacterial interspecies interaction and biofilm formation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023056/ https://www.ncbi.nlm.nih.gov/pubmed/31906541 http://dx.doi.org/10.3390/microorganisms8010070 |
work_keys_str_mv | AT shokeenbhumika roleoffadiinfusobacterialinterspeciesinteractionandbiofilmformation AT parkjane roleoffadiinfusobacterialinterspeciesinteractionandbiofilmformation AT duongemily roleoffadiinfusobacterialinterspeciesinteractionandbiofilmformation AT rambhiasonam roleoffadiinfusobacterialinterspeciesinteractionandbiofilmformation AT paulmanash roleoffadiinfusobacterialinterspeciesinteractionandbiofilmformation AT weinbergaaron roleoffadiinfusobacterialinterspeciesinteractionandbiofilmformation AT shiwenyuan roleoffadiinfusobacterialinterspeciesinteractionandbiofilmformation AT luxrenate roleoffadiinfusobacterialinterspeciesinteractionandbiofilmformation |