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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...

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Autores principales: Shokeen, Bhumika, Park, Jane, Duong, Emily, Rambhia, Sonam, Paul, Manash, Weinberg, Aaron, Shi, Wenyuan, Lux, Renate
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
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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.
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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
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