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Recent progress in experimental and human disease-associated multi-species biofilms

Human bodies are colonized by trillions of microorganisms, which are often referred to as human microbiota and play important roles in human health. Next generation sequencing studies have established links between the genetic content of human microbiota and various human diseases. However, it remai...

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Detalles Bibliográficos
Autores principales: Bai, Fang, Cai, Zhao, Yang, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944735/
https://www.ncbi.nlm.nih.gov/pubmed/31921390
http://dx.doi.org/10.1016/j.csbj.2019.09.010
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author Bai, Fang
Cai, Zhao
Yang, Liang
author_facet Bai, Fang
Cai, Zhao
Yang, Liang
author_sort Bai, Fang
collection PubMed
description Human bodies are colonized by trillions of microorganisms, which are often referred to as human microbiota and play important roles in human health. Next generation sequencing studies have established links between the genetic content of human microbiota and various human diseases. However, it remains largely unknown about the spatial organizations and interspecies interactions of individual species within the human microbiota. Bacterial cells tend to form surface-attached biofilms in many natural environments, which enable intercellular communications and interactions in a microbial ecosystem. In this review, we summarize the recent progresses on the experimental and human disease-associated multi-species biofilm studies. We hypothesize that engineering biofilm structures and interspecies interactions might provide a tool for manipulating the composition and function of human microbiota.
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spelling pubmed-69447352020-01-09 Recent progress in experimental and human disease-associated multi-species biofilms Bai, Fang Cai, Zhao Yang, Liang Comput Struct Biotechnol J Review Article Human bodies are colonized by trillions of microorganisms, which are often referred to as human microbiota and play important roles in human health. Next generation sequencing studies have established links between the genetic content of human microbiota and various human diseases. However, it remains largely unknown about the spatial organizations and interspecies interactions of individual species within the human microbiota. Bacterial cells tend to form surface-attached biofilms in many natural environments, which enable intercellular communications and interactions in a microbial ecosystem. In this review, we summarize the recent progresses on the experimental and human disease-associated multi-species biofilm studies. We hypothesize that engineering biofilm structures and interspecies interactions might provide a tool for manipulating the composition and function of human microbiota. Research Network of Computational and Structural Biotechnology 2019-10-25 /pmc/articles/PMC6944735/ /pubmed/31921390 http://dx.doi.org/10.1016/j.csbj.2019.09.010 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Bai, Fang
Cai, Zhao
Yang, Liang
Recent progress in experimental and human disease-associated multi-species biofilms
title Recent progress in experimental and human disease-associated multi-species biofilms
title_full Recent progress in experimental and human disease-associated multi-species biofilms
title_fullStr Recent progress in experimental and human disease-associated multi-species biofilms
title_full_unstemmed Recent progress in experimental and human disease-associated multi-species biofilms
title_short Recent progress in experimental and human disease-associated multi-species biofilms
title_sort recent progress in experimental and human disease-associated multi-species biofilms
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944735/
https://www.ncbi.nlm.nih.gov/pubmed/31921390
http://dx.doi.org/10.1016/j.csbj.2019.09.010
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