Cargando…

Commensal Neisseria cinerea impairs Neisseria meningitidis microcolony development and reduces pathogen colonisation of epithelial cells

It is increasingly being recognised that the interplay between commensal and pathogenic bacteria can dictate the outcome of infection. Consequently, there is a need to understand how commensals interact with their human host and influence pathogen behaviour at epithelial surfaces. Neisseria meningit...

Descripción completa

Detalles Bibliográficos
Autores principales: Custodio, Rafael, Johnson, Errin, Liu, Guangyu, Tang, Christoph M., Exley, Rachel M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092958/
https://www.ncbi.nlm.nih.gov/pubmed/32208456
http://dx.doi.org/10.1371/journal.ppat.1008372
_version_ 1783510204026978304
author Custodio, Rafael
Johnson, Errin
Liu, Guangyu
Tang, Christoph M.
Exley, Rachel M.
author_facet Custodio, Rafael
Johnson, Errin
Liu, Guangyu
Tang, Christoph M.
Exley, Rachel M.
author_sort Custodio, Rafael
collection PubMed
description It is increasingly being recognised that the interplay between commensal and pathogenic bacteria can dictate the outcome of infection. Consequently, there is a need to understand how commensals interact with their human host and influence pathogen behaviour at epithelial surfaces. Neisseria meningitidis, a leading cause of sepsis and meningitis, exclusively colonises the human nasopharynx and shares this niche with several other Neisseria species, including the commensal Neisseria cinerea. Here, we demonstrate that during adhesion to human epithelial cells N. cinerea co-localises with molecules that are also recruited by the meningococcus, and show that, similar to N. meningitidis, N. cinerea forms dynamic microcolonies on the cell surface in a Type four pilus (Tfp) dependent manner. Finally, we demonstrate that N. cinerea colocalises with N. meningitidis on the epithelial cell surface, limits the size and motility of meningococcal microcolonies, and impairs the effective colonisation of epithelial cells by the pathogen. Our data establish that commensal Neisseria can mimic and affect the behaviour of a pathogen on epithelial cell surfaces.
format Online
Article
Text
id pubmed-7092958
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-70929582020-04-01 Commensal Neisseria cinerea impairs Neisseria meningitidis microcolony development and reduces pathogen colonisation of epithelial cells Custodio, Rafael Johnson, Errin Liu, Guangyu Tang, Christoph M. Exley, Rachel M. PLoS Pathog Research Article It is increasingly being recognised that the interplay between commensal and pathogenic bacteria can dictate the outcome of infection. Consequently, there is a need to understand how commensals interact with their human host and influence pathogen behaviour at epithelial surfaces. Neisseria meningitidis, a leading cause of sepsis and meningitis, exclusively colonises the human nasopharynx and shares this niche with several other Neisseria species, including the commensal Neisseria cinerea. Here, we demonstrate that during adhesion to human epithelial cells N. cinerea co-localises with molecules that are also recruited by the meningococcus, and show that, similar to N. meningitidis, N. cinerea forms dynamic microcolonies on the cell surface in a Type four pilus (Tfp) dependent manner. Finally, we demonstrate that N. cinerea colocalises with N. meningitidis on the epithelial cell surface, limits the size and motility of meningococcal microcolonies, and impairs the effective colonisation of epithelial cells by the pathogen. Our data establish that commensal Neisseria can mimic and affect the behaviour of a pathogen on epithelial cell surfaces. Public Library of Science 2020-03-24 /pmc/articles/PMC7092958/ /pubmed/32208456 http://dx.doi.org/10.1371/journal.ppat.1008372 Text en © 2020 Custodio 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 (http://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
Custodio, Rafael
Johnson, Errin
Liu, Guangyu
Tang, Christoph M.
Exley, Rachel M.
Commensal Neisseria cinerea impairs Neisseria meningitidis microcolony development and reduces pathogen colonisation of epithelial cells
title Commensal Neisseria cinerea impairs Neisseria meningitidis microcolony development and reduces pathogen colonisation of epithelial cells
title_full Commensal Neisseria cinerea impairs Neisseria meningitidis microcolony development and reduces pathogen colonisation of epithelial cells
title_fullStr Commensal Neisseria cinerea impairs Neisseria meningitidis microcolony development and reduces pathogen colonisation of epithelial cells
title_full_unstemmed Commensal Neisseria cinerea impairs Neisseria meningitidis microcolony development and reduces pathogen colonisation of epithelial cells
title_short Commensal Neisseria cinerea impairs Neisseria meningitidis microcolony development and reduces pathogen colonisation of epithelial cells
title_sort commensal neisseria cinerea impairs neisseria meningitidis microcolony development and reduces pathogen colonisation of epithelial cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092958/
https://www.ncbi.nlm.nih.gov/pubmed/32208456
http://dx.doi.org/10.1371/journal.ppat.1008372
work_keys_str_mv AT custodiorafael commensalneisseriacinereaimpairsneisseriameningitidismicrocolonydevelopmentandreducespathogencolonisationofepithelialcells
AT johnsonerrin commensalneisseriacinereaimpairsneisseriameningitidismicrocolonydevelopmentandreducespathogencolonisationofepithelialcells
AT liuguangyu commensalneisseriacinereaimpairsneisseriameningitidismicrocolonydevelopmentandreducespathogencolonisationofepithelialcells
AT tangchristophm commensalneisseriacinereaimpairsneisseriameningitidismicrocolonydevelopmentandreducespathogencolonisationofepithelialcells
AT exleyrachelm commensalneisseriacinereaimpairsneisseriameningitidismicrocolonydevelopmentandreducespathogencolonisationofepithelialcells