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Transient internalization of Campylobacter jejuni in Amoebae enhances subsequent invasion of human cells

The ubiquitous unicellular eukaryote, Acanthamoeba, is known to play a role in the survival and dissemination of Campylobacter jejuni. C. jejuni is the leading cause of bacterial foodborne gastroenteritis world-wide and is a major public health problem. The ability of C. jejuni to interact and poten...

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Autores principales: Nasher, Fauzy, Wren, Brendan W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941996/
https://www.ncbi.nlm.nih.gov/pubmed/35175913
http://dx.doi.org/10.1099/mic.0.001143
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author Nasher, Fauzy
Wren, Brendan W.
author_facet Nasher, Fauzy
Wren, Brendan W.
author_sort Nasher, Fauzy
collection PubMed
description The ubiquitous unicellular eukaryote, Acanthamoeba, is known to play a role in the survival and dissemination of Campylobacter jejuni. C. jejuni is the leading cause of bacterial foodborne gastroenteritis world-wide and is a major public health problem. The ability of C. jejuni to interact and potentially invade epithelial cells is thought to be key for disease development in humans. We examined C. jejuni grown under standard laboratory conditions, 11168H(CBA) with that harvested from within Acanthamoeba castellanii (11168H(AC/CBA)) or Acanthamoeba polyphaga (11168H(AP/CBA)), and compared their ability to invade different cell lines. C. jejuni harvested from within amoebae had a ~3.7-fold increase in invasiveness into T84 human epithelial cells and a striking ~11-fold increase for re-entry into A. castellanii cells. We also investigated the invasiveness and survivability of six diverse representative C. jejuni strains within Acanthamoeba spp., our results confirm that invasion and survivability is likely host-cell-dependent. Our survival assay data led us to conclude that Acanthamoeba spp. are a transient host for C. jejuni and that survival within amoebae pre-adapts C. jejuni and enhances subsequent cell invasion. This study provides new insight into C. jejuni interactions with amoebae and its increased invasiveness potential in mammalian hosts.
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spelling pubmed-89419962022-03-29 Transient internalization of Campylobacter jejuni in Amoebae enhances subsequent invasion of human cells Nasher, Fauzy Wren, Brendan W. Microbiology (Reading) Microbial Interactions and Communities The ubiquitous unicellular eukaryote, Acanthamoeba, is known to play a role in the survival and dissemination of Campylobacter jejuni. C. jejuni is the leading cause of bacterial foodborne gastroenteritis world-wide and is a major public health problem. The ability of C. jejuni to interact and potentially invade epithelial cells is thought to be key for disease development in humans. We examined C. jejuni grown under standard laboratory conditions, 11168H(CBA) with that harvested from within Acanthamoeba castellanii (11168H(AC/CBA)) or Acanthamoeba polyphaga (11168H(AP/CBA)), and compared their ability to invade different cell lines. C. jejuni harvested from within amoebae had a ~3.7-fold increase in invasiveness into T84 human epithelial cells and a striking ~11-fold increase for re-entry into A. castellanii cells. We also investigated the invasiveness and survivability of six diverse representative C. jejuni strains within Acanthamoeba spp., our results confirm that invasion and survivability is likely host-cell-dependent. Our survival assay data led us to conclude that Acanthamoeba spp. are a transient host for C. jejuni and that survival within amoebae pre-adapts C. jejuni and enhances subsequent cell invasion. This study provides new insight into C. jejuni interactions with amoebae and its increased invasiveness potential in mammalian hosts. Microbiology Society 2022-02-17 /pmc/articles/PMC8941996/ /pubmed/35175913 http://dx.doi.org/10.1099/mic.0.001143 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License. This article was made open access via a Publish and Read agreement between the Microbiology Society and the corresponding author’s institution.
spellingShingle Microbial Interactions and Communities
Nasher, Fauzy
Wren, Brendan W.
Transient internalization of Campylobacter jejuni in Amoebae enhances subsequent invasion of human cells
title Transient internalization of Campylobacter jejuni in Amoebae enhances subsequent invasion of human cells
title_full Transient internalization of Campylobacter jejuni in Amoebae enhances subsequent invasion of human cells
title_fullStr Transient internalization of Campylobacter jejuni in Amoebae enhances subsequent invasion of human cells
title_full_unstemmed Transient internalization of Campylobacter jejuni in Amoebae enhances subsequent invasion of human cells
title_short Transient internalization of Campylobacter jejuni in Amoebae enhances subsequent invasion of human cells
title_sort transient internalization of campylobacter jejuni in amoebae enhances subsequent invasion of human cells
topic Microbial Interactions and Communities
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941996/
https://www.ncbi.nlm.nih.gov/pubmed/35175913
http://dx.doi.org/10.1099/mic.0.001143
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