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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Microbiology Society
2022
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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. |
format | Online Article Text |
id | pubmed-8941996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
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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