Cargando…

Genome-wide fitness analyses of the foodborne pathogen Campylobacter jejuni in in vitro and in vivo models

Campylobacter is the most common cause of foodborne bacterial illness worldwide. Faecal contamination of meat, especially chicken, during processing represents a key route of transmission to humans. There is a lack of insight into the mechanisms driving C. jejuni growth and survival within hosts and...

Descripción completa

Detalles Bibliográficos
Autores principales: de Vries, Stefan P., Gupta, Srishti, Baig, Abiyad, Wright, Elli, Wedley, Amy, Jensen, Annette Nygaard, Lora, Lizeth LaCharme, Humphrey, Suzanne, Skovgård, Henrik, Macleod, Kareen, Pont, Elsa, Wolanska, Dominika P., L’Heureux, Joanna, Mobegi, Fredrick M., Smith, David G. E., Everest, Paul, Zomer, Aldert, Williams, Nicola, Wigley, Paul, Humphrey, Thomas, Maskell, Duncan J., Grant, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430854/
https://www.ncbi.nlm.nih.gov/pubmed/28455506
http://dx.doi.org/10.1038/s41598-017-01133-4
_version_ 1783236312351899648
author de Vries, Stefan P.
Gupta, Srishti
Baig, Abiyad
Wright, Elli
Wedley, Amy
Jensen, Annette Nygaard
Lora, Lizeth LaCharme
Humphrey, Suzanne
Skovgård, Henrik
Macleod, Kareen
Pont, Elsa
Wolanska, Dominika P.
L’Heureux, Joanna
Mobegi, Fredrick M.
Smith, David G. E.
Everest, Paul
Zomer, Aldert
Williams, Nicola
Wigley, Paul
Humphrey, Thomas
Maskell, Duncan J.
Grant, Andrew J.
author_facet de Vries, Stefan P.
Gupta, Srishti
Baig, Abiyad
Wright, Elli
Wedley, Amy
Jensen, Annette Nygaard
Lora, Lizeth LaCharme
Humphrey, Suzanne
Skovgård, Henrik
Macleod, Kareen
Pont, Elsa
Wolanska, Dominika P.
L’Heureux, Joanna
Mobegi, Fredrick M.
Smith, David G. E.
Everest, Paul
Zomer, Aldert
Williams, Nicola
Wigley, Paul
Humphrey, Thomas
Maskell, Duncan J.
Grant, Andrew J.
author_sort de Vries, Stefan P.
collection PubMed
description Campylobacter is the most common cause of foodborne bacterial illness worldwide. Faecal contamination of meat, especially chicken, during processing represents a key route of transmission to humans. There is a lack of insight into the mechanisms driving C. jejuni growth and survival within hosts and the environment. Here, we report a detailed analysis of C. jejuni fitness across models reflecting stages in its life cycle. Transposon (Tn) gene-inactivation libraries were generated in three C. jejuni strains and the impact on fitness during chicken colonisation, survival in houseflies and under nutrient-rich and –poor conditions at 4 °C and infection of human gut epithelial cells was assessed by Tn-insertion site sequencing (Tn-seq). A total of 331 homologous gene clusters were essential for fitness during in vitro growth in three C. jejuni strains, revealing that a large part of its genome is dedicated to growth. We report novel C. jejuni factors essential throughout its life cycle. Importantly, we identified genes that fulfil important roles across multiple conditions. Our comprehensive screens showed which flagella elements are essential for growth and which are vital to the interaction with host organisms. Future efforts should focus on how to exploit this knowledge to effectively control infections caused by C. jejuni.
format Online
Article
Text
id pubmed-5430854
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-54308542017-05-16 Genome-wide fitness analyses of the foodborne pathogen Campylobacter jejuni in in vitro and in vivo models de Vries, Stefan P. Gupta, Srishti Baig, Abiyad Wright, Elli Wedley, Amy Jensen, Annette Nygaard Lora, Lizeth LaCharme Humphrey, Suzanne Skovgård, Henrik Macleod, Kareen Pont, Elsa Wolanska, Dominika P. L’Heureux, Joanna Mobegi, Fredrick M. Smith, David G. E. Everest, Paul Zomer, Aldert Williams, Nicola Wigley, Paul Humphrey, Thomas Maskell, Duncan J. Grant, Andrew J. Sci Rep Article Campylobacter is the most common cause of foodborne bacterial illness worldwide. Faecal contamination of meat, especially chicken, during processing represents a key route of transmission to humans. There is a lack of insight into the mechanisms driving C. jejuni growth and survival within hosts and the environment. Here, we report a detailed analysis of C. jejuni fitness across models reflecting stages in its life cycle. Transposon (Tn) gene-inactivation libraries were generated in three C. jejuni strains and the impact on fitness during chicken colonisation, survival in houseflies and under nutrient-rich and –poor conditions at 4 °C and infection of human gut epithelial cells was assessed by Tn-insertion site sequencing (Tn-seq). A total of 331 homologous gene clusters were essential for fitness during in vitro growth in three C. jejuni strains, revealing that a large part of its genome is dedicated to growth. We report novel C. jejuni factors essential throughout its life cycle. Importantly, we identified genes that fulfil important roles across multiple conditions. Our comprehensive screens showed which flagella elements are essential for growth and which are vital to the interaction with host organisms. Future efforts should focus on how to exploit this knowledge to effectively control infections caused by C. jejuni. Nature Publishing Group UK 2017-04-28 /pmc/articles/PMC5430854/ /pubmed/28455506 http://dx.doi.org/10.1038/s41598-017-01133-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
de Vries, Stefan P.
Gupta, Srishti
Baig, Abiyad
Wright, Elli
Wedley, Amy
Jensen, Annette Nygaard
Lora, Lizeth LaCharme
Humphrey, Suzanne
Skovgård, Henrik
Macleod, Kareen
Pont, Elsa
Wolanska, Dominika P.
L’Heureux, Joanna
Mobegi, Fredrick M.
Smith, David G. E.
Everest, Paul
Zomer, Aldert
Williams, Nicola
Wigley, Paul
Humphrey, Thomas
Maskell, Duncan J.
Grant, Andrew J.
Genome-wide fitness analyses of the foodborne pathogen Campylobacter jejuni in in vitro and in vivo models
title Genome-wide fitness analyses of the foodborne pathogen Campylobacter jejuni in in vitro and in vivo models
title_full Genome-wide fitness analyses of the foodborne pathogen Campylobacter jejuni in in vitro and in vivo models
title_fullStr Genome-wide fitness analyses of the foodborne pathogen Campylobacter jejuni in in vitro and in vivo models
title_full_unstemmed Genome-wide fitness analyses of the foodborne pathogen Campylobacter jejuni in in vitro and in vivo models
title_short Genome-wide fitness analyses of the foodborne pathogen Campylobacter jejuni in in vitro and in vivo models
title_sort genome-wide fitness analyses of the foodborne pathogen campylobacter jejuni in in vitro and in vivo models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430854/
https://www.ncbi.nlm.nih.gov/pubmed/28455506
http://dx.doi.org/10.1038/s41598-017-01133-4
work_keys_str_mv AT devriesstefanp genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT guptasrishti genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT baigabiyad genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT wrightelli genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT wedleyamy genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT jensenannettenygaard genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT loralizethlacharme genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT humphreysuzanne genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT skovgardhenrik genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT macleodkareen genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT pontelsa genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT wolanskadominikap genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT lheureuxjoanna genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT mobegifredrickm genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT smithdavidge genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT everestpaul genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT zomeraldert genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT williamsnicola genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT wigleypaul genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT humphreythomas genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT maskellduncanj genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels
AT grantandrewj genomewidefitnessanalysesofthefoodbornepathogencampylobacterjejuniininvitroandinvivomodels