Cargando…

Investigating the Campylobacter jejuni Transcriptional Response to Host Intestinal Extracts Reveals the Involvement of a Widely Conserved Iron Uptake System

Campylobacter jejuni is a pathogenic bacterium that causes gastroenteritis in humans yet is a widespread commensal in wild and domestic animals, particularly poultry. Using RNA sequencing, we assessed C. jejuni transcriptional responses to medium supplemented with human fecal versus chicken cecal ex...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Martha M., Boinett, Christine J., Chan, Anson C. K., Parkhill, Julian, Murphy, Michael E. P., Gaynor, Erin C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083913/
https://www.ncbi.nlm.nih.gov/pubmed/30087169
http://dx.doi.org/10.1128/mBio.01347-18
_version_ 1783346067438305280
author Liu, Martha M.
Boinett, Christine J.
Chan, Anson C. K.
Parkhill, Julian
Murphy, Michael E. P.
Gaynor, Erin C.
author_facet Liu, Martha M.
Boinett, Christine J.
Chan, Anson C. K.
Parkhill, Julian
Murphy, Michael E. P.
Gaynor, Erin C.
author_sort Liu, Martha M.
collection PubMed
description Campylobacter jejuni is a pathogenic bacterium that causes gastroenteritis in humans yet is a widespread commensal in wild and domestic animals, particularly poultry. Using RNA sequencing, we assessed C. jejuni transcriptional responses to medium supplemented with human fecal versus chicken cecal extracts and in extract-supplemented medium versus medium alone. C. jejuni exposed to extracts had altered expression of 40 genes related to iron uptake, metabolism, chemotaxis, energy production, and osmotic stress response. In human fecal versus chicken cecal extracts, C. jejuni displayed higher expression of genes involved in respiration (fdhTU) and in known or putative iron uptake systems (cfbpA, ceuB, chuC, and CJJ81176_1649–1655 [here designated 1649–1655]). The 1649–1655 genes and downstream overlapping gene 1656 were investigated further. Uncharacterized homologues of this system were identified in 33 diverse bacterial species representing 6 different phyla, 21 of which are associated with human disease. The 1649 and 1650 (p19) genes encode an iron transporter and a periplasmic iron binding protein, respectively; however, the role of the downstream 1651–1656 genes was unknown. A Δ1651–1656 deletion strain had an iron-sensitive phenotype, consistent with a previously characterized Δp19 mutant, and showed reduced growth in acidic medium, increased sensitivity to streptomycin, and higher resistance to H(2)O(2) stress. In iron-restricted medium, the 1651–1656 and p19 genes were required for optimal growth when using human fecal extracts as an iron source. Collectively, this implicates a function for the 1649–1656 gene cluster in C. jejuni iron scavenging and stress survival in the human intestinal environment.
format Online
Article
Text
id pubmed-6083913
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-60839132018-08-24 Investigating the Campylobacter jejuni Transcriptional Response to Host Intestinal Extracts Reveals the Involvement of a Widely Conserved Iron Uptake System Liu, Martha M. Boinett, Christine J. Chan, Anson C. K. Parkhill, Julian Murphy, Michael E. P. Gaynor, Erin C. mBio Research Article Campylobacter jejuni is a pathogenic bacterium that causes gastroenteritis in humans yet is a widespread commensal in wild and domestic animals, particularly poultry. Using RNA sequencing, we assessed C. jejuni transcriptional responses to medium supplemented with human fecal versus chicken cecal extracts and in extract-supplemented medium versus medium alone. C. jejuni exposed to extracts had altered expression of 40 genes related to iron uptake, metabolism, chemotaxis, energy production, and osmotic stress response. In human fecal versus chicken cecal extracts, C. jejuni displayed higher expression of genes involved in respiration (fdhTU) and in known or putative iron uptake systems (cfbpA, ceuB, chuC, and CJJ81176_1649–1655 [here designated 1649–1655]). The 1649–1655 genes and downstream overlapping gene 1656 were investigated further. Uncharacterized homologues of this system were identified in 33 diverse bacterial species representing 6 different phyla, 21 of which are associated with human disease. The 1649 and 1650 (p19) genes encode an iron transporter and a periplasmic iron binding protein, respectively; however, the role of the downstream 1651–1656 genes was unknown. A Δ1651–1656 deletion strain had an iron-sensitive phenotype, consistent with a previously characterized Δp19 mutant, and showed reduced growth in acidic medium, increased sensitivity to streptomycin, and higher resistance to H(2)O(2) stress. In iron-restricted medium, the 1651–1656 and p19 genes were required for optimal growth when using human fecal extracts as an iron source. Collectively, this implicates a function for the 1649–1656 gene cluster in C. jejuni iron scavenging and stress survival in the human intestinal environment. American Society for Microbiology 2018-08-07 /pmc/articles/PMC6083913/ /pubmed/30087169 http://dx.doi.org/10.1128/mBio.01347-18 Text en Copyright © 2018 Liu et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Liu, Martha M.
Boinett, Christine J.
Chan, Anson C. K.
Parkhill, Julian
Murphy, Michael E. P.
Gaynor, Erin C.
Investigating the Campylobacter jejuni Transcriptional Response to Host Intestinal Extracts Reveals the Involvement of a Widely Conserved Iron Uptake System
title Investigating the Campylobacter jejuni Transcriptional Response to Host Intestinal Extracts Reveals the Involvement of a Widely Conserved Iron Uptake System
title_full Investigating the Campylobacter jejuni Transcriptional Response to Host Intestinal Extracts Reveals the Involvement of a Widely Conserved Iron Uptake System
title_fullStr Investigating the Campylobacter jejuni Transcriptional Response to Host Intestinal Extracts Reveals the Involvement of a Widely Conserved Iron Uptake System
title_full_unstemmed Investigating the Campylobacter jejuni Transcriptional Response to Host Intestinal Extracts Reveals the Involvement of a Widely Conserved Iron Uptake System
title_short Investigating the Campylobacter jejuni Transcriptional Response to Host Intestinal Extracts Reveals the Involvement of a Widely Conserved Iron Uptake System
title_sort investigating the campylobacter jejuni transcriptional response to host intestinal extracts reveals the involvement of a widely conserved iron uptake system
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083913/
https://www.ncbi.nlm.nih.gov/pubmed/30087169
http://dx.doi.org/10.1128/mBio.01347-18
work_keys_str_mv AT liumartham investigatingthecampylobacterjejunitranscriptionalresponsetohostintestinalextractsrevealstheinvolvementofawidelyconservedironuptakesystem
AT boinettchristinej investigatingthecampylobacterjejunitranscriptionalresponsetohostintestinalextractsrevealstheinvolvementofawidelyconservedironuptakesystem
AT chanansonck investigatingthecampylobacterjejunitranscriptionalresponsetohostintestinalextractsrevealstheinvolvementofawidelyconservedironuptakesystem
AT parkhilljulian investigatingthecampylobacterjejunitranscriptionalresponsetohostintestinalextractsrevealstheinvolvementofawidelyconservedironuptakesystem
AT murphymichaelep investigatingthecampylobacterjejunitranscriptionalresponsetohostintestinalextractsrevealstheinvolvementofawidelyconservedironuptakesystem
AT gaynorerinc investigatingthecampylobacterjejunitranscriptionalresponsetohostintestinalextractsrevealstheinvolvementofawidelyconservedironuptakesystem