Cargando…

Transducer-Like Protein in Campylobacter jejuni With a Role in Mediating Chemotaxis to Iron and Phosphate

Chemotaxis-mediated motility enables Campylobacter jejuni to navigate through complex environmental gradients and colonize diverse niches. C. jejuni is known to possess several methyl accepting chemotaxis proteins (MCPs), also called transducer-like proteins (Tlps). While the role of some of the Tlp...

Descripción completa

Detalles Bibliográficos
Autores principales: Chandrashekhar, Kshipra, Srivastava, Vishal, Hwang, Sunyoung, Jeon, Byeonghwa, Ryu, Sangryeol, Rajashekara, Gireesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250842/
https://www.ncbi.nlm.nih.gov/pubmed/30505293
http://dx.doi.org/10.3389/fmicb.2018.02674
_version_ 1783372990512103424
author Chandrashekhar, Kshipra
Srivastava, Vishal
Hwang, Sunyoung
Jeon, Byeonghwa
Ryu, Sangryeol
Rajashekara, Gireesh
author_facet Chandrashekhar, Kshipra
Srivastava, Vishal
Hwang, Sunyoung
Jeon, Byeonghwa
Ryu, Sangryeol
Rajashekara, Gireesh
author_sort Chandrashekhar, Kshipra
collection PubMed
description Chemotaxis-mediated motility enables Campylobacter jejuni to navigate through complex environmental gradients and colonize diverse niches. C. jejuni is known to possess several methyl accepting chemotaxis proteins (MCPs), also called transducer-like proteins (Tlps). While the role of some of the Tlps in chemotaxis has been identified, their regulation and role in virulence is still not very clear. Here, we investigated the contribution of Tlp2 to C. jejuni chemotaxis, stress survival and colonization of the chicken gastrointestinal tract. The Δtlp2 deletion mutant showed decreased chemotaxis toward aspartate, pyruvate, inorganic phosphate (Pi), and iron (FeSO(4)). Transcriptional analysis of tlp2 with a promoter fusion reporter assay revealed that the tlp2 promoter (P(tlp2)) was induced by Pi and iron, both in the ferrous (Fe(2+)) and ferric form (Fe(3+)). RT-PCR analysis using overlapping primers indicated that the phoX gene, located immediately downstream of tlp2, is co-transcribed with tlp2. A transcription start site was identified at 53 bp upstream of the tlp2 start codon. The Δtlp2 mutant showed decreased colonization of the chicken gastrointestinal tract. Collectively, our findings revealed that the tlp2 plays a role in C. jejuni pathogenesis and colonization in the chicken host and its expression is regulated by iron.
format Online
Article
Text
id pubmed-6250842
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-62508422018-11-30 Transducer-Like Protein in Campylobacter jejuni With a Role in Mediating Chemotaxis to Iron and Phosphate Chandrashekhar, Kshipra Srivastava, Vishal Hwang, Sunyoung Jeon, Byeonghwa Ryu, Sangryeol Rajashekara, Gireesh Front Microbiol Microbiology Chemotaxis-mediated motility enables Campylobacter jejuni to navigate through complex environmental gradients and colonize diverse niches. C. jejuni is known to possess several methyl accepting chemotaxis proteins (MCPs), also called transducer-like proteins (Tlps). While the role of some of the Tlps in chemotaxis has been identified, their regulation and role in virulence is still not very clear. Here, we investigated the contribution of Tlp2 to C. jejuni chemotaxis, stress survival and colonization of the chicken gastrointestinal tract. The Δtlp2 deletion mutant showed decreased chemotaxis toward aspartate, pyruvate, inorganic phosphate (Pi), and iron (FeSO(4)). Transcriptional analysis of tlp2 with a promoter fusion reporter assay revealed that the tlp2 promoter (P(tlp2)) was induced by Pi and iron, both in the ferrous (Fe(2+)) and ferric form (Fe(3+)). RT-PCR analysis using overlapping primers indicated that the phoX gene, located immediately downstream of tlp2, is co-transcribed with tlp2. A transcription start site was identified at 53 bp upstream of the tlp2 start codon. The Δtlp2 mutant showed decreased colonization of the chicken gastrointestinal tract. Collectively, our findings revealed that the tlp2 plays a role in C. jejuni pathogenesis and colonization in the chicken host and its expression is regulated by iron. Frontiers Media S.A. 2018-11-16 /pmc/articles/PMC6250842/ /pubmed/30505293 http://dx.doi.org/10.3389/fmicb.2018.02674 Text en Copyright © 2018 Chandrashekhar, Srivastava, Hwang, Jeon, Ryu and Rajashekara. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Chandrashekhar, Kshipra
Srivastava, Vishal
Hwang, Sunyoung
Jeon, Byeonghwa
Ryu, Sangryeol
Rajashekara, Gireesh
Transducer-Like Protein in Campylobacter jejuni With a Role in Mediating Chemotaxis to Iron and Phosphate
title Transducer-Like Protein in Campylobacter jejuni With a Role in Mediating Chemotaxis to Iron and Phosphate
title_full Transducer-Like Protein in Campylobacter jejuni With a Role in Mediating Chemotaxis to Iron and Phosphate
title_fullStr Transducer-Like Protein in Campylobacter jejuni With a Role in Mediating Chemotaxis to Iron and Phosphate
title_full_unstemmed Transducer-Like Protein in Campylobacter jejuni With a Role in Mediating Chemotaxis to Iron and Phosphate
title_short Transducer-Like Protein in Campylobacter jejuni With a Role in Mediating Chemotaxis to Iron and Phosphate
title_sort transducer-like protein in campylobacter jejuni with a role in mediating chemotaxis to iron and phosphate
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250842/
https://www.ncbi.nlm.nih.gov/pubmed/30505293
http://dx.doi.org/10.3389/fmicb.2018.02674
work_keys_str_mv AT chandrashekharkshipra transducerlikeproteinincampylobacterjejuniwitharoleinmediatingchemotaxistoironandphosphate
AT srivastavavishal transducerlikeproteinincampylobacterjejuniwitharoleinmediatingchemotaxistoironandphosphate
AT hwangsunyoung transducerlikeproteinincampylobacterjejuniwitharoleinmediatingchemotaxistoironandphosphate
AT jeonbyeonghwa transducerlikeproteinincampylobacterjejuniwitharoleinmediatingchemotaxistoironandphosphate
AT ryusangryeol transducerlikeproteinincampylobacterjejuniwitharoleinmediatingchemotaxistoironandphosphate
AT rajashekaragireesh transducerlikeproteinincampylobacterjejuniwitharoleinmediatingchemotaxistoironandphosphate