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dc.contributor.authorEsson, D
dc.contributor.authorMather, AE
dc.contributor.authorScanlan, E
dc.contributor.authorGupta, S
dc.contributor.authorde Vries, SPW
dc.contributor.authorBailey, D
dc.contributor.authorHarris, SR
dc.contributor.authorMcKinley, TJ
dc.contributor.authorMéric, G
dc.contributor.authorBerry, SK
dc.contributor.authorMastroeni, P
dc.contributor.authorSheppard, SK
dc.contributor.authorChristie, G
dc.contributor.authorThomson, NR
dc.contributor.authorParkhill, J
dc.contributor.authorMaskell, DJ
dc.contributor.authorGrant, AJ
dc.date.accessioned2017-02-01T15:08:28Z
dc.date.available2017-02-01T15:08:28Z
dc.date.issued2016-12-02
dc.identifier.issn2045-2322
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/262218
dc.description.abstract$\textit{Campylobacter jejuni}$, the most common cause of bacterial diarrhoeal disease, is normally helical. However, it can also adopt straight rod, elongated helical and coccoid forms. Studying how helical morphology is generated, and how it switches between its different forms, is an important objective for understanding this pathogen. Here, we aimed to determine the genetic factors involved in generating the helical shape of $\textit{Campylobacter}$. A C. $\textit{jejuni}$ transposon (Tn) mutant library was screened for non-helical mutants with inconsistent results. Whole genome sequence variation and morphological trends within this Tn library, and in various C. $\textit{jejuni}$ wild type strains, were compared and correlated to detect genomic elements associated with helical and rod morphologies. All rod-shaped C. $\textit{jejuni}$ Tn mutants and all rod-shaped laboratory, clinical and environmental C. $\textit{jejuni}$ and $\textit{Campylobacter coli}$ contained genetic changes within the $\textit{pgp1}$ or $\textit{pgp2}$ genes, which encode peptidoglycan modifying enzymes. We therefore confirm the importance of Pgp1 and Pgp2 in the maintenance of helical shape and extended this to a wide range of C. $\textit{jejuni}$ and C. $\textit{coli}$ isolates. Genome sequence analysis revealed variation in the sequence and length of homopolymeric tracts found within these genes, providing a potential mechanism of phase variation of cell shape.
dc.description.sponsorshipThis work was funded by The Wellcome Trust through a PhD training studentship awarded to DE, and was supported by an Isaac Newton Trust/Wellcome Trust ISSF/University of Cambridge joint research grant awarded to AJG. SG and SPWDV were funded by BBSRC grant BB/K004514/1. AEM, SH, NRT and JP were supported by the Wellcome Trust grant number 098051. AEM was also supported by BBSRC grant BB/M014088/1. SKS was funded by Biotechnology and Biological Sciences Research Council grant BB/I02464X/1, Medical Research Council grant MR/L015080/1 and Wellcome Trust grant 088786/C/09/Z. GM was supported by a National Institute for Social Care and Health Research Fellowship (HF-14-13).
dc.languageeng
dc.language.isoen
dc.publisherNature Publishing Group
dc.rightsAttribution 4.0 International
dc.rightsAttribution 4.0 International
dc.rightsAttribution 4.0 International
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectAnimals
dc.subjectBacterial Proteins
dc.subjectCampylobacter Infections
dc.subjectCampylobacter coli
dc.subjectCampylobacter jejuni
dc.subjectChickens
dc.subjectDNA Transposable Elements
dc.subjectGene Expression Regulation, Bacterial
dc.subjectGene Library
dc.subjectGenome, Bacterial
dc.subjectHumans
dc.subjectMutagenesis, Site-Directed
dc.subjectMutation
dc.subjectPeptidoglycan
dc.subjectPoultry Diseases
dc.subjectWhole Genome Sequencing
dc.titleGenomic variations leading to alterations in cell morphology of $\textit{Campylobacter}$ spp
dc.typeArticle
prism.number38303
prism.publicationDate2016
prism.publicationNameScientific Reports
prism.volume6
dc.identifier.doi10.17863/CAM.7473
dcterms.dateAccepted2016-11-07
rioxxterms.versionofrecord10.1038/srep38303
rioxxterms.versionVoR
rioxxterms.licenseref.urihttp://creativecommons.org/licenses/by/4.0/
rioxxterms.licenseref.startdate2016-12-02
dc.contributor.orcidde Vries, Stefan [0000-0002-0823-208X]
dc.contributor.orcidBerry, Sophia [0000-0002-2184-1074]
dc.contributor.orcidMastroeni, Pietro [0000-0003-3838-4962]
dc.contributor.orcidChristie, Graham [0000-0001-7177-9646]
dc.contributor.orcidParkhill, Julian [0000-0002-7069-5958]
dc.contributor.orcidMaskell, Duncan [0000-0002-5065-653X]
dc.contributor.orcidGrant, Andrew [0000-0001-9746-2989]
dc.identifier.eissn2045-2322
rioxxterms.typeJournal Article/Review
pubs.funder-project-idMedical Research Council (G1100102)
pubs.funder-project-idBiotechnology and Biological Sciences Research Council (BB/I002189/1)
pubs.funder-project-idBiotechnology and Biological Sciences Research Council (BB/M014088/1)
pubs.funder-project-idBiotechnology and Biological Sciences Research Council (BB/K004514/1)
cam.issuedOnline2016-12-02
cam.orpheus.successThu Jan 30 12:57:04 GMT 2020 - The item has an open VoR version.
rioxxterms.freetoread.startdate2100-01-01


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Attribution 4.0 International
Except where otherwise noted, this item's licence is described as Attribution 4.0 International