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In silico scrutiny of genes revealing phylogenetic congruence with clinical prevalence or tropism properties of Chlamydia trachomatis strains

dc.contributor.authorFerreira, R.
dc.contributor.authorAntelo, M.
dc.contributor.authorNunes, A.
dc.contributor.authorBorges, V.
dc.contributor.authorDamião, V.
dc.contributor.authorBorrego, M.J.
dc.contributor.authorGomes, João Paulo
dc.date.accessioned2015-09-24T15:27:41Z
dc.date.available2015-09-24T15:27:41Z
dc.date.issued2014-11-05
dc.description.abstractMicrobes possess a multiplicity of virulence factors that confer them the ability to specifically infect distinct biological niches. Contrary to what is known for other bacteria, for the obligate intracellular human pathogen Chlamydia trachomatis, the knowledge of the molecular basis underlying serovars’ tissue specificity is scarce. We examined all ~900 genes to evaluate the association between individual phylogenies and cell-appetence or ecological success of C. trachomatis strains. Only ~1% of the genes presented a tree topology showing the segregation of all three disease groups (ocular, urogenital, and lymphatic) into three wellsupported clades. Approximately 28% of the genes, which include the majority of the genes encoding putative type III secretion system effectors and Inc proteins, present a phylogenetic tree where only lymphogranuloma venereum strains form a clade. Similarly, an exclusive phylogenetic segregation of the most prevalent genital serovars was observed for 61 proteins. Curiously, these serovars are phylogenetically cosegregated with the lymphogranuloma venereum serovars for ~20% of the genes. Some clade-specific pseudogenes were identified (novel findings include the conserved hypothetical protein CT037 and the predicted a-hemolysin CT473), suggesting their putative expendability for the infection of particular niches. Approximately 3.5% of the genes revealed a significant overrepresentation of nonsynonymous mutations, and the majority encode proteins that directly interact with the host. Overall, this in silico scrutiny of genes whose phylogeny is congruent with clinical prevalence or tissue specificity of C. trachomatis strains may constitute an important database of putative targets for future functional studies to evaluate their biological role in chlamydial infections.por
dc.description.sponsorshipThis work was supported by a grant, ERA-PTG/0004/2010, from Fundação para a Ciência e a Tecnologia (FCT) (to J.P.G.), in the frame of ERA-NET PathoGenoMics. A.N. is recipient of a FCT post-doctoral fellowship (SFRH/BPD/75295/2010), V.B. and R.F. are recipients of Ph.D. fellowships (SFRH/BD/68527/2010 and SFRH/BD/68532/2010, respectively) from FCT, and V.D. is a recipient of fellowship on behalf of the grant ERA-PTG/0004/2010.por
dc.identifier.citationG3 (Bethesda). 2014 Nov 5;5(1):9-19. doi: 10.1534/g3.114.015354por
dc.identifier.doi10.1534/g3.114.015354
dc.identifier.issn2160-1836
dc.identifier.urihttp://hdl.handle.net/10400.18/3161
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherGenetics Society of America
dc.relation.publisherversionhttp://www.g3journal.org/content/5/1/9.longpor
dc.subjectChlamydia Trachomatispor
dc.subjectPhylogenypor
dc.subjectTropismpor
dc.subjectInfecções Sexualmente Transmissíveispor
dc.titleIn silico scrutiny of genes revealing phylogenetic congruence with clinical prevalence or tropism properties of Chlamydia trachomatis strainspor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage19por
oaire.citation.startPage9por
oaire.citation.titleG3 : genes - genomes - geneticspor
oaire.citation.volume5(1)por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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