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Normalization strategies for real-time expression data in Chlamydia trachomatis

dc.contributor.authorBorges, V.
dc.contributor.authorFerreira, R.
dc.contributor.authorNoguerira, P.
dc.contributor.authorNunes, A.
dc.contributor.authorBorrego, M.J.
dc.contributor.authorGomes, João Paulo
dc.date.accessioned2012-02-24T18:16:28Z
dc.date.available2012-02-24T18:16:28Z
dc.date.issued2011-03
dc.description.abstractSince Chlamydia trachomatis is a genetically non-tractable pathogen, transcriptomics assumes a fundamental role for the better understanding of its biology. However, the suitability of endogenous controls for normalization of transcriptomic data in this bacterium still needs validation. We aimed to assess the stability of 10 genes for their potential use as endogenous controls in qPCR at both normal and stress (antibiotic treatment) growth conditions throughout the developmental cycle of three strains with different cell-appetence. Normalization was performed using the quantified bacterial genomes. We also tested the applicability of two widely used softwares (geNorm and Normfinder) to our data. For all strains, we found that 16SrRNA was the most stably expressed gene throughout the normal developmental cycle, but it was highly unstable under antibiotic exposure, suggesting prudence when using ribosomal genes as endogenous controls in expression experiments involving stress environments. The geNorm and Normfinder algorithms revealed contrasting results and seem inappropriate for the selected pool of genes. Considering the multiplicity of experimental conditions, there should be an in loco validation of endogenous controls, where 16SrRNA appears to be in the front line. Alternatively, normalization of expression data against genomic DNA, which is less influenced by experimental constraints (especially relevant for intracellular organisms) and stress conditions, likely constitutes a good option. The present study constitutes the first evaluation of putative endogenous controls for real-time expression assays in C. trachomatispor
dc.identifier.urihttp://hdl.handle.net/10400.18/636
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpor
dc.subjectInfecções Sexualmente Transmissíveispor
dc.subjectChlamydia Trachomatispor
dc.subjectReal-time PCRpor
dc.subjectNormalizationpor
dc.subject16SrRNApor
dc.titleNormalization strategies for real-time expression data in Chlamydia trachomatispor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceRedondo Beach, California - EUApor
oaire.citation.title5th Biennial Meeting of the Chlamydia Basic Research Society (CBRS), 18 March 2011por
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor

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