OpaR controls a network of downstream transcription factors in Vibrio parahaemolyticus BB22OP
| Autor: | Alison, Kernell Burke, Leah T C, Guthrie, Thero, Modise, Guy, Cormier, Roderick V, Jensen, Linda L, McCarter, Ann M, Stevens |
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| Rok vydání: | 2014 |
| Předmět: |
Reverse Transcriptase Polymerase Chain Reaction
Virulence Factors Blotting Western High-Throughput Nucleotide Sequencing Quorum Sensing Electrophoretic Mobility Shift Assay Gene Expression Regulation Bacterial Regulatory Sequences Nucleic Acid Real-Time Polymerase Chain Reaction Regulon Bacterial Proteins Humans RNA Messenger Vibrio parahaemolyticus Promoter Regions Genetic Transcription Factors Research Article |
| Zdroj: | PLoS ONE |
| ISSN: | 1932-6203 |
| Popis: | Vibrio parahaemolyticus is an emerging world-wide human pathogen that is associated with food-borne gastroenteritis when raw or undercooked seafood is consumed. Expression of virulence factors in this organism is modulated by the phenomenon known as quorum sensing, which permits differential gene regulation at low versus high cell density. The master regulator of quorum sensing in V. parahaemolyticus is OpaR. OpaR not only controls virulence factor gene expression, but also the colony and cellular morphology associated with growth on a surface and biofilm formation. Whole transcriptome Next Generation sequencing (RNA-Seq) was utilized to determine the OpaR regulon by comparing strains BB22OP (opaR +, LM5312) and BB22TR (∆opaR1, LM5674). This work, using the published V. parahaemolyticus BB22OP genome sequence, confirms and expands upon a previous microarray analysis for these two strains that used an Affymetrix GeneChip designed from the closely related V. parahaemolyticus RIMD2210633 genome sequence. Overall there was excellent correlation between the microarray and RNA-Seq data. Eleven transcription factors under OpaR control were identified by both methods and further confirmed by quantitative reverse transcription PCR (qRT-PCR) analysis. Nine of these transcription factors were demonstrated to be direct OpaR targets via in vitro electrophoretic mobility shift assays with purified hexahistidine-tagged OpaR. Identification of the direct and indirect targets of OpaR, including small RNAs, will enable the construction of a network map of regulatory interactions important for the switch between the nonpathogenic and pathogenic states. |
| Databáze: | OpenAIRE |
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