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Small Regulatory RNAs of Rickettsia conorii

Small regulatory RNAs comprise critically important modulators of gene expression in bacteria, yet very little is known about their prevalence and functions in Rickettsia species. R. conorii, the causative agent of Mediterranean spotted fever, is a tick-borne pathogen that primarily infects microvas...

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Autores principales: Narra, Hema P., Schroeder, Casey L. C., Sahni, Abha, Rojas, Mark, Khanipov, Kamil, Fofanov, Yuriy, Sahni, Sanjeev K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105140/
https://www.ncbi.nlm.nih.gov/pubmed/27834404
http://dx.doi.org/10.1038/srep36728
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author Narra, Hema P.
Schroeder, Casey L. C.
Sahni, Abha
Rojas, Mark
Khanipov, Kamil
Fofanov, Yuriy
Sahni, Sanjeev K.
author_facet Narra, Hema P.
Schroeder, Casey L. C.
Sahni, Abha
Rojas, Mark
Khanipov, Kamil
Fofanov, Yuriy
Sahni, Sanjeev K.
author_sort Narra, Hema P.
collection PubMed
description Small regulatory RNAs comprise critically important modulators of gene expression in bacteria, yet very little is known about their prevalence and functions in Rickettsia species. R. conorii, the causative agent of Mediterranean spotted fever, is a tick-borne pathogen that primarily infects microvascular endothelium in humans. We have determined the transcriptional landscape of R. conorii during infection of Human Microvascular Endothelial Cells (HMECs) by strand-specific RNA sequencing to identify 4 riboswitches, 13 trans-acting (intergenic), and 22 cis-acting (antisense) small RNAs (termed ‘Rc_sR’s). Independent expression of four novel trans-acting sRNAs (Rc_sR31, Rc_sR33, Rc_sR35, and Rc_sR42) and known bacterial sRNAs (6S, RNaseP_bact_a, ffs, and α-tmRNA) was next confirmed by Northern hybridization. Comparative analysis during infection of HMECs vis-à-vis tick AAE2 cells revealed significantly higher expression of Rc_sR35 and Rc_sR42 in HMECs, whereas Rc_sR31 and Rc_sR33 were expressed at similar levels in both cell types. We further predicted a total of 502 genes involved in all important biological processes as potential targets of Rc_sRs and validated the interaction of Rc_sR42 with cydA (cytochrome d ubiquinol oxidase subunit I). Our findings constitute the first evidence of the existence of post-transcriptional riboregulatory mechanisms in R. conorii and interactions between a novel Rc_sR and its target mRNA.
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spelling pubmed-51051402016-11-17 Small Regulatory RNAs of Rickettsia conorii Narra, Hema P. Schroeder, Casey L. C. Sahni, Abha Rojas, Mark Khanipov, Kamil Fofanov, Yuriy Sahni, Sanjeev K. Sci Rep Article Small regulatory RNAs comprise critically important modulators of gene expression in bacteria, yet very little is known about their prevalence and functions in Rickettsia species. R. conorii, the causative agent of Mediterranean spotted fever, is a tick-borne pathogen that primarily infects microvascular endothelium in humans. We have determined the transcriptional landscape of R. conorii during infection of Human Microvascular Endothelial Cells (HMECs) by strand-specific RNA sequencing to identify 4 riboswitches, 13 trans-acting (intergenic), and 22 cis-acting (antisense) small RNAs (termed ‘Rc_sR’s). Independent expression of four novel trans-acting sRNAs (Rc_sR31, Rc_sR33, Rc_sR35, and Rc_sR42) and known bacterial sRNAs (6S, RNaseP_bact_a, ffs, and α-tmRNA) was next confirmed by Northern hybridization. Comparative analysis during infection of HMECs vis-à-vis tick AAE2 cells revealed significantly higher expression of Rc_sR35 and Rc_sR42 in HMECs, whereas Rc_sR31 and Rc_sR33 were expressed at similar levels in both cell types. We further predicted a total of 502 genes involved in all important biological processes as potential targets of Rc_sRs and validated the interaction of Rc_sR42 with cydA (cytochrome d ubiquinol oxidase subunit I). Our findings constitute the first evidence of the existence of post-transcriptional riboregulatory mechanisms in R. conorii and interactions between a novel Rc_sR and its target mRNA. Nature Publishing Group 2016-11-11 /pmc/articles/PMC5105140/ /pubmed/27834404 http://dx.doi.org/10.1038/srep36728 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Narra, Hema P.
Schroeder, Casey L. C.
Sahni, Abha
Rojas, Mark
Khanipov, Kamil
Fofanov, Yuriy
Sahni, Sanjeev K.
Small Regulatory RNAs of Rickettsia conorii
title Small Regulatory RNAs of Rickettsia conorii
title_full Small Regulatory RNAs of Rickettsia conorii
title_fullStr Small Regulatory RNAs of Rickettsia conorii
title_full_unstemmed Small Regulatory RNAs of Rickettsia conorii
title_short Small Regulatory RNAs of Rickettsia conorii
title_sort small regulatory rnas of rickettsia conorii
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105140/
https://www.ncbi.nlm.nih.gov/pubmed/27834404
http://dx.doi.org/10.1038/srep36728
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