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Temperature-dependent sRNA transcriptome of the Lyme disease spirochete

BACKGROUND: Transmission of Borrelia burgdorferi from its tick vector to a vertebrate host requires extensive reprogramming of gene expression. Small regulatory RNAs (sRNA) have emerged in the last decade as important regulators of bacterial gene expression. Despite the widespread observation of sRN...

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Autores principales: Popitsch, Niko, Bilusic, Ivana, Rescheneder, Philipp, Schroeder, Renée, Lybecker, Meghan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216591/
https://www.ncbi.nlm.nih.gov/pubmed/28056764
http://dx.doi.org/10.1186/s12864-016-3398-3
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author Popitsch, Niko
Bilusic, Ivana
Rescheneder, Philipp
Schroeder, Renée
Lybecker, Meghan
author_facet Popitsch, Niko
Bilusic, Ivana
Rescheneder, Philipp
Schroeder, Renée
Lybecker, Meghan
author_sort Popitsch, Niko
collection PubMed
description BACKGROUND: Transmission of Borrelia burgdorferi from its tick vector to a vertebrate host requires extensive reprogramming of gene expression. Small regulatory RNAs (sRNA) have emerged in the last decade as important regulators of bacterial gene expression. Despite the widespread observation of sRNA-mediated gene regulation, only one sRNA has been characterized in the Lyme disease spirochete B. burgdorferi. We employed an sRNA-specific deep-sequencing approach to identify the small RNA transcriptome of B. burgdorferi at both 23 °C and 37 °C, which mimics in vitro the transmission from the tick vector to the mammalian host. RESULTS: We identified over 1000 sRNAs in B. burgdorferi revealing large amounts of antisense and intragenic sRNAs, as well as characteristic intergenic and 5′ UTR-associated sRNAs. A large fraction of the novel sRNAs (43%) are temperature-dependent and differentially expressed at the two temperatures, suggesting a role in gene regulation for adaptation during transmission. In addition, many genes important for maintenance of Borrelia during its enzootic cycle are associated with antisense RNAs or 5′ UTR sRNAs. RNA-seq data were validated for twenty-two of the sRNAs via Northern blot analyses. CONCLUSIONS: Our study demonstrates that sRNAs are abundant and differentially expressed by environmental conditions suggesting that gene regulation via sRNAs is a common mechanism utilized in B. burgdorferi. In addition, the identification of antisense and intragenic sRNAs impacts the broadly used loss-of-function genetic approach used to study gene function and increases the coding potential of a small genome. To facilitate access to the analyzed RNA-seq data we have set-up a website at http://www.cibiv.at/~niko/bbdb/ that includes a UCSC browser track hub. By clicking on the respective link, researchers can interactively inspect the data in the UCSC genome browser (Kent et al., Genome Res 12:996-1006, 2002). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3398-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-52165912017-01-09 Temperature-dependent sRNA transcriptome of the Lyme disease spirochete Popitsch, Niko Bilusic, Ivana Rescheneder, Philipp Schroeder, Renée Lybecker, Meghan BMC Genomics Research Article BACKGROUND: Transmission of Borrelia burgdorferi from its tick vector to a vertebrate host requires extensive reprogramming of gene expression. Small regulatory RNAs (sRNA) have emerged in the last decade as important regulators of bacterial gene expression. Despite the widespread observation of sRNA-mediated gene regulation, only one sRNA has been characterized in the Lyme disease spirochete B. burgdorferi. We employed an sRNA-specific deep-sequencing approach to identify the small RNA transcriptome of B. burgdorferi at both 23 °C and 37 °C, which mimics in vitro the transmission from the tick vector to the mammalian host. RESULTS: We identified over 1000 sRNAs in B. burgdorferi revealing large amounts of antisense and intragenic sRNAs, as well as characteristic intergenic and 5′ UTR-associated sRNAs. A large fraction of the novel sRNAs (43%) are temperature-dependent and differentially expressed at the two temperatures, suggesting a role in gene regulation for adaptation during transmission. In addition, many genes important for maintenance of Borrelia during its enzootic cycle are associated with antisense RNAs or 5′ UTR sRNAs. RNA-seq data were validated for twenty-two of the sRNAs via Northern blot analyses. CONCLUSIONS: Our study demonstrates that sRNAs are abundant and differentially expressed by environmental conditions suggesting that gene regulation via sRNAs is a common mechanism utilized in B. burgdorferi. In addition, the identification of antisense and intragenic sRNAs impacts the broadly used loss-of-function genetic approach used to study gene function and increases the coding potential of a small genome. To facilitate access to the analyzed RNA-seq data we have set-up a website at http://www.cibiv.at/~niko/bbdb/ that includes a UCSC browser track hub. By clicking on the respective link, researchers can interactively inspect the data in the UCSC genome browser (Kent et al., Genome Res 12:996-1006, 2002). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3398-3) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-05 /pmc/articles/PMC5216591/ /pubmed/28056764 http://dx.doi.org/10.1186/s12864-016-3398-3 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Popitsch, Niko
Bilusic, Ivana
Rescheneder, Philipp
Schroeder, Renée
Lybecker, Meghan
Temperature-dependent sRNA transcriptome of the Lyme disease spirochete
title Temperature-dependent sRNA transcriptome of the Lyme disease spirochete
title_full Temperature-dependent sRNA transcriptome of the Lyme disease spirochete
title_fullStr Temperature-dependent sRNA transcriptome of the Lyme disease spirochete
title_full_unstemmed Temperature-dependent sRNA transcriptome of the Lyme disease spirochete
title_short Temperature-dependent sRNA transcriptome of the Lyme disease spirochete
title_sort temperature-dependent srna transcriptome of the lyme disease spirochete
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216591/
https://www.ncbi.nlm.nih.gov/pubmed/28056764
http://dx.doi.org/10.1186/s12864-016-3398-3
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