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Genome-Wide Transcriptional Start Site Mapping and sRNA Identification in the Pathogen Leptospira interrogans
Leptospira are emerging zoonotic pathogens transmitted from animals to humans typically through contaminated environmental sources of water and soil. Regulatory pathways of pathogenic Leptospira spp. underlying the adaptive response to different hosts and environmental conditions remains elusive. In...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243855/ https://www.ncbi.nlm.nih.gov/pubmed/28154810 http://dx.doi.org/10.3389/fcimb.2017.00010 |
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author | Zhukova, Anna Fernandes, Luis Guilherme Hugon, Perrine Pappas, Christopher J. Sismeiro, Odile Coppée, Jean-Yves Becavin, Christophe Malabat, Christophe Eshghi, Azad Zhang, Jun-Jie Yang, Frank X. Picardeau, Mathieu |
author_facet | Zhukova, Anna Fernandes, Luis Guilherme Hugon, Perrine Pappas, Christopher J. Sismeiro, Odile Coppée, Jean-Yves Becavin, Christophe Malabat, Christophe Eshghi, Azad Zhang, Jun-Jie Yang, Frank X. Picardeau, Mathieu |
author_sort | Zhukova, Anna |
collection | PubMed |
description | Leptospira are emerging zoonotic pathogens transmitted from animals to humans typically through contaminated environmental sources of water and soil. Regulatory pathways of pathogenic Leptospira spp. underlying the adaptive response to different hosts and environmental conditions remains elusive. In this study, we provide the first global Transcriptional Start Site (TSS) map of a Leptospira species. RNA was obtained from the pathogen Leptospira interrogans grown at 30°C (optimal in vitro temperature) and 37°C (host temperature) and selectively enriched for 5′ ends of native transcripts. A total of 2865 and 2866 primary TSS (pTSS) were predicted in the genome of L. interrogans at 30 and 37°C, respectively. The majority of the pTSSs were located between 0 and 10 nucleotides from the translational start site, suggesting that leaderless transcripts are a common feature of the leptospiral translational landscape. Comparative differential RNA-sequencing (dRNA-seq) analysis revealed conservation of most pTSS at 30 and 37°C. Promoter prediction algorithms allow the identification of the binding sites of the alternative sigma factor sigma 54. However, other motifs were not identified indicating that Leptospira consensus promoter sequences are inherently different from the Escherichia coli model. RNA sequencing also identified 277 and 226 putative small regulatory RNAs (sRNAs) at 30 and 37°C, respectively, including eight validated sRNAs by Northern blots. These results provide the first global view of TSS and the repertoire of sRNAs in L. interrogans. These data will establish a foundation for future experimental work on gene regulation under various environmental conditions including those in the host. |
format | Online Article Text |
id | pubmed-5243855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52438552017-02-02 Genome-Wide Transcriptional Start Site Mapping and sRNA Identification in the Pathogen Leptospira interrogans Zhukova, Anna Fernandes, Luis Guilherme Hugon, Perrine Pappas, Christopher J. Sismeiro, Odile Coppée, Jean-Yves Becavin, Christophe Malabat, Christophe Eshghi, Azad Zhang, Jun-Jie Yang, Frank X. Picardeau, Mathieu Front Cell Infect Microbiol Microbiology Leptospira are emerging zoonotic pathogens transmitted from animals to humans typically through contaminated environmental sources of water and soil. Regulatory pathways of pathogenic Leptospira spp. underlying the adaptive response to different hosts and environmental conditions remains elusive. In this study, we provide the first global Transcriptional Start Site (TSS) map of a Leptospira species. RNA was obtained from the pathogen Leptospira interrogans grown at 30°C (optimal in vitro temperature) and 37°C (host temperature) and selectively enriched for 5′ ends of native transcripts. A total of 2865 and 2866 primary TSS (pTSS) were predicted in the genome of L. interrogans at 30 and 37°C, respectively. The majority of the pTSSs were located between 0 and 10 nucleotides from the translational start site, suggesting that leaderless transcripts are a common feature of the leptospiral translational landscape. Comparative differential RNA-sequencing (dRNA-seq) analysis revealed conservation of most pTSS at 30 and 37°C. Promoter prediction algorithms allow the identification of the binding sites of the alternative sigma factor sigma 54. However, other motifs were not identified indicating that Leptospira consensus promoter sequences are inherently different from the Escherichia coli model. RNA sequencing also identified 277 and 226 putative small regulatory RNAs (sRNAs) at 30 and 37°C, respectively, including eight validated sRNAs by Northern blots. These results provide the first global view of TSS and the repertoire of sRNAs in L. interrogans. These data will establish a foundation for future experimental work on gene regulation under various environmental conditions including those in the host. Frontiers Media S.A. 2017-01-19 /pmc/articles/PMC5243855/ /pubmed/28154810 http://dx.doi.org/10.3389/fcimb.2017.00010 Text en Copyright © 2017 Zhukova, Fernandes, Hugon, Pappas, Sismeiro, Coppée, Becavin, Malabat, Eshghi, Zhang, Yang and Picardeau. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Zhukova, Anna Fernandes, Luis Guilherme Hugon, Perrine Pappas, Christopher J. Sismeiro, Odile Coppée, Jean-Yves Becavin, Christophe Malabat, Christophe Eshghi, Azad Zhang, Jun-Jie Yang, Frank X. Picardeau, Mathieu Genome-Wide Transcriptional Start Site Mapping and sRNA Identification in the Pathogen Leptospira interrogans |
title | Genome-Wide Transcriptional Start Site Mapping and sRNA Identification in the Pathogen Leptospira interrogans |
title_full | Genome-Wide Transcriptional Start Site Mapping and sRNA Identification in the Pathogen Leptospira interrogans |
title_fullStr | Genome-Wide Transcriptional Start Site Mapping and sRNA Identification in the Pathogen Leptospira interrogans |
title_full_unstemmed | Genome-Wide Transcriptional Start Site Mapping and sRNA Identification in the Pathogen Leptospira interrogans |
title_short | Genome-Wide Transcriptional Start Site Mapping and sRNA Identification in the Pathogen Leptospira interrogans |
title_sort | genome-wide transcriptional start site mapping and srna identification in the pathogen leptospira interrogans |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243855/ https://www.ncbi.nlm.nih.gov/pubmed/28154810 http://dx.doi.org/10.3389/fcimb.2017.00010 |
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