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Characterization of LE3 and LE4, the only lytic phages known to infect the spirochete Leptospira
Leptospira is a phylogenetically unique group of bacteria, and includes the causative agents of leptospirosis, the most globally prevalent zoonosis. Bacteriophages in Leptospira are largely unexplored. To date, a genomic sequence is available for only one temperate leptophage called LE1. Here, we se...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078989/ https://www.ncbi.nlm.nih.gov/pubmed/30082683 http://dx.doi.org/10.1038/s41598-018-29983-6 |
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author | Schiettekatte, Olivier Vincent, Antony T. Malosse, Christian Lechat, Pierre Chamot-Rooke, Julia Veyrier, Frédéric J. Picardeau, Mathieu Bourhy, Pascale |
author_facet | Schiettekatte, Olivier Vincent, Antony T. Malosse, Christian Lechat, Pierre Chamot-Rooke, Julia Veyrier, Frédéric J. Picardeau, Mathieu Bourhy, Pascale |
author_sort | Schiettekatte, Olivier |
collection | PubMed |
description | Leptospira is a phylogenetically unique group of bacteria, and includes the causative agents of leptospirosis, the most globally prevalent zoonosis. Bacteriophages in Leptospira are largely unexplored. To date, a genomic sequence is available for only one temperate leptophage called LE1. Here, we sequenced and analysed the first genomes of the lytic phages LE3 and LE4 that can infect the saprophyte Leptospira biflexa using the lipopolysaccharide O-antigen as receptor. Bioinformatics analysis showed that the 48-kb LE3 and LE4 genomes are similar and contain 62% genes whose function cannot be predicted. Mass spectrometry led to the identification of 21 and 23 phage proteins in LE3 and LE4, respectively. However we did not identify significant similarities with other phage genomes. A search for prophages close to LE4 in the Leptospira genomes allowed for the identification of a related plasmid in L. interrogans and a prophage-like region in the draft genome of a clinical isolate of L. mayottensis. Long-read whole genome sequencing of the L. mayottensis revealed that the genome contained a LE4 phage-like circular plasmid. Further isolation and genomic comparison of leptophages should reveal their role in the genetic evolution of Leptospira. |
format | Online Article Text |
id | pubmed-6078989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60789892018-08-09 Characterization of LE3 and LE4, the only lytic phages known to infect the spirochete Leptospira Schiettekatte, Olivier Vincent, Antony T. Malosse, Christian Lechat, Pierre Chamot-Rooke, Julia Veyrier, Frédéric J. Picardeau, Mathieu Bourhy, Pascale Sci Rep Article Leptospira is a phylogenetically unique group of bacteria, and includes the causative agents of leptospirosis, the most globally prevalent zoonosis. Bacteriophages in Leptospira are largely unexplored. To date, a genomic sequence is available for only one temperate leptophage called LE1. Here, we sequenced and analysed the first genomes of the lytic phages LE3 and LE4 that can infect the saprophyte Leptospira biflexa using the lipopolysaccharide O-antigen as receptor. Bioinformatics analysis showed that the 48-kb LE3 and LE4 genomes are similar and contain 62% genes whose function cannot be predicted. Mass spectrometry led to the identification of 21 and 23 phage proteins in LE3 and LE4, respectively. However we did not identify significant similarities with other phage genomes. A search for prophages close to LE4 in the Leptospira genomes allowed for the identification of a related plasmid in L. interrogans and a prophage-like region in the draft genome of a clinical isolate of L. mayottensis. Long-read whole genome sequencing of the L. mayottensis revealed that the genome contained a LE4 phage-like circular plasmid. Further isolation and genomic comparison of leptophages should reveal their role in the genetic evolution of Leptospira. Nature Publishing Group UK 2018-08-06 /pmc/articles/PMC6078989/ /pubmed/30082683 http://dx.doi.org/10.1038/s41598-018-29983-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Schiettekatte, Olivier Vincent, Antony T. Malosse, Christian Lechat, Pierre Chamot-Rooke, Julia Veyrier, Frédéric J. Picardeau, Mathieu Bourhy, Pascale Characterization of LE3 and LE4, the only lytic phages known to infect the spirochete Leptospira |
title | Characterization of LE3 and LE4, the only lytic phages known to infect the spirochete Leptospira |
title_full | Characterization of LE3 and LE4, the only lytic phages known to infect the spirochete Leptospira |
title_fullStr | Characterization of LE3 and LE4, the only lytic phages known to infect the spirochete Leptospira |
title_full_unstemmed | Characterization of LE3 and LE4, the only lytic phages known to infect the spirochete Leptospira |
title_short | Characterization of LE3 and LE4, the only lytic phages known to infect the spirochete Leptospira |
title_sort | characterization of le3 and le4, the only lytic phages known to infect the spirochete leptospira |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078989/ https://www.ncbi.nlm.nih.gov/pubmed/30082683 http://dx.doi.org/10.1038/s41598-018-29983-6 |
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