Cargando…

A window into lysogeny: revealing temperate phage biology with transcriptomics

Prophages are integrated phage elements that are a pervasive feature of bacterial genomes. The fitness of bacteria is enhanced by prophages that confer beneficial functions such as virulence, stress tolerance or phage resistance, and these functions are encoded by ‘accessory’ or ‘moron’ loci. Whilst...

Descripción completa

Detalles Bibliográficos
Autores principales: Owen, Siân V., Canals, Rocío, Wenner, Nicolas, Hammarlöf, Disa L., Kröger, Carsten, Hinton, Jay C. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067206/
https://www.ncbi.nlm.nih.gov/pubmed/32022660
http://dx.doi.org/10.1099/mgen.0.000330
_version_ 1783505369055625216
author Owen, Siân V.
Canals, Rocío
Wenner, Nicolas
Hammarlöf, Disa L.
Kröger, Carsten
Hinton, Jay C. D.
author_facet Owen, Siân V.
Canals, Rocío
Wenner, Nicolas
Hammarlöf, Disa L.
Kröger, Carsten
Hinton, Jay C. D.
author_sort Owen, Siân V.
collection PubMed
description Prophages are integrated phage elements that are a pervasive feature of bacterial genomes. The fitness of bacteria is enhanced by prophages that confer beneficial functions such as virulence, stress tolerance or phage resistance, and these functions are encoded by ‘accessory’ or ‘moron’ loci. Whilst the majority of phage-encoded genes are repressed during lysogeny, accessory loci are often highly expressed. However, it is challenging to identify novel prophage accessory loci from DNA sequence data alone. Here, we use bacterial RNA-seq data to examine the transcriptional landscapes of five Salmonella prophages. We show that transcriptomic data can be used to heuristically enrich for prophage features that are highly expressed within bacterial cells and represent functionally important accessory loci. Using this approach, we identify a novel antisense RNA species in prophage BTP1, STnc6030, which mediates superinfection exclusion of phage BTP1. Bacterial transcriptomic datasets are a powerful tool to explore the molecular biology of temperate phages.
format Online
Article
Text
id pubmed-7067206
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Microbiology Society
record_format MEDLINE/PubMed
spelling pubmed-70672062020-03-17 A window into lysogeny: revealing temperate phage biology with transcriptomics Owen, Siân V. Canals, Rocío Wenner, Nicolas Hammarlöf, Disa L. Kröger, Carsten Hinton, Jay C. D. Microb Genom Research Article Prophages are integrated phage elements that are a pervasive feature of bacterial genomes. The fitness of bacteria is enhanced by prophages that confer beneficial functions such as virulence, stress tolerance or phage resistance, and these functions are encoded by ‘accessory’ or ‘moron’ loci. Whilst the majority of phage-encoded genes are repressed during lysogeny, accessory loci are often highly expressed. However, it is challenging to identify novel prophage accessory loci from DNA sequence data alone. Here, we use bacterial RNA-seq data to examine the transcriptional landscapes of five Salmonella prophages. We show that transcriptomic data can be used to heuristically enrich for prophage features that are highly expressed within bacterial cells and represent functionally important accessory loci. Using this approach, we identify a novel antisense RNA species in prophage BTP1, STnc6030, which mediates superinfection exclusion of phage BTP1. Bacterial transcriptomic datasets are a powerful tool to explore the molecular biology of temperate phages. Microbiology Society 2020-02-05 /pmc/articles/PMC7067206/ /pubmed/32022660 http://dx.doi.org/10.1099/mgen.0.000330 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License. This article was made open access via a Publish and Read agreement between the Microbiology Society and the corresponding author’s institution.
spellingShingle Research Article
Owen, Siân V.
Canals, Rocío
Wenner, Nicolas
Hammarlöf, Disa L.
Kröger, Carsten
Hinton, Jay C. D.
A window into lysogeny: revealing temperate phage biology with transcriptomics
title A window into lysogeny: revealing temperate phage biology with transcriptomics
title_full A window into lysogeny: revealing temperate phage biology with transcriptomics
title_fullStr A window into lysogeny: revealing temperate phage biology with transcriptomics
title_full_unstemmed A window into lysogeny: revealing temperate phage biology with transcriptomics
title_short A window into lysogeny: revealing temperate phage biology with transcriptomics
title_sort window into lysogeny: revealing temperate phage biology with transcriptomics
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067206/
https://www.ncbi.nlm.nih.gov/pubmed/32022660
http://dx.doi.org/10.1099/mgen.0.000330
work_keys_str_mv AT owensianv awindowintolysogenyrevealingtemperatephagebiologywithtranscriptomics
AT canalsrocio awindowintolysogenyrevealingtemperatephagebiologywithtranscriptomics
AT wennernicolas awindowintolysogenyrevealingtemperatephagebiologywithtranscriptomics
AT hammarlofdisal awindowintolysogenyrevealingtemperatephagebiologywithtranscriptomics
AT krogercarsten awindowintolysogenyrevealingtemperatephagebiologywithtranscriptomics
AT hintonjaycd awindowintolysogenyrevealingtemperatephagebiologywithtranscriptomics
AT owensianv windowintolysogenyrevealingtemperatephagebiologywithtranscriptomics
AT canalsrocio windowintolysogenyrevealingtemperatephagebiologywithtranscriptomics
AT wennernicolas windowintolysogenyrevealingtemperatephagebiologywithtranscriptomics
AT hammarlofdisal windowintolysogenyrevealingtemperatephagebiologywithtranscriptomics
AT krogercarsten windowintolysogenyrevealingtemperatephagebiologywithtranscriptomics
AT hintonjaycd windowintolysogenyrevealingtemperatephagebiologywithtranscriptomics