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Campylobacter bacteriophage DA10: an excised temperate bacteriophage targeted by CRISPR-cas
BACKGROUND: Lytic bacteriophages that infect Campylobacter spp. have been utilized to develop therapeutic/decontamination techniques. However, the association of Campylobacter spp. and bacteriophages has been the focus of several strands of research aimed at understanding the complex relationships t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291426/ https://www.ncbi.nlm.nih.gov/pubmed/32532247 http://dx.doi.org/10.1186/s12864-020-06808-3 |
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author | Hooton, Steven D’Angelantonio, Daniela Hu, Yang Connerton, Phillippa L. Aprea, Giuseppe Connerton, Ian F. |
author_facet | Hooton, Steven D’Angelantonio, Daniela Hu, Yang Connerton, Phillippa L. Aprea, Giuseppe Connerton, Ian F. |
author_sort | Hooton, Steven |
collection | PubMed |
description | BACKGROUND: Lytic bacteriophages that infect Campylobacter spp. have been utilized to develop therapeutic/decontamination techniques. However, the association of Campylobacter spp. and bacteriophages has been the focus of several strands of research aimed at understanding the complex relationships that have developed between predators and prey over evolutionary time. The activities of endogenous temperate bacteriophages have been used to evaluate genomic rearrangements and differential protein expression in host cells, and mechanisms of resistance to bacteriophage infection in campylobacters such as phase variation and CRISPR-mediated immunity. RESULTS: Temperate bacteriophage DA10 represents a novel excised and infective virus capable of replication in a restricted set of C. jejuni and C. coli hosts. Whole genome sequencing reveals that DA10 (35,379 bp) forms part of a novel group of temperate bacteriophages that have limited distribution among database host genome sequences. Analysis of potential host genomes reveals a robust response against DA10 and DA10-like bacteriophages is driven by CRISPR-mediated immunity with 75% of DA10 ORFs represented as ~ 30 bp spacer sequences in numerous Campylobacter Type II-C CRISPR arrays. Several DA10-like homologues have been identified in a small sub-set of C. jejuni and C. coli genome sequences (ranging from near complete integrated prophage sequences to fragments recognisable in the sequence read archive). CONCLUSIONS: A complete intact DA10-like prophage in C. jejuni CJ677CC520 provides evidence that the associations between host and DA10-like bacteriophages are long-standing in evolutionary timescales. Extensive nucleotide substitution and loss can be observed in the integrated DA10-like prophage of CJ677CC520 compared to other relatives as observed through pairwise genome comparisons. Examining factors that have limited the population expansion of the prophage, while others appear to have thrived and prospered (Mu-like, CJIE-like, and lytic Campylobacter bacteriophages) will assist in identifying the underlying evolutionary processes in the natural environment. |
format | Online Article Text |
id | pubmed-7291426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72914262020-06-12 Campylobacter bacteriophage DA10: an excised temperate bacteriophage targeted by CRISPR-cas Hooton, Steven D’Angelantonio, Daniela Hu, Yang Connerton, Phillippa L. Aprea, Giuseppe Connerton, Ian F. BMC Genomics Research Article BACKGROUND: Lytic bacteriophages that infect Campylobacter spp. have been utilized to develop therapeutic/decontamination techniques. However, the association of Campylobacter spp. and bacteriophages has been the focus of several strands of research aimed at understanding the complex relationships that have developed between predators and prey over evolutionary time. The activities of endogenous temperate bacteriophages have been used to evaluate genomic rearrangements and differential protein expression in host cells, and mechanisms of resistance to bacteriophage infection in campylobacters such as phase variation and CRISPR-mediated immunity. RESULTS: Temperate bacteriophage DA10 represents a novel excised and infective virus capable of replication in a restricted set of C. jejuni and C. coli hosts. Whole genome sequencing reveals that DA10 (35,379 bp) forms part of a novel group of temperate bacteriophages that have limited distribution among database host genome sequences. Analysis of potential host genomes reveals a robust response against DA10 and DA10-like bacteriophages is driven by CRISPR-mediated immunity with 75% of DA10 ORFs represented as ~ 30 bp spacer sequences in numerous Campylobacter Type II-C CRISPR arrays. Several DA10-like homologues have been identified in a small sub-set of C. jejuni and C. coli genome sequences (ranging from near complete integrated prophage sequences to fragments recognisable in the sequence read archive). CONCLUSIONS: A complete intact DA10-like prophage in C. jejuni CJ677CC520 provides evidence that the associations between host and DA10-like bacteriophages are long-standing in evolutionary timescales. Extensive nucleotide substitution and loss can be observed in the integrated DA10-like prophage of CJ677CC520 compared to other relatives as observed through pairwise genome comparisons. Examining factors that have limited the population expansion of the prophage, while others appear to have thrived and prospered (Mu-like, CJIE-like, and lytic Campylobacter bacteriophages) will assist in identifying the underlying evolutionary processes in the natural environment. BioMed Central 2020-06-12 /pmc/articles/PMC7291426/ /pubmed/32532247 http://dx.doi.org/10.1186/s12864-020-06808-3 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Hooton, Steven D’Angelantonio, Daniela Hu, Yang Connerton, Phillippa L. Aprea, Giuseppe Connerton, Ian F. Campylobacter bacteriophage DA10: an excised temperate bacteriophage targeted by CRISPR-cas |
title | Campylobacter bacteriophage DA10: an excised temperate bacteriophage targeted by CRISPR-cas |
title_full | Campylobacter bacteriophage DA10: an excised temperate bacteriophage targeted by CRISPR-cas |
title_fullStr | Campylobacter bacteriophage DA10: an excised temperate bacteriophage targeted by CRISPR-cas |
title_full_unstemmed | Campylobacter bacteriophage DA10: an excised temperate bacteriophage targeted by CRISPR-cas |
title_short | Campylobacter bacteriophage DA10: an excised temperate bacteriophage targeted by CRISPR-cas |
title_sort | campylobacter bacteriophage da10: an excised temperate bacteriophage targeted by crispr-cas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291426/ https://www.ncbi.nlm.nih.gov/pubmed/32532247 http://dx.doi.org/10.1186/s12864-020-06808-3 |
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