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Core defense hotspots within Pseudomonas aeruginosa are a consistent and rich source of anti-phage defense systems
Bacteria use a diverse arsenal of anti-phage immune systems, including CRISPR-Cas and restriction enzymes. Recent advances in anti-phage system discovery and annotation tools have unearthed many unique systems, often encoded in horizontally transferred defense islands, which can be horizontally tran...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250203/ https://www.ncbi.nlm.nih.gov/pubmed/37140042 http://dx.doi.org/10.1093/nar/gkad317 |
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author | Johnson, Matthew C Laderman, Eric Huiting, Erin Zhang, Chi Davidson, Alan Bondy-Denomy, Joseph |
author_facet | Johnson, Matthew C Laderman, Eric Huiting, Erin Zhang, Chi Davidson, Alan Bondy-Denomy, Joseph |
author_sort | Johnson, Matthew C |
collection | PubMed |
description | Bacteria use a diverse arsenal of anti-phage immune systems, including CRISPR-Cas and restriction enzymes. Recent advances in anti-phage system discovery and annotation tools have unearthed many unique systems, often encoded in horizontally transferred defense islands, which can be horizontally transferred. Here, we developed Hidden Markov Models (HMMs) for defense systems and queried microbial genomes on the NCBI database. Out of the 30 species with >200 completely sequenced genomes, our analysis found Pseudomonas aeruginosa exhibits the greatest diversity of anti-phage systems, as measured by Shannon entropy. Using network analysis to identify the common neighbors of anti-phage systems, we identified two core defense hotspot loci (cDHS1 and cDHS2). cDHS1 is up to 224 kb (median: 26 kb) with varied arrangements of more than 30 distinct immune systems across isolates, while cDHS2 has 24 distinct systems (median: 6 kb). Both cDHS regions are occupied in a majority of P. aeruginosa isolates. Most cDHS genes are of unknown function potentially representing new anti-phage systems, which we validated by identifying a novel anti-phage system (Shango) commonly encoded in cDHS1. Identifying core genes flanking immune islands could simplify immune system discovery and may represent popular landing spots for diverse MGEs carrying anti-phage systems. |
format | Online Article Text |
id | pubmed-10250203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102502032023-06-10 Core defense hotspots within Pseudomonas aeruginosa are a consistent and rich source of anti-phage defense systems Johnson, Matthew C Laderman, Eric Huiting, Erin Zhang, Chi Davidson, Alan Bondy-Denomy, Joseph Nucleic Acids Res Genomics Bacteria use a diverse arsenal of anti-phage immune systems, including CRISPR-Cas and restriction enzymes. Recent advances in anti-phage system discovery and annotation tools have unearthed many unique systems, often encoded in horizontally transferred defense islands, which can be horizontally transferred. Here, we developed Hidden Markov Models (HMMs) for defense systems and queried microbial genomes on the NCBI database. Out of the 30 species with >200 completely sequenced genomes, our analysis found Pseudomonas aeruginosa exhibits the greatest diversity of anti-phage systems, as measured by Shannon entropy. Using network analysis to identify the common neighbors of anti-phage systems, we identified two core defense hotspot loci (cDHS1 and cDHS2). cDHS1 is up to 224 kb (median: 26 kb) with varied arrangements of more than 30 distinct immune systems across isolates, while cDHS2 has 24 distinct systems (median: 6 kb). Both cDHS regions are occupied in a majority of P. aeruginosa isolates. Most cDHS genes are of unknown function potentially representing new anti-phage systems, which we validated by identifying a novel anti-phage system (Shango) commonly encoded in cDHS1. Identifying core genes flanking immune islands could simplify immune system discovery and may represent popular landing spots for diverse MGEs carrying anti-phage systems. Oxford University Press 2023-05-04 /pmc/articles/PMC10250203/ /pubmed/37140042 http://dx.doi.org/10.1093/nar/gkad317 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Genomics Johnson, Matthew C Laderman, Eric Huiting, Erin Zhang, Chi Davidson, Alan Bondy-Denomy, Joseph Core defense hotspots within Pseudomonas aeruginosa are a consistent and rich source of anti-phage defense systems |
title | Core defense hotspots within Pseudomonas aeruginosa are a consistent and rich source of anti-phage defense systems |
title_full | Core defense hotspots within Pseudomonas aeruginosa are a consistent and rich source of anti-phage defense systems |
title_fullStr | Core defense hotspots within Pseudomonas aeruginosa are a consistent and rich source of anti-phage defense systems |
title_full_unstemmed | Core defense hotspots within Pseudomonas aeruginosa are a consistent and rich source of anti-phage defense systems |
title_short | Core defense hotspots within Pseudomonas aeruginosa are a consistent and rich source of anti-phage defense systems |
title_sort | core defense hotspots within pseudomonas aeruginosa are a consistent and rich source of anti-phage defense systems |
topic | Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250203/ https://www.ncbi.nlm.nih.gov/pubmed/37140042 http://dx.doi.org/10.1093/nar/gkad317 |
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