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Comparative Genomics Reveals the Core Gene Toolbox for the Fungus-Insect Symbiosis
Modern genomics has shed light on many entomopathogenic fungi and expanded our knowledge widely; however, little is known about the genomic features of the insect-commensal fungi. Harpellales are obligate commensals living in the digestive tracts of disease-bearing insects (black flies, midges, and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954228/ https://www.ncbi.nlm.nih.gov/pubmed/29764946 http://dx.doi.org/10.1128/mBio.00636-18 |
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author | Wang, Yan Stata, Matt Wang, Wei Stajich, Jason E. White, Merlin M. Moncalvo, Jean-Marc |
author_facet | Wang, Yan Stata, Matt Wang, Wei Stajich, Jason E. White, Merlin M. Moncalvo, Jean-Marc |
author_sort | Wang, Yan |
collection | PubMed |
description | Modern genomics has shed light on many entomopathogenic fungi and expanded our knowledge widely; however, little is known about the genomic features of the insect-commensal fungi. Harpellales are obligate commensals living in the digestive tracts of disease-bearing insects (black flies, midges, and mosquitoes). In this study, we produced and annotated whole-genome sequences of nine Harpellales taxa and conducted the first comparative analyses to infer the genomic diversity within the members of the Harpellales. The genomes of the insect gut fungi feature low (26% to 37%) GC content and large genome size variations (25 to 102 Mb). Further comparisons with insect-pathogenic fungi (from both Ascomycota and Zoopagomycota), as well as with free-living relatives (as negative controls), helped to identify a gene toolbox that is essential to the fungus-insect symbiosis. The results not only narrow the genomic scope of fungus-insect interactions from several thousands to eight core players but also distinguish host invasion strategies employed by insect pathogens and commensals. The genomic content suggests that insect commensal fungi rely mostly on adhesion protein anchors that target digestive system, while entomopathogenic fungi have higher numbers of transmembrane helices, signal peptides, and pathogen-host interaction (PHI) genes across the whole genome and enrich genes as well as functional domains to inactivate the host inflammation system and suppress the host defense. Phylogenomic analyses have revealed that genome sizes of Harpellales fungi vary among lineages with an integer-multiple pattern, which implies that ancient genome duplications may have occurred within the gut of insects. |
format | Online Article Text |
id | pubmed-5954228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-59542282018-05-23 Comparative Genomics Reveals the Core Gene Toolbox for the Fungus-Insect Symbiosis Wang, Yan Stata, Matt Wang, Wei Stajich, Jason E. White, Merlin M. Moncalvo, Jean-Marc mBio Research Article Modern genomics has shed light on many entomopathogenic fungi and expanded our knowledge widely; however, little is known about the genomic features of the insect-commensal fungi. Harpellales are obligate commensals living in the digestive tracts of disease-bearing insects (black flies, midges, and mosquitoes). In this study, we produced and annotated whole-genome sequences of nine Harpellales taxa and conducted the first comparative analyses to infer the genomic diversity within the members of the Harpellales. The genomes of the insect gut fungi feature low (26% to 37%) GC content and large genome size variations (25 to 102 Mb). Further comparisons with insect-pathogenic fungi (from both Ascomycota and Zoopagomycota), as well as with free-living relatives (as negative controls), helped to identify a gene toolbox that is essential to the fungus-insect symbiosis. The results not only narrow the genomic scope of fungus-insect interactions from several thousands to eight core players but also distinguish host invasion strategies employed by insect pathogens and commensals. The genomic content suggests that insect commensal fungi rely mostly on adhesion protein anchors that target digestive system, while entomopathogenic fungi have higher numbers of transmembrane helices, signal peptides, and pathogen-host interaction (PHI) genes across the whole genome and enrich genes as well as functional domains to inactivate the host inflammation system and suppress the host defense. Phylogenomic analyses have revealed that genome sizes of Harpellales fungi vary among lineages with an integer-multiple pattern, which implies that ancient genome duplications may have occurred within the gut of insects. American Society for Microbiology 2018-05-15 /pmc/articles/PMC5954228/ /pubmed/29764946 http://dx.doi.org/10.1128/mBio.00636-18 Text en © Crown copyright 2018. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Wang, Yan Stata, Matt Wang, Wei Stajich, Jason E. White, Merlin M. Moncalvo, Jean-Marc Comparative Genomics Reveals the Core Gene Toolbox for the Fungus-Insect Symbiosis |
title | Comparative Genomics Reveals the Core Gene Toolbox for the Fungus-Insect Symbiosis |
title_full | Comparative Genomics Reveals the Core Gene Toolbox for the Fungus-Insect Symbiosis |
title_fullStr | Comparative Genomics Reveals the Core Gene Toolbox for the Fungus-Insect Symbiosis |
title_full_unstemmed | Comparative Genomics Reveals the Core Gene Toolbox for the Fungus-Insect Symbiosis |
title_short | Comparative Genomics Reveals the Core Gene Toolbox for the Fungus-Insect Symbiosis |
title_sort | comparative genomics reveals the core gene toolbox for the fungus-insect symbiosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954228/ https://www.ncbi.nlm.nih.gov/pubmed/29764946 http://dx.doi.org/10.1128/mBio.00636-18 |
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