<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sahu N</submitter><funding>European Research Council</funding><pagination>1668-1681</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7615209</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(9)</volume><pubmed_abstract>The fungal genus Armillaria contains necrotrophic pathogens and some of the largest terrestrial organisms that cause tremendous losses in diverse ecosystems, yet how they evolved pathogenicity in a clade of dominantly non-pathogenic wood degraders remains elusive. Here we show that Armillaria species, in addition to gene duplications and de novo gene origins, acquired at least 1,025 genes via 124 horizontal gene transfer events, primarily from Ascomycota. Horizontal gene transfer might have affected plant biomass degrading and virulence abilities of Armillaria, and provides an explanation for their unusual, soft rot-like wood decay strategy. Combined multi-species expression data revealed extensive regulation of horizontally acquired and wood-decay related genes, putative virulence factors</pubmed_abstract><journal>Nature microbiology</journal><pubmed_title>Vertical and horizontal gene transfer shaped plant colonization and biomass degradation in the fungal genus Armillaria.</pubmed_title><pmcid>PMC7615209</pmcid><funding_grant_id>758161</funding_grant_id><pubmed_authors>Ahrendt S</pubmed_authors><pubmed_authors>Slot J</pubmed_authors><pubmed_authors>Andreopoulos B</pubmed_authors><pubmed_authors>Sahu N</pubmed_authors><pubmed_authors>Pangilinan J</pubmed_authors><pubmed_authors>Monk TL</pubmed_authors><pubmed_authors>Balint B</pubmed_authors><pubmed_authors>Ford KL</pubmed_authors><pubmed_authors>Tsai IJ</pubmed_authors><pubmed_authors>Bugge Harder C</pubmed_authors><pubmed_authors>Papanicolaou A</pubmed_authors><pubmed_authors>Riley R</pubmed_authors><pubmed_authors>Foster GD</pubmed_authors><pubmed_authors>Yan M</pubmed_authors><pubmed_authors>Grigoriev IV</pubmed_authors><pubmed_authors>Ke HM</pubmed_authors><pubmed_authors>Kocsube S</pubmed_authors><pubmed_authors>Rigling D</pubmed_authors><pubmed_authors>Plett KL</pubmed_authors><pubmed_authors>Koriabine M</pubmed_authors><pubmed_authors>Plett J</pubmed_authors><pubmed_authors>Drula E</pubmed_authors><pubmed_authors>LaButti K</pubmed_authors><pubmed_authors>Viragh M</pubmed_authors><pubmed_authors>Indic B</pubmed_authors><pubmed_authors>Sipos G</pubmed_authors><pubmed_authors>Martin FM</pubmed_authors><pubmed_authors>Barry K</pubmed_authors><pubmed_authors>Nagy LG</pubmed_authors><pubmed_authors>Henrissat B</pubmed_authors><pubmed_authors>Lipzen A</pubmed_authors><pubmed_authors>Champramary S</pubmed_authors><pubmed_authors>Wong-Bajracharya J</pubmed_authors><pubmed_authors>Merenyi Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Vertical and horizontal gene transfer shaped plant colonization and biomass degradation in the fungal genus Armillaria.</name><description>The fungal genus Armillaria contains necrotrophic pathogens and some of the largest terrestrial organisms that cause tremendous losses in diverse ecosystems, yet how they evolved pathogenicity in a clade of dominantly non-pathogenic wood degraders remains elusive. Here we show that Armillaria species, in addition to gene duplications and de novo gene origins, acquired at least 1,025 genes via 124 horizontal gene transfer events, primarily from Ascomycota. Horizontal gene transfer might have affected plant biomass degrading and virulence abilities of Armillaria, and provides an explanation for their unusual, soft rot-like wood decay strategy. Combined multi-species expression data revealed extensive regulation of horizontally acquired and wood-decay related genes, putative virulence factors</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Sep</publication><modification>2026-05-29T06:05:24.564Z</modification><creation>2025-02-18T23:51:51.606Z</creation></dates><accession>S-EPMC7615209</accession><cross_references><pubmed>37550506</pubmed><doi>10.1038/s41564-023-01448-1</doi></cross_references></HashMap>