<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Teng L</submitter><pubmed_abstract>&lt;i>Talaromyces amestolkiae&lt;/i> is an important fungal species owing to its ubiquity in soils, plants, air, and food. In this study, we identified a novel six-segmented polymycovirus, &lt;i>Talaromyces amestolkiae&lt;/i> polymycovirus 1 (TaPmV-1). Each of the double-stranded (ds) RNA segments of TaPmV-1 contained a single open reading frame, and the proteins encoded by dsRNA1, dsRNA2, dsRNA3, and dsRNA 5 shared significant amino acid identities of 56, 40, 47, and 43%, respectively, with the corresponding proteins of &lt;i>Aspergillus fumigatus&lt;/i> polymycovirus-1(AfuPmV-1). DsRNA1, dsRNA3, and dsRNA5 of TaPmV-1 encoded an RNA-dependent RNA polymerase (RdRp), a viral methyltransferase, and a PAS-rich protein, respectively. The functions of the proteins encoded by dsRNA2, dsRNA4, and dsRNA6 have not been elucidated. Comparison of the virus-infected strain LSH3 with virus-cured strain LSHVF revealed that infection with TaPmV-l may reduce the production of red pigments and induce the clustering of fungal sclerotia. Furthermore, transcriptomic analyses demonstrated that infection with TaPmV-l downregulated the expression of transcripts related to metabolism, and may correlate with the reduced production of red pigments and clustering of sclerotia in &lt;i>T. amestolkiae&lt;/i>. These results of this study provide novel insights into the mechanism of fungal gene regulation by polymycovirus infections at the transcriptome level, and this study is the first to report a novel polymycovirus of &lt;i>T. amestolkiae&lt;/i>.</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>1008409</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9645161</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Molecular characterization and transcriptomic analysis of a novel polymycovirus in the fungus &lt;i>Talaromyces amestolkiae&lt;/i>.</pubmed_title><pmcid>PMC9645161</pmcid><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Zhang T</pubmed_authors><pubmed_authors>Hu Z</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Teng L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular characterization and transcriptomic analysis of a novel polymycovirus in the fungus &lt;i>Talaromyces amestolkiae&lt;/i>.</name><description>&lt;i>Talaromyces amestolkiae&lt;/i> is an important fungal species owing to its ubiquity in soils, plants, air, and food. In this study, we identified a novel six-segmented polymycovirus, &lt;i>Talaromyces amestolkiae&lt;/i> polymycovirus 1 (TaPmV-1). Each of the double-stranded (ds) RNA segments of TaPmV-1 contained a single open reading frame, and the proteins encoded by dsRNA1, dsRNA2, dsRNA3, and dsRNA 5 shared significant amino acid identities of 56, 40, 47, and 43%, respectively, with the corresponding proteins of &lt;i>Aspergillus fumigatus&lt;/i> polymycovirus-1(AfuPmV-1). DsRNA1, dsRNA3, and dsRNA5 of TaPmV-1 encoded an RNA-dependent RNA polymerase (RdRp), a viral methyltransferase, and a PAS-rich protein, respectively. The functions of the proteins encoded by dsRNA2, dsRNA4, and dsRNA6 have not been elucidated. Comparison of the virus-infected strain LSH3 with virus-cured strain LSHVF revealed that infection with TaPmV-l may reduce the production of red pigments and induce the clustering of fungal sclerotia. Furthermore, transcriptomic analyses demonstrated that infection with TaPmV-l downregulated the expression of transcripts related to metabolism, and may correlate with the reduced production of red pigments and clustering of sclerotia in &lt;i>T. amestolkiae&lt;/i>. These results of this study provide novel insights into the mechanism of fungal gene regulation by polymycovirus infections at the transcriptome level, and this study is the first to report a novel polymycovirus of &lt;i>T. amestolkiae&lt;/i>.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2024-11-10T02:22:08.127Z</modification><creation>2024-11-10T02:22:08.127Z</creation></dates><accession>S-EPMC9645161</accession><cross_references><pubmed>36386701</pubmed><doi>10.3389/fmicb.2022.1008409</doi></cross_references></HashMap>