Ruby Ye , Megan Biango-Daniels , Jacob L. Steenwyk , Antonis Rokas , Nicolas L. Louw , Robert Nardella , Benjamin E. Wolfe
{"title":"奶酪外皮微生物组中青霉物种的基因组、转录组和生态多样性","authors":"Ruby Ye , Megan Biango-Daniels , Jacob L. Steenwyk , Antonis Rokas , Nicolas L. Louw , Robert Nardella , Benjamin E. Wolfe","doi":"10.1016/j.fgb.2023.103862","DOIUrl":null,"url":null,"abstract":"<div><p>Although <em>Penicillium</em> molds can have significant impacts on agricultural, industrial, and biomedical systems, the ecological roles of <em>Penicillium</em> species in many microbiomes are not well characterized. Here we utilized a collection of 35 <em>Penicillium</em> strains isolated from cheese rinds to broadly investigate the genomic potential for secondary metabolism in cheese-associated <em>Penicillium</em> species, the impact of <em>Penicillium</em> on bacterial community assembly, and mechanisms of <em>Penicillium</em>-bacteria interactions. Using antiSMASH, we identified 1558 biosynthetic gene clusters, 406 of which were mapped to known pathways, including several mycotoxins and antimicrobial compounds. By measuring bacterial abundance and fungal mRNA expression when culturing representative <em>Penicillium</em> strains with a cheese rind bacterial community, we observed divergent impacts of different <em>Penicillium</em> strains, from strong inhibitors of bacterial growth to those with no impact on bacterial growth or community composition. Through differential mRNA expression analyses, <em>Penicillium</em> strains demonstrated limited differential gene expression in response to the bacterial community. We identified a few shared responses between the eight tested <em>Penicillium</em> strains, primarily upregulation of nutrient metabolic pathways, but we did not identify a conserved fungal response to growth in a multispecies community. These results in tandem suggest high variation among cheese-associated <em>Penicillium</em> species in their ability to shape bacterial community development and highlight important ecological diversity within this iconic genus.</p></div>","PeriodicalId":55135,"journal":{"name":"Fungal Genetics and Biology","volume":null,"pages":null},"PeriodicalIF":2.4000,"publicationDate":"2024-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genomic, transcriptomic, and ecological diversity of Penicillium species in cheese rind microbiomes\",\"authors\":\"Ruby Ye , Megan Biango-Daniels , Jacob L. Steenwyk , Antonis Rokas , Nicolas L. Louw , Robert Nardella , Benjamin E. Wolfe\",\"doi\":\"10.1016/j.fgb.2023.103862\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Although <em>Penicillium</em> molds can have significant impacts on agricultural, industrial, and biomedical systems, the ecological roles of <em>Penicillium</em> species in many microbiomes are not well characterized. Here we utilized a collection of 35 <em>Penicillium</em> strains isolated from cheese rinds to broadly investigate the genomic potential for secondary metabolism in cheese-associated <em>Penicillium</em> species, the impact of <em>Penicillium</em> on bacterial community assembly, and mechanisms of <em>Penicillium</em>-bacteria interactions. Using antiSMASH, we identified 1558 biosynthetic gene clusters, 406 of which were mapped to known pathways, including several mycotoxins and antimicrobial compounds. By measuring bacterial abundance and fungal mRNA expression when culturing representative <em>Penicillium</em> strains with a cheese rind bacterial community, we observed divergent impacts of different <em>Penicillium</em> strains, from strong inhibitors of bacterial growth to those with no impact on bacterial growth or community composition. Through differential mRNA expression analyses, <em>Penicillium</em> strains demonstrated limited differential gene expression in response to the bacterial community. We identified a few shared responses between the eight tested <em>Penicillium</em> strains, primarily upregulation of nutrient metabolic pathways, but we did not identify a conserved fungal response to growth in a multispecies community. These results in tandem suggest high variation among cheese-associated <em>Penicillium</em> species in their ability to shape bacterial community development and highlight important ecological diversity within this iconic genus.</p></div>\",\"PeriodicalId\":55135,\"journal\":{\"name\":\"Fungal Genetics and Biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2024-01-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fungal Genetics and Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1087184523000932\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fungal Genetics and Biology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1087184523000932","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Genomic, transcriptomic, and ecological diversity of Penicillium species in cheese rind microbiomes
Although Penicillium molds can have significant impacts on agricultural, industrial, and biomedical systems, the ecological roles of Penicillium species in many microbiomes are not well characterized. Here we utilized a collection of 35 Penicillium strains isolated from cheese rinds to broadly investigate the genomic potential for secondary metabolism in cheese-associated Penicillium species, the impact of Penicillium on bacterial community assembly, and mechanisms of Penicillium-bacteria interactions. Using antiSMASH, we identified 1558 biosynthetic gene clusters, 406 of which were mapped to known pathways, including several mycotoxins and antimicrobial compounds. By measuring bacterial abundance and fungal mRNA expression when culturing representative Penicillium strains with a cheese rind bacterial community, we observed divergent impacts of different Penicillium strains, from strong inhibitors of bacterial growth to those with no impact on bacterial growth or community composition. Through differential mRNA expression analyses, Penicillium strains demonstrated limited differential gene expression in response to the bacterial community. We identified a few shared responses between the eight tested Penicillium strains, primarily upregulation of nutrient metabolic pathways, but we did not identify a conserved fungal response to growth in a multispecies community. These results in tandem suggest high variation among cheese-associated Penicillium species in their ability to shape bacterial community development and highlight important ecological diversity within this iconic genus.
期刊介绍:
Fungal Genetics and Biology, formerly known as Experimental Mycology, publishes experimental investigations of fungi and their traditional allies that relate structure and function to growth, reproduction, morphogenesis, and differentiation. This journal especially welcomes studies of gene organization and expression and of developmental processes at the cellular, subcellular, and molecular levels. The journal also includes suitable experimental inquiries into fungal cytology, biochemistry, physiology, genetics, and phylogeny.
Fungal Genetics and Biology publishes basic research conducted by mycologists, cell biologists, biochemists, geneticists, and molecular biologists.
Research Areas include:
• Biochemistry
• Cytology
• Developmental biology
• Evolutionary biology
• Genetics
• Molecular biology
• Phylogeny
• Physiology.