Jack Wess, Yiheng Hu, Sambasivam Periyannan, Ashley Jones, John P Rathjen
{"title":"一种新型咖啡青霉菌分离物在小麦条锈病真菌(锈病菌)上生长过程中的转录组变化。","authors":"Jack Wess, Yiheng Hu, Sambasivam Periyannan, Ashley Jones, John P Rathjen","doi":"10.1016/j.fgb.2024.103956","DOIUrl":null,"url":null,"abstract":"<p><p>Wheat stripe rust caused by the fungus Puccinia striiformis f. sp. tritici (Pst) is currently the most destructive disease of wheat. The major control methods which include the deployment of resistant wheat cultivars and application of chemical fungicides are losing efficiency as the fungus evolves. Natural antagonists of Pst may be an avenue for alternative and environmentally sustainable control of the disease in the field. Here we describe a novel fungus found growing on Pst pustules. We identified the fungus as a novel isolate of the plant endophyte Penicillium coffeae. We present a high-quality reference genome and a comparative transcriptomic analysis used to investigate how the fungus deploys its genes during growth amongst Pst spores. The gene content of the P. coffeae ANU01 genome is suggestive of a generalist that makes use of diverse substrates. An abundance of genes related to lipid, amino acid and carbohydrate metabolism indicate that P. coffeae ANU01 has evolved the ability to exploit nutrient stores in Pst urediniospores. P. coffeae ANU01 deploys a number of biosynthetic gene clusters during growth on Pst spores, potentially to inhibit urediniospores germination and halt defence responses. A number of genes encoding carbohydrate active enzymes are also highly upregulated, suggesting targeting and degradation of Pst urediniospores structures. Alongside carbohydrates, P. coffeae ANU01 appears to target spore lipids as a nutrient source, secreting several highly upregulated lipases. Our findings broaden the understanding of growth associated with rust spores as an evolutionary strategy and provide insight into the genes potentially required for this process.</p>","PeriodicalId":55135,"journal":{"name":"Fungal Genetics and Biology","volume":"176 ","pages":"103956"},"PeriodicalIF":2.4000,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Global transcriptome changes during growth of a novel Penicillium coffeae isolate on the wheat stripe rust fungus, Puccinia striiformis f. sp. tritici.\",\"authors\":\"Jack Wess, Yiheng Hu, Sambasivam Periyannan, Ashley Jones, John P Rathjen\",\"doi\":\"10.1016/j.fgb.2024.103956\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Wheat stripe rust caused by the fungus Puccinia striiformis f. sp. tritici (Pst) is currently the most destructive disease of wheat. The major control methods which include the deployment of resistant wheat cultivars and application of chemical fungicides are losing efficiency as the fungus evolves. Natural antagonists of Pst may be an avenue for alternative and environmentally sustainable control of the disease in the field. Here we describe a novel fungus found growing on Pst pustules. We identified the fungus as a novel isolate of the plant endophyte Penicillium coffeae. We present a high-quality reference genome and a comparative transcriptomic analysis used to investigate how the fungus deploys its genes during growth amongst Pst spores. The gene content of the P. coffeae ANU01 genome is suggestive of a generalist that makes use of diverse substrates. An abundance of genes related to lipid, amino acid and carbohydrate metabolism indicate that P. coffeae ANU01 has evolved the ability to exploit nutrient stores in Pst urediniospores. P. coffeae ANU01 deploys a number of biosynthetic gene clusters during growth on Pst spores, potentially to inhibit urediniospores germination and halt defence responses. A number of genes encoding carbohydrate active enzymes are also highly upregulated, suggesting targeting and degradation of Pst urediniospores structures. Alongside carbohydrates, P. coffeae ANU01 appears to target spore lipids as a nutrient source, secreting several highly upregulated lipases. 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Global transcriptome changes during growth of a novel Penicillium coffeae isolate on the wheat stripe rust fungus, Puccinia striiformis f. sp. tritici.
Wheat stripe rust caused by the fungus Puccinia striiformis f. sp. tritici (Pst) is currently the most destructive disease of wheat. The major control methods which include the deployment of resistant wheat cultivars and application of chemical fungicides are losing efficiency as the fungus evolves. Natural antagonists of Pst may be an avenue for alternative and environmentally sustainable control of the disease in the field. Here we describe a novel fungus found growing on Pst pustules. We identified the fungus as a novel isolate of the plant endophyte Penicillium coffeae. We present a high-quality reference genome and a comparative transcriptomic analysis used to investigate how the fungus deploys its genes during growth amongst Pst spores. The gene content of the P. coffeae ANU01 genome is suggestive of a generalist that makes use of diverse substrates. An abundance of genes related to lipid, amino acid and carbohydrate metabolism indicate that P. coffeae ANU01 has evolved the ability to exploit nutrient stores in Pst urediniospores. P. coffeae ANU01 deploys a number of biosynthetic gene clusters during growth on Pst spores, potentially to inhibit urediniospores germination and halt defence responses. A number of genes encoding carbohydrate active enzymes are also highly upregulated, suggesting targeting and degradation of Pst urediniospores structures. Alongside carbohydrates, P. coffeae ANU01 appears to target spore lipids as a nutrient source, secreting several highly upregulated lipases. Our findings broaden the understanding of growth associated with rust spores as an evolutionary strategy and provide insight into the genes potentially required for this process.
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.