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

IF 2.4 3区 生物学 Q3 GENETICS & HEREDITY Fungal Genetics and Biology Pub Date : 2024-01-11 DOI:10.1016/j.fgb.2023.103862
Ruby Ye , Megan Biango-Daniels , Jacob L. Steenwyk , Antonis Rokas , Nicolas L. Louw , Robert Nardella , Benjamin E. Wolfe
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引用次数: 0

摘要

虽然青霉对农业、工业和生物医学系统有重大影响,但青霉物种在许多微生物组中的生态作用还没有得到很好的描述。在这里,我们利用从奶酪皮中分离出的 35 株青霉菌株,广泛研究了奶酪相关青霉物种二次代谢的基因组潜力、青霉对细菌群落组装的影响以及青霉-细菌相互作用的机制。利用反SMASH,我们发现了1558个生物合成基因簇(BGC),其中406个基因簇与已知的途径相匹配,包括几种霉菌毒素和抗菌化合物。通过测量具有代表性的青霉菌株与奶酪外皮细菌群落培养时的细菌丰度和真菌 mRNA 表达量,我们观察到不同青霉菌株对奶酪外皮群落的影响各不相同,有的对细菌生长有强烈抑制作用,有的则对细菌生长或群落组成没有影响。通过差异 mRNA 表达分析,青霉菌株对细菌群落的反应表现出有限的差异基因表达。我们在 8 个受测青霉菌株之间发现了一些共同的反应,主要是营养代谢途径的上调,但我们并没有发现真菌对多物种群落生长的一致反应。这些结果共同表明,与奶酪相关的青霉菌种在影响细菌群落发展的能力方面存在很大差异,并凸显了这一标志性菌属中重要的生态多样性。
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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.

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来源期刊
Fungal Genetics and Biology
Fungal Genetics and Biology 生物-遗传学
CiteScore
6.20
自引率
3.30%
发文量
66
审稿时长
85 days
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.
期刊最新文献
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