Domestication in dry-cured meat Penicillium fungi: Convergent specific phenotypes and horizontal gene transfers without strong genetic subdivision

IF 3.5 2区 生物学 Q1 EVOLUTIONARY BIOLOGY
Ying-Chu Lo, Jade Bruxaux, Ricardo C. Rodríguez?de?la?Vega, Samuel O'Donnell, Alodie Snirc, Monika Coton, Mélanie Le?Piver, Stéphanie Le?Prieur, Daniel Roueyre, Jo?lle Dupont, Jos Houbraken, Robert Debuchy, Jeanne Ropars, Tatiana Giraud, Antoine Branca
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引用次数: 2

Abstract

Some fungi have been domesticated for food production, with genetic differentiation between populations from food and wild environments, and food populations often acquiring beneficial traits through horizontal gene transfers (HGTs). Studying their adaptation to human-made substrates is of fundamental and applied importance for understanding adaptation processes and for further strain improvement. We studied here the population structures and phenotypes of two distantly related Penicillium species used for dry-cured meat production, P. nalgiovense, the most common species in the dry-cured meat food industry, and P. salamii, used locally by farms. Both species displayed low genetic diversity, lacking differentiation between strains isolated from dry-cured meat and those from other environments. Nevertheless, the strains collected from dry-cured meat within each species displayed slower proteolysis and lipolysis than their wild conspecifics, and those of P. nalgiovense were whiter. Phenotypically, the non-dry-cured meat strains were more similar to their sister species than to their conspecific dry-cured meat strains, indicating an evolution of specific phenotypes in dry-cured meat strains. A comparison of available Penicillium genomes from various environments revealed HGTs, particularly between P. nalgiovense and P. salamii (representing almost 1.5 Mb of cumulative length). HGTs additionally involved P. biforme, also found in dry-cured meat products. We further detected positive selection based on amino acid changes. Our findings suggest that selection by humans has shaped the P. salamii and P. nalgiovense populations used for dry-cured meat production, which constitutes domestication. Several genetic and phenotypic changes were similar in P. salamii, P. nalgiovense and P. biforme, indicating convergent adaptation to the same human-made environment. Our findings have implications for fundamental knowledge on adaptation and for the food industry: the discovery of different phenotypes and of two mating types paves the way for strain improvement by conventional breeding, to elucidate the genomic bases of beneficial phenotypes and to generate diversity.

Abstract Image

干腌肉青霉真菌的驯化:聚合特异性表型和水平基因转移
一些真菌已被驯化用于食品生产,来自食物和野生环境的种群之间存在遗传分化,食物种群通常通过水平基因转移(HGT)获得有益性状。研究它们对人造基质的适应对于理解适应过程和进一步改善应变具有基础和应用重要性。我们在这里研究了两种用于干腌肉生产的亲缘关系较远的青霉的种群结构和表型,这两种青霉是干腌肉食品行业中最常见的P.nalgiovense和当地农场使用的P.salamii。这两个物种都表现出较低的遗传多样性,从干腊肉中分离的菌株与从其他环境中分离的毒株之间缺乏分化。然而,从每个物种的干腌腊肉中采集的菌株表现出比野生同种更慢的蛋白水解和脂解,而P.nalgiovense的菌株则更白。从表型上看,非干腌肉菌株与其姊妹物种比其同种干腌肉品种更相似,这表明干腌肉菌种中的特定表型发生了进化。对不同环境中可用的青霉菌基因组的比较显示了HGT,特别是在P.nalgiovense和P.salamii之间(约1.5 累积长度的Mb)。HGTs还涉及双型疟原虫,也在干腌肉制品中发现。我们进一步检测到基于氨基酸变化的阳性选择。我们的发现表明,人类的选择塑造了用于干腌腊肉生产的蝾螈和纳焦文氏蝾螈种群,这构成了驯化。蝾螈、纳焦文氏蝾螈和双形蝾螈的一些遗传和表型变化相似,表明它们对同一人类环境的趋同适应。我们的发现对适应和食品工业的基础知识有启示:不同表型和两种交配类型的发现为通过传统育种改良菌株、阐明有益表型的基因组基础和产生多样性铺平了道路。
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来源期刊
Evolutionary Applications
Evolutionary Applications 生物-进化生物学
CiteScore
8.50
自引率
7.30%
发文量
175
审稿时长
6 months
期刊介绍: Evolutionary Applications is a fully peer reviewed open access journal. It publishes papers that utilize concepts from evolutionary biology to address biological questions of health, social and economic relevance. Papers are expected to employ evolutionary concepts or methods to make contributions to areas such as (but not limited to): medicine, agriculture, forestry, exploitation and management (fisheries and wildlife), aquaculture, conservation biology, environmental sciences (including climate change and invasion biology), microbiology, and toxicology. All taxonomic groups are covered from microbes, fungi, plants and animals. In order to better serve the community, we also now strongly encourage submissions of papers making use of modern molecular and genetic methods (population and functional genomics, transcriptomics, proteomics, epigenetics, quantitative genetics, association and linkage mapping) to address important questions in any of these disciplines and in an applied evolutionary framework. Theoretical, empirical, synthesis or perspective papers are welcome.
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