Borneman Anthony R, Zeppel Ryan, Chambers Paul J, Curtin Chris D
The Australian Wine Research Institute, Adelaide, Australia.
The Australian Wine Research Institute, Adelaide, Australia ; University of Adelaide, Adelaide, Australia.
PLoS Genet. 2014 Feb 13;10(2):e1004161. doi: 10.1371/journal.pgen.1004161. eCollection 2014 Feb.
The yeast Dekkera bruxellensis is a major contaminant of industrial fermentations, such as those used for the production of biofuel and wine, where it outlasts and, under some conditions, outcompetes the major industrial yeast Saccharomyces cerevisiae. In order to investigate the level of inter-strain variation that is present within this economically important species, the genomes of four diverse D. bruxellensis isolates were compared. While each of the four strains was shown to contain a core diploid genome, which is clearly sufficient for survival, two of the four isolates have a third haploid complement of chromosomes. The sequences of these additional haploid genomes were both highly divergent from those comprising the diploid core and divergent between the two triploid strains. Similar to examples in the Saccharomyces spp. clade, where some allotriploids have arisen on the basis of enhanced ability to survive a range of environmental conditions, it is likely these strains are products of two independent hybridisation events that may have involved multiple species or distinct sub-species of Dekkera. Interestingly these triploid strains represent the vast majority (92%) of isolates from across the Australian wine industry, suggesting that the additional set of chromosomes may confer a selective advantage in winery environments that has resulted in these hybrid strains all-but replacing their diploid counterparts in Australian winery settings. In addition to the apparent inter-specific hybridisation events, chromosomal aberrations such as strain-specific insertions and deletions and loss-of-heterozygosity by gene conversion were also commonplace. While these events are likely to have affected many phenotypes across these strains, we have been able to link a specific deletion to the inability to utilise nitrate by some strains of D. bruxellensis, a phenotype that may have direct impacts in the ability for these strains to compete with S. cerevisiae.
酵母酒香酵母(Dekkera bruxellensis)是工业发酵过程中的主要污染物,例如在生物燃料和葡萄酒生产中使用的发酵过程,在这些过程中它比主要的工业酵母酿酒酵母(Saccharomyces cerevisiae)存活时间更长,并且在某些条件下能胜过酿酒酵母。为了研究这个具有重要经济意义的物种中存在的菌株间变异水平,对四种不同的酒香酵母分离株的基因组进行了比较。虽然四个菌株中的每一个都显示含有一个核心二倍体基因组,这显然足以维持生存,但四个分离株中的两个具有第三条单倍体染色体互补。这些额外单倍体基因组的序列与构成二倍体核心的序列高度不同,并且在两个三倍体菌株之间也存在差异。类似于酿酒酵母属(Saccharomyces spp.)分支中的例子,其中一些异源三倍体是基于在一系列环境条件下增强的生存能力而产生的,很可能这些菌株是两个独立杂交事件的产物,这两个事件可能涉及酒香酵母的多个物种或不同亚种。有趣的是,这些三倍体菌株占澳大利亚葡萄酒行业分离株的绝大多数(92%),这表明额外的一组染色体可能在酿酒厂环境中赋予了选择性优势,导致这些杂交菌株在澳大利亚酿酒厂环境中几乎取代了它们的二倍体对应物。除了明显的种间杂交事件外,染色体畸变如菌株特异性插入和缺失以及通过基因转换导致的杂合性丧失也很常见。虽然这些事件可能影响了这些菌株的许多表型,但我们已经能够将一个特定的缺失与一些酒香酵母菌株无法利用硝酸盐联系起来,这种表型可能对这些菌株与酿酒酵母竞争的能力产生直接影响。