Pattemore Julie A, Hane James K, Williams Angela H, Wilson Bree A L, Stodart Ben J, Ash Gavin J
Graham Centre for Agricultural Innovation, School of Agricultural and Wine Sciences, Charles Sturt University, Locked Bag 588, Wagga Wagga 2650, NSW, Australia.
BMC Genomics. 2014 Aug 7;15(1):660. doi: 10.1186/1471-2164-15-660.
Metarhizium anisopliae is an important fungal biocontrol agent of insect pests of agricultural crops. Genomics can aid the successful commercialization of biopesticides by identification of key genes differentiating closely related species, selection of virulent microbial isolates which are amenable to industrial scale production and formulation and through the reduction of phenotypic variability. The genome of Metarhizium isolate ARSEF23 was recently published as a model for M. anisopliae, however phylogenetic analysis has since re-classified this isolate as M. robertsii. We present a new annotated genome sequence of M. anisopliae (isolate Ma69) and whole genome comparison to M. robertsii (ARSEF23) and M. acridum (CQMa 102).
Whole genome analysis of M. anisopliae indicates significant macrosynteny with M. robertsii but with some large genomic inversions. In comparison to M. acridum, the genome of M. anisopliae shares lower sequence homology. While alignments overall are co-linear, the genome of M. acridum is not contiguous enough to conclusively observe macrosynteny. Mating type gene analysis revealed both MAT1-1 and MAT1-2 genes present in M. anisopliae suggesting putative homothallism, despite having no known teleomorph, in contrast with the putatively heterothallic M. acridum isolate CQMa 102 (MAT1-2) and M. robertsii isolate ARSEF23 (altered MAT1-1). Repetitive DNA and RIP analysis revealed M. acridum to have twice the repetitive content of the other two species and M. anisopliae to be five times more RIP affected than M. robertsii. We also present an initial bioinformatic survey of candidate pathogenicity genes in M. anisopliae.
The annotated genome of M. anisopliae is an important resource for the identification of virulence genes specific to M. anisopliae and development of species- and strain- specific assays. New insight into the possibility of homothallism and RIP affectedness has important implications for the development of M. anisopliae as a biopesticide as it may indicate the potential for greater inherent diversity in this species than the other species. This could present opportunities to select isolates with unique combinations of pathogenicity factors, or it may point to instability in the species, a negative attribute in a biopesticide.
绿僵菌是农作物害虫的一种重要真菌生物防治剂。基因组学可通过鉴定区分密切相关物种的关键基因、选择适合工业规模生产和制剂的高毒力微生物分离株以及减少表型变异性,来助力生物农药的成功商业化。绿僵菌分离株ARSEF23的基因组最近作为绿僵菌的一个模型被发表,然而系统发育分析后来将该分离株重新分类为罗伯茨绿僵菌。我们展示了绿僵菌(分离株Ma69)的一个新的注释基因组序列,并与罗伯茨绿僵菌(ARSEF23)和蝗绿僵菌(CQMa 102)进行了全基因组比较。
绿僵菌的全基因组分析表明与罗伯茨绿僵菌有显著的宏观共线性,但存在一些大的基因组倒位。与蝗绿僵菌相比,绿僵菌的基因组具有较低的序列同源性。虽然总体比对是共线性的,但蝗绿僵菌的基因组连续性不足,无法确凿地观察到宏观共线性。交配型基因分析显示绿僵菌中同时存在MAT1-1和MAT1-2基因,这表明尽管没有已知的有性型,但推测其为同宗配合,这与推测为异宗配合的蝗绿僵菌分离株CQMa 102(MAT1-2)和罗伯茨绿僵菌分离株ARSEF23(改变的MAT1-1)形成对比。重复DNA和RIP分析显示,蝗绿僵菌的重复含量是其他两个物种的两倍,绿僵菌受RIP影响的程度是罗伯茨绿僵菌的五倍。我们还展示了对绿僵菌中候选致病基因的初步生物信息学调查。
绿僵菌的注释基因组是鉴定绿僵菌特异性毒力基因以及开发物种和菌株特异性检测方法的重要资源。对同宗配合可能性和RIP影响的新见解对绿僵菌作为生物农药的开发具有重要意义,因为这可能表明该物种比其他物种具有更大的内在多样性潜力。这可能为选择具有独特致病因子组合的分离株提供机会,或者可能表明该物种的不稳定性,这在生物农药中是一个负面属性。