Carnes Jason, Anupama Atashi, Balmer Oliver, Jackson Andrew, Lewis Michael, Brown Rob, Cestari Igor, Desquesnes Marc, Gendrin Claire, Hertz-Fowler Christiane, Imamura Hideo, Ivens Alasdair, Kořený Luděk, Lai De-Hua, MacLeod Annette, McDermott Suzanne M, Merritt Chris, Monnerat Severine, Moon Wonjong, Myler Peter, Phan Isabelle, Ramasamy Gowthaman, Sivam Dhileep, Lun Zhao-Rong, Lukeš Julius, Stuart Ken, Schnaufer Achim
Seattle Biomedical Research Institute, Seattle, United States of America.
Swiss Tropical and Public Health Institute, Basel, Switzerland.
PLoS Negl Trop Dis. 2015 Jan 8;9(1):e3404. doi: 10.1371/journal.pntd.0003404. eCollection 2015 Jan.
Two key biological features distinguish Trypanosoma evansi from the T. brucei group: independence from the tsetse fly as obligatory vector, and independence from the need for functional mitochondrial DNA (kinetoplast or kDNA). In an effort to better understand the molecular causes and consequences of these differences, we sequenced the genome of an akinetoplastic T. evansi strain from China and compared it to the T. b. brucei reference strain. The annotated T. evansi genome shows extensive similarity to the reference, with 94.9% of the predicted T. b. brucei coding sequences (CDS) having an ortholog in T. evansi, and 94.6% of the non-repetitive orthologs having a nucleotide identity of 95% or greater. Interestingly, several procyclin-associated genes (PAGs) were disrupted or not found in this T. evansi strain, suggesting a selective loss of function in the absence of the insect life-cycle stage. Surprisingly, orthologous sequences were found in T. evansi for all 978 nuclear CDS predicted to represent the mitochondrial proteome in T. brucei, although a small number of these may have lost functionality. Consistent with previous results, the F1FO-ATP synthase γ subunit was found to have an A281 deletion, which is involved in generation of a mitochondrial membrane potential in the absence of kDNA. Candidates for CDS that are absent from the reference genome were identified in supplementary de novo assemblies of T. evansi reads. Phylogenetic analyses show that the sequenced strain belongs to a dominant group of clonal T. evansi strains with worldwide distribution that also includes isolates classified as T. equiperdum. At least three other types of T. evansi or T. equiperdum have emerged independently. Overall, the elucidation of the T. evansi genome sequence reveals extensive similarity of T. brucei and supports the contention that T. evansi should be classified as a subspecies of T. brucei.
无需舌蝇作为必需传播媒介,以及无需功能性线粒体DNA(动质体或动质体DNA)。为了更好地理解这些差异的分子原因及后果,我们对来自中国的一株无动质体的伊氏锥虫菌株进行了基因组测序,并将其与布氏锥虫指名亚种参考菌株进行比较。注释后的伊氏锥虫基因组与参考基因组显示出广泛的相似性,布氏锥虫预测的编码序列(CDS)中有94.9%在伊氏锥虫中有直系同源物,94.6%的非重复直系同源物的核苷酸同一性达到95%或更高。有趣的是,在该伊氏锥虫菌株中,几个前环素相关基因(PAGs)被破坏或未被发现,这表明在没有昆虫生命周期阶段的情况下功能发生了选择性丧失。令人惊讶的是,在伊氏锥虫中发现了布氏锥虫预测代表线粒体蛋白质组的所有978个核CDS的直系同源序列,尽管其中少数可能已丧失功能。与之前的结果一致,发现F1FO - ATP合酶γ亚基有A281缺失,这与在没有动质体DNA的情况下线粒体膜电位的产生有关。在伊氏锥虫reads的补充从头组装中鉴定出了参考基因组中不存在的CDS候选序列。系统发育分析表明,测序菌株属于伊氏锥虫克隆菌株的一个优势群体,该群体在全球分布,其中还包括被归类为马媾疫锥虫的分离株。至少还有其他三种类型的伊氏锥虫或马媾疫锥虫是独立出现的。总体而言,伊氏锥虫基因组序列的阐明揭示了布氏锥虫的广泛相似性,并支持将伊氏锥虫归类为布氏锥虫亚种的观点。