Molecular Pathology Division, Seribiotech Research Laboratory, Central Silk Board, CSB Campus, Carmelaram Post, Kodathi, Bangalore, Karnataka, 560035, India.
Proteomics Division, Seribiotech Research Laboratory, Central Silk Board, CSB Campus, Carmelaram Post, Kodathi, Bangalore, Karnataka, 560035, India.
J Mol Evol. 2020 May;88(4):345-360. doi: 10.1007/s00239-020-09936-2. Epub 2020 Mar 12.
Intracellular microsporidian Nosema mylitta infects Indian wild silkworm Antheraea mylitta causing pebrine disease. Genetic structure and phylogeny of N. mylitta are analysed using nucleotide variability in 5S ribosomal DNA and intergenic spacer (IGS) sequence from 20 isolates collected from Southern, Northern and Central regions of Jharkhand State. Nucleotide diversity (π) and genetic differentiation Gst were highest in the Central isolates whereas lowest in the North. Among the isolates, absence of nucleotides, transitions and transversions were observed. Haplotyping showed nucleotide variability at 83 positions in IGS and 13 positions in 5S rDNA. Haplotype-based genetic differentiation was 0.96 to 0.97 whereas nucleotide sequence-based genetic differentiation was higher (Ks = 22.29) between Southern and Central isolates. Bottleneck analysis showed negative value for Tajima's D and other summary statistics revealing induction of loss of rare alleles and population explosion. From IGS, 17 ancestral sequences were inferred by Network algorithm. Core of nine closely related nodes having ancient nucleotides and peripheral nodes with highly divergent nucleotides were derived. Most diverged peripheral haplotype was Bero (H11) from the Central region whereas Deoghar (H3) of the Northern region diverged early. Phylogeny of N. mylitta grouped Southern and Northern isolates together revealed weak phylogenetic signal for these locations. Phylogeny of N. mylitta with Nosema sp. infecting other lepidopterans clustered N. mylitta isolates with N. antheraea and N. philosamiae of China indicating genetic similarity whereas other species were dissimilar showing diversity irrespective of country of origin.
细胞内微孢子虫 Nosema mylitta 感染印度野生家蚕 Antheraea mylitta,导致微粒子病。使用来自印度恰尔康得邦南部、北部和中部地区的 20 个分离株的 5S 核糖体 DNA 和基因间 spacer (IGS) 序列中的核苷酸变异性分析了 N. mylitta 的遗传结构和系统发育。核苷酸多样性 (π) 和遗传分化 Gst 在中部分离株中最高,而在北部分离株中最低。在这些分离株中,观察到核苷酸缺失、转换和颠换。单倍型分析显示 IGS 中有 83 个位置和 5S rDNA 中有 13 个位置存在核苷酸变异。基于单倍型的遗传分化为 0.96 至 0.97,而基于核苷酸序列的遗传分化在南部和中部分离株之间更高 (Ks=22.29)。瓶颈分析显示 Tajima's D 和其他汇总统计量的负值表明稀有等位基因的丧失和种群爆发的诱导。通过网络算法推断出 IGS 中的 17 个祖先序列。得出了具有古老核苷酸的 9 个紧密相关节点的核心和具有高度分化核苷酸的外围节点。最分化的外围单倍型是来自中部地区的 Bero (H11),而来自北部地区的 Deoghar (H3) 则较早分化。N. mylitta 的系统发育将南部和北部分离株聚在一起,表明这些地点的系统发育信号较弱。与感染其他鳞翅目昆虫的 Nosema sp. 的 N. mylitta 系统发育将 N. mylitta 分离株与中国的 N. antheraea 和 N. philosamiae 聚在一起,表明遗传相似性,而其他物种则不同,显示出与起源国无关的多样性。