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首页> 外文期刊>Nematology >Phylogeny of Meloidogyne spp. based on 18S rDNA and the intergenic region of mitochondrial DNA sequences.
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Phylogeny of Meloidogyne spp. based on 18S rDNA and the intergenic region of mitochondrial DNA sequences.

机译:根结线虫属的系统发育。基于18S rDNA和线粒体DNA序列的基因间区域。

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摘要

The 18S rDNA of 19 populations of Meloidogyne spp. was amplified and directly sequenced. The region of mitochondrial DNA, located in the 3' portion of the gene that codes for cytochrome oxidase subunit II (COII) through a portion of the 16S rRNA (lRNA) gene, from 16 of these populations was cloned and sequenced. Heteroplasmic sequences were identified from both rDNA and mtDNA regions for several taxa. Several sequences sampled from nominal taxa differed from previously published accounts. Phylogenetic trees based on alignments of these sequences were constructed using distance, parsimony and likelihood optimality criteria. For 18S rDNA data, three main clades were identified. One well supported clade (86-91% bootstrap) included the most common and widely disseminated species, e.g., M. arenaria, M. javanica and M. incognita, some recently described or redescribed species (M. floridensis, M. paranaensis, and M. ethiopica) plus numerous unidentified isolates. All mitotic parthenogenetic species, except for M. oryzae, were included in this clade. Other, less well supported clades included the amphimictic and facultative meiotic species M. hapla, M. microtyla, M. maritima and M. duytsi. One such clade comprised three meiotic parthenogens (M. exigua, M. graminicola and M. chitwoodi) and M. oryzae. This clade was moderately supported (77% bootstrap) but the relationships within this clade were poor. For mitochondrial DNA data, only the species in clade I from rDNA analysis, and M. hapla were analysed. These species formed a well supported clade (100% bootstrap) to the exclusion of M. mayaguensis and M. hapla. The addition of taxa and mtDNA data to publicly available records improved the discrimination sensitivity of species and atypical, non-identified, isolates..
机译:19个根结线虫属种群的18S rDNA。被扩增并直接测序。从这些种群中的16个种群中克隆了线粒体DNA的区域,该区域位于通过16S rRNA(lRNA)基因的一部分编码细胞色素氧化酶亚基II(COII)的基因的3'部分,并进行了测序。从rDNA和mtDNA区域中鉴定了几个类群的异质序列。从名义分类单元中采样的几个序列与以前发布的帐户不同。使用距离,简约性和似然性最佳标准构建基于这些序列比对的系统发育树。对于18S rDNA数据,确定了三个主要进化枝。一种支撑良好的进化枝(86-91%的靴带)包括最常见且广泛传播的物种,例如,沙参分枝杆菌,爪哇分枝杆菌和隐孢子虫,一些最近描述或重新描述的物种(莫氏分支杆菌,巴拉那分枝杆菌和M. ethiopica)和许多未鉴定的分离株。除米曲霉外,所有有丝分裂孤雌生殖物种都包括在该进化枝中。其他较少得到支持的进化枝包括两亲和兼性减数分裂物种M. hapla,M。microtyla,M。maritima和M. duytsi。一个这样的进化枝包含三种减数分裂的孤雌生殖(M. exigua,M。graminicola和M. chitwoodi)和M. oryzae。该分支得到了中等程度的支持(77%的引导程序),但是该分支之间的关系很差。对于线粒体DNA数据,仅分析了来自rDNA的进化枝I中的物种和ha。Mpla。这些物种形成了一个支撑良好的进化枝(100%引导),从而排除了玛雅支原体和hapla支原体。将分类单元和mtDNA数据添加到可公开获得的记录中,提高了物种和非典型,未识别分离株的区分敏感性。

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