首页> 外文期刊>Journal of Invertebrate Pathology >Genetic variation and virulence of Autographa californica multiple nucleopolyhedrovirus and Trichoplusia ni single nucleopolyhedrovirus isolates.
【24h】

Genetic variation and virulence of Autographa californica multiple nucleopolyhedrovirus and Trichoplusia ni single nucleopolyhedrovirus isolates.

机译:加州产卷纹夜蛾多核多角体病毒和 Trichoplusia ni单核多角体病毒分离株的遗传变异和毒力。

获取原文
获取原文并翻译 | 示例
           

摘要

To determine the genetic diversity within the baculovirus species Autographa calfornica multiple nucleopolyhedrovirus (AcMNPV; Baculoviridae: Alphabaculovirus), a PCR-based method was used to identify and classify baculoviruses found in virus samples from the lepidopteran host species A. californica, Autographa gamma, Trichoplusia ni, Rachiplusia ou, Anagrapha falcifera, Galleria mellonella, and Heliothis virescens. Alignment and phylogenetic inference from partial nucleotide sequences of three highly conserved genes (lef-8, lef-9, and polh) indicated that 45 of 74 samples contained isolates of AcMNPV, while six samples contained isolates of Rachiplusia ou multiple nucleopolyhedrovirus strain R1 (RoMNPV-R1) and 25 samples contained isolates of the species Trichoplusia ni single nucleopolyhedrovirus (TnSNPV; Alphabaculovirus). One sample from A. californica contained a previously undescribed NPV related to alphabaculoviruses of the armyworm genus Spodoptera. Data from PCR and sequence analysis of the ie-2 gene and a region containing ORF ac86 in samples from the AcMNPV and RoMNPV clades indicated a distinct group of viruses, mostly from G. mellonella, that are characterized by an unusual ie-2 gene previously found in the strain Plutella xylostella multiple nucleopolyhedrovirus CL3 (PlxyMNPV-CL3) and a large deletion within ac86 previously described in the AcMNPV isolate 1.2 and PlxyMNPV-CL3. PCR and sequence analysis of baculovirus repeated ORF (bro) genes revealed that the bro gene ac2 was split into two separate bro genes in some samples from the AcMNPV clade. Comparison of sequences in this region suggests that ac2 was formed by a deletion that fused the two novel bro genes together. In bioassays of a selection of isolates against T. ni, significant differences were observed in the insecticidal properties of individual isolates, but no trends were observed among the AcMNPV, TnSNPV, or RoMNPV groups of isolates. This study expands on what we know about the variation of AcMNPV, AcMNPV-like and TnSNPV viruses, provides novel information on the distinct groups in which AcMNPV isolates occur, and contributes to data useful for the registration, evaluation, and improvement of AcMNPV, AcMNPV-like, and TnSNPV isolates as biological control agents.
机译:为了确定杆状病毒种类中的遗传多样性,使用基于PCR的方法对杆状线虫多核多角体病毒(AcMNPV;杆状病毒科:杆状病毒)进行遗传多样性分析。对鳞翅目宿主物种 A的病毒样品中发现的杆状病毒进行鉴定和分类。加利福尼亚州, Autographa gamma , Trichoplusia ni , Rachiplusia ou , Anagrapha falcifera , Galleria mellonella 和 Heliothis virescens 。从三个高度保守的基因( lef-8 , lef-9 和 polh )的部分核苷酸序列进行比对和系统发育推断。 74个样品包含AcMNPV的分离株,而6个样品包含 Rachiplusia ou 多核多角体病毒株R1(RoMNPV-R1)的分离株,而25个样品则包含了 plus虫单核多角体病毒种的分离株。 (TnSNPV; α杆状病毒)。来自 A的一个样本。 californica 包含以前未描述的与粘虫 Spodoptera 的杆状病毒有关的NPV。来自AcMNPV和RoMNPV进化枝样本中 ie-2 基因和包含ORF ac86 的区域的PCR和序列分析数据表明,病毒的类型明显不同,主要来自< i> G。 mellonella ,其特征是先前在 Plutella xylostella 多核多角体病毒CL3(PlxyMNPV-CL3)菌株中发现了一个不寻常的 ie-2 基因,并且在先前在AcMNPV分离物1.2和PlxyMNPV-CL3中描述的 ac86 。杆状病毒重复ORF ( bro )基因的PCR和序列分析表明, bro 基因 ac2 被分为两个从AcMNPV进化枝的一些样本中分离出 bro 基因。该区域中序列的比较表明, 是通过将两个新的 bro 基因融合在一起的缺失而形成的。在针对i的分离株选择的生物测定中。另外,在各个分离株的杀虫特性上观察到显着差异,但是在分离株的AcMNPV,TnSNPV或RoMNPV组之间没有观察到趋势。这项研究扩大了我们对AcMNPV,类AcMNPV和TnSNPV病毒变异的了解,提供了有关AcMNPV分离株出现的不同组的新颖信息,并有助于对AcMNPV,AcMNPV的注册,评估和改进有用的数据类和TnSNPV分离作为生物防治剂。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号