俄罗斯欧洲地区棉铃虫(鳞翅目:夜蛾科)局部种群内共生分子的检测

A. K. Kononchuk*, S. Malysh, A. C. Rumiantseva, D. S. Kireeva, A. Gerus, V. Zhuravlyov
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引用次数: 1

摘要

棉铃虫(Helicoverpa armigera)是世界上食性最广的害虫之一。细胞内共生生物在鳞翅目中广泛存在,在鳞翅目的动态中起着重要的作用。未对俄罗斯棉铃虫内共生菌的流行情况进行调查。本研究于2018-2020年在克拉斯诺达尔地区、沃罗涅日和萨拉托夫地区采集棉虫幼虫和成虫(131 ~ 170只),采用PCR方法对杆状病毒(基因座lef8)、沃尔巴克氏菌属细菌(基因座wsp)和微孢子虫(基因座SSU rRNA)进行群体特异性引物分析。2018年在克拉斯诺达尔地区的铁姆约克地区收集的32名样本中,杆状病毒感染水平为16%。整个样本170人的感染率为2.9%。左8位点与棉铃虫和美洲棉铃虫多角体病毒核分离株的序列相似性为98.7 ~ 99.6%。131只检测昆虫中未检出沃尔巴克氏菌属细菌。PCR检测结果显示,2019年在克拉斯诺达尔地区克拉斯诺阿尔梅斯克区采集的19只昆虫中,1只幼虫呈阳性,患病率为5%。SSU rRNA和最大亚基RNA聚合酶II编码基因的部分测序使鉴定新分离物为bombycis。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular detection of endosymbionts in local populations of Helicoverpa armigera (Lepidoptera: Noctuidae) in European part of Russia
Cotton bollworm Helicoverpa armigera is one of the most polyphagous and cosmopolitan pests. Intracellular endosymbionts are widespread in Lepidoptera, often playing an important role in their dynamics. The prevalence of endosymbionts of cotton bollworm in Russia was not investigated. Cotton bollworm larvae and adults were collected in 2018–2020 in Krasnodar Area, and in Voronezh and Saratov Regions (from 131 to 170 insects) and analyzed by PCR using sets of group-specific primers for baculoviruses (locus lef8), bacteria of the genus of Wolbachia (locus wsp), and microsporidia (locus SSU rRNA). Level of infection with baculoviruses was 16 % for the sample of 32 individuals collected in Temryuk District of Krasnodar Area in 2018. The infection rate of the entire sample of 170 individuals was 2.9 %. The lef8 locus demonstrated 98.7–99.6 % of sequence similarity to the nuclear polyhedrosis virus isolates from the cotton bollworm and American bollworm. Among the tested 131 insects, bacteria of the genus of Wolbachia were not detected. PCR screening for microsporidia revealed one positive larvae among 19 insects collected in Krasnoarmeysk District of Krasnodar Area in 2019, which corresponded to the prevalence of 5 %. Partial sequencing of the genes coding for SSU rRNA and largest subunit RNA polymerase II made it possible to identify the new isolate as N. bombycis.
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