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Issue:ISSN 2095-1353
           CN 11-6020/Q
Director:Chinese Academy of Sciences
Sponsored by:Chinese Society of Entomological;institute of zoology, chinese academy of sciences;
Address:Chaoyang District No. 1 Beichen West Road, No. 5 hospital,Beijing City,100101, China
Your Position :Home->Past Journals Catalog->2016年53 No.4

Molecular detection and sequence analysis of Wolbachia strains inEctropis obliqua and Ectropis grisescens (Lepidoptera: Geometridae)
Author of the article:ZHOU Xiao-Gui1, 2, 3** FU Jian-Yu2, 3 LIU Shou-An2, 3MAO Teng-Fei2, 3 XIAO Qiang2, 3*** CHEN Xue
Author's Workplace:1. Institute of Insect Sciences, Zhejiang University, Hangzhou 310058, China;2. Tea Research Institute, Chinese Academy of Agricultural Sciences, Hangzhou 310008, China; 3. Key Laboratory of Tea Biology and Resources Utilization, Ministry of Agriculture, Hangzhou 310008, China
Key Words: Ectropis obliqua, Ectropis grisescens, Wolbachia, 16S rRNA, ftsZ, wsp, sequence analysis

 [Objectives]  The infection rates and taxonomic relationships between Wolbachia strains in the sister species Ectropis obliqua and E. grisescens (Lepidoptera: Geometridae) were identified by molecular methods in order to reveal the potential effects of this endosymbiont on these species. [Methods]  Wolbachia infection in three populations of E. obliqua (Hangzhou and Yuhang, Zhejiang province; Wuxi, Jiangsu Province) and three populations of E. grisescens (Xinchang, Zhejiang Province; Xishui, Hubei Province; and Nanchang, Jiangxi Province) were detected using PCR with three specific primers for Wolbachia 16S rRNA and the Wolbachia ftsZ and wsp genes. All Wolbachia 16S rRNA, ftsZ and wsp genes from the three E. grisescens populations and some Wolbachia 16S rRNA and wsp genes from the three E. obliqua populations, were sequenced and analyzed. [Results]  All E. obliqua and E. grisescens populations were infected with Wolbachia. Infection rates of the three E. grisescens populations were all 100%, but ranged from 22% to 95% among the three E. obliqua populations, with positive PCRs showing only weak bands in the electrophoretogram. There were no intra- and interspecific differences in the wsp sequences of E. obliqua and E. grisescens, however, intra- and interspecific differences in 16S rRNA sequences were between 0.362% and 0.727%, respectively. There was a 1.647% difference in two ftsZ haplotypes from E. grisescens, moreover, we were unable to successfully amplify ftsZ from all E. obliqua individuals. A phylogenetic tree based on the 16S rRNA and wsp sequences showed that all strains of Wolbachia detected belong to the Pip subgroup of the B group. [Conclusion]  All three E. obliqua and E. grisescens populations tested are infected with Wolbachia strains belonging to the Pip subgroup of the B group, but the infection rate varies significantly between E. obliqua and E. grisescens. These results provide the basis for future study of the effects of Wolbachia on the biology and ecology of E. obliqua and E. grisescens.

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