我国麦蚜体内的沃尔巴克氏体(Wolbachia)的检测

沃尔巴克氏体是广泛分布于节肢动物体内的一类共生细菌 ,它们参与多种调控其寄主生殖活动的机制。本研究通过wsp基因的特异性扩增证实了沃尔巴克氏体在麦长管蚜Sitobionavenae(Fabricius)体内的共生。而且在麦长管蚜的两种体色型 (绿色型和红色型 )中都检测到了沃尔巴克氏体的共生。     

抗生素处理对感染Wolbachia的丽蚜小蜂生殖的影响

Wolbachia是一类广泛存在于节肢动物体内, 可以对寄主的生殖力及生殖行为产生影响的共生菌。用抗生素可以有效除去寄主体内的Wolbachia。本实验通过喂食浓度分别为1, 5和10 mg盐酸四环素/mL蔗糖水, 结合PCR检测丽蚜小蜂Encarsia formosa体内Wolbachia的去除效果; 解剖观察丽蚜小蜂F0代及F1, F2和F3代怀卵量和卵巢管数量, 评价Wolbachia对丽蚜小蜂生殖的影响。结果显示： 抗生素处理去除Wolbachia后F0代蜂的卵巢管数量与未处理蜂之间无显著差异（P=0.12）, 但F1, F2和F3代蜂的卵巢管均为6条, 显著少于F0代蜂的卵巢管数量（P<0.001）。抗生素处理去除Wolbachia后的F0代蜂怀卵量与未处理蜂相比显著下降, 但显著高于经抗生素处理去除Wolbachia后的F1, F2和F3代蜂怀卵量（P<0.001）, 后代（F1, F2, F3）蜂之间怀卵量无显著差异（P=0.59）。去除Wolbachia后, 丽蚜小蜂可以产生雄性后代, 但未见交配行为, 且雌蜂可不经交配而产生雌性后代。结果说明, Wolbachia不仅直接影响丽蚜小蜂的怀卵量, 而且还可以通过影响丽蚜小蜂卵巢管的发育影响丽蚜小蜂的怀卵量; 然而, 去除Wolbachia不改变雌蜂的孤雌生殖方式。     

小麦和大豆蚜虫中内共生菌Wolbachia的感染检测和系统发育分析

Wolbachia是一类在节肢动物中广泛感染的胞内共生菌。为了了解其在我国蚜虫中的感染情况, 本研究通过扩增wsp基因片段对采集自我国多个地区的3种小麦蚜虫（荻草谷网蚜Sitobion miscanthi、 麦二叉蚜Schizaphis graminum和禾谷缢管蚜Rhopalosiphum padi）和1种大豆蚜虫（大豆蚜Aphis glycines）样品进行了内共生菌Wolbachia的感染检测。结果显示： 3种小麦蚜虫中均未检测出Wolabchia。大豆蚜也仅在采集自北京和杭州的种群中发现了Wolbachia的感染, 感染率分别为95.8%和22.9%, 并且所检测的个体均为单株系感染。wsp基因序列的比对分析显示, 大豆蚜感染的Wolbachia株系与多个亲缘关系较远的昆虫物种中所感染的Wolbachia株系间具有高度一致的基因序列。wsp基因序列构建的系统发育关系和序列一致性均表明大豆蚜感染的Wolbachia株系属于B大组CauB组。本研究为今后探讨Wolbachia在我国蚜虫中的寄主范围和株系多样性提供了数据支持。     

米蛾体内Wolbachia的wsp基因序列测定与系统发育分析

Wolbachia是广泛分布于节肢动物体内的一类共生菌, 它们参与多种调控寄主的生殖活动机制。通过对wsp基因的特异性扩增和测序,发现了Wolbachia在米蛾Corcyra cephalonica (Stainton)体内的感染。利用所测序列和其他已发表的序列建立系统树,结果表明米蛾体内Wolbachia属于B大组的Pip类群,与其寄生物茧蜂及赤眼蜂中的Wolbachia各株系遗传距离相差较远。据此推测米蛾体内感染的Wolbachia不是由寄生物（茧蜂、赤眼蜂）水平传播所致。     

三色书虱体内共生微生物Wolbachia的wsp基因的分子检测

采用常规PCR和巢式PCR方法对三色书虱Liposcelis tricolor体内的共生微生物Wolbachia的wsp基因进行分子检测;通过Wolbachia的通用引物以及A、B亚群引物分别比较了常规PCR和巢式PCR对wsp基因扩增的灵敏性。从三色书虱体内扩增出了610bp的Wolbachia的wsp基因片段,500bp的WolbachiaA亚群的wsp基因片段和450bp的Wolbachia B亚群的wsp基因片段。扩增结果说明三色书虱被A和B两个亚群的Wolbachia混合感染;巢式PCR比常规PCR更为灵敏。     

首次发现沃尔巴克氏体Wolbachia对我国南亚果实蝇的感染现象

沃尔巴克氏体Wolbachia是广泛分布于节肢动物体生殖组织内的一类共生细菌,泰国等已发现Wolbachia感染南亚果实蝇Bactrocera(Zeugodacus)tau(Walker)的现象。利用沃尔巴克氏体wsp基因的1对通用引物(81F,691R)从我国南亚果实蝇的总DNA中扩增到1段500 bp左右的wsp基因片段,并克隆得到了Wolbachia相关序列,首次发现了沃尔巴克氏体对我国南亚果实蝇的感染现象。     

中国部分地区柑桔木虱体内感染Wolbachia的检测及其系统发育分析

Wolbachia是一种广泛分布于节肢动物体内的共生细菌, 该共生菌经寄主卵的细胞质传播并参与多种寄主生殖活动调控, 对节肢动物的物种进化有着重要意义并可能应用于害虫的生物防治。本研究以柑桔黄龙病（Huanglongbing, HLB）的主要传播媒介——柑桔木虱Diaphorina citri为研究对象, 通过Wolbachia的16S rDNA、 细胞分裂基因（ftsZ）、 表面蛋白基因（wsp）的特异引物对来自于中国广西北海、 广西柳州、 广东深圳、 广东阳春、 福建福州5个地区的柑桔木虱进行PCR扩增, 并对扩增产物进行克隆测序, 与GenBank中相关序列进行比对分析, 建立了柑桔木虱共生Wolbachia的系统发育树。结果显示上述5个地区的柑桔木虱均存在Wolbachia感染, 通过Wolbachia的16S rDNA, ftsZ基因和wsp基因DNA序列的系统发育分析表明, 5个地区的柑桔木虱体内的Wolbachia均属于B组; 基于wsp基因的系统发育分析进一步表明5个地区的亚洲柑桔木虱体内的Wolbachia属于B组的Con亚组, 且不同地区柑桔木虱体内的Wolbachia的16S rDNA, ftsZ基因和wsp基因序列差异不明显。研究结果为认识柑桔黄龙病传播媒介昆虫的进化及其综合防治提供了重要的参考依据。     

河南不同地区棉蚜种群共生菌Wolbachia的检测及系统发育分析

【目的】本研究旨在揭示河南省不同地区棉蚜Aphis gossypii种群共生菌Wolbachia的感染情况,明确Wolbachia的感染类型及分类地位。【方法】2016-2017年间采集河南省不同地区的13个棉蚜种群,通过扩增COI基因片段对其进行种类鉴定;通过扩增棉蚜种群中Wolbachia的wsp基因片段对其进行Wolbachia感染率的检测,应用neighbor-joining法构建系统进化树进行棉蚜种群中Wolbachia的系统发育分析。【结果】对河南省内不同地区采集的13个棉蚜种群的Wolbachia感染率而言,郑州(ZZ)种群最高(46.67%),信阳2(XY2)种群最低(6.67%),13个种群Wolbachia的感染率范围为6.67%～46.67%,平均感染率为28.35%。基于wsp基因构建的系统发育树表明,安阳和信阳的棉蚜种群感染的Wolbachia株系属于B大组,其余地区棉蚜种群感染的Wolbachia株系属于A大组。【结论】河南省不同地区的棉蚜种群Wolbachia感染率差别较大,且不同种群感染的Wolbachia株系分别属于A大组或B大组。     

High incidences and similar patterns of Wolbachia infection in fig wasp communities from three different continents

Abstract Wolbachia are endosymbiotic bacteria that infect numerous arthropod species. Previous studies in Panama and Australia revealed that the majority of fig wasp species harbor Wolbachia infections, but that similar patterns of incidence have evolved independently with different wasp species and Wolbachia strains on the two continents. We found Wolbachia infections in 25/47 species (53%) of fig wasp associated with 25 species of Chinese figs. Phylogenetic analyses of Wolbachia wsp sequences indicated that very similar strains are not obviously found in either closely related or ecologically linked fig wasps species. The extremely high prevalence of Wolbachia in fig wasps (over 50% of species infected) is not constrained by geographical origin and is a recurrent theme of fig wasp/Wolbachia interactions.     

Hidden Wolbachia diversity in field populations of the European cherry fruit fly, Rhagoletis cerasi (Diptera, Tephritidae)

The European cherry fruit fly Rhagoletis cerasi has been a field model for cytoplasmic incompatibility since the mid 1970s. Two Wolbachia strains were detected in this tephritid species and w Cer2 was described as the CI inducing agent dividing European populations into two unidirectional incompatible groups, i.e. southern females produce viable offspring with northern males, whereas the reciprocal cross results in incompatibility. We detected three new Wolbachia strains by sequencing a multitude of plasmids derived from Wolbachia surface protein gene ( wsp ) polymerase chain reaction (PCR) products. Strain-specific primers were developed allowing individual diagnosis without need for cloning. Hybridization of specific PCR products with a wsp oligonucleotide enhanced the detection limit significantly and revealed the presence of low-titre infections in some strains, in different ontogenetic stages and in adults of different age. We then performed a survey of strain prevalence and infection frequency in eight European regions. w Cer1 was fixed in all populations, whereas w Cer2 was detected only in the South. w Cer3 frequency was the lowest without a clear distribution pattern. The abundance of w Cer4 was homogenous across Europe. Like w Cer2, w Cer5 showed significant differences in spatial distribution. Our new findings of previously undetected and recombinant Wolbachia strains in R. cerasi reveal a major caveat to the research community not to overlook hidden Wolbachia diversity in field populations. Low-titres and geographical variability in Wolbachia diversity are expected to influence the outcome of Wolbachia population dynamics and Wolbachia- based insect population control and may create invasion barriers for expanding and artificially introduced Wolbachia strains.