Varaldi J, Lepetit D
Laboratoire de Biométrie et Biologie Evolutive (UMR CNRS 5558),University Lyon 1 - University of Lyon,43 boulevard du 11 novembre 1918,69622 Villeurbanne cedex,France.
Parasitology. 2018 Dec;145(14):1979-1989. doi: 10.1017/S0031182018000835. Epub 2018 May 28.
Behaviour manipulation imposed by parasites is a fascinating phenomenon but our understanding is still very limited. We studied the interaction between a virus and the parasitic wasp Leptopilina boulardi that attacks Drosophila larvae. Wasps usually refrain to lay eggs into already parasitized hosts (superparasitism avoidance). On the contrary, females infected by the Leptopilina boulardi Filamentous Virus (LbFV) are much more incline to superparasitize. Interestingly, the host-sharing induced by this behaviour modification leads to the horizontal transmission of the virus, thus increasing its fitness at the expense of that of the wasp. To better understand the mechanisms underlying this behaviour manipulation, we studied by RNA sequencing the meta-transcriptome of LbFV and the parasitic wasp both in the abdomen and in the head. We found that the abundance of viral transcripts was independent of the wasp strain but strongly differed between tissues. Based on the tissue pattern of expression, we identified a set of 20 viral genes putatively involved in the manipulation process. In addition, we identified a set of wasp genes deregulated in the presence of the virus either in the abdomen or in the head, including genes with annotations suggesting involvement in behaviour (i.e. Potassium-channel protein). This dataset gives new insights into the behaviour manipulation and on the genetic basis of superparasitism in parasitoids.
寄生虫引发的行为操纵是一种引人入胜的现象,但我们对此的了解仍然非常有限。我们研究了一种病毒与寄生黄蜂巴氏细蜂(Leptopilina boulardi)之间的相互作用,这种黄蜂会攻击果蝇幼虫。黄蜂通常不会在已经被寄生的宿主中产卵(避免重复寄生)。相反,感染了巴氏细蜂丝状病毒(LbFV)的雌蜂更倾向于重复寄生。有趣的是,这种行为改变引发的宿主共享导致了病毒的水平传播,从而以黄蜂的适应性为代价提高了病毒的适应性。为了更好地理解这种行为操纵背后的机制,我们通过RNA测序研究了LbFV和寄生黄蜂在腹部和头部的元转录组。我们发现病毒转录本的丰度与黄蜂品系无关,但在不同组织之间有很大差异。基于表达的组织模式,我们鉴定出一组可能参与操纵过程的20个病毒基因。此外,我们还鉴定出一组在病毒存在时在腹部或头部中表达失调的黄蜂基因,包括一些注释表明参与行为的基因(即钾通道蛋白)。该数据集为行为操纵以及寄生蜂重复寄生的遗传基础提供了新的见解。