Dheilly Nolwenn M, Maure Fanny, Ravallec Marc, Galinier Richard, Doyon Josée, Duval David, Leger Lucas, Volkoff Anne-Nathalie, Missé Dorothée, Nidelet Sabine, Demolombe Vincent, Brodeur Jacques, Gourbal Benjamin, Thomas Frédéric, Mitta Guillaume
UMR 5244, Ecologie et Evolution des Interactions (2EI), CNRS, Université de Perpignan, Perpignan 66860, France MIVEGEC (UMR CNRS/IRD/UM1/UM2 5290), 911 Avenue Agropolis, BP 64501, Montpellier Cedex 5 34394, France
MIVEGEC (UMR CNRS/IRD/UM1/UM2 5290), 911 Avenue Agropolis, BP 64501, Montpellier Cedex 5 34394, France Département de Sciences Biologiques, Institut de Recherche en Biologie Végétale, Université de Montréal, 4101 rue Sherbrooke est, Montréal, Québec, Canada H1X 2B2.
Proc Biol Sci. 2015 Mar 22;282(1803):20142773. doi: 10.1098/rspb.2014.2773.
Many parasites modify their host behaviour to improve their own transmission and survival, but the proximate mechanisms remain poorly understood. An original model consists of the parasitoid Dinocampus coccinellae and its coccinellid host, Coleomegilla maculata; during the behaviour manipulation, the parasitoid is not in contact with its host anymore. We report herein the discovery and characterization of a new RNA virus of the parasitoid (D. coccinellae paralysis virus, DcPV). Using a combination of RT-qPCR and transmission electron microscopy, we demonstrate that DcPV is stored in the oviduct of parasitoid females, replicates in parasitoid larvae and is transmitted to the host during larval development. Next, DcPV replication in the host's nervous tissue induces a severe neuropathy and antiviral immune response that correlate with the paralytic symptoms characterizing the behaviour manipulation. Remarkably, virus clearance correlates with recovery of normal coccinellid behaviour. These results provide evidence that changes in ladybeetle behaviour most likely result from DcPV replication in the cerebral ganglia rather than by manipulation by the parasitoid. This offers stimulating prospects for research on parasitic manipulation by suggesting for the first time that behaviour manipulation could be symbiont-mediated.
许多寄生虫会改变宿主行为以提高自身传播率和生存率,但其直接机制仍知之甚少。一个典型的例子是寄生蜂双斑侧沟茧蜂及其瓢虫宿主黄斑盘瓢虫;在行为操纵过程中,寄生蜂不再与宿主接触。我们在此报告寄生蜂一种新RNA病毒(双斑侧沟茧蜂麻痹病毒,DcPV)的发现及特性。通过实时定量逆转录聚合酶链反应(RT-qPCR)和透射电子显微镜相结合的方法,我们证明DcPV存储在寄生蜂雌性的输卵管中,在寄生蜂幼虫中复制,并在幼虫发育期间传播给宿主。接下来,DcPV在宿主神经组织中的复制会引发严重的神经病变和抗病毒免疫反应,这与行为操纵所特有的麻痹症状相关。值得注意的是,病毒清除与瓢虫正常行为的恢复相关。这些结果表明,瓢虫行为的改变很可能是由DcPV在脑神经节中的复制引起的,而非寄生蜂的操纵。这首次表明行为操纵可能是由共生体介导的,为寄生操纵的研究提供了令人兴奋的前景。