Department of Nutrition, Genetics and Ethology, Ghent University, B-9820, Merelbeke, Belgium.
Department of Biochemistry and Microbiology, Ghent University, B-9000, Ghent, Belgium.
Sci Rep. 2019 May 24;9(1):7794. doi: 10.1038/s41598-019-44254-8.
Host-parasite co-evolution history is lacking when parasites switch to novel hosts. This was the case for Western honey bees (Apis mellifera) when the ectoparasitic mite, Varroa destructor, switched hosts from Eastern honey bees (Apis cerana). This mite has since become the most severe biological threat to A. mellifera worldwide. However, some A. mellifera populations are known to survive infestations, largely by suppressing mite population growth. One known mechanism is suppressed mite reproduction (SMR), but the underlying genetics are poorly understood. Here, we take advantage of haploid drones, originating from one queen from the Netherlands that developed Varroa-resistance, whole exome sequencing and elastic-net regression to identify genetic variants associated with SMR in resistant honeybees. An eight variants model predicted 88% of the phenotypes correctly and identified six risk and two protective variants. Reproducing and non-reproducing mites could not be distinguished using DNA microsatellites, which is in agreement with the hypothesis that it is not the parasite but the host that adapted itself. Our results suggest that the brood pheromone-dependent mite oogenesis is disrupted in resistant hosts. The identified genetic markers have a considerable potential to contribute to a sustainable global apiculture.
当寄生虫转移到新宿主时,就会缺乏宿主-寄生虫共同进化的历史。西方蜜蜂(Apis mellifera)的情况就是如此,当时外寄生螨瓦螨(Varroa destructor)从东方蜜蜂(Apis cerana)转移到了西方蜜蜂。从那时起,这种螨虫就成为了全世界对 A. mellifera 最严重的生物威胁。然而,一些 A. mellifera 种群已知能够在感染中存活下来,主要是通过抑制螨虫的种群增长。一个已知的机制是抑制螨虫繁殖(SMR),但潜在的遗传学知之甚少。在这里,我们利用来自荷兰的一只具有抗瓦螨特性的蜂王所产生的单倍体雄蜂,进行全外显子组测序和弹性网络回归,以鉴定与抗性蜜蜂 SMR 相关的遗传变异。一个包含八个变体的模型正确预测了 88%的表型,并鉴定出六个风险变体和两个保护变体。使用 DNA 微卫星无法区分繁殖和非繁殖的螨虫,这与寄生虫适应宿主的假设是一致的。我们的结果表明,在抗性宿主中,与幼虫信息素有关的螨虫卵发生被破坏。鉴定出的遗传标记具有很大的潜力,为可持续的全球养蜂业做出贡献。