Doremus Matthew R, Stouthamer Corinne M, Kelly Suzanne E, Schmitz-Esser Stephan, Hunter Martha S
Graduate Interdisciplinary Program in Entomology and Insect Science, University of Arizona, Tucson, AZ, United States.
Department of Entomology, University of Arizona, Tucson, AZ, United States.
Front Microbiol. 2020 Dec 10;11:606399. doi: 10.3389/fmicb.2020.606399. eCollection 2020.
Arthropods harbor heritable intracellular symbionts that may manipulate host reproduction to favor symbiont transmission. In cytoplasmic incompatibility (CI), the symbiont sabotages the reproduction of infected males such that high levels of offspring mortality result when they mate with uninfected females. In crosses with infected males and infected females, however (the "rescue" cross), normal numbers of offspring are produced. A common CI-inducing symbiont, , causes variable levels of CI mortality in the parasitoid wasp, Previous work correlated CI-induced mortality with male development time in this system, although the timing of CI-induction and the relationship between development time and CI mortality was not well understood. Here, using a combination of crosses, manipulation of development time, and fluorescence microscopy, we identify the localization and the timing of the CI-induction step in the system. Antibiotic treatment of adult -infected males did not reduce the mortality associated with the CI phenotype, suggesting that CI-alteration occurs prior to adulthood. Our results suggest that the alteration step occurs during the pupal period, and is limited by the duration of pupal development: 1) produces most sperm prior to adulthood, 2) FISH localization of in testes showed an association with sperm nuclei throughout spermatogenesis but not with mature sperm, and 3) two methods of prolonging the pupal period (cool temperatures and the juvenile hormone analog methoprene) both caused greater CI mortality, suggesting the degree of alteration is limited by the duration of the pupal stage. Based on these results, we compare two models for potential mechanisms of sperm modification in the context of what is known about analogous mechanisms of , a more extensively studied CI-inducing symbiont.
节肢动物体内携带着可遗传的细胞内共生体,这些共生体可能会操纵宿主的繁殖,以利于共生体的传播。在细胞质不相容性(CI)中,共生体破坏受感染雄性的繁殖,以至于当它们与未受感染的雌性交配时,会导致大量后代死亡。然而,在受感染雄性与受感染雌性的杂交中(“挽救”杂交),会产生正常数量的后代。一种常见的诱导CI的共生体,在寄生蜂中会导致不同程度的CI死亡率。此前的研究将该系统中CI诱导的死亡率与雄性发育时间相关联,尽管CI诱导的时间以及发育时间与CI死亡率之间的关系尚不清楚。在这里,我们结合杂交、发育时间操纵和荧光显微镜技术,确定了该系统中CI诱导步骤的定位和时间。用抗生素处理成年感染的雄性,并没有降低与CI表型相关的死亡率,这表明CI改变发生在成年之前。我们的结果表明,改变步骤发生在蛹期,并且受蛹期发育持续时间的限制:1)在成年之前产生大部分精子;2)在睾丸中对进行荧光原位杂交(FISH)定位显示,在整个精子发生过程中与精子核相关,但与成熟精子无关;3)两种延长蛹期的方法(低温和保幼激素类似物烯虫酯)都导致了更高的CI死亡率,这表明改变的程度受蛹期持续时间的限制。基于这些结果,我们在已知的一种研究更广泛的诱导CI的共生体的类似机制的背景下,比较了两种关于精子修饰潜在机制的模型。