Global Health Institute, School of Life Sciences, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Nature. 2018 May;557(7704):252-255. doi: 10.1038/s41586-018-0086-2. Epub 2018 May 2.
Several lineages of symbiotic bacteria in insects selfishly manipulate host reproduction to spread in a population , often by distorting host sex ratios. Spiroplasma poulsonii is a helical and motile, Gram-positive symbiotic bacterium that resides in a wide range of Drosophila species . A notable feature of S. poulsonii is male killing, whereby the sons of infected female hosts are selectively killed during development. Although male killing caused by S. poulsonii has been studied since the 1950s, its underlying mechanism is unknown. Here we identify an S. poulsonii protein, designated Spaid, whose expression induces male killing. Overexpression of Spaid in D. melanogaster kills males but not females, and induces massive apoptosis and neural defects, recapitulating the pathology observed in S. poulsonii-infected male embryos. Our data suggest that Spaid targets the dosage compensation machinery on the male X chromosome to mediate its effects. Spaid contains ankyrin repeats and a deubiquitinase domain, which are required for its subcellular localization and activity. Moreover, we found a laboratory mutant strain of S. poulsonii with reduced male-killing ability and a large deletion in the spaid locus. Our study has uncovered a bacterial protein that affects host cellular machinery in a sex-specific way, which is likely to be the long-searched-for factor responsible for S. poulsonii-induced male killing.
昆虫体内的几种共生细菌自私地操纵宿主繁殖,以在种群中传播,通常通过扭曲宿主的性别比例。螺旋体 poulsonii 是一种螺旋形和能动的革兰氏阳性共生细菌,存在于广泛的果蝇物种中。S. poulsonii 的一个显著特征是雄性致死,即感染雌性宿主的儿子在发育过程中被选择性杀死。尽管自 20 世纪 50 年代以来就已经研究了 S. poulsonii 引起的雄性致死,但它的潜在机制尚不清楚。在这里,我们鉴定了一种 S. poulsonii 蛋白,命名为 Spaid,其表达诱导雄性致死。在 D. melanogaster 中过表达 Spaid 会杀死雄性但不杀死雌性,并诱导大量细胞凋亡和神经缺陷,再现了在 S. poulsonii 感染的雄性胚胎中观察到的病理学。我们的数据表明,Spaid 靶向雄性 X 染色体上的剂量补偿机制来介导其作用。Spaid 含有锚蛋白重复序列和去泛素化酶结构域,这对于其亚细胞定位和活性是必需的。此外,我们发现了一种 S. poulsonii 的实验室突变株,其雄性致死能力降低,并且在 spaid 基因座处有一个大的缺失。我们的研究揭示了一种细菌蛋白,它以性别特异性的方式影响宿主细胞机制,这很可能是长期以来寻找的导致 S. poulsonii 诱导雄性致死的因素。