Imperial College London, South Kensington, United Kingdom.
MRC Centre for Outbreak Analysis and Modelling, Department of Infectious Disease Epidemiology, Imperial College London, London, United Kingdom.
PLoS Pathog. 2019 Nov 7;15(11):e1008063. doi: 10.1371/journal.ppat.1008063. eCollection 2019 Nov.
Mating causes dramatic changes in female physiology, behaviour, and immunity in many insects, inducing oogenesis, oviposition, and refractoriness to further mating. Females from the Anopheles gambiae species complex typically mate only once in their lifetime during which they receive sperm and seminal fluid proteins as well as a mating plug that contains the steroid hormone 20-hydroxyecdysone. This hormone, which is also induced by blood-feeding, plays a major role in activating vitellogenesis for egg production. Here we show that female Anopheles coluzzii susceptibility to Plasmodium falciparum infection is significantly higher in mated females compared to virgins. We also find that mating status has a major impact on the midgut transcriptome, detectable only under sugar-fed conditions: once females have blood-fed, the transcriptional changes that are induced by mating are likely masked by the widespread effects of blood-feeding on gene expression. To determine whether increased susceptibility to parasites could be driven by the additional 20E that mated females receive from males, we mimicked mating by injecting virgin females with 20E, finding that these females are significantly more susceptible to human malaria parasites than virgin females injected with the control 20E carrier. Further RNAseq was carried out to examine whether the genes that change upon 20E injection in the midgut are similar to those that change upon mating. We find that 79 midgut-expressed genes are regulated in common by both mating and 20E, and 96% (n = 76) of these are regulated in the same direction (up vs down in 20E/mated). Together, these findings show that male Anopheles mosquitoes induce changes in the female midgut that can affect female susceptibility to P. falciparum. This implies that in nature, males might contribute to malaria transmission in previously unappreciated ways, and that vector control strategies that target males may have additional benefits towards reducing transmission.
交配会导致许多昆虫的雌性生理、行为和免疫力发生剧烈变化,从而诱导卵发生、产卵和对进一步交配产生抗性。冈比亚按蚊复合体的雌性一生中通常只交配一次,在此期间,它们会接收精子和精液蛋白,以及一个含有类固醇激素 20-羟基蜕皮酮的交配栓。这种激素也会被吸血诱导,在激活卵黄生成以产生卵子方面起着主要作用。在这里,我们发现与处女蝇相比,交配后的雌性按蚊对恶性疟原虫感染的易感性显著增加。我们还发现,交配状态对中肠转录组有重大影响,只有在喂食糖的情况下才能检测到:一旦雌性吸血,交配诱导的转录变化很可能被吸血对基因表达的广泛影响所掩盖。为了确定增加对寄生虫的易感性是否可以归因于雄性提供的额外 20E,我们通过向处女蝇注射 20E 来模拟交配,发现这些雌性对人类疟原虫的易感性明显高于注射对照 20E 载体的处女蝇。进一步进行 RNAseq 以检查 20E 注射后中肠发生变化的基因是否与交配后变化的基因相似。我们发现,79 个中肠表达基因受到 20E 注射和交配的共同调节,并且这些基因中有 96%(n = 76)以相同的方向(20E/交配时上调或下调)调节。总之,这些发现表明,雄性按蚊会诱导雌性中肠发生变化,从而影响雌性对恶性疟原虫的易感性。这意味着在自然界中,雄性可能以以前未被认识到的方式促进疟疾传播,而针对雄性的病媒控制策略可能会对减少传播产生额外的好处。