Kumari Seena, Chauhan Charu, Tevatiya Sanjay, Singla Deepak, De Tanwee Das, Sharma Punita, Thomas Tina, Rani Jyoti, Savargaonkar Deepali, Pandey Kailash C, Pande Veena, Dixit Rajnikant
Laboratory of Host-Parasite Interaction Studies, ICMR-National Institute of Malaria Research, Dwarka, New Delhi, 110077, India.
School of Agricultural Biotechnology, Punjab Agricultural University, Ludhiana, Punjab, India.
Curr Res Immunol. 2021 Feb 20;2:12-22. doi: 10.1016/j.crimmu.2021.02.002. eCollection 2021.
Recently, we showed how an early restriction of gut flora proliferation by favors immune-suppression and survival in the gut lumen (Sharma et al., 2020). Here, we asked post gut invasion how interacts with individual tissues such as the midgut, hemocyte, and salivary glands, and manages its survival in the mosquito host. Our data from tissue-specific comparative RNA-Seq analysis and extensive temporal/spatial expression profiling of selected mosquito transcripts in the uninfected and infected mosquito's tissues indicated that (i) a transient suppression of gut metabolic machinery by early oocysts; (ii) enriched expression of nutritional responsive proteins and immune proteins against late oocysts, together may ensure optimal parasite development and gut homeostasis restoration; (iii) pre-immune activation of hemocyte by early gut-oocysts infection REL induction (p < 0.003); and altered expression of hemocyte-encoded immune proteins may cause rapid removal of free circulating sporozoites from hemolymph; (iv) while a strong suppression of salivary metabolic activities, and elevated expression of salivary specific secretory, as well as immune proteins together, may favor the long-term storage and survival of invaded sporozoites. Finally, our RNA-Seq-based discovery of 4449 transcripts of origin, and their developmental stage-specific expression modulation in the corresponding infected mosquito tissues, predicts a possible mechanism of mosquito responses evasion by . Conclusively, our system-wide RNA-Seq analysis provides the first genetic evidence of direct mosquito- interaction and establishes a functional correlation.
最近,我们展示了肠道菌群增殖的早期限制如何有利于免疫抑制和肠道腔内的生存(Sharma等人,2020年)。在这里,我们研究了肠道入侵后如何与中肠、血细胞和唾液腺等单个组织相互作用,并在蚊子宿主中维持其生存。我们来自组织特异性比较RNA测序分析的数据,以及对未感染和感染蚊子组织中选定蚊子转录本的广泛时空表达谱分析表明:(i)早期卵囊对肠道代谢机制有短暂抑制作用;(ii)针对晚期卵囊的营养反应蛋白和免疫蛋白的表达富集,共同可确保寄生虫的最佳发育和肠道内环境稳定的恢复;(iii)早期肠道卵囊感染通过REL诱导对血细胞进行免疫前激活(p < 0.003);血细胞编码的免疫蛋白表达改变可能导致从血淋巴中快速清除游离循环的子孢子;(iv)虽然唾液代谢活动受到强烈抑制,同时唾液特异性分泌蛋白以及免疫蛋白的表达升高,可能有利于入侵子孢子的长期储存和生存。最后,我们基于RNA测序发现了4449个起源的转录本,以及它们在相应感染蚊子组织中的发育阶段特异性表达调控,预测了逃避蚊子反应的可能机制。总之,我们全系统的RNA测序分析提供了蚊子与直接相互作用的首个遗传证据,并建立了功能相关性。