Rani Jyoti, Chauhan Charu, Das De Tanwee, Kumari Seena, Sharma Punita, Tevatiya Sanjay, Patel Karan, Mishra Ashwani K, Pandey Kailash C, Singh Namita, Dixit Rajnikant
Laboratory of Host-Parasite Interaction Studies, ICMR-National Institute of Malaria, Research, Dwarka, New Delhi 110077, India; Department of Bio and Nanotechnology, Guru Jambheshwar University of Science and Technology, Hisar, Haryana, India.
Laboratory of Host-Parasite Interaction Studies, ICMR-National Institute of Malaria, Research, Dwarka, New Delhi 110077, India.
Gene. 2021 Sep 25;798:145810. doi: 10.1016/j.gene.2021.145810. Epub 2021 Jul 2.
Anopheles stephensi and Anopheles culicifacies are dominant malarial vectors in urban and rural India, respectively. Both species carry significant biological differences in their behavioral adaptation and immunity, but the genetic basis of these variations are still poorly understood. Here, we uncovered the genetic differences of immune blood cells, that influence several immune-physiological responses. We generated, analyzed and compared the hemocyte RNA-Seq database of both mosquitoes. A total of 5,837,223,769 assembled bases collapsed into 7,595 and 3,791 transcripts, originating from hemocytes of laboratory-reared 3-4 days old naïve (sugar-fed) mosquitoes, Anopheles stephensi and Anopheles culicifacies respectively. Comparative GO annotation analysis revealed that both mosquito hemocytes encode similar proteins. Furthermore, while An. stephensi hemocytes showed a higher percentage of immune transcripts encoding APHAG (Autophagy), IMD (Immune deficiency pathway), PRDX (Peroxiredoxin), SCR (Scavenger receptor), IAP (Inhibitor of apoptosis), GALE (galactoside binding lectins), BGBPs (1,3 beta D glucan binding proteins), CASPs (caspases) and SRRP (Small RNA regulatory pathway), An. culicifacies hemocytes yielded a relatively higher percentage of transcripts encoding CLIP (Clip domain serine protease), FREP (Fibrinogen related proteins), PPO (Prophenol oxidase), SRPN (Serpines), ML (Myeloid differentiation 2-related lipid recognition protein), Toll path and TEP (Thioester protein), family proteins. However, a detailed comparative Interproscan analysis showed An. stephensi mosquito hemocytes encode proteins with increased repeat numbers as compared to An. culicifacies. Notably, we observed an abundance of transcripts showing significant variability of encoded proteins with repeats such as LRR (Leucine rich repeat), WD40 (W-D dipeptide), Ankyrin, Annexin, Tetratricopeptide and Mitochondrial substrate carrier repeat-containing family proteins, which may have a direct influence on species-specific immune-physiological responses. Summarily, our deep sequencing analysis unraveled that An. stephensi evolved with an expansion of repeat sequences in hemocyte proteins as compared to An. culicifacies, possibly providing an advantage for better adaptation to diverse environments.
斯氏按蚊和库氏按蚊分别是印度城市和农村地区的主要疟疾传播媒介。这两种按蚊在行为适应性和免疫力方面存在显著的生物学差异,但这些差异的遗传基础仍知之甚少。在此,我们揭示了影响多种免疫生理反应的免疫血细胞的遗传差异。我们生成、分析并比较了这两种蚊子的血细胞RNA测序数据库。总共5,837,223,769个组装碱基汇聚成7,595个和3,791个转录本,分别源自实验室饲养的3 - 4日龄未接触过病原体(以糖为食)的斯氏按蚊和库氏按蚊的血细胞。比较基因本体注释分析表明,两种蚊子的血细胞编码相似的蛋白质。此外,虽然斯氏按蚊血细胞中编码自噬相关蛋白(APHAG)、免疫缺陷通路蛋白(IMD)、过氧化物还原酶(PRDX)、清道夫受体(SCR)、凋亡抑制蛋白(IAP)、半乳糖苷结合凝集素(GALE)、1,3-β-D-葡聚糖结合蛋白(BGBPs)、半胱天冬酶(CASPs)和小RNA调控通路蛋白(SRRP)的免疫转录本比例较高,但库氏按蚊血细胞中编码clip结构域丝氨酸蛋白酶(CLIP)、纤维蛋白原相关蛋白(FREP)、前酚氧化酶(PPO)、丝氨酸蛋白酶抑制剂(SRPN)、髓系分化2相关脂质识别蛋白(ML)、Toll通路蛋白和硫酯蛋白(TEP)家族蛋白的转录本比例相对较高。然而,详细的比较Interproscan分析表明,与库氏按蚊相比,斯氏按蚊的血细胞编码的蛋白质重复次数增加。值得注意的是,我们观察到大量转录本显示出编码具有重复序列的蛋白质存在显著变异性,如富含亮氨酸重复序列(LRR)、W-D二肽(WD40)、锚蛋白、膜联蛋白、四肽重复序列和含线粒体底物载体重复序列的家族蛋白,这可能对物种特异性免疫生理反应有直接影响。总之,我们的深度测序分析表明,与库氏按蚊相比,斯氏按蚊血细胞蛋白中的重复序列有所扩展,这可能为其更好地适应多样环境提供了优势。