Mohanty Ajeet Kumar, Deshpande Dipti, Shah Disha, Balabaskaran Nina Praveen, Karmodiya Krishanpal
Field Station, ICMR-National Institute of Malaria Research, DHS Building, Campal, Panaji, Goa, India, 403001.
Department of Biology, Indian Institute of Science Education and Research, Dr. Homi Bhabha Road, Pashan, Pune, 411008, Maharashtra, India.
BMC Genomics. 2025 Jul 11;26(1):658. doi: 10.1186/s12864-025-11530-z.
The urban malaria vector, Anopheles stephensi, originally limited to South Asia and the Arabian Peninsula has now expanded to several countries in Africa. Despite the continuous insecticide pressure and changing urban landscapes, An. stephensi has been able to adapt, sustain, and expand. The expansion of this remarkably sturdy vector poses a grave public health threat to millions in urban Africa. Research efforts across the globe have mainly focused on understanding the genes that support and limit the development of Plasmodium in An. stephensi. Understanding the genes that are critical for adaptation and survival is important for focused An. stephensi's control and elimination efforts. Balancing selection is an evolutionary mechanism adapted by organisms to maintain genetic diversity, especially for immune-related genes. Here, we sequenced and analyzed the genome of laboratory-reared isofemale once every 25 th generation-0 (Wild type), 25 th, 50 th, 75 th, 100 th, 125 th, and 150 th to identify loci and genes undergoing balancing selection-information that could aid in vector control.
Tajima's D and beta scores were used to identify the signatures of selection in the genomes of seven isofemale An. stephensi from 0 - 150 th generation. Based on the beta scores, the top five genes undergoing balancing selection include ASTEI04624, ASTEI04623 (sensory perception), ASTEI10474 (carbohydrate metabolism), ASTEI03792 (Actin binding), and ASTEI01081 (yet to be functionally characterized).
For its survival, a certain amount of heterozygosity and balancing selection in specific loci, especially in genes involved in carbohydrate metabolism and chemoreception is maintained by the inbred laboratory-reared isofemale An. stephensi. This could be a functional adaptation to the glucose-based diet they are fed in the laboratory.
城市疟疾传播媒介斯氏按蚊原本局限于南亚和阿拉伯半岛,如今已扩散至非洲的多个国家。尽管面临持续的杀虫剂压力和不断变化的城市环境,斯氏按蚊仍能够适应、生存并扩散。这种极具适应性的传播媒介的扩散对非洲城市的数百万人构成了严重的公共卫生威胁。全球的研究工作主要集中在了解支持和限制疟原虫在斯氏按蚊体内发育的基因。了解对适应和生存至关重要的基因对于针对性地控制和消除斯氏按蚊的工作具有重要意义。平衡选择是生物体采用的一种进化机制,用于维持遗传多样性,尤其是对于免疫相关基因。在此,我们对实验室饲养的同系雌蚊每隔25代(第0代(野生型)、第25代、第50代、第75代、第100代、第125代和第150代)进行基因组测序和分析,以确定经历平衡选择的基因座和基因——这些信息有助于病媒控制。
利用 Tajima's D 和 beta 分数来识别来自第0 - 150代的七只同系雌蚊斯氏按蚊基因组中的选择特征。基于 beta 分数,经历平衡选择的前五个基因包括 ASTEI04624、ASTEI04623(感官感知)、ASTEI10474(碳水化合物代谢)、ASTEI03792(肌动蛋白结合)和 ASTEI01081(功能尚未明确)。
实验室饲养的近交同系雌蚊斯氏按蚊为了生存,在特定基因座,尤其是参与碳水化合物代谢和化学感受的基因中维持了一定程度的杂合性和平衡选择。这可能是对实验室喂养的基于葡萄糖的饮食的一种功能适应性。