The microbiota, the malarial parasite, and the mosquito [MMM] – A three-sided relationship

IF 1.4 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Sathishkumar Vinayagam , Devianjana Rajendran , Kathirvel Sekar , Kaviyarasi Renu , Kamaraj Sattu
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引用次数: 2

Abstract

The mosquito gut microbiota is vital to the proper functioning of the host organism. Mosquitoes may benefit from this microbiota in their guts because it promotes factors including blood digestion, fecundity, metamorphosis, and living habitat and inhibits malarial parasites (Plasmodium) growth or transmission. In this overview, we analyzed how mosquitoes acquire their gut microbiota, characterized those bacteria, and discussed the functions they provide. We also investigated the effects of microbiota on malaria vectors, with a focus on the mosquito species Anopheles, as well as the relationship between microbiota and Plasmodium, the aspects in which microbiota influences Plasmodium via immune response, metabolism, and redox mechanisms, and the strategies in which gut bacteria affect the life cycle of malaria vectors and provide the ability to resist insecticides. This article explores the difficulties in studying triadic interactions, such as the interplay between Mosquitoes, Malarial parasite, and the Microbiota that dwell in the mosquitoes' guts, and need additional research for a better understanding of these multiple connections to implement an exact vector control strategies using Gut microbiota in malaria control.

微生物群、疟疾寄生虫和蚊子[MMM]——三方关系
蚊子肠道微生物群对宿主生物的正常功能至关重要。蚊子可能从肠道中的这种微生物群中受益,因为它促进血液消化、生殖能力、变态和生活栖息地等因素,并抑制疟疾寄生虫(疟原虫)的生长或传播。在这篇综述中,我们分析了蚊子是如何获得肠道微生物群的,对这些细菌进行了表征,并讨论了它们提供的功能。我们还研究了微生物群对疟疾媒介的影响,重点是蚊子物种按蚊,以及微生物群与疟原虫之间的关系,微生物群通过免疫反应、代谢和氧化还原机制影响疟原虫的各个方面,以及肠道细菌影响疟疾媒介生命周期并提供抗药性的策略。这篇文章探讨了研究三元相互作用的困难,例如蚊子、疟疾寄生虫和蚊子肠道中的微生物群之间的相互作用,需要进一步的研究来更好地理解这些多重联系,以便在疟疾控制中使用肠道微生物群实施准确的媒介控制策略。
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来源期刊
CiteScore
2.90
自引率
0.00%
发文量
51
审稿时长
63 days
期刊介绍: The journal provides a medium for rapid publication of investigations of the molecular biology and biochemistry of parasitic protozoa and helminths and their interactions with both the definitive and intermediate host. The main subject areas covered are: • the structure, biosynthesis, degradation, properties and function of DNA, RNA, proteins, lipids, carbohydrates and small molecular-weight substances • intermediary metabolism and bioenergetics • drug target characterization and the mode of action of antiparasitic drugs • molecular and biochemical aspects of membrane structure and function • host-parasite relationships that focus on the parasite, particularly as related to specific parasite molecules. • analysis of genes and genome structure, function and expression • analysis of variation in parasite populations relevant to genetic exchange, pathogenesis, drug and vaccine target characterization, and drug resistance. • parasite protein trafficking, organelle biogenesis, and cellular structure especially with reference to the roles of specific molecules • parasite programmed cell death, development, and cell division at the molecular level.
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