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CRISPR/Cas9 敲除埃及伊蚊中偏雌性表达的基因 AeAct-4 或 myo-fem 会导致雌性而非雄性蚊子丧失飞行能力。

CRISPR/Cas9 knockout of female-biased genes AeAct-4 or myo-fem in Ae. aegypti results in a flightless phenotype in female, but not male mosquitoes.

机构信息

Department of Entomology, Texas A&M University, College Station, Texas, United States of America.

Interdisciplinary Program in Genetics, Texas A&M University, College Station, Texas, United States of America.

出版信息

PLoS Negl Trop Dis. 2020 Dec 18;14(12):e0008971. doi: 10.1371/journal.pntd.0008971. eCollection 2020 Dec.

Abstract

Aedes aegypti is a vector of dengue, chikungunya, and Zika viruses. Current vector control strategies such as community engagement, source reduction, and insecticides have not been sufficient to prevent viral outbreaks. Thus, interest in novel strategies involving genetic engineering is growing. Female mosquitoes rely on flight to mate with males and obtain a bloodmeal from a host. We hypothesized that knockout of genes specifically expressed in female mosquitoes associated with the indirect flight muscles would result in a flightless female mosquito. Using CRISPR-Cas9 we generated loss-of-function mutations in several genes hypothesized to control flight in mosquitoes, including actin (AeAct-4) and myosin (myo-fem) genes expressed specifically in the female flight muscle. Genetic knockout of these genes resulted in 100% flightless females, with homozygous males able to fly, mate, and produce offspring, albeit at a reduced rate when compared to wild type males. Interestingly, we found that while AeAct-4 was haplosufficient, with most heterozygous individuals capable of flight, this was not the case for myo-fem, where about half of individuals carrying only one intact copy could not fly. These findings lay the groundwork for developing novel mechanisms of controlling Ae. aegypti populations, and our results suggest that this mechanism could be applicable to other vector species of mosquito.

摘要

埃及伊蚊是登革热、基孔肯雅热和寨卡病毒的传播媒介。目前的病媒控制策略,如社区参与、源头减少和杀虫剂的使用,还不足以预防病毒的爆发。因此,人们对涉及基因工程的新策略越来越感兴趣。雌性蚊子依靠飞行来与雄性交配,并从宿主那里获取血液。我们假设,敲除与雌性蚊子间接飞行肌肉相关的特定表达基因,会导致雌性蚊子无法飞行。我们使用 CRISPR-Cas9 技术,在几个被认为控制蚊子飞行的基因上产生了功能丧失突变,包括在雌性飞行肌肉中特异性表达的肌动蛋白(AeAct-4)和肌球蛋白(myo-fem)基因。这些基因的遗传敲除导致 100%的雌性蚊子无法飞行,而纯合雄性蚊子能够飞行、交配并产生后代,尽管与野生型雄性相比,其繁殖率降低。有趣的是,我们发现虽然 AeAct-4 是半合子充分的,大多数杂合子个体能够飞行,但 myo-fem 并非如此,只有一半左右的个体携带一个完整的拷贝无法飞行。这些发现为开发新型控制埃及伊蚊种群的机制奠定了基础,我们的结果表明,这种机制可能适用于其他蚊子传播物种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adcd/7781531/41acd464ef7e/pntd.0008971.g001.jpg

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