Lysinibacillus sphaericus exposure impedes Anopheles dirus's oviposition via downregulating vitellogenin.

IF 3 2区 医学 Q1 PARASITOLOGY
Shasha Yu, Zhilong Liu, Jing Wang, Hong Zheng, Shiqian Han, Feifei Zheng, Dan Zheng, Caizhi Zhao, Xin Li, Tingting Liu, Xuesen Yang, Ying Wang
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Abstract

Background: Vector control using Lysinibacillus sphaericus is an effective strategy for preventing the transmission of mosquito-borne diseases. Our previous study demonstrated that exposure to L. sphaericus during the larval stage of Anopheles dirus significantly reduced the fecundity of surviving adult mosquitoes. However, the underlying mechanisms driving this reduction remain unclear. Sublethal doses of L. sphaericus, often resulting from insufficient or delayed application, can still impact mosquito populations. Therefore, this study aimed to investigate how sublethal doses of L. sphaericus inhibit the reproductive capacity of An. dirus mosquitoes.

Methods: First, the staining method was used to detect L. sphaericus in surviving adult mosquitoes that had been exposed to sublethal doses during the larval stage. Second, adult mosquitoes were fed a sucrose solution containing L. sphaericus, and the effects on the reproductive capacity were observed. Third, transcriptome sequencing and qPCR were employed to identify and validate genes associated with oviposition suppression in An. dirus following treatment with sublethal doses of L. sphaericus. Finally, we assessed the effects of sublethal doses and direct feeding of L. sphaericus on vitellogenin (Vg) expression and activation of the target of rapamycin (TOR) signaling pathway using qPCR and Western blotting.

Results: Our findings demonstrated that L. sphaericus persists in adult An. dirus mosquitoes that survived larval exposure to sublethal doses. Additionally, feeding adult female mosquitoes with L. sphaericus significantly suppressed their oviposition ability. Transcriptome analysis revealed substantial alterations in gene expression profiles among surviving mosquitoes exposed to sublethal doses of L. sphaericus. Notably, L. sphaericus inhibit lysosomal function and lipid metabolism, which are critical for mosquito physiology. Furthermore, L. sphaericus significantly downregulated the Akt-TOR signaling pathway and Vg expression in adult mosquitoes.

Conclusions: Exposure An. dirus larvae to L. sphaericus resulted in the persistence of L. sphaericus in surviving adult mosquitoes and significantly suppressed female oviposition by downregulating Vg expression via inhibition of lysosomal function and the TOR signaling pathway. This study offers novel insights into the interaction between L. sphaericus and its mosquito host and identifies potential molecular targets for controlling mosquito population density by modulating oviposition behavior.

通过下调卵黄素,暴露于溶血芽孢杆菌会阻碍按蚊的产卵。
背景:利用来苏比特芽孢杆菌(Lysinibacillus sphaericus)控制病媒是预防蚊媒疾病传播的有效策略。我们之前的研究表明,在疟蚊幼虫期暴露于史氏赖氏菌可显著降低存活成蚊的繁殖力。然而,导致这种降低的根本机制仍不清楚。亚致死剂量的 L. sphaericus 通常是施用不足或延迟施用造成的,但仍会对蚊子种群产生影响。因此,本研究旨在调查亚致死剂量的海星蚊虫如何抑制弧蚊的繁殖能力:方法:首先,使用染色法检测幼虫期暴露于亚致死剂量的存活成蚊中的矛尖鳋。其次,给成蚊喂食含有螺旋体的蔗糖溶液,观察其对繁殖能力的影响。第三,采用转录组测序和 qPCR 方法,鉴定和验证了在使用亚致死剂量的海星酵母菌处理后,与海星蚊产卵抑制有关的基因。最后,我们利用 qPCR 和 Western 印迹技术评估了亚致死剂量和直接饲喂海鞘酵母菌对卵黄素(Vg)表达和雷帕霉素靶标(TOR)信号通路激活的影响:结果:我们的研究结果表明,L. sphaericus 在幼虫暴露于亚致死剂量后存活下来的成蚊体内持续存在。此外,给成年雌蚊喂食海鞘酵母菌会显著抑制它们的产卵能力。转录组分析表明,暴露于亚致死剂量海鞘酵母的存活蚊子的基因表达谱发生了很大变化。值得注意的是,螺旋体抑制溶酶体功能和脂质代谢,这对蚊子的生理机能至关重要。此外,褐飞虱还能显著下调成蚊体内的 Akt-TOR 信号通路和 Vg 表达:结论:将褐飞虱幼虫暴露于褐飞虱(L. sphaericus)会导致褐飞虱持续存在于存活的成蚊体内,并通过抑制溶酶体功能和 TOR 信号通路下调 Vg 的表达,从而显著抑制雌蚊的排卵。这项研究为我们提供了新的视角,使我们能够深入了解褐飞虱与蚊子宿主之间的相互作用,并确定了通过调节排卵行为来控制蚊子种群密度的潜在分子靶标。
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来源期刊
Parasites & Vectors
Parasites & Vectors 医学-寄生虫学
CiteScore
6.30
自引率
9.40%
发文量
433
审稿时长
1.4 months
期刊介绍: Parasites & Vectors is an open access, peer-reviewed online journal dealing with the biology of parasites, parasitic diseases, intermediate hosts, vectors and vector-borne pathogens. Manuscripts published in this journal will be available to all worldwide, with no barriers to access, immediately following acceptance. However, authors retain the copyright of their material and may use it, or distribute it, as they wish. Manuscripts on all aspects of the basic and applied biology of parasites, intermediate hosts, vectors and vector-borne pathogens will be considered. In addition to the traditional and well-established areas of science in these fields, we also aim to provide a vehicle for publication of the rapidly developing resources and technology in parasite, intermediate host and vector genomics and their impacts on biological research. We are able to publish large datasets and extensive results, frequently associated with genomic and post-genomic technologies, which are not readily accommodated in traditional journals. Manuscripts addressing broader issues, for example economics, social sciences and global climate change in relation to parasites, vectors and disease control, are also welcomed.
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