First-male sperm precedence in polyandrous Spodoptera frugiperda allows sterile males induce population suppression

bioRxiv Pub Date : 2024-07-16 DOI:10.1101/2024.07.10.602994
Hao Sun, Ling-Ao Bu, Xin-Yue Zhang, Zhi-Ruo Zhang, Ling-Yi Zhu, Shao-Cong Su, Di Guo, Gao Hu, Cong-Fen Gao, S. R. Palli, J. Champer, Shun-Fan Wu
{"title":"First-male sperm precedence in polyandrous Spodoptera frugiperda allows sterile males induce population suppression","authors":"Hao Sun, Ling-Ao Bu, Xin-Yue Zhang, Zhi-Ruo Zhang, Ling-Yi Zhu, Shao-Cong Su, Di Guo, Gao Hu, Cong-Fen Gao, S. R. Palli, J. Champer, Shun-Fan Wu","doi":"10.1101/2024.07.10.602994","DOIUrl":null,"url":null,"abstract":"Males respond to intense sperm competition by adapting reproductive strategies to promote fertilization success, which is critical for population reproduction. Thus, investigating the patterns and mechanisms of sperm competition is crucial for the development and application of pest population management techniques. In this study, we analyzed the sperm precedence pattern of a major pest, the fall armyworm, and used this pattern to manage the pest population. First, we found that females had a post-mating response and did not gain direct benefit through multiple mating. Next, in a double mating experiment, we used a molecular marker created by CRISPR/Cas9 to determine that most females use only the sperm of the first male to produce offspring. To further explore the role of fertilizing sperm in sperm competition, we constructed a sterile male line with eupyrene sperm defect by knocking out the B2t gene. Interestingly, two round mating assays showed that first mating with B2t-null males inhibited sperm fertilization from a second wild-type male. In other words, prior mating with B2t-null males significantly reduced the fertility and fecundity of females. Based on this finding, we continued to explore whether sperm-deficient sterile males could be used in the management of FAW populations. Cage experiments and mathematical modeling analyses showed that the release of excess B2t-null males induced population suppression. Our study expands our knowledge of sperm competition patterns in lepidopteran. In addition, our study provides a paradigm to develop and apply genetic control methods based on sperm competition outcome in polyandrous pests. Significance Sperm competition is essential for maintaining population reproduction. Understanding patterns and mechanisms of sperm competition facilitates the development of appropriate pest genetic control methods. Here, we describe that a globally major pest, the fall armyworm displays the first-male sperm precedence pattern. Interestingly, first mating with B2t-null males, which produces non-functional eupyrene sperm, significantly reduces the fertility and fecundity of females. That means that the ejaculate of the first male, even if its eupyrene sperm are defective, can inhibit sperm fertilization from a second wild-type male. Based on this, the release of excess B2t-null males significantly suppresses FAW populations. These results suggest that future development of genetic control techniques based on targeting nucleated sperm can effectively control FAW populations.","PeriodicalId":9124,"journal":{"name":"bioRxiv","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.07.10.602994","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Males respond to intense sperm competition by adapting reproductive strategies to promote fertilization success, which is critical for population reproduction. Thus, investigating the patterns and mechanisms of sperm competition is crucial for the development and application of pest population management techniques. In this study, we analyzed the sperm precedence pattern of a major pest, the fall armyworm, and used this pattern to manage the pest population. First, we found that females had a post-mating response and did not gain direct benefit through multiple mating. Next, in a double mating experiment, we used a molecular marker created by CRISPR/Cas9 to determine that most females use only the sperm of the first male to produce offspring. To further explore the role of fertilizing sperm in sperm competition, we constructed a sterile male line with eupyrene sperm defect by knocking out the B2t gene. Interestingly, two round mating assays showed that first mating with B2t-null males inhibited sperm fertilization from a second wild-type male. In other words, prior mating with B2t-null males significantly reduced the fertility and fecundity of females. Based on this finding, we continued to explore whether sperm-deficient sterile males could be used in the management of FAW populations. Cage experiments and mathematical modeling analyses showed that the release of excess B2t-null males induced population suppression. Our study expands our knowledge of sperm competition patterns in lepidopteran. In addition, our study provides a paradigm to develop and apply genetic control methods based on sperm competition outcome in polyandrous pests. Significance Sperm competition is essential for maintaining population reproduction. Understanding patterns and mechanisms of sperm competition facilitates the development of appropriate pest genetic control methods. Here, we describe that a globally major pest, the fall armyworm displays the first-male sperm precedence pattern. Interestingly, first mating with B2t-null males, which produces non-functional eupyrene sperm, significantly reduces the fertility and fecundity of females. That means that the ejaculate of the first male, even if its eupyrene sperm are defective, can inhibit sperm fertilization from a second wild-type male. Based on this, the release of excess B2t-null males significantly suppresses FAW populations. These results suggest that future development of genetic control techniques based on targeting nucleated sperm can effectively control FAW populations.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
多雌性鞘翅目昆虫的第一雄性精子优先权允许不育雄性诱导种群抑制
雄虫通过调整生殖策略来应对激烈的精子竞争,从而提高受精成功率,这对种群繁衍至关重要。因此,研究精子竞争的模式和机制对于开发和应用害虫种群管理技术至关重要。在这项研究中,我们分析了一种主要害虫--秋绵羊的精子优先模式,并利用这种模式来管理害虫种群。首先,我们发现雌虫有交配后反应,并不会通过多次交配直接获益。接下来,在双交配实验中,我们利用 CRISPR/Cas9 创建的分子标记确定,大多数雌虫只使用第一只雄虫的精子来繁殖后代。为了进一步探索受精精子在精子竞争中的作用,我们通过敲除 B2t 基因构建了一个具有优生精子缺陷的不育雄性品系。有趣的是,两轮交配试验表明,首先与B2t基因缺失的雄性交配会抑制第二个野生型雄性的精子受精。换句话说,先与 B2t 基因无效的雄性交配会显著降低雌性的生育能力和繁殖力。基于这一发现,我们继续探索是否可以利用精子缺陷不育雄性来管理一窝蜂种群。笼中实验和数学建模分析表明,释放过量的B2t-null雄性可诱导种群抑制。我们的研究拓展了我们对鳞翅目昆虫精子竞争模式的认识。此外,我们的研究还为基于多雄性害虫精子竞争结果的遗传控制方法的开发和应用提供了范例。意义 精子竞争对维持种群繁殖至关重要。了解精子竞争的模式和机制有助于开发适当的害虫遗传控制方法。在这里,我们描述了一种全球主要害虫--秋天军虫--的首雄精子优先模式。有趣的是,首先与 B2t 缺失的雄虫交配(产生无功能的优胜精子)会显著降低雌虫的生育能力和繁殖力。这意味着,即使第一只雄性的优胜劣汰精子有缺陷,其射精也能抑制第二只野生型雄性的精子受精。基于这一点,释放过量的 B2t 缺失雄性能显著抑制 FAW 群体。这些结果表明,未来基于有核精子的基因控制技术的发展可以有效控制一窝蜂的数量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
DGTS overproduced in seed plants is excluded from plastid membranes and promotes endomembrane expansion A distant TANGO1 family member promotes vitellogenin export from the ER in C. elegans Diet-induced obesity mediated through Estrogen-Related Receptor α is independent of intestinal function The Rbfox1/LASR complex controls alternative pre-mRNA splicing by recognition of multi-part RNA regulatory modules The Once and Future Fish: 1300 years of Atlantic herring population structure and demography revealed through ancient DNA and mixed-stock analysis
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1