寄生蜂的寄主范围与寄主对其互生病毒共生体的易感性有关。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
K. A. Coffman, A. N. Kauwe, N. E. Gillette, G. R. Burke, S. M. Geib
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引用次数: 0

摘要

寄生蜂是地球上物种最丰富的动物群体之一,因为它们能够成功地寄生于几乎所有类型的昆虫。与大多数专门寄生于一种或几种寄主物种的已知寄生蜂不同,Diachasmimorpha longicaudata 是一种通性寄生蜂,可以在多个栉水母果蝇寄主属中生存,其中包括许多全球重要的害虫物种。因此,Diachasmimorpha longicaudata 被广泛释放,作为热带和亚热带农业生态系统生物防治工作的一部分,用于抑制害虫种群。在这项研究中,我们调查了互利性痘病毒在三个农业害虫属中影响长尾蝇寄主范围的作用:其中两个属是长尾蝇寄生的容许寄主,一个属是非容许寄主。我们发现,寄主Ceratitis capitata和Bactrocera dorsalis对人工注射病毒高度敏感,病毒复制迅速,大量苍蝇死亡。然而,非允许性宿主Zeugodacus curbitae在很大程度上克服了病毒感染,表现出极低的死亡率和无病毒复制。对病毒感染过程中转录动态的研究表明,与允许感染的物种相比,非允许感染的宿主体内病毒基因表达受阻,苍蝇基因表达的变化有限,这表明病毒共生体的宿主范围可能会影响长角胡蜂的宿主范围。这些发现还揭示了病毒共生体的活动可能是长尾蝇黄蜂成功成为寄生虫通才物种和全球成功的生物控制剂的主要原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Host range of a parasitoid wasp is linked to host susceptibility to its mutualistic viral symbiont

Host range of a parasitoid wasp is linked to host susceptibility to its mutualistic viral symbiont

Parasitoid wasps are one of the most species-rich groups of animals on Earth, due to their ability to successfully develop as parasites of nearly all types of insects. Unlike most known parasitoid wasps that specialize towards one or a few host species, Diachasmimorpha longicaudata is a generalist that can survive within multiple genera of tephritid fruit fly hosts, including many globally important pest species. Diachasmimorpha longicaudata has therefore been widely released to suppress pest populations as part of biological control efforts in tropical and subtropical agricultural ecosystems. In this study, we investigated the role of a mutualistic poxvirus in shaping the host range of D. longicaudata across three genera of agricultural pest species: two of which are permissive hosts for D. longicaudata parasitism and one that is a nonpermissive host. We found that permissive hosts Ceratitis capitata and Bactrocera dorsalis were highly susceptible to manual virus injection, displaying rapid virus replication and abundant fly mortality. However, the nonpermissive host Zeugodacus cucurbitae largely overcame virus infection, exhibiting substantially lower mortality and no virus replication. Investigation of transcriptional dynamics during virus infection demonstrated hindered viral gene expression and limited changes in fly gene expression within the nonpermissive host compared with the permissive species, indicating that the host range of the viral symbiont may influence the host range of D. longicaudata wasps. These findings also reveal that viral symbiont activity may be a major contributor to the success of D. longicaudata as a generalist parasitoid species and a globally successful biological control agent.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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