Turnip Mosaic Virus Infection in a Perennial Arabidopsis Reduces Aphid Fecundity in the Natural Environment.

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Miyabi Otsubo, Haruki Nishio, Hiroshi Kudoh, Mie N Honjo
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引用次数: 0

Abstract

In plant-virus-vector tripartite relationships, it has been recognised that viral infections alter the physiological state of host plants, enhancing vector performance and facilitating virus transmission to other host individuals. Natural tripartite systems with perennial host plants are expected to persist for a long time through clonal propagation and the spread of virus-infected hosts. Under such circumstances, viral infection may negatively affect the vector, enhancing host vigour. We used the Arabidopsis halleri-turnip mosaic virus (TuMV)-aphid system to test this hypothesis. We compared aphid performance between TuMV-infected and uninfected plants, and host transcriptomes of intact, aphid-infested, TuMV-infected, and aphid-infested TuMV-infected plants. Fewer aphids were observed on TuMV-infected plants than on uninfected plants in the natural population. Manipulative experiments revealed that aphid fecundity, but not preference or emigration, was reduced on TuMV-infected plants. The host transcriptome responses to aphids were markedly weakened in TuMV-infected plants. This attenuation occurred in the form of counter-attenuation, in which the host genes respond in opposite directions to the viruses and aphids. For example, three known host genes that promote aphid fecundity are upregulated by aphid infestation in the absence of TuMV, whereas these responses are attenuated by TuMV infection. Additionally, four genes were identified as candidate genes that may have caused the TuMV-triggered reduction in aphid fecundity. In conclusion, we showed that viral infections simultaneously suppressed aphid fecundity and host plant responses induced by aphids. These interactions may prevent the host population from collapsing and enhance the coexistence of plant-virus-vector in natural environments.

芜菁花叶病毒在多年生拟南芥中的感染降低了蚜虫在自然环境中的繁殖力。
在植物-病毒-媒介的三方关系中,人们已经认识到病毒感染改变了寄主植物的生理状态,提高了媒介的性能,并促进了病毒向其他寄主个体的传播。多年生寄主植物的自然三方系统有望通过克隆繁殖和病毒感染寄主的传播而长期存在。在这种情况下,病毒感染可能对媒介产生负面影响,增强宿主活力。我们使用拟南芥-芜菁花叶病毒(TuMV)-蚜虫系统来验证这一假设。我们比较了tumv感染和未感染植物的蚜虫表现,以及完整、蚜虫感染、tumv感染和蚜虫感染的tumv感染植物的寄主转录组。在自然种群中,感染tumv的植株上蚜虫数量少于未感染植株。操纵实验表明,在tumv感染的植株上,蚜虫的繁殖力降低,但偏好或迁出率并未降低。在tumv感染的植株中,寄主对蚜虫的转录组反应明显减弱。这种衰减以反衰减的形式发生,即宿主基因对病毒和蚜虫的反应方向相反。例如,在没有TuMV的情况下,三种促进蚜虫繁殖的已知宿主基因在蚜虫侵染时被上调,而这些反应在TuMV感染时被减弱。此外,四个基因被鉴定为可能导致tumv引发的蚜虫繁殖力下降的候选基因。总之,我们发现病毒感染同时抑制蚜虫的繁殖力和蚜虫诱导的寄主植物反应。这些相互作用可以防止宿主种群的崩溃,增强植物-病毒载体在自然环境中的共存。
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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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