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[具体物质]对叶螨病毒限制的潜在影响。 (这里原文“Potential effect of on virus restriction in the spider mite.”中“of”后面缺少具体内容,所以翻译时补充了“[具体物质]”)

Potential effect of on virus restriction in the spider mite .

作者信息

Ferreira Lucas Yago Melo, Santos João Pedro Nunes, Souza David Gabriel do Nascimento, Orellana Lixsy Celeste Bernardez, de Santana Sabrina Ferreira, Sousa Anderson Gonçalves, Fonseca Paula Luize Camargos, Silva Amanda Gabrielly Santana, Santos Vinicius Castro, de Faria Isaque João da Silva, Olmo Roenick Proveti, Pacheco Luis Gustavo Carvalho, Costa Marcio Gilberto Cardoso, Pirovani Carlos Priminho, Oliveira Anibal Ramadan, Aguiar Eric Roberto Guimarães Rocha

机构信息

Center of Biotechnology and Genetics, Department of Biological Sciences, Universidade Estadual de Santa Cruz, Ilhéus, Bahia, Brazil.

Department of Genetics, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.

出版信息

Front Microbiol. 2025 May 29;16:1570606. doi: 10.3389/fmicb.2025.1570606. eCollection 2025.

Abstract

The mite is a significant agricultural pest and may serve as a potential vector for viral transmission. However, the virome of remains understudied. Through metatranscriptomic analyses of publicly available data, we uncovered a diverse range of viruses associated with the spider mite, including crop-infecting pathogenic species such as and , and fourteen previously unknown viruses across several families (e.g., , , , , and ). Taking advantage of mite samples under different conditions, we also assessed the impact of biotic ( and infection) and abiotic stresses (pesticide exposure and temperature stress) on the virome. Interestingly, appeared to restrict viral infections in by reducing viral diversity and abundance, with a pronounced effect on dicistroviruses. Surprisingly, a similar effect also observed with . However, the viral restriction phenotype vanishes in co-infected mites. Transcriptomics analysis of singly-infected mites revealed upregulation of piRNA and autophagy-related genes, while lipid metabolism processes-related genes were downregulated, indicating an endosymbiont-sharing mechanisms of viral interference. Although the impact of abiotic stressors on the virome was not statistically significant, and TtDV-2 viruses were absent in abamectin-exposed mites, suggesting a potential reduction in the viral diversity, while heat-stressed mites exhibited slightly higher viral diversity compared to those raised at regular temperatures. Overall, our work provides a detailed analysis of the virome, shedding light on how endosymbionts and environmental factors shape viral dynamics and offering potential insights for pest management strategies.

摘要

这种螨是一种重要的农业害虫,可能是病毒传播的潜在媒介。然而,其病毒组仍未得到充分研究。通过对公开可用数据进行宏转录组分析,我们发现了与叶螨相关的多种病毒,包括感染作物的致病物种,如[具体物种1]和[具体物种2],以及跨几个科的14种先前未知的病毒(例如,[科名1]、[科名2]、[科名3]、[科名4]和[科名5])。利用不同条件下的螨样本,我们还评估了生物胁迫([具体生物1]和[具体生物2]感染)和非生物胁迫(农药暴露和温度胁迫)对叶螨病毒组的影响。有趣的是,[具体生物1]似乎通过降低病毒多样性和丰度来限制叶螨中的病毒感染,对双顺反子病毒有显著影响。令人惊讶的是,[具体生物2]也观察到了类似的效果。然而,在共同感染的螨中病毒限制表型消失。对单感染螨的转录组分析显示,piRNA和自噬相关基因上调,而脂质代谢过程相关基因下调,表明存在病毒干扰的内共生体共享机制。尽管非生物胁迫因素对病毒组的影响在统计学上不显著,但在接触阿维菌素的螨中不存在[具体病毒1]和TtDV - 2病毒,这表明病毒多样性可能会降低,而热胁迫螨与在正常温度下饲养的螨相比,病毒多样性略高。总体而言,我们的工作对叶螨病毒组进行了详细分析,揭示了内共生体和环境因素如何塑造病毒动态,并为害虫管理策略提供了潜在的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a1a/12159000/c18dd507b480/fmicb-16-1570606-g001.jpg

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