Potential effect of Wolbachia on virus restriction in the spider mite T. truncatus.

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2025-05-29 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1570606
Lucas Yago Melo Ferreira, João Pedro Nunes Santos, David Gabriel do Nascimento Souza, Lixsy Celeste Bernardez Orellana, Sabrina Ferreira de Santana, Anderson Gonçalves Sousa, Paula Luize Camargos Fonseca, Amanda Gabrielly Santana Silva, Vinicius Castro Santos, Isaque João da Silva de Faria, Roenick Proveti Olmo, Luis Gustavo Carvalho Pacheco, Marcio Gilberto Cardoso Costa, Carlos Priminho Pirovani, Anibal Ramadan Oliveira, Eric Roberto Guimarães Rocha Aguiar
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引用次数: 0

Abstract

The mite T. truncatus is a significant agricultural pest and may serve as a potential vector for viral transmission. However, the virome of T. truncatus 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 Potato virus Y and Cherry virus A, and fourteen previously unknown viruses across several families (e.g., Virgaviridae, Dicistroviridae, Kitaviridae, Betaflexiviridae, and Nudiviridae). Taking advantage of mite samples under different conditions, we also assessed the impact of biotic (Wolbachia and Spiroplasma infection) and abiotic stresses (pesticide exposure and temperature stress) on the T. truncatus virome. Interestingly, Wolbachia appeared to restrict viral infections in T. truncatus by reducing viral diversity and abundance, with a pronounced effect on dicistroviruses. Surprisingly, a similar effect also observed with Spiroplasma. 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, Potato virus Y 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 T. truncatus virome, shedding light on how endosymbionts and environmental factors shape viral dynamics and offering potential insights for pest management strategies.

沃尔巴克氏体对猴爪螨体内病毒抑制的潜在影响。
截尾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,截尾绦虫的病毒体仍未得到充分的研究。通过对公开数据的超转录组学分析,我们发现了与蜘蛛螨相关的多种病毒,包括作物感染致病性物种,如马铃薯病毒Y和樱桃病毒a,以及14种以前未知的病毒,分布在几个科(如Virgaviridae, Dicistroviridae, Kitaviridae, Betaflexiviridae和Nudiviridae)。利用不同条件下的螨类样本,我们还评估了生物胁迫(沃尔巴克氏体和螺旋体感染)和非生物胁迫(农药暴露和温度胁迫)对T. truncatus病毒的影响。有趣的是,沃尔巴克氏体似乎通过减少病毒的多样性和丰度来限制T. truncatus的病毒感染,对双股病毒有明显的影响。令人惊讶的是,在螺旋体中也观察到类似的效果。然而,病毒限制性表型在共感染螨中消失。单次感染螨的转录组学分析显示,piRNA和自噬相关基因上调,脂质代谢过程相关基因下调,提示病毒干扰的内共生共享机制。尽管非生物胁迫源对病毒体的影响在统计学上不显著,但暴露于阿巴菌素的螨虫中不存在马铃薯病毒Y和TtDV-2病毒,这表明病毒多样性可能减少,而热应激的螨虫比常温下的螨虫表现出略高的病毒多样性。总的来说,我们的工作提供了对T. truncatus病毒的详细分析,揭示了内共生体和环境因素如何影响病毒动力学,并为害虫管理策略提供了潜在的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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