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本文引用的文献

1
Reproductive incompatibility between the B and Q biotypes of the whitefly Bemisia tabaci in China: genetic and behavioural evidence.中国烟粉虱B型和Q型生物型之间的生殖不相容性:遗传和行为证据
Bull Entomol Res. 2011 Apr;101(2):211-20. doi: 10.1017/S0007485310000416. Epub 2010 Nov 1.
2
Bemisia tabaci: a statement of species status.烟粉虱:物种状况声明。
Annu Rev Entomol. 2011;56:1-19. doi: 10.1146/annurev-ento-112408-085504.
3
An invasive whitefly feeding on a virus-infected plant increased its egg production and realized fecundity.一种吸食受病毒感染植物的入侵性粉虱增加了其产卵量并实现了繁殖力。
PLoS One. 2010 Jul 22;5(7):e11713. doi: 10.1371/journal.pone.0011713.
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De novo characterization of a whitefly transcriptome and analysis of its gene expression during development.从头鉴定粉虱转录组及其在发育过程中的基因表达分析。
BMC Genomics. 2010 Jun 24;11:400. doi: 10.1186/1471-2164-11-400.
5
Reproductive incompatibility among genetic groups of Bemisia tabaci supports the proposition that the whitefly is a cryptic species complex.烟粉虱遗传群体间的生殖不相容性支持了粉虱是一个隐存物种复合体的观点。
Bull Entomol Res. 2010 Jun;100(3):359-66. doi: 10.1017/S0007485310000015. Epub 2010 Feb 24.
6
Transcriptomic analysis of intestinal genes following acquisition of pea enation mosaic virus by the pea aphid Acyrthosiphon pisum.豌豆蚜 Acyrthosiphon pisum 获得豌豆卷叶病毒后的肠道基因转录组分析。
J Gen Virol. 2010 Mar;91(Pt 3):802-8. doi: 10.1099/vir.0.012856-0. Epub 2009 Nov 18.
7
Begomovirus coat protein interacts with a small heat-shock protein of its transmission vector (Bemisia tabaci).双生病毒外壳蛋白与介体昆虫(烟粉虱)的一个小分子热休克蛋白相互作用。
Insect Mol Biol. 2009 Nov;18(6):693-703. doi: 10.1111/j.1365-2583.2009.00906.x. Epub 2009 Oct 8.
8
Viruses and autophagy.病毒与自噬。
Rev Med Virol. 2009 Nov;19(6):359-78. doi: 10.1002/rmv.630.
9
Deep sequencing of the zebrafish transcriptome response to mycobacterium infection.斑马鱼转录组对分枝杆菌感染反应的深度测序
Mol Immunol. 2009 Sep;46(15):2918-30. doi: 10.1016/j.molimm.2009.07.002. Epub 2009 Jul 24.
10
Short-read sequencing technologies for transcriptional analyses.用于转录分析的短读长测序技术。
Annu Rev Plant Biol. 2009;60:305-33. doi: 10.1146/annurev.arplant.043008.092032.

全球分析烟粉虱对番茄黄曲叶病毒的转录反应揭示了共同进化适应的关系。

Global analysis of the transcriptional response of whitefly to tomato yellow leaf curl China virus reveals the relationship of coevolved adaptations.

机构信息

Ministry of Agriculture Key Laboratory of Molecular Biology of Crop Pathogens and Insects, Institute of Insect Sciences, Zhejiang University, Hangzhou 310029, China.

出版信息

J Virol. 2011 Apr;85(7):3330-40. doi: 10.1128/JVI.02507-10. Epub 2011 Jan 26.

DOI:10.1128/JVI.02507-10
PMID:21270146
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3067855/
Abstract

The begomoviruses are the largest and most economically important group of plant viruses transmitted exclusively by the whitefly Bemisia tabaci in a circulative, persistent manner. The circulation of the viruses within the insect vectors involves complex interactions between virus and vector components; however, the molecular mechanisms of these interactions remain largely unknown. Here we investigated the transcriptional response of the invasive B. tabaci Middle East-Asia Minor 1 species to Tomato yellow leaf curl China virus (TYLCCNV) using Illumina sequencing technology. Results showed that 1,606 genes involved in 157 biochemical pathways were differentially expressed in the viruliferous whiteflies. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis indicated that TYLCCNV can perturb the cell cycle and primary metabolism in the whitefly, which explains the negative effect of this virus on the longevity and fecundity of B. tabaci. Our data also demonstrated that TYLCCNV can activate whitefly immune responses, such as autophagy and antimicrobial peptide production, which might lead to a gradual decrease of viral particles within the body of the viruliferous whitefly. Furthermore, PCR results showed that TYLCCNV can invade the ovary and fat body tissues of the whitefly, and Lysotracker and Western blot analyses revealed that the invasion of TYLCCNV induced autophagy in both the ovary and fat body tissues. Surprisingly, TYLCCNV also suppressed the whitefly immune responses by downregulating the expression of genes involved in Toll-like signaling and mitogen-activated protein kinase (MAPK) pathways. Taken together, these results reveal the relationship of coevolved adaptations between begomoviruses and whiteflies and will provide a road map for future investigations into the complex interactions between plant viruses and their insect vectors.

摘要

双生病毒是最大和最重要的植物病毒组,它们仅通过粉虱烟粉虱以循环和持续的方式传播。病毒在昆虫载体中的循环涉及病毒和载体成分之间的复杂相互作用;然而,这些相互作用的分子机制在很大程度上仍然未知。在这里,我们使用 Illumina 测序技术研究了入侵的烟粉虱中东-亚洲 1 种对番茄黄曲叶病毒(TYLCCNV)的转录反应。结果表明,1606 个涉及 157 种生化途径的基因在带毒粉虱中差异表达。京都基因与基因组百科全书(KEGG)途径分析表明,TYLCCNV 可以扰乱粉虱的细胞周期和初级代谢,这解释了该病毒对烟粉虱寿命和繁殖力的负面影响。我们的数据还表明,TYLCCNV 可以激活粉虱的免疫反应,如自噬和抗菌肽的产生,这可能导致体内带毒粉虱的病毒颗粒逐渐减少。此外,PCR 结果表明,TYLCCNV 可以入侵粉虱的卵巢和脂肪体组织,Lysotracker 和 Western blot 分析表明,TYLCCNV 的入侵诱导了卵巢和脂肪体组织中的自噬。令人惊讶的是,TYLCCNV 通过下调参与 Toll 样信号和丝裂原活化蛋白激酶(MAPK)途径的基因的表达,也抑制了粉虱的免疫反应。总之,这些结果揭示了双生病毒和粉虱之间共同进化适应的关系,并为未来研究植物病毒与其昆虫载体之间的复杂相互作用提供了路线图。