Pandey Sudeep, Catto Michael, Roberts Phillip, Bag Sudeep, Jacobson Alana L, Srinivasan Rajagopalbabu
Department of Entomology, University of Georgia, Griffin, GA, United States.
Department of Entomology, University of Georgia, Athens, GA, United States.
Front Plant Sci. 2024 Mar 8;15:1341781. doi: 10.3389/fpls.2024.1341781. eCollection 2024.
Upon acquisition of persistent circulative viruses such as poleroviruses, the virus particles transcytose through membrane barriers of aphids at the midgut and salivary glands via hemolymph. Such intricate interactions can influence aphid behavior and fitness and induce associated gene expression in viruliferous aphids. Differential gene expression can be evaluated by omics approaches such as transcriptomics. Previously conducted aphid transcriptome studies used only one host species as the source of virus inoculum. Viruses typically have alternate hosts. Hence, it is not clear how alternate hosts infected with the same virus isolate alter gene expression in viruliferous vectors. To address the question, this study conducted a transcriptome analysis of viruliferous aphids that acquired the virus from different host species. A polerovirus, cotton leafroll dwarf virus (CLRDV), which induced gene expression in the cotton aphid, Glover, was assessed using four alternate hosts, viz., cotton, hibiscus, okra, and prickly sida. Among a total of 2,942 differentially expressed genes (DEGs), 750, 310, 1,193, and 689 genes were identified in that acquired CLRDV from infected cotton, hibiscus, okra, and prickly sida, respectively, compared with non-viruliferous aphids that developed on non-infected hosts. A higher proportion of aphid genes were overexpressed than underexpressed following CLRDV acquisition from cotton, hibiscus, and prickly sida. In contrast, more aphid genes were underexpressed than overexpressed following CLRDV acquisition from okra plants. Only four common DEGs (, , and two unannotated genes) were identified among viruliferous aphids from four alternate hosts. Gene ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) annotations indicated that the acquisition of CLRDV induced DEGs in aphids associated with virus infection, signal transduction, immune systems, and fitness. However, these induced changes were not consistent across four alternate hosts. These data indicate that alternate hosts could differentially influence gene expression in aphids and presumably aphid behavior and fitness despite being infected with the same virus isolate.
在获取持久性循环病毒(如马铃薯卷叶病毒)后,病毒粒子通过血淋巴跨细胞穿过蚜虫中肠和唾液腺的膜屏障。这种复杂的相互作用会影响蚜虫的行为和适应性,并在带毒蚜虫中诱导相关基因表达。差异基因表达可以通过转录组学等组学方法进行评估。此前进行的蚜虫转录组研究仅使用一种寄主物种作为病毒接种源。病毒通常有交替寄主。因此,尚不清楚感染相同病毒分离株的交替寄主如何改变带毒介体中的基因表达。为了解决这个问题,本研究对从不同寄主物种获取病毒的带毒蚜虫进行了转录组分析。使用棉花、木槿、秋葵和刺蒴麻这四种交替寄主,评估了一种能在棉蚜(Glover)中诱导基因表达的马铃薯卷叶病毒——棉花卷叶矮化病毒(CLRDV)。在总共2942个差异表达基因(DEG)中,与在未感染寄主上发育的无毒蚜虫相比,分别从感染棉花、木槿、秋葵和刺蒴麻中获取CLRDV的蚜虫中鉴定出750、310、1193和689个基因。从棉花、木槿和刺蒴麻获取CLRDV后,蚜虫中过表达的基因比例高于低表达的基因。相比之下,从秋葵植株获取CLRDV后,蚜虫中低表达的基因比过表达的基因更多。在来自四种交替寄主的带毒蚜虫中仅鉴定出四个共同的差异表达基因(、和两个未注释基因)。基因本体(GO)富集分析和京都基因与基因组百科全书(KEGG)注释表明,获取CLRDV会在蚜虫中诱导与病毒感染、信号转导、免疫系统和适应性相关的差异表达基因。然而,这些诱导变化在四种交替寄主中并不一致。这些数据表明,尽管感染相同的病毒分离株,但交替寄主可能会对蚜虫中的基因表达产生不同影响,大概也会影响蚜虫的行为和适应性。