Temporal and spatial profiling of Aedes albopictus immune responses to chikungunya virus infection.

IF 3.4 2区 医学 Q1 PARASITOLOGY
PLoS Neglected Tropical Diseases Pub Date : 2025-10-03 eCollection Date: 2025-10-01 DOI:10.1371/journal.pntd.0013588
Maria Greta Dipaola, Claudia Fortuna, Francesco Severini, Giulia Bevivino, Marco Di Luca, Tony Nolan, Marco Salvemini, Bruno Arcà, Fabrizio Lombardo
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引用次数: 0

Abstract

The global expansion of Aedes albopictus from Southeast Asia to various regions worldwide poses a significant public health concern due to its role as a vector for several pathogens, including chikungunya virus (CHIKV), which infects over one million people annually. In this study, aimed at understanding the molecular interactions between Ae. albopictus and CHIKV, we analyzed by RNA sequencing CHIKV-infected and uninfected control mosquitoes. We focused our attention on key mosquito organs at one- and five-days post-blood meal ingestion, which correspond to viral entry and dissemination, and found specific transcriptional changes involving various pathways during the CHIKV lifecycle. The mosquito midgut plays a crucial role in the early stages, when the virus enters along with human blood components, encounters the resident microbiota, interacts with the developing peritrophic matrix, and counteracts the mosquito's digestive enzymes. We found that RNA interference (RNAi) was predominantly activated in the midgut during the initial virus invasion. Additionally, several key enzymes involved in autophagy and ubiquitination were also more abundant in infected midguts compared to controls. At later time points, after viral dissemination into the hemocoel, key immune responses are triggered in the hemolymph and, accordingly, immune mechanisms such as the activation of leucine-rich repeats (LRRs) proteins, secretion of antimicrobial peptides (e.g., holotricin), and melanization (mediated by phenoloxidase, PO) were the most prominent. RNA-seq results were validated by RT-qPCR on selected candidates in different tissues and a catalogue of Ae. albopictus immune genes (891 contigs) grouped into 24 different immune and immune-related families was compiled. This study explores the molecular interactions between Ae. albopictus and CHIKV across developmental stages, providing key insights into arbovirus transmission dynamics and mosquito vector competence.

白纹伊蚊对基孔肯雅病毒感染免疫反应的时空分析。
白纹伊蚊从东南亚向全球各区域的全球扩张引起了重大的公共卫生关注,因为它是几种病原体的媒介,包括每年感染100多万人的基孔肯雅病毒(CHIKV)。在本研究中,旨在了解Ae.;对感染和未感染的对照蚊进行RNA测序分析。我们将注意力集中在摄入血液后1天和5天的关键蚊子器官上,这些器官与病毒的进入和传播相对应,并发现了CHIKV生命周期中涉及各种途径的特定转录变化。蚊子的中肠在早期阶段起着至关重要的作用,此时病毒随人体血液成分进入,遇到常驻的微生物群,与发育中的营养基质相互作用,并抵消蚊子的消化酶。我们发现RNA干扰(RNAi)在病毒入侵初期主要在中肠被激活。此外,与对照组相比,受感染的肠道中参与自噬和泛素化的几种关键酶也更丰富。在较晚的时间点,病毒传播到血液后,关键的免疫反应在血淋巴中被触发,因此,诸如富含亮氨酸重复序列(lrr)蛋白的激活、抗菌肽(如holotricin)的分泌和黑色素化(由酚氧化酶(PO)介导)等免疫机制是最突出的。RNA-seq结果通过RT-qPCR在不同组织和伊蚊目录中选择候选者进行验证。汇编了白纹伊蚊免疫基因(891个contigs),分为24个不同的免疫和免疫相关家族。本研究探讨了Ae。白纹伊蚊和CHIKV跨越发育阶段,为虫媒病毒传播动力学和蚊子媒介能力提供关键见解。
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
PLoS Neglected Tropical Diseases
PLoS Neglected Tropical Diseases PARASITOLOGY-TROPICAL MEDICINE
自引率
10.50%
发文量
723
期刊介绍: PLOS Neglected Tropical Diseases publishes research devoted to the pathology, epidemiology, prevention, treatment and control of the neglected tropical diseases (NTDs), as well as relevant public policy. The NTDs are defined as a group of poverty-promoting chronic infectious diseases, which primarily occur in rural areas and poor urban areas of low-income and middle-income countries. Their impact on child health and development, pregnancy, and worker productivity, as well as their stigmatizing features limit economic stability. All aspects of these diseases are considered, including: Pathogenesis Clinical features Pharmacology and treatment Diagnosis Epidemiology Vector biology Vaccinology and prevention Demographic, ecological and social determinants Public health and policy aspects (including cost-effectiveness analyses).
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