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罗斯河病毒在蚊子中引发差异表达的 microRNA 和 RNA 干扰反应。

Ross River Virus Provokes Differentially Expressed MicroRNA and RNA Interference Responses in Mosquitoes.

机构信息

Australian Infectious Disease Research Centre, School of Biological Sciences, The University of Queensland, Brisbane, QLD 4072, Australia.

出版信息

Viruses. 2020 Jun 27;12(7):695. doi: 10.3390/v12070695.

Abstract

Alphaviruses are globally distributed and predominately transmitted by mosquitoes. species are common vectors for the clinically important alphaviruses-Chikungunya, Sindbis, and Ross River (RRV) viruses-with also being a vector for the flaviviruses dengue, Yellow Fever, and Zika viruses. was putatively implicated in the large 1979-1980 South Pacific Islands outbreak of RRV-the leading cause of arboviral disease in Australia today. The RNA interference (RNAi) defense response in mosquitoes involves a number of small RNAs, with their kinetics induced by alphaviruses being poorly understood, particularly at the tissue level. We compared the small RNA profiles between RRV-infected and noninfected midgut and fat body tissues at 2, 6, and 12 days post-inoculation (dpi). RRV induced an incremental RNAi response, yielding short interfering and P-element-induced-wimpy-testis (PIWI)-interacting RNAs. Fourteen host microRNAs were differentially expressed due to RRV with the majority in the fat body at 2 dpi. The largely congruent pattern of microRNA regulation with previous reports for alphaviruses and divergence from those for flaviviruses suggests a degree of conservation, whereas patterns of microRNA expression unique to this study provide novel insights into the tissuespecific hostvirus attributes of responses to this previously unexplored oldworld alphavirus.

摘要

甲病毒在全球范围内分布,并主要通过蚊子传播。 是引起基孔肯雅热、辛德毕斯和罗斯河病毒(RRV)等重要临床病毒的常见媒介,也是登革热、黄热病和寨卡病毒等黄病毒的媒介。 被推测与 1979-1980 年南太平洋岛屿爆发的 RRV 大流行有关,这是当今澳大利亚虫媒病毒病的主要原因。蚊子中的 RNA 干扰(RNAi)防御反应涉及多种小 RNA,而它们对甲病毒的反应动力学还了解甚少,特别是在组织水平上。我们比较了 RRV 感染和未感染的 中肠和脂肪体组织在接种后 2、6 和 12 天的小 RNA 谱。RRV 诱导了一种递增的 RNAi 反应,产生了短干扰 RNA 和 P 元素诱导的软绵绵睾丸(PIWI)相互作用 RNA。由于 RRV,有 14 个宿主 microRNA 表达差异,其中大多数在 2 dpi 时在脂肪体中。microRNA 调控的模式与先前报道的甲病毒基本一致,与黄病毒的模式不同,表明存在一定程度的保守性,而本研究中 microRNA 表达模式的独特性为研究 对这种以前未探索的旧世界甲病毒的组织特异性宿主-病毒属性提供了新的见解。

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