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piRNA Profiling of Dengue Virus Type 2-Infected Asian Tiger Mosquito and Midgut Tissues

机译:登革热病毒2型感染亚洲虎蚊和中肠组织的piRNA分析

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The Asian tiger mosquito, Aedes albopictus , is a competent vector for the majority of arboviruses. The mosquito innate immune response is a primary determinant for arthropod-borne virus transmission, and the midgut is the first barrier to pathogen transmission. Mosquito antiviral immunity is primarily mediated by the small interfering RNA pathway. However, the roles that the P-element induced wimpy testis (PIWI)-interacting RNA (piRNA) pathway play in antiviral immunity in Ae. albopictus and its midgut still need further exploration. This study aimed to explore the profiles of both viral-derived and host-originated piRNAs in the whole body and midgut infected with Dengue virus 2 (DENV-2) in Ae. albopictus , and to elucidate gene expression profile differences of the PIWI protein family between adult females and their midguts. A deep sequencing-based method was used to identify and analyze small non-coding RNAs, especially the piRNA profiles in DENV-2-infected Ae. albopictus and its midgut. The top-ranked, differentially-expressed piRNAs were further validated using Stem-loop qRT-PCR. Bioinformatics analyses and reverse-transcription PCR (RT-PCR) methods were used to detect PIWI protein family members, and their expression profiles. DENV-2 derived piRNAs (vpiRNA, 24–30 nts) were observed in both infected Ae. albopictus and its midgut; however, only vpiRNA in the whole-body library had a weak preference for adenine at position 10 (10A) in the sense molecules as a feature of secondary piRNA. These vpiRNAs were not equally distributed, instead they were derived from a few specific regions of the genome, especially several hot spots, and displayed an obvious positive strand bias. We refer to the differentially expressed host piRNAs after DENV infection as virus-induced host endogenous piRNAs (vepiRNAs). However, we found that vepiRNAs were abundant in mosquito whole-body tissue, but deficient in the midgut. A total of eleven PIWI family genes were identified in Ae. albopictus ; however, only AalPiwi5–7 and AalAgo3(1–2) were readily detected in the midgut. The characteristics of piRNAs in DENV-2-infected Ae. albopictus adult females were similar to those previously described for flavivirus infections but were not observed in the midgut. The reduced levels of vepiRNAs and incomplete expression of PIWI pathway genes in midgut samples from DENV-2-infected Ae. albopictus suggests that viral regulation of host piRNAs may not be an important factor in the midgut.
机译:亚洲虎蚊,白纹伊蚊,是大多数虫媒病毒的有效媒介。蚊子的先天免疫应答是节肢动物传播的病毒传播的主要决定因素,而中肠是病原体传播的第一个障碍。蚊子的抗病毒免疫力主要由小干扰RNA途径介导。但是,P元素诱导的imp弱睾丸(PIWI)相互作用RNA(piRNA)途径在Ae的抗病毒免疫中发挥了作用。白带及其中肠仍需进一步探索。这项研究旨在探讨在Ae感染登革热病毒2(DENV-2)的全身和中肠中病毒来源和宿主来源的piRNA的概况。并阐明成年雌性和中肠之间PIWI蛋白家族的基因表达谱差异。基于深度测序的方法用于鉴定和分析小的非编码RNA,尤其是DENV-2感染的Ae中的piRNA图谱。白化病及其中肠。使用Stem-loop qRT-PCR进一步验证了排名最高,差异表达的piRNA。使用生物信息学分析和逆转录PCR(RT-PCR)方法检测PIWI蛋白家族成员及其表达谱。在两个被感染的Ae中均观察到DENV-2衍生的piRNA(vpiRNA,24–30 nt)。白化病及其中肠;然而,在全身文库中,只有vpiRNA对有义分子中第10位(10A)的腺嘌呤具有较弱的偏好,这是次级piRNA的特征。这些vpiRNA分布不均,而是源自基因组的几个特定区域,尤其是几个热点,并表现出明显的正链偏向。我们将DENV感染后差异表达的宿主piRNA称为病毒诱导的宿主内源性piRNA(vepiRNA)。但是,我们发现vepiRNAs在蚊子的全身组织中丰富,但在中肠中却不足。在Ae中总共鉴定出11个PIWI家族基因。白化病;但是,在中肠中仅能轻易检测到AalPiwi5-7和AalAgo3(1-2)。 DENV-2感染的Ae中piRNA的特征。白化成年雌性与先前描述的黄病毒感染相似,但未在中肠观察到。在感染DENV-2的Ae中肠样品中,vepiRNA的水平降低,PIWI途径基因的表达不完全。 albopictus表明宿主piRNA的病毒调节可能不是中肠的重要因素。

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