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利用高通量小 RNA 测序技术在野外捕获的蚊子中发现 DNA 病毒。

Discovery of DNA viruses in wild-caught mosquitoes using small RNA high throughput sequencing.

机构信息

State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, China.

出版信息

PLoS One. 2011;6(9):e24758. doi: 10.1371/journal.pone.0024758. Epub 2011 Sep 20.

Abstract

BACKGROUND

Mosquito-borne infectious diseases pose a severe threat to public health in many areas of the world. Current methods for pathogen detection and surveillance are usually dependent on prior knowledge of the etiologic agents involved. Hence, efficient approaches are required for screening wild mosquito populations to detect known and unknown pathogens.

METHODOLOGY/PRINCIPAL FINDINGS: In this study, we explored the use of Next Generation Sequencing to identify viral agents in wild-caught mosquitoes. We extracted total RNA from different mosquito species from South China. Small 18-30 bp length RNA molecules were purified, reverse-transcribed into cDNA and sequenced using Illumina GAIIx instrumentation. Bioinformatic analyses to identify putative viral agents were conducted and the results confirmed by PCR. We identified a non-enveloped single-stranded DNA densovirus in the wild-caught Culex pipiens molestus mosquitoes. The majority of the viral transcripts (.>80% of the region) were covered by the small viral RNAs, with a few peaks of very high coverage obtained. The +/- strand sequence ratio of the small RNAs was approximately 7∶1, indicating that the molecules were mainly derived from the viral RNA transcripts. The small viral RNAs overlapped, enabling contig assembly of the viral genome sequence. We identified some small RNAs in the reverse repeat regions of the viral 5'- and 3' -untranslated regions where no transcripts were expected.

CONCLUSIONS/SIGNIFICANCE: Our results demonstrate for the first time that high throughput sequencing of small RNA is feasible for identifying viral agents in wild-caught mosquitoes. Our results show that it is possible to detect DNA viruses by sequencing the small RNAs obtained from insects, although the underlying mechanism of small viral RNA biogenesis is unclear. Our data and those of other researchers show that high throughput small RNA sequencing can be used for pathogen surveillance in wild mosquito vectors.

摘要

背景

蚊媒传染病对世界许多地区的公共卫生构成严重威胁。目前的病原体检测和监测方法通常依赖于对相关病原体的预先了解。因此,需要有效的方法来筛选野生蚊子种群,以检测已知和未知的病原体。

方法/主要发现:在这项研究中,我们探索了使用下一代测序技术来识别野生捕获蚊子中的病毒。我们从中国南方不同的蚊子物种中提取总 RNA。纯化小的 18-30bp 长 RNA 分子,反转录成 cDNA,并用 Illumina GAIIx 仪器进行测序。进行了生物信息学分析以鉴定可能的病毒,并通过 PCR 进行了验证。我们在野生捕获的致倦库蚊中鉴定出一种非包膜的单链 DNA 浓核病毒。大多数病毒转录物(占该区域的>80%)被小病毒 RNA 覆盖,只有少数几个高覆盖峰。小 RNA 的 +/- 链序列比约为 7∶1,表明这些分子主要来自病毒 RNA 转录物。小 RNA 重叠,从而能够组装病毒基因组序列的连续序列。我们在病毒 5'和 3'非翻译区的反向重复区中鉴定出一些小 RNA,而这些区域预计没有转录物。

结论/意义:我们的结果首次证明,高通量测序小 RNA 可用于鉴定野生捕获蚊子中的病毒。我们的结果表明,通过测序从昆虫中获得的小 RNA 可以检测 DNA 病毒,尽管小病毒 RNA 生物发生的潜在机制尚不清楚。我们的数据和其他研究人员的数据表明,高通量小 RNA 测序可用于野生蚊媒病原体监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d34f/3176773/63016edc0dc1/pone.0024758.g001.jpg

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