Suppr超能文献

无文化基因组全位点序列分型(GLST)为克氏锥虫传播和感染复杂性提供了新的视角。

Culture-free genome-wide locus sequence typing (GLST) provides new perspectives on Trypanosoma cruzi dispersal and infection complexity.

机构信息

Institute of Biodiversity, Animal Health & Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.

Centro de Investigación para la Salud en América Latina, Pontificia Universidad Católica del Ecuador, Quito, Ecuador.

出版信息

PLoS Genet. 2020 Dec 16;16(12):e1009170. doi: 10.1371/journal.pgen.1009170. eCollection 2020 Dec.

Abstract

Analysis of genetic polymorphism is a powerful tool for epidemiological surveillance and research. Powerful inference from pathogen genetic variation, however, is often restrained by limited access to representative target DNA, especially in the study of obligate parasitic species for which ex vivo culture is resource-intensive or bias-prone. Modern sequence capture methods enable pathogen genetic variation to be analyzed directly from host/vector material but are often too complex and expensive for resource-poor settings where infectious diseases prevail. This study proposes a simple, cost-effective 'genome-wide locus sequence typing' (GLST) tool based on massive parallel amplification of information hotspots throughout the target pathogen genome. The multiplexed polymerase chain reaction amplifies hundreds of different, user-defined genetic targets in a single reaction tube, and subsequent agarose gel-based clean-up and barcoding completes library preparation at under 4 USD per sample. Our study generates a flexible GLST primer panel design workflow for Trypanosoma cruzi, the parasitic agent of Chagas disease. We successfully apply our 203-target GLST panel to direct, culture-free metagenomic extracts from triatomine vectors containing a minimum of 3.69 pg/μl T. cruzi DNA and further elaborate on method performance by sequencing GLST libraries from T. cruzi reference clones representing discrete typing units (DTUs) TcI, TcIII, TcIV, TcV and TcVI. The 780 SNP sites we identify in the sample set repeatably distinguish parasites infecting sympatric vectors and detect correlations between genetic and geographic distances at regional (< 150 km) as well as continental scales. The markers also clearly separate TcI, TcIII, TcIV and TcV + TcVI and appear to distinguish multiclonal infections within TcI. We discuss the advantages, limitations and prospects of our method across a spectrum of epidemiological research.

摘要

遗传多态性分析是流行病学监测和研究的有力工具。然而,由于难以获得有代表性的目标 DNA,病原体遗传变异的强大推断往往受到限制,尤其是在研究需要资源密集型或有偏差的专性寄生物种时。现代序列捕获方法可直接从宿主/载体材料中分析病原体遗传变异,但对于流行传染病的资源匮乏环境来说,这些方法通常过于复杂且昂贵。本研究提出了一种简单、具有成本效益的“全基因组定位序列分型”(GLST)工具,该工具基于在目标病原体基因组中的信息热点进行大规模平行扩增。多重聚合酶链反应在单个反应管中扩增数百个不同的、用户定义的遗传靶标,随后进行琼脂糖凝胶为基础的清理和条形码标记,可在每个样本不到 4 美元的情况下完成文库制备。本研究针对恰加斯病的寄生虫病原体克氏锥虫(Trypanosoma cruzi),生成了一种灵活的 GLST 引物面板设计工作流程。我们成功地将我们的 203 个靶标 GLST 面板应用于无培养的三锥虫载体宏基因组提取物,该提取物至少包含 3.69 pg/μl 的 T. cruzi DNA,并且通过对代表离散分型单位(DTU)TcI、TcIII、TcIV、TcV 和 TcVI 的 T. cruzi 参考克隆的 GLST 文库进行测序,进一步阐述了方法的性能。我们在样本集中鉴定了 780 个 SNP 位点,这些位点可重复性地区分感染同域载体的寄生虫,并在区域(<150km)和大陆尺度上检测到遗传和地理距离之间的相关性。这些标记还可清晰区分 TcI、TcIII、TcIV 和 TcV+TcVI,并似乎可区分 TcI 中的多克隆感染。我们讨论了我们的方法在一系列流行病学研究中的优势、限制和前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d4b/7743988/c55ba14ee22b/pgen.1009170.g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验