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LupiQuant:一种基于实时 PCR 的检测方法,用于确定盘尾丝虫病样本中盘尾丝虫和宿主犬科动物狼的宿主-寄生虫 DNA 比值。

LupiQuant: A real-time PCR based assay for determining host-to-parasite DNA ratios of Onchocerca lupi and host Canis lupus from onchocercosis samples.

机构信息

The Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ, United States of America.

School of Informatics, Computing, and Cyber Systems, Northern Arizona University, Flagstaff, AZ, United States of America.

出版信息

PLoS One. 2022 Nov 21;17(11):e0276916. doi: 10.1371/journal.pone.0276916. eCollection 2022.

DOI:10.1371/journal.pone.0276916
PMID:36409718
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9678315/
Abstract

Onchocerca lupi is a filarial nematode that causes ocular onchocercosis in canines globally including North America and areas of Europe, North Africa, and the Middle East. Reported incidence of this parasite in canines has continued to steadily escalate since the early 21st century and was more recently documented in humans. Whole genome sequencing (WGS) of this parasite can provide insight into gene content, provide novel surveillance targets, and elucidate the origin and range expansion. However, past attempts of whole genome sequencing of other Onchocerca species reported a substantial portion of their data unusable due to the variable over-abundance of host DNA in samples. Here, we have developed a method to determine the host-to-parasite DNA ratio using a quantitative PCR (qPCR) approach that relies on two standard plasmids each of which contains a single copy gene specific to the parasite genus Onchocerca (major body wall myosin gene, myosin) or a single copy gene specific to the canine host (polycystin-1 precursor, pkd1). These plasmid standards were used to determine the copy number of the myosin and pkd1 genes within a sample to calculate the ratio of parasite and host DNA. Furthermore, whole genome sequence (WGS) data for three O. lupi isolates were consistent with our host-to-parasite DNA ratio results. Our study demonstrates, despite unified DNA extraction methods, variable quantities of host DNA within any one sample which will likely affect downstream WGS applications. Our quantification assay of host-to-parasite genome copy number provides a robust and accurate method of assessing canine host DNA load in an O. lupi specimen that will allow informed sample selection for WGS. This study has also provided the first whole genome draft sequence for this species. This approach is also useful for future focused WGS studies of other parasites.

摘要

犬恶丝虫是一种丝虫,可引起全球犬类眼部盘尾丝虫病,包括北美和欧洲部分地区、北非和中东地区。自 21 世纪初以来,这种寄生虫在犬类中的报告发病率持续稳步上升,最近在人类中也有记录。该寄生虫的全基因组测序(WGS)可以深入了解基因组成,提供新的监测靶点,并阐明起源和范围扩展。然而,过去对其他盘尾丝虫物种的全基因组测序尝试报告说,由于样本中宿主 DNA 的大量可变丰度,其大部分数据不可用。在这里,我们开发了一种使用定量 PCR(qPCR)方法确定宿主与寄生虫 DNA 比值的方法,该方法依赖于两个标准质粒,每个质粒都包含一个特定于寄生虫属盘尾丝虫(主要体壁肌球蛋白基因,肌球蛋白)或特定于犬宿主的单个拷贝基因(多囊蛋白-1 前体,pkd1)的单一拷贝基因。这些质粒标准品用于确定样品中肌球蛋白和 pkd1 基因的拷贝数,以计算寄生虫和宿主 DNA 的比值。此外,三个 O. lupi 分离株的全基因组序列(WGS)数据与我们的宿主与寄生虫 DNA 比值结果一致。我们的研究表明,尽管采用了统一的 DNA 提取方法,但任何一个样本中的宿主 DNA 数量都存在差异,这可能会影响下游 WGS 应用。我们对宿主与寄生虫基因组拷贝数的定量检测提供了一种可靠而准确的方法,可用于评估 O. lupi 样本中的犬宿主 DNA 负荷,从而为 WGS 提供知情的样本选择。本研究还提供了该物种的第一个全基因组草案序列。这种方法对于其他寄生虫的未来重点 WGS 研究也很有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dfd/9678315/81b5ec0c5d86/pone.0276916.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dfd/9678315/81b5ec0c5d86/pone.0276916.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dfd/9678315/81b5ec0c5d86/pone.0276916.g001.jpg

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