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基于重组酶聚合酶扩增技术的粪便中土源性线虫感染的敏感和半定量检测。

Sensitive and semiquantitative detection of soil-transmitted helminth infection in stool using a recombinase polymerase amplification-based assay.

机构信息

PATH, Seattle, Washington, United States of America.

TwistDx Limited, Norman Way, Cambridge, United Kingdom.

出版信息

PLoS Negl Trop Dis. 2021 Sep 13;15(9):e0009782. doi: 10.1371/journal.pntd.0009782. eCollection 2021 Sep.

Abstract

BACKGROUND

Soil-transmitted helminths (STHs) are parasitic nematodes that inhabit the human intestine. They affect more than 1.5 billion people worldwide, causing physical and cognitive impairment in children. The global strategy to control STH infection includes periodic mass drug administration (MDA) based on the results of diagnostic testing among populations at risk, but the current microscopy method for detecting infection has diminished sensitivity as the intensity of infection decreases. Thus, improved diagnostic tools are needed to support decision-making for STH control programs.

METHODOLOGY

We developed a nucleic acid amplification test based on recombinase polymerase amplification (RPA) technology to detect STH in stool. We designed primers and probes for each of the four STH species, optimized the assay, and then verified its performance using clinical stool samples.

PRINCIPAL FINDINGS

Each RPA assay was as sensitive as a real-time polymerase chain reaction (PCR) assay in detecting copies of cloned target DNA sequences. The RPA assay amplified the target in DNA extracted from human stool samples that were positive for STH based on the Kato-Katz method, with no cross-reactivity of the non-target genomic DNA. When tested with clinical stool samples from patients with infections of light, moderate, and heavy intensity, the RPA assays demonstrated performance comparable to that of real-time PCR, with better results than Kato-Katz. This new rapid, sensitive and field-deployable method for detecting STH infections can help STH control programs achieve their goals.

CONCLUSIONS

Semi-quantitation of target by RPA assay is possible and is comparable to real-time PCR. With proper instrumentation, RPA assays can provide robust, semi-quantification of STH DNA targets as an alternative field-deployable indicator to counts of helminth eggs for assessing infection intensity.

摘要

背景

土壤传播性蠕虫(STH)是寄生在人类肠道中的线虫。它们影响着全球超过 15 亿人,导致儿童身体和认知受损。控制 STH 感染的全球战略包括根据高危人群的诊断检测结果定期进行大规模药物治疗(MDA),但目前用于检测感染的显微镜方法随着感染强度的降低而降低了敏感性。因此,需要改进诊断工具来支持 STH 控制计划的决策。

方法

我们开发了一种基于重组酶聚合酶扩增(RPA)技术的核酸扩增检测方法,用于检测粪便中的 STH。我们为每一种 STH 物种设计了引物和探针,对检测方法进行了优化,然后使用临床粪便样本验证了其性能。

主要发现

每个 RPA 检测在检测克隆靶 DNA 序列的拷贝时与实时聚合酶链反应(PCR)检测一样敏感。RPA 检测扩增了基于加藤法检测为 STH 阳性的人粪便样本中 DNA 提取的靶标,无非靶标基因组 DNA 的交叉反应性。用来自轻度、中度和重度感染的患者的临床粪便样本进行测试时,RPA 检测与实时 PCR 的性能相当,优于加藤法。这种新的快速、敏感和现场可部署的 STH 感染检测方法可以帮助 STH 控制计划实现其目标。

结论

通过 RPA 检测进行靶标半定量是可能的,并且与实时 PCR 相当。在适当的仪器设备下,RPA 检测可以提供可靠的 STH DNA 靶标半定量,作为替代现场部署的指标,用于评估感染强度的蠕虫卵计数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44a5/8459997/fd33a322687e/pntd.0009782.g001.jpg

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