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在区分链状艾氏类圆线虫与粪类圆线虫后改进类圆线虫病的分子流行病学监测。

Improving Molecular Epidemiological Surveillance of Strongyloidiasis Upon Differentiation of Strongyloides fuelleborni fuelleborni From Strongyloides stercoralis.

作者信息

Cunningham Lucas J, Nevin William D, Verweij Jaco J, Buonfrate Dora, Scarso Salvatore, Khieu Virak, O'Ferrall Angus M, Rollason Sarah, Stothard J Russell

机构信息

Department of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, Merseyside, United Kingdom.

Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, Merseyside, United Kingdom.

出版信息

J Infect Dis. 2025 Jul 30;232(1):e169-e173. doi: 10.1093/infdis/jiaf237.

Abstract

Molecular epidemiological surveillance for zoonotic strongyloidiasis is confounded by a genus-specific TaqMan probe assay that conflates Strongyloides fuelleborni fuelleborni with Strongyloides stercoralis. To improve surveillance, we developed and validated a novel duplex species-specific TaqMan probe assay, screening a representative collection of available clinical samples. Our assay was highly discriminatory, evidencing no cross-reactivity, and had a lowest DNA detection limit of 1 pg/µL. However, as the genus-specific DNA assay has greater detection ability, we propose a 2-step protocol where samples are first screened with this assay then, if positive, screened with our species-specific assay, discriminating (co)infections between each threadworm species.

摘要

人兽共患类圆线虫病的分子流行病学监测因一种属特异性TaqMan探针检测法而变得复杂,该检测法将斐氏类圆线虫与粪类圆线虫混淆。为了改进监测,我们开发并验证了一种新型的双链种特异性TaqMan探针检测法,对一批具有代表性的现有临床样本进行了筛查。我们的检测法具有高度的鉴别力,无交叉反应,DNA最低检测限为1 pg/µL。然而,由于属特异性DNA检测法具有更强的检测能力,我们提出了一个两步方案,即首先用该检测法对样本进行筛查,若呈阳性,则再用我们的种特异性检测法进行筛查,以区分每种线虫之间的(混合)感染情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87a1/12308652/fe63b35af4c8/jiaf237f1.jpg

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