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本文引用的文献

1
Validation of a new test for Schistosoma haematobium based on detection of Dra1 DNA fragments in urine: evaluation through latent class analysis.基于尿液中 Dra1 DNA 片段检测的新型曼氏血吸虫检测方法的验证:应用潜类别分析进行评估。
PLoS Negl Trop Dis. 2012 Jan;6(1):e1464. doi: 10.1371/journal.pntd.0001464. Epub 2012 Jan 3.
2
Diagnosis of Schistosoma haematobium by detection of specific DNA fragments from filtered urine samples.从过滤尿液样本中检测特异性 DNA 片段诊断埃及血吸虫病。
Am J Trop Med Hyg. 2011 Jun;84(6):998-1001. doi: 10.4269/ajtmh.2011.10-0691.
3
Application of a circulating-cathodic-antigen (CCA) strip test and real-time PCR, in comparison with microscopy, for the detection of Schistosoma haematobium in urine samples from Ghana.与显微镜检查相比,循环阴极抗原(CCA)试纸条检测和实时荧光定量PCR在加纳尿液样本中检测埃及血吸虫的应用。
Ann Trop Med Parasitol. 2008 Oct;102(7):625-33. doi: 10.1179/136485908X337490.
4
Current status of vaccines for schistosomiasis.血吸虫病疫苗的现状
Clin Microbiol Rev. 2008 Jan;21(1):225-42. doi: 10.1128/CMR.00046-07.
5
Multiplex real-time PCR for the detection and quantification of Schistosoma mansoni and S. haematobium infection in stool samples collected in northern Senegal.用于检测和定量塞内加尔北部采集的粪便样本中曼氏血吸虫和埃及血吸虫感染的多重实时聚合酶链反应。
Trans R Soc Trop Med Hyg. 2008 Feb;102(2):179-85. doi: 10.1016/j.trstmh.2007.10.011. Epub 2008 Jan 3.
6
Simultaneous detection and quantification of Ancylostoma duodenale, Necator americanus, and Oesophagostomum bifurcum in fecal samples using multiplex real-time PCR.使用多重实时荧光定量PCR同时检测和定量粪便样本中的十二指肠钩口线虫、美洲板口线虫和分岔食道口线虫。
Am J Trop Med Hyg. 2007 Oct;77(4):685-90.
7
Differentiation of Schistosoma haematobium from related schistosomes by PCR amplifying an inter-repeat sequence.通过聚合酶链式反应扩增重复序列间序列来区分埃及血吸虫与相关血吸虫。
Am J Trop Med Hyg. 2007 May;76(5):950-5.
8
Multiplex detection of Enterocytozoon bieneusi and Encephalitozoon spp. in fecal samples using real-time PCR.使用实时荧光定量聚合酶链反应对粪便样本中的微小隐孢子虫和脑炎微孢子虫属进行多重检测。
Diagn Microbiol Infect Dis. 2007 Feb;57(2):163-7. doi: 10.1016/j.diagmicrobio.2006.08.009. Epub 2006 Oct 3.
9
Human schistosomiasis.人类血吸虫病
Lancet. 2006 Sep 23;368(9541):1106-18. doi: 10.1016/S0140-6736(06)69440-3.
10
Real-time PCR in clinical microbiology: applications for routine laboratory testing.临床微生物学中的实时聚合酶链反应:在常规实验室检测中的应用
Clin Microbiol Rev. 2006 Jan;19(1):165-256. doi: 10.1128/CMR.19.1.165-256.2006.

加纳在校儿童尿液样本中的血吸虫感染的分子诊断。

Molecular diagnosis of Schistosoma infections in urine samples of school children in Ghana.

机构信息

Parasitology Department, Noguchi Memorial Institute for Medical Research, University of Ghana, Accra, Ghana.

出版信息

Am J Trop Med Hyg. 2013 Jun;88(6):1028-31. doi: 10.4269/ajtmh.12-0571. Epub 2013 Mar 25.

DOI:10.4269/ajtmh.12-0571
PMID:23530072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3752797/
Abstract

Recent studies using an internal transcribed spacer (ITS)-based real-time polymerase chain reaction (PCR) for the detection of Schistosoma DNA in urine samples has shown high sensitivity and specificity when performed on controls and known microscopy-positive samples. In this study, using 730 urine samples collected from children in five primary schools from different communities in the Greater Accra region of Ghana, specific detection of Schistosoma DNA showed excellent sensitivity of 100% and 85.2% in urines with > 50 eggs/10 mL urine and ≤ 50 eggs/10 mL of urine, respectively. Additionally, Schistosoma-specific DNA was amplified in 102 of 673 samples in which Schistosoma eggs could not be detected with microscopy. Taking microscopy and/or PCR-positive samples as true positives, the negative predictive value calculated was 94.6-100% for each school sampled as compared with 54.3-95.7% using microscopy. This ITS-based real-time PCR proves to be a powerful tool in epidemiological surveys of schistosomiasis providing more precise and sensitive results than microscopy.

摘要

最近的研究使用基于内部转录间隔区(ITS)的实时聚合酶链反应(PCR)检测尿液样本中的血吸虫 DNA,在对对照和已知显微镜阳性样本进行检测时显示出高灵敏度和特异性。在这项研究中,使用从加纳大阿克拉地区五个不同社区的 730 名儿童采集的尿液样本,特异性检测血吸虫 DNA 在尿液中 > 50 个卵/10 毫升尿液和 ≤ 50 个卵/10 毫升尿液时的灵敏度分别为 100%和 85.2%。此外,在显微镜无法检测到血吸虫卵的 673 个样本中,有 102 个样本扩增出了血吸虫特异性 DNA。以显微镜和/或 PCR 阳性样本作为真阳性,与显微镜相比,每个采样学校的阴性预测值计算为 94.6-100%,为 54.3-95.7%。这种基于 ITS 的实时 PCR 证明是血吸虫病流行病学调查的有力工具,提供比显微镜更精确和敏感的结果。