• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

用于诊断马达加斯加恶性疟原虫疟疾的非同位素DNA检测试剂盒的评估

Evaluation of a nonisotopic DNA assay kit for diagnosing Plasmodium falciparum malaria in Madagascar.

作者信息

McLaughlin G L, Subramanian S, Lepers J P, Raharimalala L, Deloron P

机构信息

Department of Veterinary Pathobiology, Purdue University, West Lafayette, Indiana.

出版信息

Am J Trop Med Hyg. 1993 Feb;48(2):211-5. doi: 10.4269/ajtmh.1993.48.211.

DOI:10.4269/ajtmh.1993.48.211
PMID:8447525
Abstract

This study evaluated a nonisotopic DNA assay kit for diagnosing Plasmodium falciparum malaria in an area of Madagascar where all Plasmodium species of human malaria are present and where malaria is endemic. Blood samples from 440 healthy children and 20 healthy adults were processed and assayed in a single day in a blind protocol. The parasitemia levels of the four Plasmodium species were determined by microscopic examinations and by counts of numbers of malaria parasites per 1,000 white blood cells. Relative to P. falciparum infections, the DNA assay results agreed with those of microscopy for 207 positive and 239 negative samples; two samples were scored as positive by the DNA probe that were not detected by microscopy, and 12 samples were scored as positive by microscopy but were not detected by the assay. Relative to microscopy, the sensitivity of the assay was 95%, the specificity was 99%, and the effective sensitivity threshold of the DNA probe assay was approximately 30 parasites/mm3 of blood. The assay did not detect infections with either P. vivax, P. malariae, or P. ovale alone, but detected mixed infections of P. falciparum with either P. vivax or P. ovale. With this nonisotopic DNA probe assay, we were able to process large numbers of samples efficiently and to detect P. falciparum malaria infections with high sensitivity and specificity in a population that did not display overt disease symptoms.

摘要

本研究评估了一种非同位素DNA检测试剂盒,用于在马达加斯加一个存在所有人类疟原虫种类且疟疾为地方病的地区诊断恶性疟原虫疟疾。来自440名健康儿童和20名健康成人的血样在一天内按照盲法方案进行处理和检测。通过显微镜检查以及每1000个白细胞中疟原虫数量的计数来确定四种疟原虫的寄生虫血症水平。相对于恶性疟原虫感染,DNA检测结果与显微镜检查结果在207份阳性和239份阴性样本上一致;有两份样本经DNA探针检测为阳性,但显微镜检查未检测到,还有12份样本经显微镜检查为阳性,但检测未检测到。相对于显微镜检查,该检测的灵敏度为95%,特异性为99%,DNA探针检测的有效灵敏度阈值约为每立方毫米血液30个寄生虫。该检测单独未检测到间日疟原虫、三日疟原虫或卵形疟原虫感染,但检测到恶性疟原虫与间日疟原虫或卵形疟原虫的混合感染。使用这种非同位素DNA探针检测方法,我们能够高效地处理大量样本,并在未表现出明显疾病症状的人群中以高灵敏度和特异性检测到恶性疟原虫疟疾感染。

相似文献

1
Evaluation of a nonisotopic DNA assay kit for diagnosing Plasmodium falciparum malaria in Madagascar.用于诊断马达加斯加恶性疟原虫疟疾的非同位素DNA检测试剂盒的评估
Am J Trop Med Hyg. 1993 Feb;48(2):211-5. doi: 10.4269/ajtmh.1993.48.211.
2
Microscopic and molecular evidence of the presence of asymptomatic Plasmodium falciparum and Plasmodium vivax infections in an area with low, seasonal and unstable malaria transmission in Ethiopia.在埃塞俄比亚疟疾传播率低、呈季节性且不稳定的地区,存在无症状恶性疟原虫和间日疟原虫感染的微观及分子证据。
BMC Infect Dis. 2015 Aug 5;15:310. doi: 10.1186/s12879-015-1070-1.
3
Comparative detection of Plasmodium vivax and Plasmodium falciparum DNA in saliva and urine samples from symptomatic malaria patients in a low endemic area.在低流行地区,对有症状的疟疾患者的唾液和尿液样本中的间日疟原虫和恶性疟原虫 DNA 进行比较检测。
Malar J. 2010 Mar 9;9:72. doi: 10.1186/1475-2875-9-72.
4
A highly sensitive, rapid, and simple polymerase chain reaction-based method to detect human malaria (Plasmodium falciparum and Plasmodium vivax) in blood samples.一种基于聚合酶链反应的高灵敏度、快速且简单的方法,用于检测血样中的人类疟疾(恶性疟原虫和间日疟原虫)。
Am J Trop Med Hyg. 1994 Sep;51(3):308-13. doi: 10.4269/ajtmh.1994.51.308.
5
Usefulness of genus-specific PCR and Southern blot species-specific hybridization for the detection of imported malaria cases in Italy.属特异性聚合酶链反应和Southern印迹物种特异性杂交在意大利输入性疟疾病例检测中的应用价值。
New Microbiol. 2001 Jan;24(1):69-76.
6
Use of the polymerase chain reaction to directly detect malaria parasites in blood samples from the Venezuelan Amazon.利用聚合酶链反应直接检测委内瑞拉亚马逊地区血样中的疟原虫。
Am J Trop Med Hyg. 1994 Feb;50(2):169-80. doi: 10.4269/ajtmh.1994.50.169.
7
Evaluation of the utility value of three diagnostic methods in the detection of malaria parasites in endemic area.三种诊断方法在疟疾流行区疟原虫检测中的实用价值评估
Malar J. 2017 May 6;16(1):189. doi: 10.1186/s12936-017-1838-4.
8
Evaluation of SYBR green I based visual loop-mediated isothermal amplification (LAMP) assay for genus and species-specific diagnosis of malaria in and endemic regions.基于SYBR绿I的可视化环介导等温扩增(LAMP)检测法在疟疾流行和非流行地区进行属和种特异性疟疾诊断的评估。
J Vector Borne Dis. 2017 Jan-Mar;54(1):54-60.
9
Co-reactivity of plasmodial histidine-rich protein 2 and aldolase on a combined immuno-chromographic-malaria dipstick (ICT) as a potential semi-quantitative marker of high Plasmodium falciparum parasitaemia.疟原虫富含组氨酸蛋白2与醛缩酶在联合免疫层析疟疾快速检测条(ICT)上的共同反应性,作为恶性疟原虫高血症潜在的半定量标志物。
Parasitol Res. 2004 Nov;94(5):384-5. doi: 10.1007/s00436-004-1213-6. Epub 2004 Sep 30.
10
Evaluation of a new plate hybridization assay for the laboratory diagnosis of imported malaria in Italy.用于意大利输入性疟疾实验室诊断的新型平板杂交检测方法的评估
New Microbiol. 2004 Apr;27(2):163-71.

引用本文的文献

1
Multispecies Plasmodium infections of humans.人类的多种疟原虫感染。
J Parasitol. 1999 Feb;85(1):12-8.
2
ACP Broadsheet no 148. July 1996. Laboratory diagnosis of malaria.《内科学年鉴》简讯第148期。1996年7月。疟疾的实验室诊断。
J Clin Pathol. 1996 Jul;49(7):533-8. doi: 10.1136/jcp.49.7.533.
3
DNA probes and PCR for diagnosis of parasitic infections.用于诊断寄生虫感染的DNA探针和聚合酶链反应
Clin Microbiol Rev. 1995 Jan;8(1):113-30. doi: 10.1128/CMR.8.1.113.