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一种新的实时聚合酶链反应,使用来自疟原虫/巴西疟原虫线粒体细胞色素b基因的种特异性引物。

A new Real Time PCR with species-specific primers from Plasmodium malariae/P. brasilianum mitochondrial cytochrome b gene.

作者信息

Dos Santos Emilly Henrique, Yamamoto Lidia, Domingues Wilson, di Santi Silvia Maria, Kanunfre Kelly Aparecida, Okay Thelma Suely

机构信息

Instituto de Medicina Tropical, Universidade de São Paulo, São Paulo, SP, Brazil.

Instituto de Medicina Tropical, Universidade de São Paulo, São Paulo, SP, Brazil; Núcleo de Estudos em Malária, Superintendência de Controle de Endemias (SUCEN), São Paulo, SP, Brazil; Departamento de Moléstias Infecciosas e Parasitárias, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.

出版信息

Parasitol Int. 2020 Jun;76:102069. doi: 10.1016/j.parint.2020.102069. Epub 2020 Feb 4.

Abstract

Plasmodium malariae mainly causes asymptomatic submicroscopic parasitemia in the endemic Amazon and non-endemic Atlantic Forest, where the number of cases and transmission of malaria through blood transfusion has increased. This study developed a P. malariae/P. brasilianum Real Time PCR (rtPCR) targeting the cytochrome b oxidase (cytb), a highly repetitive gene (20-150 copies/parasite) that should detect more cases than the 18S rRNA (4-8 copies/parasite) gene-based amplification systems. Cytb from human and non-human Plasmodium species (including P. brasilianum) aligned to the only 20 African P. malariae cytb sequences identified polymorphic regions within which we designed P. malariae species-specific primers. Non-human Plasmodium species, related parasites, anemia-causing microorganisms, normal human DNA and 47 blood bank donors samples that were truly negative to malaria accessed rtPCR specificity. Truly positive samples (n = 101) with species identification by semi-nested, nested or TaqMan PCR, and four samples from the Atlantic Forest that were suspected of malaria but three of them had negative genus TaqMan and 18S rRNA nested PCR. The cloned amplification product used in standard curves determined qPCR detection limit (0.5-1 parasite equivalent/μL). The 10 positive P. malariae samples among truly positives yielded positive rtPCR results and more importantly, rtPCR detected the four samples suspected of malaria from the Atlantic Forest. The rtPCR specificity was 100%, reproducibility 11.1% and repeatability 6.7%. In conclusion, the proposed rtPCR is fast, apparently more sensitive than all 18S rRNA amplification systems for detecting extremely low parasitemia. The rtPCR is also specific to P. malariae/P. brasilianum species. This new molecular tool could be applied to the detection of P. malariae/brasilianum infections with submicroscopic parasitemias in the context of epidemiological studies and blood bank safety programs.

摘要

在疟疾流行的亚马逊地区和非流行的大西洋森林地区,间日疟原虫主要引起无症状的亚显微寄生虫血症,在这些地区,疟疾病例数量以及通过输血传播疟疾的情况有所增加。本研究开发了一种针对细胞色素b氧化酶(cytb)的间日疟原虫/巴西疟原虫实时荧光定量聚合酶链反应(rtPCR),细胞色素b氧化酶是一种高度重复的基因(每个寄生虫有20 - 150个拷贝),与基于18S核糖体RNA(每个寄生虫有4 - 8个拷贝)基因的扩增系统相比,该基因应能检测到更多病例。来自人类和非人类疟原虫物种(包括巴西疟原虫)的细胞色素b与仅有的20条非洲间日疟原虫细胞色素b序列比对,确定了多态性区域,我们在这些区域设计了间日疟原虫物种特异性引物。非人类疟原虫物种、相关寄生虫、导致贫血的微生物、正常人DNA以及47份对疟疾检测呈真阴性的血库供者样本用于检测rtPCR的特异性。通过半巢式、巢式或TaqMan PCR进行物种鉴定的真阳性样本(n = 101),以及来自大西洋森林的4份疑似疟疾的样本,其中3份TaqMan属和18S rRNA巢式PCR检测为阴性。用于标准曲线的克隆扩增产物确定了qPCR的检测限(0.5 - 1个寄生虫当量/μL)。在真阳性样本中的10份间日疟原虫阳性样本产生了阳性rtPCR结果,更重要的是,rtPCR检测到了来自大西洋森林的4份疑似疟疾样本。rtPCR的特异性为100%,重现性为11.1%,重复性为6.7%。总之,所提出的rtPCR速度快,在检测极低寄生虫血症方面显然比所有基于18S rRNA的扩增系统更敏感。rtPCR对间日疟原虫/巴西疟原虫物种也具有特异性。这种新的分子工具可应用于在流行病学研究和血库安全计划背景下检测具有亚显微寄生虫血症的间日疟原虫/巴西疟原虫感染。

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