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机构地区:[1]苏州医学院寄生虫学教研室,苏州215007 [2]江苏省寄生虫病防治研究所,无锡214064
出 处:《中国寄生虫学与寄生虫病杂志》1999年第6期380-383,共4页Chinese Journal of Parasitology and Parasitic Diseases
摘 要:目的: 建立在同一次扩增中即可鉴别患者感染的疟原虫虫种的复式PCR检测方法。方法: 根据恶性疟原虫(P.f.)中度重复基因序列pBRK1-14 和间日疟原虫(P.v.)线粒体细胞色素C氧化酶基因COIII合成引物,采用经优化的PCR反应体系, 对疟原虫DNA模板进行扩增。结果: P.f.与P.v.分别被扩增出206 和370 bp 大小的DNA片段,与人白细胞DNA 无交叉;用该反应体系至少可检测出原虫血症为5×10- 7的P.f.感染和1.02×10- 6 P.v.感染; 自云南疟疾流行区采集的783份滤纸干血滴样本中, 复式PCR法阳性检出率为85.8% , 误诊率为0, 漏诊率为0.1% , 而镜检法依次分别为84.9% 、3.1% 和1.0% , 两者符合率为95.8% 。结论: 本复式PCR检测疟原虫较镜检敏感、特异, 适用于我国恶性疟与间日疟混合流行区的疟疾诊断、流行病学调查、药物的疗效考核和献血员的筛选等。AIM: To establish a sensitive and specific PCR\|based method to detect Plasmodium falciparum and P.vivax in blood samples in a single amplification reaction. METHODS: Malaria parasite DNA in blood was amplified by the multiplex polymerase chain reaction using two sets of primers derived from the P.f. moderately\|repetitive DNA sequence and COIII gene of P.v. RESULTS: A 206\| bp product for P.f. and a 370\| bp product for P.v. were amplified by multiplex PCR, being able to detect parasitemia level as low as 5×10\+\{-7\} for P.f. and 1\^02×10\+\{-6\} for P.v. and having no cross\|reaction with human leucocyte DNA. A total of 783 blood samples on the filter paper collected from patients attending to malaria clinics in malaria endemic areas were detected. The positive rate of multiplex PCR was 85\^8%, the misdiagnosis rate was 0, and the under\|diagnosis rate was 0\^1%, while these three rates of microscopic examination were 84\^9%, 3\^1% and 1\^0%, respectively. The concordance between the two methods was 95\^8%. CONCLUSION: The multiplex PCR method made the malaria detection more sensitive and specific than the microscopic examination and should be suitable for the diagnosis of malaria in mixed endemic areas, large\|scale epidemiological studies, follow\|up of drug treatment and donor blood screenig.\;
分 类 号:R382.31[医药卫生—医学寄生虫学] R531.304[医药卫生—基础医学]
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