Lucena W A, Dhalia R, Abath F G, Nicolas L, Regis L N, Furtado A F
Departamento de Entomologia, Centro de Pesquisas Aggeu Magalhães-FIOCRUZ, Recife, PE, Brasil.
Trans R Soc Trop Med Hyg. 1998 May-Jun;92(3):290-3. doi: 10.1016/s0035-9203(98)91016-1.
A sensitive and specific polymerase chain reaction (PCR) based on a highly repeated deoxyribonucleic acid (DNA) sequence (188 bp; SspI repeat) was tested for the detection of Wuchereria bancrofti DNA in blood and urine samples collected during the day from individuals in Coque, Recife, Brazil, an endemic area for W. bancrofti. All microfilaraemic individuals were also positive by PCR, irrespective of the samples used. The PCR system was capable of detecting W. bancrofti DNA in amicrofilaraemic individuals: c. 93% were positive by PCR when day blood samples were used and 59.7% when urine samples collected at 07:00 were used. Thus, nocturnally periodic W. bancrofti infection can be detected in blood samples collected during the day, which is convenient for large-scale screening. In addition, non-invasive urine collection provided suitable samples for PCR, which is clearly advantageous for preliminary mass diagnosis.
在巴西累西腓科克地区(班氏丝虫病的流行区),对从白天采集的血液和尿液样本中检测班氏丝虫DNA的一种基于高度重复脱氧核糖核酸(DNA)序列(188bp;SspI重复序列)的灵敏且特异的聚合酶链反应(PCR)进行了测试。所有微丝蚴血症个体无论使用何种样本,PCR检测均为阳性。该PCR系统能够检测无微丝蚴血症个体中的班氏丝虫DNA:使用白天血液样本时约93%的个体PCR检测呈阳性,使用07:00采集的尿液样本时59.7%的个体呈阳性。因此,在白天采集的血液样本中可以检测到夜现周期性班氏丝虫感染,这便于大规模筛查。此外,非侵入性尿液采集为PCR提供了合适的样本,这显然有利于初步大规模诊断。