首页> 外文期刊>The American Journal of Tropical Medicine and Hygiene >Detection of DNA of nocturnally periodic Brugia malayi in night and day blood samples by a polymerase chain reaction-ELISA-based method using an internal control DNA.
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Detection of DNA of nocturnally periodic Brugia malayi in night and day blood samples by a polymerase chain reaction-ELISA-based method using an internal control DNA.

机译:使用内部对照DNA,通过基于聚合酶链反应-ELISA的方法检测夜间和白天血液样本中夜间周期性马来虫的DNA。

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An internal control was used in a polymerase chain reaction (PCR)-ELISA-based technique to detect the Hha I repeat of the filarial parasite Brugia malayi. A single microfilaria added to 200 microl of blood was reliably detected. The assay was evaluated on field samples from persons living in an area endemic for Anopheles-transmitted, nocturnally periodic B. malayi in central Sulawesi, Indonesia. Examination of night blood of 138 individuals for the presence of microfilariae by filtration revealed 44 microfilaria carriers. All microfilaria carriers were also positive in the PCR-ELISA and, in addition, 14 more samples were proven to contain parasite DNA. The sensitivity of both methods was compared on night and on day blood samples collected from 113 persons. Whereas 37 microfilaria carriers were identified by filtration of night blood, no microfilariae were observed in the corresponding day blood samples. The PCR-ELISA result was positive in all 37 night blood samples of microfilaria carriers and in an additional 13 night blood samples without microfilariae. Parasite DNA was detected in 31 day blood samples of microfilaria carriers and in 3 day blood samples of amicrofilaremic persons. Assuming a sensitivity of the PCR-ELISA on night blood of 100%, the sensitivity of night blood filtration is 74% and that of the PCR-ELISA on day blood is 68%. These data suggest that the described PCR-ELISA method is capable of detecting infections with nocturnally periodic B. malayi in day blood samples. Therefore, this method may facilitate both the identification of endemic areas and the monitoring of control programs.
机译:内部对照用于基于聚合酶链反应(PCR)-ELISA的技术中,以检测丝状寄生虫马来氏布鲁氏菌的Hha I重复序列。可靠地检测到添加到200微升血液中的单个微丝aria。对印度尼西亚苏拉威西省中部按蚊传播的夜间周期性疟原虫的流行地区居民的现场样本进行了评估。通过过滤检查138个人的夜间血液中是否存在微丝aria,发现有44个微丝aria携带者。所有微丝虫携带者在PCR-ELISA中也呈阳性,此外,另外14个样品被证明含有寄生虫DNA。在夜间和白天从113人采集的血液样本中比较了这两种方法的敏感性。通过夜间血液过滤鉴定出37种微丝虫携带者,而在相应的白天血液样本中未观察到微丝虫。在所有37个微丝aria携带者的夜间血样中,以及另外13个没有微丝aria的夜间血样中,PCR-ELISA结果均为阳性。在31天的微丝aria携带者血样和3天的微丝fil虫病患者血样中检测到了寄生虫DNA。假设PCR-ELISA对夜间血液的敏感性为100%,则夜间血液过滤的敏感性为74%,而PCR-ELISA对白天血液的敏感性为68%。这些数据表明,所描述的PCR-ELISA方法能够检测日间血液样品中夜间周期性的B. malayi感染。因此,该方法可以促进流行区域的识别和控制程序的监视。

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