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Vector Surveillance for Dengue Virus Detection in the Archipelago of Fernando de Noronha, Brazil

机译:巴西费尔南多·迪诺罗尼亚群岛登革热病毒载体监测

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摘要

Aedes aegypti (L.) has become an efficient vector of important arboviruses due to its anthropophilic and domiciliary behaviors. Since the 1980s, dengue affects thousands of people every year in Brazil; in Fernando de Noronha (FN), a touristic archipelago, dengue cases have occurred since 2001. Once Ae. aegypti populations are well established in the inhabited areas of FN, the threat of dengue or another arbovirus epidemic is continuously imminent. This study aimed to monitor the DENV serotypes in mosquito samples collected in FN, where at least one resident was clinically diagnosed as dengue patient. Entomological surveillance was conducted in 2011 and 2012. Mosquitoes were sorted by sex and location and were stored in pools. DENV detection was performed using polymerase chain reaction with reverse transcription (RT-PCR) and the Platelia Dengue NS1 Ag. RNA integrity was checked by RT-PCR using rpL8 primers, and the minimum infection rate (MIR) was calculated. In total, 339 pools were analyzed, and only one was positive (DENV-1) by Multiplex RT-PCR (MIR = 1.53). When considering only pools with RNA integrity, the MIR was 2.92. Using the Platelia kit, the MIR was 9.18 (considering all the pools) and 17.54 (only 140 pools with RNA integrity). Our results showed the importance of a constant entomological surveillance in that area, the need to improve storage and transportation protocols, and an endogenous control in the RT-PCR to avoid false-negative results. Finally, our study indicated that the NS1-Ag detection was the most sensitive method and should be used routinely for DENV surveillance in mosquitoes if the serotype identification is not required.
机译:埃及伊蚊(Aedes aegypti(L.))由于其嗜人和定居行为,已成为重要虫媒病毒的有效载体。自1980年代以来,登革热每年在巴西影响成千上万人。自2001年以来,在旅游群岛的费尔南多·迪诺罗尼亚群岛(FN),发生了登革热病例。在FN的居民区,埃及人的种群已经建立,登革热或其他虫媒病毒流行的威胁不断迫在眉睫。这项研究旨在监测FN中收集的蚊子样本中的DENV血清型,其中至少一名居民被临床诊断为登革热患者。在2011年和2012年进行了昆虫学监测。按性别和位置对蚊子进行分类,并将其存储在水池中。 DENV检测使用具有逆转录功能的聚合酶链反应(RT-PCR)和Platelia Dengue NS1 Ag进行。使用rpL8引物通过RT-PCR检查RNA完整性,并计算最小感染率(MIR)。总共分析了339个池,通过多重RT-PCR(MIR = 1.53)只有一个阳性(DENV-1)。仅考虑具有RNA完整性的库时,MIR为2.92。使用Platelia试剂盒,MIR为9.18(考虑所有库)和17.54(只有140个具有RNA完整性的库)。我们的结果表明,在该区域进行持续的昆虫学监测非常重要,需要改进存储和运输协议,并且在RT-PCR中进行内源性控制以避免假阴性结果。最后,我们的研究表明,NS1-Ag检测是最灵敏的方法,如果不需要血清型鉴定,则应常规用于蚊子的DENV监测。

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