Swiss Tropical and Public Health Institute, Basel, Switzerland.
University of Basel, Basel, Switzerland.
PLoS Negl Trop Dis. 2016 Oct 5;10(10):e0005010. doi: 10.1371/journal.pntd.0005010. eCollection 2016 Oct.
One root cause of the neglect of rabies is the lack of adequate diagnostic tests in the context of low income countries. A rapid, performance friendly and low cost method to detect rabies virus (RABV) in brain samples will contribute positively to surveillance and consequently to accurate data reporting, which is presently missing in the majority of rabies endemic countries.
METHODOLOGY/PRINCIPAL FINDINGS: We evaluated a rapid immunodiagnostic test (RIDT) in comparison with the standard fluorescent antibody test (FAT) and confirmed the detection of the viral RNA by real time reverse transcription polymerase chain reaction (RT-qPCR). Our analysis is a multicentre approach to validate the performance of the RIDT in both a field laboratory (N'Djamena, Chad) and an international reference laboratory (Institut Pasteur, Paris, France). In the field laboratory, 48 samples from dogs were tested and in the reference laboratory setting, a total of 73 samples was tested, representing a wide diversity of RABV in terms of animal species tested (13 different species), geographical origin of isolates with special emphasis on Africa, and different phylogenetic clades. Under reference laboratory conditions, specificity was 93.3% and sensitivity was 95.3% compared to the gold standard FAT test. Under field laboratory conditions, the RIDT yielded a higher reliability than the FAT test particularly on fresh and decomposed samples. Viral RNA was later extracted directly from the test filter paper and further used successfully for sequencing and genotyping.
CONCLUSION/SIGNIFICANCE: The RIDT shows excellent performance qualities both in regard to user friendliness and reliability of the result. In addition, the test cassettes can be used as a vehicle to ship viral RNA to reference laboratories for further laboratory confirmation of the diagnosis and for epidemiological investigations using nucleotide sequencing. The potential for satisfactory use in remote locations is therefore very high to improve the global knowledge of rabies epidemiology. However, we suggest some changes to the protocol, as well as careful further validation, before promotion and wider use.
在低收入国家,由于缺乏足够的诊断检测手段,导致狂犬病被忽视。一种快速、性能友好且低成本的方法来检测脑组织样本中的狂犬病病毒(RABV),将有助于监测,从而有助于准确报告数据,而目前大多数狂犬病流行国家都缺乏这一数据。
方法/主要发现:我们评估了一种快速免疫诊断检测(RIDT),并将其与标准荧光抗体检测(FAT)进行比较,并通过实时逆转录聚合酶链反应(RT-qPCR)确认了病毒 RNA 的检测。我们的分析是一种多中心方法,旨在验证 RIDT 在现场实验室(乍得恩贾梅纳)和国际参考实验室(法国巴斯德研究所)中的性能。在现场实验室中,对 48 份犬样本进行了检测,在参考实验室中,共检测了 73 份样本,这些样本代表了广泛的 RABV 多样性,包括所检测的动物物种(13 个不同物种)、分离株的地理来源,特别强调非洲,以及不同的系统发育分支。在参考实验室条件下,与金标准 FAT 检测相比,RIDT 的特异性为 93.3%,敏感性为 95.3%。在现场实验室条件下,RIDT 的可靠性高于 FAT 检测,特别是在新鲜和分解样本上。随后,从测试滤纸上提取病毒 RNA,并成功用于测序和基因分型。
结论/意义:RIDT 在易用性和结果可靠性方面都具有出色的性能。此外,测试卡可以作为一种载体,将病毒 RNA 运送到参考实验室,以进一步确认诊断,并进行基于核苷酸测序的流行病学调查。因此,在偏远地区进行令人满意的使用具有很高的潜力,以提高对狂犬病流行病学的全球认识。然而,在推广和更广泛的应用之前,我们建议对方案进行一些修改,并进行仔细的进一步验证。