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作为一种工具的实验室间比对试验,用于提高撒哈拉以南非洲兽医实验室的狂犬病诊断能力。

An inter-laboratory trial as a tool to increase rabies diagnostic capabilities of Sub-Saharan African Veterinary laboratories.

机构信息

FAO and National Reference Centre for Rabies, OIE Collaborating Centre for Diseases at the Animal-Human Interface, Istituto Zooprofilattico Sperimentale delle Venezie, Legnaro (PD), Italy.

Laboratory Unit-Emergency Prevention System (EMPRES), Animal Health Service, Food and Agriculture Organization of the United Nations (FAO-UN), Rome, Italy.

出版信息

PLoS Negl Trop Dis. 2020 Feb 10;14(2):e0008010. doi: 10.1371/journal.pntd.0008010. eCollection 2020 Feb.

Abstract

To achieve the goal of eliminating dog-mediated human rabies deaths by 2030, many African countries have agreed to list rabies as a priority zoonotic disease and to undertake both short and long-term control programs. Within this context, reliable local diagnosis is essential for the success of field surveillance systems. However, a harmonized, sustainable and supportive diagnostic offer has yet to be achieved in the continent. We herewith describe the organization and outcome of a proficiency test (PT) for the post-mortem diagnosis of rabies in animals, involving thirteen veterinary laboratories and one public health laboratory in Africa. Participants were invited to assess both the performance of the Direct Fluorescent Antibody (DFA) test and of a conventional RT-PCR. From the submitted results, while thirteen laboratories proved to be able to test the samples through DFA test, eleven performed the RT-PCR method; ten applied both techniques. Of note, the number of laboratories able to apply rabies RT-PCR had increased from four to ten after the exercise. Importantly, results showed a higher proficiency in applying the molecular test compared to the DFA test (concordance, sensitivity and specificity: 98.2%, 96.97% and 100% for RT-PCR; 87.69%, 89.23% and 86.15% for DFA test), indicating the feasibility of molecular methods to diagnose animal pathogens in Africa. Another positive outcome of this approach was that negative and positive controls were made available for further in-house validation of new techniques; in addition, a detailed questionnaire was provided to collect useful and relevant information on the diagnostic procedures and biosafety measures applied at laboratory level.

摘要

为实现 2030 年消除犬介导的人类狂犬病死亡的目标,许多非洲国家已同意将狂犬病列为优先动物传染病,并开展短期和长期控制规划。在这种情况下,可靠的本地诊断对于现场监测系统的成功至关重要。然而,非洲大陆尚未实现协调、可持续和支持性的诊断方案。我们在此描述了一项在非洲的动物狂犬病死后诊断能力验证测试(PT)的组织和结果,涉及 13 个兽医实验室和 1 个公共卫生实验室。邀请参与者评估直接荧光抗体(DFA)检测和常规 RT-PCR 的性能。从提交的结果来看,虽然有 13 个实验室能够通过 DFA 检测来测试样本,但有 11 个实验室能够进行 RT-PCR 方法;有 10 个实验室同时应用了这两种技术。值得注意的是,在进行该测试后,能够应用狂犬病 RT-PCR 的实验室数量从 4 个增加到 10 个。重要的是,结果显示与 DFA 检测相比,应用分子检测的熟练度更高(RT-PCR 的一致性、敏感性和特异性分别为 98.2%、96.97%和 100%;DFA 检测分别为 87.69%、89.23%和 86.15%),表明分子方法在非洲诊断动物病原体的可行性。这种方法的另一个积极结果是,为进一步在内部验证新技术提供了阴性和阳性对照;此外,还提供了一份详细的调查问卷,以收集有关实验室层面应用的诊断程序和生物安全措施的有用和相关信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6be2/7010240/d665e0679d7b/pntd.0008010.g001.jpg

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