Abstract

Rift Valley fever (RVF) is a viral zoonosis that primarily affects animals resulting in considerable economic losses due to death and abortions among infected livestock. RVF also affects humans with clinical symptoms ranging from an influenza-like illness to a hemorrhagic fever. Over the past years, RVF virus (RVFV) has caused severe outbreaks in livestock and humans throughout Africa and regions of the world previously regarded as free of the virus. This situation prompts the need to evaluate the diagnostic capacity and performance of laboratories worldwide. Diagnostic methods for RVFV detection include virus isolation, antigen and antibody detection methods, and nucleic acid amplification techniques. Molecular methods such as reverse-transcriptase polymerase chain reaction and other newly developed techniques allow for a rapid and accurate detection of RVFV. This study aims to assess the efficiency and accurateness of RVFV molecular diagnostic methods used by expert laboratories worldwide. Thirty expert laboratories from 16 countries received a panel of 14 samples which included RVFV preparations representing several genetic lineages, a specificity control and negative controls. In this study we present the results of the first international external quality assessment (EQA) for the molecular diagnosis of RVF. Optimal results were reported by 64% of the analyses, 21% of the analyses achieved acceptable results and 15% of the results revealed that there is need for improvement. Evenly good performances were achieved by specific protocols which can therefore be recommended as an accurate molecular protocol for the diagnosis of RVF. Other protocols showed uneven performances revealing the need for improved optimization and standardization of these protocols.

Highlights

  • Rift Valley fever (RVF) is a mosquito-borne viral zoonosis that primarily affects animals and has the capacity to infect humans

  • In this study we present the results of the first international external quality assessment (EQA) for the molecular diagnosis of RVF

  • Optimal results were reported by 64% (n = 25) of the analyses; 21% (n = 8) of the analyses achieved acceptable results due to the inability to detect one positive sample, and 15% (n = 6) revealed several false negative and/or one or more false positive results indicating that there is still need for improvement (Table 2 and 3)

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Summary

Introduction

Rift Valley fever (RVF) is a mosquito-borne viral zoonosis that primarily affects animals and has the capacity to infect humans. The disease is less fatal to humans as most human infections are asymptomatic and when clinical symptoms appear they are in majority influenza-like. Some cases may develop a severe RVF disease with variable clinical signs. The number of identified viral lineages of RVFV has increased from 3 in an early analysis [3] to 7 in a 2007 study [4], and in the most recent report 15 distinct genetic groups were reported [5]. Phylogenetic analysis shows that the virus emerged in the mid-19th century, but it was first identified in 1930 during an outbreak of abortions and deaths among sheep in the

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