Abstract

In 2014, Ebola hemorrhagic fever broke out in West Africa. As contact between China and West Africa is frequent, the possibility that Ebola virus would enter China was high. Thus, an external assessment of the quality of Ebola virus detection was organized by the National Center for Clinical Laboratories in China. Virus-like particles encapsulating known sequences of epidemic strains of Ebola virus from 2014 were prepared as positive quality controls. The sample panel, which was composed of seven positive and three negative samples, was dispatched to 19 laboratories participating in this assessment of Ebola virus detection. Accurate detection was reported at 14 of the 19 participating laboratories, with a sensitivity of 91.43% and a specificity of 100%. Four participants (21.05%) reported false-negative results and were classified as “acceptable.” One participant (5.26%) did not detect any positive samples and was thus classified as “improvable.” Based on the results returned, the ability to detect weakly positive Ebola specimens should be improved. Furthermore, commercial assays and the standard primers offered by the Chinese Centers for Disease Control and Prevention were found to be most accurate and dependable for Ebola detection. A two-target detection approach is recommended for Ebola screening; this approach could reduce the probability of false-negative results. Additionally, standardization of operations and punctual adjustment of instruments are necessary for the control and prevention of Ebola virus.

Highlights

  • From 2013 to 2015, the outbreak of Ebola hemorrhagic fever (EHF) caused over 22,000 cases of infection, including nearly 9,000 deaths [1] in West Africa

  • Nucleotide sequences of the epidemic strain of Zaire Ebola virus from West Africa were obtained from GenBank (KJ660346, KJ660347, and KJ660348) [3]

  • From 2014 to 2015, the number of people suffering from Ebola hemorrhagic fever (EHF) increased continually in West Africa [13], and at one point the situation was out of control primers and probes

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Summary

Introduction

From 2013 to 2015, the outbreak of Ebola hemorrhagic fever (EHF) caused over 22,000 cases of infection, including nearly 9,000 deaths (as of February 4, 2015) [1] in West Africa. The Ebola virus has an 18–19 kb, non-segmented, single-stranded negative-RNA genome that encodes seven structural proteins (nucleoprotein (NP), virion structural protein (VP), VP40, glycoprotein (GP), VP30, VP24, and RNA-dependent RNA polymerase (L)) [2]. Virological research and analysis recently identified the epidemic agent as Zaire Ebola virus (EBOV) [3].

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