Panning Marcus, Laue Thomas, Olschlager Stephan, Eickmann Markus, Becker Stephan, Raith Sabine, Courbot Marie-Claude Georges, Nilsson Mikael, Gopal Robin, Lundkvist Ake, di Caro Antonino, Brown David, Meyer Hermann, Lloyd Graham, Kummerer Beate M, Gunther Stephan, Drosten Christian
Bernhard-Nocht Institute for Tropical Medicine, Hamburg 20359, Germany.
J Infect Dis. 2007 Nov 15;196 Suppl 2(Suppl 2):S199-204. doi: 10.1086/520600.
A network of European biosafety level 4 laboratories has designed the first industry-standard molecular assay for all filoviruses species, based on the strain collections of all participants. It uses 5 optimized L gene primers and 3 probes, as well as an internal control with a separate detection probe. Detection limits (probit analysis, 95% detection chance) were as follows: Zaire ebolavirus, 487 copies/mL of plasma; Sudan ebolavirus Maleo, 586 copies/mL; Sudan ebolavirus Gulu, 1128 copies/mL; Cote d'Ivoire ebolavirus, 537 copies/mL; Reston ebolavirus, 4546 copies/mL; Lake Victoria marburgvirus Musoke, 860 copies/mL; and Lake Victoria marburgvirus Ravn, 1551 copies/mL. The assay facilitates reliable detection or exclusion screening of filovirus infections.
一个欧洲生物安全4级实验室网络基于所有参与者的毒株收集,设计了首个针对所有丝状病毒物种的行业标准分子检测方法。它使用5种优化的L基因引物和3种探针,以及带有单独检测探针的内部对照。检测限(概率分析,95%检测机会)如下:扎伊尔埃博拉病毒,血浆中487拷贝/毫升;苏丹埃博拉病毒马莱奥株,586拷贝/毫升;苏丹埃博拉病毒古卢株,1128拷贝/毫升;科特迪瓦埃博拉病毒,537拷贝/毫升;雷斯顿埃博拉病毒,4546拷贝/毫升;维多利亚湖马尔堡病毒穆索凯株,860拷贝/毫升;以及维多利亚湖马尔堡病毒拉夫恩株,1551拷贝/毫升。该检测方法有助于可靠地检测或排除丝状病毒感染的筛查。