コンテンツへスキップ
Merck

Identification of interferon-stimulated genes that attenuate Ebola virus infection.

Nature communications (2020-06-13)
Makoto Kuroda, Peter J Halfmann, Lindsay Hill-Batorski, Makoto Ozawa, Tiago J S Lopes, Gabriele Neumann, John W Schoggins, Charles M Rice, Yoshihiro Kawaoka
要旨

The West Africa Ebola outbreak was the largest outbreak ever recorded, with over 28,000 reported infections; this devastating epidemic emphasized the need to understand the mechanisms to counteract virus infection. Here, we screen a library of nearly 400 interferon-stimulated genes (ISGs) against a biologically contained Ebola virus and identify several ISGs not previously known to affect Ebola virus infection. Overexpression of the top ten ISGs attenuates virus titers by up to 1000-fold. Mechanistic studies demonstrate that three ISGs interfere with virus entry, six affect viral transcription/replication, and two inhibit virion formation and budding. A comprehensive study of one ISG (CCDC92) that shows anti-Ebola activity in our screen reveals that CCDC92 can inhibit viral transcription and the formation of complete virions via an interaction with the viral protein NP. Our findings provide insights into Ebola virus infection that could be exploited for the development of therapeutics against this virus.

材料
製品番号
ブランド
製品内容

Sigma-Aldrich
Triton X-100, laboratory grade
Sigma-Aldrich
ANTI-FLAG®抗体、ラットモノクロナール, clone 6F7, purified from hybridoma cell culture
Sigma-Aldrich
抗BTN3A3抗体 ウサギ宿主抗体, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution
Sigma-Aldrich
MISSION® esiRNA, targeting human BTN3A3