High-throughput screening of active compounds against human respiratory syncytial virus

被引:8
作者
Fu, Yuan-Hui [1 ]
Xu, Zhu-Xin [1 ]
Jiang, Nan [1 ]
Zheng, Yan-Peng [1 ]
Rameix-Welti, Marie-Anne [2 ,3 ]
Jiao, Yue-Ying [1 ]
Peng, Xiang-Lei [1 ]
Wang, Ye [1 ]
Eleouet, Jean-Francois [4 ]
Cen, Shan [5 ]
He, Jin-Sheng [1 ]
机构
[1] Beijing Jiaotong Univ, Coll Life Sci & Bioengn, Beijing 100044, Peoples R China
[2] UVSQ, UFR Sci Sante Simone Veil, INSERM, U1173,UMR,I2, Montigny Le Bretonneux, France
[3] Hop Ambroise Pare, AP HP, Lab Microbiol, F-92104 Boulogne, France
[4] Univ Paris Saclay, INRA, Unite Virol & Immunol Mol UR892, F-78350 Jouy En Josas, France
[5] Chinese Acad Med Sci, Inst Med Biotechnol, Beijing 100050, Peoples R China
关键词
Human respiratory syncytial virus; High-throughput screening; RSV inhibitor; Azathioprine; 6-Mercaptopurine; INHIBITOR; IDENTIFICATION; REPLICATION; DISCOVERY; MECHANISM; GS-5806; TARGET; ASSAY;
D O I
10.1016/j.virol.2019.07.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human respiratory syncytial virus (RSV) is one of the predominant pathogens causing lower respiratory tract infection in infants and young children worldwide, whereas there is so far no vaccine or drug against RSV infection for clinical use. In this work, we developed and validated a fluorescence-based high-throughput screening (HTS) assay to identify compounds active against RSV, using RSV-mGFP, a recombinant RSV encoding enhanced green fluorescent protein (EGFP). Thereafter, among 54,800 compounds used for our screen, we obtained 62 compounds active against RSV. Among these hits, azathioprine (AZA) and 6-mercaptopurine (6-MP) were identified as RSV inhibitors with half maximal inhibitory concentration (IC50) values of 6.69 +/- 1.41 and 3.13 +/- 0.98 mu M respectively. Further experiments revealed that they functioned by targeting virus transcription or/and genome replication. In conclusion, the established HTS assay is suitable to screen anti-RSV compounds, and the screened two hits of AZA and 6-MP, as potential anti-RSV agents targeting RSV genome replication/transcription, are worthy of further investigation on their anti-RSV activity in vivo.
引用
收藏
页码:171 / 178
页数:8
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