A BSL-4 High-Throughput Screen Identifies Sulfonamide Inhibitors of Nipah Virus

被引:26
作者
Tigabu, Bersabeh [1 ]
Rasmussen, Lynn [3 ]
White, E. Lucile [3 ]
Tower, Nichole [3 ]
Saeed, Mohammad [3 ]
Bukreyev, Alexander [1 ,2 ]
Rockx, Barry [2 ]
LeDuc, James W. [1 ]
Noah, James W. [3 ]
机构
[1] Univ Texas Med Branch, Galveston Natl Lab, Dept Microbiol & Immunol, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Galveston Natl Lab, Dept Pathol, Galveston, TX 77555 USA
[3] So Res Inst, Drug Discovery Div, Birmingham, AL 35205 USA
关键词
SMALL-MOLECULE INHIBITOR; VALIDATION; ASSAY; ENCEPHALITIS; REPLICATION; DISCOVERY; EBOLA;
D O I
10.1089/adt.2013.567
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nipah virus is a biosafety level 4 (BSL-4) pathogen that causes severe respiratory illness and encephalitis in humans. To identify novel small molecules that target Nipah virus replication as potential therapeutics, Southern Research Institute and Galveston National Laboratory jointly developed an automated high-throughput screening platform that is capable of testing 10,000 compounds per day within BSL-4 biocontainment. Using this platform, we screened a 10,080-compound library using a cell-based, high-throughput screen for compounds that inhibited the virus-induced cytopathic effect. From this pilot effort, 23 compounds were identified with EC50 values ranging from 3.9 to 20.0 mu M and selectivities >10. Three sulfonamide compounds with EC50 values <12 mu M were further characterized for their point of intervention in the viral replication cycle and for broad antiviral efficacy. Development of HTS capability under BSL-4 containment changes the paradigm for drug discovery for highly pathogenic agents because this platform can be readily modified to identify prophylactic and postexposure therapeutic candidates against other BSL-4 pathogens, particularly Ebola, Marburg, and Lassa viruses.
引用
收藏
页码:155 / 161
页数:7
相关论文
共 29 条
[1]   Development and validation of a chemiluminescent immunodetection assay amenable to high throughput screening of antiviral drugs for Nipah and Hendra virus [J].
Aljofan, Moharnad ;
Porotto, Matteo ;
Moscona, Anne ;
Mungall, Bruce A. .
JOURNAL OF VIROLOGICAL METHODS, 2008, 149 (01) :12-19
[2]  
Amal N. M., 2000, Southeast Asian Journal of Tropical Medicine and Public Health, V31, P301
[3]  
[Anonymous], 25661567 CID
[4]  
[Anonymous], 17483530 CID
[5]   Ebola and Marburg virus-like particles activate human myeloid dendritic cells [J].
Bosio, CM ;
Moore, BD ;
Warfield, KL ;
Ruthel, G ;
Mohamadzadeh, M ;
Aman, MJ ;
Bavari, S .
VIROLOGY, 2004, 326 (02) :280-287
[6]   Ebola and Marburg viruses replicate in monocyte-derived dendritic cells without inducing the production of cytokines and full maturation [J].
Bosio, CM ;
Aman, MJ ;
Grogan, C ;
Hogan, R ;
Ruthel, G ;
Negley, D ;
Mohamadzadeh, M ;
Bavari, S ;
Schmaljohn, A .
JOURNAL OF INFECTIOUS DISEASES, 2003, 188 (11) :1630-1638
[7]   Nipah virus-assodiated encephalitis outbreak, Siliguri, India [J].
Chadha, MS ;
Comer, JA ;
Lowe, L ;
Rota, PA ;
Rollin, PE ;
Bellini, WJ ;
Ksiazek, TG ;
Mishra, AC .
EMERGING INFECTIOUS DISEASES, 2006, 12 (02) :235-240
[8]  
Che PL, 2009, INT J CLIN EXP MED, V2, P363
[9]   Risk factors for Nipah virus infection among abattoir workers in Singapore [J].
Chew, MHL ;
Arguin, PM ;
Shay, DK ;
Goh, KT ;
Rollin, PE ;
Shieh, WJ ;
Zaki, SR ;
Rota, PA ;
Ling, AE ;
Ksiazek, TG ;
Chew, SK ;
Anderson, LJ .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (05) :1760-1763
[10]   Fatal encephalitis due to Nipah virus among pig-farmers in Malaysia [J].
Chua, KB ;
Goh, KJ ;
Wong, KT ;
Kamarulzaman, A ;
Tan, PSK ;
Ksiazek, TG ;
Zaki, SR ;
Paul, G ;
Lam, SK ;
Tan, CT .
LANCET, 1999, 354 (9186) :1257-1259