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Journal of Virology, February 2004, p. 1289-1300, Vol. 78, No. 3
0022-538X/04/$08.00+0 DOI: 10.1128/JVI.78.3.1289-1300.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Boris Feld,1 Jonathan D. Bloom,3 and John O'Connell1
Infectious Disease Section,1 Biological Chemistry,2 Chemical Sciences, Wyeth Research, Pearl River, New York 109653
Received 20 June 2003/ Accepted 6 October 2003
A novel small molecule inhibitor of human cytomegalovirus (HCMV) was identified as the result of screening a chemical library by using a whole-virus infected-cell assay. Synthetic chemistry efforts yielded the analog designated CFI02, a compound whose potency had been increased about 100-fold over an initial inhibitor. The inhibitory concentration of CFI02 in various assays is in the low nanomolar range. CFI02 is a selective and potent inhibitor of HCMV; it has no activity against other CMVs, alphaherpesviruses, or unrelated viruses. Mechanism-of-action studies indicate that CFI02 acts very early in the replication cycle, inhibiting virion envelope fusion with the cell plasma membrane. Mutants resistant to CFI02 have mutations in the abundant virion envelope glycoprotein B that are sufficient to confer resistance. Taken together, the data suggest that CFI02 inhibits glycoprotein B-mediated HCMV virion fusion. Furthermore, CFI02 inhibits the cell-cell spread of HCMV. This is the first study of a potent and selective small molecule inhibitor of CMV fusion and cell-cell spread.
Present address: Department of Biology, Indiana UniversityPurdue University at Fort Wayne, Fort Wayne, IN 46805.
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