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Antimicrobial Agents and Chemotherapy, July 2004, p. 2760-2765, Vol. 48, No. 7
0066-4804/04/$08.00+0 DOI: 10.1128/AAC.48.7.2760-2765.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Center for Comparative Medicine,1 Department of Veterinary Molecular Biosciences,2 Department of Medical Pathology, University of California, Davis, Davis, California 95616,3 Interdepartmental Graduate Program in Medicinal Chemistry, College of Pharmacy,4 Department of Biologic and Materials Sciences, School of Dentistry, University of Michigan, Ann Arbor, Ann Arbor, Michigan 481095
Received 6 November 2003/ Returned for modification 8 January 2004/ Accepted 15 March 2004
Rhesus and human cytomegalovirus (RhCMV and HCMV, respectively) exhibit comparable inhibition by benzimidazole nucleosides, including 2,5,6-trichloro-(1-ß-D-ribofuranosyl)benzimidazole (TCRB), and pyrrolo[2,3-d]pyrimidines. The two HCMV protein targets of TCRB, UL89 and UL56, are highly conserved with their RhCMV homologues. These data indicate that infection of rhesus macaques with RhCMV represents a useful model to test novel anti-HCMV drugs.
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