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Antimicrobial Agents and Chemotherapy, June 2006, p. 2210-2213, Vol. 50, No. 6
0066-4804/06/$08.00+0 doi:10.1128/AAC.01447-05
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Botswana-Harvard School of Public Health AIDS Initiative Partnership for HIV Research and Education, Gaborone, Botswana,1 McGill University AIDS Centre, Lady Davis Institute for Medical Research, Montreal, Quebec, Canada,2 Infectious Disease Care Clinic, Princess Marina Hospital, Gaborone, Botswana,3 Harvard School of Public Health, Boston, Massachusetts4
Received 9 November 2005/ Returned for modification 9 January 2006/ Accepted 23 March 2006
Among 16 human immunodeficiency virus-infected (subtype C) Batswana patients who failed nelfinavir (NFV)-containing regimens, the most prevalent mutation observed was D30N (54%), followed by L90M (31%). L89I, K20T/I, and E35D polymorphic changes were also identified. These findings suggest that subtype C viruses in Botswana may develop resistance to NFV via subtype-specific pathways.
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