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Antimicrobial Agents and Chemotherapy, December 2006, p. 4182-4185, Vol. 50, No. 12
0066-4804/06/$08.00+0 doi:10.1128/AAC.00714-06
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, Jewish General Hospital, Montreal, Quebec, Canada,2 Infectious Disease Care Clinic, Princess Marina Hospital, Gaborone, Botswana,3 Harvard School of Public Health, Boston, Massachusetts4
Received 8 June 2006/ Returned for modification 24 July 2006/ Accepted 21 September 2006
We analyzed the reverse transcriptase genotypes of human immunodeficiency virus type 1 subtype C viruses isolated from 23 patients in Botswana treated with didanosine-based regimens. The K65R mutation was selected either alone or together with the Q151M, S68G, or F116Y substitution in viruses from seven such individuals. The results of in vitro passage experiments were consistent with an apparent increased propensity of subtype C viruses to develop the K65R substitution.
Published ahead of print on 2 October 2006.
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