Abstract: Among those with recent infection, the most common RAMs to nucleoside reverse transcriptase inhibitors (NRTIs) were M184I/V and T215D/E/F/I/S/Y (1.1%), to non-NRTIs was Y181C (1.3%), and to PIs was M46I (1.5%).
Abstract: Of patients with chronic infection, T215D/E/F/I/S/Y (0.8%; NRTI), Y181C (0.5%; non-NRTI), and M46I (0.4%; PI) were the most common RAMs.
Result: <
Trends in Genotypic HIV-1 Antiretroviral Resistance between 2006 and 2012 in South African Patients Receiving First- and Second-Line Antiretroviral Treatment Regimens.
Result: (ii) K65N, which occurred in one patient receiving TDF; (iii) T69D, V75M, and V75T, which occurred in 1.3%, 2.5%, and 0.3% respectively; (iv) T215I occurred in 1.4% of patients; and (v) K219R and K219N, occurred in 1.6% and 0.9% respectively.
Increased risk of Q151M and K65R mutations in patients failing stavudine-containing first-line antiretroviral therapy in Cambodia.
Abstract: RT subtype B virus isolates tended to acquire different ZDV resistance mutations (Q151M and D67N or T215Y, D67D/N and F214L) compared to subtype C (D67N, K70R, T215I or T215F).
Result: The first mutation (D67N) was replaced by T215I at day 91 (2 microM), after the virus reached a VL level comparable to that before selection.
Result: The mutation T215I (ATY or ATC) is an intermediary mutation between T215 (ACC) and T215F (TTT).
Result: Three final resistance profiles were de
Zidovudine (AZT) monotherapy selects for the A360V mutation in the connection domain of HIV-1 reverse transcriptase.
Result: Other NRTI-associated mutations detected included T69A/N/S (n=21), V75L, V118I and T215A/I.
Presence of drug resistance mutations among drug-naive patients in Morocco.
PMID: 21087198
2011
AIDS research and human retroviruses
Abstract: The presence of DRMs was found in four (5.06%) of 91 patients; resistance mutations to NRTIs were M184V and T215I/S revertant mutations; resistance to NNRTIs was associated with K103N and resistance to PIs with V82A.
Dynamics of HIV-1 quasispecies during antiviral treatment dissected using ultra-deep pyrosequencing.
Abstract: CONCLUSIONS: With this highly sensitive UDPS protocol preexisting drug resistance was infrequently observed; only M184I, T215A and T215I were detected at very low levels.
Abstract: Other resistance mutations, except T215A and T215I were below the detection limit.
Introduction: Thus, only M184I, T215A and T215I were found at very low levels.
Introduction: We also studied so called T215 reversion mutations (T215A/C/D/E/G/H/I/L/N/S/V).
Result: Our results show that T215A and T215I not only evolve following treatmen
Transmission networks of drug resistance acquired in primary/early stage HIV infection.
Abstract: The transmission of nucleoside analogue mutations and 215 resistant variants (T215C/D/I/F/N/S/Y) declined with clustering (7.9 vs.
Result: As shown, viral variants harbouring mutations to NRTIs, including revertants at codon 215 (T215C/D/I/N/S), thymidine analogue mutations, and M184V, as well as to PIs were less frequent in clustered transmissions.