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. 2006 Dec 20;45(2):477–487. doi: 10.1128/JCM.01708-06

TABLE 5.

Susceptibilities of seven patient-derived viral isolates to representative drugs assayed using R5-MaRBLE cells

Strain or isolate (subtype) Tropismb RT mutation(s) Protease mutation(s) IC50 (nM) ± SD (change, n-fold) of:
Zidovudine Lamivudine Efavirenz Lopinavir
JRCSF (B) R5 None L63P 1.4 ± 0.6 (1) 13.6 ± 4.6 (1) 0.9 ± 0.1 (1) 19.3 ± 8.4 (1)
1 (B) R5 None L63P/T, A71A/V, V77I 1.2 (0.7) 4.2 (0.3) 1.5 (1.8) 6.8 (0.5)
2 (B) X4, R5 M41L, D67N, K70R, K101Q, M184V, L210L/W, T215F, K219Q L10I, L33F, M46I, F53L, I54V, L63P, A71V, G73S/T, V77I, V82F, L90M 56.1 (32.9) >5,000 (>380.7) 1.1 (1.3) >1,000 (>76.5)
3 (F) X4, R5 M41L, E44E/D, D67N, K101K/E, V118I, L210W, T215Y K20T, D30N, M36I, M46M/L, L63P, A71V, N88D 195.1 (114.5) 34.5 (2.6) 0.1 (0.2) NDc (ND)
4 (B) X4, R5 M41L, E44A, D67N, V118I, L210W, T215Y L10V, K20T, D30N, M36I, I54V, L63T, A71V, V77V/I, N88D, L90M 326.5 (191.7) 13.5 (1.0) 0.2 (0.2) 123.4 (9.4)
5 (B) X4, R5 M41L, E44D, D67N, V118I, M184V, L210W, T215Y L10V, K20R, V32I, M36I, M46L, F53F/L, I54V, L63P, A71V, V82A, L90M 177.4 (104.1) >5,000 (>380.7) 0.5 (0.6) 986.8 (75.5)
6 (F) R5 M41L, E44D, D67N, V118I, L210W, T215Y L10I, K20T, M36I, M46I, F53L, L63L/I/T/P, A71V, I84V, L90M 381.7 (224.0) 88.0 (6.7) 0.3 (0.4) 190.6 (14.6)
7Ra (B) X4 K103N L63C, V77I 2.1 (1.5) 22.3 (1.6) 60.2 (66.8) 7.6 (0.4)
a

Recombinant HXB2 with patient-derived protease and RT sequences.

b

The tropism of each virus was determined by using X4-GHOST and R5-GHOST cells.

c

ND, not determined.