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. 2019 Mar 27;63(4):e02205-18. doi: 10.1128/AAC.02205-18

TABLE 1.

Prevalence of HCV GT NS3, NS5A, and NS5B polymorphisms at clinically relevant residue positions associated with drug resistance

Polymorphisms (n) ina:
NS3 sequences (n = 104) NS5A sequences (n = 130) NS5B sequencesb (n = 104)
V36 Y56 K80 A156 D168 I170 L28 R30 L31 T58 T93 L159 S282 L392 V421 V494 P495
V (78) Y (93) Q (81) A (103) D (102) V (70) V (52) S (58) L (126) P (65) T (109) L (100) S (102) L (96) V (103) A (77) P (103)
L (20) F (11) K (22) V (1) E (2) I (33) L (36) R (38) I (2) T(46) S (18) F (3) C (1) I (8) A (1) V (25) L (1)
I (6) L (1) A (1) F (14) A (28) M (2) G (5) I (2) ? (1) ? (1) M (2)
T (13) N (4) S (6) ? (1)
A (6) E (1) A (4)
M (6) T (1) ? (1)
? (2) L (2)
G (1) L/Pc (1)
a

The first row depicts the GT-6a consensus sequence (determined from alignment of 24 NS3, 36 NS5A, and 24 NS5B sequences). Underlining indicates polymorphisms previously shown to be associated with DAA resistance (21, 33, 3537, 48); ?, undefined polymorphism. Only GT-6a reference polymorphisms were observed at NS3 (T54, V55, and R155), NS5A (P29 and P32), and NS5B (V321 and A499) resistance-associated residue positions. NS5A-A92P was detected in 1/130 NS5A sequences.

b

BCV-associated RASs include L392I, A421V, V494A, L495L/S, and A499T; SOF-associated RASs were found at L159F, S282T, and V321I.

c

One patient-derived NS5A sequence had a mixture of polymorphisms detected at T58. Each of these polymorphisms (L58 and P58) represented ≥15% of the viral population.