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. 2015 May 20;89(15):7758–7775. doi: 10.1128/JVI.00039-15

TABLE 1.

Coding mutations of serially passaged Core-NS2 SA13 (5a) JFH1-based recombinantsg

graphic file with name zjv9990906130008.jpg

a

Positions are numbered according to the sequence of pSA13/JFH1 (24) (GenBank accession no. FJ393024). Corresponding H77 absolute reference numbers are given. Only positions with coding mutations present as a 50/50 quasispecies or dominant in at least one isolate are shown. Dashes indicate identity with original plasmid sequence. Positions with quasispecies are written with the dominant sequence in uppercase and the minor sequence in lowercase. The 50/50 quasispecies are shown with two uppercase letters. Shaded positions were introduced back into pSA13/JFH1orig in different combinations. Positions shaded in black represent SA13/JFH1orig cell culture-adaptive mutations described previously (24).

b

Common 17th passage used for subsequent flask and plate lineage.

c

Virus stocks are designated according to their passage and the well number used to infect culture. Accordingly, a 31st-passage virus stock derived from well C5 of a 96-well plate is designated p31/C5.

d

Adapted virus stock received from the University of Birmingham (United Kingdom).

e

Positions of individual amino acid changes within the given HCV protein are shown as H77 absolute reference numbers.

f

HCV infectivity titers were determined as described in Materials and Methods. Peak infectivity titers are displayed as log10 focus-forming units per milliliter.

g

In addition to the mutations shown in the table, the following noncoding nucleotide changes (positions are given as H77 absolute reference numbers, GenBank accession no. AF009606) were observed in the ORFs of the various sequenced virus stocks: G350T, T791C, T2337T/C, T2405C/t, C2468T/c, T2636C, G2807C/g, C3881T/C, A3914G, A4367G, T5231C, T5648C/T, C5750T, T7202C, A7485G/A, T7540C, C7540A/c, T7932C, and A8573G.