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. 2017 Dec 14;92(1):e01682-17. doi: 10.1128/JVI.01682-17

TABLE 1.

Nucleotide changes in K33S-GPC rCan upon serial passage in the presence and absence of 1 mM AmCl

Nucleotide(s) (nt) Stock
p11 no AmCl
p21 AmCl
nt changea (% reads) Amino acid change nt change (% reads) Amino acid change nt change (% reads) Amino acid change
S RNA
    5′ end 1–8 missing 1–8 missing 1–8 missing
    186–202; 217 K33S oligonucleotideb (≥98) K33S oligonucleotide (≥98) K33S oligonucleotide (≥98)
    590 G→A (55) GP1 A168T
    863–883 Delete codons T259DSSGKD265 GP2 ΔFP
    1127 A→T (88) GP2 I347F
    1146 T→C (39) GP2 V353A
    1401 T→C (19) GP2 F438S
    1535 A→G (35) GP2 R483G
    1655 G→A (51) NP A560T
    2382 T→C (40) NP S317 silent
    3406 (3′-UTR) A→T (56) A→T (38)
    3′ end 3407–3413 missing 3411–3413 missing
L RNA
    5′ end 1–4 missing 1–5 missing
    150 G→A (90) Z A23T
    4687 A→G (49) L N800D
    3′ end 7111–7114 missing 7111–7114 missing
a

Changes present in ≥10% of reads relative to the sequence of reverse genetics plasmids used to construct rCan viruses (28). The raw RNA-Seq data originally were aligned to Candid#1 S and L RNA reference genomes (AY746353.1 and AY746354.1, respectively).

b

In addition to the K33S mutation, the mutagenic oligonucleotide introduced 4 synonymous nucleotide changes and an I35V change (see Materials and Methods and the text).