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. 2019 Aug 13;10(4):e01698-19. doi: 10.1128/mBio.01698-19

TABLE 3.

Mutations identified in PA14-1 RSCVs

Sample
Driver mutation
Secondary mutation
Day RSCV no. Wound no. Gene Mutationa Frequency (%) Gene Mutation
3 1 1 wspA 285-298del pslO-pslE Δ14,299 bp
2 2 wspA 285-298del
pslO-pslE Δ14,299 bp
4 1 wspA 285-298del PA14_13130/PA14_13140 TNN→TGC
fabI/ppiD TTC→TCC
Day 3 summary wspA 285-298del 100
14 3 4 wspA 285-298del
6 4 wspA 285-298del
7 4 wspA 285-298del
8 4 wspA 285-298del
9 4 wspA 285-298del
10 4 wspA 285-298del
12 4 wspA 285-298del CRISPR–Cas1/hpb +60bp
13 1 wspA 285-298del Glutamyl-tRNA reductase L71L (CTG→TTG)
14 4 wspA 285-298del fabI/ppiD TTC→TCC
16 4 wspA 285-298del
17 4 wspA 285-298del
20 4 wspF V154fs
24 1 wspA 285-298del
27 1 wspA 285-298del
28 2 wspA 285-298del
36 3 wspF V154fs
37 3 wspA 285-298del
38 3 wspF V154fs
86 3 wspA 285-298del CRISPR–Cas1/hp +60bp
Day 14 summary wspA 285-298del 84.2
wspF V154fs 15.8
28 G→TT 585bp
wspD CT→AG 588-589bp
40 1 wspA 285-298del S197S (TCG→TCA)
PA14_54090 A248V (GCG→GTG)
42 3 wspA 285-298del
43 3 wspA 285-298del
45 3 wspA 285-298del
87 2 wspA 285-298del
Day 28 summary wspA 285-298del 100
a

Deleted amino acid residues are indicated. del, deletion; fs, frameshift.

b

hp, hypothetical protein.