TABLE 4.
Isolate | Accession no. and point mutations for genea:
|
|||
---|---|---|---|---|
CgERG4 | CgERG5 | CgERG6 | CgERG11 | |
21231 | AY942649; A-429T,b T-322C,bT842A, T947C,b G1490A | AY942651; A-373G,b G-367X,b G-314A, T-35C,b X-34A, C-33T, A-32T, C-27T | AY942653; G-268A,b A-209X,bA524G,bG1064A, C1196Tb | DQ060157; T767C,bC836T, A1022G,bT1556Ab |
21229 | AY942648; A-429T,b T-322C,bT947C,bG1394A | AY942650; A-373G,b G-367X,b A-311G, T-36A, T-35C,b C-33X, C-31T, C426T, A1156G | AY942652; G-268A,b A-209X,b C-199G, T-136A, T515C, A524G,bG592T, C1196Tb | AY942647; C677T, T767C,bA1022G,bT1274C, T1520A, T1556Ab |
Mutations are described as follows. The first letter corresponds to the nucleotide present in the GenBank database sequence for the corresponding gene (accession numbers NC005967, NC006036, NC006031, and L40389 for CgERG4, CgERG5, CgERG6, and CgERG11, respectively), the number represents the relative position from the start of the ORF, and the second letter represents the nucleotide found in the ERG gene sequence of isolate 21231 or 21229. Mutations located inside the coding sequences are in boldface type, and the missense mutation found in the isolate 21229 CgERG6 gene sequence is underlined. Other mutations correspond to polymorphisms outside the coding sequences. The letter X placed after the number indicates a deletion of the corresponding nucleotide, and the same letter placed before the number corresponds to an insertion.
Mutations shared by isolates 21231 and 21229.