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. 2011 Feb;49(2):491–499. doi: 10.1128/JCM.01274-10

Table 2.

Genes studiedc

Gene(s) Size of analyzed fragment (bp) %G+C No. of polymorphic sites No. of alleles dN/dS Maximum % of nt divergencea % of nt divergence between type strain sequencesb
MabsT versus MmasT MabsT versus MbolT MbolT versus MmasT
argH 480 66.8 40 19 0.1529 5.47 4.58 3.54 2.92
cya 510 68.2 31 25 0.0029 3.62 1.96 1.96 2.75
glpK 534 62.7 25 16 0.0380 2.48 1.69 1.31 0.94
gnd 480 65.2 33 20 0.0307 4.73 2.29 4.58 3.54
murC 537 68.6 39 16 0.1259 4.44 2.05 3.54 3.35
pgm 495 62.2 29 25 0.1900 2.02 1.41 1.41 0.81
pta 486 66.1 20 20 0.0110 2.74 1.85 1.65 2.26
purH 549 65.6 31 21 0.0502 2.98 1.82 2.00 0.18
All MLSA genes 4,071 65.7 248 79 ND 2.85 2.19 2.43 2.01
rpoB 752 65.6 43 22 0.0827 4.79 3.32 4.12 1.46
a

Maximum nucleotide divergence found between the 123 strains studied.

b

M. abscessus CIP 104536T, M. massiliense CIP 108297T, and M. bolletii CIP 108541T.

c

ND, not done; dN/dS, ratio of the rate of nonsynonymous substitutions (dN) to the rate of synonymous substitutions (dS); MabsT, M. abscessus type strain sequence; MbolT, M. bolletii type strain sequence; MmasT, M. massiliense type strain sequence.