TABLE 2.
Nucleotide sequence identities between partial sequences of inlA genes ( positions 799 to 1531 bp) and deduced theoretical molecular masses of InlA of L. monocytogenes strains H1, H17, H32, H34, and LO28 and the epidemic reference strains Scott A (serotype 4b) and EGD-e (serotype 1/2a)
| Strain (serotype) | % Nucleotide sequence identity (no. of nucleotide differences) (n = 733)
|
Theoretical molecular mass (kDa) of InlAa | ||
|---|---|---|---|---|
| Scott A | EGD-e LO28 | H1, H32, and H34 | ||
| Scott A (4b) | 80 | |||
| EGD-e (1/2a) | 95.91 (30) | 100.00 | 80 | |
| LO28 | 95.91 (30) | 100.00 | 63 (1636∧1637insA)b | |
| H1, H32, and H34 | 97.27 (20) | 98.23 (13) | 100.00 | 47 (1414 C→T) |
| H17 | 97.14 (21) | 98.09 (14) | 99.86 (1) | 47 (1414 C→T) |
The nucleotide change implicated in synthesis of a truncated form of InlA is given in parentheses. The position of the first translated codon is denoted as +1.
Results are from the partial sequences of inlA from Jonquieres et al. (22).