Table 2. Nucleotide polymorphisms in the sequences of putative virulence factors found in the genome of Clavibacter michiganensis subsp. nebraskensis strains GIL1 and HF4. PCR primers flanking each locus were used in sequencing reactions to obtain the complete sequence of each gene.
Locus in Cmn genome (Isolate NCPPB 2581) | Putative function | Nucleotide differences |
---|---|---|
Cmn 00734 | Chloride anion channel | No difference |
Cmn 00144 | Secreted cellulase A | Indel (18 nucleotides) |
Cmn 02650 | Endoglucanase | 3 SNPs |
Cmn 02651 | Endoglucanase | Indel (66 nucleotides) |
Cmn 00792 | Translocase glycosyl hydrolase | No difference |
Cmn 01115 | Polysaccharide deacetylase | No difference |
Xys A | Endo-1, 4-beta xylanase A | No difference |
Xys B | Endo-1, 4-beta xylanase B | 6 SNPs |
Pga A | Polygalacturonase A | No difference |
Cmn 01173 | Secreted serine peptidase | No difference |
Cmn ppaF | Secreted serine peptidase | No difference |
Cmn 457 | Secreted serine peptidase | No difference |
Cmn sbtC | Serine peptidase | No difference |
Cmn sbtB | Serine peptidase | No difference |
Cmn 2417 | Secreted serine peptidase | No difference |
Cmn 2381 | Secreted serine peptidase | No difference |
Cmn 2235 | Secreted serine peptidase | No difference |
Cmn 1337 | Secreted serine peptidase | No difference |
Cmn 1248 | Secreted serine peptidase | No difference |
Cmn 00106 | Toxin-antitoxin system | No difference |
Cmn 00626 | Toxin-antitoxin system | No difference |
Cmn 00771 | Toxin-antitoxin system | No difference |
Cmn 01077 | Toxin-antitoxin system | No difference |
Cmn 01078 | Toxin-antitoxin system | No difference |
Cmn 02136 | RTX toxin | No difference |
Cmn 02626 | Toxin component | No difference |
Cmn 02669 | Toxin component | No difference |
Cmn 02707 | Toxin gene | No difference |
Cmn 00414 | Protein kinase | No difference |
Cmn 0118 | Exported toxin | No difference |
Cmn 02101 | TetR lipase/esterase | No difference |
Cmn 00283 | Glycosyl transferase | No difference |
Cmn 02654 | Pectate lyase | I SNP |
Sequences were aligned and examined for nucleotide sequence differences. Primers were designed from reference strain NCPPB 2581 genomic sequence.