Genes
The Campylobacter lari MLST scheme uses internal fragments of the following seven house-keeping genes:
adk (adenylate kinase)
atpA (ATP synthase alpha subunit)
glnA (glutamine synthetase)
glyA (serine hydroxy methyl transferase)
pgi (glucose-6-phosphate isomerase)
pgm (phospho glucomutase)
tkt (transketolase)
PCR Amplification and sequencing
The primer pairs used for the PCR amplification and sequencing are detailed below:
adk
Forward
adkF: TGAAAGAATTRTTTTTAATCATAGG
Reverse
adkR: CTTTCATRTCWGCHACGATAGGTTC
atpA
Forward
atpAF: GWCAAGGDGTTATYTGTATWTATGTTGC
Reverse
atpAR: TTTAADAVYTCAACCATTCTTTGTCC
glnA
Forward
glnAF: TGATAGGMACTTGGCAYCATATYAC
Reverse
glnAR: ARRCTCATATGMACATGCATACCA
glyA
Forward
glyAF: ATTCAGGTTCTCAAGCTAATCAAGG
Reverse
glyAR: GCTAAATCYGCATCTTTKCCRCTAAA
pgi
Forward
pgiF1: TAGTGGGWATGGGAGGDTCAAGTT
Reverse
pgiR1: CCAATDAGWGCDATAGGAGTTAAACC
pgm
Forward
pgmF3: CGTGTTGTTTTAGATGTGGCTCA
Reverse
pgmR3: ATAGCGAAACAAACTAGCAATTCCT
tkt
Forward
tktF2: GCCTTTGGGTTTAGCRGATATTATG
Reverse
tktR: TTTTAATHAVHTCTTCRCCCAAAGGT
Reaction conditions - PCR
Denaturation: 94ºC 30 s
Annealing: 53ºC 30 s
Extension: 72ºC 2 minutes
30 cycles