Primers used for MLST of Campylobacter helveticus

Genes

The Campylobacter helveticus MLST scheme uses internal fragments of the following seven house-keeping genes:

aspA (aspartase)

atpA (ATP synthase alpha subunit)

glnA (glutamine synthetase)

gltA (citrate synthase)

glyA (serine hydroxy methyl transferase)

pgm (phospho glucomutase)

tkt (transketolase)

PCR Amplification and sequencing

The primer pairs used for the PCR amplification and sequencing are detailed below:

aspA

Forward

aspAF2: GAAGCWAAAGCWAAAGAATAYAAAGAT

Reverse

aspAR2: GAGTTTTTTGCAWGCTTCWGGATT

atpA

Forward

atpAF: GWCAAGGDGTTATYTGTATWTATGTTGC

Reverse

atpAR: TTTAADAVYTCAACCATTCTTTGTCC

glnA

Forward

glnAF: TGATAGGMACTTGGCAYCATATYAC

Reverse

glnAR: ARRCTCATATGMACATGCATACCA

gltA

Forward

gltAF: GARTGGCTTGCKGAAAAYAARCTTT

Reverse

gltAR: TATAAACCCTATGYCCAAAGCCCAT

glyA

Forward

glyAF: ATTCAGGTTCTCAAGCTAATCAAGG

Reverse

glyAR: GCTAAATCYGCATCTTTKCCRCTAAA

pgm

Forward

pgmF2: ATGTGGCWCAYGGAGCRGCTTATAA

Reverse

pgmR2: GGCTATTRATRCCCTTTTTATCAAG

tkt

Forward

tktF1: GCAAAYTCAGGMCAYCCAGGTGC

Reverse

tktR: TTTTAATHAVHTCTTCRCCCAAAGGT

Reaction conditions - PCR

Denaturation: 94ºC 30 s

Annealing: 53ºC 30 s

Extension: 72ºC 2 minutes

30 cycles