Primers used for MLST of Campylobacter upsaliensis

Genes

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

adk (adenylate kinase)

aspA (aspartase)

atpA (ATP synthase alpha subunit)

glnA (glutamine synthetase)

glyA (serine hydroxy methyl transferase)

pgi (glucose-6-phosphate isomerase)

tkt (transketolase)

PCR Amplification and sequencing

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

adk

Forward

adkF: TGAAAGAATTRTTTTTAATCATAGG

Reverse

adkR: CTTTCATRTCWGCHACGATAGGTTC

aspA

Forward

aspAF2: GAAGCWAAAGCWAAAGAATAYAAAGAT

Reverse

aspAR2: GAGTTTTTTGCAWGCTTCWGGATT

atpA

Forward

atpAF: GWCAAGGDGTTATYTGTATWTATGTTGC

Reverse

atpAR: TTTAADAVYTCAACCATTCTTTGTCC

glnA

Forward

glnAF: TGATAGGMACTTGGCAYCATATYAC

Reverse

glnAR: ARRCTCATATGMACATGCATACCA

glyA

Forward

glyAF: ATTCAGGTTCTCAAGCTAATCAAGG

Reverse

glyAR: GCTAAATCYGCATCTTTKCCRCTAAA

pgi

Forward

pgiF2: TTTAGTGGGWATGGGTGGKTCAAGT

Reverse

pgiR3: TCTCTAGCACCAATGAGAGCTATGG

tkt

Forward

tktF1: GCAAAYTCAGGMCAYCCAGGTGC

Reverse

tktR: TTTTAATHAVHTCTTCRCCCAAAGGT

Reaction conditions - PCR

Denaturation: 94ºC 30 s

Annealing: 53ºC 30 s

Extension: 72ºC 2 minutes

30 cycles