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Table 1 Primers used for multiplex PCR to detect and differentiate Salmonella enterica serogroups and serovars

From: Rapid screening of Salmonella entericaserovars Enteritidis, Hadar, Heidelberg and Typhimurium using a serologically-correlative allelotyping PCR targeting the O and H antigen alleles

Target gene1

Nucleotide sequence

Expected Size (bp)

O-antigen multiplex

  

abe1 (B)

F: GGCTTCCGGCTTTATTGG

561

 

R: TCTCTTATCTGTTCGCCTGTTG

 

wbaD-manC (C1)

F: ATTTGCCCAGTTCGGTTTG

341

 

R: CCATAACCGACTTCCATTTCC

 

abe2 (C2)

F: CGTCCTATAACCGAGCCAAC

397

 

R: CTGCTTTATCCCTCTCACCG

 

prt (A/D1)

F: ATGGGAGCGTTTGGGTTC

624

 

R: CGCCTCTCCACTACCAACTTC

 

wzx – wzy (E1)

F: GATAGCAACGTTCGGAAATTC

281

 

R: CCCAATAGCAATAAACCAAGC

 

H1-1 multiplex

  

fliC (i)

F: AACGAAATCAACAACAACCTGC

508

 

R: TAGCCATCTTTACCAGTTCCC

 

fliC (g,m)

F: GCAGCAGCACCGGATAAAG

309

 

R: CATTAACATCCGTCGCGCTAG

 

H1-2 multiplex

  

fliC (r)

F: CCTGCTATTACTGGTGATC

169

 

R: GTTGAAGGGAAGCCAGCAG

 

fliC (z10)

F: GCACTGGCGTTACTCAATCTC

363

 

R: GCATCAGCAATACCACTCGC

 

H2 multiplex

  

fljB (I: 1,2; 1,5; 1,6; 1,7)

F: AGAAAGCGTATGATGTGAAA

294

 

R: ATTGTGGTTTTAGTTGCGCC

 

fljB (II: e,n,x; e,n,z15)

F: TAACTGGCGATACATTGACTG

152

 

R: TAGCACCGAATGATACAGCC

 
  1. 1Indicates the unique genes or the junctions between the two genes used for designing PCR primers. () = antigen(s) detected.