Skip to main content
. 2002 Feb;40(2):633–636. doi: 10.1128/JCM.40.2.633-636.2002

TABLE 1.

Primers for multiplex PCR amplification of Salmonella enterica serovars Typhi and Paratyphi A

Gene and primer (oligonucleotide sequence) Length (bp) Amplified fragment size (bp) Sourceb
tyv (rfbE)
tyv-s (5"-GAG GAA GGG AAA TGA AGC TTT T-3") 22 615 M29682
tyv-as (5"-TAG CAA ACT GTC TCC CAC CAT AC-3") 23 M29682
prt (rfbS)
parat-s (5"-CTT GCT ATG GAA GAC ATA ACG AAC C-3") 25 258 M29682
parat-as, (5"-CGT CTC CAT CAA AAG CTC CAT AGA-3") 24 M29682
viaB
vi-s (5"-GTT ATT TCA GCA TAA GGA G-3") 19 439 D14156
vi-as (5"-CTT CCA TAC CAC TTT CCG-3") 18 D14156
fliC
fliCcom-s (5"-AAT CAA CAA CAA CCT GCA GCG-3") 21 L21912
fliCd-as (5"-GCA TAG CCA CCA TCA ATA ACC-3") 21 L21912
fliCa-as (5"-TAG TGC TTA ATG TAG CCG AAG G-3") 22 X03393
fliCcom-fliCd-as 750 (489)a
fliCcom-fliCa-as 329
a

Number in parentheses represents size of PCR product of H:j gene.

b

Primers were designed using sequences corresponding to indicated GenBank-EMBL-DDBL nucleotide sequence database accession numbers.