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. 2010 Jul 7;48(9):3295–3300. doi: 10.1128/JCM.00750-10

TABLE 1.

Primers and annealing temperatures for the detection of B. henselae by PCR

Target gene and assay (segment amplified) Primer name Primer sequence (5′-3′) Annealing temp (°C) Amplicon size (bp) Reference(s)
htrA
    Assay I (nt 1209-1372) 3+ (outer forward) GTG CGT TAA TTA CCG ATC CA 58.0 163 3, 5
4− (outer reverse) CCA AAC TCC TAA GGT TAC TGT TTC 58.0 5
1+ (inner forward) GCT GGT ATC AAG GCA GGT G 58.0 82 5
2− (inner reverse) GCA ATA CGC TTT GCT AGA TCAC 58.0 5
    Assay II (nt 1250-1332) 6+ (outer forward) CCA GAT CAA CAT CCC TTG AAA 58.0 182 5
5− (outer reverse) GCG TAA CTT GTG CCA TCA GA 58.0 5
7+ (inner forward) TTT GCA ACG TTC GCA TAG ACT 58.0 93 5
8− (inner reverse) CAG AAA TCA CAT GAT TAT TGG TCAC 58.0 5
gltA (nt 504-1178) f1 (outer forward) GGT CCC AAC TCT TGC CGC TAT G 65.0 675 34
r1 (outer reverse) CAG CCG ACA CTG CGT GCT AAT G 65.0 34
f2 (inner forward) ATG CCT AAA AAT GTT ACA AGA 58.0 354 34
r2 (inner reverse) CGT GCT AAT GCA AAA AGA AC 58.0 34