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. 2014 May;52(5):1664–1671. doi: 10.1128/JCM.03437-13

TABLE 3.

Primers used for the M. hyorhinis real-time PCR assay, for the sequencing of the p37 gene, and for the MLST scheme

Gene Primer Sequence (5′→3′)a Start position (in HUB-1 genome) Amplicon size (bp) Seq. sizeb (bp)
p37 gene Mhr-p37-RT-F TATCTCATTGACCTTGACTAAC 768070 89
Mhr-p37-RT-R ATTTTCGCCAATAGCATTTG
Mhr-p37-Probe FAMa-CATCCTCTTGCTTGACTACTCCTG-BHQ1b
p37-A1F TTTTCCTTGGCCTGATGAAC 766864 836 1,278
p37-A1R TTCAGATCCACTTGTAAAAATTGC
p37-A2F AGCTTGAACAGTTGGATCGT 764
p37-A2R GGGTGCTGTAAAAGGCTGAG
dnaA dnaA_F CCAGAAGTCTTAGGTGGTTTTGA 612 495 435
dnaA_R ATGATCCTTGCCTCCAAAAA
rpoB rpoB_F CAACGTCAAGCTGTTCCATT 71189 563 496
rpoB_R CCTGCACTAACTTCTGATCCAA
gyrB gyrB_F CCGATTCTGATGGTTCACAT 316687 399 291
gyrB_R TTTTTGCATATTTTGCATTTTCTT
gltX gltX_F GCTGAAAGACTCTCAAAATCACC 415737 493 370
gltX_R CAAGCCTTTTTGAAATTAGTTCTTT
adk adk_F GCGATGGCATCTAATTCTTTT 488754 484 277
adk_R ACTCAGGCAAAGTTTTTAGAACA
gmk gmk_F TTGCGCCTGTTTCTGTTAAT 522045 499 435
gmk_R AAGAGACAAAAGACCTAATGAAGTAGA
a

FAM, 6-carboxyfluorescein, fluorescence reporter dye; BHQ, Black Hole Quencher.

b

Size of sequenced fragment.