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Table 2 Primers used for amplification of each gene in this study

From: Molecular detection and genetic characterization of Mycoplasma gallisepticum, Mycoplama synoviae, and infectious bronchitis virus in poultry in Myanmar

Target gene

Primer name

Primer sequences (5′ – 3′)

Size in nucleotides (bp)

References

For detection of each pathogen

 pMGA1.2

  1st

pMGAFo

GTG AAG AAA AAA AAC ATA TTA AAG TTT

1,900

Mardassi et al., 2005 [15]

pMGARo

CTA AGA TGG ATT TGA AAC ATT AGT

  2nd

pMGAF1i

CTA GTT AAT ACT AGT GAT CAA GTG AAA CTA

500

Mardassi et al., 2005 [15]

pMGAR1i

TTG AAC ATT GTT CTT TGG AAC CAT CAT

 MS2/12

  1st

MS1.2Fo

AAA CTA CAA AAC TTT GTA ATG GCT

1,200

Mardassi et al., 2005 [15]

MS1.2Ro

TTA CAA GTA CGG TGT TTA ATC AAT

  2nd

MS1.2F1i

ATT ACC AAG CAG ATG GTT ACG ACG T

450

Mardassi et al., 2005 [15]

MS1.2R2i

AGT TAT AGT AAC TCC GTT TGT TCC A

 S1

IBV-S1

AGG AAT GGT AAG TTR CTR GTW AGA G

620–640

Mase et al., 2004 [16]

IBV-S2

GCG CAG TAC CRT TRA YAA AAT AAG C

For sequence analysis

 gapA

gapA 3F

TTC TAG CGC TTT AGC CCT AAA CCC

332

Ferguson et al., 2005 [17]

gapA 4R

CTT GTG GAA CAG CAA CGT ATT CGC

 vlhA

vlhA f

TAC TAT TAG CAG CTA GTG C

350 / 400

Dijkman et al., 2016 [18]

vlhA R

AGT AAC CGA TCC GCT TAA T