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Table 4 Primer sequences and specific thermal cycling conditions used for the PCR reactions

From: Goose parvovirus, goose hemorrhagic polyomavirus and goose circovirus infections are prevalent in commercial geese flocks in Poland and contribute to overall health and production outcomes: a two-year observational study

Assay target

Primer sequence (5’→3’)

Thermal cycling conditions

Product size bp

Reference

GPV detection

F: ACC GGA AGT CAC GTG AC

50 °C–2 min, (95 °C–10 min, 94 °C–15 s, 60 °C–1 min) x 40

123

[12]

R: GTT CGT TCG TTC GAA CC

Probe: 6-FAM ACC GGA AGC AyG TGA CCG GAA TAMRA(Q)

GHPV detection

F: ACC CGT GCT TCC ATT CAC AA

95 °C–3 min, (94 °C–20 s, 62 °C–30 s, 72 °C–20 s) x 30, 72 °C–3 min

379

[2]

R: CTG CTC CCC AAA CCT GTC AA

GoCV detection

F: TAA ATG CGA GTT TGA TGT GTC T

95 °C–3 min, (94 °C–20 s, 60 °C–30 s, 72 °C–20 s) x 30, 72 °C–3 min

565

[42]

R: CAT TTA ACC CCT TCC AAA GAG T

GPV sequencing

F: TTG CGA TTC CCA ATG GAT G

98 °C–3 min, (98 °C–10 s, 61 °C–20 s, 72 °C–1 min) x 40, 72 °C–5 min

1171

[49]

R: CCC AAA TAG GTC CCT GTA GAT A

GHPV sequencing

F1: GGA TGC TGC CTC TAA TTC TA

98 °C–3 min, (98 °C–10 s, 55 °C–20 s, 72 °C–1 min) x 40, 72 °C–5 min

1232

[26]

R1: CGC AGT TAA TCA GCT TAC AA

F2: GCC CCT ACT ATG AAG GAT CT

1290

R2: GGC TAA AGC CAT TAT CAG TG

GoCV

sequencing

F1: CGT CCG ATG TGT AGC CTT CGT

98 °C–3 min, (98 °C–10 s, 57 °C–20 s, 72 °C–1 min) x 40, 72 °C–5 min

1091

Nucleotide position 1-930 and 1661–1821

This study

R1: CAT AAA CTC GGG GGC GGG TG

F2: TAA ATG CGA GTT TGA TGT GTC T

98 °C–3 min, (98 °C–10 s, 60 °C–20 s, 72 °C–1 min) x 40, 72 °C–5 min

564

Nucleotide position 837–1400

[42]

R2: CAT TTA ACC CCT TCC AAA GAG T

F3: GCC CAG TCC ATT GTC CGA ATC

98 °C–3 min, (98 °C–10 s, 57 °C–20 s, 72 °C–1 min) x 40, 72 °C–5 min

749

Nucleotide position 1020–1768

This study

R3: GCC CAT CAT GCC GCT GTA TCG