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Table 2 Primer sequences for the amplification of T. equi and/or B. caballi

From: First report of genetic diversity and risk factor analysis of equine piroplasm infection in equids in Jilin, China

Organism-s

Target gene

Assay

Product size (bp)

Primer

Sequence 5′–3′

Annealing temperature (°C)

Reference

T. equi

18S rRNA

PCR

435

P1

TCGAAGACGATCAGATACCGTCG

60

[14]

P2

TGCCTTAAACTTCCTTGCGAT

B. caballi

BC48

Nested PCR

454

P3

ACGAATTCCCACAACAGCCGTGTT

55

[15]

P4

ACGAATTCGTAAAGCGTGGCCATG

P5

GGGCGACGTGACTAAGACCTTATT

P6

GTTCTCAATGTCAGTAGCATCCGC

T. equi/B. caballi

18S rRNA

Nested PCR

~ 1400

P7

GAAAYTGCGAATGGCTCATTAM

57

[13]

P8

CACCGGATCACTCGATCGGTAGG

P9

GGATAACCGTGSTAATTSTAGGGC

P10

GTGTGTACAAAGGGCAGGGACG