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Table 1 Target genes, primers sequence, PCR methods used for pathogens identification

From: Tick-borne pathogens and associated co-infections in ticks collected from domestic animals in central China

Pathogens

Method

Target gene

Primers sequence (5′-3′)

Product size (bp)

Reference

Babesia/Theileria

Nested PCR

18S rRNA

RIB-19(CGGGATCCAACCTGGTTGATCCTGC)

1700

[28]

RIB-20(CCGAATTCCTTGTTACGACTTCTC)

BAB-F(ACCTCACCAGGTCCAGACAG)

430

BAB-R(GTACAAAGGGCAGGGACGTA)

Anaplasma/Ehrlichia

Nested PCR

16S rRNA

Eh-out1 (TTGAGAGTTTGATCCTGGCTCAGAACG)

653

[29]

Eh-out2 (CACCTCTACACTAGGAATTCCGCTATC)

Eh-gs1 (GTAATACTGTATAATCCCTG)

282

 

Eh-gs2 (TATAGGTACCGTCATTATCTTCCCTAC)

TBEV

Nested PCR

Non-structural protein NS5

FSM1 (GAGGCTGAACAACTGCACGA)

357

[32]

FSM2 (GAACACGTCCATTCCTGATCT)

FSM1i (ACGGAACGTGACAAGGCTAG)

251

FSM2i (GCTTGTTACCATCTTTGGAG)

Rickettsia spp.

Nested PCR

groEL

Gro1 (AAGAAGGCGTGATAAC)

200

[30]

Gro2 (ACTTCCGTAGCACC)

SF (GATAGAAGAAAAGCAATGATG)

250

SR (CAGCTATTTGAGATTTAATTTG)

B. burgdorferi s. l.

Nested PCR

Flagellin

Outer1 (CTGCTGGCATGGGAGTTTCT)

730

[31]

Outer2 (TCAATTGCATACTCAGTACT)

Inner1 (AAGGAATTGGCAGTTCAATC )

290

Inner2 (ACAGCAATAGCTTCATCTTG )

Leishmania infantum

PCR

kDNA

RV1(CTTTTCTGGTCCCGCGGGTAGG)

183

[27]

   

RV2(CCACCTGGCCTATTTTACACCA)

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