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Table 1 Primers and thermal conditions used for PCR detection and genetic characterization of Anaplasma and ticks

From: Wild deer (Pudu puda) from Chile harbor a novel ecotype of Anaplasma phagocytophilum

Organisms

Gene

PCR

Primer

Sequence

To (°C)

Expected length (in bp)

Reference

Mammals

GAPDH

Conventional

gapdh F

CCTTCATTGACCTCAACTACAT

52

400

[25]

gapdh R

CCAAAGTTGTCATGGATGACC

Ticks

Mitochondrial 16S rRNA (rrs)

Conventional

16S + 1

CCGGTCTCAACTCAGATCAAGT

 

460

[26]

16S − 1

GCTCAATGATTTTTTAAATTGCTGT

  

Anaplasma

16S rRNA (rrs)

Conventional

EC9

TACCTTGTTACGACTT

48

1300

[27]

EC12A

TGATCCTGGCTCAGAACGAACG

  

[28]

Nested

A17a

GCGGCAAGCCTCCCACAT

54

1200

[29]

IS58-1345r

CACCAGCTTCGAGTTAAACC

   

groEl

Conventional

HS1a

AYTGGGCTGGTAYTGAAAT

47

1614

[30]

GroEl_2R

CGTTCTTACTAGGAACATCAAC

  

[31]

Nested

Gro677F

ATTACTCAGAGTGCTTCTCARTG

53

942

[32]

GroEL_rev2

GCCGACTTTTAGTACAGCAA

  

[33]

Heminested

GroEl_2F

TGTAAAGGCGCCTGGTTTCG

55

772

[31]

GroEl_2R

CGTTCTTACTAGGAACATCAAC

  

[31]

gltA

Conventional

F4b

CCAGGCTTTATGTCAACTGC

55

800

[34]

R1b

CGATGACCAAAACCCAT

   

Nested

EHR-CS136F

TTYATGTCYACTGCTGCKTG

55

650

 

EHR-CS778R

GCNCCMCCATGMGCTGG

   
  1. GAPDH Glyceraldehyde-3-phosphate dehydrogenase, gltA citrate synthase gene, groEL heat-shock operon