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Table 1 Details of the PCR primers used in the present study, with the respective positive control DNA used in the reactions

From: Novel genotypes of Hepatozoon spp. in small mammals, Brazil

Genes

Target organisms

Primers

Sequence (5′–3′)

Amplicon size (bp)

References

Positive control in the PCR assay

18S rRNA

Hepatozoon spp.

HEP2 144–169 (F)

GGTAATTCTAGAGCTAATACATGAGC

574

[41]

Hepatozoon canis

  

HEP2 743–718 (R)

ACAATAAAGTAAAAAACAYTTCAAAG

   
  

HAM-1(F)

GCCAGTAGTCATATGCTTGTC

1750

[42]

H. canis

  

HPF-2(R)

GACTTCTCCTTCGTCTAAG

   
  

HEP-1(F)

CGCGAAATTACCCAATTa

   
  

HEP-2(R)

CAGACCGGTTACTTTYAGCAGa

   
  

HEP-4(R)

TAAGGTGCTGAAGGAGTCGTTTATa

   
  

HPF-1(F)

CTATGCCGACTAGAGATTGa

   

18S rRNA

Piroplasmorida

BAB2 143–167 (F)

CCGTGCTAATTGTAGGGCTAATACA

551

[41]

Babesia vogeli

  

BAB2 694–667 (R)

GCTTGAAACACTCTARTTTTCTCAAAG

   

16S rRNA

Anaplasmataceae

EHR 16SD (F)

GGTACCYACAGAAGAAGTCC

344

[43]

Ehrlichia canis

  

EHR 16SD (R)

TAGCACTCATCGTTTACAG

   
  1. aInternal primers used only for DNA sequencing