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. 2014 Oct 29;7:490. doi: 10.1186/s13071-014-0490-x

Table 1.

Primers and conditions for PCR detection of pathogen DNA

Organism Target gene Primer Sequence (5' to 3') Amplicon Annealing temperature (°C) Reference
size (bp)
Rickettsia spp gltA RpCS.780p GACCATGAGCAGAATGCTTCT 600 48 [8]
RpCS.877p GGGGACCTGCTCACGGCGG 480 54
RpCS.1273r CATAACCAGTGTAAAGCTG
Anaplasma sp.. 16S rDNA EHR16SD GGTACCYACAGAAGAAGTCC 345 53 [9]
EHR16SR TAGCACTCATCGTTTACAGC
Coxiella burnetii IS1111 Trans 1 TATGTATCCACCGTAGCCAGTC 687 60 [10]
Trans 2 CCCAACAACACCTCCTTATTC
Borrelia spp. fla gene BflaPAD GATCA(G/A)GC(T/A)CAA(C/T)ATAACCA(A/T)ATGCA 55 [11]
BflaPDU AGATTCAAGTCTGTTTTGGAAAGC
BflaPBU,nest GCTGAAGAGCTTGGAATGCAACC 340 55
BflaPCR,nest TGATCAGTTATCATTCTAATAGCA
B. microti 18S rDNA Babl CTTAGTATAAGCTTTTATACAGC 238 55 [12]
Bab4 ATAGGTCAGAAACTTGAATGATACA
Trypanosoma spp. ITS1 rDNA ITS1 CF CCGGAAGTTCACCGATATTG Variable 58 [13]
ITS1 BR TTGCTGCGTTCTTCAACGAA
Leishmania spp. kDNA minicircle L.MC-1S CTRGGGGTTGGTGTAAAATAG- 700 55 [14]
L.MC-1R TWTGAACGGGRTTTCTG
Plasmodium spp. Cytb DW2 &DW4 DW2; TAATGCCTAGACGTATTCCTGATTATCCAG 1253 60 [15]
DW4; TGTTTGCTTGGGAGCTGTAATCATAATGTG
Cytb1 & Cytb2 CYTb1; CTCTATTAATTTAGTTAAAGCACA 939 50
Tb2; ACAGAATAATCTCTAGCACC