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Table 1 Details of the qPCR/PCR assays used in the study for the detection of tick-borne pathogens

From: Anaplasma phagocytophilum, Bartonella spp., haemoplasma species and Hepatozoon spp. in ticks infesting cats: a large-scale survey

Target species (target gene)

PCR primer and probe sequences (5'–3')

Product size (bp)

Reference

Anaplasma phagocytophilum (msp2)

F: ATGGAAGGTAGTGTTGGTTATGGTATT

77

[7]

R: TTGGTCTTGAAGCGCTCGTA

FAM-TGGTGCCAGGGTTGAGCTTGAGATTG-BHQ1

Bartonella henselae (alr-gcvP intergenic spacer)

F: GAGGGAAATGACTCTCTCAGTAAAA

110

[9]a

R: TGAACAGGATGTGGAAGAAGG

FAM-CAGCCAAATATACGGGCTATCCATCAA-BHQ1

Bartonella spp. (ssrA)

F: GCTATGGTAATAAATGGACAATGAAATAA

299

[8]b

R: GGCTTCTGTTGCCAGGTG

FAM-ACCCCGCTTAAACCTGCGACG-BHQ1

Candidatus Mycoplasma haemominutum” (16S rRNA gene)

F: TGATCTATTGTKAAAGGCACTTGCT

135

[10]

R: TTAGCCTCYGGTGTTCCTCAA

FAM-TTCAATGTGTAGCGGTGGAATGCGT-BHQ1

Candidatus Mycoplasma turicensis” (16S rRNA gene)

F: AGAGGCGAAGGCGAAAACT

138

[10]

R: ACGTAAGCTACAACGCCGAAA

FAM-CGTAAACGATGGGTATTAGATGTCGGGAT-BHQ1

Feline genomic DNA (28S rRNA)

F: AGCAGGAGGTGTTGGAAGAG

100

[10]

R: AGGGAGAGCCTAAATCAAAGG

Texas Red-TGG CTT GTG GCA GCC AAG TGT-BHQ2

Hepatozoon. spp. (18S rRNA gene)

F: AAACGGCTACCACATNTAAGGA

522

[11]

R: AATACAAATGCCCCCAACTNT

Mycoplasma haemofelis (16S rRNA gene)

F: GTGCTACAATGGCGAACACA

80

[10]

R: TCCTATCCGAACTGAGACGAA

FAM-TGTGTTGCAAACCAGCGATGGT-BHQ1

  1. aThe reverse and probe sequences in the original paper are incorrectly labelled; the correct sequences are cited in this table
  2. bThe reverse primer has been modified compared to the one described in the paper
  3. Abbreviations: F, forward primer sequence; R, reverse primer sequence; FAM, 6-carboxyfluorescein; BHQ, black hole quencher (1 or 2 as indicated)