Skip to main content

Table 1 Target pathogens, molecular method, target genes and primers used in this study

From: Ticks are more suitable than red foxes for monitoring zoonotic tick-borne pathogens in northeastern Italy

Target

Method

Gene

Primer

Amplicon size (bp)

Reference

B. burgdorferi (s.l.)

Traditional PCR

Flagellin

FLA1; FLA2

482

[51]

Candidatus N. mikurensis”

Traditional PCR

groEL

NM-350s (5'-GTG TAA TGA CAA AGT TGG TGA TGG-3'); NM-1152as

802

This study; [52]

A. phagocytophilum

SYBR green rPCR

msp2

msp2-3f ; msp2-3r

334

[53]

Rickettsia spp.

SYBR green rPCR

OmpB

rompB OFm; rompB ORm

489

[54]

Babesia spp.

SYBR green rPCR

18S rRNA

BJ1; BN2

411–452

[55]

DNA extraction control

Traditional PCR

18S rRNA

18SU; 18SD

488

[37]

TBE virus

TaqMan rRT-PCR

3' non-coding region

F-TBE 1; R-TBE 1 TBE-Probe-WT

67

[38]

RNA extraction control

TaqMan rRT-PCR

16S rRNA

F-16sIxodes; R-16sIxodes; 16s-Ixodes-Probe

97

[38]