“…For virF, ail, inv, ymoA, ystA, ystB and myfA, the primers and cycling parameters described by Bhagat and Virdi (2007) were used. For rovA the protocols defined by Divya and Varadaraj (2011) and for yadA the protocols by Thoerner et al (2003) were used (Table 1). Two microliters of template was added to 28 µL of reaction mixture consisting of 1 X× PCR buffer (Solis BioDyne, Tartu, Estonia), 2.5 mM MgCl 2 (Solis BioDyne, Tartu, Estonia), 200 µM dNTPS (Roche, Rotkreuz, Switzerland), 0.25 µL FIREPol DNA polymerase (Solis BioDyne, Tartu, Estonia) and primers (Microsynth, Balgach, Switzerland) at a final concentration of 0.25 µM.…”