TABLE 2.

Primer sequences and amplification cycling conditions for the different PCR-based genomic DNA fingerprints

Primer set	Primer	Nucleotide sequence	References	Amplification cycling conditions
ERIC	ERIC-1R ERIC-2	5′-ATG TAA GCT CCT GGG GAT TCA C-3′ 5′-AAG TAA GTG ACT GGG GTG AGC G-3′	1, 19, 30	Initial denaturation 95°C for 2 min, 92°C for 30 s; 35 cycles of 92°C for 30 s, 50°C for 80 s, and 68°C for 200 s, final extension at 68°C for 8 min, final 4°C soak
REP	REP 1R DT REP 2-DT	5′-III ICG ICG ICA TCI GGC-3′ 5′-ICG ICT TAT CIG GGC TAC-3′	1, 30	Initial denaturation at 95°C for 2 min, 92°C for 30 s, 35 cycles of 92°C for 30 s, 38°C for 80 s, and 68°C for 200 s, final extension at 68°C for 8 min, final 4°C soak
BOXAIR		5′-CTA CGG CAA GGC GAC GCT GAC G-3′	2, 24	Initial denaturation 95°C for 2 min, 94°C for 3 s; 30 cycles of 92°C for 30 s, 50°C for 1 min, and 65°C for 8 min; final extension at 68°C for 8 min, final 4°C soak