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. 2019 May 8;20(3):e26. doi: 10.4142/jvs.2019.20.e26

Table 1. Sequences of oligonucleotide primers used to detect putative virulence genes in Enterococcus isolates.

Virulence gene Gene description Primer Sequence (5′ to 3′) Amplicon size (bp)
fsr Regulator of gelE and sprE expression Forward primer CAA GGC ACT ATT TCT TAC TTA GG 1,016
Reverse primer AGC GCA TAA ATC AAC CAA G
efm E. faecium-specific cell wall adhesin Forward primer GAA AAG TTG TCA GTC GTG G 818
Reverse primer TGT TTG TGA CAA ACC TTC ATG
esp Enterococcal surface protein Forward primer CAT CTT TGA TTC TTG GTT GTC G 695
Reverse primer GTT ATA GGT ACG TAT GTT GCA TCA
cylA Hemolysin Forward primer GAG TTA GAT GAA TAT GGT CAT GGT 521
Reverse primer AGA AAC TAG CGA TGT AGG GTA ATA
cad1 Pheromone cAD1 precursor lipoprotein Forward primer TTC CAA AAC TAC GCA CAA CA 423
Reverse primer CTT TTT CAG CAG CAT TCA CTA ATT
ace Collagen-binding cell wall protein Forward primer ATA GAA ACG GAT TTC GGA ACA G 298
Reverse primer TCA AAC TCG GCA AGT GAA ATA T
gelE Gelatinase Forward primer TAT GAC AAT GCT TTT TGG GAT G 208
Reverse primer GCA CCC GAA ATA ATA TAA CCC
asa1 Aggregation substance Forward primer AAC AAG CTT GGT CTG TGT ATC 168
Reverse primer TCT TCC CCT TTC TTG TTA TGA AC