“…Among 386 S. caprae isolates reported in the literature, 17 of 22 were well identified by API Staph [7,9,13,15,18,20,23,40], [8,10,14,[18][19][20]23,38,41], 64 of 85 were well identified by Vitek [3,16,29,30,39,41], none of 15 were well identified by Microscan [3,29], nine were well identified by Phoenik [30], five of eight were well identified by 16S PCR (plus two false positives) [6,13,27,41], seven were well identified by soda gene sequencing [6,22], four were well-identified by tuf gene sequencing [6,41], 65 of 74 were well identified by ribotyping 16S-23S printer [4,8,23,40], 17 of 19 were well identified by internal transcribed spacer PCR [12,42], 17 of 19 were well identified by multiplex-PCR [32], four of five were well identified by pulsed-field gel electrophoresis [15], one was well identified by rpoB gene sequencing [31], one was well identified by autolysin gene sequencing [43], and 88 of 89 were w...…”