“…Detection of M. ovipneumoniae was conducted with the real‐time PCR method as described by Ziegler et al (; TBL, WADDL, WYL) or conventional PCR as described by McAuliffe et al (; CPW, DBL, TBL, WYL) or by Weiser et al (; DBL, GWL). For detection of lktA broadly among Pasteurellaceae, participating laboratories also used several different PCR methods, including those described by Fisher et al (; GWL, TBL), Fox et al (; CPW, TBL), and Dassanayake et al (; WYL). The WADDL and TBL used a recently developed real‐time Taqman PCR procedure utilizing primers lktAF (5′‐CCGCTTATTTGGTGGTAAAGGC‐3′), lktAR (5′‐CGCCTTGACGGTGAACGAAA‐3′), and probe 5′‐FAM‐TCGATGGCGGTAAAGGCAATGACCT‐MGB‐3′, with the following cycling parameters: 1) hold 50° C, 2 min; 2) hold 95° C, 600 s; 3) 38 cycles of denaturation (95° C, 15 s) and annealing–extension (61° C, 60 s).…”