Abstract:
Fish disease surveillance methods can be complicated and time consuming, which limits their value for timely intervention strategies on aquaculture farms. Novel molecular-based assays using droplet digital Polymerase Chain Reaction (ddPCR) can produce immediate results and enable high sample throughput with the ability to multiplex several targets using different fluorescent dyes. A ddPCR tetraplex assay was developed for priority salmon diseases for farmers in New Zealand including New Zealand <i>Rickettsia</i>-like organism 1 (NZ-RLO1), NZ-RLO2, <i>Tenacibaculum maritimum</i>, and <i>Yersinia ruckeri</i>. The limit of detection in singleplex and tetraplex assays was reached for most targets at 10<sup>-9</sup> ng/μl with, respectively, NZ-RLO1 = 0.931 and 0.14 copies/μl, NZ-RLO2 = 0.162 and 0.21 copies/μl, <i>T. maritimum =</i> 0.345 and 0.93 copies/μl, while the limit of detection for <i>Y. ruckeri</i> was 10<sup>-8</sup> with 1.0 copies/μl and 0.7 copies/μl. While specificity of primers was demonstrated in previous studies, we detected cross-reactivity of <i>T. maritimum</i> with some strains of <i>Tenacibaculum dicentrarchi</i> and <i>Y. ruckeri</i> with <i>Serratia liquefaciens</i>, respectively. The tetraplex assay was applied as part of a commercial fish disease surveillance program in New Zealand for 1 year to demonstrate the applicability of tetraplex tools for the salmonid aquaculture industry.