Commercial Vaccines Do Not Confer Protection against Two Genogroups of Piscirickettsia salmonis, LF-89 and EM-90, in Atlantic Salmon

Biology (Basel). 2022 Jun 30;11(7):993. doi: 10.3390/biology11070993.

Abstract

In Atlantic salmon, vaccines have failed to control and prevent Piscirickettsiosis, for reasons that remain elusive. In this study, we report the efficacy of two commercial vaccines developed with the Piscirickettsia salmonis isolates AL100005 and AL 20542 against another two genogroups which are considered highly and ubiquitously prevalent in Chile: LF-89 and EM-90. Two cohabitation trials were performed to mimic field conditions and vaccine performance: (1) post-smolt fish were challenged with a single infection of LF-89, (2) adults were coinfected with EM-90, and a low level coinfection of sea lice. In the first trial, the vaccine delayed smolt mortalities by two days; however, unvaccinated and vaccinated fish did not show significant differences in survival (unvaccinated: 60.3%, vaccinated: 56.7%; p = 0.28). In the second trial, mortality started three days later for vaccinated fish than unvaccinated fish. However, unvaccinated and vaccinated fish did not show significant differences in survival (unvaccinated: 64.6%, vaccinated: 60.2%, p = 0.58). Thus, we found no evidence that the evaluated vaccines confer effective protection against the genogroups LF-89 and EM-90 of P. salmonis with estimated relative survival proportions (RPSs) of -9% and -12%, respectively. More studies are necessary to evaluate whether pathogen heterogeneity is a key determinant of the lack of vaccine efficacy against P. salmonis.

Keywords: Piscirickettsiosis; Salmo salar; bacterin vaccine; cohabitation; live attenuated vaccine; monovalent vaccine; pentavalent vaccine; sea lice; vaccine efficacy.

Grants and funding

This research study was funded by CONICYT-Chile through the project FONDECYT No. 1140772 awarded to J.A.G. and P.C. Furthermore, J.A.G. was supported by the Cooperative Research Program Fellowships of OECD—PCI 2015-CONICYT. C.F. was supported by PUCV and CONICYT-Chile through a Postdoctoral fellowship (Proyecto VRIEA-PUCV Postdoctorado and FONDECYT No. 3170744). D.T. was supported by ANID-Chile through a Postdoctoral fellowship (Fondecyt No. 3210502). B.M.-L. was supported by the Postdoctoral program from the National Research and Development Agency of Chile (ANID-Chile No. 74200139).