Animals (Sep 2022)

Effect of Feeding <i>Saccharomyces cerevisiae boulardii</i> CNCM I-1079 to Sows and Piglets on Piglets’ Immune Response after Vaccination against <i>Actinobacillus pleuropneumoniae</i>

  • Fernando Bravo de Laguna,
  • Carolina Cabrera,
  • Ana Belén González,
  • Clara de Pascual,
  • Francisco José Pallarés,
  • Eric Chevaux,
  • Mathieu Castex,
  • David Saornil,
  • Pierre Lebreton,
  • Guillermo Ramis

DOI
https://doi.org/10.3390/ani12192513
Journal volume & issue
Vol. 12, no. 19
p. 2513

Abstract

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The aim of this study was to assess the effect that feeding Saccharomyces cerevisiae boulardii CNCM I-1079 (LSB) to lactating sows and their progeny has on inflammatory response and mucosal immunity after vaccination against Actinobacillus pleuropneumoniae. Sixty-seven Danbred sows were allotted into two treatments when they entered the farrowing room seven days before the expected farrowing date: control (CON: lactation diet) and LSB (CON + 12 × 109 colony forming units (CFU)/d until weaning). At weaning, piglets were equally allotted into two experimental diets according to sow diet: control (CON: 2-phase post-weaning diets) and LSB (CON + 2 × 109 CFU/kg and 1 × 109 CFU/kg in phases 1 and 2, respectively). The piglets were vaccinated at days 26 and 49 post-weaning. Growth performance and number of IgA producing cells and cytokine’s gene expression in lung, lymph node, and intestine samples at day 70 post-weaning were assessed and analyzed in SPSS Statistics 26: performance with a general linear model with sex, room, sow diet, piglet diet, and their interactions as main effects, and immunity with a Kruskal–Wallis test for k unrelated samples. Piglets from LSB-fed sows displayed a higher average daily gain (ADG; p p p p p Saccharomyces cerevisiae boulardii CNCM I-1079 to sows improved piglet performance during lactation and showed a clear reduction in the inflammatory status of the lungs after vaccination against A. pleuropneumoniae, suggesting that there was a maternal imprinting effect on mucosal protection and a cross-talk between the gut microbiota and the lung.

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