Protein deficiency reduces efficacy of oral attenuated human rotavirus vaccine in a human infant fecal microbiota transplanted gnotobiotic pig model

Vaccine. 2018 Oct 8;36(42):6270-6281. doi: 10.1016/j.vaccine.2018.09.008. Epub 2018 Sep 12.

Abstract

Background: Low efficacy of rotavirus (RV) vaccines in developing African and Asian countries, where malnutrition is prevalent, remains a major concern and a challenge for global health.

Methods: To understand the effects of protein malnutrition on RV vaccine efficacy, we elucidated the innate, T cell and cytokine immune responses to attenuated human RV (AttHRV) vaccine and virulent human RV (VirHRV) challenge in germ-free (GF) pigs or human infant fecal microbiota (HIFM) transplanted gnotobiotic (Gn) pigs fed protein-deficient or -sufficient bovine milk diets. We also analyzed serum levels of tryptophan (TRP), a predictor of malnutrition, and kynurenine (KYN).

Results: Protein-deficient pigs vaccinated with oral AttHRV vaccine had lower protection rates against diarrhea post-VirHRV challenge and significantly increased fecal virus shedding titers (HIFM transplanted but not GF pigs) compared with their protein-sufficient counterparts. Reduced vaccine efficacy in protein-deficient pigs coincided with altered serum IFN-α, TNF-α, IL-12 and IFN-γ responses to oral AttHRV vaccine and the suppression of multiple innate immune parameters and HRV-specific IFN-γ producing T cells post-challenge. In protein-deficient HIFM transplanted pigs, decreased serum KYN, but not TRP levels were observed throughout the experiment, suggesting an association between the altered TRP metabolism and immune responses.

Conclusion: Collectively, our findings confirm the negative effects of protein deficiency, which were exacerbated in the HIFM transplanted pigs, on innate, T cell and cytokine immune responses to HRV and on vaccine efficacy, as well as on TRP-KYN metabolism.

Keywords: Innate immunity; Malnutrition; Microbiota; Rotavirus; T cell; Vaccine.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Feces / microbiology*
  • Germ-Free Life*
  • Humans
  • Infant
  • Microbiota / immunology
  • Protein Deficiency / complications*
  • Protein Deficiency / immunology
  • Protein Deficiency / metabolism
  • Rotavirus / immunology
  • Rotavirus / pathogenicity
  • Rotavirus Vaccines / therapeutic use
  • Swine
  • Tryptophan / metabolism
  • Vaccines, Attenuated / therapeutic use*

Substances

  • Rotavirus Vaccines
  • Vaccines, Attenuated
  • Tryptophan