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Early and late gut microbiota signatures of stroke in high salt-fed stroke-prone spontaneously hypertensive rats

  • Silvia Bencivenni,
  • Sara Roggiani,
  • Augusta Zannoni,
  • Gabriele Conti,
  • Marco Fabbrini,
  • Maria Cotugno,
  • Rosita Stanzione,
  • Donatella Pietrangelo,
  • Margherita Litterio,
  • Maurizio Forte,
  • Carla Letizia Busceti,
  • Francesco Fornai,
  • Massimo Volpe,
  • Silvia Turroni,
  • Patrizia Brigidi,
  • Monica Forni,
  • Speranza Rubattu,
  • Federica D’Amico

摘要

The high salt-fed stroke-prone spontaneously hypertensive rat (SHRSP) is a suitable tool to study the mechanisms underlying stroke pathogenesis. Salt intake modifies the gut microbiota (GM) in rats and humans and alterations of the GM have previously been associated with increased stroke occurrence. We aimed to characterize the GM profile in SHRSPs fed a high-salt stroke-permissive diet (Japanese diet, JD), compared to the closely related stroke-resistant control (SHRSR), to identify possible changes associated with stroke occurrence. SHRSPs and SHRSRs were fed a regular diet or JD for 4 weeks (short-term, ST) or a maximum of 10 weeks (long-term, LT). Stroke occurred in SHRSPs on JD-LT, preceded by proteinuria and diarrhoea. The GM of JD-fed SHRSPs underwent early and late compositional changes compared to SHRSRs. An overrepresentation of Streptococcaceae and an underrepresentation of Lachnospiraceae were observed in SHRSPs JD-ST, while in SHRSPs JD-LT short-chain fatty acid producers, e.g. Lachnobacterium and Faecalibacterium, decreased and pathobionts such as Coriobacteriaceae and Desulfovibrio increased. Occludin gene expression behaved differently in SHRSPs and SHRSRs. Calprotectin levels were unchanged. In conclusion, the altered GM in JD-fed SHRSPs may be detrimental to gut homeostasis and contribute to stroke occurrence.