PLoS Biology (Dec 2019)

Human sperm displays rapid responses to diet.

  • Daniel Nätt,
  • Unn Kugelberg,
  • Eduard Casas,
  • Elizabeth Nedstrand,
  • Stefan Zalavary,
  • Pontus Henriksson,
  • Carola Nijm,
  • Julia Jäderquist,
  • Johanna Sandborg,
  • Eva Flinke,
  • Rashmi Ramesh,
  • Lovisa Örkenby,
  • Filip Appelkvist,
  • Thomas Lingg,
  • Nicola Guzzi,
  • Cristian Bellodi,
  • Marie Löf,
  • Tanya Vavouri,
  • Anita Öst

DOI
https://doi.org/10.1371/journal.pbio.3000559
Journal volume & issue
Vol. 17, no. 12
p. e3000559

Abstract

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The global rise in obesity and steady decline in sperm quality are two alarming trends that have emerged during recent decades. In parallel, evidence from model organisms shows that paternal diet can affect offspring metabolic health in a process involving sperm tRNA-derived small RNA (tsRNA). Here, we report that human sperm are acutely sensitive to nutrient flux, both in terms of sperm motility and changes in sperm tsRNA. Over the course of a 2-week diet intervention, in which we first introduced a healthy diet followed by a diet rich in sugar, sperm motility increased and stabilized at high levels. Small RNA-seq on repeatedly sampled sperm from the same individuals revealed that tsRNAs were up-regulated by eating a high-sugar diet for just 1 week. Unsupervised clustering identified two independent pathways for the biogenesis of these tsRNAs: one involving a novel class of fragments with specific cleavage in the T-loop of mature nuclear tRNAs and the other exclusively involving mitochondrial tsRNAs. Mitochondrial involvement was further supported by a similar up-regulation of mitochondrial rRNA-derived small RNA (rsRNA). Notably, the changes in sugar-sensitive tsRNA were positively associated with simultaneous changes in sperm motility and negatively associated with obesity in an independent clinical cohort. This rapid response to a dietary intervention on tsRNA in human sperm is attuned with the paternal intergenerational metabolic responses found in model organisms. More importantly, our findings suggest shared diet-sensitive mechanisms between sperm motility and the biogenesis of tsRNA, which provide novel insights about the interplay between nutrition and male reproductive health.