The effects of sugar in drinking water on Streptococcus pyogenes colonisation in a murine nasopharyngeal infection

Farina Nor Hashimi1,2, Julie Bennett1,3, Michael G Baker3,2

  • 1Department of Molecular Medicine and Pathology, School of Medical Sciences, University of Auckland, Private Bag 92019, Auckland, 1023, New Zealand.

Scientific Reports
|October 22, 2022
PubMed

Insights

High sugar intake may increase the risk of acute rheumatic fever by promoting Streptococcus pyogenes growth. This study found increased bacterial load in mice fed sucrose, suggesting a biological link.

Area of Science:

  • Microbiology
  • Immunology
  • Nutritional Science

Background:

  • Acute rheumatic fever (ARF) is an autoimmune disease linked to Streptococcus pyogenes infections.
  • Previous epidemiological studies suggest a correlation between sugar-sweetened beverage consumption and ARF risk.
  • The underlying biological mechanisms for this association remain unclear.

Purpose of the Study:

  • To investigate a potential biological basis for the association between sugar-sweetened beverage intake and ARF.
  • To determine if sucrose consumption influences Streptococcus pyogenes nasopharyngeal colonization in a mouse model.

Main Methods:

  • Utilized a mouse model to study Streptococcus pyogenes nasopharyngeal colonization.
  • Implemented a dietary intervention involving sucrose in drinking water post-infection.
  • Quantified bacterial load in the nasopharynx.

Main Results:

  • Mice receiving sucrose drinking water exhibited an increased bacterial load in the nasopharynx after S. pyogenes infection.
  • This suggests that high sucrose intake supports the growth and/or survival of Streptococcus pyogenes.
  • The findings provide evidence for a direct biological link between sucrose and bacterial colonization.

Conclusions:

  • High sucrose intake may promote Streptococcus pyogenes colonization in the nasopharynx.
  • This mechanism could contribute to the observed association between sugar-sweetened beverage consumption and acute rheumatic fever risk in humans.
  • Further research is warranted to confirm these findings and explore therapeutic implications.

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