Streptococcus mutans supernatant affects the virulence of Candida albicans

Maíra Terra Garcia1, Jéssica Diane Dos Santos2, Paulo Henrique Fonseca do Carmo2

  • 1Department of Biosciences and Oral Diagnosis, São Paulo State University (UNESP), Institute of Science and Technology, Av. Engenheiro Francisco José Longo, 777, São José dos Campos, SP, 12245-000, Brazil. maa.terra@hotmail.com.

Insights

Metabolites from Streptococcus mutans (SM-S) reduce Candida albicans virulence. Pretreated C. albicans showed inhibited growth, adhesion, and biofilm formation, leading to reduced infection in Galleria mellonella larvae.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Antimicrobial Research

Background:

  • Candida albicans is a major human pathogen causing candidiasis.
  • Limited antifungal agents necessitate novel therapeutic strategies.
  • Streptococcus mutans metabolites show potential antifungal activity.

Purpose of the Study:

  • To investigate the impact of Streptococcus mutans supernatant (SM-S) on Candida albicans virulence factors.
  • To assess the modified virulence and infectivity of C. albicans surviving SM-S pretreatment.
  • To evaluate the potential of SM-S in developing new candidiasis therapies.

Main Methods:

  • Streptococcus mutans supernatant (SM-S) was prepared.
  • Candida albicans cells were pretreated with SM-S for 24 hours.
  • In vitro assays evaluated hyphal growth, adhesion, biofilm formation, and proteolytic activity.
  • In vivo assays used Galleria mellonella larvae to assess infectivity and hemocyte response.

Main Results:

  • SM-S pretreatment significantly inhibited C. albicans hyphal growth, altered adhesion, and impaired biofilm formation.
  • Proteolytic activity of C. albicans remained unaffected by SM-S.
  • In vivo, pretreated C. albicans showed reduced infectivity in G. mellonella.
  • A higher number of circulating hemocytes was observed in G. mellonella infected with pretreated C. albicans.

Conclusions:

  • Streptococcus mutans supernatant (SM-S) effectively inhibits key virulence factors of Candida albicans.
  • SM-S pretreatment reduces the pathogenicity of C. albicans in a G. mellonella infection model.
  • These findings suggest SM-S as a promising candidate for novel candidiasis therapeutic strategies.