pdh modulate virulence through reducing stress tolerance and biofilm formation of Streptococcus suis serotype 2

Virulence. 2019 Dec;10(1):588-599. doi: 10.1080/21505594.2019.1631661.

Abstract

Streptococcus suis serotype 2 (S. suis 2) is a zoonotic pathogen. It causes meningitis, arthritis, pneumonia and sepsis in pigs, leading to extremely high mortality, which seriously affects public health and the development of the pig industry. Pyruvate dehydrogenase (PDH) is an important sugar metabolism enzyme that is widely present in microorganisms, mammals and higher plants. It catalyzes the irreversible oxidative decarboxylation of pyruvate to acetyl-CoA and reduces NAD+ to NADH. In this study, we found that the virulence of the S. suis ZY05719 sequence type 7 pdh deletion strain (Δpdh) was significantly lower than the wild-type strain (WT) in the mouse infection model. The distribution of viable bacteria in the blood and organs of mice infected with the Δpdh was significantly lower than those infected with WT. Bacterial survival rates were reduced in response to temperature stress, salt stress and oxidative stress. Additionally, compared to WT, the ability to adhere to and invade PK15 cells, biofilm formation and stress resistance of Δpdh were significantly reduced. Moreover, real-time PCR results showed that pdh deletion reduced the expression of multiple adhesion-related genes. However, there was no significant difference in the correlation biological analysis between the complemented strain (CΔpdh) and WT. Moreover, the survival rate of Δpdh in RAW264.7 macrophages was significantly lower than that of the WT strain. This study shows that PDH is involved in the pathogenesis of S. suis 2 and reduction in virulence of Δpdh may be related to the decreased ability to resist stress of the strain.

Keywords: Streptococcus suis; adhesion; biofilm formation; pyruvate dehydrogenase; stress; virulence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins / genetics
  • Biofilms / growth & development*
  • Female
  • Gene Expression Regulation, Bacterial
  • Mice
  • Oxidative Stress*
  • Pyruvate Dehydrogenase Complex / genetics*
  • Serogroup
  • Specific Pathogen-Free Organisms
  • Streptococcus suis / enzymology
  • Streptococcus suis / genetics*
  • Streptococcus suis / pathogenicity*
  • Virulence

Substances

  • Bacterial Proteins
  • Pyruvate Dehydrogenase Complex

Grants and funding

This work was supported by the National Key Research and Development Program of China (2018YFD0500100), the National Natural Science Foundation of China (31772761, 31540095), the Natural Science Foundation of Henan Province (182300410047, 162300410067).