Streptococcus agalactiae impairs cerebral bioenergetics in experimentally infected silver catfish

Microb Pathog. 2017 Oct:111:28-32. doi: 10.1016/j.micpath.2017.08.013. Epub 2017 Aug 12.

Abstract

It is becoming evident that bacterial infectious diseases affect brain energy metabolism, where alterations of enzymatic complexes of the mitochondrial respiratory chain and creatine kinase (CK) lead to an impairment of cerebral bioenergetics which contribute to disease pathogenesis in the central nervous system (CNS). Based on this evidence, the aim of this study was to evaluate whether alterations in the activity of complex IV of the respiratory chain and CK contribute to impairment of cerebral bioenergetics during Streptococcus agalactiae infection in silver catfish (Rhamdia quelen). The activity of complex IV of the respiratory chain in brain increased, while the CK activity decreased in infected animals compared to uninfected animals. Brain histopathology revealed inflammatory demyelination, gliosis of the brain and intercellular edema in infected animals. Based on this evidence, S. agalactiae infection causes an impairment in cerebral bioenergetics through the augmentation of complex IV activity, which may be considered an adaptive response to maintain proper functioning of the electron respiratory chain, as well as to ensure ongoing electron flow through the electron transport chain. Moreover, inhibition of cerebral CK activity contributes to lower availability of ATP, contributing to impairment of cerebral energy homeostasis. In summary, these alterations contribute to disease pathogenesis linked to the CNS.

Keywords: Adenosine triphosphate; Brain; Energy metabolism; Group B streptococcus.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Brain / metabolism*
  • Brain / microbiology
  • Brain / pathology
  • Brazil
  • Catfishes / microbiology
  • Central Nervous System / metabolism
  • Central Nervous System / microbiology
  • Central Nervous System / pathology
  • Creatine Kinase / metabolism
  • Creatine Kinase, Mitochondrial Form / metabolism*
  • Demyelinating Diseases
  • Disease Models, Animal
  • Electron Transport / physiology*
  • Electron Transport Complex IV / metabolism*
  • Energy Metabolism*
  • Fish Diseases / enzymology
  • Fish Diseases / microbiology
  • Fish Diseases / pathology
  • Gliosis / pathology
  • Homeostasis
  • Humans
  • Neutrophils / microbiology
  • Neutrophils / pathology
  • Streptococcal Infections / metabolism*
  • Streptococcal Infections / microbiology
  • Streptococcus agalactiae / pathogenicity*

Substances

  • Adenosine Triphosphate
  • Electron Transport Complex IV
  • Creatine Kinase
  • Creatine Kinase, Mitochondrial Form