Selective Inhibition of Coxiella burnetii Replication by the Steroid Hormone Progesterone

Infect Immun. 2020 Nov 16;88(12):e00894-19. doi: 10.1128/IAI.00894-19. Print 2020 Nov 16.

Abstract

Coxiella burnetii is a zoonotic bacterial obligate intracellular parasite and the cause of query (Q) fever. During natural infection of female animals, C. burnetii shows tropism for the placenta and is associated with late-term abortion, at which time the pathogen titer in placental tissue can exceed one billion bacteria per gram. During later stages of pregnancy, placental trophoblasts serve as the major source of progesterone, a steroid hormone known to affect the replication of some pathogens. During infection of placenta-derived JEG-3 cells, C. burnetii showed sensitivity to progesterone but not the immediate precursor pregnenolone or estrogen, another major mammalian steroid hormone. Using host cell-free culture, progesterone was determined to have a direct inhibitory effect on C. burnetii replication. Synergy between the inhibitory effect of progesterone and the efflux pump inhibitors verapamil and 1-(1-naphthylmethyl)-piperazine is consistent with a role for efflux pumps in preventing progesterone-mediated inhibition of C. burnetii activity. The sensitivity of C. burnetii to progesterone, but not structurally related molecules, is consistent with the ability of progesterone to influence pathogen replication in progesterone-producing tissues.

Keywords: Coxiella burnetii; axenic; efflux pumps; intracellular replication; progesterone; steroid hormone.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins / chemistry
  • Cell Line
  • Cell Survival / drug effects
  • Coxiella burnetii / drug effects*
  • Coxiella burnetii / growth & development*
  • DNA Replication / drug effects
  • Drug Synergism
  • Escherichia coli Proteins / chemistry
  • Estrogens / pharmacology
  • Ethidium / chemistry
  • Female
  • Host-Pathogen Interactions*
  • Humans
  • Membrane Proteins / chemistry
  • Membrane Transport Proteins / chemistry
  • Membrane Transport Proteins / drug effects
  • Membrane Transport Proteins / metabolism
  • Piperazines / pharmacology
  • Placenta / drug effects
  • Placenta / microbiology*
  • Pregnancy
  • Pregnenolone / pharmacology
  • Progesterone / pharmacology*
  • Protein Kinases / chemistry
  • Verapamil / pharmacology

Substances

  • 1-(1-naphthylmethyl)piperazine
  • Bacterial Proteins
  • EmrB protein, E coli
  • Escherichia coli Proteins
  • Estrogens
  • Membrane Proteins
  • Membrane Transport Proteins
  • MtrD protein, Neisseria gonorrhoeae
  • Piperazines
  • Progesterone
  • Pregnenolone
  • Verapamil
  • Protein Kinases
  • arcB protein, E coli
  • Ethidium