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In Vivo Targets of Pasteurella Multocida Toxin.

Abstract
Many Pasteurella multocida strains are carried as commensals, while some cause disease in animals and humans. Some type D strains cause atrophic rhinitis in pigs, where the causative agent is known to be the Pasteurella multocida toxin (PMT). PMT activates three families of G-proteins-Gq/11, G12/13, and Gi/o-leading to cellular mitogenesis and other sequelae. The effects of PMT on whole animals in vivo have been investigated previously, but only at the level of organ-specific pathogenesis. We report here the first study to screen all the organs targeted by the toxin by using the QE antibody that recognizes only PMT-modified G-proteins. Under our experimental conditions, short-term treatment of PMT is shown to have multiple in vivo targets, demonstrating G-alpha protein modification, stimulation of proliferation markers and expression of active β-catenin in a tissue- and cell-specific manner. This highlights the usefulness of PMT as an important tool for dissecting the specific roles of different G-alpha proteins in vivo.
AuthorsArshiya Banu, Alistair J Lax, Agamemnon E Grigoriadis
JournalInternational journal of molecular sciences (Int J Mol Sci) Vol. 21 Issue 8 (Apr 15 2020) ISSN: 1422-0067 [Electronic] Switzerland
PMID32326543 (Publication Type: Journal Article)
Chemical References
  • Bacterial Proteins
  • Bacterial Toxins
  • Pasteurella multocida toxin
  • Recombinant Proteins
  • beta Catenin
  • GTP-Binding Protein alpha Subunits, Gq-G11
Topics
  • Animals
  • Bacterial Proteins (genetics, toxicity)
  • Bacterial Toxins (genetics, toxicity)
  • Cell Proliferation (drug effects)
  • Endometrium (drug effects, metabolism)
  • Female
  • GTP-Binding Protein alpha Subunits, Gq-G11 (metabolism)
  • Immunohistochemistry
  • Mice
  • Pasteurella multocida (metabolism)
  • Recombinant Proteins (genetics, metabolism)
  • Signal Transduction (drug effects)
  • Spleen (drug effects, metabolism)
  • Thymus Gland (drug effects, metabolism)
  • Uterus (drug effects, metabolism)
  • beta Catenin (metabolism)

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