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.
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Authors | Arshiya Banu, Alistair J Lax, Agamemnon E Grigoriadis |
Journal | International journal of molecular sciences
(Int J Mol Sci)
Vol. 21
Issue 8
(Apr 15 2020)
ISSN: 1422-0067 [Electronic] Switzerland |
PMID | 32326543
(Publication Type: Journal Article)
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Chemical References |
- Bacterial Proteins
- Bacterial Toxins
- Pasteurella multocida toxin
- Recombinant Proteins
- beta Catenin
- GTP-Binding Protein alpha Subunits, Gq-G11
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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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