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In Vivo Targets of Pasteurella Multocida Toxin

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—G(q/11), G(12/...

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Autores principales: Banu, Arshiya, Lax, Alistair J., Grigoriadis, Agamemnon E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215291/
https://www.ncbi.nlm.nih.gov/pubmed/32326543
http://dx.doi.org/10.3390/ijms21082739
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author Banu, Arshiya
Lax, Alistair J.
Grigoriadis, Agamemnon E.
author_facet Banu, Arshiya
Lax, Alistair J.
Grigoriadis, Agamemnon E.
author_sort Banu, Arshiya
collection PubMed
description 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—G(q/11), G(12/13), and G(i/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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spelling pubmed-72152912020-05-18 In Vivo Targets of Pasteurella Multocida Toxin Banu, Arshiya Lax, Alistair J. Grigoriadis, Agamemnon E. Int J Mol Sci Article 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—G(q/11), G(12/13), and G(i/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. MDPI 2020-04-15 /pmc/articles/PMC7215291/ /pubmed/32326543 http://dx.doi.org/10.3390/ijms21082739 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Banu, Arshiya
Lax, Alistair J.
Grigoriadis, Agamemnon E.
In Vivo Targets of Pasteurella Multocida Toxin
title In Vivo Targets of Pasteurella Multocida Toxin
title_full In Vivo Targets of Pasteurella Multocida Toxin
title_fullStr In Vivo Targets of Pasteurella Multocida Toxin
title_full_unstemmed In Vivo Targets of Pasteurella Multocida Toxin
title_short In Vivo Targets of Pasteurella Multocida Toxin
title_sort in vivo targets of pasteurella multocida toxin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215291/
https://www.ncbi.nlm.nih.gov/pubmed/32326543
http://dx.doi.org/10.3390/ijms21082739
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