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Characterization of Coxiella burnetii Dugway Strain Host-Pathogen Interactions In Vivo

Coxiella burnetii is a Gram-negative, intracellular bacterium that causes the zoonosis Q fever. Among the many natural isolates of C. burnetii recovered from various sources, the Dugway group exhibits unique genetic characteristics, including the largest C. burnetii genomes. These strains were isola...

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Autores principales: Tesfamariam, Mahelat, Binette, Picabo, Cockrell, Diane, Beare, Paul A., Heinzen, Robert A., Shaia, Carl, Long, Carrie Mae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692954/
https://www.ncbi.nlm.nih.gov/pubmed/36422331
http://dx.doi.org/10.3390/microorganisms10112261
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author Tesfamariam, Mahelat
Binette, Picabo
Cockrell, Diane
Beare, Paul A.
Heinzen, Robert A.
Shaia, Carl
Long, Carrie Mae
author_facet Tesfamariam, Mahelat
Binette, Picabo
Cockrell, Diane
Beare, Paul A.
Heinzen, Robert A.
Shaia, Carl
Long, Carrie Mae
author_sort Tesfamariam, Mahelat
collection PubMed
description Coxiella burnetii is a Gram-negative, intracellular bacterium that causes the zoonosis Q fever. Among the many natural isolates of C. burnetii recovered from various sources, the Dugway group exhibits unique genetic characteristics, including the largest C. burnetii genomes. These strains were isolated during 1954–1958 from wild rodents from the Utah, USA desert. Despite retaining phase I lipopolysaccharide and the type 4B secretion system, two critical virulence factors, avirulence has been reported in a guinea pig infection model. Using guinea pig models, we evaluated the virulence, whole-cell vaccine (WCV) efficacy, and post-vaccination hypersensitivity (PVH) potential of a representative Dugway strain. Consistent with prior reports, Dugway appeared to be highly attenuated compared to a virulent strain. Indeed, Dugway-infected animals showed similarly low levels of fever, body weight loss, and splenomegaly like Nine Mile II-infected animals. When compared to a human Q fever vaccine, QVax(®), Dugway WCV exhibited analogous protection against a heterologous Nine Mile I challenge. PVH was investigated in a skin-testing model which revealed significantly decreased maximum erythema in Dugway Δdot/icm WCV-skin-tested animals compared to that of QVax(®). These data provide insight into this unique bacterial strain and implicate its potential use as a mutated WCV candidate.
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spelling pubmed-96929542022-11-26 Characterization of Coxiella burnetii Dugway Strain Host-Pathogen Interactions In Vivo Tesfamariam, Mahelat Binette, Picabo Cockrell, Diane Beare, Paul A. Heinzen, Robert A. Shaia, Carl Long, Carrie Mae Microorganisms Article Coxiella burnetii is a Gram-negative, intracellular bacterium that causes the zoonosis Q fever. Among the many natural isolates of C. burnetii recovered from various sources, the Dugway group exhibits unique genetic characteristics, including the largest C. burnetii genomes. These strains were isolated during 1954–1958 from wild rodents from the Utah, USA desert. Despite retaining phase I lipopolysaccharide and the type 4B secretion system, two critical virulence factors, avirulence has been reported in a guinea pig infection model. Using guinea pig models, we evaluated the virulence, whole-cell vaccine (WCV) efficacy, and post-vaccination hypersensitivity (PVH) potential of a representative Dugway strain. Consistent with prior reports, Dugway appeared to be highly attenuated compared to a virulent strain. Indeed, Dugway-infected animals showed similarly low levels of fever, body weight loss, and splenomegaly like Nine Mile II-infected animals. When compared to a human Q fever vaccine, QVax(®), Dugway WCV exhibited analogous protection against a heterologous Nine Mile I challenge. PVH was investigated in a skin-testing model which revealed significantly decreased maximum erythema in Dugway Δdot/icm WCV-skin-tested animals compared to that of QVax(®). These data provide insight into this unique bacterial strain and implicate its potential use as a mutated WCV candidate. MDPI 2022-11-15 /pmc/articles/PMC9692954/ /pubmed/36422331 http://dx.doi.org/10.3390/microorganisms10112261 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tesfamariam, Mahelat
Binette, Picabo
Cockrell, Diane
Beare, Paul A.
Heinzen, Robert A.
Shaia, Carl
Long, Carrie Mae
Characterization of Coxiella burnetii Dugway Strain Host-Pathogen Interactions In Vivo
title Characterization of Coxiella burnetii Dugway Strain Host-Pathogen Interactions In Vivo
title_full Characterization of Coxiella burnetii Dugway Strain Host-Pathogen Interactions In Vivo
title_fullStr Characterization of Coxiella burnetii Dugway Strain Host-Pathogen Interactions In Vivo
title_full_unstemmed Characterization of Coxiella burnetii Dugway Strain Host-Pathogen Interactions In Vivo
title_short Characterization of Coxiella burnetii Dugway Strain Host-Pathogen Interactions In Vivo
title_sort characterization of coxiella burnetii dugway strain host-pathogen interactions in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9692954/
https://www.ncbi.nlm.nih.gov/pubmed/36422331
http://dx.doi.org/10.3390/microorganisms10112261
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