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Examining the safety of respiratory and intravenous inoculation of Bdellovibrio bacteriovorus and Micavibrio aeruginosavorus in a mouse model

Bdellovibrio spp. and Micavibrio spp. are Gram-negative predators that feed on other Gram-negative bacteria, making predatory bacteria potential alternatives to antibiotics for treating multi-drug resistant infections. While the ability of predatory bacteria to control bacterial infections in vitro...

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Autores principales: Shatzkes, Kenneth, Chae, Richard, Tang, Chi, Ramirez, Gregory C., Mukherjee, Somdatta, Tsenova, Liana, Connell, Nancy D., Kadouri, Daniel E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528228/
https://www.ncbi.nlm.nih.gov/pubmed/26250699
http://dx.doi.org/10.1038/srep12899
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author Shatzkes, Kenneth
Chae, Richard
Tang, Chi
Ramirez, Gregory C.
Mukherjee, Somdatta
Tsenova, Liana
Connell, Nancy D.
Kadouri, Daniel E.
author_facet Shatzkes, Kenneth
Chae, Richard
Tang, Chi
Ramirez, Gregory C.
Mukherjee, Somdatta
Tsenova, Liana
Connell, Nancy D.
Kadouri, Daniel E.
author_sort Shatzkes, Kenneth
collection PubMed
description Bdellovibrio spp. and Micavibrio spp. are Gram-negative predators that feed on other Gram-negative bacteria, making predatory bacteria potential alternatives to antibiotics for treating multi-drug resistant infections. While the ability of predatory bacteria to control bacterial infections in vitro is well documented, the in vivo effect of predators on a living host has yet to be extensively examined. In this study, respiratory and intravenous inoculations were used to determine the effects of predatory bacteria in mice. We found no reduction in mouse viability after intranasal or intravenous inoculation of B. bacteriovorus 109J, HD100 or M. aeruginosavorus. Introducing predators into the respiratory tract of mice provoked a modest inflammatory response at 1 hour post-exposure, but was not sustained at 24 hours, as measured by RT-qPCR and ELISA. Intravenous injection caused an increase of IL-6 in the kidney and spleen, TNF in the liver and CXCL-1/KC in the blood at 3 hours post-exposure, returning to baseline levels by 18 hours. Histological analysis of tissues showed no pathological changes due to predatory bacteria. Furthermore, qPCR detected predators were cleared from the host quickly and efficiently. This work addresses some of the safety concerns regarding the potential use of predatory bacteria as a live antibiotic.
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spelling pubmed-45282282015-08-07 Examining the safety of respiratory and intravenous inoculation of Bdellovibrio bacteriovorus and Micavibrio aeruginosavorus in a mouse model Shatzkes, Kenneth Chae, Richard Tang, Chi Ramirez, Gregory C. Mukherjee, Somdatta Tsenova, Liana Connell, Nancy D. Kadouri, Daniel E. Sci Rep Article Bdellovibrio spp. and Micavibrio spp. are Gram-negative predators that feed on other Gram-negative bacteria, making predatory bacteria potential alternatives to antibiotics for treating multi-drug resistant infections. While the ability of predatory bacteria to control bacterial infections in vitro is well documented, the in vivo effect of predators on a living host has yet to be extensively examined. In this study, respiratory and intravenous inoculations were used to determine the effects of predatory bacteria in mice. We found no reduction in mouse viability after intranasal or intravenous inoculation of B. bacteriovorus 109J, HD100 or M. aeruginosavorus. Introducing predators into the respiratory tract of mice provoked a modest inflammatory response at 1 hour post-exposure, but was not sustained at 24 hours, as measured by RT-qPCR and ELISA. Intravenous injection caused an increase of IL-6 in the kidney and spleen, TNF in the liver and CXCL-1/KC in the blood at 3 hours post-exposure, returning to baseline levels by 18 hours. Histological analysis of tissues showed no pathological changes due to predatory bacteria. Furthermore, qPCR detected predators were cleared from the host quickly and efficiently. This work addresses some of the safety concerns regarding the potential use of predatory bacteria as a live antibiotic. Nature Publishing Group 2015-08-07 /pmc/articles/PMC4528228/ /pubmed/26250699 http://dx.doi.org/10.1038/srep12899 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Shatzkes, Kenneth
Chae, Richard
Tang, Chi
Ramirez, Gregory C.
Mukherjee, Somdatta
Tsenova, Liana
Connell, Nancy D.
Kadouri, Daniel E.
Examining the safety of respiratory and intravenous inoculation of Bdellovibrio bacteriovorus and Micavibrio aeruginosavorus in a mouse model
title Examining the safety of respiratory and intravenous inoculation of Bdellovibrio bacteriovorus and Micavibrio aeruginosavorus in a mouse model
title_full Examining the safety of respiratory and intravenous inoculation of Bdellovibrio bacteriovorus and Micavibrio aeruginosavorus in a mouse model
title_fullStr Examining the safety of respiratory and intravenous inoculation of Bdellovibrio bacteriovorus and Micavibrio aeruginosavorus in a mouse model
title_full_unstemmed Examining the safety of respiratory and intravenous inoculation of Bdellovibrio bacteriovorus and Micavibrio aeruginosavorus in a mouse model
title_short Examining the safety of respiratory and intravenous inoculation of Bdellovibrio bacteriovorus and Micavibrio aeruginosavorus in a mouse model
title_sort examining the safety of respiratory and intravenous inoculation of bdellovibrio bacteriovorus and micavibrio aeruginosavorus in a mouse model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528228/
https://www.ncbi.nlm.nih.gov/pubmed/26250699
http://dx.doi.org/10.1038/srep12899
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