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Elevated Carbon Monoxide in the Exhaled Breath of Mice during a Systemic Bacterial Infection
Blood is the specimen of choice for most laboratory tests for diagnosis and disease monitoring. Sampling exhaled breath is a noninvasive alternative to phlebotomy and has the potential for real-time monitoring at the bedside. Improved instrumentation has advanced breath analysis for several gaseous...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3729689/ https://www.ncbi.nlm.nih.gov/pubmed/23936104 http://dx.doi.org/10.1371/journal.pone.0069802 |
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author | Barbour, Alan G. Hirsch, Charlotte M. Ghalyanchi Langeroudi, Arash Meinardi, Simone Lewis, Eric R. G. Estabragh, Azadeh Shojaee Blake, Donald R. |
author_facet | Barbour, Alan G. Hirsch, Charlotte M. Ghalyanchi Langeroudi, Arash Meinardi, Simone Lewis, Eric R. G. Estabragh, Azadeh Shojaee Blake, Donald R. |
author_sort | Barbour, Alan G. |
collection | PubMed |
description | Blood is the specimen of choice for most laboratory tests for diagnosis and disease monitoring. Sampling exhaled breath is a noninvasive alternative to phlebotomy and has the potential for real-time monitoring at the bedside. Improved instrumentation has advanced breath analysis for several gaseous compounds from humans. However, application to small animal models of diseases and physiology has been limited. To extend breath analysis to mice, we crafted a means for collecting nose-only breath samples from groups and individual animals who were awake. Samples were subjected to gas chromatography and mass spectrometry procedures developed for highly sensitive analysis of trace volatile organic compounds (VOCs) in the atmosphere. We evaluated the system with experimental systemic infections of severe combined immunodeficiency Mus musculus with the bacterium Borrelia hermsii. Infected mice developed bacterial densities of ∼10(7) per ml of blood by day 4 or 5 and in comparison to uninfected controls had hepatosplenomegaly and elevations of both inflammatory and anti-inflammatory cytokines. While 12 samples from individual infected mice on days 4 and 5 and 6 samples from uninfected mice did not significantly differ for 72 different VOCs, carbon monoxide (CO) was elevated in samples from infected mice, with a mean (95% confidence limits) effect size of 4.2 (2.8–5.6), when differences in CO(2) in the breath were taken into account. Normalized CO values declined to the uninfected range after one day of treatment with the antibiotic ceftriaxone. Strongly correlated with CO in the breath were levels of heme oxygenase-1 protein in serum and HMOX1 transcripts in whole blood. These results (i) provide further evidence of the informativeness of CO concentration in the exhaled breath during systemic infection and inflammation, and (ii) encourage evaluation of this noninvasive analytic approach in other various other rodent models of infection and for utility in clinical management. |
format | Online Article Text |
id | pubmed-3729689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37296892013-08-09 Elevated Carbon Monoxide in the Exhaled Breath of Mice during a Systemic Bacterial Infection Barbour, Alan G. Hirsch, Charlotte M. Ghalyanchi Langeroudi, Arash Meinardi, Simone Lewis, Eric R. G. Estabragh, Azadeh Shojaee Blake, Donald R. PLoS One Research Article Blood is the specimen of choice for most laboratory tests for diagnosis and disease monitoring. Sampling exhaled breath is a noninvasive alternative to phlebotomy and has the potential for real-time monitoring at the bedside. Improved instrumentation has advanced breath analysis for several gaseous compounds from humans. However, application to small animal models of diseases and physiology has been limited. To extend breath analysis to mice, we crafted a means for collecting nose-only breath samples from groups and individual animals who were awake. Samples were subjected to gas chromatography and mass spectrometry procedures developed for highly sensitive analysis of trace volatile organic compounds (VOCs) in the atmosphere. We evaluated the system with experimental systemic infections of severe combined immunodeficiency Mus musculus with the bacterium Borrelia hermsii. Infected mice developed bacterial densities of ∼10(7) per ml of blood by day 4 or 5 and in comparison to uninfected controls had hepatosplenomegaly and elevations of both inflammatory and anti-inflammatory cytokines. While 12 samples from individual infected mice on days 4 and 5 and 6 samples from uninfected mice did not significantly differ for 72 different VOCs, carbon monoxide (CO) was elevated in samples from infected mice, with a mean (95% confidence limits) effect size of 4.2 (2.8–5.6), when differences in CO(2) in the breath were taken into account. Normalized CO values declined to the uninfected range after one day of treatment with the antibiotic ceftriaxone. Strongly correlated with CO in the breath were levels of heme oxygenase-1 protein in serum and HMOX1 transcripts in whole blood. These results (i) provide further evidence of the informativeness of CO concentration in the exhaled breath during systemic infection and inflammation, and (ii) encourage evaluation of this noninvasive analytic approach in other various other rodent models of infection and for utility in clinical management. Public Library of Science 2013-07-31 /pmc/articles/PMC3729689/ /pubmed/23936104 http://dx.doi.org/10.1371/journal.pone.0069802 Text en © 2013 Barbour et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Barbour, Alan G. Hirsch, Charlotte M. Ghalyanchi Langeroudi, Arash Meinardi, Simone Lewis, Eric R. G. Estabragh, Azadeh Shojaee Blake, Donald R. Elevated Carbon Monoxide in the Exhaled Breath of Mice during a Systemic Bacterial Infection |
title | Elevated Carbon Monoxide in the Exhaled Breath of Mice during a Systemic Bacterial Infection |
title_full | Elevated Carbon Monoxide in the Exhaled Breath of Mice during a Systemic Bacterial Infection |
title_fullStr | Elevated Carbon Monoxide in the Exhaled Breath of Mice during a Systemic Bacterial Infection |
title_full_unstemmed | Elevated Carbon Monoxide in the Exhaled Breath of Mice during a Systemic Bacterial Infection |
title_short | Elevated Carbon Monoxide in the Exhaled Breath of Mice during a Systemic Bacterial Infection |
title_sort | elevated carbon monoxide in the exhaled breath of mice during a systemic bacterial infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3729689/ https://www.ncbi.nlm.nih.gov/pubmed/23936104 http://dx.doi.org/10.1371/journal.pone.0069802 |
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