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Non invasive real-time monitoring of bacterial infection & therapeutic effect of anti-microbials in five mouse models
BACKGROUND & OBJECTIVES: In vivo imaging system has contributed significantly to the understanding of bacterial infection and efficacy of drugs in animal model. We report five rapid, reproducible, and non invasive murine pulmonary infection, skin and soft tissue infection, sepsis, and meningitis...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249968/ https://www.ncbi.nlm.nih.gov/pubmed/22199109 http://dx.doi.org/10.4103/0971-5916.90997 |
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author | Barman, Tarani Kanta Rao, Madhvi Bhati, Ashish Kishore, Krishna Shukla, Gunjan Kumar, Manoj Mathur, Tarun Pandya, Manisha Upadhyay, Dilip J. |
author_facet | Barman, Tarani Kanta Rao, Madhvi Bhati, Ashish Kishore, Krishna Shukla, Gunjan Kumar, Manoj Mathur, Tarun Pandya, Manisha Upadhyay, Dilip J. |
author_sort | Barman, Tarani Kanta |
collection | PubMed |
description | BACKGROUND & OBJECTIVES: In vivo imaging system has contributed significantly to the understanding of bacterial infection and efficacy of drugs in animal model. We report five rapid, reproducible, and non invasive murine pulmonary infection, skin and soft tissue infection, sepsis, and meningitis models using Xenogen bioluminescent strains and specialized in vivo imaging system (IVIS). METHODS: The progression of bacterial infection in different target organs was evaluated by the photon intensity and target organ bacterial counts. Genetically engineered bioluminescent bacterial strains viz. Staphylococcus aureus Xen 8.1, 29 and 31; Streptococcus pneumoniae Xen 9 and 10 and Pseudomonas aeruginosa Xen-5 were used to induce different target organs infection and were validated with commercially available antibiotics. RESULTS: The lower limit of detection of colony forming unit (cfu) was 1.7-log(10) whereas the lower limit of detection of relative light unit (RLU) was 4.2-log(10). Recovery of live bacteria from different target organs showed that the bioluminescent signal correlated to the live bacterial count. INTERPRETATION & CONCLUSIONS: This study demonstrated the real time monitoring and non-invasive analysis of progression of infection and pharmacological efficacy of drugs. These models may be useful for pre-clinical discovery of new antibiotics. |
format | Online Article Text |
id | pubmed-3249968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-32499682012-01-05 Non invasive real-time monitoring of bacterial infection & therapeutic effect of anti-microbials in five mouse models Barman, Tarani Kanta Rao, Madhvi Bhati, Ashish Kishore, Krishna Shukla, Gunjan Kumar, Manoj Mathur, Tarun Pandya, Manisha Upadhyay, Dilip J. Indian J Med Res Original Article BACKGROUND & OBJECTIVES: In vivo imaging system has contributed significantly to the understanding of bacterial infection and efficacy of drugs in animal model. We report five rapid, reproducible, and non invasive murine pulmonary infection, skin and soft tissue infection, sepsis, and meningitis models using Xenogen bioluminescent strains and specialized in vivo imaging system (IVIS). METHODS: The progression of bacterial infection in different target organs was evaluated by the photon intensity and target organ bacterial counts. Genetically engineered bioluminescent bacterial strains viz. Staphylococcus aureus Xen 8.1, 29 and 31; Streptococcus pneumoniae Xen 9 and 10 and Pseudomonas aeruginosa Xen-5 were used to induce different target organs infection and were validated with commercially available antibiotics. RESULTS: The lower limit of detection of colony forming unit (cfu) was 1.7-log(10) whereas the lower limit of detection of relative light unit (RLU) was 4.2-log(10). Recovery of live bacteria from different target organs showed that the bioluminescent signal correlated to the live bacterial count. INTERPRETATION & CONCLUSIONS: This study demonstrated the real time monitoring and non-invasive analysis of progression of infection and pharmacological efficacy of drugs. These models may be useful for pre-clinical discovery of new antibiotics. Medknow Publications & Media Pvt Ltd 2011-11 /pmc/articles/PMC3249968/ /pubmed/22199109 http://dx.doi.org/10.4103/0971-5916.90997 Text en Copyright: © The Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Barman, Tarani Kanta Rao, Madhvi Bhati, Ashish Kishore, Krishna Shukla, Gunjan Kumar, Manoj Mathur, Tarun Pandya, Manisha Upadhyay, Dilip J. Non invasive real-time monitoring of bacterial infection & therapeutic effect of anti-microbials in five mouse models |
title | Non invasive real-time monitoring of bacterial infection & therapeutic effect of anti-microbials in five mouse models |
title_full | Non invasive real-time monitoring of bacterial infection & therapeutic effect of anti-microbials in five mouse models |
title_fullStr | Non invasive real-time monitoring of bacterial infection & therapeutic effect of anti-microbials in five mouse models |
title_full_unstemmed | Non invasive real-time monitoring of bacterial infection & therapeutic effect of anti-microbials in five mouse models |
title_short | Non invasive real-time monitoring of bacterial infection & therapeutic effect of anti-microbials in five mouse models |
title_sort | non invasive real-time monitoring of bacterial infection & therapeutic effect of anti-microbials in five mouse models |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249968/ https://www.ncbi.nlm.nih.gov/pubmed/22199109 http://dx.doi.org/10.4103/0971-5916.90997 |
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