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Modelling of cerebral tuberculosis in BALB/c mice using clinical strain from patients with CNS tuberculosis infection
BACKGROUND & OBJECTIVES: Central nervous system (CNS) infection caused by Mycobacterium tuberculosis (MTB) is the most severe form of extrapulmonary tuberculosis (EPTB) due to a high level of mortality and morbidity. Limited studies are available on CNS-TB animal model development. The present s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674554/ https://www.ncbi.nlm.nih.gov/pubmed/29067986 http://dx.doi.org/10.4103/ijmr.IJMR_1930_15 |
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author | Husain, Aliabbas A. Gupta, Umesh Datta Gupta, Pushpa Nayak, Amit R. Chandak, Nitin H. Daginawla, Hatim F. Singh, Lokendra Kashyap, Rajpal Singh |
author_facet | Husain, Aliabbas A. Gupta, Umesh Datta Gupta, Pushpa Nayak, Amit R. Chandak, Nitin H. Daginawla, Hatim F. Singh, Lokendra Kashyap, Rajpal Singh |
author_sort | Husain, Aliabbas A. |
collection | PubMed |
description | BACKGROUND & OBJECTIVES: Central nervous system (CNS) infection caused by Mycobacterium tuberculosis (MTB) is the most severe form of extrapulmonary tuberculosis (EPTB) due to a high level of mortality and morbidity. Limited studies are available on CNS-TB animal model development. The present study describes the development of a murine model of CNS-TB using a clinical strain (C3) isolated from the cerebrospinal fluid (CSF) of CNS-TB patients. METHODS: Groups of mice were infected by the intravenous route with MTB C3 strain isolated from the CSF of CNS-TB patients. Brain and lung tissue were evaluated for bacterial burden, histopathology and surrogate markers of TB infection at 30 and 50 days post-infection. RESULTS: Mice infected intravenously with MTB C3 strains showed progressive development of CNS disease with high bacillary burden in lungs at the initial stage (30 days), which eventually disseminated to the brain at a later stage (50 days). Similarly, high mortality (60%) was associated in mice infected with C3 strain compared to control. INTERPRETATION & CONCLUSIONS: The study showed development of a novel murine model of CNS-TB using the C3 strain of MTB that replicated events of extrapulmonary dissemination. The developed model would be helpful in understanding the pathogenesis of CNS-TB infection for the development of improved therapeutic interventions in future. |
format | Online Article Text |
id | pubmed-5674554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56745542017-11-17 Modelling of cerebral tuberculosis in BALB/c mice using clinical strain from patients with CNS tuberculosis infection Husain, Aliabbas A. Gupta, Umesh Datta Gupta, Pushpa Nayak, Amit R. Chandak, Nitin H. Daginawla, Hatim F. Singh, Lokendra Kashyap, Rajpal Singh Indian J Med Res Original Article BACKGROUND & OBJECTIVES: Central nervous system (CNS) infection caused by Mycobacterium tuberculosis (MTB) is the most severe form of extrapulmonary tuberculosis (EPTB) due to a high level of mortality and morbidity. Limited studies are available on CNS-TB animal model development. The present study describes the development of a murine model of CNS-TB using a clinical strain (C3) isolated from the cerebrospinal fluid (CSF) of CNS-TB patients. METHODS: Groups of mice were infected by the intravenous route with MTB C3 strain isolated from the CSF of CNS-TB patients. Brain and lung tissue were evaluated for bacterial burden, histopathology and surrogate markers of TB infection at 30 and 50 days post-infection. RESULTS: Mice infected intravenously with MTB C3 strains showed progressive development of CNS disease with high bacillary burden in lungs at the initial stage (30 days), which eventually disseminated to the brain at a later stage (50 days). Similarly, high mortality (60%) was associated in mice infected with C3 strain compared to control. INTERPRETATION & CONCLUSIONS: The study showed development of a novel murine model of CNS-TB using the C3 strain of MTB that replicated events of extrapulmonary dissemination. The developed model would be helpful in understanding the pathogenesis of CNS-TB infection for the development of improved therapeutic interventions in future. Medknow Publications & Media Pvt Ltd 2017-06 /pmc/articles/PMC5674554/ /pubmed/29067986 http://dx.doi.org/10.4103/ijmr.IJMR_1930_15 Text en Copyright: © 2017 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Husain, Aliabbas A. Gupta, Umesh Datta Gupta, Pushpa Nayak, Amit R. Chandak, Nitin H. Daginawla, Hatim F. Singh, Lokendra Kashyap, Rajpal Singh Modelling of cerebral tuberculosis in BALB/c mice using clinical strain from patients with CNS tuberculosis infection |
title | Modelling of cerebral tuberculosis in BALB/c mice using clinical strain from patients with CNS tuberculosis infection |
title_full | Modelling of cerebral tuberculosis in BALB/c mice using clinical strain from patients with CNS tuberculosis infection |
title_fullStr | Modelling of cerebral tuberculosis in BALB/c mice using clinical strain from patients with CNS tuberculosis infection |
title_full_unstemmed | Modelling of cerebral tuberculosis in BALB/c mice using clinical strain from patients with CNS tuberculosis infection |
title_short | Modelling of cerebral tuberculosis in BALB/c mice using clinical strain from patients with CNS tuberculosis infection |
title_sort | modelling of cerebral tuberculosis in balb/c mice using clinical strain from patients with cns tuberculosis infection |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674554/ https://www.ncbi.nlm.nih.gov/pubmed/29067986 http://dx.doi.org/10.4103/ijmr.IJMR_1930_15 |
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