Abstract

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.

Details

Title
Modelling of cerebral tuberculosis in BALB/c mice using clinical strain from patients with CNS tuberculosis infection
Author
Husain, Aliabbas 1 ; Gupta, Umesh 2 ; Gupta, Pushpa 2 ; Nayak, Amit 1 ; Chandak, Nitin 3 ; Daginawla, Hatim 1 ; Singh, Lokendra 4 ; Kashyap, Rajpal 1 

 Biochemistry Research Laboratory, Central India Institute of Medical Sciences, Nagpur 
 ICMR- National JALMA Institute for Leprosy & Other Mycobacterial Diseases, Agra 
 Department of Neurology, Central India Institute of Medical Sciences, Nagpur 
 Department of Neurosurgery, Central India Institute of Medical Sciences, Nagpur 
Pages
833-839
Publication year
2017
Publication date
Jun 2017
Publisher
Scientific Scholar
ISSN
0971-5916
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2258206099
Copyright
© 2017. This work is published under https://creativecommons.org/licenses/by-nc-sa/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.