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Comparative neuropathology of major Indian Bluetongue virus serotypes in a neonatal BALB/c mouse model

Anjaneya, A.; Singh, K.P.; Cherian, S.; Saminathan, M.; Singh, R.; Ramakrishnan, M.A.; Maan, S.; Maan, N.S.; Hemadri, D.; Rao, P.P.; Putty, K.; Krishnajyothi, Y.; Mertens, P.P.

Authors

A. Anjaneya

K.P. Singh

S. Cherian

M. Saminathan

R. Singh

M.A. Ramakrishnan

S. Maan

N.S. Maan

D. Hemadri

P.P. Rao

K. Putty

Y. Krishnajyothi



Abstract

Bluetongue virus (BTV) is neurotropic in nature, especially in ruminant fetuses and in-utero infection results in abortion and congenital brain malformations. The aim of the present study was to compare the neuropathogenicity of major Indian BTV serotypes 1, 2, 10, 16 and 23 by gross and histopathological lesions and virus distribution in experimentally infected neonatal BALB/c mice. Each BTV serotype (20 μl of inoculum containing 1 × 105 tissue culture infectious dose [TCID]50/ml of virus) was inoculated intracerebrally into 3-day-old mice, while a control group was inoculated with mock-infected cell culture medium. Infection with BTV serotypes 1, 2 and 23 led to 65–70% mortality at 7–9 days post infection (dpi) and caused severe necrotizing encephalitis with neurodegenerative changes in neurons, swelling and proliferation of vascular endothelial cells in the cerebral cortex, cerebellum, midbrain and brainstem. In contrast, infection with BTV serotypes 10 and 16 led to 25–30% mortality at 9–11 dpi and caused mild neuropathological lesions. BTV antigen was detected by immunohistochemistry, direct fluorescence antibody technique and confocal microscopy in the cytoplasm of neuronal cells of the hippocampus, grey matter of the cerebral cortex and vascular endothelial cells in the midbrain and brainstem of BTV-1, -2, -10, -16 and -23 infected groups from 3 to 20 dpi. BTV nucleic acid was detected in the infected brain tissues from as early as 24 h up to 20 dpi by VP7 gene segment-based one-step reverse transcriptase polymerase chain reaction. This study of the relative neurovirulence of BTV serotypes is likely to help design suitable vaccination and control strategies for the disease.

Citation

Anjaneya, A., Singh, K., Cherian, S., Saminathan, M., Singh, R., Ramakrishnan, M., …Mertens, P. (2018). Comparative neuropathology of major Indian Bluetongue virus serotypes in a neonatal BALB/c mouse model. Journal of Comparative Pathology, 162, 18-28. https://doi.org/10.1016/j.jcpa.2018.06.001

Journal Article Type Article
Acceptance Date Jun 1, 2018
Online Publication Date Jul 3, 2018
Publication Date 2018-07
Deposit Date Aug 10, 2018
Journal Journal of Comparative Pathology
Print ISSN 0021-9975
Electronic ISSN 1532-3129
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 162
Pages 18-28
DOI https://doi.org/10.1016/j.jcpa.2018.06.001
Keywords BALB/c mice; bluetongue virus; histopathology; neuropathogenicity
Public URL https://nottingham-repository.worktribe.com/output/914309
Publisher URL https://www.sciencedirect.com/science/article/pii/S0021997518300653
Additional Information This article is maintained by: Elsevier; Article Title: Comparative Neuropathology of Major Indian Bluetongue Virus Serotypes in a Neonatal BALB/c Mouse Model; Journal Title: Journal of Comparative Pathology; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.jcpa.2018.06.001; Content Type: article; Copyright: © 2018 Elsevier Ltd. All rights reserved.