Pathological and immunological characterization of bluetongue virus serotype 1 infection in type I interferons blocked immunocompetent adult mice

Bibliographic Details
Title: Pathological and immunological characterization of bluetongue virus serotype 1 infection in type I interferons blocked immunocompetent adult mice
Authors: Mani Saminathan, Karam Pal Singh, Madhulina Maity, Sobharani Vineetha, Gundallhalli Bayyappa Manjunathareddy, Kuldeep Dhama, Yashpal Singh Malik, Muthannan Andavar Ramakrishnan, Jyoti Misri, Vivek Kumar Gupta
Source: Journal of Advanced Research, Vol 31, Iss , Pp 137-153 (2021)
Publisher Information: Elsevier, 2021.
Publication Year: 2021
Collection: LCC:Medicine (General)
LCC:Science (General)
Subject Terms: Bluetongue virus serotype 1, Adult mouse, Type I IFNs blockade, MAR1-5A3 antibody, Sequential pathology, Immune responses, Medicine (General), R5-920, Science (General), Q1-390
More Details: Introduction: Wild-type adult mice with intact interferon (IFN) system were neither susceptible to bluetongue virus (BTV) infection nor showed signs of morbidity/mortality. Establishment of immunologically competent wild-type adult mouse model with type I IFNs blockade is necessary to assess the pathogenesis, immune responses and testing of BTV vaccines. Objectives: Present study aimed to establish and characterize BTV serotype 1 infection in immunocompetent adult mice with type I IFNs blockade at the time of infection by studying immune responses and sequential pathology. Methods: Adult mice were administered with anti-mouse IFN-α/β receptor subunit-1 (IFNAR1) blocking antibody (Clone: MAR1-5A3) 24 h before and after BTV serotype 1 infection, and sacrificed at various time points. Sequential pathology, BTV localization by immunohistochemistry and quantification by qRT-PCR, immune cell kinetics and apoptosis by flow cytometry, and cytokines estimation by c-ELISA and qRT-PCR were studied. Results: IFNAR blocked-infected mice developed clinical signs and typical lesions of BT; whereas, isotype-infected control mice did not develop any disease. The IFNAR blocked-infected mice showed enlarged, edematous, and congested lymph nodes (LNs) and spleen, and vascular (congestion and hemorrhage) and pneumonic lesions in lungs. Histopathologically, marked lymphoid depletion with “starry-sky pattern” due to lymphocytes apoptosis was noticed in the LNs and spleen. BTV antigen was detected and quantified in lymphoid organs, lungs, and other organs at various time points. Initial leukopenia (increased CD4+/CD8+ T cells ratio) followed by leukocytosis (decreased CD4+/CD8+ T cells ratio) and significantly increased biochemical values were noticed in IFNAR blocked-infected mice. Increased apoptotic cells in PBMCs and tissues coincided with viral load and levels of different cytokines in blood, spleen and draining LNs and notably varied between time points in IFNAR blocked-infected mice. Conclusion: Present study is first to characterize BTV serotype 1 infection in immunocompetent adult mouse with type I IFNs blockade. The findings will be useful for studying pathogenesis and testing the efficacy of BTV vaccines.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2090-1232
Relation: http://www.sciencedirect.com/science/article/pii/S209012322100014X; https://doaj.org/toc/2090-1232
DOI: 10.1016/j.jare.2021.01.007
Access URL: https://doaj.org/article/c92d5a28548d45e2b8f153817a2cae98
Accession Number: edsdoj.92d5a28548d45e2b8f153817a2cae98
Database: Directory of Open Access Journals
More Details
ISSN:20901232
DOI:10.1016/j.jare.2021.01.007
Published in:Journal of Advanced Research
Language:English