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      An updated review on bluetongue virus: epidemiology, pathobiology, and advances in diagnosis and control with special reference to India

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          Abstract

          Bluetongue (BT) is an economically important, non-contagious viral disease of domestic and wild ruminants. BT is caused by BT virus (BTV) and it belongs to the genus Orbivirus and family Reoviridae. BTV is transmitted by Culicoides midges and causes clinical disease in sheep, white-tailed deer, pronghorn antelope, bighorn sheep, and subclinical manifestation in cattle, goats and camelids. BT is a World Organization for Animal Health (OIE) listed multispecies disease and causes great socio-economic losses. To date, 28 serotypes of BTV have been reported worldwide and 23 serotypes have been reported from India. Transplacental transmission (TPT) and fetal abnormalities in ruminants had been reported with cell culture adopted live-attenuated vaccine strains of BTV. However, emergence of BTV-8 in Europe during 2006, confirmed TPT of wild-type/field strains of BTV. Diagnosis of BT is more important for control of disease and to ensure BTV-free trade of animals and their products. Reverse transcription polymerase chain reaction, agar gel immunodiffusion assay and competitive enzyme-linked immunosorbent assay are found to be sensitive and OIE recommended tests for diagnosis of BTV for international trade. Control measures include mass vaccination (most effective method), serological and entomological surveillance, forming restriction zones and sentinel programs. Major hindrances with control of BT in India are the presence of multiple BTV serotypes, high density of ruminant and vector populations. A pentavalent inactivated, adjuvanted vaccine is administered currently in India to control BT. Recombinant vaccines with DIVA strategies are urgently needed to combat this disease. This review is the first to summarise the seroprevalence of BTV in India for 40 years, economic impact and pathobiology.

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          Since the discovery, over a decade and a half ago, that genetically engineered DNA can be delivered in vaccine form and elicit an immune response, there has been much progress in understanding the basic biology of this platform. A large amount of data has been generated in preclinical model systems, and more sustained cellular responses and more consistent antibody responses are being observed in the clinic. Four DNA vaccine products have recently been approved, all in the area of veterinary medicine. These results suggest a productive future for this technology as more optimized constructs, better trial designs and improved platforms are being brought into the clinic.
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            Genetic control of mosquitoes.

            Genetics can potentially provide new, species-specific, environmentally friendly methods for mosquito control. Genetic control strategies aim either to suppress target populations or to introduce a harm-reducing novel trait. Different approaches differ considerably in their properties, especially between self-limiting strategies, where the modification has limited persistence, and self-sustaining strategies, which are intended to persist indefinitely in the target population and may invade other populations. Several methods with different molecular biology are under development and the first field trials have been completed successfully.
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              The pathology and pathogenesis of bluetongue.

              Bluetongue (BT) is an insect-transmitted viral disease of wild and domestic ruminants and, occasionally, other species. Amongst domestic livestock, BT is most common in certain breeds of sheep whereas asymptomatic BT virus (BTV) infection of cattle is typical in enzootic regions. BT in cattle can be a feature of specific outbreaks, notably the current epizootic in Europe caused by BTV serotype 8. BTV replicates within mononuclear phagocytic and endothelial cells, lymphocytes and possibly other cell types in lymphoid tissues, the lungs, skin and other tissues. Infected ruminants may exhibit a prolonged but not persistent viraemia and BTV is associated with erythrocytes during the late stages of this prolonged viraemia. The pathogenesis of BT involves injury to small blood vessels in target tissues, but the relative contributions of direct virus-induced cytolysis and virus-induced vasoactive mediators in causing endothelial injury and dysfunction are presently unclear. The lesions of BT are characteristic and include: haemorrhage and ulcers in the oral cavity and upper gastrointestinal tract; necrosis of skeletal and cardiac muscle; coronitis; subintimal haemorrhage in the pulmonary artery; oedema of the lungs, ventral subcutis, and fascia of the muscles of the neck and abdominal wall; and pericardial, pleural and abdominal effusions. Transplacental transmission of BTV in ruminants, with subsequent fetal infection, is a property of specific virus strains, especially those propagated in embryonated eggs or cell culture. The outcome of BTV infection of fetal ruminants is age-dependent, with distinctive cavitating lesions of the central nervous system in animals that survive infection in early gestation. Immune competence to BTV arises by mid-gestation, and animals infected in late gestation can be born viraemic and without significant brain malformations.
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                Author and article information

                Journal
                Vet Q
                Vet Q
                The Veterinary Quarterly
                Taylor & Francis
                0165-2176
                1875-5941
                10 November 2020
                2020
                : 40
                : 1
                : 258-321
                Affiliations
                [a ]Division of Pathology, ICAR-Indian Veterinary Research Institute , Izatnagar, Bareilly, Uttar Pradesh, India
                [b ]Animal Science Division, Indian Council of Agricultural Research , New Delhi, India
                [c ]Division of Biological Standardization, ICAR-Indian Veterinary Research Institute , Izatnagar, Bareilly, Uttar Pradesh, India
                [d ]Centre for Animal Disease Research and Diagnosis, ICAR-Indian Veterinary Research Institute , Izatnagar, Bareilly, Uttar Pradesh, India
                [e ]Director, ICAR-Indian Veterinary Research Institute , Izatnagar, Bareilly, Uttar Pradesh, India
                Author notes
                [*]

                These

                authors contributed equally to this work.

                CONTACT Mani Saminathan, Karam Pal Singh, Kuldeep Dhama drswamyvet@ 123456gmail.com , karam.singh@ 123456rediffmail.com , kdhama@ 123456rediffmail.com Division of Pathology, ICAR-Indian Veterinary Research Institute , Izatnagar, Bareilly-243122, Uttar Pradesh, India
                Author information
                https://orcid.org/0000-0003-0557-7194
                https://orcid.org/0000-0002-2832-4854
                https://orcid.org/0000-0001-7469-4752
                Article
                1831708
                10.1080/01652176.2020.1831708
                7655031
                33003985
                0eb420f2-e66b-477f-9d41-a22be9e1d2bf
                © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                Page count
                Figures: 5, Tables: 3, Pages: 64, Words: 50560
                Categories
                Review

                cattle,sheep,goat,bluetongue virus,epidemiology,indian scenario,pathogenesis,pathology,immune responses,mice model,diagnosis,vaccination,control

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