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      Evidence for Transmission of Bluetongue Virus Serotype 26 through Direct Contact

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          Abstract

          The aim of this study was to assess the mechanisms of transmission of bluetongue virus serotype 26 (BTV-26) in goats. A previous study, which investigated the pathogenicity and infection kinetics of BTV-26 in goats, unexpectedly revealed that one control goat may have been infected through a direct contact transmission route. To investigate the transmission mechanisms of BTV-26 in more detail an experimental infection study was carried out in which three goats were infected with BTV-26, three goats were kept uninfected, but were housed in direct contact with the infected goats, and an additional four goats were kept in indirect contact separated from infected goats by metal gates. This barrier allowed the goats to have occasional face-to-face contact in the same airspace, but feeding, watering, sampling and environmental cleaning was carried out separately. The three experimentally infected goats did not show clinical signs of BTV, however high levels of viral RNA were detected and virus was isolated from their blood. At 21 dpi viral RNA was detected in, and virus was isolated from the blood of the three direct contact goats, which also seroconverted. The four indirect barrier contact goats remained uninfected throughout the duration of the experiment. In order to assess replication in a laboratory model species of Culicoides biting midge, more than 300 Culicoides sonorensis were fed a BTV-26 spiked blood meal and incubated for 7 days. The dissemination of BTV-26 in individual C. sonorensis was inferred from the quantity of virus RNA and indicated that none of the insects processed at day 7 possessed transmissible infections. This study shows that BTV-26 is easily transmitted through direct contact transmission between goats, and the strain does not seem to replicate in C. sonorensis midges using standard incubation conditions.

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          Bluetongue in Europe: past, present and future.

          The recent arrival in Northern and Western (NW) Europe of bluetongue virus (BTV), which causes the ruminant disease 'bluetongue', has raised the profile of this vector-borne ruminant disease and sparked discussions on the reasons for its sudden emergence so far north. This expansion has not happened in isolation and the disease has been expanding into Southern and Eastern Europe for the last decade. This shifting disease distribution is being facilitated by a number of different introduction mechanisms including the movement of infected livestock, the passive movement of infected Culicoides on the wind and, in NW Europe, an unknown route of introduction. The expansion of BTV in Europe has forced a re-evaluation of the importance of Palaearctic Culicoides species in transmission, as well as the importance of secondary transmission routes, such as transplacental transmission, in facilitating the persistence of the virus. The current European outbreak of BTV-8 is believed to have caused greater economic damage than any previous single-serotype outbreak. Although attempts are being made to improve the capacity of European countries to cope with future BTV incursions, the options available are limited by a lack of basic entomological data and limited virological surveillance.
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            Temperature Dependence of the Extrinsic Incubation Period of Orbiviruses in Culicoides Biting Midges

            Background The rate at which viruses replicate and disseminate in competent arthropod vectors is limited by the temperature of their environment, and this can be an important determinant of geographical and seasonal limits to their transmission by arthropods in temperate regions. Methodology/Principal Findings Here, we present a novel statistical methodology for estimating the relationship between temperature and the extrinsic incubation period (EIP) and apply it to both published and novel data on virus replication for three internationally important orbiviruses (African horse sickness virus (AHSV), bluetongue virus (BTV) and epizootic haemorrhagic disease virus (EHDV)) in their Culicoides vectors. Our analyses show that there can be differences in vector competence for different orbiviruses in the same vector species and for the same orbivirus in different vector species. Both the rate of virus replication (approximately 0.017-0.021 per degree-day) and the minimum temperature required for replication (11-13°C), however, were generally consistent for different orbiviruses and across different Culicoides vector species. The estimates obtained in the present study suggest that previous publications have underestimated the replication rate and threshold temperature because the statistical methods they used included an implicit assumption that all negative vectors were infected. Conclusions/Significance Robust estimates of the temperature dependence of arbovirus replication are essential for building accurate models of transmission and for informing policy decisions about seasonal relaxations to movement restrictions. The methodology developed in this study provides the required robustness and is superior to methods used previously. Importantly, the methods are generic and can readily be applied to other arbovirus-vector systems, as long as the assumptions described in the text are valid.
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              Evidence for transplacental and contact transmission of bluetongue virus in cattle.

              This paper presents evidence that a field strain of bluetongue virus serotype 8 (BTV-8) was transmitted transplacentally and that it was also spread by a direct contact route. Twenty pregnant heifers were imported from the Netherlands into Northern Ireland during the midge-free season. Tests before and after the animals were imported showed that eight of them had antibodies to bluetongue virus, but no viral RNA was detected in any of them by reverse transcriptase-PCR (RT-PCR). Two of the seropositive heifers gave birth to three calves that showed evidence of bluetongue virus infection (RT-PCR-positive), and one of the calves was viraemic. Two further viraemic animals (one newly calved Dutch heifer, and one milking cow originally from Scotland) were also found to have been infected with BTV-8 and evidence is presented that these two animals may have been infected by direct contact, possibly through the ingestion of placentas infected with BTV-8.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2014
                5 May 2014
                : 9
                : 5
                : e96049
                Affiliations
                [1 ]Non Vesicular Reference Laboratory, The Pirbright Institute, Woking, Surrey, United Kingdom
                [2 ]Entomology, The Pirbright Institute, Woking, Surrey, United Kingdom
                [3 ]Centre for Integrative Biology, The Pirbright Institute, Woking, Surrey, United Kingdom
                [4 ]Vaccinology, The Pirbright Institute, Woking, Surrey, United Kingdom
                [5 ]School of Veterinary Medicine, Faculty of Health and Medical Sciences, University of Surrey, Guildford, United Kingdom
                [6 ]School of Veterinary Medicine, University of the West Indies, St. Augustine, Trinidad and Tobago
                The University of Texas Medical Branch, United States of America
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: CB KD EV CO. Performed the experiments: CB KD MH PF EV S. Graves LF. Analyzed the data: CB EV S. Gubbins MH LF. Contributed reagents/materials/analysis tools: CB MH LF S. Graves S. Gubbins PF EV. Wrote the paper: CB KD EV CO S. Gubbins MH LF.

                Article
                PONE-D-13-43942
                10.1371/journal.pone.0096049
                4010411
                24797910
                7c6316fa-200e-4b61-a381-ccd8a1c7765c
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 25 October 2013
                : 3 April 2014
                Page count
                Pages: 7
                Funding
                The work was funded by the European Union ( http://europa.eu/index_en.htm) and Department for Environment, Food and Rural Affairs (Defra) ( http://www.defra.gov.uk/) and carried out using facilities funded by the Biotechnology and Biological Sciences Research Council (BBSRC) ( http://www.bbsrc.ac.uk/home/home.aspx). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Microbiology
                Virology
                Viral Transmission and Infection
                Viral Vectors
                Viral Disease Diagnosis
                Population Biology
                Veterinary Science
                Veterinary Diseases
                Veterinary Virology
                Veterinary Epidemiology
                Veterinary Microbiology
                Medicine and Health Sciences
                Epidemiology
                Infectious Disease Epidemiology

                Uncategorized
                Uncategorized

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