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      Analysis of vaccine‐like lumpy skin disease virus from flies near the western border of China

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          MEGA6: Molecular Evolutionary Genetics Analysis version 6.0.

          We announce the release of an advanced version of the Molecular Evolutionary Genetics Analysis (MEGA) software, which currently contains facilities for building sequence alignments, inferring phylogenetic histories, and conducting molecular evolutionary analysis. In version 6.0, MEGA now enables the inference of timetrees, as it implements the RelTime method for estimating divergence times for all branching points in a phylogeny. A new Timetree Wizard in MEGA6 facilitates this timetree inference by providing a graphical user interface (GUI) to specify the phylogeny and calibration constraints step-by-step. This version also contains enhanced algorithms to search for the optimal trees under evolutionary criteria and implements a more advanced memory management that can double the size of sequence data sets to which MEGA can be applied. Both GUI and command-line versions of MEGA6 can be downloaded from www.megasoftware.net free of charge.
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            Quantification of lumpy skin disease virus following experimental infection in cattle.

            Lumpy skin disease along with sheep pox and goatpox are the most serious poxvirus diseases of livestock, and are caused by viruses that belong to the genus Capripoxvirus within the subfamily Chordopoxvirinae, family Poxviridae. To facilitate the study of lumpy skin disease pathogenesis, we inoculated eight 4- to 6-month-old Holstein calves intravenously with lumpy skin disease virus (LSDV) and collected samples over a period of 42 days for analysis by virus isolation, real-time PCR and light microscopy. Following inoculation, cattle developed fever and skin nodules, with the extent of infection varying between animals. Skin nodules remained visible until the end of the experiment on day post-inoculation (DPI) 42. Viremia measured by real-time PCR and virus isolation was not observed in all animals but was detectable between 6 and 15 DPI. Low levels of viral shedding were observed in oral and nasal secretions between 12 and 18 DPI. Several tissues were assessed for the presence of virus at DPI 3, 6, 9, 12, 15, 18 and 42 by virus isolation and real-time PCR. Virus was consistently detected by real-time PCR and virus isolation at high levels in skin nodules indicating LSDV has a tropism for skin. In contrast, relatively few lesions were observed systemically. Viral DNA was detected by real-time PCR in skin lesions collected on DPI 42. Cattle developing anti-capripoxvirus antibodies starting at DPI 21 was detected by serum neutralization. The disease in this study varied from mild with few secondary skin nodules to generalized infection of varying severity, and was characterized by morbidity with no mortality.
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              Mechanical transmission of lumpy skin disease virus by Aedes aegypti (Diptera: Culicidae).

              Aedes aegypti female mosquitoes are capable of the mechanical transmission of lumpy skin disease virus (LSDV) from infected to susceptible cattle. Mosquitoes that had fed upon lesions of LSDV-infected cattle were able to transmit virus to susceptible cattle over a period of 2-6 days post-infective feeding. Virus was isolated from the recipient animals in 5 out of 7 cases. The clinical disease recorded in the animals exposed to infected mosquitoes was generally of a mild nature, with only one case being moderate. LSDV has long been suspected to be insect transmitted, but these findings are the first to demonstrate this unequivocally, and they suggest that mosquito species are competent vectors.
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                Author and article information

                Contributors
                Journal
                Transboundary and Emerging Diseases
                Transbounding Emerging Dis
                Wiley
                1865-1674
                1865-1682
                June 04 2021
                Affiliations
                [1 ]Department of Animal Center, Chongqing Key Laboratory of Pediatrics, and Ministry of Education Key Lab of Child Development and Disorders, and National Clinical Research Center for Child Health and Disorders, and China International Science and Technology Cooperation base of Child Development and Critical Disorders Children's Hospital of Chongqing Medical University Chongqing China
                [2 ]Animal Inspection and Quarantine Laboratory Technical Center of Chong‐Qing Custom Chongqing China
                [3 ]Animal Quarantine Laboratory Technical Center of Yi‐Ning Custom Yining China
                [4 ]School of Life Sciences Chongqing University Chongqing China
                [5 ]Animal Quarantine Laboratory Technical Center of Haikou Custom Haikou China
                [6 ]Animal Quarantine Laboratory Technical Center of Chengdu Custom Chengdu China
                Article
                10.1111/tbed.14159
                34033246
                a1497a64-30ff-4732-a57d-a296e79ccaae
                © 2021

                http://onlinelibrary.wiley.com/termsAndConditions#vor

                http://doi.wiley.com/10.1002/tdm_license_1.1

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