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      Quantifying and Modeling the Acquisition and Retention of Lumpy Skin Disease Virus by Hematophagus Insects Reveals Clinically but Not Subclinically Affected Cattle Are Promoters of Viral Transmission and Key Targets for Control of Disease Outbreaks

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          Abstract

          Lumpy skin disease virus (LSDV) causes a severe systemic disease characterized by cutaneous nodules in cattle. LSDV is a rapidly emerging pathogen, having spread since 2012 into Europe and Russia and across Asia.

          ABSTRACT

          Lumpy skin disease virus (LSDV) is a vector-transmitted poxvirus that causes disease in cattle. Vector species involved in LSDV transmission and their ability to acquire and transmit the virus are poorly characterized. Using a highly representative bovine experimental model of lumpy skin disease, we fed four model vector species ( Aedes aegypti, Culex quinquefasciatus, Stomoxys calcitrans, and Culicoides nubeculosus) on LSDV-inoculated cattle in order to examine their acquisition and retention of LSDV. Subclinical disease was a more common outcome than clinical disease in the inoculated cattle. Importantly, the probability of vectors acquiring LSDV from a subclinical animal (0.006) was very low compared with that from a clinical animal (0.23), meaning an insect feeding on a subclinical animal was 97% less likely to acquire LSDV than one feeding on a clinical animal. All four potential vector species studied acquired LSDV from the host at a similar rate, but Aedes aegypti and Stomoxys calcitrans retained the virus for a longer time, up to 8 days. There was no evidence of virus replication in the vector, consistent with mechanical rather than biological transmission. The parameters obtained in this study were combined with data from studies of LSDV transmission and vector life history parameters to determine the basic reproduction number of LSDV in cattle mediated by each of the model species. This reproduction number was highest for Stomoxys calcitrans (19.1), followed by C. nubeculosus (7.1) and Ae. aegypti (2.4), indicating that these three species are potentially efficient transmitters of LSDV; this information can be used to inform LSD control programs.

          IMPORTANCE Lumpy skin disease virus (LSDV) causes a severe systemic disease characterized by cutaneous nodules in cattle. LSDV is a rapidly emerging pathogen, having spread since 2012 into Europe and Russia and across Asia. The vector-borne nature of LSDV transmission is believed to have promoted this rapid geographic spread of the virus; however, a lack of quantitative evidence about LSDV transmission has hampered effective control of the disease during the current epidemic. Our research shows subclinical cattle play little part in virus transmission relative to clinical cattle and reveals a low probability of virus acquisition by insects at the preclinical stage. We have also calculated the reproductive number of different insect species, therefore identifying efficient transmitters of LSDV. This information is of utmost importance, as it will help to define epidemiological control measures during LSDV epidemics and of particular consequence in resource-poor regions where LSD vaccination may be less than adequate.

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            Factors that make an infectious disease outbreak controllable.

            The aim of this study is to identify general properties of emerging infectious agents that determine the likely success of two simple public health measures in controlling outbreaks, namely (i) isolating symptomatic individuals and (ii) tracing and quarantining their contacts. Because these measures depend on the recognition of specific disease symptoms, we investigate the relative timing of infectiousness and the appearance of symptoms by using a mathematical model. We show that the success of these control measures is determined as much by the proportion of transmission occurring prior to the onset of overt clinical symptoms (or via asymptomatic infection) as the inherent transmissibility of the etiological agent (measured by the reproductive number R(0)). From published studies, we estimate these quantities for two moderately transmissible viruses, severe acute respiratory syndrome coronavirus and HIV, and for two highly transmissible viruses, smallpox and pandemic influenza. We conclude that severe acute respiratory syndrome and smallpox are easier to control using these simple public health measures. Direct estimation of the proportion of asymptomatic and presymptomatic infections is achievable by contact tracing and should be a priority during an outbreak of a novel infectious agent.
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              Asymptomatic humans transmit dengue virus to mosquitoes.

              Three-quarters of the estimated 390 million dengue virus (DENV) infections each year are clinically inapparent. People with inapparent dengue virus infections are generally considered dead-end hosts for transmission because they do not reach sufficiently high viremia levels to infect mosquitoes. Here, we show that, despite their lower average level of viremia, asymptomatic people can be infectious to mosquitoes. Moreover, at a given level of viremia, DENV-infected people with no detectable symptoms or before the onset of symptoms are significantly more infectious to mosquitoes than people with symptomatic infections. Because DENV viremic people without clinical symptoms may be exposed to more mosquitoes through their undisrupted daily routines than sick people and represent the bulk of DENV infections, our data indicate that they have the potential to contribute significantly more to virus transmission to mosquitoes than previously recognized.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                J Virol
                J Virol
                jvi
                jvi
                JVI
                Journal of Virology
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                0022-538X
                1098-5514
                10 February 2021
                12 April 2021
                May 2021
                12 April 2021
                : 95
                : 9
                : e02239-20
                Affiliations
                [a ]The Pirbright Institute, Pirbright, Surrey, United Kingdom
                [b ]The Roslin Institute, Edinburgh, United Kingdom
                [c ]MSD Animal Health, Walton, Milton Keynes, United Kingdom
                University of Illinois at Urbana Champaign
                Author notes
                Address correspondence to Philippa M. Beard, pip.beard@ 123456pirbright.ac.uk .
                [*]

                Present address: Adriana V. Diaz, The Royal Veterinary College, Hatfield, United Kingdom; Mia White, Genomics, National Infection Service, Public Health England, Porton Down, United Kingdom.

                Simon Gubbins and Philippa M. Beard contributed equally to this study.

                Citation Sanz-Bernardo B, Haga IR, Wijesiriwardana N, Basu S, Larner W, Diaz AV, Langlands Z, Denison E, Stoner J, White M, Sanders C, Hawes PC, Wilson AJ, Atkinson J, Batten C, Alphey L, Darpel KE, Gubbins S, Beard PM. 2021. Quantifying and modeling the acquisition and retention of lumpy skin disease virus by hematophagus insects reveals clinically but not subclinically affected cattle are promoters of viral transmission and key targets for control of disease outbreaks. J Virol 95:e02239-20. https://doi.org/10.1128/JVI.02239-20.

                Author information
                https://orcid.org/0000-0001-6965-3497
                https://orcid.org/0000-0002-2285-810X
                Article
                02239-20
                10.1128/JVI.02239-20
                8104101
                33568514
                c965c05f-86eb-4898-b75b-d0d004cd5962
                Copyright © 2021 Sanz-Bernardo et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                : 19 November 2020
                : 2 February 2021
                Page count
                Figures: 8, Tables: 5, Equations: 26, References: 83, Pages: 26, Words: 16064
                Funding
                Funded by: MSD Animal Health;
                Award Recipient :
                Funded by: UKRI | Biotechnology and Biological Sciences Research Council (BBSRC), https://doi.org/10.13039/501100000268;
                Award ID: BBS/E/I/00007033
                Award Recipient : Award Recipient : Award Recipient : Award Recipient :
                Funded by: UKRI | Biotechnology and Biological Sciences Research Council (BBSRC), https://doi.org/10.13039/501100000268;
                Award ID: BBS/E/I/00007037
                Award Recipient : Award Recipient : Award Recipient : Award Recipient :
                Funded by: UKRI | Biotechnology and Biological Sciences Research Council (BBSRC), https://doi.org/10.13039/501100000268;
                Award ID: BBS/E/I/00007038
                Award Recipient : Award Recipient : Award Recipient : Award Recipient :
                Funded by: UKRI | Biotechnology and Biological Sciences Research Council (BBSRC), https://doi.org/10.13039/501100000268;
                Award ID: BBS/E/I/00007039
                Award Recipient : Award Recipient : Award Recipient : Award Recipient :
                Funded by: UKRI | Biotechnology and Biological Sciences Research Council (BBSRC), https://doi.org/10.13039/501100000268;
                Award ID: BBE/I/00007036
                Award Recipient : Award Recipient : Award Recipient : Award Recipient :
                Funded by: UKRI | Biotechnology and Biological Sciences Research Council (BBSRC), https://doi.org/10.13039/501100000268;
                Award ID: BB/R002606/1
                Award Recipient : Award Recipient : Award Recipient : Award Recipient : Award Recipient : Award Recipient :
                Funded by: Wellcome, https://doi.org/10.13039/100004440;
                Award ID: 200171/Z/15/Z
                Award Recipient :
                Categories
                Pathogenesis and Immunity
                Custom metadata
                May 2021

                Microbiology & Virology
                poxvirus,lumpy skin disease virus,vector transmission
                Microbiology & Virology
                poxvirus, lumpy skin disease virus, vector transmission

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