Cargando…
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
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...
Autores principales: | , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104101/ https://www.ncbi.nlm.nih.gov/pubmed/33568514 http://dx.doi.org/10.1128/JVI.02239-20 |
_version_ | 1783689422165770240 |
---|---|
author | Sanz-Bernardo, Beatriz Haga, Ismar R. Wijesiriwardana, Najith Basu, Sanjay Larner, Will Diaz, Adriana V. Langlands, Zoë Denison, Eric Stoner, Joanne White, Mia Sanders, Christopher Hawes, Philippa C. Wilson, Anthony J. Atkinson, John Batten, Carrie Alphey, Luke Darpel, Karin E. Gubbins, Simon Beard, Philippa M. |
author_facet | Sanz-Bernardo, Beatriz Haga, Ismar R. Wijesiriwardana, Najith Basu, Sanjay Larner, Will Diaz, Adriana V. Langlands, Zoë Denison, Eric Stoner, Joanne White, Mia Sanders, Christopher Hawes, Philippa C. Wilson, Anthony J. Atkinson, John Batten, Carrie Alphey, Luke Darpel, Karin E. Gubbins, Simon Beard, Philippa M. |
author_sort | Sanz-Bernardo, Beatriz |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8104101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-81041012021-05-21 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 Sanz-Bernardo, Beatriz Haga, Ismar R. Wijesiriwardana, Najith Basu, Sanjay Larner, Will Diaz, Adriana V. Langlands, Zoë Denison, Eric Stoner, Joanne White, Mia Sanders, Christopher Hawes, Philippa C. Wilson, Anthony J. Atkinson, John Batten, Carrie Alphey, Luke Darpel, Karin E. Gubbins, Simon Beard, Philippa M. J Virol Pathogenesis and Immunity 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. American Society for Microbiology 2021-04-12 /pmc/articles/PMC8104101/ /pubmed/33568514 http://dx.doi.org/10.1128/JVI.02239-20 Text en Copyright © 2021 Sanz-Bernardo et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Pathogenesis and Immunity Sanz-Bernardo, Beatriz Haga, Ismar R. Wijesiriwardana, Najith Basu, Sanjay Larner, Will Diaz, Adriana V. Langlands, Zoë Denison, Eric Stoner, Joanne White, Mia Sanders, Christopher Hawes, Philippa C. Wilson, Anthony J. Atkinson, John Batten, Carrie Alphey, Luke Darpel, Karin E. Gubbins, Simon Beard, Philippa M. 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 |
title | 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 |
title_full | 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 |
title_fullStr | 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 |
title_full_unstemmed | 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 |
title_short | 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 |
title_sort | 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 |
topic | Pathogenesis and Immunity |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104101/ https://www.ncbi.nlm.nih.gov/pubmed/33568514 http://dx.doi.org/10.1128/JVI.02239-20 |
work_keys_str_mv | AT sanzbernardobeatriz quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT hagaismarr quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT wijesiriwardananajith quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT basusanjay quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT larnerwill quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT diazadrianav quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT langlandszoe quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT denisoneric quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT stonerjoanne quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT whitemia quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT sanderschristopher quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT hawesphilippac quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT wilsonanthonyj quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT atkinsonjohn quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT battencarrie quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT alpheyluke quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT darpelkarine quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT gubbinssimon quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks AT beardphilippam quantifyingandmodelingtheacquisitionandretentionoflumpyskindiseasevirusbyhematophagusinsectsrevealsclinicallybutnotsubclinicallyaffectedcattlearepromotersofviraltransmissionandkeytargetsforcontrolofdiseaseoutbreaks |