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In Situ Hybridization (RNAscope) Detection of Bluetongue Virus Serotypes 10 and 17 in Experimentally Co-Infected Culicoides sonorensis

Bluetongue virus (BTV) is a segmented, double-stranded RNA virus transmitted by Culicoides biting midges. Infection of domestic and wild ruminants with BTV can result in a devastating disease and significant economic losses. As a virus with a segmented genome, reassortment among the BTV serotypes th...

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Autores principales: Carpenter, Molly, Benavides Obon, AnaMario, Kopanke, Jennifer, Lee, Justin, Reed, Kirsten, Sherman, Tyler, Rodgers, Case, Stenglein, Mark, McDermott, Emily, Mayo, Christie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10609982/
https://www.ncbi.nlm.nih.gov/pubmed/37887723
http://dx.doi.org/10.3390/pathogens12101207
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author Carpenter, Molly
Benavides Obon, AnaMario
Kopanke, Jennifer
Lee, Justin
Reed, Kirsten
Sherman, Tyler
Rodgers, Case
Stenglein, Mark
McDermott, Emily
Mayo, Christie
author_facet Carpenter, Molly
Benavides Obon, AnaMario
Kopanke, Jennifer
Lee, Justin
Reed, Kirsten
Sherman, Tyler
Rodgers, Case
Stenglein, Mark
McDermott, Emily
Mayo, Christie
author_sort Carpenter, Molly
collection PubMed
description Bluetongue virus (BTV) is a segmented, double-stranded RNA virus transmitted by Culicoides biting midges. Infection of domestic and wild ruminants with BTV can result in a devastating disease and significant economic losses. As a virus with a segmented genome, reassortment among the BTV serotypes that have co-infected a host may increase genetic diversity, which can alter BTV transmission dynamics and generate epizootic events. The objective of this study was to determine the extent of dissemination and characterize the tropism of BTV serotypes 10 and 17 in co-infected Culicoides sonorensis. Midges were exposed to both BTV serotypes via blood meal and processed for histologic slides 10 days after infection. An in situ hybridization approach was employed using the RNAscope platform to detect the nucleic acid segment 2 of both serotypes. Observations of the mosaic patterns in which serotypes did not often overlap suggest that co-infection at the cellular level may not be abundant with these two serotypes in C. sonorensis. This could be a consequence of superinfection exclusion. Understanding BTV co-infection and its biological consequences will add an important dimension to the modeling of viral evolution and emergence.
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spelling pubmed-106099822023-10-28 In Situ Hybridization (RNAscope) Detection of Bluetongue Virus Serotypes 10 and 17 in Experimentally Co-Infected Culicoides sonorensis Carpenter, Molly Benavides Obon, AnaMario Kopanke, Jennifer Lee, Justin Reed, Kirsten Sherman, Tyler Rodgers, Case Stenglein, Mark McDermott, Emily Mayo, Christie Pathogens Article Bluetongue virus (BTV) is a segmented, double-stranded RNA virus transmitted by Culicoides biting midges. Infection of domestic and wild ruminants with BTV can result in a devastating disease and significant economic losses. As a virus with a segmented genome, reassortment among the BTV serotypes that have co-infected a host may increase genetic diversity, which can alter BTV transmission dynamics and generate epizootic events. The objective of this study was to determine the extent of dissemination and characterize the tropism of BTV serotypes 10 and 17 in co-infected Culicoides sonorensis. Midges were exposed to both BTV serotypes via blood meal and processed for histologic slides 10 days after infection. An in situ hybridization approach was employed using the RNAscope platform to detect the nucleic acid segment 2 of both serotypes. Observations of the mosaic patterns in which serotypes did not often overlap suggest that co-infection at the cellular level may not be abundant with these two serotypes in C. sonorensis. This could be a consequence of superinfection exclusion. Understanding BTV co-infection and its biological consequences will add an important dimension to the modeling of viral evolution and emergence. MDPI 2023-09-30 /pmc/articles/PMC10609982/ /pubmed/37887723 http://dx.doi.org/10.3390/pathogens12101207 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Carpenter, Molly
Benavides Obon, AnaMario
Kopanke, Jennifer
Lee, Justin
Reed, Kirsten
Sherman, Tyler
Rodgers, Case
Stenglein, Mark
McDermott, Emily
Mayo, Christie
In Situ Hybridization (RNAscope) Detection of Bluetongue Virus Serotypes 10 and 17 in Experimentally Co-Infected Culicoides sonorensis
title In Situ Hybridization (RNAscope) Detection of Bluetongue Virus Serotypes 10 and 17 in Experimentally Co-Infected Culicoides sonorensis
title_full In Situ Hybridization (RNAscope) Detection of Bluetongue Virus Serotypes 10 and 17 in Experimentally Co-Infected Culicoides sonorensis
title_fullStr In Situ Hybridization (RNAscope) Detection of Bluetongue Virus Serotypes 10 and 17 in Experimentally Co-Infected Culicoides sonorensis
title_full_unstemmed In Situ Hybridization (RNAscope) Detection of Bluetongue Virus Serotypes 10 and 17 in Experimentally Co-Infected Culicoides sonorensis
title_short In Situ Hybridization (RNAscope) Detection of Bluetongue Virus Serotypes 10 and 17 in Experimentally Co-Infected Culicoides sonorensis
title_sort in situ hybridization (rnascope) detection of bluetongue virus serotypes 10 and 17 in experimentally co-infected culicoides sonorensis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10609982/
https://www.ncbi.nlm.nih.gov/pubmed/37887723
http://dx.doi.org/10.3390/pathogens12101207
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