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Pathogenesis of West Nile Virus Lineage 2 in Domestic Geese after Experimental Infection
West Nile virus (WNV) is an emerging infectious pathogen circulating between mosquitoes and birds but also infecting mammals. WNV has become autochthonous in Germany, causing striking mortality rates in avifauna and occasional diseases in humans and horses. We therefore wanted to assess the possible...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9230372/ https://www.ncbi.nlm.nih.gov/pubmed/35746790 http://dx.doi.org/10.3390/v14061319 |
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author | Reemtsma, Hannah Holicki, Cora M. Fast, Christine Bergmann, Felicitas Eiden, Martin Groschup, Martin H. Ziegler, Ute |
author_facet | Reemtsma, Hannah Holicki, Cora M. Fast, Christine Bergmann, Felicitas Eiden, Martin Groschup, Martin H. Ziegler, Ute |
author_sort | Reemtsma, Hannah |
collection | PubMed |
description | West Nile virus (WNV) is an emerging infectious pathogen circulating between mosquitoes and birds but also infecting mammals. WNV has become autochthonous in Germany, causing striking mortality rates in avifauna and occasional diseases in humans and horses. We therefore wanted to assess the possible role of free-ranging poultry in the WNV transmission cycle and infected 15 goslings with WNV lineage 2 (German isolate). The geese were monitored daily and sampled regularly to determine viremia, viral shedding, and antibody development by molecular and serological methods. Geese were euthanized at various time points post-infection (pi). All infected geese developed variable degrees of viremia from day 1 to day 10 (maximum) and actively shed virus from days 2 to 7 post-infection. Depending on the time of death, the WN viral genome was detected in all examined tissue samples in at least one individual by RT-qPCR and viable virus was even re-isolated, except for in the liver. Pathomorphological lesions as well as immunohistochemically detectable viral antigens were found mainly in the brain. Furthermore, all of the geese seroconverted 6 days pi at the latest. In conclusion, geese are presumably not functioning as important amplifying hosts but are suitable sentinel animals for WNV surveillance. |
format | Online Article Text |
id | pubmed-9230372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92303722022-06-25 Pathogenesis of West Nile Virus Lineage 2 in Domestic Geese after Experimental Infection Reemtsma, Hannah Holicki, Cora M. Fast, Christine Bergmann, Felicitas Eiden, Martin Groschup, Martin H. Ziegler, Ute Viruses Article West Nile virus (WNV) is an emerging infectious pathogen circulating between mosquitoes and birds but also infecting mammals. WNV has become autochthonous in Germany, causing striking mortality rates in avifauna and occasional diseases in humans and horses. We therefore wanted to assess the possible role of free-ranging poultry in the WNV transmission cycle and infected 15 goslings with WNV lineage 2 (German isolate). The geese were monitored daily and sampled regularly to determine viremia, viral shedding, and antibody development by molecular and serological methods. Geese were euthanized at various time points post-infection (pi). All infected geese developed variable degrees of viremia from day 1 to day 10 (maximum) and actively shed virus from days 2 to 7 post-infection. Depending on the time of death, the WN viral genome was detected in all examined tissue samples in at least one individual by RT-qPCR and viable virus was even re-isolated, except for in the liver. Pathomorphological lesions as well as immunohistochemically detectable viral antigens were found mainly in the brain. Furthermore, all of the geese seroconverted 6 days pi at the latest. In conclusion, geese are presumably not functioning as important amplifying hosts but are suitable sentinel animals for WNV surveillance. MDPI 2022-06-16 /pmc/articles/PMC9230372/ /pubmed/35746790 http://dx.doi.org/10.3390/v14061319 Text en © 2022 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 Reemtsma, Hannah Holicki, Cora M. Fast, Christine Bergmann, Felicitas Eiden, Martin Groschup, Martin H. Ziegler, Ute Pathogenesis of West Nile Virus Lineage 2 in Domestic Geese after Experimental Infection |
title | Pathogenesis of West Nile Virus Lineage 2 in Domestic Geese after Experimental Infection |
title_full | Pathogenesis of West Nile Virus Lineage 2 in Domestic Geese after Experimental Infection |
title_fullStr | Pathogenesis of West Nile Virus Lineage 2 in Domestic Geese after Experimental Infection |
title_full_unstemmed | Pathogenesis of West Nile Virus Lineage 2 in Domestic Geese after Experimental Infection |
title_short | Pathogenesis of West Nile Virus Lineage 2 in Domestic Geese after Experimental Infection |
title_sort | pathogenesis of west nile virus lineage 2 in domestic geese after experimental infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9230372/ https://www.ncbi.nlm.nih.gov/pubmed/35746790 http://dx.doi.org/10.3390/v14061319 |
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