Analysis of avian Usutu virus infections in Germany from 2011 to 2018 with focus on dsRNA detection to demonstrate viral infections

• Published in: Scientific Reports
• Main Authors: Störk, Theresa, de le Roi, Madeleine, Haverkamp, Ann-Kathrin, Jesse, Sonja T., Peters, Martin, Fast, Christine, Gregor, Katharina M., Könenkamp, Laura, Steffen, Imke, Ludlow, Martin, Beineke, Andreas, Hansmann, Florian, Wohlsein, Peter, Osterhaus, Albert D. M. E., Baumgärtner, Wolfgang
• Format: Article in Journal/Newspaper
• Language: English
• Published: 2021
• Subjects: Text; ddc:570; great grey owl
• Online Access: https://doi.org/10.1038/s41598-021-03638-5; https://www.openagrar.de/receive/openagrar_mods_00076723; https://www.openagrar.de/servlets/MCRFileNodeServlet/openagrar_derivate_00043763/SD2021576.pdf; https://www.nature.com/articles/s41598-021-03638-5.pdf; https://www.nature.com/articles/s41598-021-03638-5

Usutu virus (USUV) is a zoonotic arbovirus causing avian mass mortalities. The first outbreak in North-Western Germany occurred in 2018. This retrospective analysis focused on combining virological and pathological findings in birds and immunohistochemistry. 25 common blackbirds, one great grey owl, and one kingfisher collected from 2011 to 2018 and positive for USUV by qRT-PCR were investigated. Macroscopically, most USUV infected birds showed splenomegaly and hepatomegaly. Histopathological lesions included necrosis and lymphohistiocytic inflammation within spleen, Bursa fabricii, liver, heart, brain, lung and intestine. Immunohistochemistry revealed USUV antigen positive cells in heart, spleen, pancreas, lung, brain, proventriculus/gizzard, Bursa fabricii, kidney, intestine, skeletal muscle, and liver. Analysis of viral genome allocated the virus to Europe 3 or Africa 2 lineage. This study investigated whether immunohistochemical detection of double-stranded ribonucleic acid (dsRNA) serves as an alternative tool to detect viral intermediates. Tissue samples of six animals with confirmed USUV infection by qRT-PCR but lacking viral antigen in liver and spleen, were further examined immunohistochemically. Two animals exhibited a positive signal for dsRNA. This could indicate either an early state of infection without sufficient formation of virus translation products, occurrence of another concurrent virus infection or endogenous dsRNA not related to infectious pathogens and should be investigated in more detail in future studies.