Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 26, Number 8—August 2020
Dispatch

Atypical Pathogenicity of Avian Influenza (H3N1) Virus Involved in Outbreak, Belgium, 2019

Mieke SteenselsComments to Author , Philippe Gelaude, Steven Van Borm, Thierry Van Den Berg, Mickaël Cargnel, Virginie Roupie, Fabienne Rauw, and Bénédicte Lambrecht
Author affiliations: Sciensano, Brussels, Belgium (M. Steensels, S. Van Borm, T. Van Den Berg, M. Cargnel, V. Roupie, F. Rauw, B. Lambrecht); Animal Health Vlaanderen, Torhout, Belgium (P. Gelaude)

Main Article

Figure 2

Viral presence in birds during experimental infection with avian influenza (H3N1) isolated from poultry in Belgium, 2019. The individual excretion values are shown (different patterns in circles and diamonds correspond to individual birds) in addition to the average group value ± SDs (error bars). Asterisks (*) indicate statistically relevant differences between time points, groups, or organs, p<0.05. Note: for diluted viral isolates the correspondence between log10 (no. copies/mL) and log10

Figure 2. Viral presence in birds during experimental infection with avian influenza (H3N1) isolated from poultry in Belgium, 2019. The individual excretion values are shown (different patterns in circles and diamonds correspond to individual birds) in addition to the average group value ± SDs (error bars). Asterisks (*) indicate statistically relevant differences between time points, groups, or organs, p<0.05. Note: for diluted viral isolates the correspondence between log10 (no. copies/mL) and log10 (50% egg infectious dose/mL) is a difference of ≈1 log less in egg infectious dose. The exact link (by determining the titer of infectious virus in the samples) was considered beyond the scope of this article. A) Viral RNA excretion of infected and sentinel birds at different points after infection, by respiratory gastrointestinal tract samples. B) Viral presence in the organs of infected and sentinel birds at time of death or the end of the experiment (21 dpi), determined by real-time reverse transcription PCR. Viral RNA excretion or presence is expressed as the logarithm of the number of viral RNA copies/mL as quantification was performed relative to an external curve during real-time reverse transcription PCR analysis. CLS, cloacal samples; dpi, days postinfection; repro, reproduction; TRS, oropharyngeal swab samples.

Main Article

Page created: June 12, 2020
Page updated: July 18, 2020
Page reviewed: July 18, 2020
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
file_external