4.5 Article

Evaluation of Feedstuffs as a Potential Carrier of Avian Influenza Virus between Feed Mills and Poultry Farms

Journal

PATHOGENS
Volume 11, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/pathogens11070755

Keywords

avian influenza virus; poultry; feed; complete layer mash; real-time polymerase chain reaction; half-life

Categories

Funding

  1. Egg Industry Center (Ames, IA, USA) [2704235]
  2. Fulbright scholarship

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The present study assessed the potential role of feedstuffs in the spread of avian influenza virus (AIV) and found that AIV survivability in feed is relatively low, thus rendering it low risk. The decay of AIV RNA was faster at higher temperatures, suggesting that maintaining feed in the cold chain is important for testing purposes. Furthermore, heat treatment of feed may be an alternative to chemical treatment when contamination is suspected.
The present study was conducted to assess the potential vector role of feedstuffs for the area spreading of avian influenza virus (AIV). Firstly, feed samples were collected from commercial poultry facilities that experienced highly pathogenic avian influenza (H5N2) in 2014-2015 for AIV testing by a real-time RT-PCR specific for the viral matrix gene. Secondly, feed materials obtained from an AIV-negative farm were spiked with various concentrations of a low pathogenic AIV H5N2. Virus-spiked cell culture media were prepared in the same manner and used for comparison. The spiked feed and media samples were tested by a multiplex real-time RT-PCR ran in a quantitative manner, either immediately or after incubation at -20, 4, 22, and 37 degrees C for 24, 48, and 72 h. Some of the feedstuffs collected from the poultry facilities or feed mills were positive for AIV RNA but negative by the virus isolation (VI) test, while all the formaldehyde-treated feedstuffs were PCR-negative. In the spiked feeds, the AIV titer was 1-3 logs lower than that in the corresponding media, even when tested immediately after spiking, suggesting that feed might have a negative impact on the virus or PCR detection. The half-life of AIV RNA was shorter at a higher temperature. A significant decay in the viral RNA over time was noted at 37 degrees C (p < 0.05), suggesting that feedstuffs should be maintained in the cold chain when testing is desired. Furthermore, the thermal degradation of AIV suggests that the heat treatment of feeds could be an alternative to chemical treatment when contamination is suspected. Collectively, the study observations indicate that AIV survivability in feed is relatively low, thus rendering it a low risk.

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