4.6 Article

Evaluating the distribution of African swine fever virus within a feed mill environment following manufacture of inoculated feed

Journal

PLOS ONE
Volume 16, Issue 8, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0256138

Keywords

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Funding

  1. NBAF Transition Funds from the state of Kansas
  2. National Pork Board [20-018]
  3. Department of Homeland Security Center of Excellence for Emerging and Zoonotic Animal Diseases [HSHQDC 16-A-B0006]
  4. AMP Core of the NIGMS COBRE Center on Emerging and Zoonotic Infectious Diseases (CEZID) [P20GM13044]

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This study evaluated the distribution of ASFV in a feed mill environment, showing a higher detection of viral genome on transient surfaces compared to other surfaces. The findings suggest that once ASFV enters the feed mill environment, it can rapidly spread, with human movement significantly contributing to the transmission of ASFV in the feed mill environment.
It is critical to understand the role feed manufacturing may have regarding potential African swine fever virus (ASFV) transmission, especially given the evidence that feed and/or ingredients may be potential vectors. The objective of the study was to evaluate the distribution of ASFV in a feed mill following manufacture of contaminated feed. To accomplish this, a pilot-scale feed mill consisting of a mixer, bucket elevator, and spouting was constructed in a BSL-3Ag facility. First, a batch of ASFV-free feed was manufactured, followed by a batch of feed that had an ASFV-contaminated ingredient added to feed, which was then mixed and discharged from the equipment. Subsequently, four additional ASFV-free batches of feed were manufactured using the same equipment. Environmental swabs from 18 locations within the BSL-3Ag room were collected after each batch of feed was discharged. The locations of the swabs were categorized into four zones: 1) feed contact surface, 2) non-feed contact surface < 1 meter away from feed, 3) non-feed contact surface > 1 meter from feed, and 4) transient surfaces. Environmental swabs were analyzed using a qPCR specific for the ASFV p72 gene and reported as genomic copy number (CN)/mL of environmental swab processing buffer. Genomic copies were transformed with a log(10) function for statistical analysis. There was no evidence of a zone x batch interaction for log(10) genomic CN/mL (P = 0.625) or cycle threshold (Ct) value (P = 0.608). Sampling zone impacted the log(10) p72 genomic CN/mL (P < 0.0001) and Ct values (P < 0.0001), with a greater amount of viral genome detected on transient surfaces compared to other surfaces (P < 0.05). This study illustrates that once ASFV enters the feed mill environment it becomes widespread and movement of people can significantly contribute to the spread of ASFV in a feed mill environment.

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