Houston Grace E, Trujillo Jessie D, Jones Cassandra K, Kwon Taeyong, Stark Charles R, Cool Konner, Paulk Chad B, Gaudreault Natasha N, Woodworth Jason C, Morozov Igor, Gallardo Carmina, Gebhardt Jordan T, Richt Jürgen A
Department of Diagnostic Medicine/Pathobiology, Kansas State University, Manhattan, KS, USA.
Center of Excellence for Emerging and Zoonotic Animal Disease, Kansas State University, Manhattan, KS, USA.
Transbound Emerg Dis. 2023 Aug 23;2023:3455128. doi: 10.1155/2023/3455128. eCollection 2023.
One way to mitigate risk of feed-based pathogens for swine diets is to quarantine feed ingredients before inclusion in complete diets. Data have been generated evaluating the stability of swine viruses in ingredients, but the stability of African swine fever virus (ASFV) in feed or in a feed manufacturing environment has not been well characterized. Therefore, this study aimed to determine the stability of ASFV DNA in swine feed and on mill surfaces over time. A pilot-scale feed mill was used to manufacture six sequential batches of feed consisting of a batch of ASFV-free feed, followed by a batch inoculated with ASFV (final concentration = 5.6 × 10 TCID/g), and then four subsequent ASFV-free batches. After each batch, 10 feed samples were aseptically collected in a double "X" pattern. During feed manufacturing, 24 steel coupons were placed on the floor of the manufacturing area and allowed to collect dust during feed manufacturing. Once feed manufacturing was completed, feed samples and steel coupons were stored at room temperature. Three of each were randomly selected from storage on 3, 7, 14, 28, 60, 90, and 180 days after feed manufacturing and analyzed for ASFV DNA. For feed samples, there was evidence of a batch × day interaction ( = 0.023) for the quantification of genomic copies/g of feed, indicating that the amount of ASFV DNA present was impacted by both the batch of feed and days held at room temperature. There were no differences of genomic copies/g in early batches, but quantity of detectable ASFV decreased with increasing storage time. In Batches 4-6, the greatest quantity of ASFV DNA was detected on the day of feed manufacturing. The lowest quantity was detected on Day 7 for Batch 4, Day 60 for Batch 5, and at 28 and 180 days for Batch 6. There was no evidence of ASFV degradation on environmental discs across holding times ( = 0.433). In conclusion, the quarantining of feed may help reduce but not eliminate the presence of ASFV DNA in feed over time. Importantly, ASFV DNA was detectable on feed manufacturing surfaces for at least 180 days with no overt evidence of reduction, highlighting the importance of bioexclusion of ASFV within feed manufacturing facilities and the need for thorough/effective decontamination and other mitigation processes in affected areas.
降低猪饲料中基于饲料的病原体风险的一种方法是在将饲料成分纳入全价日粮之前进行隔离。已经产生了评估猪病毒在饲料成分中的稳定性的数据,但非洲猪瘟病毒(ASFV)在饲料或饲料生产环境中的稳定性尚未得到充分表征。因此,本研究旨在确定ASFV DNA在猪饲料和工厂表面随时间的稳定性。使用中试规模的饲料厂生产六批连续的饲料,一批不含ASFV的饲料,然后一批接种ASFV(最终浓度 = 5.6×10 TCID/g),随后是四批不含ASFV的饲料。每批生产后,以双“X”模式无菌采集10个饲料样本。在饲料生产过程中,将24个钢片放置在生产区域的地面上,在饲料生产过程中收集灰尘。饲料生产完成后,将饲料样本和钢片在室温下储存。在饲料生产后的第3、7、14、28、60、90和180天,从储存中随机选择其中三个进行ASFV DNA分析。对于饲料样本,在每克饲料基因组拷贝数的定量分析中存在批次×天数的交互作用( = 0.023),这表明存在的ASFV DNA量受到饲料批次和室温保存天数的影响。早期批次中每克基因组拷贝数没有差异,但可检测到的ASFV数量随着储存时间的增加而减少。在第4 - 6批中,在饲料生产当天检测到的ASFV DNA量最大。第4批在第7天、第5批在第60天、第6批在第28天和第180天检测到的量最低。在整个保存时间内,环境圆盘上没有ASFV降解的迹象( = 0.433)。总之,饲料隔离可能有助于随着时间的推移减少但不能消除饲料中ASFV DNA的存在。重要的是,在饲料生产表面至少180天可检测到ASFV DNA,且没有明显减少的迹象,这突出了在饲料生产设施内对ASFV进行生物排除的重要性,以及在受影响地区进行彻底/有效去污和其他缓解措施的必要性。