共 4 条
Survival of a surrogate African swine fever virus-like algal virus in feed matrices using a 23-day commercial United States truck transport model
被引:8
|作者:
Palowski, Amanda
[1
]
Balestreri, Cecilia
[1
]
Urriola, Pedro E.
[2
]
van de Ligt, Jennifer L. G.
[1
]
Sampedro, Fernando
[3
]
Dee, Scott
[4
]
Shah, Apoorva
[5
]
Yancy, Haile F.
[6
]
Shurson, Gerald C.
[2
]
Schroeder, Declan C.
[1
,7
]
机构:
[1] Univ Minnesota, Coll Vet Med, Dept Vet Populat Med, St Paul, MN 55455 USA
[2] Univ Minnesota, Coll Food Agr & Nat Resource Sci, Dept Anim Sci, St Paul, MN 55455 USA
[3] Univ Minnesota, Sch Publ Hlth, Environm Hlth Sci Div, Minneapolis, MN USA
[4] Pipestone Vet Serv, Pipestone Appl Res, Pipestone, MN USA
[5] SAM Nutr, Eden Prairie, MN USA
[6] US FDA, Ctr Vet Med, Off Res, Laurel, MD USA
[7] Univ Reading, Sch Biol Sci, Reading, England
关键词:
African swine fever virus;
Emiliania huxleyi virus;
NCLDVs;
feed;
transport;
viability PCR;
FAMILIES;
INFECTS;
D O I:
10.3389/fmicb.2022.1059118
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
African swine fever virus (ASFV) is a member of the nucleocytoplasmic large DNA viruses (NCLDVs) and is stable in a variety of environments, including animal feed ingredients as shown in previous laboratory experiments and simulations. Emiliania huxleyi virus (EhV) is another member of the NCLDVs, which has a restricted host range limited to a species of marine algae called Emiliania huxleyi. This algal NCLDV has many similar morphological and physical characteristics to ASFV thereby making it a safe surrogate, with results that are applicable to ASFV and suitable for use in real-world experiments. Here we inoculated conventional soybean meal (SBMC), organic soybean meal (SBMO), and swine complete feed (CF) matrices with EhV strain 86 (EhV-86) at a concentration of 6.6 x 10(7) virus g(-1), and then transported these samples in the trailer of a commercial transport vehicle for 23 days across 10,183 km covering 29 states in various regions of the United States. Upon return, samples were evaluated for virus presence and viability using a previously validated viability qPCR (V-qPCR) method. Results showed that EhV-86 was detected in all matrices and no degradation in EhV-86 viability was observed after the 23-day transportation event. Additionally, sampling sensitivity (we recorded unexpected increases, as high as 49% in one matrix, when virus was recovered at the end of the sampling period) rather than virus degradation best explains the variation of virus quantity observed after the 23-day transport simulation. These results demonstrate for the first time that ASFV-like NCLDVs can retain viability in swine feed matrices during long-term transport across the continental United States.
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