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Inactivation of Highly Transmissible Livestock and Avian Viruses Including Influenza A and Newcastle Disease Virus for Molecular Diagnostics

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Journal Front Vet Sci
Date 2024 Mar 22
PMID 38515532
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Abstract

There is a critical need for an inactivation method that completely inactivates pathogens at the time of sample collection while maintaining the nucleic acid quality required for diagnostic PCR testing. This inactivation method is required to alleviate concerns about transmission potential, minimize shipping complications and cost, and enable testing in lower containment laboratories, thereby enhancing disease diagnostics through improved turn-around time. This study evaluated a panel of 10 surrogate viruses that represent highly pathogenic animal diseases. These results showed that a commercial PrimeStore® molecular transport media (PSMTM) completely inactivated all viruses tested by >99.99%, as determined by infectivity and serial passage assays. However, the detection of viral nucleic acid by qRT-PCR was comparable in PSMTM and control-treated conditions. These results were consistent when viruses were evaluated in the presence of biological material such as sera and cloacal swabs to mimic diagnostic sample conditions for non-avian and avian viruses, respectively. The results of this study may be utilized by diagnostic testing laboratories for highly pathogenic agents affecting animal and human populations. These results may be used to revise guidance for select agent diagnostic testing and the shipment of infectious substances.

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References
1.
Powers A . Resurgence of Interest in Eastern Equine Encephalitis Virus Vaccine Development. J Med Entomol. 2021; 59(1):20-26. DOI: 10.1093/jme/tjab135. View

2.
Joshi V, Chaudhary D, Bansal N, Singh R, Maan S, Mahajan N . Prevalence of Newcastle Disease Virus in Commercial and Backyard Poultry in Haryana, India. Front Vet Sci. 2021; 8:725232. PMC: 8600042. DOI: 10.3389/fvets.2021.725232. View

3.
Daum L, Worthy S, Yim K, Nogueras M, Schuman R, Choi Y . A clinical specimen collection and transport medium for molecular diagnostic and genomic applications. Epidemiol Infect. 2011; 139(11):1764-73. DOI: 10.1017/S0950268810002384. View

4.
Koonin E, Yutin N . Origin and evolution of eukaryotic large nucleo-cytoplasmic DNA viruses. Intervirology. 2010; 53(5):284-92. PMC: 2895762. DOI: 10.1159/000312913. View

5.
Charlier J, Barkema H, Becher P, De Benedictis P, Hansson I, Hennig-Pauka I . Disease control tools to secure animal and public health in a densely populated world. Lancet Planet Health. 2022; 6(10):e812-e824. DOI: 10.1016/S2542-5196(22)00147-4. View