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.2021 Nov 12;17(11):e1009952.
doi: 10.1371/journal.ppat.1009952. eCollection 2021 Nov.

An outbreak of SARS-CoV-2 with high mortality in mink (Neovison vison) on multiple Utah farms

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An outbreak of SARS-CoV-2 with high mortality in mink (Neovison vison) on multiple Utah farms

Chrissy D Eckstrand et al. PLoS Pathog..

Abstract

The breadth of animal hosts that are susceptible to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and may serve as reservoirs for continued viral transmission are not known entirely. In August 2020, an outbreak of SARS-CoV-2 occurred on five mink farms in Utah and was associated with high mink mortality (35-55% of adult mink) and rapid viral transmission between animals. The premise and clinical disease information, pathology, molecular characterization, and tissue distribution of virus within infected mink during the early phase of the outbreak are provided. Infection spread rapidly between independently housed animals and farms, and caused severe respiratory disease and death. Disease indicators were most notably sudden death, anorexia, and increased respiratory effort. Gross pathology examination revealed severe pulmonary congestion and edema. Microscopically there was pulmonary edema with moderate vasculitis, perivasculitis, and fibrinous interstitial pneumonia. Reverse transcriptase polymerase chain reaction (RT-PCR) of tissues collected at necropsy demonstrated the presence of SARS-CoV-2 viral RNA in multiple organs including nasal turbinates, lung, tracheobronchial lymph node, epithelial surfaces, and others. Localization of viral RNA by in situ hybridization revealed a more localized infection, particularly of the upper respiratory tract. Whole genome sequencing from multiple mink was consistent with published SARS-CoV-2 genomes with few polymorphisms. The Utah mink SARS-CoV-2 strains fell into Clade GH, which is unique among mink and other animal strains sequenced to date. While sharing the N501T mutation which is common in mink, the Utah strains did not share other spike RBD mutations Y453F and F486L found in nearly all mink from the United States. Mink in the outbreak reported herein had high levels of SARS-CoV-2 in the upper respiratory tract associated with symptomatic respiratory disease and death.

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Clinical and gross necropsy findings in SARS-CoV-2 infected mink.
A. A mucopurulent nasal discharge, indicative of rhinitis, stains the fur surrounding the nares in a SARS-CoV-2 infected mink. B. Gross image of severe pulmonary congestion and edema of an infected mink.
Fig 2
Fig 2. Pulmonary histopathology of SARS-CoV-2 infected mink.
A. Lung from an adult mink with large cuffs of mononuclear inflammatory cells and edema multifocally surrounding pulmonary vessels. 20x H&E. B. Alveolar spaces are multifocally filled with eosinophilic edema fluid. 40x H&E. C. Bronchioles are lined with proliferative, slightly disorganized hyperplastic epithelium and type II pneumocyte hyperplasia is present in alveoli associated with increased intra-alveolar inflammation. 100x H&E. D. Neutrophils, fewer macrophages, and strands of fibrin are multifocally present in alveoli. 200x H&E.
Fig 3
Fig 3. Detection of SARS-CoV-2 RNA in tissues by RT-PCR and ISH.
Tissues where viral RNA was not detected (ND) or not tested (NT) by RT-PCR are present below the lower horizontal black line. Circles represent samples that were SARS-CoV-2 tested by RT-PCR, and SARS-CoV-2 RNA was not detected by ISH in FFPE. Triangles represent samples that were SARS-CoV-2 tested by RT-PCR, and demonstrated positive detection of SARS-Co-2 RNA by ISH. Diamonds represent samples that were not tested (not available) by RT-PCR, and SARS-CoV-2 was positively detected by ISH on FFPE tissue. Squares represent samples in which SARS-CoV-2 tested by RT-PCR, however FFPE tissues was not tested (not available) for ISH. Stars represent cases in which tissue was unavailable for both SARS-CoV-2 RT-PCR and ISH.
Fig 4
Fig 4. Detection of SARS-CoV-2 RNA in tissues by ISH.
Fig A-C. Nasal turbinate samples from SARS-CoV-2 infected mink 5. A. H&E image of suppurative and histiocytic rhinitis filling the nasal passage. B. Detection of SARS-CoV-2 RNA in the nasal exudate. C. No detection of FIPV RNA in nasal turbinate of SARS-CoV-2 infected mink (negative control). D. Nasal turbinate samples from SARS-CoV-2 infected mink 5 demonstrating mild rhinitis in the caudal nasal passage and mild disorganization of respiratory epithelial cells E. Detection of SARS-CoV-2 viral RNA within respiratory epithelial cells of mink 5. F. No detection of FIPV RNA in nasal turbinate epithelial cells of SARS-CoV-2 infected mink (negative control). Fig G-H Lung samples from SARS-CoV-2 infected mink 1. G. H&E image of bronchus with attenuation and multifocal loss of respiratory epithelial cells. H. Detection of SARS-CoV-2 viral RNA within respiratory epithelial cells of the bronchus. Fig I-J Trachea samples from SARS-CoV-2 infected mink 1. I. H&E image of trachea with mild attenuation and multifocal disorganization of respiratory epithelial cells. J. Detection of SARS-CoV-2 viral RNA within respiratory epithelial cells of the trachea.
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References

    1. Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020; doi: 10.1016/S0140-6736(20)30183-5 - DOI - PMC - PubMed
    1. Zhou P, Yang X Lou, Wang XG, Hu B, Zhang L, Zhang W, et al. A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature. Springer US; 2020;579: 270–273. doi: 10.1038/s41586-020-2012-7 - DOI - PMC - PubMed
    1. Lu R, Zhao X, Li J, Niu P, Yang B, Wu H, et al. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. Lancet. Elsevier Ltd; 2020;395: 565–574. doi: 10.1016/S0140-6736(20)30251-8 - DOI - PMC - PubMed
    1. Olival KJ, Cryan PM, Amman BR, Baric RS, Blehert DS, Brook CE, et al. Possibility for reverse zoonotic transmission of SARS-CoV-2 to free-ranging wildlife: A case study of bats. PLoS Pathog. 2020;In Press: 1–19. doi: 10.1371/journal.ppat.1008758 - DOI - PMC - PubMed
    1. Martina BEE, Haagmans BL, Kuiken T, Fouchier RAM, Rimmelzwaan GF, Van Amerongen G, et al. SARS virus infection of cats and ferrets. Nature. 2003;425: 915. doi: 10.1038/425915a - DOI - PMC - PubMed

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