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Intranasal exposure of African green monkeys to SARS-CoV-2 results in acute phase pneumonia with shedding and lung injury still present in the early convalescence phase.
Cross, Robert W; Agans, Krystle N; Prasad, Abhishek N; Borisevich, Viktoriya; Woolsey, Courtney; Deer, Daniel J; Dobias, Natalie S; Geisbert, Joan B; Fenton, Karla A; Geisbert, Thomas W.
  • Cross RW; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, 77555, USA.
  • Agans KN; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, 77555, USA.
  • Prasad AN; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, 77555, USA.
  • Borisevich V; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, 77555, USA.
  • Woolsey C; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, 77555, USA.
  • Deer DJ; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, 77555, USA.
  • Dobias NS; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, 77555, USA.
  • Geisbert JB; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, 77555, USA.
  • Fenton KA; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, 77555, USA.
  • Geisbert TW; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, 77555, USA.
Virol J ; 17(1): 125, 2020 08 18.
Article in English | MEDLINE | ID: covidwho-719595
Preprint
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ABSTRACT
We recently reported the development of the first African green monkey (AGM) model for COVID-19 based on a combined liquid intranasal (i.n.) and intratracheal (i.t.) exposure to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Here, we followed up on this work by assessing an i.n. particle only route of exposure using the LMA mucosal atomization device (MAD). Six AGMs were infected with SARS-CoV-2; three animals were euthanized near the peak stage of virus replication (day 5) and three animals were euthanized during the early convalescence period (day 34). All six AGMs supported robust SARS-CoV-2 replication and developed respiratory disease. Evidence of coagulation dysfunction as noted by a transient increases in aPTT and circulating levels of fibrinogen was observed in all AGMs. The level of SARS-CoV-2 replication and lung pathology was not quite as pronounced as previously reported with AGMs exposed by the combined i.n. and i.t. routes; however, SARS-CoV-2 RNA was detected in nasal swabs of some animals as late as day 15 and rectal swabs as late as day 28 after virus challenge. Of particular importance to this study, all three AGMs that were followed until the early convalescence stage of COVID-19 showed substantial lung pathology at necropsy as evidenced by multifocal chronic interstitial pneumonia and increased collagen deposition in alveolar walls despite the absence of detectable SARS-CoV-2 in any of the lungs of these animals. These findings are consistent with human COVID-19 further demonstrating that the AGM faithfully reproduces the human condition.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Coronavirus Infections / Betacoronavirus Limits: Animals Language: English Journal: Virol J Journal subject: Virology Year: 2020 Document Type: Article Affiliation country: S12985-020-01396-w

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Coronavirus Infections / Betacoronavirus Limits: Animals Language: English Journal: Virol J Journal subject: Virology Year: 2020 Document Type: Article Affiliation country: S12985-020-01396-w