Predictive Value of Precision-Cut Lung Slices for the Susceptibility of Three Animal Species for SARS-CoV-2 and Validation in a Refined Hamster Model.

Nora M Gerhards1 Jan B W J Cornelissen1 Lucien J M van Keulen1 José Harders-Westerveen1 Rianka Vloet1 Bregtje Smid1 Stéphanie Vastenhouw1 Sophie van Oort1 Renate W Hakze-van der Honing1 Jose L Gonzales1 Norbert Stockhofe-Zurwieden1 Rineke de Jong1 Wim H M van der Poel1 Sandra Vreman1 Jeroen Kortekaas1,2 Paul J Wichgers Schreur1 Nadia Oreshkova1
Affiliations 2 institutions
  1. Wageningen Bioveterinary Research, Houtribweg 39, 8221 RA Lelystad, The Netherlands.
  2. Laboratory of Virology, Wageningen University, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands.

Abstract

In assessing species susceptibility for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and in the search for an appropriate animal model, multiple research groups around the world inoculated a broad range of animal species using various SARS-CoV-2 strains, doses and administration routes. Although in silico analyses based on receptor binding and diverse in vitro cell cultures were valuable, exact prediction of species susceptibility based on these tools proved challenging. Here, we assessed whether precision-cut lung slices (PCLS) could facilitate the selection of animal models, thereby reducing animal experimentation. Pig, hamster and cat PCLS were incubated with SARS-CoV-2 and virus replication was followed over time. Virus replicated efficiently in PCLS from hamsters and cats, while no evidence of replication was obtained for pig PCLS. These data corroborate the findings of many research groups that have investigated the susceptibility of hamsters, pigs and cats towards infection with SARS-CoV-2. Our findings suggest that PCLS can be used as convenient tool for the screening of different animal species for sensitivity to newly emerged viruses. To validate our results obtained in PCLS, we employed the hamster model. Hamsters were inoculated with SARS-CoV-2 via the intranasal route. Susceptibility to infection was evaluated by body weight loss, viral loads in oropharyngeal swabs and respiratory tissues and lung pathology. The broadly used hamster model was further refined by including activity tracking of the hamsters by an activity wheel as a very robust and sensitive parameter for clinical health. In addition, to facilitate the quantification of pathology in the lungs, we devised a semi-quantitative scoring system for evaluating the degree of histological changes in the lungs. The inclusion of these additional parameters refined and enriched the hamster model, allowing for the generation of more data from a single experiment.

Supporting text Virus Host Location
activity 1 hamster model 1 histology scores 1 precision-cut lung slices 1 SARS-CoV-2 550

Evidence records

1 total
Experimental Infection
1 records · 1 evidence types
Evidence type
1 records
OVE4932
Key finding

SARS-CoV-2 replicated efficiently in precision-cut lung slices from hamsters and cats, but not in those from pigs.

Virus
Host
Location
Not specified
Supporting text

Pig, hamster and cat PCLS were incubated with SARS-CoV-2 and virus replication was followed over time. Virus replicated efficiently in PCLS from hamsters and cats, while no evidence of replication was obtained for pig PCLS.

Method
viral incubation | virus replication monitoring over time
Sample type
precision-cut lung slices
Experimental system
ex vivo precision-cut lung slice infection assay