Tracking Ovine Pulmonary Adenocarcinoma Development Using an Experimental Jaagsiekte Sheep Retrovirus Infection Model

Author:

Cousens Chris1ORCID,Meehan James2ORCID,Collie David2,Wright Steven2,Chang Ziyuan2,Todd Helen1,Moore Jo1,Grant Lynn2,Daniel Carola R.2,Tennant Peter2,Ritchie Adrian2,Nixon James2,Proudfoot Chris2,Guido Stefano2,Brown Helen2,Gray Calum D.3ORCID,MacGillivray Tom J.4,Clutton R. Eddie2,Greenhalgh Stephen N.2ORCID,Gregson Rachael2,Griffiths David J.1ORCID,Spivey James5,Storer Nicole5,Eckert Chad E.5,Gray Mark2ORCID

Affiliation:

1. Moredun Research Institute, Pentlands Science Park, Bush Loan, Penicuik EH26 0PZ, UK

2. The Royal (Dick) School of Veterinary Studies and Roslin Institute, University of Edinburgh, Easter Bush, Roslin, Edinburgh EH25 9RG, UK

3. Edinburgh Imaging Facility, Queen’s Medical Research Institute, University of Edinburgh, 47 Little France Crescent, Edinburgh EH16 4TJ, UK

4. Centre for Clinical Brain Sciences, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, EH16 4SB, UK

5. Interventional Oncology, Johnson & Johnson Enterprise Innovation, Inc., One Johnson & Johnson Plaza, New Brunswick, NJ 08933, USA

Abstract

Ovine pulmonary adenocarcinoma (OPA) is an infectious, neoplastic lung disease of sheep that causes significant animal welfare and economic issues throughout the world. Understanding OPA pathogenesis is key to developing tools to control its impact. Central to this need is the availability of model systems that can monitor and track events after Jaagsiekte sheep retrovirus (JSRV) infection. Here, we report the development of an experimentally induced OPA model intended for this purpose. Using three different viral dose groups (low, intermediate and high), localised OPA tumour development was induced by bronchoscopic JSRV instillation into the segmental bronchus of the right cardiac lung lobe. Pre-clinical OPA diagnosis and tumour progression were monitored by monthly computed tomography (CT) imaging and trans-thoracic ultrasound scanning. Post mortem examination and immunohistochemistry confirmed OPA development in 89% of the JSRV-instilled animals. All three viral doses produced a range of OPA lesion types, including microscopic disease and gross tumours; however, larger lesions were more frequently identified in the low and intermediate viral groups. Overall, 31% of JSRV-infected sheep developed localised advanced lesions. Of the sheep that developed localised advanced lesions, tumour volume doubling times (calculated using thoracic CT 3D reconstructions) were 14.8 ± 2.1 days. The ability of ultrasound to track tumour development was compared against CT; the results indicated a strong significant association between paired CT and ultrasound measurements at each time point (R2 = 0.799, p < 0.0001). We believe that the range of OPA lesion types induced by this model replicates aspects of naturally occurring disease and will improve OPA research by providing novel insights into JSRV infectivity and OPA disease progression.

Funder

Johnson & Johnson

Publisher

MDPI AG

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