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

Authors :
Cousens, Chris
Meehan, James
Collie, David
Wright, Steven
Chang, Ziyuan
Todd, Helen
Moore, Jo
Grant, Lynn
Daniel, Carola R.
Tennant, Peter
Ritchie, Adrian
Nixon, James
Proudfoot, Chris
Guido, Stefano
Brown, Helen
Gray, Calum D.
MacGillivray, Tom J.
Clutton, R. Eddie
Greenhalgh, Stephen N.
Gregson, Rachael
Source :
Genes. Aug2024, Vol. 15 Issue 8, p1019. 21p.
Publication Year :
2024

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20734425
Volume :
15
Issue :
8
Database :
Academic Search Index
Journal :
Genes
Publication Type :
Academic Journal
Accession number :
179354032
Full Text :
https://doi.org/10.3390/genes15081019