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利用实验性贾第虫绵羊反转录病毒感染模型跟踪绵羊肺腺癌的发展。

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

机构信息

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

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

出版信息

Genes (Basel). 2024 Aug 2;15(8):1019. doi: 10.3390/genes15081019.

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 (R = 0.799, < 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.

摘要

绵羊肺腺癌(OPA)是一种感染性、肿瘤性的绵羊肺部疾病,在全球范围内给动物福利和经济带来了重大影响。了解 OPA 的发病机制是开发控制其影响的工具的关键。为此,需要有能够监测和跟踪 Jaagsiekte 绵羊逆转录病毒(JSRV)感染后事件的模型系统。在这里,我们报告了一种为此目的而开发的实验性诱导 OPA 模型。使用三个不同的病毒剂量组(低、中、高),通过支气管镜将 JSRV 注入右心叶段支气管,诱导局部 OPA 肿瘤发展。通过每月进行计算机断层扫描(CT)成像和经胸超声扫描来监测临床前 OPA 的诊断和肿瘤进展。尸检和免疫组织化学证实,89%的 JSRV 注入动物中发展出了 OPA。三种病毒剂量均产生了一系列 OPA 病变类型,包括显微镜下疾病和大体肿瘤;然而,在低和中剂量病毒组中更常发现较大的病变。总体而言,31%的 JSRV 感染绵羊发展为局部晚期病变。在发展为局部晚期病变的绵羊中,肿瘤体积倍增时间(使用胸部 CT 3D 重建计算)为 14.8±2.1 天。超声检测肿瘤发展的能力与 CT 进行了比较;结果表明,在每个时间点,CT 和超声测量之间存在强烈的显著相关性(R=0.799,<0.0001)。我们相信,该模型诱导的 OPA 病变类型范围复制了自然发生疾病的某些方面,通过为 JSRV 感染性和 OPA 疾病进展提供新的见解,将改善 OPA 研究。

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