Mammary transmission of caprine arthritis encephalitis virus: a 3D model for in vitro study.

Christian Le Jan, Claire Bellaton, Timothy Greenland, Jean-François Mornex
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引用次数: 14

Abstract

Transmission of Caprine Arthritis Encephalitis virus (CAEV) from the mother to offspring is principally mediated by infected cells from colostrum and milk. The infection of the dam is often sub-clinical, and results in increased cellularity of milk, sometimes exacerbated by bacterial co-infections. Although monocytes are the major viral host cells, several other cell types, including epithelial mammary cells, fibroblasts and endothelial cells show low levels of in vivo infection. In vitro, however, all phenotypes of mammary gland cells are individually highly sensitive to CAEV infection. This suggests that local mechanisms act to control viral expression. Our goal is to analyse the mechanisms regulating local virus infection, including the physiological status of the mammary gland and bacterial co-infections. In this work, we present the development of a model for the in vitro reconstitution of mammary gland tissue using 3D cultures in Matrigel. Mononuclear cells from the blood are added to the 3D cultures in vitro. In these experimental conditions, the mammary cells spontaneously organize into mammospheres. Blood leucocytes migrate into the culture gel, and localize particularly at the periphery of the mammospheres. Mammospheres were susceptible to infection in vitro by CAEV, as shown by a cytopathic effect and expression of late CAEV antigen p30. This model will allow the in vitro study of virus expression, transfer of infection to mammary gland cells and interactions between the mammary gland cells, infected monocytes and immunocompetent cells. It will allow the study of mechanisms participating in the control of passage of pathogens into milk, according to the physiological and CAEV-infection status of the animal, microenvironment and the presence of bacterial co-infections.

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山羊关节炎脑炎病毒的乳腺传播:体外研究的3D模型。
羊关节炎脑炎病毒(CAEV)由母体向后代的传播主要是由初乳和乳汁中的感染细胞介导的。乳腺炎的感染通常是亚临床的,导致乳汁细胞增多,有时因细菌联合感染而加剧。虽然单核细胞是主要的病毒宿主细胞,但其他几种细胞类型,包括乳腺上皮细胞、成纤维细胞和内皮细胞,在体内感染水平较低。然而,在体外,所有表型的乳腺细胞都对CAEV感染高度敏感。这表明局部机制控制病毒的表达。我们的目标是分析调节局部病毒感染的机制,包括乳腺的生理状态和细菌共感染。在这项工作中,我们提出了一个模型的发展,乳腺组织的体外重建使用3D培养在Matrigel。将血液中的单个核细胞添加到体外3D培养物中。在这些实验条件下,乳腺细胞自发组织成乳腺球。血液中的白细胞迁移到培养凝胶中,特别是在乳腺球的周围。乳房微球易受CAEV体外感染,表现为细胞病变效应和CAEV晚期抗原p30的表达。该模型将允许在体外研究病毒表达、感染转移到乳腺细胞以及乳腺细胞、受感染单核细胞和免疫活性细胞之间的相互作用。根据动物的生理和caev感染状况、微环境和细菌共感染的存在,它将允许研究参与控制病原体进入牛奶的机制。
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