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体外暴露于牛疱疹病毒1和溶血曼氏杆菌的牛支气管上皮细胞的基因表达谱分析

Gene expression profiling of bovine bronchial epithelial cells exposed in vitro to bovine herpesvirus 1 and Mannheimia haemolytica.

作者信息

N'jai Alhaji U, Rivera Jose, Atapattu Dhammika N, Owusu-Ofori Kwadwo, Czuprynski Charles J

机构信息

Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, 2015 Linden Drive-West, WI 52706, United States.

出版信息

Vet Immunol Immunopathol. 2013 Sep 15;155(3):182-9. doi: 10.1016/j.vetimm.2013.06.012. Epub 2013 Jul 1.

Abstract

Bovine respiratory disease (BRD) often occurs when active respiratory virus infections (BHV-1, etc.) impair resistance to Mannheimia haemolytica infection in the lower respiratory tract. The interactions that occur when the respiratory epithelium encounters these viral and bacterial pathogens are poorly understood. We used Agilent bovine gene microarray chips containing 44,000 transcripts to elucidate bovine bronchial epithelial cell (BBEC) responses following in vitro exposure to BHV-1 alone, M. haemolytica alone, or both BHV-1 and M. haemolytica. Microarray analysis revealed differential regulation (>2-fold) of 978 transcripts by BHV-1 alone, 2040 transcripts by M. haemolytica alone, and 2189 genes by BHV-1 and M. haemolytica in combination. M. haemolytica treatment produced significantly greater inductions (>10-fold) of several inflammation associated genes, such as CXCL2, IL-6, IL-1α, e-selectin, and IL-8, than to BHV-1 alone. Functional analysis of the microarray data revealed a significant upregulation of genes involved in important biological processes such as inflammation (TNF-α, IL-8, Tlr-2, IL-1, CXCL2, CSF2), vascular functions (VEGF, EDN2) and leukocyte migration (ICAM1, IL-16) during a co-infection with BHV-1 and M. haemolytica compared to either pathogen alone. This study provides evidence to support that lung epithelial cells are a source of mediators that may promote inflammatory changes observed during bovine respiratory disease.

摘要

牛呼吸道疾病(BRD)通常发生在活跃的呼吸道病毒感染(如BHV-1等)损害下呼吸道对溶血曼氏杆菌感染的抵抗力时。呼吸道上皮细胞遇到这些病毒和细菌病原体时发生的相互作用目前还知之甚少。我们使用了包含44000个转录本的安捷伦牛基因微阵列芯片,以阐明体外单独暴露于BHV-1、单独暴露于溶血曼氏杆菌或同时暴露于BHV-1和溶血曼氏杆菌后牛支气管上皮细胞(BBEC)的反应。微阵列分析显示,单独BHV-1可使978个转录本差异调节(>2倍),单独溶血曼氏杆菌可使2040个转录本差异调节,BHV-1和溶血曼氏杆菌共同作用可使2189个基因差异调节。与单独BHV-1相比,溶血曼氏杆菌处理对几个炎症相关基因(如CXCL2、IL-6、IL-1α、e-选择素和IL-8)产生了显著更高的诱导(>10倍)。微阵列数据的功能分析显示,与单独感染任何一种病原体相比,BHV-1和溶血曼氏杆菌共同感染期间,参与重要生物学过程(如炎症(TNF-α、IL-8、Tlr-2、IL-1、CXCL2、CSF2)、血管功能(VEGF、EDN2)和白细胞迁移(ICAM1、IL-16))的基因显著上调。本研究提供了证据支持肺上皮细胞是可能促进牛呼吸道疾病期间观察到的炎症变化的介质来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4814/7127263/81ab342fdedd/gr1.jpg

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