Comparative transcriptomic analysis of bovine papillomatosis

被引:6
|
作者
Barreto, Debora M. [1 ]
Barros, Gerlane S. [1 ]
Santos, Lucas A. B. O. [1 ]
Soares, Rosilene C. [2 ]
Batista, Marcus V. A. [1 ]
机构
[1] Univ Fed Sergipe, Ctr Biol & Hlth Sci, Dept Biol, Lab Mol Genet & Biotechnol, Sao Cristovao, Sergipe, Brazil
[2] Univ Fed Sergipe, Dept Morphol, Sao Cristovao, Sergipe, Brazil
来源
BMC GENOMICS | 2018年 / 19卷
关键词
Bovine papillomavirus; RNA-seq; Differently expressed genes; Keratinocyte; Apoptosis; Immune response; PAPILLOMAVIRUS DNA; BLOOD;
D O I
10.1186/s12864-018-5361-y
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
BackgroundBovine papillomavirus (BPV) belongs to the Papillomaviridae family and infects epithelial cells of bovines and closely related animals, causing hyperproliferative lesions known as warts or papillomas, which may regress or progress to form benign or malignant tumors. The virus enters the host cell and interacts with it by altering the regulation of genes that are responsible for controlling the cell cycle, thus triggering lesion formation. It is not yet known which host genes are regulated by viral infection. Therefore, the objective of this study was to make use of next-generation RNA sequencing methods to identify differentially expressed genes associated with BPV infection, which might elucidate possible marker genes that could be used to control the disease.ResultsTranscriptome analysis revealed that 1343 genes were differentially regulated (FDR<0.05). A comparison of gene expression in infected and noninfected cows indicated that 655 genes were significantly upregulated, and 688 genes were significantly downregulated. Most differentially expressed genes were associated with BPV infection pathways, which supports the hypothesis that viral infection was the mechanism associated with this regulation.ConclusionsThis is the first study that focused on a large-scale evaluation of gene expression associated with BPV infection, which is important to identify possible metabolic pathways regulated by host genes for lesion development. In addition, novel targets could be identified in order to find ligands that interact with BPV, with the aim of interrupting the infection cycle.
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页数:9
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