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Experimental challenge with bovine respiratory syncytial virus in dairy calves: bronchial lymph node transcriptome response

机译:牛犊牛呼吸道合胞病毒的实验挑战:支气管淋巴结转录组反应

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摘要

Bovine Respiratory Disease (BRD) is the leading cause of mortality in calves. The objective of this study was to examine the response of the host’s bronchial lymph node transcriptome to Bovine Respiratory Syncytial Virus (BRSV) in a controlled viral challenge. Holstein-Friesian calves were either inoculated with virus (103.5 TCID50/ml × 15 ml) (n = 12) or mock challenged with phosphate buffered saline (n = 6). Clinical signs were scored daily and blood was collected for haematology counts, until euthanasia at day 7 post-challenge. RNA was extracted and sequenced (75 bp paired-end) from bronchial lymph nodes. Sequence reads were aligned to the UMD3.1 bovine reference genome and differential gene expression analysis was performed using EdgeR. There was a clear separation between BRSV challenged and control calves based on gene expression changes, despite an observed mild clinical manifestation of the disease. Therefore, measuring host gene expression levels may be beneficial for the diagnosis of subclinical BRD. There were 934 differentially expressed genes (DEG) (p < 0.05, FDR <0.1, fold change >2) between the BRSV challenged and control calves. Over-represented gene ontology terms, pathways and molecular functions, among the DEG, were associated with immune responses. The top enriched pathways included interferon signaling, granzyme B signaling and pathogen pattern recognition receptors, which are responsible for the cytotoxic responses necessary to eliminate the virus.
机译:牛呼吸系统疾病(BRD)是犊牛死亡的主要原因。这项研究的目的是检查宿主的支气管淋巴结转录组在病毒控制下对牛呼吸道合胞病毒(BRSV)的反应。用病毒(10 3.5 TCID50 / ml××15 ml)(n = 12)接种荷斯坦-弗里斯牛犊或用磷酸盐缓冲液(n = 6)模拟攻击。每天对临床体征进行评分,并收集血液用于血液学计数,直到攻击后第7天安乐死。从支气管淋巴结中提取RNA并测序(75 bp对末端)。将序列读数与UMD3.1牛参考基因组比对,并使用EdgeR进行差异基因表达分析。尽管观察到该病的轻度临床表现,但根据基因表达变化,BRSV攻击小牛和对照牛之间仍存在明显的分离。因此,测量宿主基因表达水平可能对亚临床BRD的诊断有益。 BRSV攻击小牛和对照牛之间存在934个差异表达基因(DEG)(p <0.05,FDR <0.1,倍数变化> 2)。 DEG中过度代表的基因本体术语,途径和分子功能与免疫反应有关。最丰富的途径包括干扰素信号传导,颗粒酶B信号传导和病原体模式识别受体,它们是消除病毒所必需的细胞毒性反应。

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