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Potential Diagnostic Value of the Peripheral Blood Mononuclear Cell Transcriptome From Cattle With Bovine Tuberculosis

机译:从牛结核牛的外周血单核细胞转录组的潜在诊断值

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Bovine tuberculosis (bTB) is a chronic disease of cattle caused by Mycobacterium bovis. During early-stage infection, M. bovis-infected cattle shed mycobacteria through nasal secretions, which can be detected via nested-polymerase chain reaction (PCR) experiments. However, little research has focused on immune responses in nested PCR-positive (bTB PCR-P) or nested PCR-negative (bTB PCR-N) M. bovis-infected cattle. Here, we investigated the transcriptomes of peripheral blood mononuclear cells (PBMCs), with or without stimulation by purified protein derivative of bovine tuberculin (PPD-B), among bTB PCR-P, bTB PCR-N, and healthy cattle using RNA-Seq. We also explored the potential value of PBMC transcripts as novel biomarkers for diagnosing bTB. Numerous differentially expressed genes were identified following pair-wise comparison of different groups, with or without PPD-B stimulation (adjusted p 0.05). Compared with healthy cattle, bTB PCR-P, and bTB PCR-N cattle shared 5 significantly dysregulated biological pathways, including Cytokine-cytokine receptor interaction, NF-kappa B signaling pathway, Hematopoietic cell lineage, Osteoclast differentiation and HTLV-I infection. Notably, dysregulated biological pathways of bTB PCR-P and bTB PCR-N cattle were associated with cell death and phagocytosis, respectively. PPD-B stimulated lymphotoxin alpha and interleukin-8 could potentially differentiate M. bovis-infected and healthy cattle, with area-under-the-curve (AUC) values of 0.9991 and 0.9343, respectively. PPD-B-stimulated B cell lymphoma 2 and chitinase 3-like 1 might enable differentiation between bTB PCR-P and bTB PCR-N, with AUC values of 0.9100 and 0.8893, respectively. Thus, the PBMC transcriptome revealed the status of bTB infection and may provide a novel sight in bTB diagnosis.
机译:牛结核病(BTB)是由Bovis引起的牛慢性疾病。在早期感染期间,通过鼻腔分泌物,M. Bovis感染的牛卵细胞脱落,可通过巢式聚合酶链式反应(PCR)实验来检测。然而,小型研究专注于巢式PCR阳性(BTB PCR-P)或嵌套的PCR-阴性(BTB PCR-N)M.感染牛中的免疫应答。在这里,我们研究了外周血单核细胞(PBMC)的转录组,或不通过牛结核蛋白(PPD-B)的纯化的蛋白质衍生物,BTB PCR-P,BTB PCR-N和使用RNA-SEQ的健康牛来刺激。我们还探讨了PBMC成绩单作为新型生物标志物的潜在价值,用于诊断BTB。鉴定多种差异表达的基因在不同基团的成对比较后,有或没有PPD-B刺激(调节P <0.05)。与健康养牛,BTB PCR-P和BTB PCR-N牛相比,共用5显着失调的生物途径,包括细胞因子 - 细胞因子受体相互作用,NF-Kappa信令途径,造血细胞谱系,破骨细胞分化和HTLV-I感染。值得注意的是,BTB PCR-P和BTB PCR-N牛的失调生物途径分别与细胞死亡和吞噬作用相关。 PPD-B受刺激的淋巴毒素α和白细胞介素-8可能分别区分肉豆感染和健康牛,分别具有0.9991和0.9343的面积曲线(AUC)值。 PPD-B刺激的B细胞淋巴瘤2和几丁质酶3样1可以使BTB PCR-P和BTB PCR-N之间的分化分别为0.9100和0.8893的AUC值。因此,PBMC转录组揭示了BTB感染的状态,并且可以在BTB诊断中提供新的视觉。

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