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牛单核细胞来源的巨噬细胞体外感染两种无乳链球菌后 microRNA 表达谱。

MicroRNA expression profiles of bovine monocyte-derived macrophages infected in vitro with two strains of Streptococcus agalactiae.

机构信息

Department of Basic Sciences and Aquatic Medicine, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, 0033, Oslo, Norway.

Department of Food Safety and Infection Biology, Faculty of Veterinary Medicine, Norwegian University of Life Sciences, 0033, Oslo, Norway.

出版信息

BMC Genomics. 2018 Apr 10;19(1):241. doi: 10.1186/s12864-018-4591-3.

Abstract

BACKGROUND

MicroRNAs (miRNAs) are short, non-coding RNAs that regulate gene expression at the post-transcriptional level and play a key role in the control of innate and adaptive immune responses. For a subclinical infection such as bovine streptococcal mastitis, early detection is a great challenge, and miRNA profiling could potentially assist in the diagnosis and contribute to the understanding of the pathogenicity and defense mechanisms. We have examined the miRNA repertoire and the transcript level of six key immune genes [tumor necrosis factor alpha (TNFα), interleukin-1 beta (IL-1β), interleukin-6 (IL-6), interleukin-8 (IL-8), interleukin-10 (IL-10) and transforming growth factor beta 1 (TGFβ1)] during the early phase response of bovine immature macrophages to in vitro infection with live Streptococcus agalactiae. Next generation sequencing of small RNA libraries from 20 cultures of blood monocyte-derived macrophages exposed to either one of two sequence types of S. agalactiae (ST103 or ST12) for 6 h in vitro and unchallenged controls was performed.

RESULTS

Analyzes of over 356 million high quality sequence reads, revealed differential expression of 17 and 44 miRNAs (P < 0.05) in macrophages infected with ST103 and ST12, respectively, versus unchallenged control cultures. We also identified the expression of 31 potentially novel bovine miRNAs. Pathway analysis of the differentially regulated miRNAs and their predicted target genes in the macrophages infected with ST12 revealed significant enrichment for inflammatory response and apoptosis, while significant enrichment for integrin and GABA signaling were found in ST103 infected macrophages. Furthermore, both bacterial strains regulated miRNAs involved in the alternative activation of macrophages. The transcript levels of TNF-α, IL-1β, IL-6, IL-8 and IL-10 were significantly up-regulated by both bacterial strains, however the expression of TGFβ1 was significantly down-regulated only by ST12.

CONCLUSIONS

Our study identified pathogen-induced differential regulation of miRNAs controlling inflammation and polarization in bovine macrophages. This implies that miRNAs have potential to serve as biomarkers for early detection of bacterial infection.

摘要

背景

微小 RNA(miRNA)是一类短的非编码 RNA,可在转录后水平调控基因表达,在先天和适应性免疫反应的调控中发挥关键作用。对于牛链球菌乳腺炎等亚临床感染,早期检测是一个巨大的挑战,miRNA 谱分析可能有助于诊断,并有助于了解致病性和防御机制。我们已经检查了牛未成熟巨噬细胞在体外感染活酿脓链球菌后早期反应中 miRNA 谱和六个关键免疫基因 [肿瘤坏死因子-α(TNFα)、白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、白细胞介素-8(IL-8)、白细胞介素-10(IL-10)和转化生长因子-β1(TGFβ1)] 的转录水平。对 20 个血液单核细胞衍生巨噬细胞培养物的小 RNA 文库进行下一代测序,这些培养物分别在体外暴露于两种酿脓链球菌序列型(ST103 或 ST12)6 小时,并与未受挑战的对照进行比较。

结果

对超过 3.56 亿个高质量序列读取的分析表明,与未受挑战的对照培养物相比,分别用 ST103 和 ST12 感染的巨噬细胞中 17 和 44 个 miRNA 的表达存在差异(P<0.05)。我们还鉴定了 31 个潜在的新的牛 miRNA。用 ST12 感染的巨噬细胞中差异表达的 miRNA 及其预测靶基因的途径分析表明,炎症反应和细胞凋亡显著富集,而整合素和 GABA 信号显著富集在 ST103 感染的巨噬细胞中。此外,两种细菌株都调节了参与巨噬细胞的替代激活的 miRNA。两种细菌株均显著上调 TNF-α、IL-1β、IL-6、IL-8 和 IL-10 的转录水平,而仅 ST12 显著下调 TGFβ1 的表达。

结论

我们的研究鉴定了病原体诱导的控制牛巨噬细胞炎症和极化的 miRNA 的差异调节。这意味着 miRNA 有可能作为细菌感染早期检测的生物标志物。

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