Shandilya Umesh K, Wu Xiang, McAllister Caitlin, Mutharia Lucy, Karrow Niel A
Department of Animal Biosciences, University of Guelph, Guelph, Ontario, Canada.
Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada.
Microbiol Spectr. 2023 Mar 13;11(2):e0439322. doi: 10.1128/spectrum.04393-22.
Toll-like receptor 4 () encodes an innate immune cell pattern-recognition receptor implicated in the recognition of Mycobacterium avium subsp. (MAP), the causative agent of Johne's disease in ruminants. Polymorphisms in have been associated with susceptibility to MAP infection. In this study, a previously developed knockout (KO) bovine mammary epithelial (MAC-T) cell line and wild-type MAC-T cells (WT) were infected with live MAP for 72 h to identify potential immunoregulatory miRNAs, inflammatory genes, and cytokines/chemokines impacted by MAP infection in the presence/absence of . Cytokines/chemokines production in culture supernatants was measured by multiplexing immunoassay. Total RNA was extracted from the remaining MAC-T cells, and quantitative PCR was performed to determine the expression of inflammatory genes and selected bovine miRNAs. Results showed that the levels of tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), CXCL8, CXCL10, CCL4, and CCL3 were significantly induced in WT MAC-T cells during MAP infection. However, KO MAC-T cells had greater secretion of CCL3, IL-6, vascular endothelial growth factor (VEGF-α), and TNF-α and decreased secretion of CXCL10 and CCL2. Moreover, the expression of inflammatory genes was induced in KO cells. The expression of miRNAs (miR133b, miR-92a, and miR-184) was increased in WT MAC-T cells post-MAP infection; however, there was no significant induction of these miRNAs in KO cells, which suggests they are involved in regulating the innate immune response to MAP infection. Target gene function analysis further suggests that miR-92a may be involved in TLR and interleukin signaling and miR-133b and miR-184 may be involved in other signaling pathways. These findings support the involvement of TLR4 in the regulation of innate immune response to MAP. Mycobacterium avium subsp. (MAP) is the causative agent for paratuberculosis or Johne's disease (JD) in ruminants, a disease clinically very similar to Crohn's disease in humans. Polymorphisms in the bovine Toll-like receptor genes (, , and ) have been shown to affect MAP recognition and host innate immune response and have been associated with increased susceptibility of cattle to paratuberculosis. Our results demonstrated that knocking out the gene in bovine MAC-T cells enhanced inflammation in response to MAP. These findings show divergent roles for TLR4 in Escherichia coli lipopolysaccharide and mycobacterial infections, and this may have important consequences for the treatment of these inflammatory diseases and for genetic selection to improve disease resistance. It advances our understanding of the role of TLR4 in the context of MAP infection.
Toll样受体4(TLR4)编码一种天然免疫细胞模式识别受体,参与识别鸟分枝杆菌副结核亚种(MAP),它是反刍动物约翰氏病的病原体。TLR4基因多态性与MAP感染易感性相关。在本研究中,用活的MAP感染先前构建的TLR4基因敲除(KO)牛乳腺上皮(MAC-T)细胞系和野生型MAC-T细胞(WT)72小时,以鉴定在有无TLR4情况下受MAP感染影响的潜在免疫调节性微小RNA(miRNA)、炎症基因以及细胞因子/趋化因子。通过多重免疫测定法检测培养上清液中细胞因子/趋化因子的产生。从剩余的MAC-T细胞中提取总RNA,并进行定量PCR以确定炎症基因和选定的牛miRNA的表达。结果显示,在MAP感染期间,野生型MAC-T细胞中肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、CXCL8、CXCL10、CCL4和CCL3的水平显著升高。然而,KO MAC-T细胞中CCL3、IL-6、血管内皮生长因子(VEGF-α)和TNF-α的分泌更多,而CXCL10和CCL2的分泌减少。此外,KO细胞中炎症基因的表达被诱导。MAP感染后,野生型MAC-T细胞中miRNA(miR133b、miR-92a和miR-184)的表达增加;然而,这些miRNA在KO细胞中没有明显诱导,这表明它们参与调节对MAP感染的天然免疫反应。靶基因功能分析进一步表明,miR-92a可能参与TLR和白细胞介素信号传导,而miR-133b和miR-184可能参与其他信号通路。这些发现支持TLR4参与对MAP感染的天然免疫反应调节。鸟分枝杆菌副结核亚种(MAP)是反刍动物副结核病或约翰氏病(JD)的病原体,这种疾病在临床上与人类的克罗恩病非常相似。牛Toll样受体基因(TLR1、TLR2和TLR4)的多态性已被证明会影响MAP识别和宿主天然免疫反应,并与牛对副结核病易感性增加有关。我们的结果表明,在牛MAC-T细胞中敲除TLR4基因会增强对MAP的炎症反应。这些发现显示了TLR4在大肠杆菌脂多糖和分枝杆菌感染中的不同作用,这可能对这些炎症性疾病的治疗以及提高抗病性的基因选择具有重要意义。它推进了我们对TLR4在MAP感染背景下作用的理解。