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恙虫病患者色氨酸 2,3-双加氧酶的激活及其在恙虫东方体生长受限中的作用。

Activation of indoleamine 2,3-dioxygenase in patients with scrub typhus and its role in growth restriction of Orientia tsutsugamushi.

机构信息

Division of Molecular Genetics, Department of Research and Development, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.

出版信息

PLoS Negl Trop Dis. 2012;6(7):e1731. doi: 10.1371/journal.pntd.0001731. Epub 2012 Jul 31.

Abstract

BACKGROUND

Our earlier genome-wide expression study revealed up-regulation of a tryptophan-catabolizing enzyme, indoleamine 2,3-dioxygenase (IDO1), in patients with scrub typhus. This gene has been previously reported to have anti-microbial activity in a variety of infectious diseases; therefore, we aimed to prove whether it is also involved in host defense against Orientia tsutsugamushi (OT) infection.

METHODOLOGY/PRINCIPAL FINDINGS: Using LC-MS, we observed an increased ratio of serum L-kynurenine to serum L-tryptophan in patients with scrub typhus, which suggests an active catalytic function of this enzyme upon the illness. To evaluate the effect of IDO1 activation on OT infection, a human macrophage-like cell line THP-1 was used as a study model. Although transcription of IDO1 was induced by OT infection, its functional activity was not significantly enhanced unless the cells were pretreated with IFN-γ, a potent inducer of IDO1. When the degree of infection was evaluated by quantitative real-time PCR, the relative number of OT 47 kDa gene per host genes, or infection index, was markedly reduced by IFN-γ treatment as compared to the untreated cultures at five days post-infection. Inhibition of IDO1 activity in IFN-γ treated cultures by 1-methyl-L-tryptophan, a competitive inhibitor of IDO1, resulted in partial restoration of infection index; while excessive supplementation of L-tryptophan in IFN-γ treated cultures raised the index to an even higher level than that of the untreated ones. Altogether, these data implied that IDO1 was partly involved in restriction of OT growth caused by IFN-γ through deprivation of tryptophan.

CONCLUSIONS/SIGNIFICANCE: Activation of IDO1 appeared to be a defensive mechanism downstream of IFN-γ that limited intracellular expansion of OT via tryptophan depletion. Our work provided not only the first link of in vivo activation of IDO1 and IFN-γ-mediated protection against OT infection but also highlighted the promise of this multifaceted gene in scrub typhus research.

摘要

背景

我们之前的全基因组表达研究表明,患有丛林斑疹伤寒的患者体内色氨酸分解酶吲哚胺 2,3-双加氧酶(IDO1)表达上调。该基因先前已被报道在多种传染病中具有抗微生物活性;因此,我们旨在证明它是否也参与宿主对恙虫东方体(OT)感染的防御。

方法/主要发现:使用 LC-MS,我们观察到患有丛林斑疹伤寒的患者血清中 L-犬尿氨酸与 L-色氨酸的比值增加,这表明该酶在疾病期间具有活跃的催化功能。为了评估 IDO1 激活对 OT 感染的影响,我们使用人巨噬细胞样细胞系 THP-1 作为研究模型。尽管 OT 感染诱导了 IDO1 的转录,但除非细胞先用 IFN-γ预处理,IFN-γ是 IDO1 的有效诱导剂,否则其功能活性不会显著增强。通过定量实时 PCR 评估感染程度时,与未处理的培养物相比,IFN-γ处理的培养物中的 OT 47 kDa 基因与宿主基因的相对数量,即感染指数,在感染后 5 天明显降低。在 IFN-γ处理的培养物中,用 IDO1 的竞争性抑制剂 1-甲基-L-色氨酸抑制 IDO1 的活性,导致感染指数部分恢复;而在 IFN-γ处理的培养物中过度补充 L-色氨酸会将指数提高到比未处理的培养物更高的水平。总之,这些数据表明,IDO1 通过耗尽色氨酸,部分参与了 IFN-γ限制 OT 生长的过程。

结论/意义:IDO1 的激活似乎是 IFN-γ下游的一种防御机制,通过耗尽色氨酸来限制 OT 在细胞内的扩张。我们的工作不仅提供了体内 IDO1 激活与 IFN-γ介导的 OT 感染保护之间的第一个联系,而且还强调了该多效基因在丛林斑疹伤寒研究中的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc94/3409113/766b4a2f5196/pntd.0001731.g001.jpg

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