从抗酸利莫斯乳酸杆菌 JCM 15950T 中提取的具有三个脂肪酸残基的脂联乳酸的免疫刺激活性。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Applied and Environmental Microbiology Pub Date : 2024-10-23 Epub Date: 2024-09-06 DOI:10.1128/aem.01197-24
Shino Yamasaki-Yashiki, Tsukasa Shiraishi, Mai Gyobu, Haruna Sasaki, Jun Kunisawa, Shin-Ichi Yokota, Yoshio Katakura
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引用次数: 0

摘要

某些乳酸菌株能调节宿主的肠道免疫系统。本研究旨在探究 TLR2 的配体--脂联素(LTA)在这些细菌细胞及其膜囊泡的免疫刺激活性中的作用。从细菌细胞中提取的 LTA 通过疏水相互作用色谱法纯化,然后通过阴离子交换色谱法分成 LTA1 和 LTA2 两部分。与LTA2相比,LTA1能诱导巨噬细胞样RAW264细胞产生更多的白细胞介素(IL)-6,而使用抗TLR2抗体中和TLR2能抑制诱导的IL-6产生。两种馏分中的 LTA 在糖脂锚中都含有两个己糖残基;然而,LTA1 尤其富含三酰 LTA。在 LTA1 中,甘油磷酸酯(GroP)重复单元中的游离羟基被 d-丙氨酸(d-Ala)和 α-葡萄糖取代,而在 LTA2 中仅被α-葡萄糖取代。LTA1 的脱乙酰化可轻微抑制 RAW264 细胞中 IL-6 的产生,而脱乙酰化则几乎完全抑制了 IL-6 的产生。此外,烷基化的LTA1诱导的IL-6产生量明显高于烷基化的LTA2诱导的IL-6产生量。这些结果表明,L. antri 衍生的 LTA 免疫刺激活性的关键分子是三个脂肪酸残基,而不是 GroP 中的 d-Ala 取代。LTA也在MV中被检测到,这表明三酰LTA而非二酰LTA能转运到MV中并赋予免疫刺激活性:一些乳酸菌通过收费样受体(TLR)2激活宿主肠道免疫系统。脂联乳酸(LTA)是一种TLR2配体;然而,由于LTA部分结构的多样性,决定其免疫刺激活性的LTA分子仍不清楚。我们发现抗利莫斯乳杆菌 JCM 15950T 有三种类型的 LTA(三酰基、二酰基和单酰基 LTA)。具体来说,对 LTAs 的结构分析表明,三酰基 LTA 在免疫刺激中起着关键作用,而脂肪酸残基对其活性至关重要。三个酰基残基是许多乳酸菌 LTAs 的特征,我们的发现可以解释乳酸菌广泛表现出的免疫刺激机制。此外,L. antri JCM 15950T 释放的膜囊泡的免疫刺激活性是由转移的 LTA 引起的,这证明了膜囊泡介导免疫刺激的新机制。
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Immunostimulatory activity of lipoteichoic acid with three fatty acid residues derived from Limosilactobacillus antri JCM 15950T.

Some strains of lactic acid bacteria can regulate the host's intestinal immune system. Bacterial cells and membrane vesicles (MVs) of Limosilactobacillus antri JCM 15950T promote immunoglobulin A (IgA) production in murine Peyer's patch cells via toll-like receptor (TLR) 2. This study aimed to investigate the role of lipoteichoic acid (LTA), a ligand of TLR2, in the immunostimulatory activity of these bacterial cells and their MVs. LTA extracted from bacterial cells was purified through hydrophobic interaction chromatography and then divided into fractions LTA1 and LTA2 through anion-exchange chromatography. LTA1 induced greater interleukin (IL)-6 production from macrophage-like RAW264 cells than LTA2, and the induced IL-6 production was suppressed by TLR2 neutralization using an anti-TLR2 antibody. The LTAs in both fractions contained two hexose residues in the glycolipid anchor; however, LTA1 was particularly rich in triacyl LTA. The free hydroxy groups in the glycerol phosphate (GroP) repeating units were substituted by d-alanine (d-Ala) and α-glucose in LTA1, but only by α-glucose in LTA2. The dealanylation of LTA1 slightly suppressed IL-6 production in RAW264 cells, whereas deacylation almost completely suppressed IL-6 production. Furthermore, IL-6 production induced by dealanylated LTA1 was markedly higher than that induced by dealanylated LTA2. These results indicated that the critical moieties for the immunostimulatory activity of L. antri-derived LTA were the three fatty acid residues rather than the substitution with d-Ala in GroP. LTA was also detected in MVs, suggesting that the triacyl LTA, but not the diacyl LTA, translocated to the MVs and conferred immunostimulatory activity.

Importance: Some lactic acid bacteria activate the host intestinal immune system via toll-like receptor (TLR) 2. Lipoteichoic acid (LTA) is a TLR2 ligand; however, the moieties of LTA that determine its immunostimulatory activity remain unclear because of the wide diversity of LTA partial structures. We found that Limosilactobacillus antri JCM 15950T has three types of LTAs (triacyl, diacyl, and monoacyl LTAs). Specifically, structural analysis of the LTAs revealed that triacyl LTA plays a crucial role in immunostimulation and that the fatty acid residues are essential for the activity. The three acyl residues are characteristic of LTAs from many lactic acid bacteria, and our findings can explain the immunostimulatory mechanisms widely exhibited by lactic acid bacteria. Furthermore, the immunostimulatory activity of membrane vesicles released by L. antri JCM 15950T is due to the transferred LTA, demonstrating a novel mechanism of membrane vesicle-mediated immunostimulation.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
期刊最新文献
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