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多聚磷酸激酶1参与生物膜的形成、形态和超微结构及其在巨噬细胞中的生存能力。

Polyphosphate kinase 1 is involved in formation, the morphology and ultramicrostructure of biofilm of and its survivability in macrophage.

作者信息

He Cailin, Li Bo, Gong Zhen, Huang Sheng, Liu Xu, Wang Jiajun, Xie Jianping, Shi Tingyu

机构信息

Medical School of Hubei Minzu University, Enshi, 445000, China.

Institute of Modern Biopharmaceuticals, School of Life Sciences, Southwest University, Chongqing, 400715, China.

出版信息

Heliyon. 2023 Mar 17;9(3):e14513. doi: 10.1016/j.heliyon.2023.e14513. eCollection 2023 Mar.

Abstract

The most unique characteristic of is persistence in the human host, and the biofilm formation is related to the persistance. Polyphosphate (polyP) kinase 1 (PPK1) is conserved in and is responsible for polyP synthesis. polyP is a chain molecule linked by high-energy phosphate bonds, which is considered to play a very important role in bacterial persistence. However, the relationship of PPK1 and mycobacterial biofilm formation is still adequately unclear. In current study, -deficient mutant (MT), -complemented (CT) and wild-type strains of mc 155 were used to investigate the formation, morphology and ultramicrostructure of the biofilm and to analyze the lipid levels and susceptibility to vancomycin antibiotic. And then WT, MT and CT strains were used to infect macrophages and to analyze the expression levels of various inflammatory factors, respectively. We found that PPK1 was required for polyP production and polyP deficiency not only attenuated the biofilm formation, but also altered the phenotype and ultramicrostructure of the biofilm and reduced the cell lipid composition (except for C16.1 and C17.1, most of the fatty acid components from C8-C24). Moreover, the -deficient mutant was also significantly more sensitive to vancomycin which targets the cell wall, and its ability to survive in macrophages was decreased, which was related to the change of the expression level of inflammatory factors in macrophage. This study demonstrates that the PPK1 can affect the biofilm structure through affecting the content of short chain fatty acid and promote intracellular survival of by altering the expression of inflammatory factors. These findings establish a basis for investigating the role of PPK1 in the persistence of , and provide clues for treating latent infection of with PPK1 as a potential drug target.

摘要

[细菌名称]最独特的特征是在人类宿主中具有持久性,且生物膜形成与之相关。多聚磷酸盐(polyP)激酶1(PPK1)在[细菌名称]中保守存在并负责多聚磷酸盐的合成。多聚磷酸盐是由高能磷酸键连接的链状分子,被认为在细菌持久性中发挥非常重要的作用。然而,PPK1与分枝杆菌生物膜形成之间的关系仍不清楚。在本研究中,使用[细菌名称]mc155的PPK1缺陷突变体(MT)、PPK1互补菌株(CT)和野生型菌株来研究生物膜的形成、形态和超微结构,并分析脂质水平及对万古霉素抗生素的敏感性。然后分别用WT、MT和CT菌株感染巨噬细胞并分析各种炎症因子的表达水平。我们发现PPK1是[细菌名称]产生多聚磷酸盐所必需的,多聚磷酸盐缺乏不仅减弱了生物膜的形成,还改变了生物膜的表型和超微结构,并降低了细胞脂质组成(除C16.1和C17.1外,大多数脂肪酸成分从C8 - C24)。此外,PPK1缺陷突变体对靶向细胞壁的万古霉素也明显更敏感,其在巨噬细胞中的存活能力下降,这与巨噬细胞中炎症因子表达水平的变化有关。本研究表明,PPK1可通过影响短链脂肪酸含量来影响生物膜结构,并通过改变炎症因子的表达促进[细菌名称]在细胞内存活。这些发现为研究PPK1在[细菌名称]持久性中的作用奠定了基础,并为以PPK1作为潜在药物靶点治疗[细菌名称]潜伏感染提供了线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa03/10034464/2a30f1d822ad/gr1.jpg

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