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BY3 复方中药渣发酵液对猪源肺炎克雷伯菌荚膜多糖的抑制作用及免疫逃逸。

Inhibition of porcine origin Klebsiella pneumoniae capsular polysaccharide and immune escape by BY3 compounded traditional Chinese medicine residue fermentation broth.

机构信息

College of Veterinary Medicine, Jilin Agricultural University, Changchun, 130118, China; The Key Laboratory of New Veterinary Drug Research and Development of Jilin Province, Jilin Agricultural University, Changchun, 130118, China.

Jilin Province Wanbang Goose Technical Service Company, Changchun, 130000, China.

出版信息

Microb Pathog. 2024 Oct;195:106853. doi: 10.1016/j.micpath.2024.106853. Epub 2024 Aug 13.

Abstract

Klebsiella pneumoniae (K. pneumoniae) is a gram-negative conditionally pathogenic bacterium that causes disease primarily in immunocompromised individuals. Recently, highly virulent K. pneumoniae strains have caused severe disease in healthy individuals, posing significant challenges to global infection control. Capsular polysaccharide (CPS), a major virulence determinant of K. pneumoniae, protects the bacteria from being killed by the host immune system, suggesting an urgent need for the development of drugs to prevent or treat K. pneumoniae infections. In this study, BY3 compounded traditional Chinese medicine residue (TCMR) was carried out using Lactobacillus rhamnosus as a fermentation strain, and BY3 compounded TCMR fermentation broth (BY3 fermentation broth) was obtained. The transcription of K. pneumoniae CPS-related biosynthesis genes after treatment with BY3 fermentation broth was detected using quantitative real-time polymerase chain reaction. The effects of BY3 fermentation broth on K. pneumoniae serum killing, macrophage phagocytosis, complement deposition and human β-defensin transcription were investigated. The therapeutic effect of BY3 fermentation broth on K. pneumoniae-infected mice was also observed, and the major active components of BY3 fermentation broth were analysed via LC‒MS analysis, network pharmacology, and molecular docking. The results showed that BY3 fermentation broth inhibited K. pneumoniae CPS production and downregulated transcription of CPS-related biosynthesis genes, which weakened bacterial resistance to serum killing and phagocytosis, while promoting bacterial surface complement C3 deposition and human β-defensin expression. BY3 fermentation broth demonstrated safety and therapeutic effects in vivo and in vitro, restoring body weight and visceral indices, significantly reducing the organ bacterial load and serum cytokine levels, and alleviating pathological organ damage in mice. In addition, three natural compounds-oleanolic acid, quercetin, and palmitoleic acid-were identified as the major active components in the BY3 fermentation broth. Therefore, BY3 fermentation broth may be a promising strategy for the prevention or treatment of K. pneumoniae infections.

摘要

肺炎克雷伯菌(Klebsiella pneumoniae)是一种条件致病性革兰氏阴性菌,主要引起免疫功能低下人群的疾病。最近,高毒力肺炎克雷伯菌菌株在健康人群中引起了严重疾病,对全球感染控制构成了重大挑战。荚膜多糖(Capsular polysaccharide,CPS)是肺炎克雷伯菌的主要毒力决定因素,可保护细菌免受宿主免疫系统的杀伤,这表明迫切需要开发预防或治疗肺炎克雷伯菌感染的药物。本研究采用鼠李糖乳杆菌作为发酵菌株对 BY3 复方中药渣(TCMR)进行发酵,获得 BY3 复方中药渣发酵液(BY3 发酵液)。采用实时荧光定量聚合酶链反应检测 BY3 发酵液处理后肺炎克雷伯菌 CPS 相关生物合成基因的转录情况。研究了 BY3 发酵液对肺炎克雷伯菌血清杀伤、巨噬细胞吞噬、补体沉积和人β防御素转录的影响。观察了 BY3 发酵液对肺炎克雷伯菌感染小鼠的治疗效果,并通过 LC-MS 分析、网络药理学和分子对接分析了 BY3 发酵液的主要活性成分。结果表明,BY3 发酵液抑制肺炎克雷伯菌 CPS 的产生,下调 CPS 相关生物合成基因的转录,从而减弱细菌对血清杀伤和吞噬的抵抗力,同时促进细菌表面补体 C3 的沉积和人β防御素的表达。BY3 发酵液在体内和体外均具有安全性和治疗效果,恢复体重和内脏指数,显著降低器官细菌负荷和血清细胞因子水平,减轻小鼠器官病理损伤。此外,鉴定出三种天然化合物——齐墩果酸、槲皮素和棕榈油酸——为 BY3 发酵液中的主要活性成分。因此,BY3 发酵液可能是预防或治疗肺炎克雷伯菌感染的一种有前途的策略。

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