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群体感应分子 N-酰基高丝氨酸内酯抑制小鼠模型中的化脓隐秘杆菌感染。

Quorum-sensing molecules N-acyl homoserine lactones inhibit Trueperella pyogenes infection in mouse model.

机构信息

Key Laboratory of Bio-resources and Eco-environment (Ministry of Education), College of Life Sciences, Sichuan University, Chengdu, China.

Sichuan Key Laboratory of Conservation Biology on Endangered Wildlife, College of Life Sciences, Sichuan University, Chengdu, China.

出版信息

Vet Microbiol. 2018 Jan;213:89-94. doi: 10.1016/j.vetmic.2017.11.029. Epub 2017 Nov 22.

Abstract

Trueperella pyogenes is a gram-positive opportunistic pathogen normally causes mastitis, liver abscesses and pneumonia of economically important livestock. It has been suggested that gram-negative bacteria can suppress the growth and virulence of T. pyogenes in vitro by using the quorum-sensing (QS) signal molecules and cause the transition of predominant species. However, whether these QS signals can be used as potential anti-virulence drugs against T. pyogenes infection is unclear. In this study, the in vivo inhibitory effect N-acyl homoserine lactones (AHLs) from Escherichia coli and Pseudomonas aeruginosa on T. pyogenes was tested by using mouse model. Mice were first peritoneally infected with T. pyogenes followed by intravenous injection of N-Octanoyl-DL-homoserine lactone (C8HSL) or N-(3-oxododecanoyl) homoserine-l-lactone (C12HSL). The results showed that C8HSL and C12HSL significantly reduced bacterial load and increased the survival rate of mice against T. pyogenes challenge. Additionally, the treatment of AHLs promoted the secretion of IL-1β, IL-6, IL-8 and TNF-α in mouse peritoneal fluid, and significantly decreased the expression levels of virulence genes of residual T. pyogenes. Importantly, murine macrophages rapidly phagocytosed bacteria when they were treated with AHLs compared to untreated cells. Collectively, our findings provide a major advance in understanding the inhibitory effect of AHLs in vivo and a promise for developing new clinical or veterinary treatments of T. pyogenes-related infection.

摘要

化脓隐秘杆菌是一种革兰阳性机会致病菌,通常可引起重要经济家畜的乳腺炎、肝脓肿和肺炎。有研究表明,革兰氏阴性菌可以通过群体感应(QS)信号分子抑制化脓隐秘杆菌的生长和毒力,并导致优势种群发生转变。然而,这些 QS 信号分子是否可以作为治疗化脓隐秘杆菌感染的潜在抗毒力药物尚不清楚。本研究通过小鼠模型测试了大肠杆菌和铜绿假单胞菌来源的 N-酰基高丝氨酸内酯(AHLs)对化脓隐秘杆菌的体内抑制作用。首先,通过腹腔注射使小鼠感染化脓隐秘杆菌,然后通过静脉注射 N-辛酰基-DL-高丝氨酸内酯(C8HSL)或 N-(3-氧代十二烷酰基)高丝氨酸-l-内酯(C12HSL)。结果表明,C8HSL 和 C12HSL 可显著降低细菌负荷并提高小鼠对化脓隐秘杆菌攻击的存活率。此外,AHLs 处理可促进小鼠腹腔液中白细胞介素-1β、白细胞介素-6、白细胞介素-8 和肿瘤坏死因子-α的分泌,并显著降低残留化脓隐秘杆菌毒力基因的表达水平。重要的是,与未处理的细胞相比,用 AHLs 处理的小鼠巨噬细胞可迅速吞噬细菌。总之,本研究结果为理解 AHLs 的体内抑制作用提供了重要进展,并为开发治疗化脓隐秘杆菌相关感染的新的临床或兽医治疗方法提供了可能。

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