Suppr超能文献

特拉唑嗪干扰群体感应和三型分泌系统,并减少细菌的“间谍活动”以减轻鼠伤寒的发病机制。

Terazosin Interferes with Quorum Sensing and Type Three Secretion System and Diminishes the Bacterial Espionage to Mitigate the Typhimurium Pathogenesis.

作者信息

Hegazy Wael A H, Salem Ibrahim M, Alotaibi Hadil Faris, Khafagy El-Sayed, Ibrahim Doaa

机构信息

Department of Microbiology and Immunology, Faculty of Pharmacy, Zagazig University, Zagazig 44519, Egypt.

Department of Medicinal Chemistry, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.

出版信息

Antibiotics (Basel). 2022 Mar 30;11(4):465. doi: 10.3390/antibiotics11040465.

Abstract

is an invasive intracellular pathogen and hires diverse systems to manipulate its survival in the host cells. could eavesdrop on the host cells, sensing and responding to the produced adrenergic hormones and other neurotransmitters, which results in the augmentation of its virulence and establishes its accommodation in host cells. The current study aims to assess the anti-virulence effect of α-adrenergic antagonist terazosin on Typhimurium. Our findings show that terazosin significantly reduced Typhimurium adhesion and biofilm formation. Furthermore, terazosin significantly decreased invasion and intracellular replication of Typhimurium. Interestingly, in vivo, terazosin protected the mice from Typhimurium pathogenesis. To understand the terazosin anti-virulence activity, its effect on quorum sensing (QS), bacterial espionage, and type three secretion system (T3SS) was studied. Strikingly, terazosin competed on the membranal sensors that sense adrenergic hormones and down-regulated their encoding genes, which indicates the ability of terazosin to diminish the bacterial eavesdropping on the host cells. Moreover, terazosin significantly reduced the QS-controlled pigment production and interfered with the QS receptor Lux-homolog SdiA, which indicates the possible terazosin-mediated anti-QS activity. Furthermore, terazosin down-regulated the expression of T3SS encoding genes. In conclusion, terazosin may mitigate Typhimurium virulence owing to its hindering QS and down-regulating T3SS encoding genes besides its inhibition of bacterial espionage.

摘要

是一种侵袭性细胞内病原体,利用多种系统来操控其在宿主细胞中的存活。它能够窃听宿主细胞,感知并响应所产生的肾上腺素能激素和其他神经递质,这会导致其毒力增强并在宿主细胞中得以立足。当前的研究旨在评估α-肾上腺素能拮抗剂特拉唑嗪对鼠伤寒沙门氏菌的抗毒力作用。我们的研究结果表明,特拉唑嗪显著降低了鼠伤寒沙门氏菌的黏附及生物膜形成。此外,特拉唑嗪显著减少了鼠伤寒沙门氏菌的侵袭及细胞内复制。有趣的是,在体内,特拉唑嗪保护小鼠免受鼠伤寒沙门氏菌致病作用的影响。为了解特拉唑嗪的抗毒力活性,研究了其对群体感应(QS)、细菌窃听及三型分泌系统(T3SS)的影响。令人惊讶的是,特拉唑嗪与感知肾上腺素能激素的膜传感器竞争,并下调其编码基因,这表明特拉唑嗪有能力减少细菌对宿主细胞的窃听。此外,特拉唑嗪显著降低了QS控制的色素产生,并干扰了QS受体Lux同源物SdiA,这表明特拉唑嗪可能介导了抗QS活性。此外,特拉唑嗪下调了T3SS编码基因的表达。总之,特拉唑嗪可能通过阻碍QS、下调T3SS编码基因以及抑制细菌窃听来减轻鼠伤寒沙门氏菌的毒力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d0b/9025009/fd49e9073e5d/antibiotics-11-00465-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验