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方酸酰胺衍生物SA2对耐甲氧西林菌的抗菌活性

Antibacterial Activity of Squaric Amide Derivative SA2 against Methicillin-Resistant .

作者信息

Yu Moxi, Hou Yachen, Cheng Meiling, Liu Yongshen, Ling Caise, Zhai Dongshen, Zhao Hui, Li Yaoyao, Chen Yamiao, Xue Xiaoyan, Ma Xue, Jia Min, Wang Bin, Wang Pingan, Li Mingkai

机构信息

Department of Pharmacology, School of Pharmacy, The Fourth Military Medical University, Xi'an 710032, China.

School of Pharmacy, Shaanxi University of Chinese Medicine, Xi'an 712046, China.

出版信息

Antibiotics (Basel). 2022 Oct 28;11(11):1497. doi: 10.3390/antibiotics11111497.

DOI:10.3390/antibiotics11111497
PMID:36358152
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9686510/
Abstract

Methicillin-resistant (MRSA)-caused infection is difficult to treat because of its resistance to commonly used antibiotic, and poses a significant threat to public health. To develop new anti-bacterial agents to combat MRSA-induced infections, we synthesized novel squaric amide derivatives and evaluated their anti-bacterial activity by determining the minimum inhibitory concentration (MIC). Additionally, inhibitory activity of squaric amide 2 (SA2) was measured using the growth curve assay, time-kill assay, and an MRSA-induced skin infection animal model. A scanning electron microscope and transmission electron microscope were utilized to observe the effect of SA2 on the morphologies of MRSA. Transcriptome analysis and real-time PCR were used to test the possible anti-bacterial mechanism of SA2. The results showed that SA2 exerted bactericidal activity against a number of MRSA strains with an MIC at 4-8 µg/mL. It also inhibited the bacterial growth curve of MRSA strains in a dose-dependent manner, and reduced the colony formation unit in 4× MIC within 4-8 h. The infective lesion size and the bacterial number in the MRSA-induced infection tissue of mice were reduced significantly within 7 days after SA2 treatment. Moreover, SA2 disrupted the bacterial membrane and alanine dehydrogenase-dependent NAD/NADH homeostasis. Our data indicates that SA2 is a possible lead compound for the development of new anti-bacterial agents against MRSA infection.

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)引起的感染由于其对常用抗生素具有耐药性而难以治疗,对公共卫生构成重大威胁。为了开发新的抗菌药物来对抗MRSA引起的感染,我们合成了新型方酸酰胺衍生物,并通过测定最低抑菌浓度(MIC)来评估它们的抗菌活性。此外,使用生长曲线测定法、时间杀菌测定法和MRSA诱导的皮肤感染动物模型来测量方酸酰胺2(SA2)的抑制活性。利用扫描电子显微镜和透射电子显微镜观察SA2对MRSA形态的影响。转录组分析和实时定量PCR用于测试SA2可能的抗菌机制。结果表明,SA2对多种MRSA菌株具有杀菌活性,MIC为4-8μg/mL。它还以剂量依赖的方式抑制MRSA菌株的细菌生长曲线,并在4-8小时内使4倍MIC下的菌落形成单位减少。SA2治疗后7天内,小鼠MRSA诱导感染组织中的感染病灶大小和细菌数量显著减少。此外,SA2破坏了细菌膜以及丙氨酸脱氢酶依赖性NAD/NADH稳态。我们的数据表明,SA2是开发针对MRSA感染的新型抗菌药物的一种可能的先导化合物。

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