从暴露于某些抗致病性多药制剂的铜绿假单胞菌和金黄色葡萄球菌的全转录组中鉴定潜在的抗毒靶点的网络分析

IF 2 Q3 PHARMACOLOGY & PHARMACY
Feny J. Ruparel, Siddhi K. Shah, Jhanvi H. Patel, Nidhi R. Thakkar, Gemini N. Gajera, Vijay O. Kothari
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引用次数: 1

摘要

抗菌素耐药性(AMR)是一个严重的全球威胁。鉴定新的抗菌靶点是迫切需要的,以帮助抗菌药物的发现计划。本研究试图鉴定两种重要病原体铜绿假单胞菌和金黄色葡萄球菌的潜在靶点。方法:对暴露于两种不同群体调节复方的铜绿假单胞菌和金黄色葡萄球菌的转录组进行网络分析,以确定最高度网络化的差异表达基因(枢纽)作为潜在的抗毒靶点。结果:与反硝化和硫代谢相关的基因是铜绿假单胞菌最重要的目标。通过体外实验也证实了铜绿假单胞菌暴露于多药配方Panchvalkal培养基中亚硝酸盐(NO2)的积累增加。产生亚硝酸盐胁迫和诱导硫饥饿似乎是有效的抗病原菌策略,以对付臭名昭著的革兰氏阴性病原体。在金黄色葡萄球菌中发现的重要靶点有转录调节因子sarA、免疫球蛋白结合蛋白Sbi、丝氨酸蛋白酶SplA、saeR/S反应调节系统以及γ -溶血素成分hlgB和hlgC。结论:通过适当的模型宿主体外和体内实验,进一步验证本研究中确定的潜在靶点是必要的。这些经过验证的靶点对全球许多抗菌药物发现项目至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Network analysis for identifying potential anti-virulence targets from whole transcriptome of Pseudomonas aeruginosa and Staphylococcus aureus exposed to certain anti-pathogenic polyherbal formulations
Introduction: Antimicrobial resistance (AMR) is a serious global threat. Identification of novel antibacterial targets is urgently warranted to help antimicrobial drug discovery programs. This study attempted identification of potential targets in two important pathogens Pseudomonas aeruginosa and Staphylococcus aureus. Methods: Transcriptomes of P. aeruginosa and S. aureus exposed to two different quorum-modulatory polyherbal formulations were subjected to network analysis to identify the most highly networked differentially expressed genes (hubs) as potential anti-virulence targets. Results: Genes associated with denitrification and sulfur metabolism emerged as the most important targets in P. aeruginosa. Increased buildup of nitrite (NO2) in P. aeruginosa culture exposed to the polyherbal formulation Panchvalkal was confirmed through in vitro assay too. Generation of nitrosative stress and inducing sulfur starvation seemed to be effective anti-pathogenic strategies against this notorious gram-negative pathogen. Important targets identified in S. aureus were the transcriptional regulator sarA, immunoglobulin-binding protein Sbi, serine protease SplA, the saeR/S response regulator system, and gamma-hemolysin components hlgB and hlgC. Conclusion: Further validation of the potential targets identified in this study is warranted through appropriate in vitro and in vivo assays in model hosts. Such validated targets can prove vital to many antibacterial drug discovery programs globally.
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来源期刊
Drug Target Insights
Drug Target Insights PHARMACOLOGY & PHARMACY-
CiteScore
2.70
自引率
0.00%
发文量
5
审稿时长
8 weeks
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