Comparative Proteomic Analysis of Capsule Proteins in Aminoglycoside-Resistant and Sensitive Mycobacterium tuberculosis Clinical Isolates: Unraveling Potential Drug Targets.

IF 1.6 Q4 INFECTIOUS DISEASES International Journal of Mycobacteriology Pub Date : 2024-04-01 Epub Date: 2024-06-15 DOI:10.4103/ijmy.ijmy_47_24
Devesh Sharma, Sakshi Gautam, Nalini Srivastava, Abdul Mabood Khan, Deepa Bisht
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Abstract

Background: Tuberculosis (TB), a global infectious threat, has seen a concerning rise in aminoglycoside-resistant Mycobacterium tuberculosis (M.tb) strains. The potential role of capsule proteins remains largely unexplored. This layer acts as the primary barrier for tubercle bacilli, attempting to infiltrate host cells and subsequent disease development.

Methods: The study aims to bridge this gap by investigating the differentially expressed capsule proteins in aminoglycoside-resistant M.tb clinical isolates compared with drug-sensitive isolates employing two-dimensional gel electrophoresis, mass spectrometry, and bioinformatic approaches.

Results: We identified eight proteins that exhibited significant upregulation in aminoglycoside-resistant isolates. Protein Rv3029c and Rv2110c were associated with intermediary metabolism and respiration; Rv2462c with cell wall and cell processes; Rv3804c with lipid metabolism; Rv2416c and Rv2623 with virulence and detoxification/adaptation; Rv0020c with regulatory functions; and Rv0639 with information pathways. Notably, the Group-based Prediction System for Prokaryotic Ubiquitin-like Protein (GPS-PUP) algorithm identified potential pupylation sites within all proteins except Rv3804c. Interactome analysis using the STRING 12.0 database revealed potential interactive partners for these proteins, suggesting their involvement in aminoglycoside resistance. Molecular docking studies revealed suitable binding between amikacin and kanamycin drugs with Rv2462c, Rv3804c, and Rv2623 proteins.

Conclusion: As a result, our findings illustrate the multifaceted nature of aminoglycoside resistance in M.tb and the importance of understanding how capsule proteins play a role in counteracting drug efficacy. Identifying the role of these proteins in drug resistance is crucial for developing more effective treatments and diagnostics for TB.

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氨基糖苷类药物耐药和敏感结核分枝杆菌临床分枝杆菌囊蛋白质的比较蛋白质组学分析:揭示潜在的药物靶点。
背景:结核病(TB)是一种全球性传染病,耐氨基糖苷类药物结核分枝杆菌(M.tb)菌株的增加令人担忧。胶囊蛋白的潜在作用在很大程度上仍未得到探索。结核分枝杆菌(M.tb)的胶囊蛋白层是结核分枝杆菌的主要屏障,它试图渗入宿主细胞,进而导致疾病的发生:本研究旨在利用二维凝胶电泳、质谱分析和生物信息学方法,研究耐氨基糖苷类药物的结核杆菌临床分离株与药物敏感的分离株中表达不同的胶囊蛋白,从而弥补这一空白:结果:我们发现耐氨基糖苷类药物的分离株中有八种蛋白质出现了明显的上调。蛋白质Rv3029c和Rv2110c与中间代谢和呼吸有关;Rv2462c与细胞壁和细胞过程有关;Rv3804c与脂质代谢有关;Rv2416c和Rv2623与毒力和解毒/适应有关;Rv0020c与调控功能有关;Rv0639与信息途径有关。值得注意的是,基于组的原核生物类泛素蛋白预测系统(GPS-PUP)算法在除 Rv3804c 以外的所有蛋白质中都发现了潜在的蛹化位点。利用 STRING 12.0 数据库进行的相互作用组分析发现了这些蛋白质的潜在相互作用伙伴,表明它们参与了氨基糖苷类药物抗性的作用。分子对接研究显示,阿米卡星和卡那霉素药物与 Rv2462c、Rv3804c 和 Rv2623 蛋白之间有合适的结合:因此,我们的研究结果表明了结核杆菌对氨基糖苷类药物耐药性的多面性,以及了解胶囊蛋白如何在抵消药效方面发挥作用的重要性。确定这些蛋白质在耐药性中的作用对于开发更有效的结核病治疗和诊断方法至关重要。
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来源期刊
CiteScore
2.20
自引率
25.00%
发文量
62
审稿时长
7 weeks
期刊最新文献
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