Integrated subtractive genomics and structure-based approach to unravel the therapeutic drug target of Leishmania species

IF 2.3 3区 生物学 Q3 MICROBIOLOGY Archives of Microbiology Pub Date : 2024-09-19 DOI:10.1007/s00203-024-04118-w
Debanjan Saha, Anupam Nath Jha
{"title":"Integrated subtractive genomics and structure-based approach to unravel the therapeutic drug target of Leishmania species","authors":"Debanjan Saha,&nbsp;Anupam Nath Jha","doi":"10.1007/s00203-024-04118-w","DOIUrl":null,"url":null,"abstract":"<div><p>Leishmaniasis is a complex vector-borne disease caused by intracellular protozoan parasites of the <i>Leishmania</i> genus. It presents a significant public health challenge in tropical and subtropical regions globally. As resistance to treatment increases, managing and controlling Leishmaniasis becomes more challenging, necessitating innovative approaches. To address this challenge, our study utilized subtractive genomics and structure-based approaches to identify common drug targets and combat antimicrobial resistance (AMR) across five <i>Leishmania</i> species strains. The subtractive genomics approach unraveled Glutamate Dehydrogenase (GDH) as a promising drug target for treating Leishmania infections. The investigation considered established methodologies observed in analogous studies, orthologous group, and druggability tests. Multiple sequence alignment revealed conserved sequences in GDH, while phylogenetic tree analysis provided insights into the evolutionary origin and close relationships of GDH across <i>Leishmania</i> species. Conserved sequences in GDH along with its function in pathogenicity provided insights into the close relationships of GDH across <i>Leishmania</i> species. Using a structure-based approach, our study showed the molecular interactions between GDH and three ligands—Bithionol, GW5074, and Hexachlorophene—through molecular docking and 100 ns molecular dynamics (MD) simulations. GW5074 exhibited a significant affinity for GDH, as indicated by stable RMSD values, a more compact conformation, and a higher number of hydrogen bonds than Bithionol. MMPBSA analysis confirmed the superior binding energy of the GW5074-GDH complex, emphasizing its potential as a potent ligand for drug development. This comprehensive analysis identified GW5074 as a promising candidate for inhibiting GDH activities in <i>Leishmania</i> species, contributing to the development of effective therapeutics against <i>Leishmania</i> infections.</p></div>","PeriodicalId":8279,"journal":{"name":"Archives of Microbiology","volume":null,"pages":null},"PeriodicalIF":2.3000,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Microbiology","FirstCategoryId":"99","ListUrlMain":"https://link.springer.com/article/10.1007/s00203-024-04118-w","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Leishmaniasis is a complex vector-borne disease caused by intracellular protozoan parasites of the Leishmania genus. It presents a significant public health challenge in tropical and subtropical regions globally. As resistance to treatment increases, managing and controlling Leishmaniasis becomes more challenging, necessitating innovative approaches. To address this challenge, our study utilized subtractive genomics and structure-based approaches to identify common drug targets and combat antimicrobial resistance (AMR) across five Leishmania species strains. The subtractive genomics approach unraveled Glutamate Dehydrogenase (GDH) as a promising drug target for treating Leishmania infections. The investigation considered established methodologies observed in analogous studies, orthologous group, and druggability tests. Multiple sequence alignment revealed conserved sequences in GDH, while phylogenetic tree analysis provided insights into the evolutionary origin and close relationships of GDH across Leishmania species. Conserved sequences in GDH along with its function in pathogenicity provided insights into the close relationships of GDH across Leishmania species. Using a structure-based approach, our study showed the molecular interactions between GDH and three ligands—Bithionol, GW5074, and Hexachlorophene—through molecular docking and 100 ns molecular dynamics (MD) simulations. GW5074 exhibited a significant affinity for GDH, as indicated by stable RMSD values, a more compact conformation, and a higher number of hydrogen bonds than Bithionol. MMPBSA analysis confirmed the superior binding energy of the GW5074-GDH complex, emphasizing its potential as a potent ligand for drug development. This comprehensive analysis identified GW5074 as a promising candidate for inhibiting GDH activities in Leishmania species, contributing to the development of effective therapeutics against Leishmania infections.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
综合减法基因组学和基于结构的方法,揭示利什曼原虫的治疗药物靶点。
利什曼病是由利什曼属细胞内原生动物寄生虫引起的一种复杂的病媒传播疾病。它对全球热带和亚热带地区的公共卫生构成重大挑战。随着抗药性的增加,利什曼病的管理和控制变得更具挑战性,需要采取创新方法。为了应对这一挑战,我们的研究采用了减法基因组学和基于结构的方法来确定共同的药物靶点,并在五个利什曼病种菌株中对抗抗菌药耐药性(AMR)。减法基因组学方法揭示了谷氨酸脱氢酶(GDH)是治疗利什曼病感染的一个有希望的药物靶点。这项研究考虑了在类比研究、同源组和可药性测试中观察到的既定方法。多重序列比对揭示了 GDH 中的保守序列,而系统发生树分析则为了解 GDH 在不同利什曼原虫物种中的进化起源和密切关系提供了见解。GDH 中的保守序列及其致病功能有助于深入了解 GDH 在不同利什曼原虫中的密切关系。我们的研究采用基于结构的方法,通过分子对接和 100 ns 分子动力学(MD)模拟,展示了 GDH 与三种配体--硫醇、GW5074 和六氯芬--之间的分子相互作用。与 Bithionol 相比,GW5074 表现出稳定的 RMSD 值、更紧凑的构象和更多的氢键,因此对 GDH 有明显的亲和力。MMPBSA 分析证实了 GW5074-GDH 复合物的超强结合能,强调了其作为药物开发的强效配体的潜力。这项综合分析确定了 GW5074 是抑制利什曼原虫 GDH 活性的有希望的候选药物,有助于开发针对利什曼原虫感染的有效疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Archives of Microbiology
Archives of Microbiology 生物-微生物学
CiteScore
4.90
自引率
3.60%
发文量
601
审稿时长
3 months
期刊介绍: Research papers must make a significant and original contribution to microbiology and be of interest to a broad readership. The results of any experimental approach that meets these objectives are welcome, particularly biochemical, molecular genetic, physiological, and/or physical investigations into microbial cells and their interactions with their environments, including their eukaryotic hosts. Mini-reviews in areas of special topical interest and papers on medical microbiology, ecology and systematics, including description of novel taxa, are also published. Theoretical papers and those that report on the analysis or ''mining'' of data are acceptable in principle if new information, interpretations, or hypotheses emerge.
期刊最新文献
Construction of engineered probiotic that adhere and display nanobody to neutralize porcine reproductive and respiratory syndrome virus Sublethal injury and recovery of Escherichia coli O157:H7 after dielectric barrier discharge plasma treatment A step-by-step procedure for analysing the 16S rRNA-based microbiome diversity using QIIME 2 and comprehensive PICRUSt2 illustration for functional prediction An improved DNA extraction method in okra for rapid PCR detection of Okra enation leaf curl virus from diverse Indian regions Exploring secretory signal sequences useful in excreting recombinant proteins in Beauveria bassiana as biocontrol fungus
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1