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一项免疫信息学与广泛分子动力学研究,旨在研发一种抗隐球菌病的多价多表位疫苗。

An immunoinformatics and extensive molecular dynamics study to develop a polyvalent multi-epitope vaccine against cryptococcosis.

作者信息

Sami Md Razwan Sardar, Rani Nurul Amin, Elahi Mohammad Mahfuz Enam, Hossain Mohammad Sajjad, Al Mueid Minhaz Abdullah, Rahim Zahidur, Patil Rajesh B, Moin Abu Tayab, Bithi Israt Jahan, Nahar Sabekun, Konika Israt Jahan, Roy Sneha, Preya Jannatul Aleya, Ahmed Jamil

机构信息

Faculty of Biotechnology and Genetic Engineering, Sylhet Agricultural University, Sylhet, Bangladesh.

Department of Pharmacy, University of Asia Pacific, Dhaka, Bangladesh.

出版信息

PLoS One. 2024 Dec 31;19(12):e0315105. doi: 10.1371/journal.pone.0315105. eCollection 2024.

Abstract

Cryptococcosis is a lethal mycosis instigated by the pathogenic species Cryptococcus neoformans and Cryptococcus gattii, primarily affects the lungs, manifesting as pneumonia, and the brain, where it presents as meningitis. Mortality rate could reach 100% if infections remain untreated in cryptococcal meningitis. Treatment options for cryptococcosis are limited and and there are no licensed vaccines clinically available to treat or prevent cryptococcosis. Our study utilizes an integrated bioinformatics approaches to develop a polyvalent multiepitope subunit vaccine focusing on the key virulent proteins Heat shock transcription factor and Chaperone DnaK of both C. neoformans and C. gatti. Then in silico analysis was done to predict highly antigenic epitopes by assessing antigenicity, transmembrane topology screening, allergenecity, toxicity, and molecular docking approaches. Following this analysis, we designed two vaccine constructs integrating a compatible adjuvant and suitable linkers. These constructs exhibited notable characteristics including high antigenicity, non-toxicity, solubility, stability, and compatibility with Toll-like receptors (TLRs). The interaction between both vaccine constructs and TLR2, TLR3, and TLR9 was assessed through molecular docking analysis. Molecular dynamics simulations and MM-PBSA calculations suggest the substantial stabilizing property and binding affinity of Vaccine Construct V1 against TLR9. Both the vaccines revealed to have a higher number of interchain hydrogen bond with TLR9. These findings serve as a crucial stepping stone towards a comprehensive solution for combating cryptococcus infections induced by both C. neoformans and C. gattii. Further validation through in vivo studies is crucial to confirm the effectiveness and potential of the vaccine to curb the spread of cryptococcosis. Subsequent validation through in vivo studies is paramount to confirm the effectiveness and potential of the vaccine in reducing the spread of cryptococcosis.

摘要

隐球菌病是一种由新型隐球菌和格特隐球菌这两种致病菌种引发的致命真菌病,主要影响肺部,表现为肺炎,也会影响大脑,表现为脑膜炎。如果隐球菌性脑膜炎感染得不到治疗,死亡率可能达到100%。隐球菌病的治疗选择有限,临床上没有可用的许可疫苗来治疗或预防隐球菌病。我们的研究利用综合生物信息学方法开发一种多价多表位亚单位疫苗,重点针对新型隐球菌和格特隐球菌的关键毒力蛋白热休克转录因子和伴侣蛋白DnaK。然后通过评估抗原性、跨膜拓扑结构筛选、过敏原性、毒性和分子对接方法进行计算机模拟分析,以预测高抗原性表位。经过该分析后,我们设计了两种整合了相容佐剂和合适连接子的疫苗构建体。这些构建体表现出显著特性,包括高抗原性、无毒性、溶解性、稳定性以及与Toll样受体(TLR)的相容性。通过分子对接分析评估了两种疫苗构建体与TLR2、TLR3和TLR9之间的相互作用。分子动力学模拟和MM-PBSA计算表明疫苗构建体V1对TLR9具有显著的稳定特性和结合亲和力。两种疫苗与TLR9都显示出较多的链间氢键。这些发现是朝着全面解决由新型隐球菌和格特隐球菌引起的隐球菌感染迈出的关键一步。通过体内研究进行进一步验证对于确认疫苗抑制隐球菌病传播的有效性和潜力至关重要。随后通过体内研究进行验证对于确认疫苗在减少隐球菌病传播方面的有效性和潜力至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d5b/11687922/dca26899378a/pone.0315105.g001.jpg

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