Ahmed Noor Maath, Suleiman Ahmed AbdulJabbar
Department of Biology, College of Science, Tikrit University, Tikrit, Saladin, Iraq.
Department of Biotechnology, College of Science, University of Anbar, Ramadi, Anbar, Iraq.
Curr Med Mycol. 2024 Apr 15;10. doi: 10.22034/cmm.2024.345180.1496. eCollection 2024.
and are highly virulent species that cause diseases, such as meningoencephalitis and pulmonary infections. The gene predominantly determines the virulence of the pathogenic species. This study aimed to examine in both pathogenic and non-pathogenic species.
This study identified species through extensive literature, retrieved sequences from UniProt, explored protein families utilizing InterPro, motif analysis by MEME, multiple sequence alignment using Clustal Omega, performance of the phylogenetic analysis with MEGA, modeled protein structures with MODELLER, and separately visualized pathogenic and non-pathogenic structures in PyMOL.
Motif analysis showed four conserved regions between the pathogenic and non-pathogenic sequences. Moreover, multiple sequence alignment revealed that pathogenic gene sequences lacked a significant portion, compared to non-pathogenic ones, with several mutations in the gene sequence of pathogenic species at highly conserved regions. The phylogenetic analysis and pairwise distance matrix revealed that is closely related to pathogenic species. Predicted protein structures were superimposed to show structural differences between pathogenic and non-pathogenic species.
In conclusion, the results suggested that non-pathogenic species may have evolved into pathogenic species since the gene sequences of the non-virulent species were longer than those of the virulent species sequences. It implies that the virulent sequences may have lost that region at some point in evolution, which additional research on capsule formation-related genes can further corroborate.
[具体物种1]和[具体物种2]是高致病性物种,可引发如脑膜脑炎和肺部感染等疾病。[具体基因]主要决定致病物种的毒力。本研究旨在检测致病和非致病物种中的[具体基因]。
本研究通过广泛查阅文献鉴定[具体物种],从UniProt检索序列,利用InterPro探索蛋白质家族,通过MEME进行基序分析,使用Clustal Omega进行多序列比对,用MEGA进行系统发育分析,用MODELLER构建蛋白质结构模型,并在PyMOL中分别可视化致病和非致病结构。
基序分析显示致病和非致病序列之间有四个保守区域。此外,多序列比对表明,与非致病序列相比,致病[具体基因]序列缺少很大一部分,致病物种[具体物种]的基因序列在高度保守区域有几个突变。系统发育分析和成对距离矩阵表明[具体物种]与致病物种密切相关。预测的[具体蛋白]结构叠加显示致病和非致病物种之间的结构差异。
总之,结果表明非致病物种可能已进化为致病物种,因为无毒力物种的[具体基因]序列比有毒力物种的序列长。这意味着有毒力序列可能在进化的某个阶段失去了该区域,关于荚膜形成相关基因的进一步研究可以进一步证实这一点。