Lian Zhong-Hao, Yang Chen-Hui, Qiu Ye, Ge Xing-Yi
Hunan Provincial Key Laboratory of Medical Virology, College of Biology, Hunan University, Changsha 410012, China.
Microorganisms. 2024 Nov 5;12(11):2239. doi: 10.3390/microorganisms12112239.
The resurgence of mpox virus (MPXV) poses a significant challenge to global public health. Currently, there is a limited understanding of the evolutionary details of MPXV during its epidemics, and no specific drugs have been developed for it. Herein, analysis of mutations and positive selection sites (PSSs) within the MPXV genomes revealed 799 mutations and 40 PSSs. Visualization analysis indicated that these mutations and PSSs may affect protein structure. Additionally, a protein-protein interaction (PPI) network between human and MPXV was established, identifying 346 MPXV-interacting human proteins (MIHPs). An interaction network involving MIHPs and other viruses confirmed that these proteins can interact with various viruses that infect humans. Functional analysis of MIHPs suggested their enrichment in host immunity pathways. Lastly, two drugs targeting MIHPs and four compounds targeting MPXV proteins were screened as candidate antivirals against MPXV. These findings not only deepen our understanding of MPXV evolution but also aid in the development of anti-MPXV drugs.
猴痘病毒(MPXV)的卷土重来对全球公共卫生构成了重大挑战。目前,人们对MPXV在其流行期间的进化细节了解有限,并且尚未开发出针对它的特效药物。在此,对MPXV基因组内的突变和正选择位点(PSS)进行分析,发现了799个突变和40个PSS。可视化分析表明,这些突变和PSS可能会影响蛋白质结构。此外,还建立了人与MPXV之间的蛋白质-蛋白质相互作用(PPI)网络,鉴定出346种与MPXV相互作用的人类蛋白质(MIHP)。一个涉及MIHP与其他病毒的相互作用网络证实,这些蛋白质可以与多种感染人类的病毒相互作用。对MIHP的功能分析表明它们在宿主免疫途径中富集。最后,筛选出两种靶向MIHP 的药物和四种靶向MPXV蛋白质的化合物作为抗MPXV的候选抗病毒药物。这些发现不仅加深了我们对MPXV进化的理解,也有助于抗MPXV药物的开发。