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I53-50: Engineered icosahedral protein cage for modular vaccine nanoplatform
Ke Liang, Shuang Wu, Sihang Dong, Tao Xu, Hongtao Wang
Received November 25, 2025  Accepted February 4, 2026  Published online April 6, 2026  
DOI: https://doi.org/10.71150/jm.2511020    [Epub ahead of print]
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  • 6 Download
AbstractAbstract PDF

I53-50 is a computationally designed, self-assembling protein nanoparticle (NP) that forms a stable icosahedral structure composed of 120 protein subunits coordinated through precise interfacial interactions. Through unique intelligent regulation, I53-50 exhibits sensitivity to environmental signals and display multimodal “nano-smart” properties. I53-50 has a variety of modifiable surface-active sites, which facilitates precise chemical modification, gene fusion, tag coupling, and other functionalizations, thereby promoting effective lymphatic uptake and optimizing the immune response. I53-50 NPs show great potential in vaccine development, drug delivery, and biomaterials, representing a model fusion of computational biology and nanomedicine and offering a versatile tool for precision medicine.

Articles
Mycobacterium tuberculosis PE_PGRS45 (Rv2615c) Promotes Recombinant Mycobacteria Intracellular Survival via Regulation of Innate Immunity, and Inhibition of Cell Apoptosis
Tao Xu , Chutong Wang , Minying Li , Jing Wei , Zixuan He , Zhongqing Qian , Xiaojing Wang , Hongtao Wang
J. Microbiol. 2024;62(1):49-62.   Published online February 9, 2024
DOI: https://doi.org/10.1007/s12275-023-00101-0
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  • 4 Web of Science
  • 4 Crossref
AbstractAbstract PDF
Tuberculosis (TB), a bacterial infectious disease caused by Mycobacterium tuberculosis (M. tuberculosis), is a significant global public health problem. Mycobacterium tuberculosis expresses a unique family of PE_PGRS proteins that have been implicated in pathogenesis. Despite numerous studies, the functions of most PE_PGRS proteins in the pathogenesis of mycobacterium infections remain unclear. PE_PGRS45 (Rv2615c) is only found in pathogenic mycobacteria. In this study, we successfully constructed a recombinant Mycobacterium smegmatis (M. smegmatis) strain which heterologously expresses the PE_PGRS45 protein. We found that overexpression of this cell wall-associated protein enhanced bacterial viability under stress in vitro and cell survival in macrophages. MS_PE_PGRS45 decreased the secretion of pro-inflammatory cytokines such as IL-1β, IL-6, IL-12p40, and TNF-α. We also found that MS_PE_PGRS45 increased the expression of the anti-inflammatory cytokine IL-10 and altered macrophage-mediated immune responses. Furthermore, PE_PGRS45 enhanced the survival rate of M. smegmatis in macrophages by inhibiting cell apoptosis. Collectively, our findings show that PE_PGRS45 is a virulent factor actively involved in the interaction with the host macrophage.

Citations

Citations to this article as recorded by  
  • Evolution of the PE_PGRS Proteins of Mycobacteria: Are All Equal or Are Some More Equal than Others?
    Bei Chen, Belmin Bajramović, Bastienne Vriesendorp, Herman Pieter Spaink
    Biology.2025; 14(3): 247.     CrossRef
  • Recent advances in research on Mycobacterium tuberculosis virulence factors and their role in pathogenesis
    Ming-Rui Sun, Jia-Yin Xing, Xiao-Tian Li, Ren Fang, Yang Zhang, Zhao-Li Li, Ning-Ning Song
    Journal of Microbiology, Immunology and Infection.2025; 58(5): 497.     CrossRef
  • Rv2741 Promotes Mycobacterium Survival by Modulating Macrophage Function via the IL-1α-MAPK Axis
    Xintong He, Yonglin He, Xichuan Deng, Nan Lu, Anlong Li, Sijia Gao, Shiyan He, Yuran Wang, Nanzhe Fu, Zijie Wang, Yuxin Nie, Lei Xu
    ACS Infectious Diseases.2025; 11(3): 676.     CrossRef
  • The PE/PPE family proteins of Mycobacterium tuberculosis: evolution, function, and prospects for tuberculosis control
    Zhijing Zhang, Le Dong, Xin Li, Taibing Deng, Qinglan Wang
    Frontiers in Immunology.2025;[Epub]     CrossRef
Exploring the oral microflora of preschool children
Wen Ren , Qun Zhang , Xuenan Liu , Shuguo Zheng , Lili Ma , Feng Chen , Tao Xu , Baohua Xu
J. Microbiol. 2017;55(7):531-537.   Published online April 22, 2017
DOI: https://doi.org/10.1007/s12275-017-6474-8
  • 539 View
  • 1 Download
  • 24 Crossref
AbstractAbstract PDF
The oral cavity is one of the most important and complicated habitats in our body and supports diverse microbial communities. In this study, we aimed to determine the bacterial diversity and composition of various oral micro-niches. Samples were collected from supragingival plaque, saliva, and tongue coating from 10 preschool children (30 samples total). 16S rRNA gene pyrosequencing dataset generated 314,639 clean reads with an average of 10,488 ± 2,787 reads per sample. The phyla Firmicutes, Proteobacteria, Actinobacteria, Bacteroidetes, and Fusobacteria were predominant, accounting for more than 90% of the total sequences. We found the highest α diversity, microbial richness, and evenness in plaque, compared with saliva and tongue coating. Plaque was also distinguished from saliva and tongue coating by phylogenetic distances (weighted UniFrac). Taxa with different relative abundances were further identified, confirming the existence of microbial differences across the three niches. Core microbiomes were defined of each niche; however, only a small proportion of operational taxonomic units (8.07%) were shared by the three niches. Coaggregation between Actinomyces spp. and Streptococcus spp. and other correlations among periodontal pathogens, such as Prevotella, Fusobacteria, Capnocytophaga, and Tannerella, were shown by a co-occurrence network. In summary, our study provides a framework of oral microbial communities in the population of preschool children as a baseline for further studies of oral diseases related to microbes.

Citations

Citations to this article as recorded by  
  • Distinct oral and fecal microbiota composition in preschool children with overweight/obesity: a cross-sectional study
    Hanguo Feng, Xinyi Zeng, Siyuan Yu, Qi Sun, Guiding Li, Yanhong Li, Juan Liu, Nanquan Rao
    Applied Microbiology and Biotechnology.2026;[Epub]     CrossRef
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    BMC Oral Health.2025;[Epub]     CrossRef
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    Tamires Timm Maske, Glenda Ávila Marques, Bruna Dalongaro Fritsch, Bruna Moraes Kremer, Maximiliano Sérgio Cenci, Pabulo Henrique Rampelotto, Rodrigo Alex Arthur
    Biofouling.2025; 41(5): 536.     CrossRef
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    Huijie Wang, Jinfeng Wang, Jinli Liu, Xiaoyang Shi, Zhichao Wang, Xu Cao
    Medicine.2025; 104(41): e45160.     CrossRef
  • The Infant Oral Microbiome: Developmental Dynamics, Modulating Factors, and Implications for Oral and Systemic Health
    Paula Olate, Ailín Martínez, Eulàlia Sans-Serramitjana, Matías Cortés, Rommy Díaz, Genisley Hernández, Erwin A. Paz, Néstor Sepúlveda, John Quiñones
    International Journal of Molecular Sciences.2025; 26(16): 7983.     CrossRef
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    Karolin C. Hoefer, Lutz T. Weber, Anna Greta Barbe, Isabelle Graf, Stefanie Thom, Angela Nowag, Claus J. Scholz, Hilmar Wisplinghoff, Michael J. Noack, Nathalie Jazmati
    Clinical Oral Investigations.2024;[Epub]     CrossRef
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    International Journal of Environmental Research and Public Health.2022; 19(18): 11403.     CrossRef
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