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在源头遏制结核病:黏附素在感染与干预中的作用

Stopping Tuberculosis at the Gate: The Role of Adhesins in Infection and Intervention.

作者信息

Yang Haoyan, Ma Yinuo, Lei Xinkui, Chai Siyu, Zhang Sigen, Su Guimin, Li Songping, Du Lin

机构信息

Research and Development Centre, Beijing Zhifei Lvzhu Biopharmaceutical Co., Ltd., Beijing 100176, China.

Beijing Bacterial Vaccine Engineering Research Centre, Beijing 100176, China.

出版信息

Vaccines (Basel). 2025 Jun 24;13(7):676. doi: 10.3390/vaccines13070676.

Abstract

The global burden of tuberculosis (TB), exacerbated by the rise of drug-resistant (), underscores the need for alternative intervention strategies. One promising approach is to block the infection at its earliest stage-bacterial adhesion to host cells-thereby preventing colonization and transmission without exerting selective pressure. Adhesins, surface-exposed molecules mediating this critical interaction, have therefore emerged as attractive targets for early prevention. This review outlines the infection process driven by bacterial adhesion and describes the architecture of the outer envelope, emphasizing components that contribute to host interaction. We comprehensively summarize both non-protein and protein adhesins, detailing their host receptors, biological roles, and experimental evidence. Recent progress in the computational prediction of adhesins, particularly neural network-based tools like SPAAN, is also discussed, highlighting its potential to accelerate adhesin discovery. Additionally, we present a detailed, generalized workflow for predicting adhesins, which synthesizes current approaches and provides a comprehensive framework for future studies. Targeting bacterial adhesion presents a therapeutic strategy that interferes with the early stages of infection while minimizing the risk of developing drug resistance. Consequently, anti-adhesion strategies may serve as valuable complements to conventional therapies and support the development of next-generation TB vaccines and treatments.

摘要

耐药性的增加加剧了全球结核病负担,这凸显了替代干预策略的必要性。一种有前景的方法是在感染的最早阶段——细菌与宿主细胞的黏附——阻断感染,从而在不施加选择压力的情况下预防定植和传播。因此,黏附素作为介导这种关键相互作用的表面暴露分子,已成为早期预防的有吸引力的靶点。本综述概述了由细菌黏附驱动的感染过程,并描述了外膜的结构,强调了有助于宿主相互作用的成分。我们全面总结了非蛋白质和蛋白质黏附素,详细介绍了它们的宿主受体、生物学作用和实验证据。还讨论了黏附素计算预测方面的最新进展,特别是像SPAAN这样基于神经网络的工具,突出了其加速黏附素发现的潜力。此外,我们提出了一种详细的、通用的黏附素预测工作流程,该流程综合了当前方法,并为未来研究提供了一个全面的框架。靶向细菌黏附提出了一种治疗策略,可以干扰感染的早期阶段,同时将产生耐药性的风险降至最低。因此,抗黏附策略可能成为传统疗法的有价值补充,并支持下一代结核病疫苗和治疗方法的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b44/12298959/3a405652e380/vaccines-13-00676-g001.jpg

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