化脓性链球菌
毒力
生物
抗生素耐药性
链球菌
免疫系统
咽炎
微生物学
免疫
青霉素
免疫学
抗生素
医学
金黄色葡萄球菌
细菌
病理
基因
生物化学
遗传学
作者
Stephan Brouwer,Tania Rivera-Hernández,Bodie F. Curren,Nichaela Harbison-Price,David M. P. De Oliveira,Magnus G. Jespersen,Mark R. Davies,Mark J. Walker
标识
DOI:10.1038/s41579-023-00865-7
摘要
Streptococcus pyogenes (Group A Streptococcus; GAS) is exquisitely adapted to the human host, resulting in asymptomatic infection, pharyngitis, pyoderma, scarlet fever or invasive diseases, with potential for triggering post-infection immune sequelae. GAS deploys a range of virulence determinants to allow colonization, dissemination within the host and transmission, disrupting both innate and adaptive immune responses to infection. Fluctuating global GAS epidemiology is characterized by the emergence of new GAS clones, often associated with the acquisition of new virulence or antimicrobial determinants that are better adapted to the infection niche or averting host immunity. The recent identification of clinical GAS isolates with reduced penicillin sensitivity and increasing macrolide resistance threatens both frontline and penicillin-adjunctive antibiotic treatment. The World Health Organization (WHO) has developed a GAS research and technology road map and has outlined preferred vaccine characteristics, stimulating renewed interest in the development of safe and effective GAS vaccines. In this Review, Brouwer et al. summarize recent developments in our understanding of Group A Streptococcus (GAS), focusing on the epidemiologic and clinical features of GAS infection and the molecular mechanisms associated with GAS virulence and drug resistance.
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