青霉素结合蛋白
金黄色葡萄球菌
SCCmec公司
抗生素
抗生素耐药性
微生物学
青霉素
耐甲氧西林金黄色葡萄球菌
内酰胺
生物
细菌
遗传学
化学
立体化学
作者
Harshad Lade,Jae‐Seok Kim
出处
期刊:Antibiotics
[MDPI AG]
日期:2023-08-24
卷期号:12 (9): 1362-1362
被引量:82
标识
DOI:10.3390/antibiotics12091362
摘要
The development of antibiotic resistance in Staphylococcus aureus, particularly in methicillin-resistant S. aureus (MRSA), has become a significant health concern worldwide. The acquired mecA gene encodes penicillin-binding protein 2a (PBP2a), which takes over the activities of endogenous PBPs and, due to its low affinity for β-lactam antibiotics, is the main determinant of MRSA. In addition to PBP2a, other genetic factors that regulate cell wall synthesis, cell signaling pathways, and metabolism are required to develop high-level β-lactam resistance in MRSA. Although several genetic factors that modulate β-lactam resistance have been identified, it remains unclear how they alter PBP2a expression and affect antibiotic resistance. This review describes the molecular determinants of β-lactam resistance in MRSA, with a focus on recent developments in our understanding of the role of mecA-encoded PBP2a and on other genetic factors that modulate the level of β-lactam resistance. Understanding the molecular determinants of β-lactam resistance can aid in developing novel strategies to combat MRSA.
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