Department of Medicinal Chemistry, University of Washington, Seattle, WA, USA.
Department of Pharmacy, University of Washington, Seattle, WA, USA.
J Antimicrob Chemother. 2020 May 1;75(5):1182-1186. doi: 10.1093/jac/dkz562.
Glycopeptides (GPs), lipopeptides (LPs) and lipoglycopeptides (LGPs) are related antimicrobials important for the management of invasive MRSA infections. Cross-resistance among these antibiotics in MRSA is well documented, as is the observation that susceptibility of MRSA to β-lactams increases as susceptibility to GPs and LPs decreases (i.e. the seesaw effect). Efforts to understand the relationship between GP/LP/LGP cross-resistance and the seesaw effect have focused on the PBPs, but the role of lipid metabolism has not been investigated.
Since the cell membrane is structurally and metabolically integrated with the cell wall and anchors associated proteins, including PBPs, we examined the relationship between membrane lipid composition and the phenomena of cross-resistance among GPs/LPs/LGPs and the β-lactam seesaw effect.
We selected for daptomycin, vancomycin and dalbavancin resistance using the USA300 strain JE2 and evaluated the resulting mutants by WGS, MS-based lipidomics and antimicrobial susceptibility testing to assess the relationship between membrane composition, cross-resistance, and the seesaw effect.
We observed cross-resistance to GPs/LPs/LGPs among the selected strains and the seesaw effect against various β-lactams, depending on the PBP targets of the particular β-lactam. We found that modification of membrane composition occurs not only in daptomycin-selected strains, but also vancomycin- and dalbavancin-selected strains. Significantly, we observed that the abundance of most phosphatidylglycerols positively correlates with MICs of GPs/LPs/LGPs and negatively correlates with the MICs of β-lactams.
These studies demonstrate a major association between membrane remodelling, cross-resistance and the seesaw effect.
糖肽类(GPs)、脂肽类(LPs)和脂糖肽类(LGPs)是与管理侵袭性 MRSA 感染相关的重要抗微生物药物。MRSA 中这些抗生素之间的交叉耐药性已有充分记录,并且观察到 MRSA 对β-内酰胺类药物的敏感性随着 GPs 和 LPs 敏感性的降低而增加(即跷跷板效应)。为了理解 GP/LP/LGP 交叉耐药性与跷跷板效应之间的关系,人们已经将重点放在 PBPs 上,但脂质代谢的作用尚未得到研究。
由于细胞膜在结构和代谢上与细胞壁融为一体,并锚定相关蛋白,包括 PBPs,因此我们研究了细胞膜脂质组成与 GPs/LPs/LGPs 之间交叉耐药性和β-内酰胺类跷跷板效应之间的关系。
我们使用 USA300 菌株 JE2 对达托霉素、万古霉素和达巴万星进行了耐药性选择,并通过 WGS、基于 MS 的脂质组学和抗菌药物敏感性测试对获得的突变体进行了评估,以评估膜组成、交叉耐药性和跷跷板效应之间的关系。
我们观察到所选菌株之间存在 GP/LP/LGP 交叉耐药性,并且针对不同的β-内酰胺类药物存在β-内酰胺类跷跷板效应,这取决于特定β-内酰胺类药物的 PBP 靶标。我们发现,不仅在达托霉素选择的菌株中,而且在万古霉素和达巴万星选择的菌株中,膜组成发生了修饰。重要的是,我们观察到大多数磷脂酰甘油的丰度与 GP/LP/LGP 的 MIC 值呈正相关,与β-内酰胺类药物的 MIC 值呈负相关。
这些研究表明,膜重塑、交叉耐药性和跷跷板效应之间存在主要关联。