Lung-Targeting Lysostaphin Microspheres for Methicillin-Resistant Staphylococcus aureus Pneumonia Treatment and Prevention

被引:40
作者
Lin, Xiuhui [1 ]
He, Jian [2 ]
Li, Wanlin [2 ]
Qi, Yuchen [2 ]
Hu, Huiqun [1 ]
Zhang, Dongxiao [2 ]
Xu, Feng [1 ]
Chen, Xiaoyuan [5 ,6 ,7 ,8 ,9 ,10 ,11 ]
Zhou, Min [1 ,2 ,3 ,4 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 2, Dept Infect Dis, Sch Med, Hangzhou 310009, Peoples R China
[2] Zhejiang Univ, Inst Translat Med, Hangzhou 310009, Peoples R China
[3] Zhejiang Univ, State Key Lab Modern Opt Instrumentat, Hangzhou 310058, Peoples R China
[4] Zhejiang Univ, Canc Ctr, Hangzhou 310009, Peoples R China
[5] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Diagnost Radiol, Singapore 119074, Singapore
[6] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Surg, Singapore 119074, Singapore
[7] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Chem & Biomol Engn, Singapore 119074, Singapore
[8] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biomed Engn, Singapore 119074, Singapore
[9] Natl Univ Singapore, Fac Engn, Singapore 119074, Singapore
[10] Natl Univ Singapore, Clin Imaging Res Ctr, Ctr Translat Med, Yong Loo Lin Sch Med, Singapore 117599, Singapore
[11] Natl Univ Singapore, NUS Ctr Nanomed, Yong Loo Lin Sch Med, Nanomed Translat Res Program, Singapore 117597, Singapore
基金
中国国家自然科学基金;
关键词
pneumonia; biofilm; MRSA; lung target; PLGA microspheres; lysostaphin; PLGA MICROSPHERES; INFECTIONS; PROMOTION; OXACILLIN; PROTEIN; DYE;
D O I
10.1021/acsnano.1c06460
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multifunctional antimicrobial strategies are urgently needed to treat methicillin-resistant Staphylococcus aureus (MRSA) caused pneumonia due to its increasing resistance, enhanced virulence, and high pathogenicity. Here, we report that lysostaphin, a bacteriolytic enzyme, encapsulated within poly(lactic-co-glycolic acid) microspheres (LyIR@MS) specially treats planktonic MRSA bacteria, mature biofilms, and related pneumonia. Optimized LyIR@MS with suitable diameters could deliver a sufficient amount of lysostaphin to the lung without a decrease in survival rate after intravenous injection. Furthermore, the degradable properties of the carrier make it safe for targeted release of lysostaphin to eliminate MRSA, repressing the expression of virulence genes and improving the sensitivity of biofilms to host neutrophils. In the MRSA pneumonia mouse model, treatment or prophylaxis with LyIR@MS significantly improved survival rate and relieved inflammatory injury without introducing adverse events. These findings suggest the clinical translational potential of LyIR@MS for the treatment of MRSA-infected lung diseases.
引用
收藏
页码:16625 / 16641
页数:17
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