Enhanced Killing of Methicillin-Resistant Staphylococcus aureus with Ceftaroline or Vancomycin in Combination with Carbapenems

万古霉素 菌血症 医学 微生物学 耐甲氧西林金黄色葡萄球菌 抗生素 厄他培南 金黄色葡萄球菌 碳青霉烯 美罗培南 抗菌剂 抗生素耐药性 生物 细菌 遗传学
作者
Allen Jankeel,Gabriel Pérez-Parra,Anuj K Khetarpal,Ivan Alvarado,Victor Nizet,George Sakoulas,Erlinda R. Ulloa
出处
期刊:The Journal of Infectious Diseases [Oxford University Press]
标识
DOI:10.1093/infdis/jiaf010
摘要

Abstract Background Methicillin-resistant Staphylococcus aureus (MRSA) bacteremia is associated with high rates of treatment failure, even when antibiotics showing in vitro susceptibility are used. Early optimization of therapy is crucial to reduce morbidity and mortality. Building on our previous research on carbapenem therapy for methicillin-susceptible S. aureus (MSSA) bacteremia, we examined the utility of adjunctive carbapenems (ertapenem or meropenem) to enhance the efficacy of ceftaroline or vancomycin for treatment of MRSA. Methods The effectiveness of combination therapy versus monotherapy against MRSA was assessed using checkerboard, time-kill, and human whole blood killing assays, as well as a murine bacteremia model. Additionally, we performed transcriptomic analysis and conducted human platelet and antimicrobial peptide killing assays on MRSA pretreated with subtherapeutic concentrations of ceftaroline and carbapenems. The supernatants from these MRSA were used to treat platelets, and cytotoxicity was assessed via LDH release assays. Results Although not typically used for MRSA, we identified striking in vitro and in vivo synergy between carbapenems and ceftaroline or vancomycin. MRSA pretreated with subtherapeutic ceftaroline-carbapenem therapy revealed transcriptional shifts indicative of reduced antibiotic resistance, virulence, and host immune evasion. Supernatants from these MRSA also caused less platelet injury compared to monotherapy. Furthermore, MRSA pretreated with ceftaroline and carbapenems demonstrated increased susceptibility to killing by human platelets and the antimicrobial peptide LL-37. Conclusion The therapeutic success of adjunctive carbapenems appears to be driven by multiple mechanisms, including direct drug-drug synergy with first-line anti-MRSA agents, attenuation of resistance and virulence factors, and enhancement of immune-mediated killing, each warranting further investigation.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
2秒前
3秒前
yyy完成签到,获得积分10
3秒前
4秒前
科研通AI5应助长情的一刀采纳,获得10
4秒前
pluto应助保住头发为科研采纳,获得10
4秒前
5秒前
bkagyin应助海森堡采纳,获得10
5秒前
香蕉觅云应助李凡采纳,获得10
5秒前
果实发布了新的文献求助10
6秒前
6秒前
yyy发布了新的文献求助10
6秒前
7秒前
小猪找库里完成签到,获得积分10
8秒前
JNL发布了新的文献求助10
8秒前
kingwill应助专一的白萱采纳,获得20
9秒前
10秒前
迅速的雅彤完成签到,获得积分10
10秒前
啦啦啦啦啦关注了科研通微信公众号
11秒前
Shulh发布了新的文献求助10
11秒前
FNNR完成签到,获得积分10
11秒前
14秒前
14秒前
科研通AI5应助果实采纳,获得10
14秒前
14秒前
调研昵称发布了新的文献求助10
15秒前
15秒前
保住头发为科研完成签到,获得积分10
16秒前
暴躁四叔应助美好斓采纳,获得30
16秒前
风华完成签到,获得积分10
17秒前
桐桐应助白日梦想家采纳,获得10
18秒前
大气海露发布了新的文献求助10
18秒前
18秒前
琪琪发布了新的文献求助10
20秒前
共享精神应助科研通管家采纳,获得10
20秒前
冷静靖荷应助科研通管家采纳,获得10
20秒前
冷静靖荷应助科研通管家采纳,获得20
21秒前
在水一方应助科研通管家采纳,获得10
21秒前
科研通AI5应助科研通管家采纳,获得10
21秒前
高分求助中
Continuum thermodynamics and material modelling 3000
Production Logging: Theoretical and Interpretive Elements 2700
Healthcare Finance: Modern Financial Analysis for Accelerating Biomedical Innovation 2000
Applications of Emerging Nanomaterials and Nanotechnology 1111
Unseen Mendieta: The Unpublished Works of Ana Mendieta 1000
Les Mantodea de Guyane Insecta, Polyneoptera 1000
工业结晶技术 880
热门求助领域 (近24小时)
化学 医学 材料科学 生物 工程类 有机化学 生物化学 纳米技术 内科学 物理 化学工程 计算机科学 复合材料 基因 遗传学 物理化学 催化作用 细胞生物学 免疫学 电极
热门帖子
关注 科研通微信公众号,转发送积分 3489857
求助须知:如何正确求助?哪些是违规求助? 3076978
关于积分的说明 9147123
捐赠科研通 2769152
什么是DOI,文献DOI怎么找? 1519630
邀请新用户注册赠送积分活动 704069
科研通“疑难数据库(出版商)”最低求助积分说明 702084