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新型抗菌肽CECT7121对难治性严重感染患者革兰氏阳性菌的体外疗效评估。

Assessment of the in vitro efficacy of the novel antimicrobial peptide CECT7121 against human Gram-positive bacteria from serious infections refractory to treatment.

作者信息

Sparo M D, Jones D G, Sánchez Bruni S F

机构信息

Parasitology Division, Moredun Research Institute, Penicuik, UK.

出版信息

Chemotherapy. 2009;55(4):270-7. doi: 10.1159/000223069. Epub 2009 Jun 2.

Abstract

BACKGROUND

Resistant Gram-positive bacteria are causing increasing concern in clinical practice. This work investigated the efficacy of AP-CECT7121 (an antimicrobial peptide isolated from an environmental strain of Enterococcus faecalis CECT7121) against various pathogenic Gram-positive bacteria.

METHODS

Strains were isolated from intensive care unit patients unresponsive to standard antibiotic treatments. Inhibitory activity of AP-CECT7121 was assessed using the agar-well diffusion method. The most resistant isolates from each species screened (Enterococcus faecium, Enterococcus faecalis,Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes, Clostridium perfringens and Clostridium difficile) were further examined in time-killing curve studies.

RESULTS

These bactericidal kinetic experiments demonstrated a rapid killing effect with no viable bacteria being detected within 30 and 90 min for enterococcal and streptococcal strains and 180 min for community-acquired methicillin-resistant S. aureus and C. perfringens: viable counts for C. difficile were threefold decreased after 90 min.

CONCLUSIONS

AP-CECT7121 may provide a novel strategy for treating potentially fatal clinical infections in hospitalized patients.

摘要

背景

耐革兰氏阳性菌在临床实践中日益引起关注。本研究调查了AP - CECT7121(一种从粪肠球菌环境菌株CECT7121中分离出的抗菌肽)对各种致病性革兰氏阳性菌的疗效。

方法

从对标准抗生素治疗无反应的重症监护病房患者中分离菌株。采用琼脂孔扩散法评估AP - CECT7121的抑制活性。对筛选出的每种细菌(屎肠球菌、粪肠球菌、金黄色葡萄球菌、肺炎链球菌、化脓性链球菌、产气荚膜梭菌和艰难梭菌)中耐药性最强的分离株进行时间 - 杀菌曲线研究。

结果

这些杀菌动力学实验表明,对于肠球菌和链球菌菌株,在30分钟和90分钟内未检测到活菌,对于社区获得性耐甲氧西林金黄色葡萄球菌和气荚膜梭菌,在180分钟内未检测到活菌,呈现出快速杀菌效果:艰难梭菌的活菌数在90分钟后减少了三倍。

结论

AP - CECT7121可能为治疗住院患者潜在致命的临床感染提供一种新策略。

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