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细菌素作为控制多重耐药葡萄球菌菌株的替代剂。

Bacteriocins as alternative agents for control of multiresistant staphylococcal strains.

作者信息

Nascimento J S, Ceotto H, Nascimento S B, Giambiagi-Demarval M, Santos K R N, Bastos M C F

机构信息

Departamento de Microbiologia Geral, Instituto de Microbiologia Prof. Paulo de Góes, Universidade Federal do Rio de Janeiro, Brazil.

出版信息

Lett Appl Microbiol. 2006 Mar;42(3):215-21. doi: 10.1111/j.1472-765X.2005.01832.x.

Abstract

AIMS

To investigate the activity of seven staphylococcins, bacteriocins produced by staphylococci, against multiresistant Staphylococcus aureus and coagulase-negative staphylococci (CNS) involved in human infections.

METHODS AND RESULTS

Four bacteriocins produced by Staph. epidermidis (Pep5, epidermin, epilancin K7 and epicidin 280) and three produced by Staph. aureus (aureocins A70, A53 and 215FN) were tested. Sixteen Staph. aureus strains, including a representative strain of the endemic Brazilian methicillin-resistant clone (MRSA), and 57 CNS strains were used as indicators. Among the staphylococcins used, Pep5 was able to inhibit 77.2% of the CNS strains and 87.5% of the Staph. aureus strains tested, including the Brazilian MRSA endemic clone, responsible for a large number of hospital-acquired infections in Brazil. On the other hand, aureocin A53 and epidermin presented a high antagonistic activity only against the Staph. aureus strains, being able to inhibit, respectively, 87.5% and 81.3% of them, including also the Brazilian MRSA endemic clone. The remaining bacteriocins inhibited only a low percentage of the nosocomial staphylococcal strains tested.

CONCLUSIONS

Aureocin A53 and epidermin have potential applications against MRSA, whereas Pep5 seems to be an attractive agent against both MRSA and CNS, including mupirocin-resistant strains and the Brazilian endemic clone of MRSA, which is also found disseminated in other countries.

SIGNIFICANCE AND IMPACT OF THE STUDY

Bacteriocins may represent alternative agents to control important nosocomial pathogens.

摘要

目的

研究七种葡萄球菌素(葡萄球菌产生的细菌素)对参与人类感染的多重耐药金黄色葡萄球菌和凝固酶阴性葡萄球菌(CNS)的活性。

方法与结果

测试了表皮葡萄球菌产生的四种细菌素(Pep5、表皮菌素、表皮兰菌素K7和表皮杀菌素280)以及金黄色葡萄球菌产生的三种细菌素(金黄色葡萄球菌素A70、A53和215FN)。使用了16株金黄色葡萄球菌菌株(包括巴西地方性耐甲氧西林克隆株的代表菌株)和57株CNS菌株作为指示菌。在所使用的葡萄球菌素中,Pep5能够抑制77.2%的CNS菌株和87.5%的测试金黄色葡萄球菌菌株,包括巴西地方性耐甲氧西林金黄色葡萄球菌克隆株,该克隆株在巴西导致大量医院获得性感染。另一方面,金黄色葡萄球菌素A53和表皮菌素仅对金黄色葡萄球菌菌株具有高拮抗活性,分别能够抑制其中的87.5%和81.3%,包括巴西地方性耐甲氧西林金黄色葡萄球菌克隆株。其余细菌素仅抑制了低比例的测试医院葡萄球菌菌株。

结论

金黄色葡萄球菌素A53和表皮菌素对耐甲氧西林金黄色葡萄球菌具有潜在应用价值,而Pep5似乎是对抗耐甲氧西林金黄色葡萄球菌和CNS的有吸引力的药物,包括对莫匹罗星耐药的菌株以及在其他国家也有传播的巴西地方性耐甲氧西林金黄色葡萄球菌克隆株。

研究的意义和影响

细菌素可能代表控制重要医院病原体的替代药物。

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