[革兰氏阳性菌对抗菌因子的耐药机制评价]。

M. Kawada-Matsuo
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引用次数: 0

摘要

在人体中观察到多种抗菌剂可预防细菌感染。在本研究中,为了阐明对人源性抗菌药物和共生菌源性细菌素的耐药机制,我们系统地评估了金黄色葡萄球菌和变形链球菌在不同部位定殖的细菌特异性双组分系统的作用。双组分系统(Two-component system, TCSs)是细菌的一种特殊调控系统,在感知和适应环境中起着重要作用。结果表明,金黄色葡萄球菌的4个TCSs和变形葡萄球菌的3个TCSs与防御素和LL37的抗微生物肽以及nisin A和nukacin ISK-1的细菌素的耐药有关。在变形链球菌中鉴定出两种单独与对细菌素nisin A (I类A型[I])和nukacin ISK-1 (I类A型[II])耐药相关的TCS,而一种TCS与对nisin A和nukacin ISK-1的主要耐药相关。提示tcs在人源性和细菌源性抗菌药物的获得中起重要作用。然而,金黄色葡萄球菌通过TCS的耐药机制与变形葡萄球菌有很大不同。其他证据表明,这些tcs是与其他产生nisin A或nukacin ISK-1的细菌共存所必需的,这意味着细菌素在不同种类的共生细菌之间的相互作用中的作用以及tcs在这一过程中的重要性。我们的研究结果将强调细菌定植在人体中的作用是建立在对来自人类和共生细菌的抗菌剂的适应上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Evaluation of resistance mechanism against antimicrobial factors in gram positive bacteria].
It is known that various antibacterial agents are observed in human for preventing bacterial infection. In this study, in order to elucidate the resistance mechanism against antimicrobial agents derived of human and bacteriocins derived of commensal bacteria, we systematically evaluated the roles of the bacteria-specific two-component systems of Staphylococcus aureus and Streptococcus mutans which colonize to different sites. Two-component systems (TCSs) are specific regulatory systems in bacteria that play an important role in sensing and adapting to the environment. As the result, four TCSs of S. aureus and three TCSs of S. mutans were associated with resistance against defensin and LL37 as antimaicrobial peptides and nisin A and nukacin ISK-1 as bacteriocins. Two TCSs that are individually associated with resistance against the bacteriocins nisin A (class I type A[I]) and nukacin ISK-1 (class I type A[II]) were identified in S. mutans, whereas one TCS is associated with main resistance against the both of nisin A and nukacin ISK-1. This result suggested that TCSs play important roles on acquisition of human- and bacteria-derived antibacterial agents. However, the resistance mechanism via TCS in S. aureus is quite different from that of in S. mutans. Additional evidence suggests that these TCSs are required for co-existence with other bacteria producing to nisin A or nukacin ISK-1, meaning that the roles of bacteriocins in the interactions between different species of commensal bacteria and the importance of TCSs in this process. Our results will highlight the roles of bacterial colonization in human being are constituted on the adaptation against antibacterial agents derived from human and commensal bacteria via TCSs.
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