Targeting Extracellular Bacterial Proteases for the Development of Novel Antivirulence Agents.

Cansu Kaya, Anna K H Hirsch
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Abstract

As resistance to clinically available antibiotics persistently increases, applying new strategies to target pathogenic bacteria are paramount to design effective drugs. Bacterial proteases play vital roles in cell viability and stress response, contributing to the pathogenicity of the resistant bacteria. Targeting these extracellular enzymes by antivirulence therapy is a prominent strategy in combating multi-drug resistant bacteria. By preventing the colonization and infiltration of the host, this method can lower selection pressure and reduce resistance development significantly. Here, we review the role of bacterial proteases, the rise of antivirulence therapy and we report on the development of novel antivirulence agents targeting two key virulence factors: elastase B (LasB) from Pseudomonas aeruginosa and collagenase H (ColH) from Clostridium histolyticum.

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以细胞外细菌蛋白酶为目标开发新型抗病毒药物。
随着临床可用抗生素的耐药性持续增加,应用新的策略来靶向致病菌对于设计有效的药物至关重要。细菌蛋白酶在细胞活力和应激反应中起着至关重要的作用,有助于耐药细菌的致病性。针对这些细胞外酶的抗毒治疗是对抗多重耐药细菌的重要策略。该方法通过阻止寄主的定植和浸润,可以显著降低选择压力,减少抗性的产生。在此,我们回顾了细菌蛋白酶的作用,抗毒治疗的兴起,并报道了针对两个关键毒力因子的新型抗毒剂的开发:铜绿假单胞菌的弹性酶B (LasB)和溶组织梭菌的胶原酶H (ColH)。
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CiteScore
1.10
自引率
0.00%
发文量
11
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