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Extended-spectrum beta-lactamases and the permeability barrier

机译:广谱β-内酰胺酶和通透性屏障

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摘要

The outer membrane of Gram-negative bacteria represents a barrier for penetration of hydrophilic compounds. Loss of porins (water-filled protein channels) contributes to antimicrobial resistance, particularly when additional mechanisms of resistance are expressed. Many studies on the structure and regulation of porins in Escherichia coli K-12 are available, but there is little information concerning clinical isolates of this species. In Klebsiella pneumoniae, two major porins, OmpK35 and OmpK36, are produced, but many extended-spectrum beta-lactamase (ESBL)-producing K. pneumoniae isolates do not express OmpK35. Loss of both OmpK35 and OmpK36 in ESBL-producing K. pneumoniae causes resistance to cefoxitin, increased resistance to expanded-spectrum cephalosporins, and decreased susceptibility to carbapenems, particularly ertapenem. Porin loss also decreases the susceptibility to other non-beta-lactam compounds, such as fluoroquinolones, of ESBL-producing organisms.
机译:革兰氏阴性细菌的外膜代表了亲水性化合物渗透的屏障。孔蛋白(充满水的蛋白质通道)的丧失有助于抗药性,特别是在表达其他抗药性机制时。目前已有许多关于大肠杆菌K-12中孔蛋白的结构和调控的研究,但是关于该种临床分离株的信息很少。在肺炎克雷伯菌中,产生了两种主要孔蛋白,OmpK35和OmpK36,但许多产生广谱β-内酰胺酶(ESBL)的肺炎克雷伯菌分离株均不表达OmpK35。产生ESBL的肺炎克雷伯菌中OmpK35和OmpK36的缺失会导致对头孢西丁的耐药性,对广谱头孢菌素的耐药性增加以及对碳青霉烯类特别是厄他培南的敏感性降低。孔蛋白的丢失还降低了产生ESBL的生物对其他非β-内酰胺化合物的敏感性,例如氟喹诺酮类。

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