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Genetic factors associated with elevated carbapenem resistance in KPC-producing Klebsiella pneumoniae.

机译:与生产KPC的肺炎克雷伯菌的碳青霉烯耐药性升高相关的遗传因素。

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In the United States, the most prevalent mechanism of carbapenem resistance among Enterobacteriaceae is the production of a Klebsiella pneumoniae carbapenemase (KPC). KPC-producing isolates often exhibit a range of carbapenem MICs. To better understand the factors that contribute to overall carbapenem resistance, we analyzed 27 KPC-producing K. pneumoniae isolates with different levels of carbapenem resistance, 11 with low-level (i.e., meropenem or imipenem MIC /= 16 mug/ml) carbapenem resistance, that were received from throughout the United States. Among 14 isolates that exhibited high-level carbapenem resistance, Western blot analysis indicated that 10 produced an elevated amount of KPC. These isolates either contained an increased bla(KPC) gene copy number (n = 3) or had deletions directly upstream of the bla(KPC) gene (n = 7). Four additional isolates lacked elevated KPC production but had high-level carbapenem resistance. Porin sequencing analysis identified 22 isolates potentially lacking a functional OmpK35 and three isolates potentially lacking a functional OmpK36. The highest carbapenem MICs were found in two isolates that lacked both functioning porins and produced elevated amounts of KPC. The 11 isolates with low-level carbapenem resistance contained neither an upstream deletion nor increased bla(KPC) copy number. These results suggest that both bla(KPC) copy number and deletions in the upstream genetic environment affect the level of KPC production and may contribute to high-level carbapenem resistance in KPC-producing K. pneumoniae, particularly when coupled with OmpK36 porin loss.
机译:在美国,肠杆菌科中最常见的碳青霉烯耐药性机制是肺炎克雷伯菌肺炎克雷伯菌(KPC)的产生。产生KPC的分离物通常表现出一系列碳青霉烯MIC。为了更好地了解影响整体碳青霉烯耐药性的因素,我们分析了27种KPC产生的肺炎克雷伯菌,其耐药性水平不同,其中11种低水平(即美洛培南或亚胺培南MIC / = 16杯/毫升的MIC)的14例状态。 Western印迹分析表明,在14个表现出高水平对碳青霉烯抗性的菌株中,有10个产生了升高的KPC量。这些分离株要么包含增加的bla(KPC)基因拷贝数(n = 3),要么直接位于bla(KPC)基因上游缺失(n = 7)。另外四个分离株缺乏提高的KPC产量,但具有高水平的碳青霉烯抗性。孔蛋白测序分析确定了22个可能缺乏功能性OmpK35的分离株和3个可能缺乏功能性OmpK36的分离株。碳青霉烯类MICs最高的是两种分离株,它们既缺乏功能性孔蛋白,又产生了升高的KPC量。具有低水平碳青霉烯抗性的11个分离株既不包含上游缺失,也不包含bla(KPC)拷贝数增加。这些结果表明,bla(KPC)的拷贝数和上游遗传环境中的缺失均会影响KPC的生产水平,并可能在生产KPC的肺炎克雷伯菌中导致高水平的碳青霉烯抗药性,特别是与OmpK36孔蛋白损失结合时。

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