首页> 外文期刊>Antimicrobial agents and chemotherapy. >Changes in the Frequencies of beta-Lactamase Genes among Enterobacteriaceae Isolates in US Hospitals, 2012 to 2014: Activity of Ceftazidime-Avibactam Tested against beta-Lactamase-Producing Isolates
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Changes in the Frequencies of beta-Lactamase Genes among Enterobacteriaceae Isolates in US Hospitals, 2012 to 2014: Activity of Ceftazidime-Avibactam Tested against beta-Lactamase-Producing Isolates

机译:美国医院中肠杆菌区分离物中β-内酰胺酶基因频率的变化,2012至2014:Ceftazidime-Avibactam的活性对β-内酰胺酶产生的分离物进行测试

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Among 15,588 Enterobacteriaceae isolates collected in 63 U.S. hospitals from 2012 to 2014, 2,129 (13.7%) displayed an extended-spectrum beta-lactamase (ESBL) phenotype. These rates were similar over time (13.2 to 13.9%); however, differences among Escherichia coli (12.7 and 15.1% in 2012 and 2014; P = 0.007) and Klebsiella pneumoniae (18.9 and 15.5% in 2012 and 2014; P = 0.006) were noted when comparing 2014 and 2012. Carbapenem-resistant Enterobacteriaceae (CRE) (2.3 and 1.8%) and carbapenem-resistant K. pneumoniae (6.8 and 5.1%; P = 0.003) rates were lower in 2014 than in 2012. Isolates carrying bla(CTX-M-15)-like genes were stable (42.1 to 42.4%), but a decrease among E. coli isolates (59.1 and 49.7%; P = 0.008) and an increase among K. pneumoniae isolates (32.7 and 41.2%; P = 0.022) in 2014 were observed. Isolates carrying bla(KPC) (304) decreased over the years (16.5 and 10.9%; P = 0.008), mainly due to the decrease in K. pneumoniae isolates harboring bla(KPC) (n = 285; 35.6 and 28.4%; P = 0.041) in hospitals in the Mid-Atlantic and South Atlantic regions, where these isolates were highly prevalent during 2012 and 2013. Isolates carrying bla(CMY-2)-like and bla(CTX-M-14-)like genes increased (8.2 and 11.9% and 9.1 and 12.9%, respectively; P = 0.04 for both), and those producing bla(SHV) ESBL decreased (24.9 and 12.7%; P < 0.001) over the studied years, due to a decreased occurrence of the enzymes among K. pneumoniae isolates. Other enzymes were detected in smaller numbers of isolates, including four K. pneumoniae isolates carrying bla(NDM-1) metallo-beta-lactamase (two in 2012 and two in 2014). Ceftazidime-avibactam, a recently approved beta-lactamase inhibitor combination, was very active against the ESBL phenotype isolates (MIC50/90, 0.12 and 1 mu g/ml; 99.7% susceptible) and CRE strains (MIC50/90, 0.5 and 2 mu g/ml; 98.5% susceptible) that displayed elevated MIC values for many comparator agents. In conclusion, significant changes were noted in the frequencies of isolates harboring various beta-lactamases among U.S. hospitals between 2012 and 2014 that will require continued monitoring.
机译:在2012年至2014年的63名美国医院收集的15,588个肠杆菌菌分离株中,2,129(13.7%)显示扩展β-内酰胺酶(ESBL)表型。这些利率随着时间的推移(13.2%至13.9%);然而,在2012年和2012年和2014年的2012年和2014年的12.7和15.1%之间的差异(12.7和15.1%; P = 0.007)和Klebsiella肺炎(18.9和15.5%; P = 0.006)在2014年和2012年的抗癌肠杆菌(Carbapenem)( CRE)(2.3和1.8%)和CarbapeNem抗性K. 2014年肺炎(6.8和5.1%; P = 0.003)率比2012年更低。携带BLA(CTX-M-15) - 尺寸基因的分离物稳定( 42.1至42.4%),但大肠杆菌分离株(59.1和49.7%; P = 0.008)中的减少,观察到2014年K.肺炎群分离物(32.7和41.2%; P = 0.022)。携带BLA(KPC)(304)的分离物多年来降低(16.5%和10.9%; P = 0.008),主要是由于患有BLA(KPC)的K.肺炎肺炎群分离物(n = 285; 35.6和28.4%; P.在大西洋中大西洋和南大西洋地区的医院中= 0.041),2012年和2013年这些分离株在普遍普遍存在。携带BLA(CMY-2)的分离物(CMY-2)和BLA(CTX-M-14-)增加( 8.2和11.9%和9.1和12.1%和12.9%; P = 0.04,产生BLA(SHV)ESBL的那些在学习年度下降(24.9%和12.7%; P <0.001),由于下降的发生K.肺炎群岛中的酶。以较少数量的分离株检测其他酶,包括携带BLA(NDM-1)金属β-内酰胺酶的四个K.肺炎群分离物(2012年两者和2014年两者)。最近批准的β-内酰胺酶抑制剂组合的Ceftazidime-Avibactam对ESBL表型分离物(MIC50 / 90,0.12和1μg/ mL; 99.7%易感)和CRE菌株(MIC50 / 90,0.5和2μm g / ml; 98.5%易感)显示了许多比较剂的升高值。总之,在2012年至2014年间,在2012年和2014年间,在2012年至2014年间,患有各种β-内酰胺酶的分离物的频率的显着变化。

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