首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Phylogenetic background and carriage of pathogenicity island-like domains in relation to antibiotic resistance profiles among Escherichia coli urosepsis isolates.
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Phylogenetic background and carriage of pathogenicity island-like domains in relation to antibiotic resistance profiles among Escherichia coli urosepsis isolates.

机译:系统发育背景和致病性岛状结构域的运输与大肠杆菌尿嘧啶分离株中的抗生素耐药性有关。

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摘要

We studied 100 well-characterized E. coli blood isolates from patients with urosepsis for their susceptibility to nalidixic acid, ampicillin and trimethoprim-sulfamethoxazole, according to prevalence of virulence factors, phylogenetic groups and subgroups, PAI II(J96)-like domains (determined by physical linkage of cnf1, hly and hra) and PAI I(CFT073)-like domains (determined by physical linkage of papGII to the hly locus). Nalidixic acid resistance was associated with a lower prevalence of sfa/foc, K1 antigen, pathogenicity island II(J96)-like domains, subgroup B2/I and a shift towards group A.
机译:我们根据毒力因子,系统发育组和亚组,PAI II(J96)样结构域(确定)的流行程度,研究了100例尿毒症患者特征明确的大肠杆菌血液分离株对萘啶酸,氨苄西林和甲氧苄氨嘧啶磺胺甲基异恶唑的敏感性(通过cnf1,hly和hra的物理连接)和PAI I(CFT073)样结构域(由papGII与hly位置的物理连接确定)。耐萘啶酸与较低的sfa / foc,K1抗原,致病岛II(J96)样结构域,B2 / I亚组和向A组的转移相关。

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