尿路致病性大肠埃希菌广谱β内酰胺酶和AmpC共存及其抗生素谱图

IF 1.2 Q3 MULTIDISCIPLINARY SCIENCES ARO-THE SCIENTIFIC JOURNAL OF KOYA UNIVERSITY Pub Date : 2022-06-21 DOI:10.14500/aro.10898
Aryan R. Ganjo
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引用次数: 0

摘要

由于各种机制导致的大肠杆菌耐药的出现使得治疗选择非常有限。本研究的目的是调查从尿路感染(uti)分离的大肠杆菌中的广谱β -内酰胺酶(ESBLs)和AmpC内酰胺酶,并评估其在卫生保健背景下的抗菌敏感性模式。在9个月期间,从临床假定的尿路感染患者病例中共分离出70株大肠杆菌。分离出细菌尿(105 CFU/ml)。表型检测到ESBL和AmpC。在70株尿路致病性大肠杆菌中,34株(48.6%)分离出ESBL, 27株(38.6%)分离出AmpC产生菌,其中14株(20%)分离出ESBL和AmpC共存表型,23株(32.9%)分离出ESBL和AmpC不产生菌。这些发现提供了有关耐药性的信息。本研究中产生ESBL-和ampc的尿路致病性大肠杆菌的耐药水平呈上升趋势;因此,严格的感染控制措施和临床实验室对产生ESBL和ampc的细菌的常规监测至关重要。
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The Coexistence of extended spectrum β lactamases and AmpC production among uropathogenic isolates of Escherichia coli and its antibiogram pattern
   Emergence of drug resistance in Escherichia coli due to various mechanisms makes the treatment choices very limited. The objective of this research was to investigate extended-spectrum beta-lactamases (ESBLs) and AmpC lactamases in E. coli isolates from urinary tract infections (UTIs) and to assess their antibacterial susceptibility patterns in a health-care context. A total of 70 E. coli isolates from clinically assumed cases of UTI patients during the 9 months period. The isolates with bacteriuria (105 CFU/ml) were identified. ESBL and AmpC were detected phenotypically. Out of the 70 isolates of uropathogenic E. coli, ESBL production was detected in 34 (48.6%) isolates and AmpC producer in 27 (38.6%) of isolates in which 14 (20%) of them showed coexistence phenotype of both ESBLs and AmpC and 23 (32.9%) E. coli isolates were both ESBL and AmpC non-producer. The findings donated information regarding drug resistance. The level of resistance recorded in ESBL- and AmpC-producing uropathogenic E. coli of this study was raising; therefore, it is crucial to have a strict infection control measures and routine monitoring of ESBL- and AmpC-producing bacteria in clinical laboratory.
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来源期刊
ARO-THE SCIENTIFIC JOURNAL OF KOYA UNIVERSITY
ARO-THE SCIENTIFIC JOURNAL OF KOYA UNIVERSITY MULTIDISCIPLINARY SCIENCES-
自引率
33.30%
发文量
33
审稿时长
16 weeks
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