在印度三级医院产生β-内酰胺酶的变形杆菌的表型检测和抗生素谱。

N Pal, S Hooja, R Sharma, R K Maheshwari
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引用次数: 15

摘要

背景:变形杆菌引起多种社区和医院获得性疾病。β-内酰胺酶的合成是β-内酰胺类抗生素耐药的主要机制。在β-内酰胺酶中,扩展谱β-内酰胺酶(ESBLs)和AmpC β-内酰胺酶最为常见。目的:本研究的目的是确定在印度一家三级保健医院的各种临床分离的变形杆菌种中ESBL和AmpC β-内酰胺酶的发生率。材料与方法:本研究从临床标本(n = 3922)中鉴定出多种变形杆菌。采用Kirby-Bauer圆盘扩散法测定药敏。采用改良双盘协同试验和间接改良三维试验检测ESBL产量,采用AmpC圆盘试验和改良霍奇试验检测AmpC β-内酰胺酶产量。结果:5.4%(101/1876)标本分离到变形杆菌。分离到的变形Proteus为mirabilis 62.4% (63/101), vulgaris 29.7% (30/101), penneri 7.9%(8/101)。两种检测均确认的ESBL生产者占88.1%(89/101)。4株菌株仅产生AmpC β-内酰胺酶。ESBL与AmpC β-内酰胺酶共产的菌株占58.4%(52/89)。12株菌株不产生β-内酰胺酶。95.1%(96/101)的菌株存在多重耐药(MDR), 50.5%(51/101)的菌株可能存在广泛耐药,无一株为泛耐药。所有菌株对哌拉西林-他唑巴坦均无耐药。penneri菌株对大多数抗生素表现出高耐药性。结论:ESBL和AmpC β-内酰胺酶高发,并发耐多药。表型法检测β-内酰胺酶简便易行,可在常规诊断实验室与药敏试验同时实施。这些数据将有助于临床医生管理和控制感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Phenotypic Detection and Antibiogram of β-lactamase-producing <i>Proteus</i> Species in a Tertiary Care Hospital, India.

Phenotypic Detection and Antibiogram of β-lactamase-producing <i>Proteus</i> Species in a Tertiary Care Hospital, India.

Phenotypic Detection and Antibiogram of β-lactamase-producing <i>Proteus</i> Species in a Tertiary Care Hospital, India.

Phenotypic Detection and Antibiogram of β-lactamase-producing Proteus Species in a Tertiary Care Hospital, India.

Background: Proteus species cause a variety of community- and hospital-acquired illnesses. Synthesis of β-lactamases is the predominant mechanism for resistance to β-lactam antibiotics. Among the β-lactamases, extended spectrum β-lactamases (ESBLs) and AmpC β-lactamases are the most common.

Aim: The objective of this study was to determine the occurrence of ESBL and AmpC β-lactamases in Proteus species among various clinical isolates at a tertiary care hospital, India.

Materials and methods: This study was done to identify various species of Proteus from clinical samples (n = 3922). Antimicrobial susceptibility was performed by Kirby-Bauer disc diffusion method. ESBL production was detected by modified double-disc synergy test and indirect modified three-dimensional tests and AmpC β-lactamase production by AmpC disc test and modified Hodge test.

Results: Proteus species were isolated in 5.4% (101/1876) specimens. Three Proteus species isolated were Proteus mirabilis 62.4% (63/101), Proteus vulgaris 29.7% (30/101), and Proteus penneri 7.9% (8/101). ESBL producers confirmed by both tests were of 88.1% (89/101). Only AmpC β-lactamase was produced by four isolates. Coproduction of ESBL and AmpC β-lactamase was observed in 58.4% (52/89) of isolates. Twelve isolates were non-β-lactamase producers. Multidrug resistance (MDR) was found in 95.1% (96/101) of isolates, 50.5% (51/101) were possibly extensively drug resistant and none were pan drug resistant. None of the isolates were resistant to piperacillin-tazobactam. P. penneri isolates exhibited high resistance to most of the antibiotics.

Conclusions: A high prevalence of ESBL and AmpC β-lactamases was found that concurrently showed MDR. Phenotypic methods for the detection of β-lactamases are easy and simple and can be implemented in routine diagnostic laboratories along with susceptibility testing. These data will assist the clinicians in the management and control of infections.

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Annals of Medical and Health Sciences Research
Annals of Medical and Health Sciences Research HEALTH CARE SCIENCES & SERVICES-
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