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首页> 外文期刊>Pathogens >First Detection of Carbapenem-Resistant Escherichia fergusonii Strains Harbouring Beta-Lactamase Genes from Clinical Samples
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First Detection of Carbapenem-Resistant Escherichia fergusonii Strains Harbouring Beta-Lactamase Genes from Clinical Samples

机译:从临床样品中首次检测到具有抗碳青霉烯类的弗氏大肠杆菌(Escherichia fergusonii)菌株,其带有β-内酰胺酶基因。

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Recently discovered extraintestinal Escherichia fergusonii obtained from non-clinical samples has exhibited the potential for acquiring multiple beta-lactamase genes, just like many extraintestinal Escherichia coli strains. Albeit, they are often omitted or classified as E. coli . This study aimed to, therefore, identify carbapenem-resistant extended-spectrum beta-lactamase (ESBL) producing E. fergusonii isolates from clinical samples, determine their evolutionary relatedness using 16S rRNA sequencing analysis and screen for beta-lactamase genes. A total of 135 septic wound samples were obtained from patients on referral at a General Hospital in Lagos, Nigeria. For the phenotypic identification of isolates from culture-positive samples, morphological, and physiological tests were carried out. Identities of the isolates harbouring beta-lactamase genes were assigned to their genus strains using the 16S rRNA sequencing. The Kirby Bauer disc diffusion technique and double-disc synergy test were used to screen isolates for multidrug resistance and ESBL production. Carbapenem-resistant ESBL producing isolates were screened for beta-lactamase genes in a polymerase chain reaction. Three E. fergusonii isolates (CR11, CR35 and CR49) were obtained during this study. E. fergusonii strains were motile, non-lactose and non-sorbitol fermenting but positive for cellobiose and adonitol fermentation. The I6S rRNA assigned the phenotypically identified isolates to E. fergusonii species. All three isolates were multidrug-resistant, carbapenem-resistant and ESBL producers. Isolates CR11 and CR35 harboured cefotaximase (CTX-M) and temoniera (TEM) beta-lactamase genes while CR49 harboured sulfhydryl variable (SHV) beta-lactamase gene. We herein report the detection of multiple beta-lactamase genes in carbapenem-resistant ESBL producing E. fergusonii from clinical samples.
机译:就像许多肠外大肠杆菌菌株一样,最近从非临床样品中获得的肠外埃希氏大肠杆菌已显示出获得多个β-内酰胺酶基因的潜力。尽管它们经常被省略或归类为大肠杆菌。因此,本研究旨在从临床样品中鉴定产生碳青霉烯抗性的广谱β-内酰胺酶(ESBL)弗格森氏大肠杆菌,使用16S rRNA测序分析确定其进化相关性并筛选β-内酰胺酶基因。从尼日利亚拉各斯一家综合医院转诊的患者中总共获得了135例化脓性伤口样本。为了从培养阳性样品中分离出的菌株进行表型鉴定,进行了形态学和生理学测试。使用16S rRNA测序,将带有β-内酰胺酶基因的分离株的身份分配给它们的属菌株。使用Kirby Bauer圆盘扩散技术和双盘协同试验来筛选分离株的多药耐药性和ESBL产生。在聚合酶链反应中筛选产生抗碳青霉烯的ESBL分离株的β-内酰胺酶基因。在此研究中获得了三个弗格森氏大肠杆菌分离株(CR11,CR35和CR49)。 Fergusonii E.菌株能活动,非乳糖和非山梨醇发酵,但纤维二糖和腺苷醇发酵呈阳性。 I6S rRNA将表型鉴定出的分离物分配给了弗氏大肠杆菌。这三个分离株均为耐多药,对碳青霉烯类耐药和ESBL产生者。分离的CR11和CR35带有头孢噻肟酶(CTX-M)和坦莫尼拉(TEM)β-内酰胺酶基因,而CR49则带有巯基可变(SHV)β-内酰胺酶基因。我们在此报告从临床样品中检测出对碳青霉烯类耐药的ESBL产生弗氏大肠杆菌的多个β-内酰胺酶基因。

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