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首页> 外文期刊>Journal of Clinical Microbiology >Direct Blood Culturing of Candida spp. on Solid Medium by a Rapid Enrichment Method with Magnetic Beads Coated with Recombinant Human Mannan-Binding Lectin
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Direct Blood Culturing of Candida spp. on Solid Medium by a Rapid Enrichment Method with Magnetic Beads Coated with Recombinant Human Mannan-Binding Lectin

机译:直接血液培养<斜体>念珠菌 SPP。通过一种快速富集法用重组人曼南结合凝集素的磁珠快速富集法

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A rapid and accurate method to identify the species and antibiotic resistance of Candida spp. in blood is vital to increase the survival rates of patients with bloodstream infections. However, the extremely low levels of Candida spp. in blood make rapid diagnosis by standard blood culture difficult. In this study, we constructed a direct blood culturing method (i.e., the M1 method) by a rapid enrichment method with magnetic beads coated with a recombined human mannan-binding lectin (rhMBL; i. ABSTRACT A rapid and accurate method to identify the species and antibiotic resistance of Candida spp. in blood is vital to increase the survival rates of patients with bloodstream infections. However, the extremely low levels of Candida spp. in blood make rapid diagnosis by standard blood culture difficult. In this study, we constructed a direct blood culturing method (i.e., the M1 method) by a rapid enrichment method with magnetic beads coated with a recombined human mannan-binding lectin (rhMBL; i.e., M1 protein), which demonstrated much higher Candida sp.-binding capacity than that of full-length MBL expressed in vitro (i.e., M2). With the M1 method, individual colonies were obtained before the standard blood culture method for each species of Candida spp. tested at?&1 CFU/ml (an average of 29 h earlier). Additionally, the clinical sensitivity of the M1 method was 90.5% compared with that of the standard blood culture method when detecting frozen plasma from patients. More significantly, the turnaround time of the M1 method for blood culture could be reduced by approximately 37 to 43 h compared with that of the standard blood culture method in clinical sample identification.
机译:一种快速准确的方法,可识别Candida SPP的物种和抗生素抗性。在血液中对增加血流感染患者的存活率至关重要。但是,极低的念珠菌水平。在血液中通过标准血液培养难以诊断。在这项研究中,我们通过一种快速富集方法构建了一种直接血液培养方法(即,M1方法),该方法具有涂有重组人类结合凝集素的磁珠(RHMBL; I.摘要一种识别物种的快速和准确的方法念珠菌SPP的抗生素抗性。在血液中,增加血流感染患者的存活率至关重要。然而,极低的Candida SPP水平。在血液中,通过标准血液文化难以诊断。在这项研究中,我们建造了一个通过涂覆有重组人类甘露结合凝集素(RHMBL;即M1蛋白)的磁珠的快速富集方法直接血液培养方法(即M1方法),其展示了比那样更高的念珠菌。结合容量全长MBL在体外表达(即,M2)。通过M1方法,在每种念珠菌SPP的标准血液培养方法之前获得单个菌落。在αα中进行了测试(AVARA预先29小时的GE)。另外,与检测患者冷冻血浆的标准血液培养方法相比,M1方法的临床敏感性为90.5%。更重要的是,与临床样本鉴定中标准血液培养方法的血液培养方法相比,M1血液培养方法的周转时间可降低约37至43小时。

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