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用于诊断类鼻疽的重组抗原评估。

Evaluation of recombinant antigens for diagnosis of melioidosis.

作者信息

Allwood Elizabeth M, Logue Carie-Anne, Hafner Gregory J, Ketheesan Natkunam, Norton Robert E, Peak Ian R, Beacham Ifor R

机构信息

Institute for Glycomics, Griffith University Gold Coast Campus, Qld, Australia.

出版信息

FEMS Immunol Med Microbiol. 2008 Oct;54(1):144-53. doi: 10.1111/j.1574-695X.2008.00464.x. Epub 2008 Jul 24.

Abstract

Burkholderia pseudomallei, the causative agent of melioidosis, is endemic to Southeast Asia and northern Australia. Clinical manifestations of the disease are diverse, ranging from chronic localized infection to acute septicaemia, with death occurring within 24-48 h after the onset of symptoms. Definitive diagnosis of melioidosis involves bacterial culture and identification, with results obtained within 3-4 days. This delayed diagnosis is a major contributing factor to high mortality rates. Rapid diagnosis is vital for successful management of the disease. This study describes the purification and evaluation of three recombinant antigenic proteins, BPSL0972, BipD and OmpA from B. pseudomallei 08, for their potential in the serodiagnosis of melioidosis using an indirect enzyme-linked immunosorbent assay (ELISA) method. The recombinant proteins were evaluated using 74 serum samples from culture-confirmed melioidosis patients from Malaysia, Thailand and Australia. In addition, 62 nonmelioidosis controls consisting of serum samples from clinically suspected melioidosis patients (n=20) and from healthy blood donors from an endemic region (n=18) and a nonendemic region (n=24) were included. The indirect ELISAs using BipD and BPSL0972 as antigens demonstrated poor to moderate sensitivities (42% and 51%, respectively) but good specificity (both 100%). In contrast, the indirect ELISA using OmpA as an antigen achieved 95% sensitivity and 98% specificity. These results highlight the potential for OmpA to be used in the serodiagnosis of melioidosis in an endemic area.

摘要

类鼻疽杆菌是类鼻疽病的病原体,在东南亚和澳大利亚北部地区呈地方性流行。该疾病的临床表现多种多样,从慢性局部感染到急性败血症不等,症状出现后24至48小时内可导致死亡。类鼻疽病的确诊需要进行细菌培养和鉴定,结果在3至4天内得出。这种诊断延迟是导致高死亡率的一个主要因素。快速诊断对于成功治疗该疾病至关重要。本研究描述了从类鼻疽杆菌08株中纯化和评估三种重组抗原蛋白BPSL0972、BipD和OmpA,并使用间接酶联免疫吸附测定(ELISA)方法评估它们在类鼻疽病血清诊断中的潜力。使用来自马来西亚、泰国和澳大利亚的经培养确诊的类鼻疽病患者的74份血清样本对重组蛋白进行了评估。此外,还纳入了62份非类鼻疽病对照样本,包括临床疑似类鼻疽病患者的血清样本(n = 20)以及来自地方性流行地区(n = 18)和非地方性流行地区(n = 24)的健康献血者的血清样本。以BipD和BPSL0972作为抗原的间接ELISA显示出低至中等的敏感性(分别为42%和51%),但特异性良好(均为100%)。相比之下,以OmpA作为抗原的间接ELISA的敏感性达到95%,特异性达到98%。这些结果突出了OmpA在地方性流行地区用于类鼻疽病血清诊断的潜力。

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