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首页> 外文期刊>BMC Infectious Diseases >Multiple-antigen ELISA for melioidosis - a novel approach to the improved serodiagnosis of melioidosis
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Multiple-antigen ELISA for melioidosis - a novel approach to the improved serodiagnosis of melioidosis

机译:乳突病的多抗原ELISA-改善乳突病血清学诊断的新方法

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Background Burkholderia pseudomallei, the causative agent of melioidosis, is endemic to Southeast Asia and northern Australia. Clinical manifestations of disease are diverse, ranging from chronic infection to acute septicaemia. The current gold standard of diagnosis involves bacterial culture and identification which is time consuming and often too late for early medical intervention. Hence, rapid diagnosis of melioidosis is crucial for the successful management of melioidosis. Methods The study evaluated 4 purified B. pseudomallei recombinant proteins (TssD-5, Omp3, smBpF4 and Omp85) as potential diagnostic agents for melioidosis. A total of 68 sera samples from Malaysian melioidosis patients were screened for the presence of specific antibodies towards these proteins using enzyme-linked immunosorbent assay (ELISA). Sera from patients with various bacterial and viral infections but negative for B. pseudomallei, as well as sera from healthy individuals, were also included as non-melioidosis controls. The Mann Whitney test was performed to compare the statistical differences between melioidosis patients and the non-melioidosis controls. Results TssD-5 demonstrated the highest sensitivity of 71% followed by Omp3 (59%), smBpF4 (41%) and Omp85 (19%). All 4 antigens showed equally high specificity (89-96%). A cocktail of all 4 antigens resulted in slightly reduced sensitivity of 65% but improved specificity (99%). Multiple-antigen ELISA provided improved sensitivity of 88.2% whilst retaining good specificity (96%). There was minimal reactivity with sera from healthy individuals proposing the utility of these antigens to demarcate diseased from non-symptomatic individuals in an endemic country. Conclusions TssD-5 demonstrated high detection sensitivity and specificity and the results were obtained within a few hours compared to time consuming culture and IFAT methods commonly used in a clinical setting. The use of multiple-antigens resulted in improved sensitivity (88.2%) whilst maintaining superior specificity. These data highlight the use of TssD-5 and other recombinant antigens tested in this study as potential serodiagnostic agents for melioidosis.
机译:背景技术类拟鼻疽伯克霍尔德菌(Burkholderia pseudomallei)是东南亚和澳大利亚北部的特有种。疾病的临床表现多种多样,从慢性感染到急性败血病。当前诊断的金标准涉及细菌培养和鉴定,这很费时,并且对于早期医学干预通常为时已晚。因此,快速诊断乳突病对于成功治疗乳突病至关重要。方法该研究评估了4种纯化的假疟原虫重组蛋白(TssD-5,Omp3,smBpF4和Omp85)作为类蚜虫病的潜在诊断剂。使用酶联免疫吸附测定(ELISA),从马来西亚类鼻疮患者的总共68份血清样品中筛选了针对这些蛋白质的特异性抗体的存在。来自患有各种细菌和病毒感染但对假苹果芽孢杆菌阴性的患者的血清,以及来自健康个体的血清,也被列为非类i虫病对照。进行了Mann Whitney检验,以比较乳突病患者和非乳突病对照之间的统计学差异。结果TssD-5的最高灵敏度为71%,其次是Omp3(59%),smBpF4(41%)和Omp85(19%)。所有4种抗原均显示出同样高的特异性(89-96%)。所有4种抗原的混合物导致敏感性降低了65%,但特异性提高了(99%)。多重抗原ELISA的灵敏度提高了88.2%,同时保留了良好的特异性(96%)。健康个体与血清的反应极少,提示这些抗原可用于区分流行国家非症状个体的疾病。结论TssD-5具有很高的检测灵敏度和特异性,与临床环境中常用的费时培养和IFAT方法相比,可以在数小时内获得结果。使用多种抗原可提高灵敏度(88.2%),同时保持出色的特异性。这些数据强调了在本研究中测试的TssD-5和其他重组抗原作为类鼻疽的潜在血清诊断药物的用途。

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