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A simple heat dissociation method increases significantly the ELISA detection sensitivity of the nonstructural-1 glycoprotein in patients infected with DENV type-4

机译:一种简单的热解离方法可显着提高DENV 4型感染患者非结构1糖蛋白的ELISA检测灵敏度

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The secreted form of the dengue virus (DENV) nonstructural-1 (NS1) glycoprotein has been shown to be useful for the diagnosis of DENV infections in patients' serum samples. In a number of studies, the sensitivity of the commercially available DENV NS1 glycoprotein detection assays was higher against some DENV serotypes (DENV-1 > DENV-3 > DENV-2 = DENV-4) than others and were also lower using patients' serum samples with secondary versus primary DENV infections. In this study, 471 DENV-4 positive acute phase patients' serum samples were selected from a large panel collected in Brazil from March 2011 to October 2012 by RT-PCR and/or virus isolation followed by serotype determination. The sera from primary (n = 228) and secondary (n = 238) DENV-4 infections were identified using IgM and IgG capture ELISAs. The sensitivity of a commercial DENV NS1 glycoprotein detection ELISA was then assessed when these serum samples were not pre-treated or pre-treated by acid or heat dissociation prior to being tested. Acid and heat dissociation of patients' serum samples with primary and secondary DENV-4 infections increased significantly the sensitivity of the DENV NS1 glycoprotein detection ELISA from 54.4% to 77.2% (p < 0.05) and 82% (p < 0.05) and from 39.1% to 63.9% (p < 0.05) and 73.1% (p < 0.05), respectively. Treatment of DENV infected patients' serum samples using simple and rapid heat dissociation step (100 C for 5 min) was, therefore, shown to be very useful for increasing the sensitivity of the DENV NS1 glycoprotein detection ELISA using serum samples from either primary or secondary DENV infected patients
机译:登革热病毒(DENV)非结构性1(NS1)糖蛋白的分泌形式已显示可用于诊断患者血清样本中的DENV感染。在许多研究中,市售的DENV NS1糖蛋白检测方法对某些DENV血清型(DENV-1> DENV-3> DENV-2 = DENV-4)的敏感性高于其他血清型,并且使用患者血清也较低继发性与原发性DENV感染的样本。在这项研究中,从2011年3月至2012年10月在巴西收集的一大批样本中,通过RT-PCR和/或病毒分离以及血清型测定,选择了471例DENV-4阳性急性期患者的血清样本。使用IgM和IgG捕获ELISA鉴定了原发性(n = 228)和继发性(n = 238)DENV-4感染的血清。当这些血清样品在测试前未经过酸或热解离预处理或预处理时,然后评估商用DENV NS1糖蛋白检测ELISA的敏感性。患有原发性和继发性DENV-4感染的患者血清样品的酸解和热解显着提高了DENV NS1糖蛋白检测ELISA的灵敏度,从54.4%增至77.2%(p <0.05)和82%(p <0.05)和39.1 %分别为63.9%(p <0.05)和73.1%(p <0.05)。因此,使用简单,快速的热解离步骤(100°C,持续5分钟)处理DENV感染患者的血清样品对于提高DENV NS1糖蛋白检测ELISA的灵敏度非常有用,该方法使用的是原发性或继发性血清DENV感染的患者

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