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首页> 外文期刊>Applied and Environmental Microbiology >Enrichment Double-Antibody Sandwich Indirect Enzyme-Linked Immunosorbent Assay That Uses a Specific Monoclonal Antibody for Sensitive Detection of Ralstonia solanacearum in Asymptomatic Potato Tubers
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Enrichment Double-Antibody Sandwich Indirect Enzyme-Linked Immunosorbent Assay That Uses a Specific Monoclonal Antibody for Sensitive Detection of Ralstonia solanacearum in Asymptomatic Potato Tubers

机译:富集双抗体夹心间接酶联免疫吸附测定,使用特异性单克隆抗体灵敏检测无症状马铃薯块茎中的Ralstonia solanacearum

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Sensitive and specific routine detection of Ralstonia solanacearum in symptomless potato tubers was achieved by efficient enrichment followed by a reliable double-antibody sandwich indirect enzyme-linked immunosorbent assay based on the specific monoclonal antibody 8B-IVIA. This monoclonal antibody reacted with 168 typical R. solanacearum strains and did not recognize 174 other pathogenic or unidentified bacteria isolated from potato. The optimized protocol included an initial enrichment step consisting of shaking the samples in modified Wilbrink broth for 72 h at 29°C. This step enabled specific detection by the enzyme-linked immunosorbent assay of 1 to 10 CFU of R. solanacearum per ml of initial potato extract. Analysis of 233 commercial potato lots by this method provided results that coincided with the results of conventional methods.
机译:通过有效富集,然后进行基于特异性单克隆抗体8B-IVIA的可靠的双抗体夹心间接酶联免疫吸附试验,可以对无症状马铃薯块茎中的青枯菌进行灵敏且特定的常规检测。该单克隆抗体与168株典型的青枯菌(R. solanacearum)菌株反应,无法识别从马铃薯中分离出的174种其他病原性或未鉴定细菌。优化的方案包括一个初始富集步骤,该步骤包括将样品在改良的Wilbrink肉汤中于29°C摇动72小时。该步骤使得能够通过酶联免疫吸附测定法对每毫升最初的马铃薯提取物中1至10 CFU的青枯菌进行特异性检测。通过这种方法对233个商业马铃薯批次进行分析,得出的结果与常规方法的结果相吻合。

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