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首页> 外文期刊>Clinical and diagnostic laboratory immunology >Expression and Refolding of Truncated Recombinant Major Outer Membrane Protein Antigen (r56) of Orientia tsutsugamushi and Its Use in Enzyme-Linked Immunosorbent Assays
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Expression and Refolding of Truncated Recombinant Major Outer Membrane Protein Antigen (r56) of Orientia tsutsugamushi and Its Use in Enzyme-Linked Immunosorbent Assays

机译:ient虫东方ient截短重组主要外膜蛋白抗原(r56)的表达,重折叠及其在酶联免疫吸附试验中的应用

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The variable 56-kDa major outer membrane protein of Orientia tsutsugamushi is the immunodominant antigen in human scrub typhus infections. The gene encoding this protein from Karp strain was cloned into the expression vector pET11a. The recombinant protein (r56) was expressed as a truncated nonfusion protein (amino acids 80 to 456 of the open reading frame) which formed an inclusion body when expressed in Escherichia coli BL21. Refolded r56 was purified and compared to purified whole-cell lysate of the Karp strain of O. tsutsugamushi by immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) for reactivity with rabbit sera prepared against eight antigenic prototypes of O. tsutsugamushi as well as several other species of Rickettsiales and nonrickettsial antigens. Refolded r56 exhibited broad reactivity with the rabbit antisera against the Orientia prototypes, and the ELISA reactions with the r56 and Karp whole-cell lysate antigens correlated well (r = 0.81, n = 22, sensitivity compared to that of standard ELISA of 91%). Refolded r56 did not react with most antisera against other rickettsial species or control antigens (specificity = 92%, n = 13) using a positive cutoff value determined with eight uninfected rabbit sera. Refolded r56 was evaluated further by ELISA, using 128 sera obtained from patients with suspected scrub typhus from Korat, Thailand, and 74 serum specimens from healthy Thai soldiers. By using the indirect immunoperoxidase assay as the reference assay, the recombinant antigen exhibited a sensitivity and specificity of 93% or greater for detection of both IgG and IgM in the ELISA at 1:400 serum dilution. These results strongly suggest that purified r56 is a suitable candidate for replacing the density gradient-purified, rickettsia-derived, whole-cell antigen currently used in the commercial dipstick assay available in the United States.
机译:东方tsu虫的可变的56kDa主要外膜蛋白是人擦洗斑疹伤寒感染的免疫显性抗原。来自Karp株的编码该蛋白的基因被克隆到表达载体pET11a中。重组蛋白(r56)被表达为截短的非融合蛋白(开放阅读框的80至456位氨基酸),当在大肠杆菌 BL21中表达时形成包涵体。纯化重新折叠的r56,并将其与 O的Karp菌株的纯化的全细胞裂解物进行比较。免疫球蛋白G(IgG)酶联免疫吸附试验(ELISA)对虫病与兔血清的反应性,针对八种 O抗原原型制备的兔血清。 tsutsugamushi 以及其他几种立克次氏菌和非立克次氏体抗原。重新折叠的r56与兔抗 Orientia 原型的血清具有广泛的反应性,并且与r56和Karp全细胞裂解物抗原的ELISA反应相关性很好( r = 0.81,< em> n = 22,相对于标准ELISA的敏感性为91%)。重新折叠的r56不能与大多数针对其他立克次氏体或对照抗原的抗血清反应(特异性= 92%, n = 13),该临界值是由八只未感染的兔子血清确定的。使用来自泰国呵叻的疑似灌木斑疹伤寒患者的128份血清和来自健康泰国士兵的74份血清标本,通过ELISA进一步评估了重折叠的r56。通过使用间接免疫过氧化物酶测定法作为参考测定法,重组抗原在以1:400的血清稀释度检测ELISA中的IgG和IgM时显示出93%或更高的灵敏度和特异性。这些结果强烈表明,纯化的r56是替代目前在美国可得的商业量油尺测定中使用的密度梯度纯化的,立克次氏体衍生的全细胞抗原的合适候选者。

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