Grewal H M, Helander A, Svennerholm A M, Bhan M K, Gaastra W, Sommerfelt H
Centre for International Health, University of Bergenn, Norway.
J Clin Microbiol. 1994 May;32(5):1295-301. doi: 10.1128/jcm.32.5.1295-1301.1994.
A polynucleotide probe comprising the gene encoding a major structural subunit protein of coli surface antigen 6 (CS6) of enterotoxigenic Escherichia coli (ETEC) was developed. Eighty-nine ETEC isolates were examined in parallel with the probe in a colony hybridization assay and in a recently developed polyclonal-antibody-based inhibition enzyme-linked immunosorbent assay (ELISA). The two assays showed a high level of concordance in the detection of CS6-positive ETEC (kappa = 0.84, P < 0.00001). Thus, 36 of the 89 ETEC isolates were identified as CS6-positive by both assays. Six strains that were negative for other colonization factor antigens were positive with the CS6 probe but negative in the ELISA, suggesting lack of surface CS6 expression in these strains. One strain was probe negative but positive in the ELISA, while the remaining 46 strains were negative in both assays. The phenotypic and genotypic assays will prove useful in vaccine-oriented studies of ETEC disease.
构建了一种多核苷酸探针,其包含编码产肠毒素大肠杆菌(ETEC)的 coli 表面抗原 6(CS6)主要结构亚基蛋白的基因。在菌落杂交试验以及最近开发的基于多克隆抗体的抑制酶联免疫吸附测定(ELISA)中,将 89 株 ETEC 分离株与该探针进行平行检测。在检测 CS6 阳性 ETEC 方面,这两种检测方法显示出高度一致性(kappa = 0.84,P < 0.00001)。因此,89 株 ETEC 分离株中有 36 株通过两种检测方法均被鉴定为 CS6 阳性。6 株对其他定植因子抗原呈阴性的菌株,用 CS6 探针检测呈阳性,但 ELISA 检测呈阴性,表明这些菌株表面缺乏 CS6 表达。1 株探针检测呈阴性但 ELISA 检测呈阳性,其余 46 株在两种检测中均呈阴性。表型和基因型检测在 ETEC 疾病的疫苗导向研究中将被证明是有用的。