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首页> 外文期刊>Applied and Environmental Microbiology >Monoclonal antibodies for detection of the H7 antigen of Escherichia coli.
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Monoclonal antibodies for detection of the H7 antigen of Escherichia coli.

机译:用于检测大肠杆菌H7抗原的单克隆抗体。

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Two murine monoclonal antibodies (MAbs) (2B7 and 46E9-9) reactive with the H7 flagellar antigen of Escherichia coli were produced and characterized. A total of 217 E. coli strains (48 O157:H7, 4 O157:NM, 23 O157:non-H7, 22 H7:non-O157, and 120 non-O157:nonH7), 17 Salmonella serovars, and 29 other gram-negative bacteria were used to evaluate the reactivities of the two MAbs by indirect enzyme-linked immunosorbent assay (ELISA). Both MAbs reacted strongly with all E. coli strains possessing the H7 antigen and with H23- and H24-positive E. coli strains. Indirect ELISA MAb specificity was confirmed by inhibition ELISA and by Western blotting (immunoblotting), using partially purified flagellins from E. coli O157:H7 and other E. coli strains. On a Western blot, MAb 46E9-9 was more reactive against H7 flagellin of E. coli O157:H7 than against H7 flagellin of E. coli O1:K1:H7. Competition ELISA suggested that MAbs 2B7 and 46E9-9 reacted with closely related H7 epitopes. When the ELISA reactivities of the MAbs and two commercially available polyclonal anti-H7 antisera were compared, both polyclonal antisera and MAbs reacted strongly with E. coli H7 bacteria. However, the polyclonal antisera cross-reacted strongly both with non-H7 E. coli and with many non-E. coli bacteria. The polyclonal antisera also reacted strongly with H23 and H24 E. coli isolates. The data suggest the need to define serotype-specific epitopes among H7, H23, and H24 E. coli flagella. The anti-H7 MAbs described in this report have the potential to serve as high-quality diagnostic reagents, used either alone or in combination with O157-specific MAbs, to identify or detect E. coli O157:H7 in food products or in human and veterinary clinical specimens.
机译:产生并鉴定了两种与大肠杆菌的H7鞭毛抗原反应的鼠单克隆抗体(MAb)(2B7和46E9-9)。总共217株大肠杆菌(48 O157:H7、4 O157:NM,23 O157:non-H7、22 H7:non-O157和120 non-O157:nonH7),17株沙门氏菌和29克-阴性细菌用于通过间接酶联免疫吸附测定(ELISA)评估两个MAb的反应性。两种MAb均与所有具有H7抗原的大肠杆菌菌株以及与H23和H24阳性的大肠杆菌菌株强烈反应。间接ELISA MAb特异性通过使用来自O157:H7大肠杆菌和其他大肠杆菌菌株的部分纯化鞭毛蛋白,通过抑制ELISA和Western blotting(免疫印迹)证实。在蛋白质印迹上,MAb 46E9-9对大肠杆菌O157:H7的H7鞭毛蛋白的反应性强于对大肠杆菌O1:K1:H7的H7鞭毛蛋白的反应性。竞争ELISA表明,单克隆抗体2B7和46E9-9与紧密相关的H7表位反应。当比较MAb和两种市售多克隆抗H7抗血清的ELISA反应性时,多克隆抗血清和MAb都与大肠杆菌H7细菌强烈反应。但是,多克隆抗血清与非H7大肠杆菌和许多非E都强烈发生交叉反应。大肠杆菌。多克隆抗血清还与H23和H24大肠杆菌分离株强烈反应。数据表明需要在H7,H23和H24大肠杆菌鞭毛中定义血清型特异性表位。本报告中描述的抗H7 MAb可以作为高质量的诊断试剂,可以单独使用或与O157特异性MAb结合使用,以鉴定或检测食品或人与人体内的大肠杆菌O157:H7。兽医临床标本。

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