Pellett S, Boehm D F, Snyder I S, Rowe G, Welch R A
Department of Medical Microbiology and Immunology, University of Wisconsin Medical School, Madison 53706.
Infect Immun. 1990 Mar;58(3):822-7. doi: 10.1128/iai.58.3.822-827.1990.
Twelve monoclonal antibodies (MAbs) produced against the Escherichia coli hemolysin (HlyA) encoded by the hemolysin recombinant plasmid pWAM04 were studied. HlyA derivatives from recombinant strains with different plasmids encoding HlyA amino-terminal and carboxy-terminal truncates, HlyA in-frame deletions, and HlyA frameshift mutations were used in immunoblots to localize the antigenic determinants for the anti-HlyA MAbs. The mapping of the MAb epitopes was also facilitated by immunoblotting analysis of HlyA polypeptide fragments derived by cyanogen bromide cleavage. The HlyA epitopes for 11 of the MAbs were mapped to relatively small linear regions of the cytolysin ranging from 28 to 160 amino acids. Five of the MAbs (C10, G8, E2, B7, and D12) neutralized HlyA hemolytic activity to varying degrees. The epitopes for these neutralizing MAbs were found to reside within the following HlyA regions: C10 and G8, amino acids 2 to 160; E2, amino acids 161 to 194; B7, amino acids 518 to 598; and D12, amino acids 626 to 726. Hemolytically active HlyA was dependent on the action of the hlyC gene product. The D12 MAb recognized only HlyA produced by strains with an intact hlyC function. MAb A10 recognized an epitope within the HlyA region from amino acids 728 to 829 where a glycine-rich repeat domain exists; however, this MAb did not neutralize HlyA hemolytic activity. A HlyA domain map showing the anti-HlyA epitope location was constructed.
对针对溶血素重组质粒pWAM04编码的大肠杆菌溶血素(HlyA)产生的12种单克隆抗体(MAb)进行了研究。来自重组菌株的HlyA衍生物,这些重组菌株带有编码HlyA氨基末端和羧基末端截短体、HlyA框内缺失以及HlyA移码突变的不同质粒,用于免疫印迹以定位抗HlyA MAb的抗原决定簇。通过对溴化氰裂解产生的HlyA多肽片段进行免疫印迹分析,也有助于MAb表位的定位。11种MAb的HlyA表位被定位到溶血素相对较小的线性区域,范围从28至160个氨基酸。其中5种MAb(C10、G8、E2、B7和D12)不同程度地中和了HlyA的溶血活性。发现这些中和性MAb的表位位于以下HlyA区域:C10和G8,氨基酸2至160;E2,氨基酸161至194;B7,氨基酸518至598;D12,氨基酸626至726。具有溶血活性的HlyA依赖于hlyC基因产物的作用。D12 MAb仅识别具有完整hlyC功能的菌株产生的HlyA。MAb A10识别HlyA区域内氨基酸728至829的一个表位,该区域存在富含甘氨酸的重复结构域;然而,该MAb未中和HlyA的溶血活性。构建了显示抗HlyA表位位置的HlyA结构域图谱。