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被单克隆抗体识别的杜克雷嗜血杆菌脂寡糖的结构确定表位。

Structurally defined epitopes of Haemophilus ducreyi lipooligosaccharides recognized by monoclonal antibodies.

作者信息

Ahmed H J, Frisk A, Månsson J E, Schweda E K, Lagergård T

机构信息

Department of Medical Microbiology and Immunology, University of Gotebörg, Sweden.

出版信息

Infect Immun. 1997 Aug;65(8):3151-8. doi: 10.1128/iai.65.8.3151-3158.1997.

Abstract

By use of enzyme-linked immunosorbent assay and immunoblotting techniques, the migration patterns and binding epitopes of lipooligosaccharides (LOS) from 10 Haemophilus ducreyi strains were investigated with two monoclonal antibodies (MAbs), MAHD6 and MAHD7, raised against LOS from H. ducreyi ITM 2665. Closely related LOS, with defined structures, from Haemophilus influenzae, Bordetella pertussis, Aeromonas spp., and synthetic glycoproteins were also included in the analyses. The MAbs bound to conserved epitopes of LOS exposed on the surface of H. ducreyi. The MAb MAHD6 reacted with 8 of the 10 LOS from H. ducreyi but with none of the other Haemophilus or Bordetella spp. with structurally defined LOS. It is suggested that MAb MAHD6 binds to a LOS epitope (-DD-Hepp-1-->6-beta-D-Glcp-). This LOS epitope is not present in the hexasaccharide structure of LOS from H. ducreyi ITM 4747 (E. K. H. Schweda, A. C. Sundström, L. M. Eriksson, J. A. Jonasson, and A. A. Lindberg, J. Biol. Chem. 269:12040-12048, 1994). Because MAb MAHD6 reacts with the epitope mentioned above, it also discriminates between the two LOS structures, the hexasaccharide group and the nonasaccharide group, of H. ducreyi strains. MAb MAHD7 recognizes the common conserved inner core region of the LOS because it reacts with all H. ducreyi strains and with LOS with minor components in the inner core epitope structure. Rabbit polyclonal sera raised against the LOS from strains CCUG 4438 and CCUG 7470 were tested with the 10 LOS from the H. ducreyi strains. The antiserum to CCUG 7470 reacted with all H. ducreyi strains as did MAb MAHD7, whereas the antiserum to CCUG 4438 reacted with only its homologous strain and strain ITM 4747. Also, the LOSs of our reference strains CCUG 4438 and CCUG 7470 were structurally analyzed by use of sugar analyses and electrospray ionization-mass spectrometry. The hexasaccharide and nonasaccharide structures obtained from LOS of strains CCUG 4438 and CCUG 7470 were identical to the described LOS structures from H. ducreyi ITM 4747 and ITM 2665, respectively. In conclusion, the MAb MAHD6 recognizes an epitope present in the nonasaccharide LOS group, whereas the MAb MAHD7 recognizes a conserved epitope on LOS of H. ducreyi, which is present in all strains of H. ducreyi tested. Two major groups of oligosaccharides were distinguished by their LOS structures and the reactivity of monoclonal as well as polyclonal antibodies. The majority of H. ducreyi strains possess a nonasaccharide structure of LOS.

摘要

运用酶联免疫吸附测定法和免疫印迹技术,使用针对杜氏嗜血杆菌ITM 2665脂寡糖(LOS)产生的两种单克隆抗体(MAb)MAHD6和MAHD7,研究了10株杜氏嗜血杆菌菌株LOS的迁移模式和结合表位。分析中还纳入了来自流感嗜血杆菌、百日咳博德特氏菌、气单胞菌属的结构明确的密切相关LOS以及合成糖蛋白。这些单克隆抗体与杜氏嗜血杆菌表面暴露的LOS保守表位结合。单克隆抗体MAHD6与10株杜氏嗜血杆菌LOS中的8株发生反应,但与其他结构明确的流感嗜血杆菌或博德特氏菌属LOS均无反应。提示单克隆抗体MAHD6与一个LOS表位(-DD-Hepp-1-->6-β-D-Glcp-)结合。该LOS表位不存在于杜氏嗜血杆菌ITM 4747的LOS六糖结构中(E. K. H. Schweda、A. C. Sundström、L. M. Eriksson、J. A. Jonasson和A. A. Lindberg,《生物化学杂志》269:12040 - 12048,1994)。由于单克隆抗体MAHD6与上述表位反应,它还能区分杜氏嗜血杆菌菌株的两种LOS结构,即六糖组和九糖组。单克隆抗体MAHD7识别LOS的共同保守内核区域,因为它与所有杜氏嗜血杆菌菌株以及内核表位结构中有少量成分的LOS发生反应。用杜氏嗜血杆菌菌株的10种LOS检测了针对CCUG 4438和CCUG 7470菌株LOS产生的兔多克隆血清。针对CCUG 7470的抗血清与所有杜氏嗜血杆菌菌株反应,与单克隆抗体MAHD7相同,而针对CCUG 4438的抗血清仅与其同源菌株及ITM 4747菌株反应。此外,通过糖分析和电喷雾电离质谱对我们的参考菌株CCUG 4438和CCUG 7470的LOS进行了结构分析。从CCUG 4438和CCUG 7470菌株LOS获得的六糖和九糖结构分别与杜氏嗜血杆菌ITM 4747和ITM 2665描述的LOS结构相同。总之,单克隆抗体MAHD6识别九糖LOS组中存在的一个表位,而单克隆抗体MAHD7识别杜氏嗜血杆菌LOS上的一个保守表位,该表位存在于所有检测的杜氏嗜血杆菌菌株中。通过LOS结构以及单克隆和多克隆抗体的反应性区分出了两大类寡糖。大多数杜氏嗜血杆菌菌株具有LOS的九糖结构。

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