Howard M D, Cox A D, Weiser J N, Schurig G G, Inzana T J
Center for Molecular Medicine and Infectious Diseases, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, USA.
J Clin Microbiol. 2000 Dec;38(12):4412-9. doi: 10.1128/JCM.38.12.4412-4419.2000.
The lipooligosaccharide (LOS) of Haemophilus somnus undergoes antigenic phase variation, which may facilitate evasion from the bovine host immune response and/or colonization and dissemination. However, LOS antigenic diversity in H. somnus has not been adequately investigated. In this study, monoclonal antibodies (MAbs) specific to various LOS epitopes were used to investigate antigenic variation and stability in LOS from H. somnus strains and phase variants. Clinical isolates of H. somnus exhibited intrastrain, as well as interstrain, antigenic heterogeneity in LOS when probed with MAbs to outer core oligosaccharide epitopes in an enzyme-linked immunosorbent assay (ELISA). However, epitopes reactive with MAbs directed predominately to the inner core heptose region were highly conserved. At least one epitope, which was expressed in few strains, was identified. One LOS component affected by phase variation was identified as phosphorylcholine (PCho), which is linked to the primary glucose residue. Inhibition ELISA, immunoblotting, and electrospray-mass spectrometry were used to confirm that MAb 5F5.9 recognized PCho. LOS reactivity with MAb 5F5.9 was associated with loss of most of the outer core oligosaccharide, indicating that reactivity with PCho was affected by phase variation of the glucose residues in this region. Our results indicate that outer core epitopes of H. somnus LOS exhibit a high degree of random, phase-variable antigenic heterogeneity and that such heterogeneity must be considered in the design of vaccines and diagnostic tests.
睡眠嗜血杆菌的脂寡糖(LOS)会发生抗原相变,这可能有助于其逃避牛宿主的免疫反应和/或实现定植与传播。然而,睡眠嗜血杆菌中LOS的抗原多样性尚未得到充分研究。在本研究中,针对各种LOS表位的单克隆抗体(MAb)被用于研究睡眠嗜血杆菌菌株及其相变变体中LOS的抗原变异和稳定性。在酶联免疫吸附测定(ELISA)中,用针对外核心寡糖表位的MAb检测时,睡眠嗜血杆菌的临床分离株在LOS中表现出菌株内以及菌株间的抗原异质性。然而,与主要针对内核心庚糖区域的MAb反应的表位高度保守。鉴定出至少一种在少数菌株中表达的表位。一种受相变影响的LOS成分被鉴定为磷酸胆碱(PCho),它与初级葡萄糖残基相连。采用抑制ELISA、免疫印迹和电喷雾质谱法来确认单克隆抗体5F5.9识别PCho。LOS与单克隆抗体5F5.9的反应性与大部分外核心寡糖的缺失有关,这表明与PCho的反应性受该区域葡萄糖残基相变的影响。我们的结果表明,睡眠嗜血杆菌LOS的外核心表位表现出高度随机的、相变可变的抗原异质性,并且在疫苗设计和诊断测试中必须考虑这种异质性。