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Investigating the candidacy of lipopolysaccharide-based glycoconjugates as vaccines to combat Mannheimia haemolytica

机译:研究基于脂多糖的糖缀合物作为对抗溶血曼海姆氏菌的疫苗的候选资格

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Inner core lipopolysaccharide (LPS) has been shown to be conserved in the majority of veterinary strains from the species Mannheimia haemolytica, Actinobacillus pleuropneumoniae and Pasteurella multocida and as such is being considered as a possible vaccine antigen. The proofin-principle that a LPS-based antigen could be considered as a vaccine candidate has been demonstrated from studies with monoclonal antibodies raised to the inner core LPS of Mannheimia haemolytica, which were shown to be both bactericidal and protective in a mouse model of disease. In this study we confirm and extend the candidacy of the inner core LPS by demonstrating that it is possible to elicit functional antibodies against Mannheimia haemolytica wild-type strains following immunisation of rabbits with glycoconjugates elaborating the conserved inner core LPS antigen. The present study describes a conjugation strategy that uses amidases produced by Dictyostelium discoideum, targeting the amino functionality created by the amidase activity as the attachment point on the LPS molecule. To protect the amino functionality on the phosphoethanolamine (PEtn) residue of the inner core, we developed a novel blocking and unblocking strategy with t-butyl oxycarbonyl. A maleimide-thiol linker strategy with the thiol linker on the carboxyl residues of the carrier protein and the maleimide linker on the carbohydrate resulted in a high loading of carbohydrates per carrier protein. Immunisation derived antisera from rabbits recognised fully extended Mannheimia haemolytica LPS and whole cells from serotypes 1 and 2, despite a somewhat immunodominant response to the linkers also being observed. Moreover, bactericidal activity was demonstrated to a strain elaborating the immunising carbohydrate antigen and crucially to wild-type cells of serotypes 1 and 2, thus further supporting the consideration of inner core LPS as a potential vaccine antigen to combat disease caused by Mannheimia haemolytica.
机译:业已证明,核心溶脂多糖(LPS)在溶血曼海姆氏菌,胸膜肺炎放线杆菌和多杀巴斯德氏菌的大多数兽医学菌株中都是保守的,因此被认为是可能的疫苗抗原。一项基于针对溶血曼海姆氏菌内在LPS的单克隆抗体的研究已证明了基于LPS的抗原可以被视为疫苗候选者的证明原则,在小鼠疾病模型中,该抗体具有杀菌和保护作用。在这项研究中,我们证实并扩展了内在保守的LPS抗原的糖缀合物对兔的免疫接种,从而证明了它有可能引发针对溶血曼海姆氏菌野生型菌株的功能性抗体,并以此扩大了内在LPS的候选资格。本研究描述了一种共轭策略,该策略使用盘基网柄菌产生的酰胺酶,靶向由酰胺酶活性产生的氨基官能团作为LPS分子上的附着点。为了保护内核的磷酸乙醇胺(PEtn)残基上的氨基官能团,我们开发了使用叔丁基氧羰基的新型封闭和非封闭策略。具有在载体蛋白的羧基残基上的硫醇接头和在碳水化合物上的马来酰亚胺接头的马来酰亚胺-硫醇接头策略导致每个载体蛋白的碳水化合物高负荷。来自兔子的免疫衍生抗血清识别出完全延长的溶血曼海姆氏菌LPS和血清型1和2的全细胞,尽管也观察到对接头的免疫显性反应。此外,已证明该菌株对精制免疫碳水化合物抗原的菌株具有杀菌活性,并且对血清型1和2的野生型细胞具有至关重要的作用,因此进一步支持了将内核LPS视为潜在的疫苗抗原来对抗溶血曼海姆氏菌引起的疾病。

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