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多杀巴斯德氏菌 Heddleston 血清型 1 和 14 表达不同的脂多糖结构,但共享相同的脂多糖生物合成外核心基因座。

Pasteurella multocida Heddleston serovars 1 and 14 express different lipopolysaccharide structures but share the same lipopolysaccharide biosynthesis outer core locus.

机构信息

Australian Research Council Centre of Excellence in Structural and Functional Microbial Genomics, Department of Microbiology, Monash University, Melbourne 3800, Australia.

出版信息

Vet Microbiol. 2011 Jun 2;150(3-4):289-96. doi: 10.1016/j.vetmic.2011.01.028. Epub 2011 Mar 3.

Abstract

Pasteurella multocida strains are classified using the Heddleston lipopolysaccharide (LPS) serotyping scheme into 16 serovars. Understanding the structural and genetic basis for this LPS typing scheme is important because protection against infections caused by P. multocida is generally considered to be serovar specific. Here we show that the serovar 14 type strain P2225 and the serovar 1 strains X73 and VP161 express similar LPS structures. However, the serovar 14 LPS lacks the terminal phosphocholine (PCho) residues present on the serovar 1 LPS and contains the 1,4-linked β-galactose but not the 1,6-linked β-galactose. Sequencing analysis of the LPS biosynthesis outer core loci of P2225 and the serovar 1 type strain X73 showed that they were nearly identical. However, the phosphocholine biosynthesis gene, pcgA of P2225 contained a 19bp nucleotide deletion. Complementation of P2225 with an intact pcgA resulted in an LPS structure identical to that expressed by serovar 1 strain VP161 and highly similar to that expressed by strain X73, with a 1,6-linked β-galactose and both terminal PCho residues. This study has shown unequivocally that strains belonging to serovar 1 and 14 share a common LPS outer core locus and that minor changes within this locus can dramatically alter the LPS structure expressed on the surface of P. multocida, and thus has implications into our understanding of the potential to generate cross-protective vaccines.

摘要

多杀巴斯德氏菌菌株根据 Heddleston 脂多糖 (LPS) 血清分型方案分为 16 个血清型。了解这种 LPS 分型方案的结构和遗传基础非常重要,因为针对多杀巴斯德氏菌感染的保护通常被认为是血清型特异性的。在这里,我们表明血清型 14 型菌株 P2225 和血清型 1 菌株 X73 和 VP161 表达相似的 LPS 结构。然而,血清型 14 LPS 缺乏存在于血清型 1 LPS 上的末端磷酸胆碱 (PCho) 残基,并且含有 1,4 连接的 β-半乳糖但不含有 1,6 连接的 β-半乳糖。对 P2225 和血清型 1 型菌株 X73 的 LPS 生物合成外核心基因座的测序分析表明,它们几乎相同。然而,P2225 的 pcgA 磷酸胆碱生物合成基因含有 19bp 核苷酸缺失。用完整的 pcgA 互补 P2225 导致 LPS 结构与血清型 1 菌株 VP161 表达的结构相同,与菌株 X73 表达的结构高度相似,具有 1,6 连接的 β-半乳糖和两个末端 PCho 残基。这项研究明确表明,属于血清型 1 和 14 的菌株共享共同的 LPS 外核心基因座,并且该基因座内的微小变化可以极大地改变多杀巴斯德氏菌表面表达的 LPS 结构,因此对我们理解产生交叉保护疫苗的潜力具有重要意义。

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