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用表达甘露庚糖荚膜的泰国伯克霍尔德菌活菌免疫后对实验性类鼻疽的保护作用。

Protection against experimental melioidosis following immunization with live Burkholderia thailandensis expressing a manno-heptose capsule.

作者信息

Scott Andrew E, Laws Thomas R, D'Elia Riccardo V, Stokes Margaret G M, Nandi Tannistha, Williamson E Diane, Tan Patrick, Prior Joann L, Atkins Timothy P

机构信息

Defence Science and Technology Laboratory, Porton Down, Salisbury, United Kingdom.

出版信息

Clin Vaccine Immunol. 2013 Jul;20(7):1041-7. doi: 10.1128/CVI.00113-13. Epub 2013 May 15.

Abstract

Melioidosis is a severe infectious disease caused by Burkholderia pseudomallei. It is highly resistant to antibiotic treatment, and there is currently no licensed vaccine. Burkholderia thailandensis is a close relative of Burkholderia pseudomallei but is essentially avirulent in mammals. In this report, we detail the protective efficacy of immunization with live B. thailandensis E555, a strain which has been shown to express an antigenic capsule similar to that of B. pseudomallei. Immunization with E555 induced significant protection against a lethal intraperitoneal B. pseudomallei challenge in a mouse model of infection, with no mice succumbing to infection over the course of the study, even with challenges of up to 6,000 median lethal doses. By comparison, mice immunized with B. thailandensis not expressing a B. pseudomallei-like capsule had significantly decreased levels of protection. E555-immunized mice had significantly higher levels of IgG than mice immunized with noncapsulated B. thailandensis, and these antibody responses were primarily directed against the capsule.

摘要

类鼻疽是由类鼻疽伯克霍尔德菌引起的一种严重传染病。它对抗生素治疗具有高度抗性,目前尚无获批的疫苗。泰国伯克霍尔德菌是类鼻疽伯克霍尔德菌的近亲,但在哺乳动物中基本无致病性。在本报告中,我们详细阐述了用活的泰国伯克霍尔德菌E555免疫的保护效果,该菌株已被证明能表达与类鼻疽伯克霍尔德菌相似的抗原性荚膜。在小鼠感染模型中,用E555免疫可诱导对致死性腹腔注射类鼻疽伯克霍尔德菌攻击产生显著保护作用,在研究过程中没有小鼠死于感染,即使受到高达6000个半数致死剂量的攻击。相比之下,用不表达类鼻疽伯克霍尔德菌样荚膜的泰国伯克霍尔德菌免疫的小鼠保护水平显著降低。用E555免疫的小鼠的IgG水平显著高于用无荚膜泰国伯克霍尔德菌免疫的小鼠,并且这些抗体反应主要针对荚膜。

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本文引用的文献

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Development of vaccines against burkholderia pseudomallei.针对伯克霍尔德氏菌的疫苗研发。
Front Microbiol. 2011 Sep 27;2:198. doi: 10.3389/fmicb.2011.00198. eCollection 2011.

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