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用源自主要外膜蛋白的合成肽对树袋熊(Phascolarctos cinereus)进行衣原体疫苗接种。

Vaccination of koalas (Phascolarctos cinereus) against Chlamydia pecorum using synthetic peptides derived from the major outer membrane protein.

机构信息

Faculty of Science, Health, Education and Engineering, University of the Sunshine Coast, Sippy Downs, Queensland, Australia.

Lone Pine Koala Sanctuary, Fig Tree Pocket, Queensland, Australia.

出版信息

PLoS One. 2018 Jun 28;13(6):e0200112. doi: 10.1371/journal.pone.0200112. eCollection 2018.

Abstract

Chlamydia pecorum is a mucosal infection, which causes debilitating disease of the urinary tract, reproductive tract and ocular sites of koalas (Phascolarctos cinereus). While antibiotics are available for treatment, they are detrimental to the koalas' gastrointestinal tract microflora leaving the implementation of a vaccine as an ideal option for the long-term management of koala populations. We have previously reported on the successes of an anti-chlamydial recombinant major outer membrane protein (rMOMP) vaccine however, recombinant protein based vaccines are not ideal candidates for scale up from the research level to small-medium production level for wider usage. Peptide based vaccines are a promising area for vaccine development, because peptides are stable, cost effective and easily produced. In this current study, we assessed, for the first time, the immune responses to a synthetic peptide based anti-chlamydial vaccine in koalas. Five healthy male koalas were vaccinated with two synthetic peptides derived from C. pecorum MOMP and another five healthy male koalas were vaccinated with full length recombinant C. pecorum MOMP (genotype G). Systemic (IgG) and mucosal (IgA) antibodies were quantified and pre-vaccination levels compared to post-vaccination levels (12 and 26 weeks). MOMP-peptide vaccinated koalas produced Chlamydia-specific IgG and IgA antibodies, which were able to recognise not only the genotype used in the vaccination, but also MOMPs from several other koala C. pecorum genotypes. In addition, IgA antibodies induced at the ocular site not only recognised recombinant MOMP protein but also, whole native chlamydial elementary bodies. Interestingly, some MOMP-peptide vaccinated koalas showed a stronger and more sustained vaccine-induced mucosal IgA antibody response than observed in MOMP-protein vaccinated koalas. These results demonstrate that a synthetic MOMP peptide based vaccine is capable of inducing a Chlamydia-specific antibody response in koalas and is a promising candidate for future vaccine development.

摘要

绵羊衣原体是一种黏膜感染,会导致考拉(Phascolarctos cinereus)的泌尿道、生殖道和眼部疾病。虽然有抗生素可供治疗,但这些抗生素对考拉的胃肠道微生物群有害,因此疫苗的实施成为考拉种群长期管理的理想选择。我们之前已经报道了抗衣原体重组主要外膜蛋白(rMOMP)疫苗的成功,但基于重组蛋白的疫苗并不适合从研究水平扩展到中小规模生产水平,以扩大使用范围。肽基疫苗是疫苗开发的一个有前途的领域,因为肽稳定、具有成本效益且易于生产。在本研究中,我们首次评估了基于合成肽的抗衣原体疫苗在考拉中的免疫反应。五头健康雄性考拉接种了两种源自 C. pecorum MOMP 的合成肽,另外五头健康雄性考拉接种了全长重组 C. pecorum MOMP(基因型 G)。系统(IgG)和黏膜(IgA)抗体进行了定量,并将预接种水平与接种后 12 周和 26 周的水平进行了比较。MOMP-肽接种的考拉产生了衣原体特异性 IgG 和 IgA 抗体,这些抗体不仅能够识别用于接种的基因型,还能够识别来自其他几种考拉 C. pecorum 基因型的 MOMP。此外,在眼部诱导的 IgA 抗体不仅能够识别重组 MOMP 蛋白,还能够识别整个原始衣原体小体。有趣的是,与 MOMP-蛋白接种的考拉相比,一些 MOMP-肽接种的考拉表现出更强、更持久的疫苗诱导黏膜 IgA 抗体反应。这些结果表明,基于合成 MOMP 肽的疫苗能够在考拉中诱导衣原体特异性抗体反应,是未来疫苗开发的有前途的候选物。

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