Tan Aimee, Atack John M, Jennings Michael P, Seib Kate L
Institute for Glycomics, Griffith University , Gold Coast, QLD , Australia.
Front Immunol. 2016 Dec 12;7:586. doi: 10.3389/fimmu.2016.00586. eCollection 2016.
Infectious diseases are a leading cause of morbidity and mortality worldwide, and vaccines are one of the most successful and cost-effective tools for disease prevention. One of the key considerations for rational vaccine development is the selection of appropriate antigens. Antigens must induce a protective immune response, and this response should be directed to stably expressed antigens so the target microbe can always be recognized by the immune system. Antigens with variable expression, due to environmental signals or phase variation (i.e., high frequency, random switching of expression), are not ideal vaccine candidates because variable expression could lead to immune evasion. Phase variation is often mediated by the presence of highly mutagenic simple tandem DNA repeats, and genes containing such sequences can be easily identified, and their use as vaccine antigens reconsidered. Recent research has identified phase variably expressed DNA methyltransferases that act as global epigenetic regulators. These phase-variable regulons, known as phasevarions, are associated with altered virulence phenotypes and/or expression of vaccine candidates. As such, genes encoding candidate vaccine antigens that have no obvious mechanism of phase variation may be subject to indirect, epigenetic control as part of a phasevarion. Bioinformatic and experimental studies are required to elucidate the distribution and mechanism of action of these DNA methyltransferases, and most importantly, whether they mediate epigenetic regulation of potential and current vaccine candidates. This process is essential to define the stably expressed antigen target profile of bacterial pathogens and thereby facilitate efficient, rational selection of vaccine antigens.
传染病是全球发病和死亡的主要原因之一,而疫苗是疾病预防最成功且最具成本效益的工具之一。合理疫苗开发的关键考虑因素之一是选择合适的抗原。抗原必须诱导保护性免疫反应,且这种反应应针对稳定表达的抗原,以便免疫系统能够始终识别目标微生物。由于环境信号或相位变异(即高频率、随机的表达切换)而具有可变表达的抗原不是理想的疫苗候选物,因为可变表达可能导致免疫逃逸。相位变异通常由高度诱变的简单串联DNA重复序列介导,含有此类序列的基因可被轻易识别,其作为疫苗抗原的用途也需重新考虑。最近的研究发现了作为全局表观遗传调节因子的相位可变表达DNA甲基转移酶。这些相位可变调控子,即所谓的相位变异体,与毒力表型改变和/或疫苗候选物的表达相关。因此,编码没有明显相位变异机制的候选疫苗抗原的基因可能作为相位变异体的一部分受到间接的表观遗传控制。需要进行生物信息学和实验研究来阐明这些DNA甲基转移酶的分布和作用机制,最重要的是,它们是否介导潜在和现有疫苗候选物的表观遗传调控。这一过程对于确定细菌病原体稳定表达的抗原靶点特征至关重要,从而有助于高效、合理地选择疫苗抗原。