Kaushik D K, Sehgal D
Molecular Immunology Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi, India.
Scand J Immunol. 2008 Jun;67(6):544-52. doi: 10.1111/j.1365-3083.2008.02107.x. Epub 2008 Apr 4.
Infectious diseases are the greatest cause of global morbidity and mortality. About half of this burden is caused by pathogenic bacteria. One of the most effective ways to prevent infectious diseases is to use vaccines. Limitations in the traditional approaches may be one of the reasons why vaccines are yet not available against some infectious bacterial agents. Recent advancements in high-throughput 'omics' technologies and the availability of complete genome sequences of microbial pathogens and multiple isolates of the same species have dramatically changed the time frame and scope for identifying novel vaccine candidates. At present, 582 microbial genomes have been sequenced and sequencing of 1733 is in progress. There are more than 50 bacterial species for which the genome sequence is available for three or more isolates. Development of tools for in silico analysis has led to the identification of novel virulence genes, metabolic pathways and cell surface proteins that represent potential new targets for anti-microbial drug and vaccine strategies. In this review, we provide an overview of the 'omics'-based techniques that can be used to advance and accelerate the discovery of vaccine candidates against extracellular bacterial pathogens. By citing specific examples, we discuss how high-throughput molecular profiling techniques, such as genomics, transcriptomics and proteomics have contributed to the discovery of novel vaccine candidates. We end by contemplating on the emerging technologies that are likely to have a high impact on the field of vaccinology in the near future.
传染病是全球发病和死亡的最大原因。约一半的负担是由致病细菌引起的。预防传染病最有效的方法之一是使用疫苗。传统方法的局限性可能是某些传染性细菌病原体尚无疫苗可用的原因之一。高通量“组学”技术的最新进展以及微生物病原体完整基因组序列和同一物种多个分离株的可得性,极大地改变了鉴定新型疫苗候选物的时间框架和范围。目前,已对582个微生物基因组进行了测序,另有1733个正在测序中。有50多种细菌的基因组序列可用于三个或更多分离株。计算机分析工具的开发已导致鉴定出新型毒力基因、代谢途径和细胞表面蛋白,这些代表了抗微生物药物和疫苗策略的潜在新靶点。在本综述中,我们概述了基于“组学”的技术,这些技术可用于推进和加速针对细胞外细菌病原体的疫苗候选物的发现。通过引用具体例子,我们讨论了高通量分子分析技术,如基因组学、转录组学和蛋白质组学如何促进新型疫苗候选物的发现。最后,我们思考了在不久的将来可能对疫苗学领域产生重大影响的新兴技术。