Meningococcal Research Department, Division of Vaccines, Center for Genetic Engineering and Biotechnology, Ave 31, Cubanacan, Habana 10600, Cuba.
Vaccine. 2009 Dec 11;28(2):532-41. doi: 10.1016/j.vaccine.2009.09.128. Epub 2009 Oct 29.
The difficulty of inducing an effective immune response against the Neisseria meningitidis serogroup B capsular polysaccharide has lead to the search for vaccines for this serogroup based on outer membrane proteins. The availability of the first meningococcal genome (MC58 strain) allowed the expansion of high-throughput methods to explore the protein profile displayed by N. meningitidis. By combining a pan-genome analysis with an extensive experimental validation to identify new potential vaccine candidates, genes coding for antigens likely to be exposed on the surface of the meningococcus were selected after a multistep comparative analysis of entire Neisseria genomes. Eleven novel putative ORF annotations were reported for serogroup B strain MC58. Furthermore, a total of 20 new predicted potential pan-neisserial vaccine candidates were produced as recombinant proteins and evaluated using immunological assays. Potential vaccine candidate coding genes were PCR-amplified from a panel of representative strains and their variability analyzed using maximum likelihood approaches for detecting positive selection. Finally, five proteins all capable of inducing a functional antibody response vs N. meningitidis strain CU385 were identified as new attractive vaccine candidates: NMB0606 a potential YajC orthologue, NMB0928 the neisserial NlpB (BamC), NMB0873 a LolB orthologue, NMB1163 a protein belonging to a curli-like assembly machinery, and NMB0938 (a neisserial specific antigen) with evidence of positive selection appreciated for NMB0928. The new set of vaccine candidates and the novel proposed functions will open a new wave of research in the search for the elusive neisserial vaccine.
诱导针对脑膜炎奈瑟菌 B 群荚膜多糖的有效免疫应答的困难促使人们寻找基于外膜蛋白的这种血清型疫苗。第一个脑膜炎球菌基因组(MC58 株)的出现使得高通量方法得以扩展,以探索脑膜炎奈瑟菌显示的蛋白质图谱。通过将泛基因组分析与广泛的实验验证相结合,以鉴定新的潜在疫苗候选物,在对整个脑膜炎奈瑟菌基因组进行多步比较分析后,选择了编码可能暴露在脑膜炎球菌表面的抗原的基因。对 B 群菌株 MC58 报告了 11 个新的推定的 ORF 注释。此外,总共产生了 20 个新的预测的潜在泛奈瑟氏球菌疫苗候选物作为重组蛋白,并使用免疫学测定进行了评估。使用最大似然方法检测正选择,从一组代表性菌株中 PCR 扩增候选疫苗编码基因,并分析其变异性。最后,鉴定出 5 种均能诱导针对 N. meningitidis 菌株 CU385 的功能性抗体反应的蛋白,作为新的有吸引力的疫苗候选物:NMB0606 是一种潜在的 YajC 同源物,NMB0928 是奈瑟氏 NlpB(BamC),NMB0873 是 LolB 同源物,NMB1163 是一种属于卷曲样组装机制的蛋白,以及 NMB0938(一种奈瑟氏特异抗原),对 NMB0928 的正选择得到了证实。这组新的候选疫苗和新提出的功能将为寻找难以捉摸的奈瑟氏菌疫苗开辟新的研究浪潮。