Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore.
Viral Research and Experimental Medicine Centre, SingHealth Duke-NUS Academic Medical Centre, Singapore, Singapore.
Genome Med. 2021 Jan 15;13(1):8. doi: 10.1186/s13073-020-00824-4.
Shigella is a major diarrheal pathogen for which there is presently no vaccine. Whole genome sequencing provides the ability to predict and derive novel antigens for use as vaccines. Here, we aimed to identify novel immunogenic Shigella antigens that could serve as Shigella vaccine candidates, either alone, or when conjugated to Shigella O-antigen.
Using a reverse vaccinology approach, where genomic analysis informed the Shigella immunome via an antigen microarray, we aimed to identify novel immunogenic Shigella antigens. A core genome analysis of Shigella species, pathogenic and non-pathogenic Escherichia coli, led to the selection of 234 predicted immunogenic Shigella antigens. These antigens were expressed and probed with acute and convalescent serum from microbiologically confirmed Shigella infections.
Several Shigella antigens displayed IgG and IgA seroconversion, with no difference in sero-reactivity across by sex or age. IgG sero-reactivity to key Shigella antigens was observed at birth, indicating transplacental antibody transfer. Six antigens (FepA, EmrK, FhuA, MdtA, NlpB, and CjrA) were identified in in vivo testing as capable of producing binding IgG and complement-mediated bactericidal antibody.
These findings provide six novel immunogenic Shigella proteins that could serve as candidate vaccine antigens, species-specific carrier proteins, or targeted adjuvants.
志贺氏菌是一种主要的腹泻病原体,目前尚无疫苗。全基因组测序提供了预测和衍生新型抗原用于疫苗的能力。在这里,我们旨在鉴定新型免疫原性志贺氏菌抗原,这些抗原可以作为志贺氏菌疫苗候选物,单独使用或与志贺氏菌 O 抗原结合使用。
使用反向疫苗学方法,通过抗原微阵列将基因组分析转化为志贺氏菌免疫组,我们旨在鉴定新型免疫原性志贺氏菌抗原。对志贺氏菌属、致病性和非致病性大肠杆菌进行核心基因组分析,选择了 234 种预测的免疫原性志贺氏菌抗原。这些抗原被表达,并与经微生物学确认的志贺氏菌感染的急性和恢复期血清进行探测。
几种志贺氏菌抗原显示 IgG 和 IgA 血清转化率,性别或年龄之间的血清反应无差异。在出生时就观察到针对关键志贺氏菌抗原的 IgG 血清反应,表明存在胎盘抗体转移。在体内试验中,有 6 种抗原(FepA、EmrK、FhuA、MdtA、NlpB 和 CjrA)被鉴定为能够产生结合 IgG 和补体介导的杀菌抗体。
这些发现提供了 6 种新型免疫原性志贺氏菌蛋白,它们可以作为候选疫苗抗原、种特异性载体蛋白或靶向佐剂。