Division of Bacteriology, ICMR- National Institute of Cholera and Enteric Diseases, P-33, C.I.T. Road, Scheme XM, Beliaghata, Kolkata-700 010, India; Center for Vaccine Development and Global Health, School of Medicine, University of Maryland, Baltimore, MD 21201, United States.
Division of Bacteriology, ICMR- National Institute of Cholera and Enteric Diseases, P-33, C.I.T. Road, Scheme XM, Beliaghata, Kolkata-700 010, India.
Microbes Infect. 2023 Jun;25(5):105100. doi: 10.1016/j.micinf.2023.105100. Epub 2023 Jan 22.
In today's world and mostly in low and middle income countries, Shigella flexneri and Shigella sonnei remains the major causative agent of clinical bacillary dysentery. Based on contemporary epidemiology, a tetravalent Outer Membrane Vesicle (OMVs) based immunogen was formulated using the most commonly circulating Shigella strains, namely, S. flexneri 2a, S. flexneri 3a, S. flexneri 6 and S. sonnei I, in a 1:1:1:1 ratio. Adult BALB/c mice were orally immunized in a prime-boost-boost manner. Tetravalent Shigella OMVs immunogen induced significant and persistent serum and mucosal antibodies against OMVs, Outer Membrane Proteins (OMPs) and lipopolysaccharides (LPS). Tetravalent OMVs also primed cell mediated immune response effectively. Protective efficacy against six heterologous Shigella strains was checked in an intra-peritoneal mouse model. Immunized mice survived lethal infection better than the non-immunized mice cohort with fewer replicating bacteria isolated from their gut. This study establishes the possibilities of tetravalent OMVs immunogen to become a potent vaccine candidate against human shigellosis, overcoming the limitations of sero-specific cross-protection of Shigella species.
在当今世界,尤其是在中低收入国家,福氏志贺菌和宋内志贺菌仍然是临床细菌性痢疾的主要病原体。基于当代流行病学,使用最常见的循环志贺菌菌株(即福氏志贺菌 2a、福氏志贺菌 3a、福氏志贺菌 6 和宋内志贺菌 I)以 1:1:1:1 的比例配制了一种四价外膜囊泡(OMV)免疫原。成年 BALB/c 小鼠经口服进行初免-加强-再加强免疫。四价志贺氏菌 OMV 免疫原诱导了针对 OMV、外膜蛋白(OMP)和脂多糖(LPS)的显著和持久的血清和粘膜抗体。四价 OMV 还能有效地引发细胞介导的免疫反应。在腹腔内小鼠模型中检查了针对六种异源志贺氏菌菌株的保护效力。与未免疫的小鼠队列相比,免疫的小鼠在致命感染中存活得更好,从其肠道中分离出的复制细菌较少。这项研究确立了四价 OMV 免疫原成为针对人类志贺氏菌病的有效疫苗候选物的可能性,克服了志贺氏菌血清特异性交叉保护的局限性。