Haloarchaeal Gas Vesicle Nanoparticles Displaying Salmonella Antigens as a Novel Approach to Vaccine Development

P. DasSarma , V.D. Negi , A. Balakrishnan , J.-M. Kim , R. Karan , D. Chakravortty , S. DasSarma
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引用次数: 15

Abstract

A safe, effective, and inexpensive vaccine against typhoid and other Salmonella diseases is urgently needed. In order to address this need, we are developing a novel vaccine platform employing buoyant, self-adjuvanting gas vesicle nanoparticles (GVNPs) from the halophilic archaeon Halobacterium sp. NRC-1, bioengineered to display highly conserved Salmonella enterica antigens. As the initial antigen for testing, we selected SopB, a secreted inosine phosphate effector protein injected by pathogenic S. enterica bacteria during infection into the host cells. Two highly conserved sopB gene segments near the 3’- region, named sopB4 and sopB5, were each fused to the gvpC gene, and resulting SopB-GVNPs were purified by centrifugally accelerated flotation. Display of SopB4 and SopB5 antigenic epitopes on GVNPs was established by Western blotting analysis using antisera raised against short synthetic peptides of SopB. Immunostimulatory activities of the SopB4 and B5 nanoparticles were tested by intraperitoneal administration of SopB-GVNPs to BALB/c mice which had been immunized with S. enterica serovar Typhimurium 14028 ΔpmrG-HM-D (DV-STM-07), a live attenuated vaccine strain. Proinflammatory cytokines IFN-γ, IL-2, and IL-9 were significantly induced in mice boosted with SopB5-GVNPs, consistent with a robust Th1 response. After challenge with virulent S. enterica serovar Typhimurium 14028, bacterial burden was found to be diminished in spleen of mice boosted with SopB4-GVNPs and absent or significantly diminished in liver, mesenteric lymph node, and spleen of mice boosted with SopB5-GVNPs, indicating that the C-terminal portions of SopB displayed on GVNPs elicit a protective response to Salmonella infection in mice. SopB antigen-GVNPs were also found to be stable at elevated temperatures for extended periods without refrigeration. The results show that bioengineered GVNPs are likely to represent a valuable platform for antigen delivery and development of improved vaccines against Salmonella and other diseases.

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显示沙门氏菌抗原的盐古菌气体囊泡纳米颗粒作为疫苗开发的新途径
目前迫切需要一种安全、有效和廉价的疫苗来预防伤寒和其他沙门氏菌疾病。为了满足这一需求,我们正在开发一种新的疫苗平台,利用来自嗜盐古菌盐杆菌NRC-1的浮力、自佐剂气体囊泡纳米颗粒(GVNPs),生物工程显示高度保守的肠沙门氏菌抗原。我们选择致病性肠链球菌在感染宿主细胞时通过注射分泌的磷酸肌苷效应蛋白SopB作为初始抗原。在3′-区附近的两个高度保守的sopB基因片段sopB4和sopB5分别与gvpC基因融合,得到的sopB - gvnps通过离心加速浮选纯化。利用合成SopB短肽的抗血清,通过Western blotting分析,在GVNPs上显示了SopB4和SopB5抗原表位。通过腹腔注射SopB-GVNPs,检测了SopB4和B5纳米颗粒对经肠炎沙门氏菌血清鼠伤寒杆菌14028 ΔpmrG-HM-D (DV-STM-07)减毒活疫苗株免疫的BALB/c小鼠的免疫刺激活性。促炎细胞因子IFN-γ、IL-2和IL-9在添加了SopB5-GVNPs的小鼠中被显著诱导,这与Th1的强烈反应一致。经强毒肠炎沙门氏菌血清型鼠伤寒杆菌14028攻毒后,经SopB4-GVNPs增强的小鼠脾脏细菌负荷减轻,而经SopB5-GVNPs增强的小鼠肝脏、肠系膜淋巴结和脾脏细菌负荷缺失或显著减少,表明GVNPs上显示的SopB c端部分引起小鼠对沙门氏菌感染的保护反应。SopB抗原- gvnps也被发现在高温下长时间不冷藏是稳定的。结果表明,生物工程GVNPs可能为抗原递送和开发针对沙门氏菌和其他疾病的改进疫苗提供了一个有价值的平台。
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Contents Production and Characterization of Human Monoclonal Antibodies from the Cells of A(H1N1)pdm2009 Influenza Virus Infected Indian Donors Editorial: Preventive Vaccination Stabilization of Outer Domain of gp120 from HIV-1 Subtype C for Vaccine Immunogen Design Haloarchaeal Gas Vesicle Nanoparticles Displaying Salmonella Antigens as a Novel Approach to Vaccine Development
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