Texas Children's Hospital Center for Vaccine Development, Departments of Pediatric Tropical Medicine and Molecular Virology and Microbiology, National School of Tropical Medicine, Baylor College of Medicine, Houston, TX, United States of America.
Department of Pathobiological Sciences, LSU School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, United States of America.
PLoS Negl Trop Dis. 2018 Oct 8;12(10):e0006772. doi: 10.1371/journal.pntd.0006772. eCollection 2018 Oct.
Parasitic nematodes produce an unusual class of fatty acid and retinol (FAR)-binding proteins that may scavenge host fatty acids and retinoids. Two FARs from Brugia malayi (Bm-FAR-1 and Bm-FAR-2) were expressed as recombinant proteins, and their ligand binding, structural characteristics, and immunogenicities examined. Circular dichroism showed that rBm-FAR-1 and rBm-FAR-2 are similarly rich in α-helix structure. Unexpectedly, however, their lipid binding activities were found to be readily differentiated. Both FARs bound retinol and cis-parinaric acid similarly, but, while rBm-FAR-1 induced a dramatic increase in fluorescence emission and blue shift in peak emission by the fluorophore-tagged fatty acid (dansyl-undecanoic acid), rBm-FAR-2 did not. Recombinant forms of the related proteins from Onchocerca volvulus, rOv-FAR-1 and rOv-FAR-2, were found to be similarly distinguishable. This is the first FAR-2 protein from parasitic nematodes that is being characterized. The relative protein abundance of Bm-FAR-1 was higher than Bm-FAR-2 in the lysates of different developmental stages of B. malayi. Both FAR proteins were targets of strong IgG1, IgG3 and IgE antibody in infected individuals and individuals who were classified as endemic normal or putatively immune. In a B. malayi infection model in gerbils, immunization with rBm-FAR-1 and rBm-FAR-2 formulated in a water-in-oil-emulsion (®Montanide-720) or alum elicited high titers of antigen-specific IgG, but only gerbils immunized with rBm-FAR-1 formulated with the former produced a statistically significant reduction in adult worms (68%) following challenge with B. malayi infective larvae. These results suggest that FAR proteins may play important roles in the survival of filarial nematodes in the host, and represent potential candidates for vaccine development against lymphatic filariasis and related filarial infections.
寄生虫线虫产生一类不寻常的脂肪酸和视黄醇 (FAR) 结合蛋白,这些蛋白可能会清除宿主的脂肪酸和视黄醇。从班氏吴策线虫 (Brugia malayi) 中表达了两种 FAR(Bm-FAR-1 和 Bm-FAR-2)作为重组蛋白,并对其配体结合、结构特征和免疫原性进行了研究。圆二色性表明 rBm-FAR-1 和 rBm-FAR-2 都富含α-螺旋结构。然而,出乎意料的是,它们的脂质结合活性很容易被区分开来。两种 FAR 都能结合视黄醇和顺式-壬烯酸,但是,当 rBm-FAR-1 诱导荧光标记脂肪酸(dansyl-十一酸)的荧光发射显著增加和峰发射蓝移时,rBm-FAR-2 则没有。来自旋盘尾丝虫 (Onchocerca volvulus) 的相关蛋白 rOv-FAR-1 和 rOv-FAR-2 的重组形式也被发现具有相似的可区分性。这是首次对寄生线虫的 FAR-2 蛋白进行特征描述。在班氏吴策线虫不同发育阶段的裂解物中,rBm-FAR-1 的相对蛋白丰度高于 rBm-FAR-2。两种 FAR 蛋白都是感染个体和被归类为地方性正常或假定免疫的个体中 IgG1、IgG3 和 IgE 抗体的靶标。在沙鼠感染班氏吴策线虫的模型中,rBm-FAR-1 和 rBm-FAR-2 与水包油乳液 (®Montanide-720) 或明矾联合免疫可引起高滴度的抗原特异性 IgG,但只有用前者与 rBm-FAR-1 免疫的沙鼠在受到班氏吴策线虫感染性幼虫的攻击后,成虫数量(68%)才会有统计学意义的降低。这些结果表明 FAR 蛋白可能在寄生虫线虫在宿主中的存活中发挥重要作用,并且代表了针对淋巴丝虫病和相关丝虫感染的疫苗开发的潜在候选物。