Muh Fauzi, Han Jin-Hee, Nyunt Myat Htut, Lee Seong-Kyun, Jeon Hye-Yoon, Ha Kwon-Soo, Park Won Sun, Hong Seok-Ho, Ahmed Md Atique, Na Sunghun, Takashima Eizo, Tsuboi Takafumi, Han Eun-Taek
Department of Medical Environmental Biology and Tropical Medicine, School of Medicine, Kangwon National University, Chuncheon, Gangwon-do, Republic of Korea.
Department of Medical Research, Yangon, Republic of the Union of Myanmar.
Malar J. 2017 Mar 28;16(1):133. doi: 10.1186/s12936-017-1760-9.
Although a number of Plasmodium vivax proteins have been identified, few have been investigated as potential vaccine candidates. This study characterized the Plasmodium vivax merozoite surface antigen 180 (PvMSA180, PVX_094920), a novel P. vivax antigenic protein.
The target gene was amplified as four overlapping domains (D1, D2, D3 and D4) to enable expression of the recombinant protein using cell-free and bacterial expression systems. The recombinant PvMSA180 proteins were used in protein microarrays to evaluate the humoral immune response of 72 vivax-infected patients and 24 vivax-naïve individuals. Antibodies produced in mice against the PvMSA180-D1 and -D4 domains were used to assess the subcellular localization of schizont-stage parasites with immunofluorescence assays. A total of 51 pvmsa180 sequences from 12 countries (41 sequences from PlasmoDB and 6 generated in this study) were used to determine the genetic diversity and genealogical relationships with DNAsp and NETWORK software packages, respectively.
PvMSA180 consists of 1603 amino acids with a predicted molecular mass of 182 kDa, and has a signal peptide at the amino-terminus. A total of 70.8% of patients (51/72) showed a specific antibody response to at least one of the PvMSA180 domains, and 20.8% (15/72) exhibited a robust antibody response to at least three of the domains. These findings suggest that PvMSA180 is targeted by the humoral immune response during natural infection with P. vivax. Immunofluorescence analysis demonstrated that PvMSA180 is localized on the merozoite surface of schizont-stage parasites, and pvmsa180 sequences originating from various geographic regions worldwide showed low genetic diversity. Twenty-two haplotypes were found, and haplotype 6 (Hap_6, 77%) of pvmsa180 was detected in isolates from six countries.
A novel P. vivax surface protein, PvMSA180, was characterized in this study. Most of P. vivax-infected patients had specific antibodies against particular antigenic domains, indicating that this protein is immunogenic in naturally exposed populations. Genetic analysis of worldwide isolates showed that pvmsa180 is less polymorphic than other well-known candidates and that some haplotypes are common to several countries. However, additional studies with a larger sample size are necessary to evaluate the antibody responses in geographically separated populations, and to identify the function of PvMSA180 during parasite invasion.
尽管已鉴定出多种间日疟原虫蛋白,但作为潜在疫苗候选物进行研究的却很少。本研究对一种新型间日疟原虫抗原蛋白——间日疟原虫裂殖子表面抗原180(PvMSA180,PVX_094920)进行了表征。
将目标基因扩增为四个重叠结构域(D1、D2、D3和D4),以便使用无细胞和细菌表达系统表达重组蛋白。重组PvMSA180蛋白用于蛋白质微阵列,以评估72例间日疟感染患者和24例未感染间日疟个体的体液免疫反应。用小鼠产生的针对PvMSA180-D1和-D4结构域的抗体,通过免疫荧光试验评估裂殖体期寄生虫的亚细胞定位。使用来自12个国家的51条pvmsa180序列(41条来自PlasmoDB,6条为本研究生成),分别用DNAsp和NETWORK软件包确定其遗传多样性和谱系关系。
PvMSA180由1603个氨基酸组成,预测分子量为182 kDa,在氨基末端有一个信号肽。共有70.8%的患者(51/72)对至少一个PvMSA180结构域表现出特异性抗体反应,20.8%(15/72)的患者对至少三个结构域表现出强烈抗体反应。这些发现表明,在间日疟原虫自然感染期间,PvMSA180是体液免疫反应的靶点。免疫荧光分析表明,PvMSA180定位于裂殖体期寄生虫的裂殖子表面,来自世界各地不同地理区域的pvmsa180序列显示出较低的遗传多样性。发现了22种单倍型,在来自六个国家的分离株中检测到pvmsa180的单倍型6(Hap_6,77%)。
本研究对一种新型间日疟原虫表面蛋白PvMSA180进行了表征。大多数间日疟感染患者对特定抗原结构域有特异性抗体,表明该蛋白在自然暴露人群中具有免疫原性。对全球分离株的遗传分析表明,pvmsa180的多态性低于其他知名候选物,且一些单倍型在几个国家中常见。然而,需要进行更多样本量更大的研究,以评估地理上分离人群中的抗体反应,并确定PvMSA180在寄生虫入侵过程中的功能。