Laboratório de Malária, Centro de Pesquisas René Rachou/Fiocruz, Belo Horizonte-MG, Brazil.
Trop Med Int Health. 2012 Aug;17(8):989-1000. doi: 10.1111/j.1365-3156.2012.03016.x. Epub 2012 May 30.
To investigate risk factors associated with the acquisition of antibodies against Plasmodium vivax Duffy binding protein (PvDBP) - a leading malaria vaccine candidate - in a well-consolidated agricultural settlement of the Brazilian Amazon Region and to determine the sequence diversity of the PvDBP ligand domain (DBP(II)) within the local malaria parasite population.
Demographic, epidemiological and clinical data were collected from 541 volunteers using a structured questionnaire. Malaria parasites were detected by conventional microscopy and PCR, and blood collection was used for antibody assays and molecular characterisation of DBP(II).
The frequency of malaria infection was 7% (6% for P. vivax and 1% for P. falciparum), with malaria cases clustered near mosquito breeding sites. Nearly 50% of settlers had anti-PvDBP IgG antibodies, as detected by enzyme-linked immunosorbent assay (ELISA) with subject's age being the only strong predictor of seropositivity to PvDBP. Unexpectedly, low levels of DBP(II) diversity were found within the local malaria parasites, suggesting the existence of low gene flow between P. vivax populations, probably due to the relative isolation of the studied settlement.
The recognition of PvDBP by a significant proportion of the community, associated with low levels of DBP(II) diversity among local P. vivax, reinforces the variety of malaria transmission patterns in communities from frontier settlements. Such studies should provide baseline information for antimalarial vaccines now in development.
在巴西亚马逊地区一个巩固的农业定居点中,调查与获得针对间日疟原虫杜菲结合蛋白(PvDBP)抗体相关的风险因素,该蛋白是一种主要的疟疾候选疫苗,并确定当地疟原虫种群中 PvDBP 配体结构域(DBP(II))的序列多样性。
使用结构化问卷收集了 541 名志愿者的人口统计学、流行病学和临床数据。通过传统显微镜和 PCR 检测疟原虫,采集血液用于抗体检测和 DBP(II)的分子特征分析。
疟疾感染率为 7%(P. vivax 为 6%,P. falciparum 为 1%),疟疾病例集中在蚊子滋生地附近。近 50%的定居者具有抗 PvDBP IgG 抗体,这是通过酶联免疫吸附试验(ELISA)检测到的,而受试者的年龄是 PvDBP 血清阳性的唯一强预测因素。出乎意料的是,在当地疟原虫中发现 DBP(II)的多样性水平较低,表明 P. vivax 种群之间的基因流动较低,这可能是由于研究定居点相对孤立。
社区中相当一部分人对 PvDBP 的识别,以及当地 P. vivax 中 DBP(II)多样性水平较低,这强化了边境定居点社区中各种疟疾传播模式的存在。此类研究应为当前正在开发的抗疟疫苗提供基线信息。