Laboratorio ICEMR-Amazonia, Laboratorios de Investigación y Desarrollo, Facultad de Ciencias y Filosofia, Universidad Peruana Cayetano Heredia, Lima, Peru.
Facultad de Salud Pública, Universidad Peruana Cayetano Heredia, Lima, Peru.
Malar J. 2017 Oct 16;16(1):415. doi: 10.1186/s12936-017-2063-x.
The incidence of malaria due both to Plasmodium falciparum and Plasmodium vivax in the Peruvian Amazon has risen in the past 5 years. This study tested the hypothesis that the maintenance and emergence of malaria in hypoendemic regions such as Amazonia is determined by submicroscopic and asymptomatic Plasmodium parasitaemia carriers. The present study aimed to precisely quantify the rate of very-low parasitaemia carriers in two sites of the Peruvian Amazon in relation to transmission patterns of P. vivax and P. falciparum in this area.
This study was carried out within the Amazonian-ICEMR longitudinal cohort. Blood samples were collected for light microscopy diagnosis and packed red blood cell (PRBC) samples were analysed by qPCR. Plasma samples were tested for total IgG reactivity against recombinant PvMSP-10 and PfMSP-10 antigens by ELISA. Occupation and age 10 years and greater were considered surrogates of occupation-related mobility. Risk factors for P. falciparum and P. vivax infections detected by PRBC-qPCR were assessed by multilevel logistic regression models.
Among 450 subjects, the prevalence of P. vivax by PRBC-PCR (25.1%) was sixfold higher than that determined by microscopy (3.6%). The prevalence of P. falciparum infection was 4.9% by PRBC-PCR and 0.2% by microscopy. More than 40% of infections had parasitaemia under 5 parasites/μL. Multivariate analysis for infections detected by PRBC-PCR showed that participants with recent settlement in the study area (AOR 2.1; 95% CI 1.03:4.2), age ≥ 30 years (AOR 3.3; 95% CI 1.6:6.9) and seropositivity to P. vivax (AOR 1.8; 95% CI 1.0:3.2) had significantly higher likelihood of P. vivax infection, while the odds of P. falciparum infection was higher for participants between 10 and 29 years (AOR 10.7; 95% CI 1.3:91.1) and with a previous P. falciparum infection (AOR 10.4; 95% CI 1.5:71.1).
This study confirms the contrasting transmission patterns of P. vivax and P. falciparum in the Peruvian Amazon, with stable local transmission for P. vivax and the source of P. falciparum to the study villages dominated by very low parasitaemia carriers, age 10 years and older, who had travelled away from home for work and brought P. falciparum infection with them.
过去 5 年来,秘鲁亚马逊地区因恶性疟原虫和间日疟原虫导致的疟疾发病率有所上升。本研究旨在验证以下假说,即在低流行地区(如亚马逊地区),疟疾的维持和出现是由亚临床和无症状的疟原虫寄生虫携带者决定的。本研究旨在精确量化两个秘鲁亚马逊地区的极低寄生虫血症携带者的比率,以及这些地区间日疟原虫和恶性疟原虫的传播模式。
本研究在亚马逊-ICEMR 纵向队列中进行。采集血样进行光学显微镜诊断,采集红细胞样本进行 qPCR 分析。通过 ELISA 检测血浆样本对重组 PvMSP-10 和 PfMSP-10 抗原的总 IgG 反应性。将职业和 10 岁及以上年龄作为与职业相关的流动性的替代指标。通过多水平逻辑回归模型评估 PRBC-qPCR 检测到的恶性疟原虫和间日疟原虫感染的危险因素。
在 450 名受试者中,PRBC-PCR 检测到的间日疟原虫患病率(25.1%)是光学显微镜检测到的患病率(3.6%)的六倍。恶性疟原虫感染率通过 PRBC-PCR 检测为 4.9%,通过光学显微镜检测为 0.2%。超过 40%的感染寄生虫血症低于 5 个寄生虫/μL。PRBC-PCR 检测到的感染的多变量分析表明,最近在研究地区定居的参与者(优势比 2.1;95%置信区间 1.03:4.2)、年龄≥30 岁(优势比 3.3;95%置信区间 1.6:6.9)和对间日疟原虫呈血清阳性(优势比 1.8;95%置信区间 1.0:3.2)的参与者更有可能感染间日疟原虫,而感染恶性疟原虫的几率更高10-29 岁的参与者(优势比 10.7;95%置信区间 1.3:91.1)和有过恶性疟原虫感染的参与者(优势比 10.4;95%置信区间 1.5:71.1)。
本研究证实了秘鲁亚马逊地区间日疟原虫和恶性疟原虫传播模式的对比,间日疟原虫在当地稳定传播,而恶性疟原虫的来源是那些年龄在 10 岁及以上、因工作而离开家园并携带恶性疟原虫感染的非常低寄生虫血症携带者。