Oyewole Tolulope A, Mohammed Nurat O, Osarenren Bright O, Tijani Muyideen K, Persson Kristina E M, Falade Mofolusho O
Cellular Parasitology Programme, Cell Biology and Genetics units, Department of Zoology, University of Ibadan, Ibadan, Nigeria.
Division of Clinical Chemistry and Pharmacology, Department of Laboratory Medicine, Lund University, 22185 Lund, Sweden.
Parasite Epidemiol Control. 2024 Jul 4;26:e00366. doi: 10.1016/j.parepi.2024.e00366. eCollection 2024 Aug.
Nigeria is a major contributor to the global malaria burden. The genetic diversity of malaria parasite populations as well as antibody responses of individuals in affected areas against antigens of the parasite can reveal the transmission intensity, a key information required to control the disease. This work was carried out to determine the allelic frequency of highly polymorphic genes and antibody responses against schizont crude antigens in an area of Ibadan, Nigeria.
Blood was collected from 147 individuals with symptoms suspected to be malaria. Malaria infection was determined using a rapid diagnostic test (RDT), and and were genotyped by a nested PCR method. In addition, levels of IgG directed against FCR3S1.2 schizont extract was measured in ELISA.
Approximately 25% (36/147) were positive for a infection in RDT, but only 32 of the positive samples were successfully genotyped. MAD20 was the most prevalent and K1 the least prevalent of the alleles. For , FC27 was more prevalent than 3D7. The mean multiplicities of infection (MOI) were 1.9 and 1.7 for and , respectively. IgG levels correlated positively with age, however there was no difference in median antibody levels between RDT-positive and RDT-negative individuals.
Low MOI has before been correlated with low/intermediate transmission intensity, however, in this study, similar levels of -specific antibodies between infected and non-infected individuals point more towards a high level of exposure and a need for further measures to control the spread of malaria in this area.
尼日利亚是全球疟疾负担的主要贡献国。疟原虫种群的遗传多样性以及受影响地区个体对疟原虫抗原的抗体反应可以揭示传播强度,这是控制该疾病所需的关键信息。开展这项工作是为了确定尼日利亚伊巴丹一个地区高度多态性基因的等位基因频率以及针对裂殖体粗抗原的抗体反应。
从147名疑似疟疾症状的个体中采集血液。使用快速诊断试验(RDT)确定疟疾感染情况,并通过巢式PCR方法对疟原虫进行基因分型。此外,在酶联免疫吸附测定(ELISA)中测量针对FCR3S1.2裂殖体提取物的IgG水平。
在RDT中,约25%(36/147)的个体为疟原虫感染阳性,但仅32份阳性样本成功进行了基因分型。在疟原虫等位基因中,MAD20最为普遍,K1最不普遍。对于间日疟原虫,FC27比3D7更普遍。恶性疟原虫和间日疟原虫的平均感染复数(MOI)分别为1.9和1.7。IgG水平与年龄呈正相关,然而RDT阳性和RDT阴性个体之间的抗体水平中位数没有差异。
低MOI之前与低/中等传播强度相关,然而,在本研究中,感染个体和未感染个体之间相似水平的疟原虫特异性抗体更表明暴露水平较高,并且需要采取进一步措施来控制该地区疟疾的传播。