Ndong Ngomo Jacques Mari, Mawili-Mboumba Denise Patricia, M'Bondoukwé Noé Patrick, Ditombi Bridy Moutombi, Koumba Lengongo Jeanne Vanessa, Batchy Ognagosso Fanny Bertrande, Bouyou-Akotet Marielle Karine
Faculty of Medicine, Department of Parasitology and Mycology, Université des Sciences de la Santé, Libreville BP 4009, Gabon.
Trop Med Infect Dis. 2023 Mar 23;8(4):184. doi: 10.3390/tropicalmed8040184.
The objective of this study was to analyze the relationship between the frequency of artemisinin-based combination (ACT) drug resistance molecular markers and clinical forms of malaria and parasitemia. A cross-sectional study was carried out between January and April 2014 at the Operational Clinical Research Unit of Melen in febrile children aged 12 to 240 months with a sp. infection. A total of 3 mL of peripheral blood collected from an EDTA tube was used for leukocyte depletion. DNA mutation detection was performed by next generation sequencing (NGS). A total of 1075 patients were screened for malaria. Among them, 384 had a infection. mono-infection was found in 98.9% of the patients. -326T mutation was found in all isolates, while 37.9% had -484I mutant allele. The highest median parasite densities were found in patients infected by parasites carrying the CVIET haplotype of the gene. The different genetic profiles found here, and their variations according to clinical and biological signs of severe malaria, are additional arguments for the surveillance of strains.
本研究的目的是分析青蒿素联合疗法(ACT)耐药分子标记物的频率与疟疾临床类型及疟原虫血症之间的关系。2014年1月至4月,在梅伦的临床研究操作单元对12至240个月的发热性疟原虫感染儿童进行了一项横断面研究。从EDTA管中采集3 mL外周血用于白细胞去除。通过下一代测序(NGS)进行DNA突变检测。共筛查了1075例疟疾患者。其中,384例感染疟原虫。98.9%的患者为单一感染。在所有分离株中均发现-326T突变,而37.9%的分离株具有-484I突变等位基因。携带疟原虫基因CVIET单倍型的患者疟原虫密度中位数最高。此处发现的不同基因谱及其根据严重疟疾临床和生物学体征的变化,是监测疟原虫菌株的额外依据。