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首页> 外文期刊>Tropical Medicine and International Health: TM and IH >Genetic diversity and genotype multiplicity of Plasmodium falciparum infections in symptomatic individuals in the maritime region of Togo
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Genetic diversity and genotype multiplicity of Plasmodium falciparum infections in symptomatic individuals in the maritime region of Togo

机译:多哥海域有症状个体恶性疟原虫感染的遗传多样性和基因型多样性

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Objective To assess the genotype prevalence and the multiplicity of Plasmodium falciparum infections in the maritime region of Togo. Methods We enrolled 309 symptomatic individuals aged from 6months to 15years from Bè/Lomé and Tsévié, two malaria endemic zones. The number and the proportions of merozoite surface proteins 1, 2 and 3 genotypes in patients were determined using capillary electrophoresis genotyping. We further investigated the possible association between transaminases and homocysteine, and the severity of the disease. Results Of the 309 samples genotyped, 210 tested positive to msp-1, 227 to msp-2 and 193 to msp-3. The nested PCR revealed 22 different alleles for the allelic family msp-1, 33 for msp-2 and 13 for msp-3. At each locus, the family distribution was 54.58% of K1, 25% of MAD20 and 20.42% of RO33 for msp-1, and 51.71% and 48.29% of FC27 and 3D7, respectively, for msp-2. For all these allelic variants, the distribution was associated with neither the severity of malaria nor the zone of habitation. Pearson correlation coefficients between either the levels of homocysteine or the transaminase and the severity of the disease were very low. Conclusion The severity of malaria was not associated with higher multiplicity of infections and did not appear restricted to particular genotypes. More comprehensive explorations including immunity, genetic factors, nutritional and sociologic status of the population could clarify the situation.
机译:目的评估多哥沿海地区恶性疟原虫感染的基因型流行率和多样性。方法我们从两个疟疾流行区的Bè/Lomé和Tsévié招募了309名有症状的个体,年龄从6个月到15岁。使用毛细管电泳基因分型法确定患者中裂殖子表面蛋白1、2和3基因型的数量和比例。我们进一步调查了转氨酶和同型半胱氨酸之间的可能联系,以及疾病的严重程度。结果在309个基因分型的样本中,有210个对msp-1呈阳性,227对msp-2呈阳性和193对msp-3呈阳性。巢式PCR显示等位基因家族msp-1有22个不同的等位基因,msp-2具有33个等位基因,msp-3具有13个等位基因。在每个位点,对于msp-1,家庭分布分别为K1的54.58%,MAD20的25%和RO33的20.42%,对于msp-2的家庭分布分别为FC27和3D7的51.71%和48.29%。对于所有这些等位基因变体,分布与疟疾的严重程度或栖息地都不相关。高半胱氨酸或转氨酶水平与疾病严重程度之间的皮尔逊相关系数非常低。结论疟疾的严重程度与较高的感染多样性无关,并且似乎并不局限于特定的基因型。人群的免疫力,遗传因素,营养和社会地位等更全面的探索可以弄清情况。

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