尼日利亚三角洲州孕妇Merozoite Surface Protein 2 (MSP2)等位基因家族频率及磺胺嘧啶-乙胺嘧啶(SP)耐药标记

Chiamaka Evan Achu, O. Nwaorgu, C. Egbuche, D. Ezeagwuna, O. Ajibaye, D. N. Aribodor
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引用次数: 2

摘要

妊娠期疟疾是一个公共卫生问题,需要用磺胺嘧啶-乙胺嘧啶(SP)药物进行预防性治疗。然而,耐sp恶性疟原虫在尼日利亚的出现和传播对这一预防性干预措施的效力和效果构成严重威胁。本研究旨在测定三角洲州Asaba市无症状孕妇恶性疟原虫MSP2等位基因家族的频率和SP耐药分子标记。使用快速诊断试验(RDT)和显微镜检查研究参与者的疟疾寄生虫感染。以恶性疟原虫MSP2为标记,采用聚合酶链式反应(PCR)技术鉴定疟原虫是否存在寄生;采用限制性片段长度多态性(RFLP)技术鉴定恶性疟原虫sp抗性分子标记,分别位于二氢叶酸还原酶(dhfr)密码子51、59、108、164和二氢叶酸合成酶(dhps)基因密码子437、540、581和431位点。首次产前登记的410名孕妇疟疾患病率分别为8.29%和17.07% (P < 0.05)。在Pfdhfr/Pfdhps基因中,C59R单突变发生率最高,为10例(21.28%)(P < 0.05)。Pfdhfr/Pfdhps的单倍型变异15个(31.91%),双倍型14个(29.79%),三倍型13个(27.66%),四倍型5个(10.64%),分别有5、8、6和3个独特的单倍型。该研究记录了研究参与者中疟疾寄生虫的存在。恶性疟原虫SP耐药基因也被检测到,这可能对妊娠期间歇性预防治疗(IPTp-SP)的有效性提出了挑战。
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Frequency of Merozoite Surface Protein 2 (MSP2) Allelic Families and Sulphadoxine-Pyrimethamine (SP) Resistance Markers Among Pregnant Women in Delta State, Nigeria)
Malaria in pregnancy is a public health problem and requires prophylactic treatment with Sulphadoxine–Pyrimethamine (SP) drug. However, the emergence and spread of SP-resistance P. falciparum parasite across Nigeria poses serious threat to the efficacy and effectiveness of this preventive intervention. This study aimed to determine the frequency of MSP2 allelic families and SP resistance molecular markers of P. falciparum among asymptomatic pregnant women in Asaba, Delta State. Rapid Diagnostic Test (RDT) and Microscopy were used to detect malaria parasite infection among the study participants. Polymerase Chain Reaction (PCR) was used to confirm parasitaemia using P. falciparum MSP2 as a marker while Restriction Fragment Length Polymorphism (RFLP) was used to identify P. falciparum SP-resistance molecular markers at codons 51, 59, 108, 164 of dihydrofolate reductase (dhfr), and codons 437, 540, 581 and 431 of dihydropteorate synthetase (dhps) genes. The prevalence of malaria from the 410 pregnant women examined at first antenatal registration were 8.29% and 17.07% using RDT and microscopy, respectively (P 0.05). Single mutation of C59R in 10 (21.28%) cases was the most prevalent haplotype in the Pfdhfr/Pfdhps genes (P < 0.05). Mutation variations of Pfdhfr/Pfdhps identified were 15 (31.91%) single, 14 (29.79%) double, 13 (27.66%) triple and 5 (10.64%) quadruple with 5, 8, 6 and 3 unique haplotypes, respectively. The study recorded the presence of malaria parasites among the study participants. P. falciparum SP resistant genes were also detected and this may present a challenge in the usefulness of Intermittent Preventive Treatment (IPTp-SP) in pregnancy.
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