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分析来自尼日利亚西南部奥贡州无症状孕妇的恶性疟原虫分离株中磺胺多辛-乙胺嘧啶耐药相关突变。

Analysis of sulphadoxine-pyrimethamine resistance-associated mutations in Plasmodium falciparum isolates obtained from asymptomatic pregnant women in Ogun State, Southwest Nigeria.

机构信息

Institute of Tropical Medicine, University of Tübingen, Germany; Department of Biomedical Sciences, Laboratory of Cytogenetics and Medical Genetics, Faculty of Health Sciences, University of Abomey-Calavi, Benin.

Department of Medical Microbiology & Parasitology, Olabisi Onabanjo University, Ago-Iwoye, Nigeria.

出版信息

Infect Genet Evol. 2020 Nov;85:104503. doi: 10.1016/j.meegid.2020.104503. Epub 2020 Aug 15.

Abstract

Intermittent preventive treatment in pregnancy with sulphadoxine-pyrimethamine (IPTp-SP) is one of the main strategies for protecting pregnant women, fetus, and their new-born against adverse effects of P. falciparum infection. The development of the drug resistance linked to mutations in P. falciparum dihydrofolate reductase gene (pfdhfr) and P. falciparum dihydropteroate synthase gene (pfdhps), is currently threatening the IPTp-SP approach. This study determined the prevalence of pfdhfr and pfdhps mutations in isolates obtained from pregnant women with asymptomatic P. falciparum infection in Nigerian. Additionally, P. falciparum genetic diversity and multiplicity of infection (MOI) was assessed by genotyping the P. falciparum merozoite surface Protein 1 and 2 (pfmsp-1 and pfmsp-2) genes. The pfdhfr and pfdhps were genotyped by direct sequencing, and the pfmsp-1 and pfmsp-2 fragment analysis by polymerase chain reaction was used to determine P. falciparum genetic diversity. Of the 406 pregnant women recruited, 123 had P. falciparum infection by PCR, and of these, 52 were successfully genotyped for pfdhfr and 42 for pfdhps genes. The pfdhfr triple-mutant parasites (N51I, C59R, and S108N) or the IRN haplotype were predominant (98%), whereas pfdhfr mutations C50R and I164L did not occur. For pfdhps gene, the prevalence of A437G, A581G, A436A, and A613S mutations were 98, 71, 55, and 36%, respectively. Nineteen (44%) isolates with quintuple mutations (CIRNI- SGKGA) had the highest combined pfdhfr-pfdhps haplotype. Isolates with sextuple mutants; CIRNI- AGKAS and CIRNI- AGKGA had a prevalence of 29 and 14%, respectively. High genetic diversity (7 pfmsp-1 alleles and 10 pfmsp-2 alleles) and monoclonal infection rate (76%) was observed. This study demonstrated a continuous high prevalence of pfdhfr mutation and an increase in pfdhps mutations associated with SP-resistance in southwest Nigeria. Continuous surveillance of IPTp-SP effectiveness and consideration of alternative IPTp strategies is recommended.

摘要

孕妇磺胺多辛-乙胺嘧啶间歇性预防疗法(IPTp-SP)是保护孕妇、胎儿及其新生儿免受恶性疟原虫感染不良影响的主要策略之一。与恶性疟原虫二氢叶酸还原酶基因(pfdhfr)和恶性疟原虫二氢蝶酸合成酶基因(pfdhps)突变相关的药物耐药性的发展,目前对 IPTp-SP 方法构成威胁。本研究确定了尼日利亚无症状恶性疟原虫感染孕妇分离株中 pfdhfr 和 pfdhps 突变的流行情况。此外,通过基因分型恶性疟原虫裂殖子表面蛋白 1 和 2(pfmsp-1 和 pfmsp-2)基因,评估了恶性疟原虫的遗传多样性和感染程度(MOI)。pfdhfr 和 pfdhps 通过直接测序进行基因分型,而 pfmsp-1 和 pfmsp-2 片段分析则通过聚合酶链反应进行,以确定恶性疟原虫的遗传多样性。在招募的 406 名孕妇中,123 名经 PCR 检测有恶性疟原虫感染,其中 52 名成功进行了 pfdhfr 基因分型,42 名进行了 pfdhps 基因分型。三重突变的 pfdhfr 寄生虫(N51I、C59R 和 S108N)或 IRN 单倍型占主导地位(98%),而 pfdhfr 突变 C50R 和 I164L 并未发生。对于 pfdhps 基因,A437G、A581G、A436A 和 A613S 突变的流行率分别为 98%、71%、55%和 36%。19 个(44%)具有五重突变(CIRNI-SGKGA)的分离株具有最高的 pfdhfr-pfdhps 单倍型。具有六重突变的分离株;CIRNI-AGKAS 和 CIRNI-AGKGA 的流行率分别为 29%和 14%。观察到高度的遗传多样性(7 个 pfmsp-1 等位基因和 10 个 pfmsp-2 等位基因)和单克隆感染率(76%)。本研究表明,在尼日利亚西南部,pfdhfr 突变持续高流行,与 SP 耐药相关的 pfdhps 突变增加。建议对 IPTp-SP 的有效性进行持续监测,并考虑替代的 IPTp 策略。

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