Suppr超能文献

尼日利亚西南部奥孙州与对不同抗疟药物耐药性相关的恶性疟原虫pfdhfr、pfdhps、pfmdr1、pfcrt和pfk13基因的突变谱

Mutational profile of pfdhfr, pfdhps, pfmdr1, pfcrt and pfk13 genes of P. falciparum associated with resistance to different antimalarial drugs in Osun state, southwestern Nigeria.

作者信息

Martín Ramírez Alexandra, Akindele Akeem Abiodun, González Mora Vicenta, García Luz, Lara Nicole, de la Torre-Capitán Matías Eva, Molina de la Fuente Irene, Nassar Sulaiman Adebayo, Ta-Tang Thuy-Huong, Benito Agustín, Berzosa Pedro

机构信息

Centro de Investigación Biomédica en Red de Enfermedades Infecciosas, Instituto de Salud Carlos III, Madrid, Spain.

National Centre of Tropical Medicine, Institute of Health Carlos III, Madrid, Spain.

出版信息

Trop Med Health. 2025 Apr 8;53(1):49. doi: 10.1186/s41182-025-00732-6.

Abstract

BACKGROUND

Nigeria accounts for the greatest burden of malaria disease globally. Malaria control requires an effective treatment after diagnosis. The efficacy of antimalarial drugs can be assessed through the analysis of genetic changes associated with reduced drug sensitivity.

METHODS

This study includes the analysis of the markers associated with artemisinin (pfk13), sulfadoxine-pyrimethamine (pfdhfr and pfdhps), and chloroquine and its derivatives (pfmdr1 and pfcrt) resistances, in blood samples collected from asymptomatic children in south-western Nigeria.

RESULTS

The 25.95% of samples showed a number of mutations in pfk13 gene. Among those, the validated, C580Y, and the candidate, R515K, mutations by WHO were detected. Twenty-seven pfdhps different haplotypes were observed, with the haplotype ISGKAA as the most prevalent (18.80%), followed by IFGKAA (12.78%) and IAGKAA (11.28%). The VAGKGS was the most common haplotype carrying the I431V mutation (10.53%). Combinations of alleles in pfdhfr and pfdhps genes provided a 40.98% of samples with the partially resistant haplotype (IRNG). No samples exhibited the 'fully resistant' or 'super resistant' pfdhprf-pfdhps combinations, but one sample contained mutations at pfdhfr 51I, 59R, and 108N with pfdhps 431V, 436A, A437G and 540E. The analysis of pfcrt 72-76 variants disclosed a 12.12% of samples with the mutant-type (CVIET). No double mutant pfmdr1 haplotypes 86Y/1246Y (YY) were detected, nor was the haplotype formed by the alleles 86Y pfmdr1 + pfcrt 76 T (YT).

CONCLUSIONS

There was no evidence of parasite genomes harbouring multilocus mutations conferring multidrug resistance, although evidence of a validated (C580Y) and a candidate (R515K) mutation in pfk13 gene, high frequency pfdhfr mutant alleles and high variability of pfdhps haplotypes were found in this study, which provides a baseline information essential in monitoring P. falciparum resistances.

摘要

背景

尼日利亚承担着全球最大的疟疾疾病负担。疟疾防控需要在诊断后进行有效治疗。抗疟药物的疗效可通过分析与药物敏感性降低相关的基因变化来评估。

方法

本研究对从尼日利亚西南部无症状儿童采集的血样中与青蒿素(pfk13)、磺胺多辛 - 乙胺嘧啶(pfdhfr和pfdhps)以及氯喹及其衍生物(pfmdr1和pfcrt)耐药性相关的标志物进行分析。

结果

25.95%的样本在pfk13基因中显示出多个突变。其中,检测到了世界卫生组织验证的C580Y突变和候选的R515K突变。观察到27种不同的pfdhps单倍型,其中单倍型ISGKAA最为常见(18.80%),其次是IFGKAA(12.78%)和IAGKAA(11.28%)。VAGKGS是携带I431V突变的最常见单倍型(10.53%)。pfdhfr和pfdhps基因中的等位基因组合使40.98%的样本具有部分耐药单倍型(IRNG)。没有样本表现出“完全耐药”或“超级耐药”的pfdhprf - pfdhps组合,但有一个样本在pfdhfr的51I、59R和108N以及pfdhps的431V、436A、A437G和540E处含有突变。对pfcrt 72 - 76变体的分析显示,12.12%的样本为突变型(CVIET)。未检测到双突变pfmdr1单倍型86Y/1246Y(YY),也未检测到由等位基因86Y pfmdr1 + pfcrt 76 T(YT)形成的单倍型。

结论

尽管本研究发现了pfk13基因中一个验证的(C580Y)和一个候选的(R515K)突变、pfdhfr突变等位基因的高频率以及pfdhps单倍型的高变异性,但没有证据表明寄生虫基因组存在赋予多药耐药性的多位点突变,这为监测恶性疟原虫耐药性提供了重要的基线信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a45b/11977893/4309e72b9212/41182_2025_732_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验