尼日利亚阿南布拉Awka地区恶性疟原虫分离株msp2和glurp基因等位基因频率分析

MalariaWorld journal Pub Date : 2025-02-18 eCollection Date: 2025-01-01 DOI:10.5281/zenodo.14886922
Moses Ikegbunam, Abone Harrison, Chukwudi Egbuche, Nwasolu Obidi, Judith Mbamalu, Enyi Emmanuel, Offojebe Kosisochukwu, Mercy Ezeunala, Nzeukwu Chibumma, Ifeyinwa Onochie-Igbinedion, Joy Igwe, Joy Nnanna, Dorothy Ezeagwuna, Vincent Duru, Frances Nworji, Charles Esimone
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引用次数: 0

摘要

恶性疟原虫的遗传多样性与其致病性相关,因此设计基于证据的干预策略以根除疟疾需要遗传多样性监测。本研究对尼日利亚Awka地区恶性疟原虫的等位基因频率和遗传多样性进行了分析。材料与方法:提取177株恶性疟原虫基因组DNA,采用巢式聚合酶链反应(nested polymerase chain reaction, PCR)对msp2和glurp基因多态性区进行分型。结果:分析了2个msp2等位基因3D7和FC27。msp2阳性分离株中以3D7等位基因家族为主,占93.55%。24株(38.71%)感染多克隆msp2。检测到21个不同的msp2等位基因,片段大小在200 ~ 1200 bp之间。3D7等位基因以300 bp等位基因片段(26.83%)为主,FC27等位基因以400 bp等位基因片段(29.54%)为主。msp2的感染多重性(multiplicity of infection, MoI)为2.03,期望杂合性(Heterozygosity, He)为0.34。69株(38.98%)glurp基因RII重复区阳性。glurp基因共检测到9个片段大小在200 ~ 1150 bp之间的等位基因,其中最常见的片段为200 bp(19%)。glurp基因的MoI和He分别为0.45和0.98。结论:本研究中观察到的高水平恶性疟原虫多克隆感染表明研究区存在广泛的遗传多样性。这些数据提供了重要的基线信息,可用于在研究地区和尼日利亚制定疟疾控制战略和消除疟疾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Allelic frequency of msp2 and glurp genes in Plasmodium falciparum isolates from Awka, Anambra, Nigeria.

Introduction: The genetic diversity of Plasmodium falciparum correlates with its pathogenicity, therefore design of evidence-based intervention strategies to eradicate malaria requires genetic diversity surveillance. This study characterised the allelic frequencies and genetic diversity of P. falciparum parasites isolated from Awka, Nigeria.

Materials and methods: Genomic DNA was extracted from 177 P. falciparum isolates and the polymorphic regions of the msp2 and glurp genes were genotyped by nested polymerase chain reaction (PCR).

Results: Two msp2 alleles (3D7 and FC27) were analysed. The 3D7 (93.55%) msp2 allelic family was predominant in msp2 positivie isolates. Polyclonal msp2 infection was observed in 24 (38.71%) isolates. Twenty-one distinct msp2 alleles were detected, with fragment sizes ranging from 200 bp to 1200 bp. The 300 bp allelic fragment (26.83%) was predominant for the 3D7 allele, while the 400 bp allelic fragment (29.54%) was predominant for the FC27 allele. The multiplicity of infection (MoI) in msp2 was 2.03, and the expected Heterozygosity (He) was 0.34. Sixty-nine isolates (38.98%) were positive for the RII repeat region of the glurp gene. For the glurp gene, nine alleles were detected for fragment sizes ranging from 200 bp to 1150 bp, and the most prevalent allelic fragment was 200 bp (19%). The MoI and He for the glurp gene were 0.45 and 0.98, respectively.

Conclusions: The high level of polyclonal infections with P. falciparum parasites observed in this study indicates extensive genetic diversity in the study area. The data provide important baseline information that can be implemented in developing malaria control strategies and elimination in the study area and Nigeria.

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