Plasmodium falciparum histidine-rich protein 2/3 gene deletions and repeat motifs in Chhattisgarh, India (2017-2018).

IF 1.9 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Shrikant Nema, Monika Kumari, Kanika Verma, Sri Krishna, Nazia A Ali, Anil Kumar Verma, Aparup Das, Anup R Anvikar, Venkatachalam Udhayakumar, Praveen Kumar Bharti
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引用次数: 0

Abstract

Background: Rapid diagnostic tests (RDTs) are vital for malaria diagnosis, especially in resource-limited areas. RDTs targeting histidine-rich protein 2 (PfHRP2) and its structural homologue PfHRP3 are commonly used for detecting Plasmodium falciparum. However, genetic deletions in these proteins can affect test accuracy. This study aims to examine the gene deletions and sequence variation in the Pfhrp2 and Pfhrp3 genes in P. falciparum isolates from Chhattisgarh, India, and assess their correlation with RDT reactivity.

Methods: A total of 264 microscopically confirmed P. falciparumpositive samples from Chhattisgarh were analyzed for deletions in the Pfhrp2 and Pfhrp3 genes. Nucleotide sequences were obtained for the Pfhrp2 (n=101) and Pfhrp3 (n=95) genes. The sequence data were analyzed for repeat motifs and correlated with the RDT performance, especially at low parasite densities.

Results: The deletion rates for Pfhrp2 and Pfhrp3 were found to be 3.8% and 14%, respectively. The Pfhrp2 gene exhibited 15 distinct repeat motifs, while the Pfhrp3 gene showed 10 repeat motifs. No significant correlation was observed between variations in repeat types 2 and 7 of Pfhrp2 and the commercial RDT performance, particularly at low parasite densities.

Conclusions: The results indicate that the deletion rates and sequence diversity of Pfhrp2 and Pfhrp3 in Chhattisgarh are below the WHO threshold of 5% for a policy change regarding Pfhrp2 gene deletion. Sequence diversity does not appear to compromise the performance of current PfHRP2-based RDTs. However, a larger-scale study encompassing other endemic regions of India is recommended for a more comprehensive understanding of the impact on RDT efficacy over time.

印度恰蒂斯加尔邦恶性疟原虫富组氨酸蛋白2/3基因缺失和重复基序(2017-2018)
背景:快速诊断检测(RDTs)对于疟疾诊断至关重要,特别是在资源有限的地区。以富组氨酸蛋白2 (PfHRP2)及其结构同源物PfHRP3为靶点的rdt常用于检测恶性疟原虫。然而,这些蛋白质的基因缺失会影响检测的准确性。本研究旨在检测印度恰蒂斯加尔邦恶性疟原虫分离株Pfhrp2和Pfhrp3基因的缺失和序列变异,并评估其与RDT反应性的相关性。方法:对来自恰蒂斯加尔邦的264份镜检恶性疟原虫阳性样本进行Pfhrp2和Pfhrp3基因缺失分析。获得Pfhrp2 (n=101)和Pfhrp3 (n=95)基因的核苷酸序列。对序列数据进行重复基序分析,并与RDT性能进行相关性分析,特别是在低寄生虫密度时。结果:Pfhrp2和Pfhrp3基因缺失率分别为3.8%和14%。Pfhrp2基因有15个不同的重复基序,而Pfhrp3基因有10个重复基序。Pfhrp2重复型2和7的变异与商业RDT性能之间没有显著的相关性,特别是在寄生虫密度低的情况下。结论:结果表明,恰蒂斯加尔邦Pfhrp2和Pfhrp3基因的缺失率和序列多样性低于世卫组织关于Pfhrp2基因缺失政策变化的阈值5%。序列多样性似乎不会影响当前基于pfhrp2的rdt的性能。然而,建议对印度其他流行地区进行更大规模的研究,以便更全面地了解随时间推移对RDT疗效的影响。
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来源期刊
Transactions of The Royal Society of Tropical Medicine and Hygiene
Transactions of The Royal Society of Tropical Medicine and Hygiene 医学-公共卫生、环境卫生与职业卫生
CiteScore
4.00
自引率
9.10%
发文量
115
审稿时长
4-8 weeks
期刊介绍: Transactions of the Royal Society of Tropical Medicine and Hygiene publishes authoritative and impactful original, peer-reviewed articles and reviews on all aspects of tropical medicine.
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