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法属圭亚那间日疟原虫msp3α和msp1_b5标记的遗传多样性

Genetic diversity of msp3alpha and msp1_b5 markers of Plasmodium vivax in French Guiana.

作者信息

Véron Vincent, Legrand Eric, Yrinesi Joséphine, Volney Béatrice, Simon Stéphane, Carme Bernard

机构信息

Laboratoire Hospitalo-Universitaire de Parasitologie et Mycologie Médicale, Equipe EA3593, UFR de Médecine de l'Université des Antilles et de la Guyane, Cayenne, French Guiana.

出版信息

Malar J. 2009 Mar 11;8:40. doi: 10.1186/1475-2875-8-40.

Abstract

BACKGROUND

Reliable molecular typing tools are required for a better understanding of the molecular epidemiology of Plasmodium vivax. The genes msp3a and msp1_block5 are highly polymorphic and have been used as markers in many P. vivax population studies. These markers were used to assess the genetic diversity of P. vivax strains from French Guiana (South America) and to develop a molecular typing protocol.

METHODS

A total of 120 blood samples from 109 patients (including 10 patients suffered from more than one malaria episode, samples were collected during each episode) with P. vivax infection were genotyped. All samples were analysed by msp3a PCR-RFLP and msp1_b5 gene sequencing was performed on 57 samples. Genotyping protocol applied to distinguish between new infection or relapse from heterologus hypnozoites and treatment failure or relapse from homologus hypnozoites was based on analysing first msp3a by PCR-RFLP and secondly, only if the genotypes of the two samples are identical, on sequencing the msp1_b5 gene.

RESULTS

msp3a alleles of three sizes were amplified by PCR: types A, B and C. Eleven different genotypes were identified among the 109 samples analysed by msp3a PCR-RFLP. In 13.8% of cases, a mixed genotype infection was observed. The sequence of msp1_b5 gene revealed 22 unique genotypes and 12.3% of cases with mixed infection. In the 57 samples analysed by both methods, 45 genotypes were found and 21% were mixed. Among ten patients with two or three malaria episodes, the protocol allowed to identify five new infections or relapses from heterologous hypnozoites and six treatment failures of relapses from homologous hypnozoites.

CONCLUSION

The study showed a high diversity of msp3a and msp1_b5 genetic markers among P. vivax strains in French Guiana with a low polyclonal infection rate. These results indicated that the P. vivax genotyping protocol presented has a good discrimination power and can be used in clinical drug trials or epidemiological studies.

摘要

背景

为了更好地了解间日疟原虫的分子流行病学,需要可靠的分子分型工具。msp3a和msp1_block5基因具有高度多态性,已在许多间日疟原虫群体研究中用作标记。这些标记用于评估来自法属圭亚那(南美洲)的间日疟原虫菌株的遗传多样性,并制定分子分型方案。

方法

对109例间日疟原虫感染患者的120份血样(包括10例经历过不止一次疟疾发作的患者,在每次发作期间采集样本)进行基因分型。所有样本均通过msp3a PCR-RFLP分析,对57份样本进行msp1_b5基因测序。用于区分新感染或来自异源休眠子的复发以及治疗失败或来自同源休眠子的复发的基因分型方案,首先基于通过PCR-RFLP分析msp3a,其次,仅当两个样本的基因型相同时,才对msp1_b5基因进行测序。

结果

通过PCR扩增出三种大小的msp3a等位基因:A、B和C型。在通过msp3a PCR-RFLP分析的109份样本中鉴定出11种不同的基因型。在13.8%的病例中观察到混合基因型感染。msp1_b5基因序列显示22种独特的基因型和12.3%的混合感染病例。在通过两种方法分析的57份样本中,发现了45种基因型,21%为混合基因型。在10例经历过两次或三次疟疾发作的患者中,该方案能够识别出5例新感染或来自异源休眠子的复发以及6例来自同源休眠子的治疗失败或复发。

结论

该研究表明,法属圭亚那的间日疟原虫菌株中msp3a和msp1_b5遗传标记具有高度多样性,多克隆感染率较低。这些结果表明,所提出的间日疟原虫基因分型方案具有良好的鉴别能力,可用于临床药物试验或流行病学研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7126/2660359/61f853613c14/1475-2875-8-40-1.jpg

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