收稿日期: 2024-03-26
修回日期: 2024-07-15
网络出版日期: 2024-10-28
基金资助
2022年度河南省医学科技攻关计划(LHGJ20220157)
Analysis of polymorphism of Pfhrp2 gene in imported Plasmodium falciparum in Henan Province in 2020
Received date: 2024-03-26
Revised date: 2024-07-15
Online published: 2024-10-28
Supported by
Joint Project of Medical Science and Technology of Henan Province of 2022(LHGJ20220157)
分析河南省2020年确诊的输入性恶性疟病例血样的恶性疟原虫富组氨酸蛋白2(Pfhrp2)基因的缺失情况和外显子2区多态性。收集2020年河南省疟疾诊断参比实验室确诊的输入性恶性疟病例信息和血样,血样DNA进行巢式PCR扩增Pfhrp2基因外显子2区,阳性扩增产物进行测序。共收集确诊的输入性恶性疟病例血样37份,Pfhrp2基因外显子2区巢式PCR扩增阳性35份,阳性率94.59%(35/37)。35份扩增阳性产物中有28份测序成功,序列平均长度为822 bp。Pfhrp2基因外显子2区序列编码的氨基酸链共包含12种重复类型,均以1型(AHHAHHVAD)作为起始、12型(AHHAA)作为结束。28条氨基酸链均含有1型、2型、4型、11型和12型重复。其他重复类型占比从高到低依次为13型(96.43%,27/28),3型(92.86%,26/28),7型(82.14%,23/28),8型(64.29%,18/28),6型(60.71%,17/28),5型(46.43%,13/28)和9型(32.14%,9/28)。本研究结果显示,2020年河南省输入性恶性疟原虫虫株的Pfhrp2基因外显子2区片段存在高度多样性,可能会造成快速诊断检测结果的差异。
李素华 , 纪鹏慧 , 王丹 , 王昊 , 周瑞敏 . 河南省2020年输入性恶性疟原虫Pfhrp2基因多态性分析[J]. 中国寄生虫学与寄生虫病杂志, 2024 , 42(5) : 664 -667 . DOI: 10.12140/j.issn.1000-7423.2024.05.016
To analyze the deletion and polymorphism of exon 2 region of Plasmodium falciparum histidine rich protein 2 (Pfhrp2) gene from the blood samples of the imported falciparum malaria cases in Henan Province in 2020. The information and blood samples of the imported falciparum malaria cases confirmed by Henan Provincial Malaria Diagnosis Reference Laboratory in 2020 were collected. Nested PCR was performed to amplify Pfhrp2 exon 2 used DNA extracted from blood samples, and the positive amplification products were sequenced. A total of 37 blood samples of confirmed imported falciparum malaria cases were collected. 35 sequences of Pfhrp2 exon 2 were amplified successfully by nested PCR and the positive rates was 94.59% (35/37). 28 of 35 positive amplification products were sequenced successfully, with an average length of 822 bp. Twelve kinds of repeat types were found in the amino acid chains encoded by Pfhrp2 exon 2. All the amino acid chains started with types 1 (AHHAHHVAD) and ended with types 12 (AHHAA), and contained type 1, 2, 4, 11 and 12. The proportion of other repeat types in descending order were type 13 (96.43%, 27/28), 3 (92.86%, 26/28), 7 (82.14%, 23/28), 8 (64.29%, 18/28), 6 (60.71%, 17/28), 5 (46.43%, 13/28) and 9 (32.14%, 9/28), respectively. The results of this study showed that there was a high diversity of Pfhrp2 exon 2 in imported Plasmodium falciparum from Henan Province in 2020, which might cause different results of rapid diagnostic tests.
Key words: Imported Plasmodium falciparum; Pfhrp2 gene; Polymorphism; Henan Province
| [1] | World Health Organization. World malaria report 2023[R]. Geneva: WHO, 2023: 8. |
| [2] | Howard RJ, Uni S, Aikawa M, et al. Secretion of a malarial histidine-rich protein (PfHRP Ⅱ) from Plasmodium falciparum-infected erythrocytes[J]. J Cell Biol, 1986, 103(4): 1269-1277. |
| [3] | Wellems TE, Howard RJ. Homologous genes encode two distinct histidine-rich proteins in a cloned isolate of Plasmodium falciparum[J]. Proc Natl AcadSci U S A, 1986, 83(16): 6065-6069. |
| [4] | Sullivan DJ Jr, Ayala YM, Goldberg DE. An unexpected 5' untranslated intron in the P. falciparum genes for histidine-rich proteins Ⅱ and Ⅲ[J]. Mol Biochem Parasitol, 1996, 83(2): 247-251. |
| [5] | Figueiredo LM, Freitas-Junior LH, Bottius E, et al. A central role for Plasmodium falciparum subtelomeric regions in spatial positioning and telomere length regulation[J]. EMBO J, 2002, 21(4): 815-824. |
| [6] | Koita OA, Doumbo OK, Ouattara A, et al. False-negative rapid diagnostic tests for malaria and deletion of the histidine-rich repeat region of the hrp2 gene[J]. Am J Trop Med Hyg, 2012, 86(2): 194-198. |
| [7] | Kumar N, Pande V, Bhatt RM, et al. Genetic deletion of HRP2 and HRP3 in Indian Plasmodium falciparum population and false negative malaria rapid diagnostic test[J]. Acta Trop, 2013, 125(1): 119-121. |
| [8] | Mussa A, Talib M, Mohamed Z, et al. Genetic diversity of Plasmodium falciparum histidine-rich protein 2 (PfHRP2) and its effect on the performance of PfHRP2-based rapid diagnostic tests[J]. BMC Res Notes, 2019, 12(1): 334. |
| [9] | Houzé S, Hubert V, Le Pessec G, et al. Combined deletions of Pfhrp2 and Pfhrp3 genes result in Plasmodium falciparum malaria false-negative rapid diagnostic test[J]. J Clin Microbiol, 2011, 49(7): 2694-2696. |
| [10] | Atroosh WM, Al-Mekhlafi HM, Al-Jasari A, et al. Genetic variation of Pfhrp2 in Plasmodium falciparum isolates from Yemen and the performance of HRP2-based malaria rapid diagnostic test[J]. Parasit Vectors, 2015, 8: 388. |
| [11] | Abdallah JF, Okoth SA, Fontecha GA, et al. Prevalence of Pfhrp2 and Pfhrp3 gene deletions in Puerto Lempira, Honduras[J]. Malar J, 2015, 14: 19. |
| [12] | Akinyi S, Hayden T, Gamboa D, et al. Multiple genetic origins of histidine-rich protein 2 gene deletion in Plasmodium falciparum parasites from Peru[J]. Sci Rep, 2013, 3: 2797. |
| [13] | Figueiredo L, Scherf A. Plasmodium telomeres and telomerase: the usual actors in an unusual scenario[J]. Chromosome Res, 2005, 13(5): 517-524. |
| [14] | Golassa L, Messele A, Amambua-Ngwa A, et al. High prevalence and extended deletions in Plasmodium falciparum hrp2/3 genomic loci in Ethiopia[J]. PLoS One, 2020, 15(11): e0241807. |
| [15] | Deme AB, Park DJ, Bei AK, et al. Analysis of Pfhrp2 genetic diversity in Senegal and implications for use of rapid diagnostic tests[J]. Malar J, 2014, 13: 34. |
| [16] | Kumar N, Singh JP, Pande V, et al. Genetic variation in histidine rich proteins among Indian Plasmodium falciparum population: possible cause of variable sensitivity of malaria rapid diagnostic tests[J]. Malar J, 2012, 11: 298. |
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