Genetic diversity of Plasmodium falciparum populations in southeast and western Myanmar

被引:27
作者
Soe, Than Naing [1 ]
Wu, Yanrui [2 ,3 ]
Tun, Myo Win [4 ]
Xu, Xin [2 ]
Hu, Yue [5 ]
Ruan, Yonghua [5 ]
Win, Aung Ye Naung [4 ]
Nyunt, Myat Htut [4 ]
Mon, Nan Cho Nwe [4 ]
Han, Kay Thwe [4 ]
Aye, Khin Myo [4 ]
Morris, James [6 ]
Su, Pincan [7 ]
Yang, Zhaoqing [2 ]
Kyaw, Myat Phone [4 ,8 ]
Cui, Liwang [2 ,9 ]
机构
[1] Minist Hlth & Sports, Dept Publ Hlth, Nay Pyi Taw, Myanmar
[2] Kunming Med Univ, Dept Pathogen Biol & Immunol, Kunming, Yunnan, Peoples R China
[3] Kunming Med Univ, Dept Cell Biol & Genet, Kunming, Yunnan, Peoples R China
[4] Dept Med Res, Yangon City, Myanmar
[5] Kunming Med Univ, Dept Pathol, Kunming, Yunnan, Peoples R China
[6] Clemson Univ, Dept Genet & Biochem, Eukaryot Pathogens Innovat Ctr, Clemson, SC USA
[7] Yunnan Kunming Blood Ctr, Transfus Med Res Dept, Kunming, Yunnan, Peoples R China
[8] Myanmar Med Assoc, Yangon, Myanmar
[9] Penn State Univ, Dept Entomol, University Pk, PA 16802 USA
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
Genetic diversity; Plasmodium falciparum; Multiclonal infection; Southeast and western Myanmar; MEROZOITE SURFACE PROTEIN-1; DIAGNOSIS; BORDER; VIVAX;
D O I
10.1186/s13071-017-2254-x
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Background: The genetic diversity of malaria parasites reflects the complexity and size of the parasite populations. This study was designed to explore the genetic diversity of Plasmodium falciparum populations collected from two southeastern areas (Shwekyin and Myawaddy bordering Thailand) and one western area (Kyauktaw bordering Bangladesh) of Myanmar. Methods: A total of 267 blood samples collected from patients with acute P. falciparum infections during 2009 and 2010 were used for genotyping at the merozoite surface protein 1 (Msp1), Msp2 and glutamate-rich protein (Glurp) loci. Results: One hundred and eighty four samples were successfully genotyped at three genes. The allelic distributions of the three genes were all significantly different among three areas. MAD20 and 3D7 were the most prevalent alleles in three areas for Msp1 and Msp2, respectively. The Glurp allele with a bin size of 700-750 bp was the most prevalent both in Shwekyin and Myawaddy, whereas two alleles with bin sizes of 800-850 bp and 900-1000 bp were the most prevalent in the western site Kyauktaw. Overall, 73.91% of samples contained multiclonal infections, resulting in a mean multiplicity of infection (MOI) of 1.94. Interestingly, the MOI level presented a rising trend with the order of Myawaddy, Kyauktaw and Shwekyin, which also paralleled with the increasing frequencies of Msp1 RO33 and Msp2 FC27 200-250 bp alleles. Msp1 and Msp2 genes displayed higher levels of diversity and higher MOI rates than Glurp. PCR revealed four samples (two from Shwekyin and two from Myawaddy) with mixed infections of P. falciparum and P. vivax. Conclusions: This study genotyped parasite clinical samples from two southeast regions and one western state of Myanmar at the Msp1, Msp2 and Glurp loci, which revealed high levels of genetic diversity and mixed-strain infections of P. falciparum populations at these sites. The results indicated that malaria transmission intensity in these regions remained high and more strengthened control efforts are needed. The genotypic data provided baseline information for monitoring the impacts of malaria elimination efforts in the region.
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页数:6
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