Plasmodium falciparum: Genetic diversity and complexity of infections in an isolated village in western Thailand

被引:8
作者
Tanabe, Kazuyuki [1 ,2 ]
Zollner, Gabriela [3 ]
Vaughan, Jefferson A. [4 ]
Sattabongkot, Jetsumon [3 ]
Khuntirat, Benjawan [3 ]
Honma, Hajime [5 ]
Mita, Toshihiro [5 ,6 ]
Tsuboi, Takafumi [7 ]
Coleman, Russell [3 ]
机构
[1] Osaka Univ, Microbial Dis Res Inst, Lab Malariol, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Microbial Dis Res Inst, Dept Mol Protozool, Suita, Osaka 5650871, Japan
[3] Armed Forces Res Inst Med Sci, US Army Med Component, Dept Entomol, Bangkok 10400, Thailand
[4] Univ N Dakota, Dept Biol, Grand Forks, ND 58202 USA
[5] Tokyo Womens Med Univ, Dept Int Affairs & Trop Med, Tokyo, Japan
[6] Juntendo Univ, Sch Med, Dept Mol & Cellular Parasitol, Tokyo 1138421, Japan
[7] Ehime Univ, Proteo Sci Ctr, Div Malaria Res, Matsuyama, Ehime 7908577, Japan
关键词
Malaria; Plasmodium falciparum; Genetic diversity; msp1; csp; ama1; SURFACE PROTEIN-1 GENE; PAPUA-NEW-GUINEA; ALLELIC DIVERSITY; MALARIA PARASITE; CIRCUMSPOROZOITE PROTEIN; POINT MUTATIONS; CHLOROQUINE USE; POPULATION; RECOMBINATION; RESISTANCE;
D O I
10.1016/j.parint.2013.09.011
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
Genetic diversity of Plasmodium falciparum is intimately associated with morbidity, mortality and malaria control strategies. It is therefore imperative to study genetic makeup and population structure of this parasite in endemic areas. In Kong Mong Tha, an isolated village in western Thailand, the majority of P. falciparum infections are asymptomatic. In this study we investigated complexity of infections and single nucleotide polymorphisms (SNPs) in the P. falciparum population of Kong Mong Tha, and compared results with those previously obtained from Mae Sod, in northwestern Thailand, where the majority of infections were symptomatic. Using PCR-based determination of the 5' merozoite surface protein 1 gene (msp1) recombinant types, we found that 39% of 59 P. falciparum isolates from Kong Mong Tha had multiple 5' recombinant types with a mean number of 1.54. These values were much lower than those obtained from Mae Sod: 96% for multiple infections and with a mean number of 3.61. Analysis of full-length sequences of two housekeeping genes, the P-type Ca2+-transporting ATPase gene (n = 33) plus adenylosuccinate lyase gene (n = 33), and three vaccine candidate antigen genes, msp1 (n = 26), the circumsporozoite protein gene, csp (n = 30) and the apical membrane antigen 1 gene, ama1 (n = 32), revealed that in all of these genes within-population SNP diversity was at similar levels between Kong Mong Tha and Mae Sod, suggesting that the extent of MOI and clinical manifestations of malaria are not strongly associated with genetic diversity. Additionally, we did not detect significant genetic differentiation between the two parasite populations, as estimated by the Wright's fixation index of inter-population variance in allele frequencies, suggesting that gene flow prevented the formation of population structuring. Thus, this study highlights unique features of P. falciparum populations in Thailand. The implications of these finding are discussed. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:260 / 266
页数:7
相关论文
共 50 条
[1]   Microsatellite markers reveal a spectrum of population structures in the malaria parasite Plasmodium falciparum [J].
Anderson, TJC ;
Haubold, B ;
Williams, JT ;
Estrada-Franco, JG ;
Richardson, L ;
Mollinedo, R ;
Bockarie, M ;
Mokili, J ;
Mharakurwa, S ;
French, N ;
Whitworth, J ;
Velez, ID ;
Brockman, AH ;
Nosten, F ;
Ferreira, MU ;
Day, KP .
MOLECULAR BIOLOGY AND EVOLUTION, 2000, 17 (10) :1467-1482
[2]   Geographical distribution of selected and putatively neutral SNPs in Southeast Asian malaria parasites [J].
Anderson, TJC ;
Nair, S ;
Sudimack, D ;
Williams, JT ;
Mayxay, M ;
Newton, PN ;
Guthmann, JP ;
Smithuis, FM ;
Hien, TT ;
van den Broek, IVF ;
White, NJ ;
Nosten, F .
MOLECULAR BIOLOGY AND EVOLUTION, 2005, 22 (12) :2362-2374
[3]   GENETIC CHANGES IN THE POPULATION OF PLASMODIUM-FALCIPARUM IN A SUDANESE VILLAGE OVER A 3-YEAR PERIOD [J].
BABIKER, HA ;
SATTI, G ;
WALLIKER, D .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1995, 53 (01) :7-15
[4]   Comparison of field and expert laboratory microscopy for active surveillance for asymptomatic Plasmodium falciparum and Plasmodium vivax in Western Thailand [J].
Coleman, RE ;
Maneechai, N ;
Rachaphaew, N ;
Kumpitak, C ;
Miller, RS ;
Soyseng, V ;
Thimasarn, K ;
Sattabongkot, J .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2002, 67 (02) :141-144
[5]   Comparison of PCR and microscopy for the detection of asymptomatic malaria in a Plasmodium falciparum/vivax endemic area in Thailand [J].
Coleman, Russell E. ;
Sattabongkot, Jetsumon ;
Promstaporm, Sommai ;
Maneechai, Nongnuj ;
Tippayachai, Bousaraporn ;
Kengluecha, Ampornpan ;
Rachapaew, Nattawan ;
Zollner, Gabriela ;
Miller, Robert Scott ;
Vaughan, Jefferson A. ;
Thimasarn, Krongtong ;
Khuntirat, Benjawan .
MALARIA JOURNAL, 2006, 5 (1)
[6]   Alterations in Plasmodium falciparum genotypes during sequential infections suggest the presence of strain specific immunity [J].
Eisen, DP ;
Saul, A ;
Fryauff, DJ ;
Reeder, JC ;
Coppel, RL .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2002, 67 (01) :8-16
[7]   Microsatellite mutations in the germline: implications for evolutionary inference [J].
Ellegren, H .
TRENDS IN GENETICS, 2000, 16 (12) :551-558
[8]   Arlequin (version 3.0): An integrated software package for population genetics data analysis [J].
Excoffier, Laurent ;
Laval, Guillaume ;
Schneider, Stefan .
EVOLUTIONARY BIOINFORMATICS, 2005, 1 :47-50
[9]   Sequence diversity and evolution of the malaria vaccine candidate merozoite surface protein-1 (MSP-1) of Plasmodium falciparum [J].
Ferreira, MU ;
Ribeiro, WL ;
Tonon, AP ;
Kawamoto, F ;
Rich, SM .
GENE, 2003, 304 :65-75
[10]   A recombinant blood-stage malaria vaccine reduces Plasmodium falciparum density and exerts selective pressure on parasite populations in a phase 1-2b trial in Papua New Guinea [J].
Genton, B ;
Betuela, I ;
Felger, I ;
Al-Yaman, F ;
Anders, RF ;
Saul, A ;
Rare, L ;
Baisor, M ;
Lorry, K ;
Brown, GV ;
Pye, D ;
Irving, DO ;
Smith, TA ;
Beck, HP ;
Alpers, MP .
JOURNAL OF INFECTIOUS DISEASES, 2002, 185 (06) :820-827