Source of drug resistant Plasmodium falciparum in a potential malaria elimination site in Saudi Arabia

被引:13
作者
Al-Farsi, Hissa M. [1 ,2 ]
Al-Hashami, Zainab S. [1 ]
Bin Dajem, Saad M. [3 ]
Al-Sheikh, Adel Ali H. [4 ]
Al-Qahtani, Ahmed [5 ,6 ,7 ]
Beja-Pereira, Albano [8 ]
Idris, Mohamed A. [2 ]
Babiker, Hamza A. [1 ,9 ]
机构
[1] Sultan Qaboos Univ, Dept Biochem, Coll Med & Hlth Sci, Muscat, Oman
[2] Sultan Qaboos Univ, Coll Med & Hlth Sci, Dept Immunol & Microbiol, Muscat, Oman
[3] King Khalid Univ, Coll Sci, Dept Biol, Abha, Saudi Arabia
[4] MOH, Natl Ctr Training & Research, Jazan, Saudi Arabia
[5] King Faisal Specialist Hosp & Res Ctr, Dept Infect, Riyadh 11211, Saudi Arabia
[6] King Faisal Specialist Hosp & Res Ctr, Immunol Res Ctr, Riyadh 11211, Saudi Arabia
[7] King Saud Univ, Liver Dis Res Ctr, Riyadh, Saudi Arabia
[8] Univ Porto, Ctr Invest Biodivers & Recursos Genet CIBIO, P-4485661 Vairao, Portugal
[9] Univ Edinburgh, Sch Biol Sci, Inst Immunol & Infect Res, Edinburgh EH9 3JT, Midlothian, Scotland
关键词
Pyrimethamine-sulfadoxine resistance; Plasmodium falciparum; Evolutionary origin; Saudi Arabia; POLYMERASE-CHAIN-REACTION; PYRIMETHAMINE RESISTANCE; DIHYDROFOLATE-REDUCTASE; EASTERN SUDAN; HIGH-LEVEL; CHLOROQUINE; SULFADOXINE; PARASITES; AREA; DHFR;
D O I
10.1016/j.meegid.2012.03.011
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
A major challenge to the success of malaria control program in Saudi Arabia is the high influx of expatriates and holy visitors from malaria endemic countries. In the present study we examined whether drug resistant parasite genotypes reported in Jazan region, southwest of Saudi Arabia are imported or developed locally. We examined 178 Plasmodium falciparum isolates for alleles of dihydropteroate synthase (dhps) and dihydrofolate reductase (dhfr), associated with Sulfadoxine-Pyrimethamine (SP) resistance, and three microsatellites flanking each gene. In addition, we examined a neutral polymorphic gene (Pfg377). We compared the dhfr and dhps haplotypes in Jazan, using network analysis, to an existing similar data set of 94 P. falciparum isolates from eastern Sudan. In Jazan, double mutant dhfr allele (511, 108N) occurred with a prevalence of 33%. The vast majority (99%) of dhps were wild-type alleles. The mean expected heterozygosity (H-e) of rnicrosatellites around mutant dhfr alleles (H-e = 0.312; n = 60) was lower (P <= 0.05) than that around the wild-type allele (H-e = 0.834; n = 116). Also, the mutant dhfr isolates showed high H-e for dhps (H-e = 0.80) and the non-drug resistance locus Pfg377 (H-e = 0.63) indicative of selection for mutant dhfr only. The predominant double mutant dhfr haplotype in Jazan (73%), was prevalent among P. falciparum in east Africa. Network analysis suggests the mutant haplotype of dhfr gene was possibly introduced into Jazan from East Africa. The absence of mutations in dhps as well as triple mutant dhfr haplotype associated with SP failure support the current use of SP as a partner with artesunate as a first line therapy in Saudi Arabia. However, the close relationship between the major mutant dhfr haplotype in Sudan and Saudi Arabia, favour the hypothesis of recent migration as a source of the major resistant dhfr lineage. Thus, regular monitoring of the dhfr and dhps haplotypes is of high priority to guard possible importation of high level SP resistant lineages. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1253 / 1259
页数:7
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