Allelic polymorphism of MSP2 gene in severe P. falciparum malaria in an area of low and seasonal transmission

Ishraga E. A-Elbasit, Gehad ElGhazali, Thoraya M.E. A-Elgadir, Amel A. Hamad, Hamza A. Babiker, Mustafa I. Elbashir, Hayder A. Giha*

*المؤلف المقابل لهذا العمل

نتاج البحث: المساهمة في مجلةمراجعة النظراء

28 اقتباسات (Scopus)

ملخص

The severe malaria (SM) and uncomplicated malaria (UM) infections are expected to have different genetic makeup. In this study, blood samples were obtained from 325 donors with SM and UM and malaria-free donors (including asymptomatic submicroscopic malaria-ASUM), from Eastern Sudan. The SM group included patients with cerebral malaria (CM), severe malarial anemia (SMA), and other complications. The MSP2 locus was exploited for parasite genotyping. We found that the genetic diversity of the parasite population was marked (51 genotypes). The overall multiplicity of infection (MOI) was 1.5, and it was comparable between SM and UM. However, the MOI in ASUM (1.0) and fatal CM (1.14) was comparable and significantly lower than in UM (1.53), SMA (1.52), and nonfatal CM (1.7). The ratio of the IC1 to FC27 allele families was comparable between SM and UM, and the distribution of the allele sizes was correlated (correlation coefficient=0.59 and 0.718; P<0.001). It is interesting to note that the FC27 genotype was overrepresented in ASUM (68.2%) and was not recognized in fatal CM, while in mixed-clone infections, the clearance of IC1 after quinine treatment was faster than FC27 clearance. Finally, the composition of the multiclone infections (IC1 and FC27) was suggesting a stronger cross-immunity within rather than between MSP2 gene families.

اللغة الأصليةEnglish
الصفحات (من إلى)29-34
عدد الصفحات6
دوريةParasitology Research
مستوى الصوت102
رقم الإصدار1
المعرِّفات الرقمية للأشياء
حالة النشرPublished - ديسمبر 2007

ASJC Scopus subject areas

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  • ???subjectarea.asjc.3400???
  • ???subjectarea.asjc.1100.1109???
  • ???subjectarea.asjc.2700.2725???

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