Asymptomatic carriage of Plasmodium falciparum by individuals with variant blood groups and haemoglobin genotypes in southern Ghana

被引:9
作者
Acquah, Festus K. [1 ,2 ]
Donu, Dickson [1 ]
Bredu, Dorcas [1 ]
Eyia-Ampah, Sophia [1 ]
Amponsah, Jones A. [1 ]
Quartey, Joseph [3 ]
Obboh, Evans K. [4 ]
Mawuli, Bernice A. [2 ]
Amoah, Linda E. [1 ,2 ]
机构
[1] Univ Ghana, Noguchi Mem Inst Med Res, Dept Immunol, POB LG 581, Legon, Accra, Ghana
[2] Univ Ghana, West African Ctr Cell Biol Infect Pathogens, Volta Rd,POB LG 54, Legon, Accra, Ghana
[3] Univ Ghana, Noguchi Mem Inst Med Res, Dept Parasitol, POB LG 581, Legon, Accra, Ghana
[4] Univ Cape Coast, Sch Med Sci, Cape Coast, Ghana
关键词
SICKLE-CELL TRAIT; INFECTED ERYTHROCYTES; MALARIA INFECTION; ABO; PROTECTION; RESISTANCE;
D O I
10.1186/s12936-020-03299-1
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
BackgroundThe ABO and the Rhesus blood group systems, as well as various abnormal haemoglobin (Hb) variants (haemoglobinopathies) are known to influence malaria parasite carriage and disease severity in individuals living in malaria endemic areas. This study identified the blood group and Hb variant distribution and Plasmodium falciparum infection status of afebrile individuals living in southern Ghana.MethodsAfebrile participants were recruited from Obom (358) in the Greater Accra Region and Ewim (100) and Simiw (329) in the Central Region of Ghana. Venous blood (1 ml) was collected into EDTA vacutainer tubes. Three 20 mu l drops of blood were used for blood group analysis using the tile method. Another 500 mu l aliquot was used for the qualitative sickling test using sodium metabisulphite and haemoglobin electrophoresis. Genomic DNA was extracted from 100 mu l of whole blood and used in P. falciparum species-specific PCR.ResultsThe most abundant blood group and abnormal haemoglobin variant in both sites was blood group O+(47.4%) and HbAS (15.8%). A total of 13 (1.7%) of the participants had full haemoglobinopathies (SS, SC and CC), whilst 196 (25.4%) were carriers (AS and AC). Although there was a significantly higher prevalence of sickling positive participants from the Central Region, genotyping identified a similar prevalence of each of the abnormal haemoglobin genes in both sites. Asymptomatic parasite carriage estimated by PCR was 40.9% in the Central Region and 41.8% in the Greater Accra Region.ConclusionsAsymptomatic carriage of P. falciparum parasite in the study population was not associated with any particular blood group variant or haemoglobin genotype.
引用
收藏
页数:8
相关论文
共 39 条
[31]  
Rathi S, 2017, NATL J INTEGR RES ME, V8, P83
[32]   Role of genetic factors and ethnicity on the multiplicity of Plasmodium falciparum infection in children with asymptomatic malaria in Yaounde, Cameroon [J].
Roman, Dongang Nana Rodrigue ;
Anne, Ngono Ngane Rosalie ;
Singh, Vineeta ;
Luther, Koanga Mogtomo Martin ;
Chantal, Ngonde Essome Marie ;
Albert, Mouelle Sone .
HELIYON, 2018, 4 (08)
[33]   The Natural History of Sickle Cell Disease [J].
Serjeant, Graham R. .
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE, 2013, 3 (10)
[34]  
Tadesse H, 2013, J VECTOR DIS, V50, P292
[35]   Evaluation of the utility value of three diagnostic methods in the detection of malaria parasites in endemic area [J].
Ugah, Uchenna Iyioku ;
Alo, Moses Nnaemeka ;
Owolabi, Jacob Oluwabusuyi ;
Okata-Nwali, Oluchi DivineGift ;
Ekejindu, Ifeoma Mercy ;
Ibeh, Nancy ;
Elom, Michael Okpara .
MALARIA JOURNAL, 2017, 16
[36]   Plasmodium falciparum malaria and ABO blood group:: is there any relationship? [J].
Uneke, C. J. .
PARASITOLOGY RESEARCH, 2007, 100 (04) :759-765
[37]   Multiplicity of Plasmodium falciparum infection in asymptomatic children in Senegal:: relation to transmission, age and erythrocyte variants [J].
Vafa, Manijeh ;
Troye-Blomberg, Marita ;
Anchang, Judith ;
Garcia, Andre ;
Migot-Nabias, Florence .
MALARIA JOURNAL, 2008, 7 (1)
[38]   Sickle cell trait and the risk of Plasmodium falciparum malaria and other childhood diseases [J].
Williams, TN ;
Mwangi, TW ;
Wambua, S ;
Alexander, ND ;
Kortok, M ;
Snow, RW ;
Marsh, K .
JOURNAL OF INFECTIOUS DISEASES, 2005, 192 (01) :178-186
[39]  
Yousuf R, 2018, MALAYS J PATHOL, V40, P27