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Distribution of the two forms of Plasmodium falciparum erythrocyte binding antigen-175 (eba-175) gene in Lao PDR
© Dittrich et al; licensee BioMed Central Ltd. 2003
Received: 16 April 2003
Accepted: 22 July 2003
Published: 22 July 2003
The erythrocyte binding antigen 175 (EBA-175) is a 175 kDa antigen of Plasmodium falciparum and plays a major role in erythrocyte recognition by the parasite. The antigen is also supposed to be partly responsible for the invasion of erythrocytes by merozoites. EBA-175 has been sequenced from the FCR-3 and CAMP strains of P. falciparum. The sequences were identical in most parts of the gene. Differences were apparent in a 423 bp segment in the FCR-3 strain, the F-Fragment, that is not found in the CAMP-strain and a 342 bp segment, the C-Fragment, which is present in the CAMP-strain but not in the FCR-3-strain. The aim of this study was to assess the distribution of the two EBA-175-alleles in the Lao PDR.
Materials & Methods
Altogether, 240 blood-samples were collected in two areas of the country: Attapeu in the south and Lung Namtha in the north. Subsequently, the material was scanned for the F-and C-fragments.
In the whole study population, 52% carried the F-fragment, and 41% the C-fragment while seven percent of the patients were infected with at least two parasite strains and showed both alleles.
Distribution of the alleles showed significant differences between the north and the south province. Reasons for this include possible importation of different parasite strains from neighbouring countries.
The erythrocyte binding antigen-175 (EBA-175) of Plasmodium falciparum is localized in the merozoites and seems to be one of the key players during the fast cascade of interactions between the parasite and host molecules before the merozoite completely invades the erythrocyte . Following initial contact of the merozoite with the erythrocyte, reorientation brings the apical end in contact with the erythrocyte surface . The content of the apical organelles, including the rhoptries and micronemes, are discharged and a tight junction is formed between the erythrocyte membrane and the surface of the merozoite . EBA-175 is localized in the micronemes and has been identified as the merozoite ligand that binds a sialic acid-dependent site on glycophorin A . It therefore acts as a "bridge" between parasite and host cell.
EBA-175 is divided into a number of domains including three cysteine-rich regions (F1, F2 and C). F1 and F2 at the N-terminus are responsible for the glycophorin A binding on the erythrocyte membrane . There is a very low amount of polymorphic regions in the cysteine-rich regions. Most EBA-175 sequences have this in common. An exception is the central part of the gene, region III. Here, sequence analysis of two different P. falciparum strains identified highly dimorphic segments, FCR-3 and CAMP [5–7]. The sequences of both strains are nearly identical, except for one dimorphic region in the FCR-3 strain (referred as F-Fragment) and one in the CAMP-stain (referred as C-Fragment).
The FCR-3 gene consists of 1462 amino acids (aa) whereas the CAMP strain gene is 1435 aa long. This length variation of 27aa is caused by differences in the 423 bp F-fragment (141aa) and the 342 bp (114aa) C-fragment. These two alleles are inserted at slightly different positions in region III of the EBA-175 gene where the F-fragment is 91aa upstream of the C-fragment. Parasite strains possess either one or the other fragment, never both . Functions and potential effects of these dimorphic regions remain unclear. Earlier studies indicated that the dimorphic regions are also involved in the invasion process following the initial binding between merozoite and red blood cell. It is assumed that proteolytic cleavage of EBA-175 is followed by binding of the dimorphic regions to the glycophorin A backbone of the erythrocyte [8, 6].
The distribution of the two EBA-175 fragments has been studied in five African populations. Results did not indicate a natural selection concerning one of the two alleles . In a serological study in The Gambia, it was shown that the C and F polymorphisms of EBA-175 were not associated with subsequent protection from clinical malaria .
The objective of this project was to study the distribution of the F- and C-fragment in a South East Asian country, the Lao PDR and to assess potential protective associations of the C and F dimorphisms in that region. Following two field studies in north and south Laos [11, 12], 240 blood samples derived from P. falciparum positive individuals were screened for EBA-175 alleles by a nested PCR method . In order to link EBA-175 alleles to pathological findings, results were correlated with clinical data.
Materials and Methods
Parasite DNA samples
All samples were obtained with informed consent from patients and guardians. Ethical clearance was received from the ethics commission of the University of Munich and from the Ministry of Health of the Lao PDR. Blood was collected from consenting volunteers on Whatman filter paper and stored as dried blood samples. To prepare the DNA, 1–2 blood-spots were cut out of the filter, transferred into a tube containing 200 μl of 5% Chelex-100 (Bio-Rad Laboratories, Munich, Germany) and mixed intensively. After incubation in boiling water for 15 minutes the tube was vortexed for 30 seconds. The Chelex was separated by centrifugation (12,000 × g for two minutes, repeated twice) and the supernatant containing the DNA was transferred to a fresh tube .
PCR amplification and product analysis
The primers to detect the different EBA-175 fragments were used as described by Touré et al. . EBA1 5'-CAAGAAGCAGTTCCTGAGGAA-3' (forward) and EBA2 5'-TCTCAACATTCATATTAACAATTC-3' (reverse) for the first amplification and EBA3 5'-GAGGAAAACACTGAAATAGCACAC-3' (forward) and EBA4 5'-CAATTCCTCC-AGACTGTTGAACAT-3' (reverse) for the second amplification. Amplification was performed under following conditions: 4 μl of DNA-Template for nest 1 and 2 μl PCR-product for nest 2, 1 μM of each Primer, 1 U Taq DNA polymerase (Qbiogene, Germany), 2 μl PCR-Buffer (Qbiogene, Germany) as supplied by the manufacturer and 200 μM dNTP in a 20 μl reaction volume. Denaturation at 94°C was performed for five minutes, followed by 29 cycles of denaturation at 94°C for one minute, primer-annealing at 56.4°C for one minute and extension at 72°C for another two minutes, with final extension at 72°C for three minutes. The outcome of the amplification was controlled by electrophoresis in an ethidium bromide-stained 1.5% agarose gel. For detection of the stained DNA, an ultraviolet transiluminator and specific detection software was used (Grabit®). A band size of 795 bp indicated the infection with the F-fragment and a band of 714 bp the infection with the C-fragment. Both bands in one lane indicated a mixed infection of the patient with at least two different parasite clones.
Statistical analysis was carried out using SPSS 11.5/SPSS Tables 11.5 for Windows. Alleles were scored separately for each of the 2 alleles. To investigate the difference between the two study sites a Chi2-test was performed (significance: p < 0.05). A Chi2-test was used to check for a correlation between fragment type and clinical outcome and fragment type and sex of the patients. In order to analyse correlations between parasitaemia on day 0, age of the patients and fragment type, the median-values were compared by Mann-Whitney-Test (significance: p < 0.05).
Fragment distribution in Southern Laos
In the region of Attapeu, 162 patients with falciparum malaria were screened for the EBA-175 fragment types of the parasites. The distribution of the EBA-175-alleles was as follows: 46% F-fragment, 45% C-fragment and 9% mixed-infections.
Fragment distribution in Northern Laos
Seventy-eight blood samples of P. falciparum positive patients were screened for the two alleles of the EBA-175 gene in the province of Luang Namtha, in the north of Lao PDR. In contrast to the region around Attapeu, the northern area (study-site: Luang Namtha) showed different frequencies. The F-fragment was more frequently present (64%) than the C-fragment (33%) and 3% of the samples had mixed infections.
Comparison of the two study-sites
Correlation of fragment type and parasitaemia on day-0/clinical outcome/sex/age
Correlation of parasitaemia at day 0 and age in the two study sites and the two allele-groups, analysed by Mann-Whitney test
Parasitaemia on day-0
A nested PCR method was used  in order to detect two alleles of EBA-175 (F-fragment and C-fragment) and to map their distribution in the Lao PDR. In this study with a combined pool of isolates derived from 240 patients in two surveys in north and south Laos, both fragment types had nearly the same distribution within the population. However, fragment types were not equally distributed between the two study sites. While isolates from Attapeu (Southern Laos) showed a almost equal distribution of the two fragments (51% F-fragment, 49% C-fragment), the F-fragment was clearly dominating in Luang Namtha, Northern Laos (65% F-fragment, 35% C-fragment) (figure 2). This difference is statistically significant when discounting mixed infections in patients who were infected with at least two different P. falciparum strains. This result confirms earlier work with samples from five African countries . As in our study, Binks et al. had found a different distribution in five countries. In four of them (Nigeria, Gambia, Gabon, S. Africa) the F-fragment dominated, whereas the C-Fragment was dominating in the Sudan.
The higher prevalence of the F-fragment EBA-175 in the north of Laos is not readily explained. One of the reasons could be a difference in the parasite populations of the different regions in Lao PDR. The province of Attapeu borders Vietnam and Cambodia whereas the province of Luang Namtha borders Myanmar and China. An exchange of parasite strains over the local borders is possible. Genetic differences in the host population may also play a role when selection of specific fragments is involved. In Laos there are about 68 ethnic minorities that exhibit major differences and often live isolated from each other. The study-site in Attapeu is dominated by groups of Lao Thung and Lao Loum while the northern province of Luang Namtha is predominantly inhabited by Lao Sung, an entirely different minority. As Binks et al.  speculate in their study of the EBA-175 allele frequency in five African countries, a genetic difference in the human host population may be a reason for fragment selection. Obviously, a random selection of allelic frequencies may also be possible. More studies on larger populations are necessary to understand the pattern distribution of EBA-175 alleles.
Correlation of fragment type and clinical data showed that there was no significant correlation between parasitaemia on day-0, age, sex, clinical outcome and fragment type. However, the observed trend towards a higher parasitaemia at day 0 in patients with a C-fragment infection is potentially interesting. Further studies should be done to investigate whether parasites expressing a C-fragment enjoy a natural advantage compared those with a F-fragment.
We thank Dr. Bounlay Phommasak (Deputy Director, Department of Hygiene and Prevention, Ministry of Health), the Center of Malariology, Parasitology and Entomology, Vientiane, the Attapeu Provincial Health Service, the Attapeu Provincial Malaria Station and all participating villagers from Attapeu for their cooperation, support and assistance in the field work.
We are also grateful to the WHO Office Vientiane for facilitating various stages of the project.
Financial support was received by the Friedrich Baur Trust, Munich, and the WHO Western Pacific Regional Office.
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