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ABSTRACT |
 TOP ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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Malaria infections are composed of a variable number of distinct genotypes, with a mean of 2–3 genotypes in one patient sample. In Malawian pregnant women, we have shown that the genotypes present in peripheral blood were frequently different from those in placental blood, suggesting that some genotypes were circulating in the peripheral blood while others were sequestered in the tissues.5 We hypothesized that parasites circulating in peripheral blood in children with severe and complicated malaria are genetically distinct from those sequestered in the brain and other organs, and that a proportion of parasites sequestered on admission would emerge into the peripheral blood over an 18–24-hour period post-admission. Data from longitudinal studies in asymptomatic children indicate that such a process occurs in children with asymptomatic malaria infections, with variations in the P. falciparum population in blood samples collected on a daily or third-day basis.6,7
Among individuals treated with parenteral quinine, parasite clearance time is frequently greater than 24 hours.8 If sequestered and circulating parasites are genetically distinct broods, as has been described in asymptomatic infection,7 one might expect to find new genotypes emerging in peripheral blood of children under quinine treatment, as a result of continuing schizogony among sequestered parasites and invasion of more erythrocytes by merozoites.
We used a nested polymerase chain reaction (PCR) to amplify genes encoding merozoite surface protein 1 (MSP-1) and MSP-2 to distinguish different genotypes in admission samples and at 18 and/or 24 hours. This method provides the advantage of great sensitivity and specificity, and distinguishes between alleles of similar serologic properties by size polymorphism.9 We asked whether parasites persisting at 18–24 hours after admission had different genotypes to those present on admission, which might indicate different broods of parasites in the periphery and in the tissues.
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MATERIALS AND METHODS |
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1% on thin blood film examination were recruited for the study. After consent was obtained from a child’s parent or guardian, clinical histories were recorded and the patients were treated with parenteral quinine (20 mg/kg loading dose, 10 mg/kg twice a day). Finger prick blood samples were collected every six hours. Malaria parasitemia was quantitated using Giemsa-stained thick and thin blood films, and 200 µL of whole blood was collected into EDTA-containing microtainers for DNA extraction. Samples with microscopically detectable parasitemia at 18 and/or 24 hours were chosen for DNA extraction. All samples were frozen at –20°C until extraction of DNA was performed. PCR analysis. DNA extraction was performed using the QIAamp DNA Mini Kit (Qiagen, Crawley, United Kingdom). DNA was eluted in 200 µL of 10 mM Tris-HCl, 0.5 mM EDTA, pH 9.0, and frozen at –20°C. Samples were genotyped by a nested PCR using primer pairs specific for amplifying the known allelic families of MSP-1 and MSP-2.11 The targeted polymorphic regions of MSP-1 and MSP-2 were amplified in a primary PCR using 1 µL of template DNA on a PTC-200 thermal cycler (MJ Research Inc., Watertown, MA) under the following conditions: 94°C for 5 minutes, 25 cycles at 94°C for 1 minute, 58°C for 2 minutes, and 72°C for 1 minute, and a final extension at 72°C for 2 minutes. All reactions were conducted in a volume of 20 µL and contained 125 µM dNTPs, 125 nM oligonucleotides, and 0.5 units of Taq polymerase. Two microliters of primary product was used to initiate a secondary reaction with specific nested oligonucleotide pairs targeting each of the allelic families of MSP-1 and MSP-2. This reaction used 30 cycles as above with an annealing temperature of 61°C. Positive and negative controls were included in all batches.
All products were analyzed by electrophoresis in 2% aga-rose gels (0.5 x Trisborate-EDTA buffer), stained with ethidium bromide, and visualized by ultraviolet transillumination. Each patient’s matched samples were run in adjacent wells in all assays. The number of bands visualized within expected size ranges11 were counted for each allelic family and summed. The minimum number of genotypes was specified as the highest total number of bands within either the MSP-1 or MSP-2 allelic families.6 All samples that resulted in different bands at 18 or 24 hours from admission samples were retested for confirmation.
Ethical approval. This study was reviewed and approved by the College of Medicine Research and Ethics Committee, University of Malawi.
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RESULTS |
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1% completed the study. Reasons for non-completion included low initial parasitemia, early clearance of parasitemia (before 18 hours), and death of the patient. Twenty-eight children had cerebral malaria alone, 19 had cerebral malaria combined with severe anemia (hematocrit < 15%), 5 had severe anemia, and 6 had non-severe malaria with or without prostration. Logistic difficulties prevented examination of samples from children who were aparasitemic by microscopy by 18 hours. DNA was extracted and PCR was performed at 0, 18, and 24 hours in 33 patients, at 0 and 24 hours in 18 patients, and 0 and 18 hours in 7 patients. Parasite genotypes studied by PCR amplification of three MSP-1 and two MSP-2 alleles showed a mean of 2–3 genotypes per patient (Table 1
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DISCUSSION |
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Rings normally grow to mature trophozoite stage by 18 hours post-invasion, when they disappear from peripheral blood and sequester in tissues. If quinine retarded parasite maturation, rings might persist for 24 hours after starting treatment. However, they appear to be resistant to quinine,15 except in the presence of high concentrations that would not be attained within the first 24 hours of treatment,16 making this explanation less likely.
There is some evidence that sequestration and schizogony continue for more than 24 hours after initial administration of quinine treatment,8 and also that quinine does not significantly reduce cytoadherence.17 Thus, repopulation of peripheral blood with progeny of sequestered parasites may continue after starting therapy. Our data suggest such repopulation is composed of parasites of the same dominant genotypes as those circulating at admission.
Changes in genotypes at one locus only could be attributed to technical problems. Our nested PCR might have failed to amplify MSP-1 or MSP-2 alleles present at levels below the threshold of sensitivity. Our results show that of 58 patients studied, only 3 (5.2%) had new genotypes detected at either the MSP-1 or MSP-2 loci. If two strains were identical at one locus, a new genotype may show only one new band. Apart from our favored explanation, that sequestered parasites are re-emerging into the circulation, other possible explanations for detection of a single new band also include variations in the quality of DNA or performance of PCR, and competition between different genotypes in our PCRs. By extracting matched samples at the same time, by repeating assays with potential new genotypes, and by running matched samples in adjacent wells in the same assay, we believe we have minimized potential artifacts as the cause of our findings.
Malaria syndrome did not appear to influence the degree of change in genotype seen, although we had relatively few samples from children with severe anemia or uncomplicated malaria. The surprising finding that the proportion of isolates showing genotype loss tended to be higher in children with unfavorable outcomes was not explained either by differences in numbers of genotype on admission, or by differences in proportions of isolates tested at 18 compared with 24 hours, and may warrant further investigation.
The results suggest that dominant clones persist in both circulating parasites and those sequestered in the tissues. These observations confirm and extend those of Missinou and others.12 In Gabon, children with single episodes of P. falciparum malaria were found to carry parasites with the same genotypes throughout the course of infection.12 The observations of genetically distinct, asynchronous broods of parasites in asymptomatic infection6,7 do not appear to be relevant to severe malaria pathogenesis, but suggest instead that relatively uniform dominant populations of genotypes may be found in both peripheral blood and tissues. Detailed comparison of peripheral blood and tissues from autopsy studies of children with fatal malaria will resolve this question.
Received May 30, 2005. Accepted for publication December 1, 2005.
Acknowledgments: We thank Professor Terrie Taylor and nursing staff (Research Ward, Department of Paediatrics, College of Medicine, University of Malawi) for collecting samples for the study, and the children and their parents and guardians for their participation.
Financial support: This study was supported by the Wellcome Trust (Senior Fellowship 063215 to Stephen J. Rogerson and project grant to 071376 to Malcolm E. Molyneux).
* Address correspondence to Stephen J. Rogerson, Department of Medicine, University of Melbourne, Post Office, Royal Melbourne Hospital, Victoria 3050, Australia. E-mail: sroger{at}unimelb.edu.au 
Authors’ addresses: Edson G Dembo, Happy T Phiri, Jacqui Montgomery, and Malcolm E Molyneux, Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Box 30096, Blantyre 3 Malawi, Telephone: 265-167-6444, Fax: 265-167-5774. Stephen J Rogerson, Department of Medicine, Post Office Royal Melbourne Hospital, Parkville, Victoria 3050, Australia, Telephone: 61-3-8344-3259, Fax: 61-3-9347-1863, E-mail: sroger{at}unimelb.edu.au.
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This article has been cited by other articles:
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  C. Dobano, S. J. Rogerson, T. E. Taylor, J. S. McBride, and M. E. Molyneux Expression of Merozoite Surface Protein Markers by Plasmodium falciparum-Infected Erythrocytes in Peripheral Blood and Tissues of Children with Fatal Malaria Infect. Immun., February 1, 2007; 75(2): 643 - 652. [Abstract] [Full Text] [PDF]
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