- Open Access
In vitro growth of Plasmodium falciparum in neonatal blood
© Sauerzopf et al.; licensee BioMed Central Ltd. 2014
- Received: 10 August 2014
- Accepted: 3 November 2014
- Published: 18 November 2014
Children below the age of six months suffer less often from malaria than older children in sub-Saharan Africa. This observation is commonly attributed to the persistence of foetal haemoglobin (HbF), which is considered not to permit growth of Plasmodium falciparum and therefore providing protection against malaria. Since this concept has recently been challenged, this study evaluated the effect of HbF erythrocytes and maternal plasma on in vitro parasite growth of P. falciparum in Central African Gabon.
Umbilical cord blood and peripheral maternal blood were collected at delivery at the Albert Schweitzer Hospital in Gabon. Respective erythrocyte suspension and plasma were used in parallel for in vitro culture. In vitro growth rates were compared between cultures supplemented with either maternal or cord erythrocytes. Plasma of maternal blood and cord blood was evaluated. Parasite growth rates were assessed by the standard HRP2-assay evaluating the increase of HRP2 concentration in Plasmodium culture.
Culture of P. falciparum using foetal erythrocytes led to comparable growth rates (mean growth rate = 4.2, 95% CI: 3.5 – 5.0) as cultures with maternal red blood cells (mean growth rate =4.2, 95% CI: 3.4 – 5.0) and those from non-malaria exposed individuals (mean growth rate = 4.6, 95% CI: 3.8 – 5.5). Standard in vitro culture of P. falciparum supplemented with either maternal or foetal plasma showed both significantly lower growth rates than a positive control using non-malaria exposed donor plasma.
These data challenge the concept of HbF serving as intrinsic inhibitor of P. falciparum growth in the first months of life. Erythrocytes containing HbF are equally permissive to P. falciparum growth in vitro. However, addition of maternal and cord plasma led to reduced in vitro growth which may translate to protection against clinical disease or show synergistic effects with HbF in vivo. Further studies are needed to elucidate the pathophysiology of innate and acquired protection against neonatal malaria.
- Plasmodium falciparum
- Neonatal haemoglobin
- Histidine-rich protein 2
- Immune plasma
Although children below five years of age are disproportionally severely affected by malaria morbidity and mortality, there is a lag time of about three months after birth, before first disease episodes occur [1–4]. This period coincides with the persistence of maternal IgG antibodies in the infant’s circulation but other protective mechanisms may also contribute to the reduced susceptibility [4–7].
Previous studies postulate a role for persisting foetal haemoglobin during the first months of life in protection against malaria . The transcription of HbF starts around the 10th week of development and ends shortly before birth. This causes a linear decline in the number of foetal red blood cells from up to 90% at time of birth to around 5% at 3 months of age . It was hypothesized that parasite strains – encountering HbF only on relatively rare occasions from an evolutionary perspective – may therefore be selected by strong adaptation to adult haemoglobin (HbA), a process resulting in limited intra-erythrocytic growth of Plasmodium falciparum in predominantly HbF containing neonatal blood [9, 10]. This paradigm of protection during early infancy – first published in 1977 – was held up since then until recently, when Amaratunga et al. failed to detect growth delays in neonatal erythrocytes and thus profoundly challenged this concept .
To further investigate potential mechanisms of protection, this study evaluated the comparative in vitro growth rates of a standardized P. falciparum clone under controlled culture conditions using either maternal, cord, or non-malaria exposed donor erythrocytes.
In addition, the growth modulating effect of maternal, cord, and non-malaria exposed donor plasma on P. falciparum growth was evaluated.
Study region and patient population
The study took place at the Centre de Recherches Médicales de Lambaréné, Albert Schweitzer Hospital and Georges Rawiri Regional Hospital in Lambaréné, Gabon. Gabon is a Central African country characterized by a tropical climate and hyperendemic malaria transmission . Participants were invited to join this study when attending the local maternity wards for delivery. Demographic data were obtained, however no validated information about intake of IPTp was available. All subjects were tested in routine antenatal care for HIV and only those with negative test result were invited to participate. The study protocol was approved by the institutional review board of the CERMEL and the ethical review committee of the Medical University of Vienna and all women provided written informed consent prior to blood sampling.
All samples were tested for sickle cell trait by haemoglobin electrophoresis and for plasmodial infection by thick smear at the time of delivery and samples were excluded in case of a positive result or when signs of haemolysis or clotting were apparent. At delivery 1.2 ml of blood was taken from the umbilical cord in an EDTA tube. Peripheral maternal venous blood was taken at the earliest convenience within three days. Non-malaria exposed donor blood was obtained from Caucasian male volunteers. Blood samples were collected in EDTA tubes and specimens were immediately centrifuged to separate red blood cells from plasma. Red blood cells were washed three times in complete parasite medium and stored at 4°C in 0.5 volume of saline adenine glucose-mannitol (150 mM NaCl, 1.25 mM adenine, 45 mM glucose, 30 mM mannitol) until further use. Plasma was immediately frozen at -80°C.
Parasite culture and growth assay
A laboratory-adapted clone of P. falciparum (3D7) repeatedly selected for presence of knob-phenotype was kept in continuous sorbitol synchronized culture throughout the course of the study. Parasites were maintained using a standard protocol in complete parasite medium (500 ml RPMI-1640, 10 mg/l gentamicin, 6 g/l (25 mM) HEPES, 292 mg/l (2 mM) L-glutamine, 50 mg/l (0.36 mM) hypoxanthine, 5 g/l Albumax II) in a candle jar at 37°C. To test the effect of erythrocytes and plasma on plasmodial growth, micro-cultures of 200 μl each were established in 96-well plates (Corning Costar-3599) in duplicates. To investigate the effect of HbF on parasite growth, micro-cultures containing cord derived red blood cells and maternal red blood cells, respectively, as well as a positive control containing donor O + red blood cells, were set up in duplicates. Parasites derived from continuous culture in adult RBC were diluted with respective test RBC (>1 : 40) to obtain at 1.5% haematocrit, 0.05% parasitaemia using 5% pooled, heat inactivated serum from AB + donors for 72 hours before growth was stopped by freezing.
Plasma derived from mothers, newborns and a malaria-naïve adult was added to cultures in complete parasite medium to assess its effect on parasite growth at 1.5% haematocrit, 0.05% parasitaemia and 10% plasma supplementation. Frozen lysates of micro-cultures were used for histidine-rich protein II enzyme linked immunosorbent assay (HRP2 ELISA) for the quantification of parasite growth [13–15]. Commercial antibodies (MPFM-55A and MPFG-55P, Immunology Consultants Laboratories, Inc) and high binding plates (Corning Costar 3590) were used. Growth rates of P. falciparum were estimated by the assessment of HRP2 concentrations in cultures. Growth was defined as an increase in optical density in the HRP2 ELISA. An at least two fold increase in HRP2 concentration from prior to post incubation was set as threshold for further analysis. Statistical analysis was performed using “R” software. Differences between groups were assessed employing the Tukey's Honestly Significant Difference test. All reagents, unless stated otherwise were obtained from Sigma-Aldrich, St. Louis.
Hundred and three pregnant women consented to participate in this study between July 2012 and June 2013, of which sixty-five were excluded from further testing (sickle cell trait: 12, clotting: 27, haemolysis after sampling: 13, Plasmodium infection: 7, presence of anti-Rhesus antibodies: 6). Thirty-eight participants finally met the criteria for analysis. Mother's age was ranging from 17 to 42 years with a mean of 25 years and a standard deviation of 7.1 years with a mean gravidity of 3.5 with a standard deviation of 2.4. Mean gestational age at delivery was 38.5 weeks of gestation with a standard deviation of 2.1 weeks and mean birth weight was 2,866 grams ranging from 1,900 to 4,400 grams. Among the recruited women, 18 paired erythrocyte samples and 22 plasma specimens were successfully used in parallel for further in vitro testing.
Maternal, neonatal, and non-malaria exposed donor erythrocytes
Mean growth rates and lower and upper margin of 95% CIs in test given test erythrocytes of high and low growth strata as well as the cumulative data
Cord derived RBC
Non malaria exposed donor RBC
Cord derived RBC
Non malaria exposed donor RBC
Cord derived RBC
Non malaria exposed donor RBC
Maternal, neonatal, and non-malaria exposed plasma
This study demonstrates that cord derived erythrocytes, harbouring a high concentration of HbF, are equally suited for P. falciparum invasion, maturation, and growth as adult erythrocytes containing predominantly HbA. Growth rates between maternal, neonatal and non-malaria exposed donor erythrocytes were very similar, and no morphological signs of growth inhibition were detected. These findings provide strong evidence that P. falciparum may similarly develop within HbF rich red blood cells and that HbF per se is no protective factor against malaria during the first months of life.
These data are in line with results published by Amaratunga et al. demonstrating normal invasion and development of P. falciparum in HbF containing red blood cells in a set of adult and six cord blood specimens. While this study focused on an overall assessment of parasite growth in a larger sample size, Amaratunga et al. could detect effects of neonatal haemoglobin, in particular in conjunction with immune IgGs, on the knob phenotype and PfEMP-1 mediated cytoadherence of parasitized red blood cells. Although erythrocytes rich in foetal haemoglobin seem to be permissive to infection with P. falciparum in vitro, reduced cytoadherence may, particularly in the presence of IgG, lead to lower parasite densities in vivo due to increased clearance of infected cells in the spleen.
To evaluate whether humoral immunity and transfer of maternal immunoglobulins or other plasmatic factors may play a protective role in newborns, cultures were supplemented with the respective plasma samples. Interestingly, a consistent growth-inhibition was observed in both maternal and neonatal plasma when compared to non-malaria exposed donor plasma. In vitro growth inhibition caused by a supplementation with immune plasma was reported previously in Thai individuals yielding comparable results to this study .
It is tempting to speculate that passive transfer of maternal antibodies to the newborn accounts for this growth inhibitory effect. However, it may not be excluded that other factors including cytokines, hormones, complement or indeed drugs with anti-malarial activity passing the placental barrier into the neonatal blood may have caused this inhibition of growth. One limitation of this study is the lack of valid information about IPTp intake of study participants – a factor potentially affecting plasma assays. In addition these data derive from experiments with one clone of P. falciparum and potential differences between wild isolates and laboratory adapted parasites may not be ruled out. Finally, behavioural factors certainly also contribute to young infants’ protection from malaria, since neonates receive special care and attention by their caregivers potentially leading to less exposure to infectious bites.
The amount of protection against malaria in early infancy might yet be caused by the interplay of several distinct factors, probably in conjunction with maternally derived antibodies. However, these data conclusively refute the hypothesis of HbF serving as an intrinsic inhibitor of P. falciparum growth in vitro, and indicate that maternal and newborn plasma show considerable inhibitory activity against in vitro growth of P. falciparum.
We thank all nurses and midwifes at the Albert Schweitzer Hospital and Georges Rawirii Regional Hospital in Lambaréné for their kind cooperation. This work was supported by Deutsche Forschungsgemeinschaft (DFG-Projekt KR 1150/6-1) and Open Access Publishing fund of the University of Tübingen, and by EU-funded project Immunological Interplay between Poverty Related Diseases and Helminth infections: An African-European Research Initiative “IDEA” (HEALTH-F3-2009-241642). We are grateful for the logistic and infrastructure support kindly provided by CANTAM.
- WHO: World Malaria Report. 2013, Geneva: World Health OrganizationGoogle Scholar
- Greenwood BM, Bojang K, Whitty CJ, Targett GA: Malaria. Lancet. 2005, 365: 1487-1498. 10.1016/S0140-6736(05)66420-3.View ArticlePubMedGoogle Scholar
- Klein Klouwenberg PMC, Oyakhirome S, Schwarz NG, Gläser B, Issifou S, Kiessling G, Klöpfer A, Kremsner PG, Längin M, Lassmann B, Necek M, Pötschke M, Ritz A, Grobusch MP: Malaria and asymptomatic parasitaemia in Gabonese infants under the age of 3 months. Acta Trop. 2005, 95: 81-85. 10.1016/j.actatropica.2005.05.003.View ArticlePubMedGoogle Scholar
- Ramharter M, Schuster K, Bouyou-Akotet MK, Adgenika AA, Schmits K, Mombo-Ngoma G, Agnandji ST, Nemeth J, Afène SN, Issifou S, Onnas IN, Kombila M, Kremsner PG: Malaria in pregnancy before and after the implementation of a national IPTp program in Gabon. Am J Trop Med Hyg. 2007, 77: 418-422.PubMedGoogle Scholar
- Riley EM, Wagner GE, Akanmori BD, Koram KA: Do maternally acquired antibodies protect infants from malaria infection?. Parasite Immunol. 2001, 23: 51-59. 10.1046/j.1365-3024.2001.00364.x.View ArticlePubMedGoogle Scholar
- Bardají A, Sigauque B, Laia B, Romagosa C, Sanz S, Mabunda S, Mandomando I, Aponte J, Sevene E, Alonso PL, Menéndez C: Clinical malaria in African pregnant women. Malar J. 2008, 7: 27-10.1186/1475-2875-7-27.PubMed CentralView ArticlePubMedGoogle Scholar
- Ramharter M, Grobusch MP, Kießling G, Adegnika AA, Möller U, Agnandji STM, Kramer M, Schwarz N, Kun JFJ, Oyakhirome S, Issifou S, Borrmann S, Lell B, Mordmüller B, Kremsner PG: Clinical and parasitological characteristics of puerperal malaria. J Infect Dis. 2005, 191: 1005-1009. 10.1086/427781.View ArticlePubMedGoogle Scholar
- Wilson RJM, Pasvol G, Weatherall DJ: Invasion and growth of Plasmodium falciparum in different types of human erythrocytes. Bull World Health Organ. 1977, 55: 79-186.Google Scholar
- Colombo B, Kim B, Atencio RP, Molina C, Terrenato L: The pattern of fetal haemoglobin disappearance after birth. Br J Haematol. 1976, 32: 79-87. 10.1111/j.1365-2141.1976.tb01877.x.View ArticlePubMedGoogle Scholar
- Pasvol G, Weatherall DJ, Wilson RJM: Effects of foetal haemoglobin on susceptibility of red cells to Plasmodium falciparum. Nature. 1977, 270: 171-173. 10.1038/270171a0.View ArticlePubMedGoogle Scholar
- Amaratunga C, Lopera-Mesa TM, Brittain NJ, Cholera R, Arie T, Fujioka H, Keefer JR, Fairhurst RM: A role for fetal hemoglobin and maternal immune IgG in infant resistance to Plasmodium falciparum malaria. PLoS One. 2011, 6: e14798-10.1371/journal.pone.0014798.PubMed CentralView ArticlePubMedGoogle Scholar
- Ramharter M, Adegnika AA, Agnandjil ST, Matsiegui PB, Grobusch MP, Winkler S, Graninger W, Krishna S, Yazdanbakhsh M, Mordmüller B, Lell B, Missinou MA, Mavoungou E, Issifou S, Kremsner PG: History and perspectives of medical research at the Albert Schweitzer Hospital in Lambaréné, Gabon. Wien Klin Wochenschr. 2007, 119: 8-12. 10.1007/s00508-007-0857-5.View ArticlePubMedGoogle Scholar
- Noedl H, Bronnert J, Yingyuen K, Attlmayr B, Kollaritsch H, Fukuda M: Simple histidine-rich protein 2 double-site sandwich enzyme-linked immunosorbent assay for use in malaria drug sensitivity testing. Antimicrob Agents Chemother. 2005, 49: 3575-3577. 10.1128/AAC.49.8.3575-3577.2005.PubMed CentralView ArticlePubMedGoogle Scholar
- Ramharter M, Noedl H, Thimasarn K, Wiedermann G, Wernsdorfer G, Wernsdorfer WH: In vitro activity of tafenoquine in combination with artemisinin against Plasmodium falciparum. Am J Trop Med Hyg. 2002, 67: 39-43.PubMedGoogle Scholar
- Ramharter M, Wernsdorfer WH, Kremsner PG: In vitro activity of quinolines against Plasmodium falciparum in Gabon. Acta Trop. 2004, 90: 55-60. 10.1016/j.actatropica.2003.11.001.View ArticlePubMedGoogle Scholar
- Monatrakul P, Mungthin M, Dondorp AM, Krudsood S, Udomsangpetch R, Wilairatana P, White NJ, Chotivanich K: Modulating effects of plasma containing anti-malarial antibodies on in vitro anti-malarial drug susceptibility in Plasmodium falciparum. Malar J. 2010, 9: 326-10.1186/1475-2875-9-326.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.