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Parasite accumulation in placenta of non-immune baboons during Plasmodium knowlesi infection
Malaria Journal volume 14, Article number: 118 (2015)
Placental malaria (PM) causes adverse pregnancy outcomes in the mother and her foetus. It is difficult to study PM directly in humans due to ethical challenges. This study set out to bridge this gap by determining the outcome of PM in non-immune baboons in order to develop a non-human primate model for the disease.
Ten pregnant baboons were acquired late in their third trimester (day 150) and randomly grouped as seven infected and three non-infected. Another group of four nulligravidae (non-pregnant) infected was also included in the analysis of clinical outcome. Malaria infection was intravenously initiated by Plasmodium knowlesi blood-stage parasites through the femoral vein on 160th day of gestation (for pregnant baboons). Peripheral smear, placental smear, haematological samples, and histological samples were collected during the study period. Median values of clinical and haematological changes were analysed using Kruskal-Wallis and Dunn’s Multiple Comparison Test. Parasitaemia profiles were analysed using Mann Whitney U test. A Spearman’s rank correlation was run to determine the relationship between the different variables of severity scores. Probability values of P <0.05 were considered significant.
Levels of white blood cells increased significantly in pregnant infected (34%) than in nulligravidae infected baboons (8%). Placental parasitaemia levels was on average 19-fold higher than peripheral parasitaemia in the same animal. Infiltration of parasitized erythrocytes and inflammatory cells were also observed in baboon placenta. Malaria parasite score increased with increase in total placental damage score (rs = 0.7650, P <0.05) and inflammatory score (rs = 0.8590, P <0.05). Although the sample size was small, absence of parasitized erythrocytes in cord blood and foetal placental region suggested lack of congenital malaria in non-immune baboons.
This study has demonstrated accumulation of parasitized red blood cells and infiltration of inflammatory cells in the placental intravillous space (IVS) of baboons that are non-immune to malaria. This is a key feature of placental falciparum malaria in humans. This presents the baboon as a new model for the characterization of malaria during pregnancy.
Every year, 125 million women are exposed to the risk of malaria worldwide . In sub-Saharan Africa where malaria burden is high, Plasmodium falciparum causes up to 10,000 cases of malaria-related deaths in pregnancy, mainly due to maternal anaemia, and approximately 200,000 infant deaths annually . In these women, malaria parasites accumulate and sequester in the placental intervillous space (IVS), a condition referred as placental malaria (PM) . PM leads to complications that threaten the lives of both mother and foetus, such as stillbirths, pre-term deliveries, low birth weights, reduction in gestation period, anaemia, and mortality [4,5]. This has socio-economic impact on the affected population .
Over the years, substantial efforts have been made to prevent and control malaria by employing different strategies [2,6,7]. These efforts have encountered major challenges, such as lack of effective vaccines, inadequate animal models and rampant drug resistance . Studies on PM immunopathology have been conducted in rodents. The shortcoming of these studies is that data obtained cannot be correlated to humans because of their difference in reproductive system [8-10]. To bridge this gap, animal models such as non-human primates whose reproductive system mimics the human situation are required in order to produce reliable data [11-13]. Baboons are good animal models for malaria in pregnancy because they have a similar host-pathogen interaction and a reproductive system that is physiologically similar to that of humans [14-18]. This study was designed to describe pathological features and clinical outcomes associated with PM in Plasmodium knowlesi-infected baboons. Results from this study will contribute to the validation of the baboon-P. knowlesi model of malaria in pregnancy.
Experimental animals and parasite isolate
Fourteen female adult baboons (Papio anubis) weighing between 12 Kg and 23 Kg were acquired from the animal facility of Institute of Primate Research (IPR), Kenya, and housed in individual squeeze-back cages (dimensions 0.6×0.6×0.68 m) in the biocontainment facility according to institutional standards. The animals were fed on a standard non-human primate diet, water provided ad libitum and their general health monitored throughout the experimental period . Prior to use, they were determined to be free from simian immunodeficiency virus (SIV), haemoprotozoan and gastrointestinal parasites. Of the 14 baboons, ten were time-mated for the first time (primigrravidae) and their pregnancies confirmed by ultrasound, while four were utilized as nulligraids (non-pregnant).
Experimental infections of baboons
Malaria infection was initiated with 2×105 P. knowlesi H strain, Pk1 (A+) clone blood stage parasites [14,19]. Four out of the ten pregnant baboons and the four nulligravidae were intravenously infected via the femoral vein. For the pregnant baboons whose gestation period is 180 days, infection was initiated on 160th day of their gestation. Prior to infection, cryopreserved P. knowlesi parasites were retrieved and cultured overnight by modification of Rowe et al. method [15,20]. Parasitaemia levels, clinical changes and haematological profiles were monitored throughout the experimental period. Caesarean section (CS) was performed on day 8 post-infection and on the 169th day of gestation for non-infected control baboons, in order to collect intact placentas. Oral treatment with pyrimethamine (1 mg/kg of body weight for three days) was initiated after CS for the pregnant animals and at peak parasitaemia for nulligravidae.
Peripheral blood samples were collected for haematological analysis at three intervals, i.e., baseline (before infection), after infection and after treatment, respectively. Intact placentas were harvested during CS according to standard operating procedures and the delivered infants taken to the nursery soon after birth. Placental and umbilical cord blood was collected according to Brustoski et al.  and Moore et al. , respectively. Umbilical cord and chorionic membrane was stripped off and the placenta placed in sterile 0.1% heparin and 2% penicillin-streptomycin saline buffer.
Parasitaemia and clinical observation
In order to assess the progression of the disease, baboons were monitored for parasitaemia and clinical symptoms, such as fever, appetite, lethargy, and weight changes. Peripheral parasitaemia was determined daily by finger-prick method from day 2 post infection. To determine placental and cord parasitaemia, blood samples collected in capillary tubes were used [21,22]. Thin blood smears were prepared for each animal and parasitaemia determined as described by Ozwara et al. .
Haematological and pathological analysis
Venous blood was collected in heparin tubes and haemoglobin (Hb), red blood cells (RBC) and white blood cells (WBC) counts determined at baseline, after infection and after treatment. Gross pathological examination was done during CS by a veterinary pathologist. Placentas were observed for any form of extensive tearing, damage or gross abnormalities. Several placental biopsy specimens of approximately 2×2 cm were obtained for each placental sample, fixed in 10% neutral buffered formalin and later stained with haematoxylin-eosin (H&E). The stained tissues were examined according to Davison et al.  with a few modifications in order to determine the level of placental damage, inflammatory infiltration, parasite infiltration, and pigmentation scores.
Data was analysed using Graph Pad Prism (version 5.0). Experimental animals were grouped as pregnant infected, nulligravidae infected and pregnant not infected. Median values of clinical and haematological changes of these groups were compared using Kruskal-Wallis statistical test and further analysed using Dunn’s multiple comparison test. Parasitaemia profiles were analysed using Mann Whitney U test. A Spearman’s rank correlation was run to determine the relationship between the different variables of severity scores. Probability values of P <0.05 were considered significant.
This study was carried out under the Malaria Research Programme at the Institute of Primate Research (IPR) located in Karen, Nairobi, Kenya. The Institutional Review Committee (IRC) comprising animal care and use committee (ACUC), scientific review and the research ethics and integrity team approved all protocols and use of animals in this study.
Clinical and haematological outcome
In this study, malaria patency was observed on days 2 and 4 post-infection (PI) in nulligravidae and pregnant infected baboons, respectively. Although peak peripheral parasitaemia (at day 8 PI) was on average 50% higher in nulligravids compared to pregnant baboons, this change was not significant (P = 0.4439) (Figure 1). Changes in weight (P = 0.0925), temperature (P = 0.651), red blood cells (RBC) (P = 0.6121), and Hb (P = 0.12379) levels were not significant. Levels of white blood cells (WBC) increased significantly (P = 0.0133). Further analysis by Dunn’s multiple comparison test revealed that increase in WBC levels was significantly higher between pregnant infected and nulligravidae infected (Figure 2).
Gross pathology in Plasmodium knowlesi-infected baboons
The harvested dams were maroon-red in colour with intact membranes. The maternal surface of the placenta had cotyledons while the foetal surface was densely distributed with blood vessels. Baboon placentas weighed on average 167.3 g and 165.9 g for the infected and non-infected groups, respectively. All animals had no fibrinoids except one (pan3233), which had slightly marked fibrinoids. Slight placental calcification was observed in all groups. Cord insertion was intact either centrally or eccentrically placed and with three blood vessels regardless of the group. Placental praevia was complete and no haemorrhage, whether retro-placental or retro-membranous was observed in all the examined placentas. These observed features present similarity of baboon placenta to human placenta.
Absence of parasitized erythrocytes in cord blood
Thin blood smears prepared from placental maternal surface, foetal surface, cord blood, and maternal peripheral circulation were observed and compared for parasitaemia levels. Placental parasitaemia (from maternal region) was on average 19-fold higher than peripheral parasitaemia in the same animal. This difference was significant (P = 0.00823). Parasitaemia differential count demonstrated the abundance of rings and late stage parasites (schizonts) in peripheral and placental (maternal side) blood samples respectively (Figure 3). In spite of high parasitaemia levels in blood smears from placental maternal section, the absence of parasitized RBC in smears from cord blood and placental foetal region was observed (Table 1). This was further confirmed by histology where H&E slides showed absence of parasitized erythrocytes on the foetal vessel and placental chorionic plate (Figures 4 and 5). Infiltration of parasitized erythrocytes and inflammatory cells such as macrophages, neutrophils and monocytes in the intravillous space (IVS) was observed in the baboon placenta (Figure 4).
Placental damage in Plasmodium knowlesi-infected baboons
H&E-stained placental biopsies were analysed by severity score ranging from 0 to 4, with 0 representing none, 1 representing minimal and 4 representing the most severe according to Davison et al.  with a few modifications. The total score for each parameter was recorded on all layers of the placenta and the average obtained. The infected group had significantly higher scores for damage and inflammation compared to the control group (Table 2). Total placental damage score consisted of fibrin necrosis of the villi (Figure 6), chorionic plate thrombosis, syncytiotrophoblast disruption and chorionic plate syncytiotrophoblast disruption. Malaria parasite score increased with increase in total placental damage score (rs = 0.7650, P <0.05) and inflammatory score (rs = 0.8590, P <0.05). This study demonstrated that placental damage and infiltration of immune cells was directly associated with P. knowlesi infection in baboons and subsequent accumulation in the placenta.
This study demonstrated, for the first time, the infiltration of parasitized RBC and inflammatory cells in the placentas of non-immune baboons. During P. knowlesi infection in pregnancy, symptomatic disease is manifested in combination with increased placental parasitaemia. Consequently, accumulation of parasites in the placental IVS combined with infiltration of inflammatory cells leads to placental damage.
In areas of stable malaria transmission, asymptomatic infections in pregnant women are common, with low clinical malaria presentation due to acquired immunity over time. In contrast, pregnant women in unstable malaria transmission areas, such as the Asia-Pacific region and South America present clinical disease because of low levels of acquired immunity . This study demonstrated higher levels (50%) of parasitaemia in nulligravids compared to pregnant infected baboons, although the difference was not significant. In addition, higher levels of placental parasitaemia were observed compared to peripheral parasitaemia in the same animal. The distribution of parasites in an infected pregnant woman varies with endemicity. The proportion of parasitized erythrocytes is often higher in the placenta than in the peripheral blood in endemic areas [24,25] because infected erythrocytes are preferentially retained in the placenta [26,27]. Haemozoin has also been frequently observed in placentas from malaria-infected women whether in the presence or absence of peripheral parasitaemia [4,28,29]. These findings correlate well with human studies.
Placental falciparum malaria in humans increases neonatal mortality by lowering birth weight while fever is associated with premature birth . Increase in body temperature and reduction in RBC and Hb levels are also observed. According to human studies, it is documented that anaemia is associated with low birth weight, a major determinant of infant mortality associated with P. falciparum . It is estimated that approximately 500,000 pregnant women develop severe anaemia due to falciparum malaria [31,32] and up to 10,000 maternal anaemia-related deaths are as a result of malaria infection in sub-Saharan Africa [33,34]. Severe anaemia is common in children and pregnant women in regions of stable, high malaria transmission such as sub-Saharan Africa, while mild anaemia is common in semi-immune or non-immune populations [35,36]. Reduced level in Hb during malaria infection is an indicator of anaemia while high parasitaemia density has been implicated for reduced Hb levels . A similar observation was demonstrated in this study as displayed by the reduced Hb and RBC levels in P. knowlesi-infected non-immune baboons.
Increased levels of WBC in peripheral circulation and inflammatory cell (monocytes, macrophages and neutrophils) infiltration in H&E-stained tissues obtained from P. knowlesi-infected baboon placentas were observed in this study. Immunosuppression during pregnancy is important in maintaining the foetal allograft. Although some murine and human studies have demonstrated that suppression of cell-mediated immune responses plays a major role in the increased susceptibility to malaria during pregnancy [24,25,38-40], a study conducted in a Plasmodium falciparum hyperendemic area in Tanzania revealed a marked increase in the levels of monocytes and macrophages and cytotoxic T cells in the IVS of placentas with active malaria infection . Findings in this baboon model indicate that placental malaria is not likely to be associated with cell-mediated immunosuppression. The role of immunosuppression in increasing risk to falciparum malarial infection as observed in pregnant women could not be clearly confirmed in this study.
Retroplacental transmission of falciparum malaria parasites from mother to her foetus is rare in humans particularly in CS deliveries. For instance, a study conducted in Burkina Faso, a region of stable malaria transmission, malaria rate in umbilical cord blood occurred in 1.4% of all newborns. This mechanism of congenital transmission was not clear, although it was attributed to several factors [42,43]. However, no such study has been conducted in areas of low or unstable malaria transmission although documented evidence indicates that malaria parasites affect the placenta selectively and are recognized in maternal erythrocytes. In addition, the placenta at full term presents an adequate barrier that prevents malaria parasites from crossing over to the foetal circulation [41,44]. This is similar to what was observed in this study. Although the sample size was small, the constant absence of parasites in placental foetal region and cord blood implies that congenital malaria in non-immune baboons is rare.
This study has also demonstrated accumulation of parasitized erythrocytes in the IVS of the baboon placenta, in addition to high levels of mature forms of the parasite in the placenta. This suggests possible cytoadherence of P. knowlesi parasites in the baboon placenta. It is documented that only the mature falciparum malaria parasites show cytoadherence properties . These parasitized erythrocytes adhere to the endothelium via parasite-derived proteins expressed on their surface . In fact, syncytiotrophoblast cells of the human placenta expresses different and variable amounts of host cell receptors onto which the parasites can bind [45,46]. The principal molecule that mediates adhesion of infected erythrocytes is P. falciparum erythrocyte membrane protein 1 (PfEMP-1), a large, highly variant parasite antigen protein, encoded by the var multigene family . The adhesion phenotypes are not homologous and as a result different parasites can bind to various numbers and combinations of host molecules, such as chondroitin sulphate A (CSA), hyaluronic acid (HA) and Fc receptors [48-50]. In seeking to identify the ligand and receptor molecules associated with accumulation of P. knowlesi infected erythrocytes in the baboon placenta, chondroitin sulphate proteoglycan (CSPG) 4 and HAPLN 1 were predicted as putative receptor molecules in the baboon with high similarity to human CSA and HA respectively. In addition, P. knowlesi erythrocyte binding proteins (EBP-alpha, EBP-beta and EBP-gamma) matched closely to the placental P. falciparum ligand Var2csa . Further work is required to demonstrate the precise ligand-receptor molecules responsible for accumulation of P. knowlesi parasites in baboon placenta.
Histopathological findings demonstrated that PM in baboons is characterized by placental damage due to fibrinous necrosis of the villi, chorionic plate thrombosis, syncytiotrophoblast disruption, chorionic plate syncytiotrophoblast disruption, and thickening of trophoblastic basement membrane. The process was also accompanied with infiltration of inflammatory cells in the placental tissue was. These findings correlate well with human studies where placental falciparum malaria pathology is characterized by excess perivillous fibrinoid deposits, excessive syncytial knotting, trophoblastic membrane thickening, which have been associated with destruction/damage of placental tissues, and proliferation of cytotrophoblastic cells [8,10,25,46,52]. It is hypothesized that placental damage, especially the thickening of the trophoblastic basement membrane, alters the maternal foetal exchange, leading to malaria-associated placental lesions and poor foetal outcomes . The same mechanism is likely to take place in P. knowlesi associated PM in the baboon.
Pathological and clinical features of knowlesi PM in baboons mimic placental falciparum malaria in humans. Compared to other non-human primates used previously, the P. knowlesi-baboon model has demonstrated accumulation of parasitized erythrocytes in the placental IVS, a key feature of placental falciparum malaria in humans. Therefore, this study presents the new baboon model for characterization of malaria in pregnancy. This will, for example, be relevant in understanding host molecular mechanisms involved in sequestration, a key determinant of pathogenesis associated with falciparum and knowlesi malaria in pregnancy.
Animal care and use committee
Chondroitin sulphate A
Chondroitin sulphate proteoglycan 4
Enhancer binding protein
Hyaluronic acid or hyaluronan
Hyaluronan and proteoglycan link protein 1
Haematoxylin and eosin
Institute of Primate Research
Institutional Review Committee
Plasmodium falciparum erythrocyte membrane protein-1
Red blood cells
Simian immunodeficiency virus
White blood cells
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We are grateful to the Director and the staff of the Department of Tropical and Infectious Diseases and the Animal Sciences Department at the Institute of Primate Research for their support and cooperation during the study.
The authors declare that they have no competing interests.
FIO participated in study design, carrying out the experiments, data analysis and drafting the manuscript preparation. OWN and FM helped in sample collection, performing the experiment and drafting the manuscript. NWM and COAO supervised the study and participated in drafting the manuscript. IOF was the pathologist in the study. CLK was the pathologist consultant in malaria and pregnancy. JMM was the northern partner, who together with HSO developed the idea into a research project and obtained funding. HSO conceived the idea, obtained the funding, participated in study and coordination and reviewed the manuscript. All authors read and approved the final manuscript. This work was supported by the research capability strengthening WHO (Grant Number: A 50075) for malaria research in Africa under the Multilateral Initiative on Malaria /Special Programme for Research and Training in Tropical Diseases (WHO-MIM/TDR), awarded to HSO.
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Onditi, F.I., Nyamongo, O.W., Omwandho, C.O. et al. Parasite accumulation in placenta of non-immune baboons during Plasmodium knowlesi infection. Malar J 14, 118 (2015). https://doi.org/10.1186/s12936-015-0631-5
- Placental malaria
- Plasmodium knowlesi