Given the widespread distribution of Plasmodium and helminth infections, and similarities of ecological requirements for disease transmission, coinfection is a common phenomenon in sub-Saharan Africa and elsewhere in the tropics. Interactions of Plasmodium falciparum and soil-transmitted helminths, including immunological responses and clinical outcomes of the host, need further scientific inquiry. Understanding the complex interactions between these parasitic infections is of public health relevance considering that control measures targeting malaria and helminthiases are going to scale.
A cross-sectional survey was carried out in April 2010 in infants, young school-aged children, and young non-pregnant women in south-central Côte d'Ivoire. Stool, urine, and blood samples were collected and subjected to standardized, quality-controlled methods. Soil-transmitted helminth infections were identified and quantified in stool. Finger-prick blood samples were used to determine Plasmodium spp. infection, parasitemia, and hemoglobin concentrations. Iron, vitamin A, riboflavin, and inflammation status were measured in venous blood samples.
Multivariate regression analysis revealed specific association between infection and demographic, socioeconomic, host inflammatory and nutritional factors. Non-pregnant women infected with P. falciparum had significantly lower odds of hookworm infection, whilst a significant positive association was found between both parasitic infections in 6- to 8-year-old children. Coinfected children had lower odds of anemia and iron deficiency than their counterparts infected with P. falciparum alone.
Our findings suggest that interaction between P. falciparum and light-intensity hookworm infections vary with age and, in school-aged children, may benefit the host through preventing iron deficiency anemia. This observation warrants additional investigation to elucidate the mechanisms and consequences of coinfections, as this information could have important implications when implementing integrated control measures against malaria and helminthiases.
In sub-Saharan Africa, parasitic worms (helminths) are among the most common chronic infections, malaria among the most deadly, and coinfection is the norm rather than the exception. Infections with hookworm and Plasmodium can decrease the level of hemoglobin and are therefore associated with anemia. Previous studies have investigated the consequences of coinfection in different age groups and settings, but results are conflicting. Indeed, there is no consensus about detrimental or beneficial effects of a coinfection for the host. We designed a cross-sectional study to determine risk factors for anemia and investigated interactions and discuss potential implications of P. falciparum and hookworm coinfection in three groups of people. Overall, 324 individuals were diagnosed for helminths and Plasmodium infections, anemia, subclinical inflammation, and micronutrient deficiencies, and household’s socioeconomic status was determined based on an asset-index. We found significant associations between hookworm and P. falciparum infections, depending on the age group. Interestingly, 6- to 8-year-old children harboring a coinfection showed significantly lower odds of anemia and iron deficiency than children infected with P. falciparum alone. This observation warrants follow-up studies, as there are important implications when implementing integrated control measures against malaria and helminthiases.
Citation: Righetti AA, Glinz D, Adiossan LG, Koua A-YG, Niamké S, et al. (2012) Interactions and Potential Implications of Plasmodium falciparum-Hookworm Coinfection in Different Age Groups in South-Central Côte d'Ivoire. PLoS Negl Trop Dis 6(11): e1889. doi:10.1371/journal.pntd.0001889
Editor: Francis Mutuku, DVBNTD/CWRU/Emory University, Kenya
Received: April 27, 2012; Accepted: September 17, 2012; Published: November 1, 2012
Copyright: © 2012 Righetti et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study received financial support from the Swiss National Science Foundation (project no. IZ70Z0_123900, http://www.snf.ch/E/Pages/default.aspx). Start-up funding for the establishment and running of the Taabo HDSS has been granted by Fairmed (http://www.fairmed.ch/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Recent estimates indicate that approximately 30% of the world's population is still exposed to malaria and that most clinical events attributable to Plasmodium falciparum are concentrated in the African region . Hookworm (Ancylostoma duodenale and Necator americanus) and other soil-transmitted helminths are also widespread, affecting more than a billion people with an estimated 200 million cases of hookworm infections found in sub-Saharan Africa . Given the widespread distribution of Plasmodium and soil-transmitted helminth infections, and the similarity of ecological requirements for disease transmission, coinfection is a common phenomenon. For instance, it has been estimated that over a quarter of school-aged children in sub-Saharan Africa, are at risk of Plasmodium-hookworm coinfection .
The interactions between soil-transmitted helminths and P. falciparum, including immunological responses and clinical outcomes of the host, are not well understood . While some studies observed an inverse relationship between helminthiases and malaria –, other studies suggest that coinfection may be more frequent than expected by chance, and hence exacerbate disease of a single infection –. These conflicting patterns have been observed in different age groups for both males and females. Importantly, since chronic helminth infection and P. falciparum can lead to anemia, the risk of anemia and iron deficiency among coinfected individuals might be exacerbated .
Risk factors and the consequences of single and multiple species parasite infection may vary depending on setting, age, infection intensity, and the host's nutritional status. A deeper understanding of such risk factors has important public health implications, and it is of considerable relevance as control interventions against malaria and helminthiases are going to scale , .
Here, we report results from a baseline cross-sectional survey as part of a 14-month prospective longitudinal surveillance of anemia in three cohorts (infants aged 6–23 months, children aged 6–8 years, and young women aged 15–25 years) implemented on the site of the recently established Taabo health demographic surveillance system (Taabo HDSS) in south-central Côte d'Ivoire. Emphasis is placed on P. falciparum and helminth infections, and micronutrient deficiencies. The specific objectives of the study reported here were (i) to assess the prevalence and intensity of P. falciparum and helminth infection, (ii) to evaluate the association between P. falciparum and helminth infections in the three population groups, and (iii) to discuss potential implications of P. falciparum-hookworm coinfection in relation to anemia in young school-aged children.
Materials and Methods
Ethical approval was granted by the ethics committee of Basel (EKBB, reference no. 252/09) and Côte d'Ivoire (reference no. 1086 MSHP/CNER). Study investigators were covered by liability insurance (GNA Assurance; Abidjan, Côte d'Ivoire, policy no. 30105811010001). Village authorities and participants were informed about the purpose, procedures, and potential risks and benefits of the study. Written informed consent was obtained from study participants and the parents/guardians of children below the age of 15 years. Suspected clinical malaria (i.e., positive rapid diagnostic test (RDT) and tympanic temperature ≥38°C), severe anemia (i.e., hemoglobin (Hb) <8 g/dl according to national guidelines of Côte d'Ivoire defining anemia requiring appropriate intervention), and helminth infections were treated according to national guidelines.
This study was carried out in the recently established Taabo HDSS, which covers Taabo sub-district located in south-central Côte d'Ivoire . Altitudes of the study area are between 50 and 250 m above sea level. The results presented here stem from the baseline cross-sectional survey of a 14-month prospective longitudinal monitoring, which aims to further the understanding of the etiology of anemia, including measures for prevention and control. The Taabo HDSS consists of a small district town (Taabo Cité), 13 main villages, and over 100 hamlets. Approximately 38,500 people are under demographic and health surveillance. The longitudinal monitoring reported here was implemented in three localities: (i) Taabo Cité, the only small town of Taabo HDSS; (ii) Ahondo, one of the 13 main villages, situated in close proximity to Lake Taabo; and (iii) Katchénou, a hamlet (subsequently designated a small village), located 50 km south of Taabo Cité.
Details of the field procedures have been described elsewhere . In brief, we designed a prospective longitudinal study pertaining to anemia and potential nutritional and parasitic risk factors in three age groups, namely (i) infants (aged 6–23 months), (ii) children in early school-age (6–8 years), and (iii) young women (aged 15–25 years). The choice of these three age groups was based on the high vulnerability of infants and women of childbearing age to the consequences of anemia, and the important exposure, yet non-immunity, of young school-aged children to parasitic infections. Based on an estimated proportion of anemia of 60% in infants and school-aged children and 40% in non-pregnant women, a drop-out rate of 20% and a confidence level of 95%, we intended to sample 137 individuals for each of the three age-groups from the readily available Taabo HDSS database, to produce an accurate estimation of the prevalence of anemia with a 9% error margin. Since the participation rate during the initial sampling phase was lower than expected, all individuals meeting our age (and sex) requirements from Ahondo and Katchénou were invited to participate. In Taabo Cité, a stepwise random sampling was employed and 120 infants, 90 children of early school-age, and 90 young non-pregnant women were selected from the Taabo HDSS database.
Overall, 732 individuals were invited to participate. Venous and finger-prick blood, stool, and urine samples were collected and subjected to standardized, quality-controlled methods to diagnose and quantify Plasmodium and helminth infections, and determine the participants' micronutrient status.
The presence of P. falciparum was determined using finger-prick blood and an RDT (ICT ML01 malaria Pf kit; ICT Diagnostics, Cape Town, South Africa). The determination of Plasmodium species was done with a thin blood film, and parasitemia assessed with a thick blood film. Hb quantification was done with a portable HemoCue Hb 301 device (HemoCue AB; Ängelholm, Sweden).
Duplicate Kato-Katz thick smears (using 41.7 mg templates) were prepared from each stool sample  and examined under a microscope for the presence of soil-transmitted helminth (Ascaris lumbricoides, hookworm, and Trichuris trichiura) and Schistosoma mansoni eggs. The number of eggs was counted and recorded for each species separately. For each individual, the egg counts of both Kato-Katz thick smears were added and multiplied by a factor 12 to obtain a standardized measure of infection intensity (i.e., eggs per gram of stool (EPG)). Urine samples were subjected to a filtration method (10 ml)  and slides quantitatively examined under a microscope for S. haematobium eggs.
For quality control, 10% of the Kato-Katz thick smears and urine filters were reexamined by a senior technician. In case of conflicting results, the slides were reexamined and results discussed with the technicians until consensus was reached.
Venous blood samples were centrifuged, aliquoted, and kept at −20°C before transfer in an ice-cold box to the Centre Suisse de Recherches Scientifiques en Côte d'Ivoire (Abidjan, Côte d'Ivoire) and then to ETH Zurich (Zurich, Switzerland). Riboflavin was measured by the erythrocyte glutathione reductase activity coefficient (EGRAC) assay, using the method of Dror et al.  with some modifications validated in our laboratory. A cut-off value >1.4 was used to define riboflavin deficiency . Serum ferritin, soluble transferrin receptor (sTfR), retinol binding protein (RBP), α1-acid glycoprotein (AGP), and C-reactive protein (CRP) were measured with a sandwich enzyme-linked immunosorbant assay (ELISA) that has been described elsewhere .
Data were entered twice using Microsoft Access version 10.0 (2007 Microsoft Corporation) and the two datasets compared with EpiInfo version 3.4.1 (Centers for Disease Control and Prevention; Atlanta, GA, USA). All statistical analyses were performed with STATA version 10 (StataCorp.; College Station, TX, USA).
Anemia was defined as Hb <11.0 g/dl for infants, <11.5 g/dl for children aged 6–8 years, and <12.0 g/dl for non-pregnant women, according to guidelines put forward by the World Health Organization (WHO) . Storage iron depletion was defined as ferritin <12 µg/l for infants without inflammation, and <15 µg/l for school-aged children and women without inflammation. For participants with AGP >1 g/l or CRP >10 mg/l, storage iron depletion was defined as ferritin <30 µg/l . Cellular iron deficiency was defined as sTfR >8.5 mg/l . Vitamin A deficiency was defined as RBP <0.825 µmol/l .
Only those individuals who had complete datasets (i.e., demographic, parasitological, and micronutrient data) were included for detailed statistical analyses (n = 324). For calculating household socioeconomic status, an asset-based index was constructed for each household of the participants with complete data records, according to a method described by Filmer and Pritchett . In brief, data on household assets (e.g., radio), housing characteristics (e.g., wall type), and number of people per room were obtained from the Taabo HDSS database. The binary data of these variables were weighted using principal component analysis (PCA), and the households were subsequently divided into five socioeconomic groups (wealth quintiles); namely (i) most poor, (ii) very poor, (iii) poor, (iv) less poor, and (v) least poor. The procedure is further explained and illustrated in technical notes provided by the Health, Nutrition, and Population (HNP) Poverty Thematic Group of the World Bank  and elsewhere .
Crude odds ratios (ORs) were calculated for variables potentially associated with P. falciparum (defined as a positive RDT or the presence of Plasmodia on blood films) and hookworm infection. To assess independent predictors of P. falciparum and hookworm infection, a multivariate logistic regression model was fitted and standard error adjusted for potential clustering within household. An independent model was computed for each age group.
Student's t-test and Wilcoxon rank-sum test were used for comparison of means and ranks, respectively. Categorical data were compared using χ2 test or Fisher's exact test, as appropriate.
From the 732 individuals invited to participate in our prospective longitudinal study, 407 (55.6%) provided written informed consent and 324 (44.3%) had complete data records (i.e., anthropometric, hematologic, parasitic, and micronutrient data). The sex ratio was balanced among infants and school-aged children who were lost to follow-up and those with complete data. There was no difference in mean age in infants, school-aged children and women who were lost to follow-up and those with complete data. There was a significant difference in participation rate across study settings (Taabo Cité: 44%, Ahondo: 34%, Katchénou: 64%; p<0.001).
Prevalence of P. falciparum Infection and Parasitemia
According to the RDT and the blood film examinations, 58.0% (95% confidence interval (CI) 52.4–63.5%) of the study participants were found infected with P. falciparum. Children aged 6–8 years showed the highest prevalence (78.2%). The respective prevalence in infants and non-pregnant women were 45.3% and 36.6% (Table 1). Among those found infected with P. falciparum, 30.2% of infants, 9.6% of school-aged children, and 3.3% of young non-pregnant women harbored >5,000 parasites/µl of blood, respectively. Four infants aged between 7 and 14 months and one 8-year-old child presented with clinical malaria.
Prevalence and Intensity of Helminth Infection
Overall, 72 of the 324 participants (22.2%) with complete data records had an infection with soil-transmitted helminths. Hookworm was the predominant species (21.6%), whereas only eight (2.5%) and four (1.2%) individuals were infected with T. trichiura and A. lumbricoides, respectively.
There were only three cases (3.2%) of soil-transmitted helminth infection in infants, whereas a prevalence of 29.9% and 30.5% was found in young school-aged children and non-pregnant women, respectively (Table 1). Among children aged 6–8 years, infection with A. lumbricoides and T. trichiura was found in three and six individuals, whereas one case of T. trichiura was found in non-pregnant women and one case of each T. trichiura and A. lumbricoides was observed among infants.
S. haematobium infection was found in 35 individuals (10.8%) with the highest prevalence observed in non-pregnant women (22.0%). The respective prevalence in school-aged children and infants was 10.2% and 2.1%.
Helminth infections were primarily of low intensity, regardless of the age groups. Only two participants, children aged 6 and 8 years, presented with heavy hookworm infection (≥4000 EPG).
Parameters Associated with P. falciparum and Helminth Infections
Tables 2 and 3 present ORs between demographic, socioeconomic, inflammatory, and micronutrient parameters and P. falciparum and hookworm infection, respectively, as determined by univariate and multivariate logistic regression analyses. Our multivariate regression model revealed that vitamin A deficiency (OR = 10.26, 95% CI 1.89–55.54), inflammation (OR = 4.74, 95% CI 1.12–20.04), and setting (OR (Katchénou) = 30.20, 95% CI 2.60–350.65) were significantly associated with P. falciparum infection in infants. Vitamin A deficiency (OR = 10.79, 95% CI 2.68–43.49), cellular iron deficiency (OR = 5.38, 95% CI 1.56–18.56), inflammation (OR = 5.36, 95% CI 1.78–16.13), and hookworm infection (OR = 7.47, 95% CI 1.84–30.32) were significantly associated with higher odds of P. falciparum infection in children aged 6–8 years. Moreover, the odds of P. falciparum infection among school-aged children were significantly lower for older children (OR (8 years) = 0.25, 95% CI 0.07–0.92). For young non-pregnant women, a concurrent hookworm infection was significantly associated with lower odds of P. falciparum infection (OR = 0.14, 95% CI 0.03–0.60). Non-pregnant women had a lower odds of P. falciparum infection if they belonged to the least poor quintile (OR = 0.06, 95% CI 0.00–0.86).
Following multivariate analysis with hookworm infection as outcome, age 8 years (OR = 4.56, 95% CI 1.11–18.69), infection with P. falciparum (OR = 7.29, 95% CI 1.36–39.23), and setting (OR (Katchénou) = 7.85, 95% CI 1.05–58.82) were significantly positively associated with hookworm infection in school-aged children. Intermediate socioeconomic status was associated with decreased odds of hookworm infection among these children. Furthermore, non-pregnant women infected with P. falciparum had lower odds of hookworm infection (OR = 0.16, 95% CI 0.05–0.55). Multivariate logistic regression showed that setting (Ahondo) was the only variable significantly associated with schistosome infection in children and women.
Prevalence and Implications of P. falciparum-Hookworm Coinfection
As shown in Table 1, P. falciparum-helminth coinfection was most prevalent among children aged 6–8 years. The prevalence of a concurrent infection with Plasmodium and hookworm was 27.9% in school-aged children, whilst the respective prevalence in young non-pregnant women and infants was 4.9% and 1.1%. The prevalence of P. falciparum-Schistosoma coinfection was low in all age groups.
Considering the overall low prevalence of P. falciparum-Schistosoma coinfection and P. falciparum-hookworm coinfection in infants and women, further investigations focused on P. falciparum-hookworm coinfection in the school-aged children. Multivariate regression analysis revealed that sex (OR (female) = 0.33, 95% CI 0.12–0.94) and setting (OR (Ahondo) = 7.53, 95% CI 1.22–46.52; OR (Katchénou) = 11.98, 95% CI 1.64–87.20), was significantly associated with P. falciparum-hookworm coinfection among school-aged children (compared to no infection or single species infection). Other demographic, parasitic, and micronutrient parameters were not significantly associated with coinfection status.
Children coinfected with hookworm and P. falciparum had significantly higher concentrations of Hb (Wilcoxon's rank-sum test, p = 0.038 (n = 115) and lower sTfR concentrations (Wilcoxon's rank-sum test, p = 0.010 (n = 115)) than children infected with P. falciparum alone. Adjusting for socioeconomic status, sex, age, P. falciparum parasitemia, stunting, inflammation status, and setting revealed that children with a coinfection had significantly lower odds of cellular iron deficiency (OR = 0.17, 95% 0.04–0.70) and anemia (OR = 0.23, 95% CI 0.06–0.83) than their counterparts harboring a single infection with P. falciparum. There was an interaction between age and infection status. Table 4 shows the hematological and inflammation data for school-aged children, stratified by 1-year age increments. Children aged 8 years with P. falciparum-hookworm coinfection had significantly higher Hb concentration and lower median values of sTfR, sTfR/log ferritin ratio, and AGP than those infected with P. falciparum alone. There was a similar trend for Hb, sTfR, and sTfR/log ferritin in children aged 7 years.
Our data derived from a baseline cross-sectional survey among three age groups in south-central Côte d'Ivoire confirm that P. falciparum and helminths co-exist with school-aged children at highest risk of coinfection , . We found significant associations between infection status and demographic parameter (age), social-ecological systems (setting and socioeconomic status), and host inflammatory and micronutrient status. Interestingly, young non-pregnant women infected with P. falciparum showed significantly lower odds of concurrent hookworm infection, whilst there was a significant positive association between both infections in children aged 6–8 years. Children coinfected with P. falciparum and hookworm had lower odds of anemia and cellular iron deficiency than their counterparts infected with P. falciparum alone. Our findings therefore underscore that the interactions between P. falciparum and hookworm are complex and may benefit the host in some circumstances.
The finding that, in school-aged children, boys had a significantly higher odds of coinfection might reflect different recreational exposures between genders. Hence, we cannot generalize our findings about parasites interactions in young women (studied here) to young men (not studied) as the two groups might be exposed differently to parasitic infection . In school-aged children, growing older was associated with lower odds of P. falciparum infection, and the infant-group showed highest P. falciparum parasitemia. Moreover, whilst P. falciparum infection was associated with inflammation in infants and school-aged children, there was no significant relationship between both variables in young non-pregnant women. These observations most likely reflect the clinical and parasitological semi-immunity that individuals living in malaria-endemic areas built up and which protect them from high parasitemia, clinical malaria, and facilitates the clearance of Plasmodium . The observation that children aged 8 years had higher odds of hookworm infection compared with their 6-year-old counterparts might be explained by a longer probability of being infected with parasitic worms. Highest helminth infection prevalence is indeed often observed among older children, adolescents, and young adults .
Our findings that children at early school-age who live in remote rural areas (i.e., in this study, Katchénou) are at higher risk of hookworm infection and P. falciparum-hookworm coinfection might be explained by the particularly poor hygiene status and suitable ecological conditions for the parasites life-cycles as well as a difficult access to health care facilities for individuals living in this setting. Indeed, at the time of our study, none of the households in Katchénou had sanitation and all of them obtained drinking water from a community pump. The nearest health center was situated in Sokrogbo, a village located approximately 5 km from Katchénou with difficult access particularly during the rainy season. The observation that remote rural setting (i.e., Katchénou) was significantly associated with P. falciparum infection in infants but not in school-aged children might be explained by the high malaria transmission in this setting, increasing the probability that young infants become infected. The high prevalence of P. falciparum in all the three study groups emphasizes the importance of implementing prevention and control measures against malaria . Among infants aged 6–23 months, 45% were infected with P. falciparum and the parasitemia level in this age group was higher than in children aged 6–8 years and in non-pregnant women aged 15–25 years. Hence, emphasis should be placed on protecting infants from mosquito bites and on effective management of malaria cases during childhood, most importantly in remote areas where prompt access to quality health care remains a formidable challenge.
With regard to micronutrients, it is not surprising that vitamin A deficiency appeared to be associated with P. falciparum infection in infants and school-aged children. Indeed, we have previously shown that P. falciparum infection and vitamin A deficiency are prevalent among infants and school-aged children living in our study area . Furthermore, although WHO does not recommend vitamin A supplementation before 6 months of age –, several studies have shown the role and the importance of vitamin A in the pathology of malaria ,  and, more generally, in the development of the immunological system during childhood –. It has also been observed that vitamin A utilization may increase during a clinical malaria episode , , suggesting a vicious cycle between deficiency in vitamin A and Plasmodium infection. The cross-sectional nature of our study, however, does not allow drawing causal inference. There are several hypotheses for the significant association we found between iron deficiency and P. falciparum infection in infants, based on the hematological and inflammatory consequences of Plasmodium infection. On the one hand, erythropoiesis rate might indirectly be increased in response to Plasmodium infection, to compensate for the loss of erythrocytes through hemolysis and splenic clearance of infected and uninfected erythrocytes. This increased erythropoiesis might, in turn, be translated to increased sTfR concentrations , . On the other hand, the effect of chronic or acute inflammation on sTfR concentrations is still being debated. Whilst several studies have suggested that inflammation inhibits erythropoiesis, others have reported higher sTfR concentrations in individuals with inflammation , . This latest observation might be explained by a secondary hematological response to hepcidin-mediated iron sequestration during inflammatory states.
Interactions and Potential Implications of P. falciparum-Hookworm Coinfection
Interestingly, our results suggest that the negative association observed between P. falciparum and hookworm infection in young non-pregnant women was independent from the social-ecological context. Indeed, multivariate regression analysis showed that this association was independent from age, socioeconomic status, and type of setting of the participating women. We did not find any significant relationship between Hb concentrations and hookworm infection intensity, but it should be kept in mind that our survey was conducted in a setting where helminth infection were primarily of light intensity, probably preventing an important intestinal blood loss in infected subjects . One hypothesis for the observed negative association between P. falciparum and hookworm infection in women is based on the distinct immunological regulations stimulated by the two parasitic infections . Indeed, helminths are known to activate the immune system with a strong polarization toward T helper 2 (Th2) responses. Furthermore, helminths are often able to survive many years in the host through the induction of immmunoregulatory mechanism resulting in an anti-inflammatory environment , . The immune responses to Plasmodium are more complex and depend on the species and the stage of infection. The host response toward early infection is rather based on Th1 activation and the production of pro-inflammatory cytokines . These non-specific reactions switch in later stage of Plasmodium infection to a Th2 cytokines profile, leading to the production of specific antibodies . Hence, one may suggest that women infected with one parasite species have a more efficient immunological system than women free of infection, leading to a more rapid clearance of a concurrent parasitic infection. Of note, many studies have reported a beneficial effect of helminth infection on malaria , , . An alternative hypothesis is that a specific parasitic infection may deprive a concurrent infection of iron or another nutrient necessary for parasite growth, leading to the elimination of the latter acquired infection. In our cohort, however, women infected with hookworm or P. falciparum singly, did not have lower concentrations of serum ferritin or sTfR than their non-infected counterparts. The observation that children aged 6–8 years coinfected with P. falciparum and hookworm had lower odds of cellular iron deficiency and anemia, compared to children infected with P. falciparum alone, adds to the current debate about Plasmodium-helminth coinfection outcomes. A protective effect on anemia has been observed in early school-aged children concurrently infected by P. vivax and soil-transmitted helminths . The observation that 7- and 8-year-old children infected with P. falciparum alone had lower Hb and higher sTfR concentrations compared with children coinfected with hookworm, whilst serum ferritin concentrations were normal in both groups, suggests that mono-infected children might be more prone to anemia due to tissue iron deficiency, potentially associated with inflammation . Of note, AGP and P. falciparum parasitemia were significantly correlated in children infected with P. falciparum alone (n = 67; Spearman's ρ: 0.27; p = 0.025) and this association was not significant for children coinfected with hookworm (n = 39; Spearman's ρ: 0.04; p = 0.807). Moreover, AGP concentrations were significantly higher in 8-year-old coinfected children than in children matched for age infected with P. falciparum only, indicating that inflammation might indeed be less important in coinfected children as compared with children infected with P. falciparum singly. The measure of hepcidin and inflammatory cytokines and implementation of an anthelmintic drug intervention trial would shed new light on this hypothesis.
In conclusion, our findings emphasize that P. falciparum and hookworm infections are associated with demographic, social-ecological, and host inflammatory and micronutrient factors. Coinfection outcomes are complex and might depend on the age and the immune system of the host. New research is needed both in the laboratory and in the field to deepen our understanding of the mechanisms and public health implications of P. falciparum-hookworm coinfection. Our observations that coinfection with P. falciparum and hookworm are particularly prone in a specific age group (i.e., school-aged children) calls for concerted action in this group. Finally, the finding that light hookworm infection may prevent anemia in children coinfected with P. falciparum should be considered when implementing integrated prevention and control measures targeting helminthiases and malaria, and call for a surveillance-response approach, so that specific interventions do not harm existing adaptive immune defense mechanisms which might exacerbate morbidity.
We are grateful to Prof. Bassirou Bonfoh, Director-General of the Centre Suisse de Recherches Scientifiques en Côte d'Ivoire, Mr. Koné Siaka, Mr. Louis Botti, Mr. Fabian Zouzou, and all other Taabo HDSS collaborators for their support and facilitation of the study. Many thanks go the whole team from the Laboratory of Animal Biology at the Unité de Formation et de Recherche Biosciences, Université de Cocody, Abidjan, for all their efforts and their dedicated work in the field and the bench. We would like to thank Mr. Christophe Zeder and Mr. Adam Krzystek for their expertise and help with the laboratory analyses conducted in Switzerland. We thank Dr. Thomas Fürst and Mr. Dimitri Hauri for their input regarding statistical issues. Last but not least, we would like to thank all the study participants for their commitment and willingness to collaborate.
Conceived and designed the experiments: AAR SN RFH RW EKN JU. Performed the experiments: AAR DG LGA AGK EKN. Analyzed the data: AAR JU. Contributed reagents/materials/analysis tools: AAR DG AGK LGA RFH RW EKN JU. Wrote the paper: AR JU.
- 1. Snow RW, Guerra CA, Noor AM, Myint HY, Hay SI (2005) The global distribution of clinical episodes of Plasmodium falciparum malaria. Nature 434: 214–217. doi: 10.1038/nature03342
- 2. de Silva NR, Brooker S, Hotez PJ, Montresor A, Engels D, et al. (2003) Soil-transmitted helminth infections: updating the global picture. Trends Parasitol 19: 547–551. doi: 10.1016/j.pt.2003.10.002
- 3. Brooker S, Clements ACA, Hotez PJ, Hay SI, Tatem AJ, et al. (2006) The co-distribution of Plasmodium falciparum and hookworm among African schoolchildren. Malar J 5: 99.
- 4. Hartgers FC, Yazdanbakhsh M (2006) Co-infection of helminths and malaria: modulation of the immune responses to malaria. Parasite Immunol 28: 497–506. doi: 10.1111/j.1365-3024.2006.00901.x
- 5. Murray J, Murray A, Murray M, Murray C (1978) The biological suppression of malaria: an ecological and nutritional interrelationship of a host and two parasites. Am J Clin Nutr 31: 1363–1366.
- 6. Brutus L, Watier L, Hanitrasoamampionona V, Razanatsoarilala H, Cot M (2007) Confirmation of the protective effect of Ascaris lumbricoides on Plasmodium falciparum infection: results of a randomized trial in Madagascar. Am J Trop Med Hyg 77: 1091–1095.
- 7. Kung'u JK, Goodman D, Haji HJ, Ramsan M, Wright VJ, et al. (2009) Early helminth infections are inversely related to anemia, malnutrition, and malaria and are not associated with inflammation in 6- to 23-month-old Zanzibari children. Am J Trop Med Hyg 81: 1062–1070. doi: 10.4269/ajtmh.2009.09-0091
- 8. Melo GC, Reyes-Lecca RC, Vitor-Silva S, Monteiro WM, Martins M, et al. (2010) Concurrent helminthic infection protects schoolchildren with Plasmodium vivax from anemia. PLoS One 5: e11206. doi: 10.1371/journal.pone.0011206
- 9. Nacher M, Singhasivanon P, Yimsamran S, Manibunyong W, Thanyavanich N, et al. (2002) Intestinal helminth infections are associated with increased incidence of Plasmodium falciparum malaria in Thailand. J Parasitol 88: 55–58. doi: 10.2307/3285390
- 10. Spiegel A, Tall A, Raphenon G, Trape JF, Druilhe P (2003) Increased frequency of malaria attacks in subjects co-infected by intestinal worms and Plasmodium falciparum malaria. Trans R Soc Trop Med Hyg 97: 198–199. doi: 10.1016/s0035-9203(03)90117-9
- 11. Yatich NJ, Yi J, Agbenyega T, Turpin A, Rayner JC, et al. (2009) Malaria and intestinal helminth co-infection among pregnant women in Ghana: prevalence and risk factors. Am J Trop Med Hyg 80: 896–901.
- 12. Pullan RL, Kabatereine NB, Bukirwa H, Staedke SG, Brooker S (2011) Heterogeneities and consequences of Plasmodium species and hookworm coinfection: a population based study in Uganda. J Infect Dis 203: 406–417. doi: 10.1093/infdis/jiq063
- 13. Brooker S, Akhwale W, Pullan R, Estambale B, Clarke SE, et al. (2007) Epidemiology of Plasmodium-helminth co-infection in Africa: populations at risk, potential impact on anemia, and prospects for combining control. Am J Trop Med Hyg 77: 88–98.
- 14. Hotez PJ, Molyneux DH, Fenwick A, Kumaresan J, Ehrlich Sachs S, et al. (2007) Control of neglected tropical diseases. N Engl J Med 357: 1018–1027. doi: 10.1056/nejmra064142
- 15. Murray CJL, Rosenfeld LC, Lim SS, Andrews KG, Foreman KJ, et al. (2012) Global malaria mortality between 1980 and 2010: a systematic analysis. Lancet 379: 413–431. doi: 10.1016/s0140-6736(12)60034-8
- 16. N'Goran EK, Diabate S, Utzinger J, Sellin B (1997) Changes in human schistosomiasis levels after the construction of two large hydroelectric dams in central Côte d'Ivoire. Bull World Health Organ 75: 541–545.
- 17. Righetti AA, Koua AYG, Adiossan LG, Glinz D, Hurrell RF, et al. (2012) Etiology of anemia among infants, school-aged children, and young non-pregnant women in different settings of south-central Côte d'Ivoire. Am J Trop Med Hyg 87: 425–434. doi: 10.4269/ajtmh.2012.11-0788
- 18. Katz N, Chaves A, Pellegrino J (1972) A simple device for quantitative stool thick-smear technique in schistosomiasis mansoni. Rev Inst Med Trop São Paulo 14: 397–400.
- 19. WHO (1991) Basic laboratory methods in medical parasitology. Geneva: World Health Organization, 121 p.
- 20. Dror Y, Stern F, Komarnitsky M (1994) Optimal and stable conditions for the determination of erythrocyte glutathione reductase activation coefficient to evaluate riboflavin status. Int J Vitam Nutr Res 64: 257–262.
- 21. Sauberlich HE (1999) Vitamin B-2. Laboratory tests for the assessment of nutritional status, 2nd ed. Boca Raton: CRC Press, pp. 55–65.
- 22. Erhardt JG, Estes JE, Pfeiffer CM, Biesalski HK, Craft NE (2004) Combined measurement of ferritin, soluble transferrin receptor, retinol binding protein, and C-reactive protein by an inexpensive, sensitive, and simple sandwich enzyme-linked immunosorbent assay technique. J Nutr 134: 3127–3132.
- 23. WHO/UNICEF/UNU (2001) Iron deficiency anemia: assessment, prevention and control: a guide for programme managers. Geneva: World Health Organization, p. 114.
- 24. Cook JD, Skikne BS, Baynes RD (1993) Serum transferrin receptor. Annu Rev Med 44: 63–74. doi: 10.1146/annurev.me.44.020193.000431
- 25. Gorstein JL, Dary O, Pongtorn, Shell-Duncan B, Quick T, et al. (2008) Feasibility of using retinol-binding protein from capillary blood specimens to estimate serum retinol concentrations and the prevalence of vitamin A deficiency in low-resource settings. Public Health Nutr 11: 513–520. doi: 10.1017/s1368980007000821
- 26. Filmer D, Pritchett LH (2001) Estimating wealth effects without expenditure data—or tears: an application to educational enrollments in states of India. Demography 38: 115–132. doi: 10.1353/dem.2001.0003
- 27. Gwatkin DR, Rutstein S, Johnson K, Suliman E, Wagstaff A, et al.. (2007) Socio-economic differences in health, nutrition, and population: Côte d'Ivoire. Washington DC: World Bank, 71 p.
- 28. O'Donnell O, van Doorslaer E, Wagstaff A, Lindelow M (2008) Analyzing health equity using household survey data. A guide to techniques and their implementation. Washington DC: World Bank, p. 220.
- 29. N'Goran EK, Utzinger J, Gnaka HN, Yapi A, N'Guessan NA, et al. (2003) Randomized, double-blind, placebo-controlled trial of oral artemether for the prevention of patent Schistosoma haematobium infections. Am J Trop Med Hyg 68: 24–32.
- 30. Becker SL, Sieto B, Silué KD, Adiossan L, Koné S, et al. (2011) Diagnosis, clinical features, and self-reported morbidity of Strongyloides stercoralis and hookworm infection in a co-endemic setting. PLoS Negl Trop Dis 5: e1292. doi: 10.1371/journal.pntd.0001292
- 31. Zuk M, McKean KA (1996) Sex differences in parasite infections: patterns and processes. Int J Parasitol 26: 1009–1023. doi: 10.1016/s0020-7519(96)80001-4
- 32. Doolan DL, Dobano C, Baird JK (2009) Acquired immunity to malaria. Clin Microbiol Rev 22: 13–36. doi: 10.1128/cmr.00025-08
- 33. Hotez PJ, Bundy DAP, Beegle K, Brooker S, Drake L, et al.. (2006) Helminth infections: soil-transmitted helminth infections and schistosomiasis. In: Jamison DT, Breman JG, Measham AR, Alleyne G, Claeson M, et al.. (eds) Disease control priorities in developing countries. 2nd edition, Washington DC: World Bank, pp. 467–482.
- 34. WHO (2011) World malaria report 2011. Geneva: World Health Organization.
- 35. WHO (1997) Vitamin A supplements: a guide to their use in the treatment and prevention of vitamin A deficiency and xerophtalmia. Geneva: World Health Orgnanization.
- 36. WHO (2011) Neonatal vitamin A supplementation. Geneva: World Health Organization.
- 37. WHO (2011) Vitamin A supplementation in infants 1–5 months of age. Geneva: World Health Organization.
- 38. Shankar AH, Genton B, Semba RD, Baisor M, Paino J, et al. (1999) Effect of vitamin A supplementation on morbidity due to Plasmodium falciparum in young children in Papua New Guinea: a randomised trial. Lancet 354: 203–209. doi: 10.1016/s0140-6736(98)08293-2
- 39. Serghides L, Kain KC (2002) Mechanism of protection induced by vitamin A in falciparum malaria. Lancet 359: 1404–1406. doi: 10.1016/s0140-6736(02)08360-5
- 40. West KP Jr, Pokhrel RP, Katz J, LeClerq SC, Khatry SK, et al. (1991) Efficacy of vitamin A in reducing preschool child mortality in Nepal. Lancet 338: 67–71. doi: 10.2307/1966692
- 41. Ross DA (1993) on behalf of the Ghana Vitamin A Supplementation Trials Study Team (1993) Vitamin A and childhood mortality. Lancet 342: 861. doi: 10.1016/0140-6736(93)92717-8
- 42. Jones G, Steketee RW, Black RE, Bhutta ZA, Morris SS (2003) How many child deaths can we prevent this year? Lancet 362: 65–71. doi: 10.1016/s0140-6736(03)13811-1
- 43. Galan P, Samba C, Luzeau R, Amedee-Manesme O (1990) Vitamin A deficiency in pre-school age Congolese children during malarial attacks. Part 2: impact of parasitic disease on vitamin A status. Int J Vitam Nutr Res 60: 224–228.
- 44. Thurnham DI, Singkamani R (1991) The acute phase response and vitamin A status in malaria. Trans R Soc Trop Med Hyg 85: 194–199. doi: 10.1016/0035-9203(91)90017-s
- 45. Mockenhaupt FP, May J, Stark K, Falusi AG, Meyer CG, et al. (1999) Serum transferrin receptor levels are increased in asymptomatic and mild Plasmodium falciparum-infection. Haematologica 84: 869–873.
- 46. Menendez C, Quinto LL, Kahigwa E, Alvarez L, Fernandez R, et al. (2001) Effect of malaria on soluble transferrin receptor levels in Tanzanian infants. Am J Trop Med Hyg 65: 138–142.
- 47. Weiss G, Goodnough LT (2005) Anemia of chronic disease. N Engl J Med 352: 1011–1023. doi: 10.1056/nejmra041809
- 48. Grant FK, Suchdev PS, Flores-Ayala R, Cole CR, Ramakrishnan U, et al. (2011) Correcting for inflammation changes estimates of iron deficiency among rural Kenyan preschool children. J Nutr 142: 105–111. doi: 10.3945/jn.111.146316
- 49. Stoltzfus RJ, Albonico M, Chwaya HM, Savioli L, Tielsch J, et al. (1996) Hemoquant determination of hookworm-related blood loss and its role in iron deficiency in African children. Am J Trop Med Hyg 55: 399–404.
- 50. Maizels RM, Yazdanbakhsh M (2003) Immune regulation by helminth parasites: cellular and molecular mechanisms. Nat Rev Immunol 3: 733–744. doi: 10.1038/nri1183
- 51. Taylor MD, LeGoff L, Harris A, Malone E, Allen JE, et al. (2005) Removal of regulatory T cell activity reverses hyporesponsiveness and leads to filarial parasite clearance in vivo. J Immunol 174: 4924–4933.
- 52. Choudhury HR, Sheikh NA, Bancroft GJ, Katz DR, De Souza JB (2000) Early nonspecific immune responses and immunity to blood-stage nonlethal Plasmodium yoelii malaria. Infect Immun 68: 6127–6132. doi: 10.1128/iai.68.11.6127-6132.2000
- 53. Langhorne J, Cross C, Seixas E, Li C, von der Weid T (1998) A role for B cells in the development of T cell helper function in a malaria infection in mice. Proc Natl Acad Sci U S A 95: 1730–1734. doi: 10.1073/pnas.95.4.1730
- 54. Lyke KE, Dabo A, Arama C, Daou M, Diarra I, et al. (2012) Reduced T regulatory cell response during acute Plasmodium falciparum infection in Malian children co-infected with Schistosoma haematobium. PLoS One 7: e31647. doi: 10.1371/journal.pone.0031647