In many parts of sub-Saharan Africa, urogenital and intestinal schistosomiasis co-occur, and mixed species infections containing both Schistosoma haematobium and S. mansoni can be common. During co-infection, interactions between these two species are possible, yet the extent to which such interactions influence disease dynamics or the outcome of control efforts remains poorly understood.
Here we analyse epidemiological data from three West African countries co-endemic for urogenital and intestinal schistosomiasis (Senegal, Niger and Mali) to test whether the impact of praziquantel (PZQ) treatment, subsequent levels of re-infection or long-term infection dynamics are altered by co-infection. In all countries, positive associations between the two species prevailed at baseline: infection by one species tended to predict infection intensity for the other, with the strength of association varying across sites. Encouragingly, we found little evidence that co-infection influenced PZQ efficacy: species-specific egg reduction rates (ERR) and cure rates (CR) did not differ significantly with co-infection, and variation in treatment success was largely geographical. In Senegal, despite positive associations at baseline, children with S. mansoni co-infection at the time of treatment were less intensely re-infected by S. haematobium than those with single infections, suggesting competition between the species may occur post-treatment. Furthermore, the proportion of schistosome infections attributable to S. mansoni increased over time in all three countries examined.
These findings suggest that while co-infection between urinary and intestinal schistosomes may not directly affect PZQ treatment efficacy, competitive interspecific interactions may influence epidemiological patterns of re-infection post-treatment. While re-infection patterns differed most strongly according to geographic location, interspecific interactions also seem to play a role, and could cause the community composition in mixed species settings to shift as disease control efforts intensify, a situation with implications for future disease management in this multi-species system.
In many parts of Africa both urinary and intestinal schistosomiasis are endemic, and mixed species infections can be common. However, little is known about potential within-host interactions between the causative parasites, S. haematobium and S. mansoni, and how these might influence treatment success and post-treatment patterns of re-infection. Here, we bring together datasets from three West African countries to examine the epidemiological evidence for interactions between these two schistosome species relevant to the impact of treatment programmes using praziquantel (PZQ). Encouragingly, PZQ efficacy (in a double 40mg/kg dose format) was not significantly altered by co-infection, though since co-infections tended to be heavier, complete clearance was less likely than for single species infections. Despite positive associations in infection intensity for these two species at baseline, Senegalese children that were successfully treated for S. haematobium showed less intense re-infection if they were co-infected with S. mansoni at the point of treatment. Furthermore, in all three settings, the proportion of infections attributable to S. mansoni increased over successive rounds of PZQ treatment. These data suggest asymmetric competition may occur between S. haematobium and S. mansoni in the context of drug treatment, which may alter schistosome species composition as PZQ-based control programmes proceed.
Citation: Knowles SCL, Webster BL, Garba A, Sacko M, Diaw OT, Fenwick A, et al. (2015) Epidemiological Interactions between Urogenital and Intestinal Human Schistosomiasis in the Context of Praziquantel Treatment across Three West African Countries. PLoS Negl Trop Dis 9(10): e0004019. https://doi.org/10.1371/journal.pntd.0004019
Editor: Giovanna Raso, Swiss Tropical and Public Health Institute, SWITZERLAND
Received: February 10, 2015; Accepted: July 30, 2015; Published: October 15, 2015
Copyright: © 2015 Knowles 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
Data Availability: Datafiles used in analysis are freely available on the DRYAD data repository through the provisional DOI number doi:10.5061/dryad.760r5.
Funding: The Senegal and Niger studies were funded by the EU grant CONTRAST (FP6 STREP contract no: 032203, http://www.eu-contrast.eu, and Mali data collection was funded by a Bill and Melinda Gates Foundation Grant to the Schistosomiasis Control Initiative (SCI). SCLK was funded by ICOSA funding from the Department for International Development (UK) to to SCI. 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.
Globally, at least 230 million people are estimated to have schistosomiasis . In sub-Saharan Africa where the disease burden is highest, Schistosoma haematobium and S. mansoni, causing urogenital and intestinal schistosomiasis respectively, frequently overlap in their geographic distribution [2–5] as do their respective snail hosts Bulinus and Biompharia spp. In such areas, mixed species infections can be common [6–10], and may be even more widespread than currently recognised if diagnostic methods with greater sensitivity than standard microscopy are applied .
Co-infection with both S. haematobium and S. mansoni generates the potential for within-host parasite interactions, whereby the presence of one species may alter the course of infection or disease caused by the other. Such interactions could arise through competition for nutrients or mates, or immune-mediated mechanisms, including cross-reactive immune responses. Immune-mediated interactions may also arise through or be affected by drug treatment, if species differ in drug susceptibility, or if the drug in question alters host immunity in a way that favours one species over another [12, 13]. Although rarely investigated, such interspecific interactions may have important implications for schistosomiasis epidemiology, associated morbidity, and the effectiveness of control measures including PZQ treatment, the cornerstone of current schistosomiasis control programmes .
Evidence for biologically relevant interactions between co-infecting S. haematobium and S. mansoni comes from studies in animal models as well as humans. These two species can engage in mate competition, since during co-infection, infertile interspecific mating pairs form resulting in the release of ectopic eggs: S. haematobium eggs in faeces or S. mansoni eggs in urine [7, 15–17]. Moreover, mixed species infections produce different morbidity profiles in humans, altering the relative levels of bladder and liver morbidity [6, 8, 15, 18, 19]. Immune-mediated competition between S. haematobium and S. mansoni has also been reported in animal models [20–22] and immunological studies suggest widespread cross-reactivity among antigenic epitopes from different schistosome species .
However, exactly how such interactions might play out in epidemiological settings, and in the context of mass PZQ treatment, remains underexplored. In parts of Africa the species composition of schistosomiasis infections has shifted notably over time. At sites in Senegal, Niger, Cameroon and Egypt, S. mansoni has been introduced through changes in irrigation (e.g. dam construction), and has been seen to increase in prevalence and subsequently ‘take over’ from S. haematobium 24–29]. While changes in the distribution and relative abundance of Biomphalaria and Bulinus snails following water resource development have undoubtedly played a key role in such shifts [25, 28, 30, 31], whether and how within-host interactions between S. haematobium and S. mansoni might influence schistosomiasis epidemiology remains to be fully investigated. PZQ treatment could also alter the relative abundance of these two species, if drug efficacy varies between species or during co-infection, or if treatment alters interspecific interactions during re-infection . With increasing momentum behind scaling up schistosomiasis control programmes across much of Africa , there is a clear need to understand how each species responds to treatment, whether these responses depend on the parasite community context, and the implications for epidemiology and morbidity.
Here, we use three epidemiological datasets from co-endemic areas of West Africa (Senegal, Niger and Mali) to investigate potential interactions between S. haematobium and S. mansoni in the context of PZQ treatment. In particular, we examine whether PZQ efficacy is altered by co-infection, the impact of co-infection on individual re-infection post-treatment, and how schistosome species composition, as well as prevalence and mean intensity of infection changes over the course of successive treatment rounds at the population level.
Study sites and datasets
Two of the datasets analysed here come from co-endemic villages in Niger  and Senegal  collected as part of the CONTRAST project, while the third comes from sentinel sites monitored as part of Mali’s schistosomiasis control programme monitoring and evaluation activities . These datasets are described in more detail below, their characteristics are summarised in Table 1, and their locations are shown in Fig 1.
Data were collected in 2007–8 from two villages (Nder and Temeye) in the Senegal River Basin (Fig 1). In previous work , village-level variation in PZQ efficacy and re-infection dynamics was documented over a one-year period at these sites. Here, we extend analysis of these data to consider the influence of individual co-infection status on PZQ efficacy, parasite clearance and re-infection dynamics. Full details on these sites and study design are given in , but a brief description of the study design follows. At baseline, children aged 5 to 15 were recruited in each village, given a unique identification number, and asked to provide a single urine and stool sample on three consecutive mornings. S. haematobium egg counts were made from filtrations of 10 ml of urine using the standard urine filtration method, and duplicate Kato-Katz thick smears were examined from each stool sample in order to calculate the number of S. mansoni eggs per gram of stool. Only children infected with either S. haematobium, S. mansoni, or both species were recruited into the follow-up study if consenting, and all infected children were then treated with two 40mg/kg doses of PZQ, spaced 3 weeks apart. Follow-up surveys were conducted at 6 weeks after baseline/the first PZQ dose (to monitor PZQ efficacy), 6 months from baseline and 12 months from baseline. All children were screened for both S. haematobium and S. mansoni at each time point, using the same diagnostics used at baseline. No treatment was given at the 6 week follow-up, but all children were given two 40mg/kg PZQ doses 3 weeks apart at both the 6 and 12 month follow ups. For S. haematobium, the number of eggs per 10ml urine was calculated for each sample, and infection intensity taken as the mean of these values across all available samples from a 3-day sampling period. For S. mansoni, infection intensity was taken as the mean number of eggs per gram of stool across all samples from the 3-day sampling period.
Data were collected in 2007–8 from two S. haematobium/S. mansoni co-endemic villages situated in the western part of the country along the Niger River—Diambala and Namarigoungou. The study design was very similar to the Senegal study described above, and is described fully in . Briefly, children aged 6 to 15 infected with either S. haematobium or S. mansoni were recruited into the study at baseline, given unique identifiers, and follow-up surveys were conducted at 6 weeks, 6 months and 12 months from baseline. As in Senegal, two 40mg/kg doses of PZQ were given to all infected children after recruitment, and to all children in the study at the 12-month sampling point, irrespective of infection status. However, unlike in Senegal, no treatment was given 6 months from baseline. At each survey time-point, all children were screened for both S. haematobium and S. mansoni using the same diagnostic techniques used in the Senegal study, with the exception that one Kato-Katz slide was read per stool sample rather than two.
The Malian data analysed here formed part of the Monitoring and Evaluation component of the Mali National Schistosomiasis Control Program, supported by the Schistosomiasis Control Initiative (SCI). In 2004, a set of 33 schools (sentinel sites) were randomly selected from all schools in three regions known a priori to be highly endemic for schistosomiasis: Bamako, Ségou, and Koulikoro. Only the 29 schools that were co-endemic for S. haematobium and S. mansoni at baseline are included in the analyses presented here, as our focus is on individual level determinants of infection traits, rather than site to site variation in co-endemicity. Baseline data were collected in 2004. At each school, 50–110 children (approximately equal numbers of boys and girls) aged 7 to 14 years old were recruited, irrespective of infection status. Participants were asked to provide a single stool sample, and two urine samples on two consecutive days. Urine filtration and Kato-Katz examinations were carried out as described in , and infection intensity was calculated as the arithmetic mean number of S. haematobium eggs per 10ml urine, or mean number of S. mansoni eggs per gram of stool. Two subsequent follow-up surveys were conducted on this cohort in 2005 and 2006, immediately prior to annual PZQ administration by the national control programme.
All statistical analyses were performed in R v3.1.1. Descriptive statistics (prevalence, mean infection intensity and confidence intervals) were calculated using the survey package , accounting for clustering of the data by school or village where necessary. The significance of model terms was assessed using likelihood ratio tests, which compared full models to models excluding the term of interest.
Baseline associations between S. haematobium and S. mansoni.
First, we tested whether the likelihood of infection by each schistosome species depended on co-infection with the other, using baseline data from Mali where children were recruited irrespective of infection status. Binomial generalized linear mixed models (GLMMs) with a logit link were performed using the glmer function in package lme4, with either S. haematobium or S. mansoni infection status as the response, and school fitted as a random intercept term. All children at the 29 co-endemic Malian schools surveyed at baseline were included. Co-infection status was coded according to WHO infection intensity categories: for S. haematobium, uninfected, light (<50 eggs/10ml urine) or heavy (≥50eggs/10ml urine) infection, and for S. mansoni, uninfected, light (1–99 epg), moderate (100–399 epg), or heavy (≥400 epg) infection. Linear and quadratic terms for age (mean-centred) were included as covariates, as well as gender and geographic region (as a 3-level factor). An interaction term between region and co-infection status was also examined to test for geographic heterogeneity in schistosome species associations. For all countries we also assessed whether baseline infection intensity was associated with co-infection, by modelling log-transformed egg counts for a given species as a function of co-infection status, age, gender and location (as a 2-level factor for village in both Senegal and Niger, and a 3-level factor for region in Mali). These infection intensity analyses included infected children only.
PZQ efficacy and parasitological cure.
Data on the immediate effect of PZQ (6 weeks after the first of two 3-week spaced treatments) were available for four villages in Senegal and Niger. To examine whether co-infection might influence PZQ efficacy, for each country we calculated the egg reduction rate (ERR) for each schistosome species, in single and co-infected individuals respectively. ERR was calculated using the formula recommended in WHO guidelines , as the difference between the (arithmetic) mean pre- and post-intervention egg counts divided by the mean pre-intervention egg count, multiplied by 100. The calculation included only individuals infected with the focal species at baseline, with known baseline co-infection status, and for which an egg count at 6 weeks post-treatment was available. Although a wide range of formulas has been used in the past to calculate ERR, this formula was used as it has been shown to be the most robust metric for evaluating drug efficacy [36, 37]. Permutation tests were used to examine whether ERR differed significantly (p<0.05) according to co-infection status. We also calculated species-specific cure rates (CR)—the proportion of infected individuals that cleared infection six weeks after the first PZQ dose, by country and co-infection status. With the exception of S. haematobium in Niger (for which parasitological cure was almost universal) we modelled factors affecting individual parasite clearance 6 weeks after PZQ using binomial GLMs. Alongside co-infection status as the key predictor of interest, a number of covariates were controlled for in these models, including initial infection intensity of the focal species (as logged epg or eggs/10ml urine) to control for differences in efficacy arising from varying infection intensity and village.
Longitudinal dynamics and re-infection.
Using the Mali dataset, we examined whether individuals’ probability of infection changed across annual rounds of PZQ treatment, according to their initial co-infection status. These analyses involved a subset of 20 schools from the original 29 co-endemic sentinel sites, as these had follow-up data for both S. haematobium and S. mansoni from all three years. We constructed a binomial GLMM, with S. haematobium or S. mansoni infection status as the response, and school and child ID included as random intercept terms. Fixed effects for baseline co-infection status (as a 3 or 4-level factor, depending on the species), year (as a 3-level factor: baseline, first and second follow-up) and their interaction term were used to examine whether temporal changes in infection for each species differed according to initial co-infection status. Region, gender and mean-centred age at baseline (linear and quadratic term) were fitted as covariates. Only children monitored at all three time-points (baseline, first and second follow-up years) were included, such that we analysed changes in infection probability over time in the same set of individuals. To examine whether drop-out from the Malian cohort might be biased according to children’s infection status at baseline, we used a binomial mixed model to test which baseline variables predicted whether children had full follow-up data. School was fitted as a random intercept term, alongside S. haematobium and S. mansoni infection categories, with region, gender and mean-centred age at baseline (linear and quadratic term) as covariates.
In Senegal and Niger it was also possible to separate effects of co-infection on parasite clearance from those on re-infection (the latter potentially including recommencement of egg-shedding by uncleared worms), since individuals were monitored six weeks after PZQ treatment. For each schistosome species, we used a binomial GLM with a logit link to test whether, among individuals infected at baseline but clear of infection 6 weeks later (after PZQ treatment), the probability of being re-infected 6 months from baseline depended on baseline co-infection status (single vs. co-infected). Covariates included were village, baseline intensity category for the focal species (2-level factor for S. haematobium: light vs. heavy; 3-level factor for S. mansoni: light, moderate or heavy), gender and mean-centred age (as a linear and quadratic term). An interaction term between village and co-infection status was also included to test for geographic heterogeneity in the influence of co-infection. Among the same individuals, we also used negative binomial GLMs (using the glm.nb function in the MASS package) to examine whether the intensity of re-infection at six months (eggs/gram stool for S. mansoni, or eggs/10ml urine for S. haematobium) was dependent on co-infection status at baseline, including the same covariates used in the binomial re-infection models.
Full details on ethical approval granted are provided in the original publications from which these data were gathered. In brief, ethical approval was obtained from the St Mary’s Hospital Local Ethics Research Committee, R&D office (part of the Imperial College, London Research Ethics Committee (ICREC; EC NO: 03.36. R&D No: 03/SB/033E) in combination with the ongoing CONTRAST and SCI activities. Within Niger, Senegal and Mali, all aspects of sample collections were carried out in the framework of the disease control activities implemented and approved by the Ministry of Health (MOH) and adopted by regional and local administrative and health authorities. In Senegal and Niger, the communities of the selected villages were informed about the objectives, the methodology of the study and the advantages. A meeting was organized with the population and verbal community consent was obtained for each selected village. Written and verbal consent was also obtained from school directors and teachers, as well as the children’s parents, prior to the recruitment of the children. Verbal assent was given by every child and their acceptance documented. Participation was voluntary and children could withdraw or be withdrawn from the study at any time without obligation. Results of the different diagnostic procedures performed on children were briefly explained to them. In Senegal and Niger, all children diagnosed as infected with schistosomiasis were immediately treated with 40mg/kg. In Mali, all children at participating schools were treated shortly after each survey, as part of the national schistosomiasis control programme activities.
Baseline associations between S. haematobium and S. mansoni
At baseline, associations between the two schistosome species were generally positive, although varied in strength across countries and regions. In Mali, infection probability for both schistosome species was positively predicted by the level of infection with the other species, after controlling for age and gender effects (Table 2). This relationship varied in strength across geographical regions (S. haematobium: S. mansoni*region interaction χ26 = 22.28, p = 0.001; S. mansoni: S. haematobium*region interaction: χ24 = 12.63, p = 0.013, Fig 2). Among infected individuals, infection intensity increased with the intensity of co-infection for both schistosome species, although again the strength of this relationship varied across countries and regions (Table 3; Fig 3). Across the 29 schools in Mali, these positive relationships for both S. haematobium and S. mansoni infection intensity were usually observed within each school, with few exceptions (Fig A in S1 Text).
Parameter estimates (on the logit scale) are from binomial mixed models. χ2 and p values are from likelihood ratio tests comparing models with and without the term in question. Age was mean-centred in both analyses. ‘ref’ indicates the reference level of each factor.
Raw data are plotted with 95% exact confidence intervals, which account for clustering of prevalence data by school. Patterns are plotted separately for each of the three regions surveyed in Mali.
Results are from Gaussian GLMs (Senegal and Niger), or GLMMs with school as a random intercept term (Mali), using log transformed egg counts among infected individuals only (eggs/10ml urine or eggs/gram stool) as the response. χ2 and p values show results of likelihood ratio tests. Parameters from full models are shown, and age was mean-centred in analyses. ‘ref’ indicates the reference level of each factor.
Co-infection and the impact of PZQ
In both Senegal and Niger, egg reduction rates 6 weeks after the first PZQ dose did not differ significantly according to co-infection status, for either S. haematobium or S. mansoni (Table 4). Thus, there was no evidence that co-infection altered the efficacy of double dose PZQ.
p-values comparing ERRs in single and co-infected subsets of individuals were derived using permutation tests. Numbers of individuals involved in each calculation are shown in brackets.
Raw cure rates for each village and schistosome species according to co-infection status are shown in Fig 4. For S. haematobium, CR was high (>90%) in Niger and showed no clear association with co-infection status. In Senegal, CR for S. haematobium was lower, particularly in Nder (where all individuals were co-infected with S. mansoni) as well as in co-infected individuals in Temeye (Fig 4A, Table 5). In a model including data from all four villages in Senegal and Niger, co-infection did not significantly explain variation in S. haematobium clearance, when controlling for significant effects of village and initial S. haematobium infection intensity (Table 5A). In Temeye, co-infected children had a lower CR than those with single infections (Fig 4A). However, models showed that this effect was equally well explained by higher S. haematobium infection intensity as by co-infection. Considering data on parasitological cure from Temeye only, both co-infection status and initial intensity had equal explanatory power in univariate models (likelihood ratio tests for co-infection: χ21 = 4.16, p = 0.041; log(eggs per 10ml): χ21 = 4.15, p = 0.042). However, neither term added significant explanatory power when the other was already present in the model (likelihood ratio test for co-infection: χ2 = 1.74, p = 0.187; log(eggs per 10ml): χ2 = 1.74, p = 0.188), suggesting that these two variables strongly confound one another in Temeye.
Parameter estimates (on the logit scale) are from binomial mixed models. χ2 and p values are from likelihood ratio tests comparing full models with and without the term in question. ‘ref’ indicates the reference level of each factor.
Raw data are plotted with exact 95% confidence intervals.
For S. mansoni, CR was lower in Niger than in Senegal, though in neither country did CR depend strongly on co-infection status (Fig 4B). In a model including data from all four villages, co-infection did not significantly explain S. mansoni clearance probability, when controlling for other effects, particularly strong variation between the two countries (Table 5B). Among those who did not clear S. mansoni entirely, the number of remaining eggs was also not predicted by S. haematobium co-infection (GLM on logged egg counts: co-infection term χ2 = 2.47, p = 0.116). In a model where clearance of all schistosome eggs of both species six weeks after PZQ was the response, there was marginal evidence that co-infected individuals were less likely to clear all parasites than those with single species infections, when controlling for differences in clearance rates between villages (Table 5C).
S. haematobium longitudinal infection dynamics
Patterns of S. haematobium infection post-treatment varied widely across sites. In Senegal, rapid re-infection with S. haematobium was seen in Temeye, though not in Nder (Fig 5A and 5B), whereas in both Nigerien villages S. haematobium re-infection was much slower (Fig 5C and 5D). In Mali, S. haematobium infection probability was higher in S. mansoni infected children at baseline, and declined less rapidly, though by the second annual follow-up, no differences in prevalence were apparent according to baseline S. mansoni status (Fig 6A; Table A in S1 Text). At the first annual follow-up (F1), an individual’s S. haematobium infection probability was predicted by their change in S. mansoni infection since baseline: while controlling for baseline S. haematobium status (i.e. predisposition to the focal species), children persistently infected with S. mansoni (at baseline and follow-up) were more likely to be infected by S. haematobium than those that never had S. mansoni, while those that either lost or gained S. mansoni since baseline had intermediate infection probabilities (S. mansoni change: χ23 = 12.06, p = 0.007, controlling for significant effects of age, gender and baseline S. haematobium infection category; Fig B in S1 Text). Among the 2197 children recruited at the 20 schools where both schistosome species were monitored for all three years, 475 (22%) were only sampled at baseline, 466 (21%) were seen in two of the three years, and 1256 (57%) were followed-up in all three years. The mean number of follow-ups was 1.36. Drop-out analysis showed that the probability of children having full follow-up data (and therefore being included in these longitudinal analyses) was not affected by baseline infection status for S. haematobium or S. mansoni, but declined with age and differed across regions (Table B in S1 Text).
Means from raw data are plotted with 95% confidence intervals. Confidence intervals for prevalence are exact, and for intensity data were calculated using a negative binomial GLM on egg counts including zero counts. Black and red lines indicate baseline single infections and co-infections with S. mansoni respectively. Solid and dashed lines represent the villages of Temeye and Nder in A and B, and Diambala and Namarigoungou in C and D respectively. There is no line for single infections in Nder because all infections in that village were co-infections.
S. haematobium re-infection isolated from lack of clearance
No S. haematobium re-infection was observed after 6 months in Nigerien co-endemic villages, so variation in S. haematobium re-infection was only examined in Senegal. Among individuals with S. haematobium at baseline that had cleared infection six weeks after PZQ treatment, six month re-infection rates were 14% in Nder (where 100% children had S. mansoni at baseline), and 98% in Temeye (96% in children co-infected with S. mansoni at baseline vs. 100% in children singly infected). In a model including data from both villages, re-infection probability was strongly predicted by village (higher in Temeye than Nder, χ21 = 133.71, p<0.001) and was also higher in individuals with heavy compared to light S. haematobium infection at baseline (χ22 = 6.17, p = 0.0130). As expected given the limited variation in re-infection rates in Temeye (the only village where co-infection showed some variation), no significant effect of baseline S. mansoni co-infection on re-infection probability was detected while controlling for village and other effects (χ21 = 1.27, p = 0.259). However, across both Senegalese villages, the intensity of S. haematobium re-infection at six months post-treatment (which varied more widely, range 0–372 eggs/10ml), was significantly lower in those individuals co-infected by S. mansoni at baseline (Table 6A, Fig 7A). The negative binomial model provided a good fit to re-infection intensity data, with observed counts closely matching expected values (Fig C in S1 Text) and a low overdispersion parameter (α = 1.2). It was not possible to test for an interaction between co-infection status and village, as all individuals in Nder were co-infected at baseline. However, when limiting the analysis to the village of Temeye, the same negative effect of S. mansoni co-infection on S. haematobium re-infection intensity was seen (χ2 = 12.02, p = 0.0005). To explore this effect further, we tested how the change in an individual’s S. mansoni infection status between baseline, 6 weeks and 6 months predicted re-infection intensity, using data from both villages. This showed that the major difference in S. haematobium re-infection intensity was between those individuals that were S. mansoni negative at baseline but gained infection by 6 months (pattern 0-0-1), compared to those that were cleared of their original S. mansoni infection (1-0-0 and 1-0-1; Table C in S1 Text). We also examined geographical variation in S. haematobium re-infection rates across all of the seven villages in Senegal and Niger assessed in our previous studies [4, 5]. We noted that village-level S. haematobium re-infection rate at six months tended to decrease with increasing baseline mean S. mansoni infection intensity (Fig 7B).
Baseline infection intensity for the focal species was retained in models even when not significant, so the effect of co-infection over and above effects of the focal species could be assessed. χ2 and p values are from likelihood ratio tests comparing full models with and without the term in question. Age was mean-centred in analyses. ‘ref’ indicates the reference level of each factor.
(A) Negative association between S. mansoni co-infection and the intensity of S. haematobium re-infection from a negative binomial GLM on Senegalese data (n = 70). Values are predicted values from the minimal model in Table 6A, for an individual of average age, living in Temeye with a light S. haematobium infection prior to treatment. Errors bars represent 1 standard error. (B) Relationship between mean S. mansoni infection intensity and the proportion of individuals re-infected with S. haematobium six months after PZQ treatment across seven villages in Niger (red dots) and Senegal (black dots).
S. mansoni longitudinal patterns
Similar to S. haematobium, re-infection for S. mansoni was much quicker in Senegalese than Nigerien villages (Fig 8). In Mali, S. mansoni prevalence declined over two annual PZQ treatments, and this pattern differed only a minor amount according to baseline S. mansoni infection status (Table B in S1 Text): S. mansoni infection probability was higher in S. haematobium positive children at baseline and declined less rapidly, though no differences according to baseline S. haematobium infection status were visible after two years (Fig 7B). After one year, similar to the pattern seen for S. haematobium, S. mansoni infection probability was weakly predicted by changes in S. haematobium infection: children persistently infected with S. haematobium (at both baseline and first follow-up) were more likely to be infected with S. mansoni than those that never had S. haematobium, with those that either lost or gained S. haematobium intermediate (S. haematobium change: χ23 = 10.22, p = 0.017, controlling for effects of age, gender, region and baseline S. mansoni infection category; Fig B in S1 Text).
Means from raw data are plotted with 95% confidence intervals. Confidence intervals for prevalence are exact, and for intensity data were calculated using a negative binomial GLM on egg counts including zero counts. Black and red lines indicate baseline single infections and co-infections with S. haematobium respectively. Solid and dashed lines represent the villages of Temeye and Nder in A and B, and Diambala and Namarigoungou in C and D respectively. There is no line for single infections in Nder because all infections in that village were co-infections.
S. mansoni re-infection isolated from lack of clearance
In the four Senegalese and Nigerien villages, among children that had S. mansoni at baseline but cleared it 6 weeks post-PZQ, re-infection probability at six months was strongly predicted by village (χ23 = 65.73, p<0.0001), largely reflecting differences between the two countries (Fig 8). S. haematobium co-infection status did not predict S. mansoni re-infection probability (χ21 = 2.312, p = 0.128), while controlling for village, baseline S. mansoni infection intensity category (χ22 = 0.799, p = 0.671), and age (Age2 χ21 = 4.883, p = 0.027). These results reflect inconsistent patterns of re-infection rate according to S. haematobium co-infection status across the four villages (single vs. co-infected in Temeye, Nder, Diambala and Namarigoungou: 100% vs. 88%, 67% vs. 97%, 33% vs. 38% and 92% vs. 59% respectively). In models of S. mansoni re-infection intensity, again the strongest effect was village (Table 6B). However, a weak main effect of S. haematobium co-infection on re-infection intensity was also detected while controlling for covariates, indicating slightly lighter S. mansoni re-infection overall among individuals co-infected with S. haematobium at baseline (Table 6B). When an interaction term between village and co-infection status was included in the model, however, this was also weakly significant (χ23 = 7.943, p = 0.047), indicating that the effect of co-infection differed somewhat across sites. This interaction term reflected a weak positive association between co-infection and S. mansoni re-infection intensity in Nder and Diambala compared to a weak negative association in Temeye and Namarigoungou (Fig D in S1 Text), though in single village analyses, the co-infection term was always non-significant (all p>0.08). Overall therefore, S. mansoni re-infection was not strongly predicted by initial S. haematobium co-infection status, and the relatively weak negative effect of co-infection on egg counts at six months was not consistent across sites. We also checked whether any potential effect of S. haematobium co-infection on re-infection intensity might depend on an individual’s initial S. mansoni infection intensity, but there was no evidence for such an interaction (χ22 = 3.451, p = 0.178).
Despite frequent co-endemicity of S. haematobium and S. mansoni across Africa, little is known about the potential for within-host interactions between these two species, or whether such interactions might affect the impact of PZQ treatment or host immunity. Here, we analyse epidemiological data from school-age children in three West African countries (Senegal, Niger and Mali), to explore whether these two species may interact with one another in the context of PZQ treatment.
At baseline, associations between urogenital and intestinal schistosomiasis were generally positive in all three countries: for both S. haematobium and S. mansoni, infection intensity increased with the degree of co-infection, while controlling for other effects such as age, gender and location, and in Mali children with one species were more likely to be infected by the other, with some geographic variation in the strength of this association. Similar positive associations prior to treatment have been previously reported from other co-endemic villages in Senegal , and Cameroon . Such positive associations may be driven by a number of processes, including correlated exposure of children to infective Bulinus and Biomphalaria snails at the same transmission sites, correlated immune susceptibility of individuals to infection by the two species, and/or facilitative interspecific interactions within the host. Few studies have examined the evidence for correlated exposure to S. haematobium and S. mansoni, and while some have in fact suggested these species may have distinct local transmission sites within villages [39, 40], further work is needed to examine the extent to which correlated exposure, or other mechanisms, may drive the positive associations between schistosome species documented here and elsewhere.
In analysing data from two efficacy studies with similar methodology in Senegal and Niger, we found that the efficacy (ERR) of two (three week spaced) PZQ doses against either S. haematobium or S. mansoni was not significantly altered by the presence of co-infection. This is encouraging, though the effect of co-infection on efficacy still requires testing for the standard, single 40mg/kg dose of PZQ widely used in control programmes. Parasitological cure rates told a somewhat different story, with clearance probability for S. haematobium reduced in mixed infections compared to single infections in Senegal, but not Niger. Further analysis showed that this effect of S. mansoni on S. haematobium clearance disappeared once initial infection intensity was controlled for, suggesting intensity differences likely underpinned reduced clearance of S. haematobium from mixed infections in Senegal. While it is well known that heavy infections are less likely to be cleared by a standard dose of PZQ [41–43], a key question arising from our findings is to what extent S. mansoni co-infection causes, or is merely correlated with, increased infection intensity for S. haematobium. The answer will determine whether co-endemicity in an area per se is cause to consider higher or more repeated doses of PZQ to get full infection clearance. Our finding of reduced overall clearance for S. haematobium/S. mansoni co-infections compared to single infections agrees with a recent meta-analysis of studies using the standard 40mg/kg PZQ dose  in suggesting mixed infections may be harder to clear. Again whether this observation is due to mixed infections simply being heavier, or other effects remains unclear. Our results did not suggest a consistent difference in PZQ efficacy against the two species: S. mansoni showed lower ERR and CR than S. haematobium in Niger , though this was not seen in Senegal . Another study with very similar methodology reported higher ERR and CR for S. mansoni than S. haematobium in co-endemic sites in Cameroon . These mixed findings echo two recent studies synthesizing cure rate data for urogenital and intestinal schistosomiasis, which showed large geographic variability but only limited species differences in PZQ-related clearance overall [43, 44]. We also show that even after controlling for differences in initial infection intensity, co-infection status and other variables, large differences in cure rates were observed between Senegal and Niger for both urogenital and intestinal schistosomiasis. Moreover, while S. haematobium ERR was similar in the Senegalese and Nigerien villages, ERR for S. mansoni was notably lower in Niger. These geographic differences may reflect intraspecific genetic differences in schistosomes, as seen across other West African countries , or geographic differences in the prevalence of cryptic hybrid schistosomes that may differ in susceptibility to PZQ , both possibilities warranting further investigation.
Patterns of re-infection for both schistosome species varied markedly between countries, and to a lesser extent among sites within each country. Variation in transmission site ecology, for example changes in the abundance of Biomphalaria and Bulinus snails, as well as seasonality are likely to play important roles in driving these differences . However, when controlling for geographic location, we revealed a somewhat counterintuitive effect of interspecific co-infection on the degree of short-term re-infection (6 months after PZQ treatment). Since baseline associations between S. haematobium and S. mansoni were generally positive, one might expect to see higher levels of re-infection among individuals that were co-infected at baseline, that would re-establish these positive associations post-treatment. However, we found the opposite pattern in data from Senegal. Despite S. mansoni co-infected individuals having higher S. haematobium egg counts at baseline, after effective treatment they had significantly lower S. haematobium egg counts six months later than those with single infections at baseline. This result could indicate some kind of asymmetric competitive interaction between S. mansoni and S. haematobium, whereby S. mansoni infection at the point of treatment limits the extent to which S. haematobium can re-infect or shed eggs after treatment. Although it was not possible to test for the same individual-level effect in Niger (since no participants were re-infected by S. haematobium at six months), we did observe at a population-level that the proportion of individuals re-infected with S. haematobium in a given location was negatively related to baseline mean intensity of S. mansoni infection. This pattern that is at least consistent with the effect seen in Senegal, though may be influenced by other factors varying across sites, such as environmental factors related to snail ecology. While there was some evidence for the reverse pattern—S. haematobium co-infection at baseline limiting S. mansoni re-infection, the effect was much weaker and geographically variable. Interestingly, a study with similar methodology in Cameroon (conducted under the same multi-country CONTRAST project as the Senegal and Niger studies reported here) also showed a reduced probability of S. haematobium re-infection among children co-infected by S. mansoni at the time of PZQ treatment, though the statistical significance of this difference was not tested . Further studies are now needed to test the generality of these patterns across a range of other co-endemic settings.
If these patterns do reflect asymmetric competition between S. mansoni and S. haematobium after treatment, a range of possible mechanisms could be responsible. First, if baseline S. mansoni co-infection is associated with faster or more intense S. mansoni re-infection, our findings could arise though interspecific competition during re-infection. Such competition could occur in the currency of mates, nutritional resources like blood (an important food source for adult schistosomes) , or immune-mediated competition via cross-immunity to cercariae, immature or adult worms. Mate competition between S. mansoni and S. haematobium has been previously documented [14–16], and competitive asymmetry could arise if S. mansoni males divert S. haematobium females away from their preferred ovipositing site more often than the reverse pattern . Competition for resources among schistosome species may also affect patterns detected here, though to our knowledge resource-based competition among schistosomes has not yet been explored. It also remains unclear to what extent S. mansoni and S. haematobium elicit cross-protective immune responses in humans. The idea of heterologous immunity in schistosomes has a long history, and there is clear evidence from animal models that challenge by one species can sometimes protect against, or at least limit egg output from, a challenge infection by another species . Challenge experiments in hamsters have shown that S. mansoni stimulates stronger cross protection than S. haematobium , and that S. mansoni competes with S. haematobium at several stages, impairing worm development, sexual maturation and egg shedding . Moreover, a recent study conducted close to our study sites in Senegal  provided preliminary evidence for cross-immunity between these two species in humans, as measured by serum cytokine production in response to egg or adult worm antigen. Intriguingly, this study also showed that S. mansoni elicited somewhat stronger heterologous responses than S. haematobium , consistent with our finding that S. mansoni was associated with reduced S. haematobium re-infection, but not necessarily the other way around. Thus cross-immunity between S. mansoni and S. haematobium may well occur, and its importance in humans warrants further investigation. To try and distinguish between mate, resource and immune-mediated competition in our analyses, we tested whether the effect of baseline S. mansoni status on S. haematobium re-infection varied according to subsequent S. mansoni clearance or re-infection. Mate competition would be expected to show the strongest effect in individuals that did not fully clear S. mansoni upon treatment, and cross-reactive immune responses against re-infecting S. mansoni would predict the strongest effect in children who were re-infected with S. mansoni six months later, compared to those with no patent infection. In fact, we found that effect of baseline S. mansoni infection was similar regardless of whether individuals were re-infected by S. mansoni six months after treatment, and was weakest in those that did not clear S. mansoni in the first place. This suggests that the legacy of S. mansoni infection, rather than active infection, is enough to generate competition with re-infecting S. haematobium, which is possible if PZQ treatment exposes S. mansoni antigen that elicit heterologous immunity. Indeed, PZQ treatment is known to alter immunity to schistosomes , an effect that could extend to heterologous immunity. While we only examined school-age children here, immunologically-driven patterns may differ depending on the length of exposure to schistosomes. Therefore, studies involving adults would also be useful to further explore the patterns reported here.
In apparent contrast to findings from Senegal, at co-endemic sentinel sites in Mali, the children most likely to have S. haematobium at the first annual follow-up were those that maintained S. mansoni infection over the same period. Children maintaining S. haematobium were also more likely to have S. mansoni at first follow-up. Despite appearing contradictory to findings from the Senegalese and Nigerien villages (where negative associations between co-infection and re-infection were seen), such positive correlations in Mali may simply reflect a lack of treatment in certain individuals: maintenance of infection with a given species could well indicate that these children missed PZQ treatment in the national treatment campaign, and therefore would also be more likely to harbor the other schistosome species at follow-up. While data from sentinel sites (where treatment coverage is imperfect), are less powerful than deliberate treatment follow-up studies for examining potential interactions between schistosome species, they can contribute to our understanding of how schistosome species composition is likely to change as preventative chemotherapy programmes advance. In this respect, it is noteworthy that in all three co-endemic West African countries examined here, among children that were infected at baseline and had complete follow-up, over time the proportion of schistosome infections attributable to S. mansoni as compared to S. haematobium, increased (Fig 9). A whole range of processes may drive such population-level trends, including altered exposure via changes in the relative abundance of Biomphalaria and Bulinus snails, or the re-infection effect we observed in Senegal, whereby S. mansoni infection appeared to limit S. haematobium re-infection after treatment. Whatever the underlying causes, it will be useful to study whether an increase in the contribution of S. mansoni to infections post-treatment is a general pattern beyond the three countries examined here.
Only children that were positive at baseline, and monitored at all follow-up occasions are included.
In conclusion, our multi-country analysis of associations between S. haematobium and S. mansoni throughout the process of PZQ treatment and re-infection provided no evidence for altered efficacy of double-dose PZQ in co-infections compared to single infections, though co-infections were sometimes heavier and less likely to clear completely after treatment. We also show that while controlling for other effects, children co-infected with S. mansoni in Senegal showed reduced S. haematobium re-infection compared to singly infected children, which we suggest may be driven by treatment-induced antigen exposure and stimulation of cross-protective immune responses. Furthermore, although the temporal dynamics of prevalence and intensity for these two species were most strongly affected by location, suggesting local environmental factors are the dominant drivers of re-infection patterns, in all three co-endemic countries examined the proportion of infections attributable to S. mansoni relative to S. haematobium increased over time post-treatment. Studies in other co-endemic areas are warranted to test the generality of these findings, which have implications for our understanding of basic schistosome biology, as well as relevance for schistosomiasis control as we move towards elimination in mixed species settings.
Figure A. Baseline patterns of schistosome infection intensity according to co-infection status in individual Malian schools. Figure B. Infection probability among Malian children in year F1 according to changes in co-infection status from baseline. Figure C. Observed and expected distribution of S. haematobium egg counts under NB2 model. Figure D. Variable relationship between S. mansoni re-infection intensity and co-infection across sites in Senegal and Niger. Table A. Model results on changes in infection probability over time in Malian children, according to baseline co-infection status. Table B. Predictors of follow-up in Malian cohort. Table C. Model results on how S. haematobium re-infection intensity in Senegal was predicted by changes in S. mansoni infection from baseline.
We would like to thank the Senegal, Niger and Mali field teams for their assistance with collecting and processing samples and all study participants for their help and cooperation. We also thank Bruno Levecke for advice on assessing drug efficacy and code for permutation tests.
Conceived and designed the experiments: JPW DR AF. Performed the experiments: OTD AG MS BLW. Analyzed the data: SCLK. Contributed reagents/materials/analysis tools: AF. Wrote the paper: SCLK JPW DR BLW.
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