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Presence and potential distribution of malaria-infected New World primates of Costa Rica

Abstract

Background

In South and Central America, Plasmodium malariae/Plasmodium brasilianum, Plasmodium vivax, Plasmodium simium, and Plasmodium falciparum has been reported in New World primates (NWP). Specifically in Costa Rica, the presence of monkeys positive to P. malariae/P brasilianum has been identified in both captivity and in the wild. The aim of the present study was to determine the presence of P. brasilianum, P. falciparum, and P. vivax, and the potential distribution of these parasites-infecting NWP from Costa Rica.

Methods

The locations with PCR (Polymerase Chain Reaction) positive results and bioclimatic predictors were used to construct ecological niche models based on a modelling environment that uses the Maxent algorithm, named kuenm, capable to manage diverse settings to better estimate the potential distributions and uncertainty indices of the potential distribution.

Results

PCR analysis for the Plasmodium presence was conducted in 384 samples of four primates (Howler monkey [n = 130], White-face monkey [n = 132], Squirrel monkey [n = 50], and red spider monkey [n = 72]), from across Costa Rica. Three Plasmodium species were detected in all primate species (P. falciparum, P. malariae/P. brasilianum, and P. vivax). Overall, the infection prevalence was 8.9%, but each Plasmodium species ranged 2.1–3.4%. The niche model approach showed that the Pacific and the Atlantic coastal regions of Costa Rica presented suitable climatic conditions for parasite infections. However, the central pacific coast has a more trustable prediction for malaria in primates.

Conclusions

The results indicate that the regions with higher suitability for Plasmodium transmission in NWP coincide with regions where most human cases have been reported. These regions were also previously identified as areas with high suitability for vector species, suggesting that enzootic and epizootic cycles occur.

Background

Malaria is a vector-borne disease caused by protozoa of the genus Plasmodium, mostly transmitted by bites of Anopheles mosquitoes. The genus Plasmodium includes more than 250 different species that infect mammals, reptiles, birds, and amphibians [1]. Four species are recognized as causing malaria in humans: Plasmodium falciparum, Plasmodium vivax, Plasmodium malariae and Plasmodium ovale. More recently, Plasmodium knowlesi and Plasmodium cynomolgi has been implicated as a cause of human malaria [2, 3]. Non-human primates are classified as important hosts of this protozoan, with at least 35 parasite species recognized as simian malaria [4, 5]. This parasite is mostly transmitted by bites of Anopheles mosquitoes. There are more than 400 different species of Anopheles mosquitoes, and approximately around 30 of these determined as malaria vectors of major importance [6, 7]. In Costa Rica at least 18 species of Anopheles were detected, being Anopheles albimanus the main vector recognized [8].

Plasmodium brasilianum and P. simium have been reported in New World primates (NWP) of the Cebidae family and are difficult to distinguish from the human P. malariae and P. vivax, respectively [9]. Plasmodium brasilianum was identified in at least 35 species of NWP in Central and South America [9,10,11]. Plasmodium brasilianum resembles P. malariae morphologically, and are nearly genetically identical, differing in mutations expected within a species. Naturally acquired infection with P. brasilianum has been found in humans [12]. In Costa Rica Calvo et al. [13] reported the presence of P. malariae/P. brasilianum in human samples, the sequences showed a 99% identity with sequences of Plasmodium species isolated from NWP in French Guiana. In Costa Rica, the analysis of genetic diversity of the monkey samples positive to malaria revealed that the P. malariae/P. brasilianum parasite found in one howler monkey was identical to that recently found in humans residing Costa Rica [11]. Plasmodium simium has been determined principally in the Atlantic Forest in southern Brazil, considered specific of NWP, and related, but distinct from P. vivax, as established recently [14]. Brasil and collaborators [15] suggest that P. vivax outbreaks reported in the Atlantic Forest of Brazil (2015, 2016) were infections caused by P. simium transmitted from monkeys to humans by mosquito bites. Plasmodium falciparum has been detected in NWP (Aotidae) from Brazil [16, 17], and it is assumed that NWP are susceptible to this malaria parasite [18]. In Costa Rica, Plasmodium has been determined both in captivity and in wild NWP. In 2006, the first report of six howler monkeys (Alouatta palliata) positive to P. brasilianum [10] was published. In 2017 five captive individuals were found positive to P. malariae/P. brasilianum [11].

Worldwide maps of malaria distribution show that Costa Rica is one of the countries with suitable conditions for stable malaria transmission [19]. However, those maps were generated at a coarse scale, so the hotspots in Costa Rica cannot be identified. Recent analysis points out that the Atlantic region of Costa Rica is one of the hot spots of human transmission [20]. Although human cases show a declining trend, there is a concern that enzootic cycles of Plasmodium elsewhere in Costa Rica could represent a spillover risk. New World Primates represent interesting populations for study, because of its distribution in areas of ideal weather and altitude in the country for the presence of vector-borne diseases, as is the case for malaria. The constant use of human altered environments by these monkeys as well as its interaction with people [21], may favour the transmission of Plasmodium between populations of monkeys or humans by way of mosquito bites. This investigation proposes to determine the presence and potential distribution of climatic suitability for the transmission of Plasmodium (P. malariae/brasilianum, P. vivax and P. falciparum,) in the four species of natural inhabitants of NWP of Costa Rica: howler (Alouatta palliata), white-faced (Cebus imitator), squirrel (Saimiri oerstedii) and spider (Ateles geoffroyi) monkeys. It has been highlighted that infection prevalence and transmission of blood parasites such as avian malaria are affected by environmental conditions and that this information is crucial to develop better risk maps [22]. It is important to emphasize that primate malaria has the potential to damper the efforts to eliminate human malaria.

Methods

Study area, sampling size and sampling

The NWP were all collected from 2000 to 2012 in forest areas, and samples from captive animals were gathered from zoos and rescue centres of Costa Rica. The geographic coordinates of each location were obtained using a GPS unit. The animals were captured in situ by chemical immobilization with darts (Type P, 1 mL, Pneu Dart Inc.), and compressed gas rifle (X-Caliber Gauged CO2, Pneu Dart Inc.) for individuals over long distances, or blowgun for individuals located at close range. Anesthetics used were Zoletil 50 (3.3–11 mg/kg) or ketamine (5–20 mg/kg), in combination with Xylazine (0.5–2 mg/kg) [23, 24]. As soon as the animal was anesthetized, a blood sample (2–4 mL) from the femoral, saphene or cephalic vein was taken. The samples were collected in tubes with EDTA and maintained at 4 °C until arrival to the laboratory, where samples were kept at −20 °C until laboratory analysis. The NWP were monitored until awakening from narcosis, and safely released into their habitat.

Molecular surveys

Total DNA was extracted from all blood samples using the DNeasy Blood & Tissue Kit (Qiagen, Hilden, Germany), according to the manufacturer’s instructions and using 100 ul of blood. Polymerase Chain Reaction (PCR) was carried out as previously described [25], where a sequence of the small ribosomal DNA subunit of Plasmodium spp. was amplified. The PCR products were visualized in 2% agarose gel electrophoresis, stained with Gel Red (Biotium Inc., Hayward, California, USA). As positive control P. malariae-DNA, P. vivax-DNA, and P. falciparum-DNA were used, which were donated by the Primatology Institute of the University of Washington, Seattle, USA, and Malaria Reference Center, INCIENSA, Tres Ríos, Costa Rica. Free nuclease water was used as a negative control. Samples with bands of 269 bp (P. malariae), 499 bp (P. vivax), and 395 bp (P. falciparum), were considered positive. Some positive samples were subsequently re-amplified, and the amplicons with adequate concentrations were sequenced with the same diagnostic primers to confirm the PCR results. Sequences derived from this study were aligned together with Plasmodium sequences from Genbank then trimmed to a common length of 269 bp, 499 bp, or 395 bp.

Data assembly and assumptions

Because of the small number of positive samples, all the infection records covering the three Plasmodium lineages were lumped together to generate a single supraspecific Plasmodium niche model as a valid taxonomic unit to model the ecological niche [26]. This was based on two criteria: (1) the three groups of Plasmodium lineages showed no specificity with the four NWP species (see “Results”); and (2) these lineages form a phylogenetically close species group of primates [27]. As a general assumption for the lumping approach, the niche conservatism hypothesis (i.e., niche traits are often conserved among closely related species; [28], were followed which has considerable evidence of lack of ecological niche differentiation at time scales comparable to close/sister species, and states that when niches show high levels of conservatism, close relatives are likely to respond similarly to environmental gradients. This is true not only for free-ranging species, but also for parasites (e. g., [29]). This approach has been assessed under different taxonomic groups that explored the contribution of using supraspecific modelling units in niche construction showing that those modelling units improved the predictive ability of the ecological niche models. Specifically, by adding the occurrences of closer taxa reduced the omission rates considerably [30].

To construct the Plasmodium niche model of NWP of Costa Rica, the Maxent's machine learning algorithm [31] was used, the most important algorithm for modelling species' ecological niches and potential distributions. Maxent has been extensively evaluated between other 15 algorithms, and has been highlighted because its high performance, especially with small (less than 20 records) data sets [32, 33]. Due to Maxent uses a generative approach, rather than discriminative, it can perform with a low amount of training data [31]. The state of art modelling package, Kuenm that uses R as a programming environment, and Maxent as a niche model algorithm [34] was used. This package allows robust model calibration processes, facilitating the creation of final models based on model significance, performance, and simplicity. This package allows the user to program different calibration settings, for instance, the use of various sets of bioclimatic predictors, various regularization parameters, which affect the model complexity [35]. By doing this, Kuenm produces thousands of models that can be compared and evaluated.

Niche model calibration

A total of 21 occurrences of primate individuals that tested positive for Plasmodium sp., were included in a primary dataset. Duplicated occurrences were eliminated (e.g., when more than one individual was positive from the same location). Afterwards, the aim was to reduce the effects of spatial autocorrelation by thinning the occurrence of records using a distance filter of 5 km between records with the spThin R package [36]. The final database included 18 occurrence records. Occurrence records were split randomly into two subsets using the “random k-fold” method: 50% of occurrences for model calibration and 50% of occurrences for final evaluation [37]. The latter method partitioned occurrence localities randomly into a user-specified number of (k) bins as described in detail in Muscarella et al. [38].

The accessible area “M” is an essential component in the biotic, abiotic, and movement (BAM) model [39], that defines the main parameters in constructing the species ecological niche model [40]. To shape this “M” area, a 50 km radius buffer was created around each occurrence point to extend the entire calibration region's limits. Each occurrence record was subsequently overlaid on the ecoregion shapefile to assess the concordance between the species occurrence and a particular ecoregion [41], as described in a previous study [42].

Fifteen variables were included in the modelling framework to construct the ENM of Plasmodium spp in Costa Rica. For this, WorldClim 2 was used because WorldClim data performed substantially better than other available climatic data in various modelling purposes (http://www.worldclim.org; [43]). From the whole list of available variables, four variables were excluded from the bioclimatic variables (Bio 8, Bio 9, Bio 18, and Bio 19) owing to their known spatial artifacts, following the protocol implemented in previous similar studies [44]. In order to know whether variable combinations are important to the geographic distribution of niche suitability of infected monkeys, four sets of bioclimatic variables were used that reflect different ecological attributes of the bioclimatic predictors: (a) set1: 15 variables from WorldClim2; (b) set2: nine variables from WorldClim2, a subset of variables with biological relevance defining the availability of thermal energy and water (e.g. the minimum, maximum and mean values of temperature and precipitation); (c) set3: a set of variables selected from a jackknife process in MaxEnt, and correlation analyses to select distinct sets of variables that contributed most to models (> 90%), eliminating one variable per pair with a correlation of (rPearson < 0.8) [37, 45], and d) set4: a set of variables selected after assessing the variance inflation factor (VIF), which is a measure of levels of multicollinearity between pairs of variables. Values of VIF > 10 denote a potentially problematic correlation with of covariates, indicating that these covariates should be carefully evaluated in model development [46]. All bioclimatic variables used are at the spatial resolution of 30 arc seconds (≈1km2 per pixel) (Table 1).

Table 1 Set of Bioclim variables used for the construction of the ecological niche modelling for Plasmodium spp

ENM was constructed using the maximum entropy algorithm implemented in MaxEnt version 3.4.1 via the kuenm R package [34]. In the Kuenm package, it is possible to configure the modelling procedure by including different parameterizations to leave the program to construct several models that can be assessed by various criteria (see below). To do this, candidate models were created by combining the four sets of environmental variables, 17 values of regularization multipliers (1, 2, 3, 4, 5, 6, 7, 8, 9, 10), and all 29 possible combinations of 5 feature classes (linear = l, quadratic = q, product = p, threshold = t, and hinge = h) [34]. The best candidate model was selected based on three criteria: (1) significance, (2) performance, and (3) the Akaike information criteria (AIC): AICc, delta AICc, and AICc weights. The criteria used to assess the model performance and select the best candidate models included first their statistical significance: partial Receiver Operating Characteristic (partial ROC) and omission rates 5% for predictive ability; and second by performance based on Akaike Information Criterion corrected (AICc) for small sample sizes [47]. Partial ROC assesses a ratio from the number of evaluation occurrences predicted correctly, and the proportion of area predicted suitable—a ratio with values ≤ 1 reflects predictions indistinguishable from random predictions, while a ratio > 1 suggests predictions better than by random [48].

The omission rate is a threshold that considers an estimate of the likely amount of error among occurrence data and thus removes 5% of occurrences with the lowest suitability values (E = 5%) [48]. The AICc provides explicit criteria for selecting models of appropriate complexity. This metric is assessed by standardizing raw scores for each ENM so that all scores within the geographic space sum to 1, and then calculating the likelihood of the data given each ENM by taking the product of the suitability scores for each grid cell containing a presence. Both training and test localities are used in calculating likelihoods. The number of parameters is measured simply by counting all parameters with a nonzero weight in the lambda file produced by Maxent, a small text file containing model details that Maxent produces as part of the modelling process [35]. Models were selected with delta AICc ≤ 2 from those that were statistically significant, and had omission rates below 5% [34]. The criteria followed was from a previous study [34] to select the final model, evaluate the model, and assess extrapolation risk. The final models of Plasmodium spp were created using ten replicates by bootstrap, with logistic outputs, and these models were transferred from the accessible area “M” to the projection area “G.”

To identify extrapolation risk in the model transfers, a mobility-oriented parity (MOP) analysis was performed comparing the environmental breadth of predictors within “M” (10% reference points sampled) with that in the projection area using the MOP function [34] available in the kuenm R package. The risk of extrapolation analysis defines the areas with strict extrapolation (i.e., places where environmental conditions are non-analogous to those in regions across which the models were calibrated) to avoid the risk of over-prediction in non-analogous environments.

Results

Throughout the study area, 384 individuals from the four species of NWP were sampled during surveys: 130 howler monkeys (Alouatta palliata), 132 white-faced monkeys (Cebus imitator), 50 squirrel monkeys (Saimiri oerstedii), and 72 red spider monkeys (Ateles geoffroyi) (Fig. 1). A total of 342 (89%) and 42 (11%) individuals were captured in free-range and captive areas, respectively. Of the 384 NWP studied 8.6% had evidence of Plasmodium presence, seven captive and 26 free-ranging individuals. Of the positive individuals, 3.4% were positive to P. falciparum, 3.1% to P. malariae/P. brasilianum, and 2.1% to P. vivax. The PCR products showed nucleotide sequence similarity to P. malariae, P. vivax, and P. falciparum, analysis to corroborate positive results (data not shown). The four species of NWP were found positive. Plasmodium positivity by monkey species was the following: howler (7.7%), white-faced (7.6%), squirrel (10%), and red spider (11.1%) (Table 2, Fig. 2). An increase in the number of positives was determined over time. Of the positive individuals seven (21%) were captive and 26 (79%) free ranging. The seven positive captive individuals were red spider monkeys, one (P. falciparum) in the Central Pacific region of Costa Rica in 2010, and six (three P. falciparum, two P. malariae, and one P. vivax) living in the Northern regions in 2005 (Table 2).

Fig. 1
figure 1

Map of Plasmodium malariae/Plasmodium brasilanum, Plasmodium vivax, and Plasmodium falciparum in positive New World primates from Costa Rica, 2000–2012. Regions: CPR—Central Pacific Region, NHR—Northern Huetar region, AHR—Atlantic Huetar region, ChR—Chorotega region, CR—Central Region, BR—Brunca Region

Table 2 New World primates and locations found Plasmodium positive, and species detected in Costa Rica, 2000–2012
Fig. 2
figure 2

Map of sampling sites of New World primates from Costa Rica, 2000–2012

The modelling framework used produced 1240 candidate models, of which 747 were statistically significant, and only six passed the three selection criteria (Table 3; Additional file 1: Fig. S1). The best models used set 2 of bioclimatic predictors (i.e., the subset of variables with biological relevance). From these six models (Additional file 2: Fig. S2), model 2 (Fig. 3) was chosen to depict the potential distribution of Plasmodium species in Costa Rica. The Pacific and the Atlantic coastal regions of Costa Rica presented suitable conditions for parasite infections (Fig. 3a); however, the Atlantic coast showed a higher variation between the chosen model's replicate outputs (Fig. 3b). This can result from a non-analogous climatic envelope to the rest of the country, as shown in the MOP analysis (Fig. 3c). The uncertainty map shows that the central pacific coast has a more trustable prediction for malaria in primates (Fig. 3d).

Table 3 Model performance under different parametrizing settings (i.e. regularization multiplier [RM] and features classes [FC]
Fig. 3
figure 3

Map of the 1st best model (see Table 1) and uncertainty for Plasmodium sp. In Costa Rica. a Ecological niche model of Plasmodium sp. In Costa Rica; b Standard deviation map; c Mobility-oriented parity (MOP) extrapolation risk analysis for the ecological niche model (see “Methods”); d Uncertainty map of Plasmodium sp. prediction

Discussion

The model of potential distribution of Plasmodium transmission in NWP of Costa Rica, indicates a higher niche suitability for the transmission in the North and Central Pacific and moderate suitability in Atlantic regions, near to where P. malariae/P. brasilianum was reported in primates living in captivity by Fuentes-Ramírez and collaborators [11] (Central Pacific, and Atlantic regions). Yet, since the Atlantic region showed high to moderate model uncertainty in the analysis, the transmission prediction in free-ranging primates in this area should be taken with caution. While the model used showed a relative week prediction for primate prediction for the Atlantic region, Chinchilla and collaborators [10], have reported the presence of P. brasilianum in howler monkeys in the Atlantic region, and with areas where there have been most reports of human malaria cases in Costa Rica [49], and areas of new autochthonous outbreaks in the country [50]. On the Pacific coast, the model of distribution indicates a high probability of occurrence in regions where the presence of evolutive stages of Plasmodium has been previously reported [49]. Therefore, the presence of Plasmodium in NWP in Costa Rica coincides with areas known as malarious for Costa Rica. Areas of incidence of malaria cases in humans will be considered given the agent's ability to infect both human and non-human primates [51]. It is possible that a high incidence of the disease in humans may reflect a high presence of positive NWP in close contact with humans, which can facilitate transmission by the vector.

The presence over time showed an increase in positive individuals, which is contrary that reported in humans, where the number of cases were decreasing during the period of this investigation [8]. Costa Rica has been a country of historically low malaria incidence. The incidence of human malaria has declined in the country since 1999. However, in recent years a greater number of imported cases have been reported, and in 2017 after five years of no reported cases native to Costa Rica [50], the Costa Rican Ministry of Health declared a sanitary alert for areas 500 m above sea level.

Plasmodium is a common agent in non-human primates, and in diverse environmental areas, that can benefit from anthropogenic changes [9]. The study of potential distribution allows the acquisition of knowledge about the factors associated with the temporal and spatial variation of agents such as Plasmodium. The great variety of microclimates and life zones of Costa Rica maintain one of the highest levels of species diversity on the planet. The country has become known for its conservation efforts. However, the forests of Costa Rica face risks from illegal logging, forest conversion for agriculture (such as pineapple and palm oil production), and cattle pasture in unprotected areas, as well as tourism and real estate development disrupting the connectivity between forest patches. Land use and climate change favour the presence of potential vectors and affect the composition of wildlife communities, which influence human and animal exposure to the parasite as well as its prevalence both at a spatial and temporal level [9]. A definite pattern with the diversity and proportion of Plasmodium species throughout the years was not observed, P. falciparum was the species most often found, followed by P. malariae/P.brasilianum, and P. vivax. When compared to the cases reported in humans of Costa Rica, most human cases reported are P. vivax, followed by P. falciparum, and specifically P. malariae/P. brasilianum cases are very rare [49], and were reported for the first time in 2015 after almost 40 years [13]. It is not possible to define a similar pattern of incidence of Plasmodium infections in NWP and humans, although a greater presence of positive individuals in areas of historically high incidence of human cases [20] was determined.

In agreement with the proposed possibility that non-human primates may be natural reservoirs for human malarias [52, 53], P. falciparum and P. vivax have not been reported in NWP of Costa Rica. The presence of P. falciparum in NWP has already been reported in Brazil [16, 17], and a possible frequent transmission of the human agent to monkeys was determined. Plasmodium vivax was the most often detected species in human cases of Costa Rica. In 2007, 99% of reported malaria cases were P. vivax, and the remaining 1% was P. falciparum [49]. Plasmodium simium, a sister species of P. vivax, has been reported to date only in NWP of Brazil, and was recently determined as a monkey specific species, distinct from P. vivax, by a differential diagnosis developed for both species [14] (de Alvarenga et al. 2018). Oliveira et al. [54] propose a process of speciation is occurring in P. simium which has adapted to sylvatic reservoirs, but can infect humans due to the presence of vectors such as Anopheles cruzii with the ability to feed on both monkeys and humans. Outbreaks of malaria diagnosed in 2015 and 2016 in Costa Rica were reported as P. vivax, it is important to investigate in future studies if native cases reported in the Atlantic region, were infections caused by P. vivax or by P. simium, transmitted from monkeys to humans by mosquito bites [15]. In Costa Rica, the analysis of genetic diversity of the monkey samples positive to malaria revealed that the P. malariae parasite found in one howler monkey was identical to that recently found in humans residing Costa Rica [11]. For this reason and considering the proven experimental replication of this Plasmodium in NWP (Aotidae and Cebidae) [55,56,57] it is relevant to determine the possibility that these species of monkeys can maintain the parasite cycle in sylvatic environments, considering the great diversity of Anopheles present in Costa Rica [8], which may act as malaria vectors for NWP.

It is expected that the vectors between monkeys and humans differ in their distribution by the habitats used [16]. Although An. albimanus is the main vector associated with the transmission of malaria in humans in Costa Rica [8], the presence of at least 18 Anopheles species has been reported [58]. Including An. neivai (Kerteszia subgenus) associated with the transmission of malaria in NWP and humans in Brazil, since its ability to be found both in the forest canopy and at ground level [59]. All positive individuals are in environments where the constant interaction between humans and NWM is commutated. Only one location with positive individuals was not in a fragmented environment, and all areas with positive cases are close to villages. This may be important, because although vectors between humans and wild animals are normally not shared, it has been established that proximity between urban and conserved areas have favoured humans and monkeys sharing malaria vectors [60, 61].

Conclusions

Here in, a first geographical approach was developed to understand the spatial patterns of malaria transmission in NWP and how this can be related with human malaria in Costa Rica. The modelling framework used allowed for the identification of areas where spillover is possible providing the coincidence between areas with climatic suitability for the primate parasite transmission with the presence of human populations. Modelling parasite-infected or diseased individuals is a challenging task since the natural infection prevalence is often low. In the presented case, several records were available of monkeys, but only 8% of infection prevalence, so there was a reduced dataset for model calibration. Although a straightforward framework was used to reduce the effect of sampling size on model quality, it was considered that for some regions the predictions must be taken with caution (i.e., in the Atlantic region) based on a limited representation. Since maps were produced for model uncertainty and the extrapolation risk, areas were identified where the model used was more or less robust. The authors encourage more research to document the spatial locations where primate infections with Plasmodium occur in order to a better to enhance the understanding of the relationship between the geographical and environmental correlates with malaria transmission, that can help plan more effective control strategies, using the natural environment cycles as disease sentinels.

Due to the great diversity of Anopheles in Latin America [7], it is a necessity to carry out studies that allow for comparing the species and abundance of Anopheles in places where NWPs are distributed. As well integrate the taxonomic determination of mosquitoes and infectivity for Plasmodium into research to establish which of these species are acting as malaria vectors for NWP, and to confirm the presence of P. simium in the country. Finally, it is recommended that an exhaustive comparison be made between free-living individuals and individuals kept in captivity to determine if captivity favours the presence of positive individuals.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

NWP:

New World primates

PCR:

Polymerase chain reaction

mg:

Milligram

kg:

Kilogram

mL:

Millilitre

°C:

Degree centigrade

bp:

Base pairs

VIF:

Variance inflation factor

ROC:

Receiver operating characteristic

AICc:

Akaike information criterion corrected

References

  1. Leclerc MC, Hugot JP, Durand P, Renaud F. Evolutionary relationships between 15 Plasmodium species from New and Old World primates (including humans): a 18SrDNA cladistic analysis. Parasitology. 2004;129:677–84.

    Article  CAS  PubMed  Google Scholar 

  2. Cox-Singh J, Singh B. Knowlesi malaria: newly emergent and of public health importance? Trends Parasitol. 2008;24:406–10.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Ta TH, Hisam S, Lanza M, Jiram AI, Ismail N, Rubio JM. First case of naturally acquired human infection with Plasmodium cynomolgi. Malar J. 2014;13:68.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Coatney GR, Collins WE, Warren M, Contacos PG. The Primate Malarias. National Institute of Health, 1971; 366 pp.

  5. Krief S, Escalante AA, Pacheco MA, Mugisha L, André C, Halbwax M, et al. On the diversity of malaria parasites in African apes and the origin of Plasmodium falciparum from Bonobos. PLoS Pathog. 2010;6:e1000765.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Tuteja R. Malaria—an overview. FEBS J. 2007;274:4670–9.

    Article  CAS  PubMed  Google Scholar 

  7. Sinka ME, Bangs MJ, Manguin S, Rubio-Palis Y, Chareonviriyaphap T, Coetzee M, et al. A global map of dominant malaria vectors. Parasit Vectors. 2012;5:69.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Ministerio de Salud-Grupo de Enfermedades Vectoriales Costa Rica. Norma de Malaria. https://www.inciensa.sa.cr/vigilancia_epidemiologica/Protocolos_Vigilancia/Norma%20de%20Malaria.pdf. 2015. Accessed 15 Mar 2021.

  9. Cormier LA. The historical ecology of human and wild primate malarias in the New World. Diversity. 2010;2:256–80.

    Article  Google Scholar 

  10. Chinchilla M, Guerrero OM, Gutiérrez G, Sánchez R. Presencia de Plasmodium brasilianum (Apicomplexa, Plasmodidae) en el mono congo (Alouatta palliata, Primates: Cebidae) de Costa Rica. Importancia epidemiológica en relación con el ser humano. Parasitol Latinoam. 2006;61:192–6.

    Article  Google Scholar 

  11. Fuentes-Ramírez A, Jiménez-Soto M, Castro R, Romero-Zuñiga JJ, Dolz G. Molecular detection of Plasmodium malariae/Plasmodium brasilianum in non-human primates in captivity in Costa Rica. PLoS One. 2017;12:e0170704.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Lalremruata A, Magris M, Vivas-Martinez S, Koehler M, Esen M, Kempaoah P, et al. Natural infection of Plasmodium brasilianum in humans: man and monkey share quartan malaria parasites in the Venezuelan Amazon. EBioMedicine. 2015;2:1186–92.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Calvo N, Morera J, Solorzano-Morales A, Herrero MV, Dolz G. Re-emergence of Plasmodium malariae in Costa Rica. Sci Postprint. 2015;1:e00049.

    Article  Google Scholar 

  14. de Alvarenga DAM, Culleton R, de Pina-Costa A, Rodrigues DF, Bianco C, Silva S, et al. An assay for the identification of Plasmodium simium infection for diagnosis of zoonotic malaria in the Brazilian Atlantic Forest. Sci Rep. 2018;8:86.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Brasil P, Zalis MG, de Pina-Costa A, Siqueira AM, Júnior CB, Silva S, et al. Outbreak of human malaria caused by Plasmodium simium in the Atlantic Forest in Rio de Janeiro: a molecular epidemiological investigation. Lancet Glob Health. 2017;5:e1038–46.

    Article  PubMed  Google Scholar 

  16. Araujo M, Messias MR, Figueiró MR, Gil LH, Probst CM, Vidal N, et al. Natural Plasmodium infection in monkeys in the state of Rondônia (Brazilian Western Amazon). Malar J. 2013;12:180.

    Article  PubMed  PubMed Central  Google Scholar 

  17. de Castro Duarte AM, dos Santos MR, Cerutti C, Curado I, de Paiva BR, Maeda AY, et al. Natural Plasmodium infections in Brazilian wild monkeys: reservoirs for human infections? Acta Trop. 2008;107:179–85.

    Article  Google Scholar 

  18. Martin MJ, Rayner JC, Gagneux P, Barnwell JW, Varki A. Evolution of human-chimpanzee differences in malaria susceptibility: relationship to human genetic loss of N-glycolylneuramidic acid. Proc Natl Acad Sci USA. 2005;102:12819–24.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Caminade C, Kovats S, Rocklov J, Tompkins AM, Morse AP, Colón-González FJ, et al. Climate change and malaria: Model intercomparison. Proc Natl Acad Sci USA. 2014;111:3286–91.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Marín-Rodríguez R, Chaves LF. Parasite removal for malaria elimination in Costa Rica. Trends Parasitol. 2019;35:585–8.

    Article  PubMed  Google Scholar 

  21. McMichael AJ, Martens WJM. The health impacts of global climate change: grasping with scenarios, predictive models and multiple uncertainties. Ecosyst Health. 1995;1:23–33.

    Google Scholar 

  22. Sehgal RN. Manifold habitat effects on the prevalence and diversity of avian blood parasites. Int J Parasitol Parasit Wildl. 2015;4:421–30.

    Article  Google Scholar 

  23. Glander KE, Fedigan LM, Fedigan C, Chapman C. Field methods for capture and measurement of three monkey species in Costa Rica. Folia Primatol (Basel). 1991;57:70–82.

    Article  CAS  Google Scholar 

  24. West G, Heard D, Caulkett N. Zoo Animal and wildlife immobilization and anesthesia. Ames, Iowa: Blackwell Publ; 2007. p. 718.

    Book  Google Scholar 

  25. Rubio JM, Post RJ, van Leeuwen WM, Henry MC, Lindergard G, Hommel M. Alternative polymerase chain reaction method to identify Plasmodium species in human blood samples: the semi-nested multiplex malaria PCR (SnM-PCR). Trans R Soc Trop Med Hyg. 2002;96:199–204.

    Article  CAS  Google Scholar 

  26. Smith AB, Godsoe W, Rodríguez-Sánchez F, Wang HH, Warren D. Niche estimation above and below the species level. Trends Ecol Evol. 2019;34(3):260–73.

    Article  PubMed  Google Scholar 

  27. Martinsen ES, Perkins SL, Schall JJ. A three-genome phylogeny of malaria parasites (Plasmodium and closely related genera): evolution of life-history traits and host switches. Mol Phylogenet Evol. 2008;47:261–73.

    Article  CAS  PubMed  Google Scholar 

  28. Peterson AT, Soberón J, Sánchez-Cordero V. Conservatism of ecological niches in evolutionary time. Science. 1999;285:1265–7.

    Article  CAS  PubMed  Google Scholar 

  29. Izeta-Alberdi A, Ibarra-Cerdeña CN, Moo-Llanes DA, Ramsey JM. Geographical, landscape and host associations of Trypanosoma cruzi DTUs and lineages. Parasit Vectors. 2016;9:631.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Castaño-Quintero S, Escobar-Luján J, Osorio-Olvera L, Peterson AT, Chiappa-Carrara X, Martínez-Meyer E, et al. Supraspecific units in correlative niche modeling improves the prediction of geographic potential of biological invasions. Peer J. 2020;8:e10454.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Phillips SJ, Anderson RP, Schapire RE. Maximum entropy modeling of species geographic distributions. Ecol Model. 2006;190:231–59.

    Article  Google Scholar 

  32. Elith J, Graham H, Anderson CP, Dudík R, Ferrier M, Guisan S, et al. Novel methods improve prediction of species’ distributions from occurrence data. Ecography. 2006;29:129–51.

    Article  Google Scholar 

  33. Valavi R, Guillera-Arroita G, Lahoz-Monfort JJ, Elith J. Predictive performance of presence-only species distribution models: a benchmark study with reproducible code. Ecol Monographs. 2021;1:e01486.

    Google Scholar 

  34. Cobos ME, Peterson AT, Barve N, Osorio-Olvera L. Kuenm: an R package for detailed development of ecological niche models using Maxent. Peer J. 2019;7:e6281.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Warren D, Seifert SN. Ecological niche modeling in MaxEnt: the importance of model complexity and the performance of model selection criteria. Ecol Appl. 2011;21:335–42.

    Article  PubMed  Google Scholar 

  36. Aiello-Lammens ME, Boria RA, Radosavljevic A, Vilela B, Anderson RP. spThin: an R package for spatial thinning of species occurrence records for use in ecological niche models. Ecography. 2015;38:541–5.

    Article  Google Scholar 

  37. Moo-Llanes DA, Pech-May A, de Oca-Aguilar ACM, Salomón OD, Ramsey JM. Niche divergence and paleo-distributions of Lutzomyia longipalpis mitochondrial haplogroups (Diptera: Psychodidae). Acta Trop. 2020;211:105607.

    Article  CAS  PubMed  Google Scholar 

  38. Muscarella R, Galante PJ, Soley-Guardia M, Boria RA, Kass JM, Uriarte M, Anderson RP. ENMeval: An R package for conducting spatially independent evaluations and estimating optimal model complexity for Maxent ecological niche models. Methods Ecol Evol. 2014;5:1198–205.

    Article  Google Scholar 

  39. Soberón J, Peterson AT. Interpretation of models of fundamental ecological niches and species’ distributional areas. Biodiversity Inform. 2005;2:1–10.

    Article  Google Scholar 

  40. Barve N, Barve V, Jiménez-Valverde A, Lira-Noriega A, Maher SP, Peterson AT, et al. The crucial role of the accessible area in ecological niche modeling and species distribution modeling. Ecol Model. 2011;222:1810–9.

    Article  Google Scholar 

  41. Olson DM, Dinerstein E, Wikramanayake ED, Burgess ND, Powell GVN, Underwood EC, et al. Terrestrial ecoregions of the world: a new map of life on Earth: a new global map of terrestrial ecoregions provides an innovative tool for conserving biodiversity. Bioscience. 2001;51:933–8.

    Article  Google Scholar 

  42. Carmona-Castro O, Moo-Llanes DA, Ramsey JM. Impact of climate change on vector transmission of Trypanosoma cruzi (Chagas, 1909) in North America. Med Vet Entomol. 2018;32:84–101.

    Article  CAS  PubMed  Google Scholar 

  43. Fick SE, Hijmans RJ. WorldClim 2: New 1-km spatial resolution climate surfaces for global land areas. Int J Climatol. 2017;37:4302–15.

    Article  Google Scholar 

  44. Escobar LE, Lira-Noriega A, Medina-Vogel G, Peterson AT. Potential for spread of the white-nose fungus (Pseudogymnoascus destructans) in the Americas: use of Maxent and NicheA to assure strict model transference. Geospat Health. 2014;9:221–9.

    Article  PubMed  Google Scholar 

  45. Moo-Llanes DA, Ibarra-Cerdeña CN, Rebollar-Téllez EA, Ibáñez-Bernal S, González C, Ramsey JM. Current and future niche of North and Central American sand flies (Diptera: Psychodidae) in climate change scenarios. PLoS Negl Trop Dis. 2013;7:e2421.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Estrada-Peña A, Estrada-Sánchez A, Estrada-Sánchez D, de la Fuente J. Assessing the effects of variables and background selection in the capture of the tick climate change. Int J Health Geograph. 2013;12:43.

    Article  Google Scholar 

  47. Nuñez-Penichet C, Osorio-Olvera L, Gonzalez V, Cobos ME, Jimenez L, DeRaad DA, et al. Geographic potential of the world’s largest hornet, Vespa mandarinia Smith (Hymenoptera: Vespidae), worldwide and particularly in North America. Peer J. 2021;9:e10690.

    Article  PubMed  PubMed Central  Google Scholar 

  48. Peterson AT, Soberón J, Pearson RG, Anderson RP, Martinez-Meyer E, Nakamura M. Ecological niches and geographic distribution. Princeton University Press. 2012, ISBN:9780691136882

  49. Avila-Aguero ML. Epidemiología de la malaria en Costa Rica. Acta Med Costarricense. 2008;50:72–4.

    Google Scholar 

  50. Ministerio de Salud. Alerta Sanitaria por casos de malaria. 2018. https://www.ministeriodesalud.go.cr/index.php/alertas/alertas-sanitarias/nacionales/3829-alerta-sanitaria-por-casos-de-malaria/file. Accessed 17 Sept 2021.

  51. Volney B, Pouliquen JF, de Thoisy B, Fandeur T. A sero-epidemiological study of malaria in human and monkey populations in French Guiana. Acta Trop. 2002;82:11–23.

    Article  PubMed  Google Scholar 

  52. Fandeur T, Volney B, Peneau C, de Thoisy B. Monkeys of the rainforest in French Guyana are natural reservoirs for P. brasilianum/P. malariae malaria. Parasitology. 2000;120:11–21.

    Article  CAS  PubMed  Google Scholar 

  53. Guimarães LO, Bajay MM, Wunderlich G, Bueno MG, Röhe F, Catão-Dias JL, et al. The genetic diversity of Plasmodium malariae and Plasmodium brasilianum from human, simian and mosquito hosts in Brazil. Acta Trop. 2012;124:27–32.

    Article  PubMed  Google Scholar 

  54. Oliveira TC, Rodrigues PT, Duarte AMRC, Rona LDP, Ferreira MU. Ongoing host-shift speciation in Plasmodium simium. Cell Press. 2021;3:940–1.

    Google Scholar 

  55. Collins WE, Chin W, Warren M, Huong AY, Jeffery GM, Skinner JC. Observations on two strains of Plasmodium falciparum from Haiti in Aotus monkeys. J Parasitol. 1981;68:657–67.

    Article  Google Scholar 

  56. Collins WE, Skinner JC, Broderson JR, Huong AY, Mehaffey PC, Stanfill PS, Sutton BB. Infection of Aotus azarae boliviensis monkeys with different strains of Plasmodium falciparum. J Parasitol. 1986;72:525–30.

    Article  CAS  PubMed  Google Scholar 

  57. Fajfar-Whetstone CJ, Collins WE, Ristic M. In vitro and in vivo adaptation of the Geneve/SGE-1 strain of Plasmodium falciparum to growth in a squirrel monkey (Saimiri sciureus) model. Am J Trop Med Hyg. 1987;36:221–7.

    Article  CAS  PubMed  Google Scholar 

  58. Organización Panamericana de la Salud & Ministerio de Salud. Diagnóstico situacional de la malaria y el DDT en Costa Rica; http://www.bvsde.paho.org/bvsdepl/fulltext/ddt/cor.pdf. 2000, Accessed 15 Mar 2021.

  59. Marelli MT, Malafronte RS, Sallum MAM, Natal D. Kerteszia subgenus of Anopheles associated with the Brazilian Atlantic rainforest: current knowledge and future challenges. Malar J. 2007;6:127.

    Article  Google Scholar 

  60. Verhulst NO, Smallegange RC, Takken W. Mosquitoes as potential bridge vectors of malaria parasites from non-human primates to humans. Front Physio. 2012;3:197.

    Article  Google Scholar 

  61. Faust C, Dobson A. Primate malarias: diversity, distribution and insights for zoonotic Plasmodium. One Health. 2015;1:66–75.

    Article  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

We are grateful to David Moo-Llanes for his help with niche modelling, and to all contributors who assisted with sampling endeavors.

Funding

This research was conducted in the framework of the project “Estudios epidemiológicos (Malaria, Dengue, Virus del Oeste del Nilo, Encefalitis Equina Venezolana), genéticos, etológicos, poblacionales y de hábitat en monos de Costa Rica” sponsored by FEES-CONARE, and with participation of UNA-ITCR-UCR-UNED.

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Authors and Affiliations

Authors

Contributions

AC and GD conceived the investigation and wrote the article. AC, SB, EO-M and GA, G-E collected samples. AC and GD conducted the laboratory analysis. AC, GN and CNI-C performed the statistical analysis. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Andrea Chaves.

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Ethics approval and consent for participate

The present study was conducted with protocols approved by the Comisión de Bienestar Animal, Universidad Nacional, Heredia (EMV-CBA-05), and adhered to the legal requirements of Costa Rica. Collection permit number: MINAET 116 SINAC Costa Rica-042-2012.

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Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Supplementary Information

Additional file 1: Fig. S1.

Omission rates and AICc values for all, non-significant, and selected “best” candidate models for the Plasmodium sp.

Additional file 2: Fig. S2.

Maps of the best models according to the performance evaluation. Maps order are the same as Table 1, (a) 1st, (b) 2nd, (c) 3rd, (d) 4th, (e) 5th, and (f) 6th.

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Chaves, A., Dolz, G., Ibarra-Cerdeña, C.N. et al. Presence and potential distribution of malaria-infected New World primates of Costa Rica. Malar J 21, 17 (2022). https://doi.org/10.1186/s12936-021-04036-y

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