Literature DB >> 29377918

Ecological suitability modeling for anthrax in the Kruger National Park, South Africa.

Pieter Johan Steenkamp1, Henriette van Heerden2, Ockert Louis van Schalkwyk2.   

Abstract

The spores of the soil-borne bacterium, Bacillus anthracis, which causes anthrax are highly resistant to adverse environmental conditions. Under ideal conditions, anthrax spores can survive for many years in the soil. Anthrax is known to be endemic in the northern part of Kruger National Park (KNP) in South Africa (SA), with occasional epidemics spreading southward. The aim of this study was to identify and map areas that are ecologically suitable for the harboring of B. anthracis spores within the KNP. Anthrax surveillance data and selected environmental variables were used as inputs to the maximum entropy (Maxent) species distribution modeling method. Anthrax positive carcasses from 1988-2011 in KNP (n = 597) and a total of 40 environmental variables were used to predict and evaluate their relative contribution to suitability for anthrax occurrence in KNP. The environmental variables that contributed the most to the occurrence of anthrax were soil type, normalized difference vegetation index (NDVI) and precipitation. Apart from the endemic Pafuri region, several other areas within KNP were classified as ecologically suitable. The outputs of this study could guide future surveillance efforts to focus on predicted suitable areas for anthrax, since the KNP currently uses passive surveillance to detect anthrax outbreaks.

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Year:  2018        PMID: 29377918      PMCID: PMC5788353          DOI: 10.1371/journal.pone.0191704

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


Introduction

Anthrax is a rapidly fatal disease caused by the spore-forming bacterium B. anthracis. The disease can affect most species, but ruminants are particularly susceptible. Multiple host and environmental factors are thought to play a role in the transmission of anthrax. Many of Africa’s wildlife reserves experience cyclic anthrax outbreaks, one such area being the KNP in SA. However, little is known about the spatial ecology and epidemiology of anthrax [1]. The general thought is that B. anthracis is an obligate in vivo pathogen and that little propagation occurs in soil. Septicaemic infection with anthrax causes impaired clotting function [2]. When an animal succumbs to anthrax, the host’s impaired clotting ability results in blood draining into the soil from any orifice. If the environmental conditions are suitable, the bacterium will rapidly form spores once outside the host. Depending on the environmental conditions, these spores can survive for decades in the soil until infection of a suitable host takes place. Soil pH and soil calcium levels are considered the most important properties for spore survival and, therefore, endemicity of B. anthracis is associated with elevated calcium and neutral-to-alkaline soils [3-7]. Although these are considered the most important factors for the long-term survival of B. anthracis in the soil, other variables such as environmental temperature, rainfall, vegetation, presence of scavengers and mechanical vectors also play a vital role in the spread of the disease [8, 9]. Anthrax is considered an indigenous and integral part of the KNP ecosystem [2, 9]. The first confirmed case of anthrax in the KNP was in 1954, but it has been in the northern region of the Park for at least 200 years, as was proven by isolation of spores from archaeological bones dating back to 1700 ± 50 BC [10]. Anthrax outbreaks in KNP appear to have a cyclical pattern of roughly 10 years and are most often associated with a dry climatological spell after a couple of years of above average rainfall [11]. In an extensive wildlife reserve, such as the KNP, it is very difficult, if not impossible, to ensure immediate and proper disposal of anthrax-infected carcasses. Contaminated areas with anthrax spores in the soil and vegetation are thus constantly created by animals dying from the disease [12, 13]. Scavengers and predators may play a role in the dissemination of spores by the opening up and dispersal of carcasses, which could also have a dilution effect at the infected carcass site, but this remains speculative due to a lack of quantitative data. Spores can also be passed in scavengers’ feces to new sites or to water sources after feeding on infected carcasses and are disseminated by insects (blowflies in KNP) [8]. Water run-off [8] and infected carcasses [13] can contaminate the grazing that is in turn ingested by herbivores. Animals can stir up and ingest spores during the dry season when congregations occur around water points. Once an epidemic starts, the maintenance and spread of the disease are determined by biotic factors. Death from anthrax is per-acute to acute, although buffalo (Syncerus caffer) and eland (Taurotragus oryx) can travel great distances (~30 km) before a new infection locus will be established [11]. The dissemination of anthrax is still poorly researched since many of the assumptions are based on observation with no or little quantitative data available. Kudu (Tragelaphus strepsiceros) are especially important in the spread of the disease since their numbers are positively correlated to food availability and therefore rainfall in the Park [14]. De Vos and Bryden [10], as well as Hugh-Jones and De Vos [8], indicated that an anthrax outbreak can be considered more likely when kudu numbers are high. This is explained by blow-flies that feed on body fluids of anthrax-infected carcasses and deposit their contaminated feces or regurgitated liquid on leaves of vegetation in the vicinity of the carcass [8, 11]. However, it has been shown that blow-flies can disperse up to 65 km from a carcass [15]. Browsing herbivores, such as kudu, that feed at a level where infected blow-fly regurgitated liquid are deposited on leaves (1–3 m) may then contract anthrax, starting a new cycle where the animal dies [11]. The identification of ecologically suitable areas for B. anthracis spores, and hence potential disease risk, is critical for the surveillance and management of the disease in wildlife, as wide scale immunization in wildlife remains untenable [16]. Passive surveillance is currently used to test potentially infected carcasses and monitor the extent of an outbreak (personal communication, State Veterinary Services, KNP, O. L. van Schalkwyk). Modeling of ecologically suitable areas for anthrax in the KNP may lead to a better understanding of anthrax ecology and epidemiology. Different, presence-only modeling approaches to predict the geographic distribution of B. anthracis have been used, such as Maxent [17] and GARP (genetic algorithm for rule-set prediction) [1, 18–20]. Tarkesh and Jetschke [21] compared correlative models including Worldclim, GARP and Maxent using the same input data and found Maxent achieved the best prediction. For the purpose of this study, ecologically suitable areas for anthrax spores were identified within KNP that are able to harbor the spores in sufficient quantities and for a period long enough to result in wildlife infection using the Maxent species distribution modeling method.

Materials and methods

Anthrax occurrence data

A database with a total of 597 confirmed positive anthrax cases in wildlife was constructed from historical records provided by the State Veterinary Services in Skukuza, KNP. These data were collected from 1988 to 2011. Maxent (version 3.3.3k, [22]) was used to determine ecological suitability for B. anthracis in the KNP. Maxent is a species distribution modelling technique that can be used with presence-only data and is considered equivalent to Poisson regression [22, 23]. To minimize model overfitting, the testing/training data set was created by classifying each pixel in the analysis framework of 18983 pixels (1 km2 resolution) as positive or negative, regardless of the number of cases in a positive pixel. A total of 219 positive pixels were identified (S1 Fig).

Environmental variables

A total of forty environmental variables were selected (S1 Table). These included nineteen climatic variables from the Worldclim dataset (S2 Table) [24]. Six environmental variables including land type, landscape, soil data, lithology, geology and bore hole locations were provided by the KNP Scientific Services. From these six variables, a further three environmental variables (calcium (Ca), pH and distance to boreholes) were derived. Two layers—caventer and phventer were created from a dataset [25] with 370 soil sampling sites from KNP [26]. Inverse Distance Weighted (IDW) interpolation was used in ArcGIS (version 9.3.1) to derive continuous Ca and pH values. Ideally, specific measured values around KNP should be used, but this was not possible from the data available. Eight soil parameters (clay, cation exchange capacity, pH, potassium, calsium, magnesium, sodium, and phosphorus) were extracted from the SOil and TERrain (SOTER) digital database [27, 28]. Three distances to water layers (seasonal, ephemeral and permanent) were created, based on the hydrological index (HI) classification by Hannart and Hughes [29], which classifies rivers with a HI of 4.39–16.10 (class 1–4) as permanent, 16.11–37.81 (class 5) as seasonal and those with a HI larger than 37.81 as ephemeral (classes 6–9). A land cover layer was provided by the Peace Parks Foundation [30]. All environmental layers were rasterised, projected and resampled to a 1 km resolution before being clipped to the extent of the KNP. All datasets were prepared in ArcGIS. Sample selection bias was factored out by providing a target background layer [31, 32]. This layer was created by only selecting ranger sections of the KNP in which anthrax cases occurred over the study period. Since there are numerous ranger sections within the Park, this method provided an easy way to select the most appropriate target background layer. All the variables were evaluated for contribution importance using multiple regression and a jackknife procedure. The best subset of variables was selected based on outputs of the jackknife procedure, Maxent model surveyor (www.phycoweb.net/software), 95% gain confidence interval evaluation [33] and response curve interpretation [22]. Simple multiple regression was used to eliminate linearly correlated variables [34]. These selected variables were used for the second (final) model.

Model parameters

A training dataset was used to build the model and an independent test dataset was used to measure how accurately the model can predict the points within this test set. A random test percentage option is also included in Maxent to indicate the percentage of data to use for testing and training. This dataset was divided into 75% training and 25% testing presence points (S1 Fig). Without this mutual exclusivity, the model would use the training data in testing, thus inflating model performance [35]. A total of 10 model runs were performed with convergence limit of 0.00001 and the maximum number of iterations set to 5000. A unique training and test dataset was created for each model run. The average value output map produced by Maxent was selected as the final output map for the model and is reported as the logistic value (continuous between zero and one, one being the highest suitability). In addition, an area under curve (AUC) measure was calculated as well as the true skill statistic (TSS). Two omissions (total and average) and commission (total and average) measures to test model performance were calculated [36]. The equal sensitivity and specificity threshold was used for the TSS calculation. TSS can be defined as sensitivity + specificity– 1 and values range from 0 to 1. A value of > 0.6 is considered ‘good’ and > 0.8 as ‘excellent’ [37]. Likewise, a successful model will have an AUC score approaching 1.0 and a model predicting no better than random will have an AUC approaching 0.5 [1, 38]. AUC analysis is independent of both threshold setting and prevalence, making it a very effective method for model evaluation when working with presence-only data [36]. Araújo and Guisan [38] defined a rough guide for classifying models based on their accuracy (AUC): 0.6–0.7 poor, 0.7–0.8 average, 0.8–0.9 good, 0.9–1 excellent. AUC analysis is independent of both threshold setting and prevalence, making it a very effective method for model evaluation when working with presence-only data [36]. A threshold of 80% was used to identify the area as suitable for the occurrence of anthrax in the environment. This threshold was chosen based upon the assumption that areas with a very high probability (>80%) of anthrax occurrence have the potential to be ecologically suitable for harbouring spores, thus anthrax is endemic. Areas with a lower probability of anthrax occurrence are most likely propagating epidemic occurrences.

Results

Twelve environmental variables were retained to construct the final Maxent model (Table 1, S2 Fig). On average, model convergence was reached after 2700 iterations. The average AUC score for the model was 0.9, which was significantly different from a line of no information (p < 0.001). The model performed very well on the test data with an average AUC of 0.8. The TSS indicated a moderate performance of the model (TSS = 0.6), based on the average of 10 partitions and the defined threshold of 1.0. However, this result still differs significantly from chance (TSS = 0). The model had a total omission of 25.8% and an average omission of 23.5%. Potentially suitable habitat was predicted with a high success rate of 79.8% for the equal sensitivity-specificity threshold and was statistically significant (p < 0.001). All accuracy metrics are summarized in Table 2.
Table 1

Environmental variables used for the final Maxent model.

Variable aType of dataSourceReferences
Integrated NDVI (indvi)bReflectance derivedMODIS-TERRA[39]
Elevation (altitude)Elevation derivedAster-DEM[40]
Distance to permanent water (permdist)Distance metricsArcGIS Spatial Analyst extension[29]
Distance to seasonal water (seasdist)Distance metricsArcGIS Spatial Analyst extension[29]
Distance to ephemeral water (ephdist)Distance metricsArcGIS Spatial Analyst extension[29]
Geology (geologyventer)cSoilsKNP Scientific Services Skukuza[25, 26, 41]
SOTER Soil ID (sotersoilid)SoilsSOTER database[27, 28]
Land Type (ltypeventer)SoilsKNP Scientific Services Skukuza[26]
Landscape (landscapegert)SoilsKNP Scientific Services Skukuza[26]
Calcium (caventer)SoilsInterpolated from Venter database[25, 27, 28, 42]
Precipitation of driest quarter (preqdryq)dClimateWorldclim[24]
Temperature seasonality (tempseasonality)ClimateWorldclim[24]

a Variable name as used in model included in parenthesis

b Measure of overall productivity and biomass as derived through the small seasonal integral of time-integrated NDVI images between 2000–2009 and is not extracted for each case’s time of death.

c Venter [25] classified the soils of Kruger National Park into 15 major classes and described the chemical composition of each.

d Precipitation is the 50 year average 1950–2000 from the Worldclim dataset.

Table 2

Accuracy metrics for the predicted distribution for Maxtent model using 12 variables.

MetricaModel specifications
Overall accuracy79.5%
N to build models165
N to test models54
Total omission25.8%
Average omission23.5%
Total commission79.8%
Average commission79.5%
TSS0.562
AUC0.857

a N indicates the number of positive point occurrences and was divided into 25% testing:75% training locations at each model subset

TSS = true skill statistic; AUC = area under curve.

a Variable name as used in model included in parenthesis b Measure of overall productivity and biomass as derived through the small seasonal integral of time-integrated NDVI images between 2000–2009 and is not extracted for each case’s time of death. c Venter [25] classified the soils of Kruger National Park into 15 major classes and described the chemical composition of each. d Precipitation is the 50 year average 1950–2000 from the Worldclim dataset. a N indicates the number of positive point occurrences and was divided into 25% testing:75% training locations at each model subset TSS = true skill statistic; AUC = area under curve. Four arbitrarily defined probability classes were used to classify the ecological suitability of the modeled prediction (Table 3) ranging from high (0.8–1), moderate (0.6–0.8), low (0.3–0.6) and not suitable (0–0.3). The highly suitable area consisted of 81.67 km2 (0.42% of total area), 702.62 km2 moderate (3.61% of total area), 3943.48 km2 low (20.24% of total area) and 14752.23 km2 not suitable (75.73% of the total area). The highly suitable areas for B. anthracis (greater than 0.8) included mainly the northern Pafuri region as well as the Shingwedzi region (south of Pafuri) and the central KNP Letaba region (Fig 1).
Table 3

Threshold point values (>0.8) for the twelve environmental variables and the three most suitable areas identified by the model in Kruger National Park for Bacillus anthracis occurrence (see Fig 1).

SectionPafuriShingwedziLetabaKruger National Park mean (range)
n pixels in area of interest16463834444718921
n cases in area of interest30213181597
n pixels containing cases689026219
n pixels > = 0.8 threshold75504134
Altitude (altitude)228.806281225.933292 (145–570)
Calcium (caventer)171.835184.626198.049148 (10–282)
Ephemeral Water Distance (ephdist)2069.046013181.5263618 (0 –20384)
Seasonal Water Distance (seasdist)3169.58707038.0074124 (0–14764)
Permanent Water Distance (permdist)2190.00046840.200733.33312461 (0–53450)
Geology Venter (geologyventer)LB, CS, ALALECLB, CS, AL, EC
INDVI (indvi)8.5899.3688.8687.34 (-775–15)
Landscape (landscapegert)25,283521,2221, 22, 25, 28, 35
Landtype (ltypeventer)Pa04,Pa05Le05Le01Le01, Le05, Pa04, Pa05
Precipitation Driest Quarter (precdryq)91423.73314.7 (8–36)
SOTER Soil ID (sotersoilid)ZA21,ZA22ZA115ZA282ZA21, ZA22, ZA115, ZA282
Temperature Seasonality (tempseasonality)3389.09736873759.93333439 (2838–3828)

LB–Karoo system; Olivine rich basalts, sub-ordinate alkali basalts, shoshonites [41]. CS–Karoo system; Fine grained sandstone, mudstone, chert (Cave sandstone and redbed stages) [41]. AL–Quarternary; Alluvium [41]. EC–Karoo system; Shale with coal seams, mudstone, grit (Ecca series) [41]. 15 –Colophospermum mopane forest. 21 –Combretum / Acacia nigrescens rugged veld. 22 –Combretum / Colophospermum mopane rugged veld. 25 –Adansonia digitata / Colophospermum mopane rugged veld. 28 –Limpopo / Luvuvhu floodplain. 35 –Salvadora angustifolia floodplains. ZA21, ZA115 –Eutric cambisols (A cambisol (CM) can be defined as having either a cambic or a mollic horizon. A cambic horizon is a weakly developed mineral soil horizon and a mollic horizon is a surface horizon of mineral soil that is dark in colour, relatively deep and contains (dry weight) at least 1% organic matter or 0.6% organic carbon) [28]. Le01: Letaba landtype; Le05: Shingwedzi Landtype; includes the Shingwedzi river; Pa04 and 05: Pafuri Landtype [25]. ZA22 –Eutric leptosols (A leptosol (LP) can be defined through a limit in depth by continuous hard rock within 25 cm from the soil surface, overlying material with a calcium carbonate equivalent of more than 40 percent within 25 cm from the soil surface or less than 10 percent (by weight) fine earth to a depth of 75 cm or more from the soil surface) [28]. ZA282 –Leptic phaeozems (Continuous rock starting between 50 and 100 cm from the soil surface with a mollic horizon and (1) a base saturation of 50 percent or more and no secondary carbonates, at least to a depth of 100 cm from the soil surface and (2) with no diagnostic horizons other than an albic, argic, cambic or vertic horizon) [28].

Fig 1

Predicted ecological suitability (>80%) for Bacillus anthracis.

The red areas (greater than 0.8 probability) indicate areas of increased Bacillus anthracis ecological suitability and black rectangles indicate the three most suitable areas (A. Pafuri, B. Shingwedzi, C. Letaba) for B. anthracis detection in Kruger National Park.

Predicted ecological suitability (>80%) for Bacillus anthracis.

The red areas (greater than 0.8 probability) indicate areas of increased Bacillus anthracis ecological suitability and black rectangles indicate the three most suitable areas (A. Pafuri, B. Shingwedzi, C. Letaba) for B. anthracis detection in Kruger National Park. LB–Karoo system; Olivine rich basalts, sub-ordinate alkali basalts, shoshonites [41]. CS–Karoo system; Fine grained sandstone, mudstone, chert (Cave sandstone and redbed stages) [41]. AL–Quarternary; Alluvium [41]. EC–Karoo system; Shale with coal seams, mudstone, grit (Ecca series) [41]. 15 –Colophospermum mopane forest. 21 –Combretum / Acacia nigrescens rugged veld. 22 –Combretum / Colophospermum mopane rugged veld. 25 –Adansonia digitata / Colophospermum mopane rugged veld. 28 –Limpopo / Luvuvhu floodplain. 35 –Salvadora angustifolia floodplains. ZA21, ZA115 –Eutric cambisols (A cambisol (CM) can be defined as having either a cambic or a mollic horizon. A cambic horizon is a weakly developed mineral soil horizon and a mollic horizon is a surface horizon of mineral soil that is dark in colour, relatively deep and contains (dry weight) at least 1% organic matter or 0.6% organic carbon) [28]. Le01: Letaba landtype; Le05: Shingwedzi Landtype; includes the Shingwedzi river; Pa04 and 05: Pafuri Landtype [25]. ZA22 –Eutric leptosols (A leptosol (LP) can be defined through a limit in depth by continuous hard rock within 25 cm from the soil surface, overlying material with a calcium carbonate equivalent of more than 40 percent within 25 cm from the soil surface or less than 10 percent (by weight) fine earth to a depth of 75 cm or more from the soil surface) [28]. ZA282 –Leptic phaeozems (Continuous rock starting between 50 and 100 cm from the soil surface with a mollic horizon and (1) a base saturation of 50 percent or more and no secondary carbonates, at least to a depth of 100 cm from the soil surface and (2) with no diagnostic horizons other than an albic, argic, cambic or vertic horizon) [28]. Of the environmental variables tested (Table 1), the most important predictor in seven out of the 12 partitions was the SOTER soil class. The land type as defined by Venter [25] ranked top in the remaining five partitions. Distance to ephemeral water, soil calcium, and the integrated NDVI value ranked next, in that order, in terms of unique information, but the precipitation during the driest quarter contributed much more to the overall model gain, making this variable the third most important. Table 3 compares the values of each environmental variable used, between the range for the entire study area and the three areas in the KNP predicted to be highly suitable for B. anthracis detection. The Pafuri region in the far north of KNP is considered endemic for anthrax with periodic outbreaks, typically occurring during late winter and spreading southward [8] but since 2008 outbreaks have been recorded in the summer after rain. This endemic area lies between the Limpopo (north) and Luvuvhu (south) rivers with the most suitable areas along these river beds. A large number of drainage channels occur into this area from the higher lying southern landscape. Areas south of the Pafuri depression with high anthrax suitability (80–100%) are displayed in Fig 2A. Areas within the Shingwedzi, Mphongolo, Phugwane and Bubube rivers (Shingwedzi river system) with high anthrax suitability (80–100%) are displayed in Fig 2B. The only highly suitable area in this section that is not associated with the Shingwedzi river system is the Nyawutsi waterhole just north of the Kostini patrol camp. In the Letaba section (Fig 2C) the Zombe waterhole has a very high suitability and similarly the N'washibejana waterhole in the Olifants ranger section.
Fig 2

Three most ecologically suitable habitats for Bacillus anthracis areas in Kruger National Park.

The following suitable areas for the harbouring of B. anthracis spores within the soil was identified using maximum entropy as a statistical model, a range of environmental predictors and anthrax occurrence data: (A) Pafuri in the northern Kruger National Park, (B) Shingwedzi river system and (C) Letaba / Olifants sections.

Three most ecologically suitable habitats for Bacillus anthracis areas in Kruger National Park.

The following suitable areas for the harbouring of B. anthracis spores within the soil was identified using maximum entropy as a statistical model, a range of environmental predictors and anthrax occurrence data: (A) Pafuri in the northern Kruger National Park, (B) Shingwedzi river system and (C) Letaba / Olifants sections.

Discussion and conclusions

This study presents the first estimate of ecologically suitable areas for anthrax spore survival in the KNP in South Africa. These ecologically suitable areas for the harboring of B. anthracis spores within the soil was identified using anthrax occurrence data, a range of environmental predictors and maximum entropy modeling. Outputs suggest there are at least three geographically distinct regions within the Park–Pafuri, Shingwedzi, and Letaba–that are highly suitable for anthrax spore survival. Our findings of low altitude (225–280 m), high soil calcium content (171–198 me/kg), low dry quarter precipitation (9–24 mm), proximity to a water source and mineral rich, eutrophic soils as essential conditions for survival of anthrax is in agreement with most similar studies on anthrax [1, 17–19, 43]. However, the lack of influence of pH layers implicitly used in this model was surprising, although this could be due to lack of information at the spatial scale at which they were employed. Calcium (Ca) sulphate and high pH were identified as important variables in other anthrax distribution studies [1, 17, 18]. As B. anthracis is a soil borne pathogen, variables related to soil (soil moisture content, soil pH, Ca sulphate and soil type) all contributed to the potential distribution of B. anthracis in these studies from different continents. Ca has been shown to be important for both spore germination and the maintenance of dormancy [7]. As the soil pH increases above 7.2, due to additional soil Ca, the "free" Ca2+ is not absorbed into the soil and can bind with other compounds [25]. The soils of Pafuri, Shingwedzi and Letaba regions (Figs 1 and 2A–2C) are characterised by high Ca levels (and concomitant high pH), which would partly explain their high suitability for anthrax spore survival. The importance of land [25] and soil types (SOTER), in conjunction with precipitation and NDVI [1, 17, 18] which ranked high in most model predictions, compliments the recent finding that infected carcass sites play an important role in spore dissemination to grazers, and that grazing (not drinking) seems to play a significant role at infected carcass sites [12, 13]. Altitude was not identified to play a major role in this study, which is likely due to the small variation in altitude within the KNP compared to variation at, for example, a continental scale [1, 19]. Anthrax outbreaks within KNP seem to be regulated by rainfall and the hydrology of the area [10]. The disease typically occurs during late winter when the environment is dry and animals congregate around water sources. However since 2010 outbreaks have been observed in the wet and dry season (personal communications, Skukuza State Veterinary office). The dry quarter precipitation variable of the model had an average value of 9 mm for Pafuri, 14 mm for Shingwedzi and 23 mm for Letaba. This suggests that dry environmental conditions are important for anthrax occurrence in KNP. As soon as the first rain occurs, the incidence of new cases starts to decrease. This is likely due to the washing away of spores and an increase in water sources leading to animal dispersal and alternate vulture bathing sites [8, 11]. Spore suitability appears to be associated with rivers, with apparent accumulation downstream (eastward) and peaking at confluences. This is most likely due to the alluvial deposition of spores after flooding. Spores have a high surface hydrophobicity, allowing clumping in water and a high buoyant density, allowing clumped organic matter to float [6] and settle in the soil, as water levels recede. No quantitative data supports this apparent association and should be investigated. The relocation of B. anthracis spores with soil through water, flooding or rain could result in a new focality [9]. Most anthrax cases in Etosha National Park (ENP) in Namibia are observed in the wet season while elephants have an anthrax mortality peak in the dry season [44]. There are numerous suppositions regarding the timing of anthrax outbreaks in endemic areas such as changes in the environment or changes in animal behaviour or variation on concentration of B. anthracis in the environment. Investigating the influence of biotic and abiotic factors on the B. anthracis is complex due to the acute nature of the disease and number of variables involve in each outbreak and ecosystem. The northern Pafuri anthrax endemic area is located at an altitude of around 228 m with an average rainfall of 400 mm per year. This area is classified by Venter [25] as the Pafuri Land Type (Pa05) and its endemicity to anthrax has previously been described by De Vos [11]. There are many small pans in the area, which during late winter usually dry up, thus creating an ideal situation for the start of an anthrax cycle. A large number of drainage channels feeds into this area from the higher lying southern landscape. Pans are replenished by run-off water after heavy rains. Soil sample analyses from the Pafuri depression clearly indicated that it acts as a catchment and accumulation area for B. anthracis spores [11]. Alluvial lowlands flank the lower Luvuvhu and Limpopo rivers with sandy to deep red silt sediments. The soil depth that anthrax spores are found at is as shallow as three centimeters during dry, high-risk outbreak conditions and as deep as 15 cm during wetter, deposition periods. Deposition periods can be defined as the time when spores are washed away during heavy rains and deposited in low-lying silt beds [11]. KNP soil profiles become shallower and soil type diversity decreases towards the north [45]. The relationship of anthrax with geographic features within the northern KNP has been described by De Vos and Bryden [10] and the effect of altitude and permanent rivers are highlighted as physical barriers to the dispersal of anthrax. The Shingwedzi river system confluence is a low-lying area with an average altitude of 260 m and an average annual rainfall of 430 mm. Significant alluvial deposits occur along this river system and various drainage channels exist in this area. The river system is not permanent and will only act as a physical barrier during wet years and after heavy rains. Very high pH and Ca levels occur along valley bottoms with predominantly dense and heterogeneous riverine vegetation. The riverine areas immediately north and west of the Shingwedzi rest camp have the highest suitability ranking in this section. With the Letaba section, the proximity of the perennial Letaba and Olifants rivers makes the spread of anthrax from these areas highly unlikely. All of the high suitability areas are associated with stagnant water sources like dams, pans, and waterholes. This study confirmed the endemicity of the Pafuri region to anthrax but also identified a number of other potential endemic sites. However, it is important to note that this is only a measure of the potential of the environment to successfully harbor anthrax spores and not the actual anthrax occurrence probability.

Worldclim variables used in Maxent model.

(DOCX) Click here for additional data file.

Overview of environmental data used in Maxent indicating the variables, type of data and source.

(DOCX) Click here for additional data file.

Spatially unique cases of Bacillus anthracis and the predicted suitability for B. anthracis occurrence.

(PNG) Click here for additional data file.

Twelve environmental variables used in the final Maxent model.

(PNG) Click here for additional data file.
  15 in total

1.  Sample selection bias and presence-only distribution models: implications for background and pseudo-absence data.

Authors:  Steven J Phillips; Miroslav Dudík; Jane Elith; Catherine H Graham; Anthony Lehmann; John Leathwick; Simon Ferrier
Journal:  Ecol Appl       Date:  2009-01       Impact factor: 4.657

2.  Dispersal, density and habitat preference of the blow-flies Chrysomyia albiceps (Wd.) and Chrysomyia marginalis (Wd.) (Diptera: Calliphoridae).

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Journal:  Onderstepoort J Vet Res       Date:  1986-03       Impact factor: 1.792

3.  Ecology of anthrax.

Authors:  G B Van Ness
Journal:  Science       Date:  1971-06-25       Impact factor: 47.728

4.  Fatal attraction: vegetation responses to nutrient inputs attract herbivores to infectious anthrax carcass sites.

Authors:  Wendy C Turner; Kyrre L Kausrud; Yathin S Krishnappa; Joris P G M Cromsigt; Holly H Ganz; Isaac Mapaure; Claudine C Cloete; Zepee Havarua; Martina Küsters; Wayne M Getz; Nils Chr Stenseth
Journal:  Proc Biol Sci       Date:  2014-11-22       Impact factor: 5.349

5.  Bacillus anthracis diversity in Kruger National Park.

Authors:  K L Smith; V DeVos; H Bryden; L B Price; M E Hugh-Jones; P Keim
Journal:  J Clin Microbiol       Date:  2000-10       Impact factor: 5.948

6.  Modeling the potential distribution of Bacillus anthracis under multiple climate change scenarios for Kazakhstan.

Authors:  Timothy Andrew Joyner; Larissa Lukhnova; Yerlan Pazilov; Gulnara Temiralyeva; Martin E Hugh-Jones; Alim Aikimbayev; Jason K Blackburn
Journal:  PLoS One       Date:  2010-03-09       Impact factor: 3.240

7.  Spatial modelling of Bacillus anthracis ecological niche in Zimbabwe.

Authors:  S M Chikerema; A Murwira; G Matope; D M Pfukenyi
Journal:  Prev Vet Med       Date:  2013-05-29       Impact factor: 2.670

Review 8.  The ecology of anthrax spores: tough but not invincible.

Authors:  D C Dragon; R P Rennie
Journal:  Can Vet J       Date:  1995-05       Impact factor: 1.008

Review 9.  The ecology of Bacillus anthracis.

Authors:  Martin Hugh-Jones; Jason Blackburn
Journal:  Mol Aspects Med       Date:  2009-08-29

10.  Ecological niche modeling of Bacillus anthracis on three continents: evidence for genetic-ecological divergence?

Authors:  Jocelyn C Mullins; Giuliano Garofolo; Matthew Van Ert; Antonio Fasanella; Larisa Lukhnova; Martin E Hugh-Jones; Jason K Blackburn
Journal:  PLoS One       Date:  2013-08-19       Impact factor: 3.240

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  6 in total

1.  Participatory mapping identifies risk areas and environmental predictors of endemic anthrax in rural Africa.

Authors:  Roman Biek; Tiziana Lembo; Olubunmi R Aminu; Taya L Forde; Divine Ekwem; Paul Johnson; Luca Nelli; Blandina T Mmbaga; Deogratius Mshanga; Mike Shand; Gabriel Shirima; Markus Walsh; Ruth N Zadoks
Journal:  Sci Rep       Date:  2022-06-22       Impact factor: 4.996

2.  Seasonality and Ecological Suitability Modelling for Anthrax (Bacillus anthracis) in Western Africa.

Authors:  Claudia Pittiglio; Sean Shadomy; Ahmed El Idrissi; Baba Soumare; Juan Lubroth; Yilma Makonnen
Journal:  Animals (Basel)       Date:  2022-04-29       Impact factor: 3.231

3.  The pattern of anthrax at the wildlife-livestock-human interface in Zimbabwe.

Authors:  Norman L Mukarati; Gift Matope; Michel de Garine-Wichatitsky; Daud N Ndhlovu; Alexandre Caron; Davies M Pfukenyi
Journal:  PLoS Negl Trop Dis       Date:  2020-10-19

4.  Potential Use for Serosurveillance of Feral Swine to Map Risk for Anthrax Exposure, Texas, USA.

Authors:  Rachel M Maison; Courtney F Pierce; Izabela K Ragan; Vienna R Brown; Michael J Bodenchuk; Richard A Bowen; Angela M Bosco-Lauth
Journal:  Emerg Infect Dis       Date:  2021-12       Impact factor: 6.883

5.  Immunological Evidence of Variation in Exposure and Immune Response to Bacillus anthracis in Herbivores of Kruger and Etosha National Parks.

Authors:  Sunday O Ochai; Jan E Crafford; Ayesha Hassim; Charles Byaruhanga; Yen-Hua Huang; Axel Hartmann; Edgar H Dekker; O Louis van Schalkwyk; Pauline L Kamath; Wendy C Turner; Henriette van Heerden
Journal:  Front Immunol       Date:  2022-02-14       Impact factor: 7.561

6.  Modeling the environmental suitability for Bacillus anthracis in the Qinghai Lake Basin, China.

Authors:  Temitope Emmanuel Arotolu; HaoNing Wang; JiaNing Lv; Kun Shi; Hein van Gils; LiYa Huang; XiaoLong Wang
Journal:  PLoS One       Date:  2022-10-14       Impact factor: 3.752

  6 in total

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