Abstract
BackgroundThe dynamics of helminth infection in African elephant populations are poorly known. We examined the effects of age, sex, social structure and the normalized difference vegetation index (NDVI) as primary drivers of infection patterns within and between elephant populations.MethodsCoprological methods were used to identify helminths and determine infection patterns in distinct elephant populations in Maasai Mara National Reserve, Tsavo East National Park, Amboseli National Park and Laikipia-Samburu Ecosystem. Gaussian finite mixture cluster analyses of egg dimensions were used to classify helminth eggs according to genera. Generalized linear models (GLM) and Chi-square analyses were used to test for variation in helminth infection patterns and to identify drivers in elephant populations.ResultsHelminth prevalence varied significantly between the studied populations. Nematode prevalence (96.3%) was over twice as high as that of trematodes (39.1%) in elephants. Trematode prevalence but not nematode prevalence varied between populations. Although we found no associations between helminth infection and elephant social groups (male vs family groups), the median helminth egg output (eggs per gram, epg) did vary between social groups: family groups had significantly higher median epg than solitary males or males in bachelor groups. Young males in mixed sex family groups had lower epg than females when controlling for population and age; these differences, however, were not statistically significant. The average NDVI over a three-month period varied between study locations. Cluster analyses based on egg measurements revealed the presence of Protofasciola sp., Brumptia sp., Murshidia sp., Quilonia sp. and Mammomonogamus sp. GLM analyses showed that the mean epg was positively influenced by a three-month cumulative mean NDVI and by social group; female social groups had higher epg than male groups. GLM analyses also revealed that epg varied between elephant populations: Samburu-Laikipia elephants had a higher and Tsavo elephants a lower epg than Amboseli elephants.ConclusionsElephants had infection patterns characterized by within- and between-population variation in prevalence and worm burden. Sociality and NDVI were the major drivers of epg but not of helminth prevalence. Gastrointestinal parasites can have a negative impact on the health of wild elephants, especially during resource scarcity. Thus, our results will be important when deciding intervention strategies.
Highlights
The dynamics of helminth infection in African elephant populations are poorly known
This model revealed that elephant populations in Kenya were infected by trematodes that can be characterized by two operational taxonomic unit (OTU)
Based on published egg dimensions of trematodes infecting African elephants, we found that trematode OTU1 had mean egg lengths and widths that were similar to those for Protofasciola robusta, while OTU2 had egg dimensions that were similar to Brumptia bicaudata (Figs. 2, 3; Table 1, Additional file 1: Table S1)
Summary
The dynamics of helminth infection in African elephant populations are poorly known. Most studies on the helminths parasitizing African elephants have in the past focused on helminth taxonomy and more recently on within population infection dynamics [1,2,3,4], but no studies have simultaneously examined inter-population and intra-population. The most common helminths infecting African elephants are nematodes and trematodes; two groups of helminths that have environmentally dependent transmission mechanisms. Species of Murshidia, Quilonia and Khalilia are the most common nematodes infecting African elephants [5]. Moisture is needed for the development and transition of larvae from soil to pasture and so rainfall and vegetation may be limiting factors on transmission and may influence patterns of inter-population variability in infection patterns [6]. Some studies have found associations between precipitation and certain qualitative measurements of egg burden (mean nematode species richness, mean number of nematode worms and infection intensity per individual host) [9,10,11]
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