Skip to main content

Ectoparasite communities of small-bodied Malagasy primates: seasonal and socioecological influences on tick, mite and lice infestation of Microcebus murinus and M. ravelobensis in northwestern Madagascar



Ectoparasitic infections are of particular interest for endangered wildlife, as ectoparasites are potential vectors for inter- and intraspecific pathogen transmission and may be indicators to assess the health status of endangered populations. Here, ectoparasite dynamics in sympatric populations of two Malagasy mouse lemur species, Microcebus murinus and M. ravelobensis, were investigated over an 11-month period. Furthermore, the animals’ body mass was determined as an indicator of body condition, reflecting seasonal and environmental challenges. Living in sympatry, the two study species experience the same environmental conditions, but show distinct differences in socioecology: Microcebus murinus sleeps in tree holes, either solitarily (males) or sometimes in groups (females only), whereas M. ravelobensis sleeps in mixed-sex groups in more open vegetation.


Both mouse lemur species hosted ticks (Haemaphysalis sp.), lice (Lemurpediculus sp.) and mites (Trombiculidae gen. sp. and Laelaptidae gen. sp.). Host species, as well as temporal variations (month and year), were identified as the main factors influencing infestation. Tick infestation peaked in the late dry season and was significantly more often observed in M. murinus (P = 0.011), while lice infestation was more likely in M. ravelobensis (P < 0.001) and showed a continuous increase over the course of the dry season. Genetic analyses identified Lemurpediculus sp. infesting both mouse lemur species. Ticks morphologically conform to H. lemuris, but genetic analysis showed a clear differentiation of the specimens collected in this study, suggesting a potentially new tick species. Host body mass decreased from the early to the late dry season, indicating nutritional stress during this period, which may render individuals more susceptible to parasitic infections.


Seasonal differences and species-specific variations in sleeping site ecology in terms of sleeping site type and sociality were determined as key factors influencing ectoparasitism in M. murinus and M. ravelobensis. This needs to be taken into account when evaluating ectoparasite infestations at a given time point. The detection of the same parasite species on two closely related and sympatric host species furthermore indicates a potential pathway for disease transmission, not only within but also between lemur species.


For millions of years, parasites and hosts have coevolved and therefore usually exist in a delicate balance [1]. However, if parasite abundance becomes exceptionally high or the host faces additional external stressors, the impact of parasite infections can be severe [2,3,4]. Ectoparasites may affect individual body condition and fitness and thereby affect population health, but also need to be considered as potential vectors for inter- and intraspecific pathogen transmission. Non-human primates are of particular importance in this context, due to their phylogenetic proximity to humans [5]. Characterization of ectoparasite communities and identification of prevalence patterns in wildlife may shed light on wildlife population health and potential risks of disease emergence, especially in the light of habitat loss and increasing human encroachment into wildlife habitats. However, a variety of biotic and abiotic factors may affect parasite communities in wildlife. Therefore, it is essential to enhance our knowledge on these complex interrelations, before any conclusions regarding the effect of anthropogenic habitat disturbance can be drawn.

Socioecological factors may have a large impact on the ectoparasite communities of different host species. The results of experimental infestation of three different bird species with the tree-hole tick Ixodes arboricola provide support for the hypothesis that host selection may be limited predominantly by host ecology rather than species specialization [6]. The interaction of group size and parasite infections has been investigated across many taxa and is summarized by Rifkin et al. [7]. On the one hand, living in groups means, inter alia, a higher local host density and possibly higher interaction rates with conspecifics, thus increasing the risk of parasitism. On the other hand, group size may also have protective properties such as the encounter-dilution effect [8] or increased allogrooming rates, leading to more effective ectoparasite disposal [9].

Furthermore, sex-specific differences in ectoparasite infestation, either due to ecological determinants, such as differences in behavior or morphology, or due to different levels of the hormone testosterone and its immunosuppressive properties, are subject to controversial debate [10]. Hormonal differences have been discussed as a potential factor favoring ectoparasite infestation [11] and may trigger ectoparasite development [12]. In addition, abiotic factors, in particular temperature and humidity, are also known to affect ectoparasite development and survival rates. Seasonal variations in climatic conditions may therefore affect ectoparasite abundance and activity [13, 14].

Here, patterns of ectoparasitism were investigated in two closely related mouse lemur species endemic to Madagascar. Even though several studies have investigated ectoparasite communities of Malagasy lemurs in recent years [15,16,17,18,19,20,21,22], the drivers and dynamics of their ectoparasite load remain largely unknown. Mouse lemurs are the world’s smallest primates and show a high cryptic species diversity with 24 species currently described [23,24,25,26]. The grey mouse lemur, Microcebus murinus, and the golden-brown mouse lemur, M. ravelobensis, are of comparable small body size, nocturnal [27], arboreal and have a seasonally changing, diverse, omnivorous diet [28, 29]. They occur sympatrically in the strongly seasonal, dry deciduous forests of the Ankarafantsika National Park in northwestern Madagascar and are thus exposed to the same environmental conditions [27, 30]. Both species have a promiscuous mating system and show a seasonal reproductive activity with mating occurring towards the end of the dry season [31, 32]. However, despite the given similarities they show distinct differences in their socioecology regarding sleeping sites. Microcebus murinus spends the days in the protected wooden shelter of tree holes, and females, in particular, show high sleeping site fidelity [33]. In contrast, M. ravelobensis prefers a broader variety of sites in open vegetation, and shifts sleeping sites more frequently [34]. Microcebus ravelobensis is usually found in mixed-sex sleeping groups [35], whereas M. murinus shows sex-specific differences in sleeping behavior, with males mostly sleeping alone while females may be found sleeping in groups [33].

These differences in socioecology may influence parasite infection rates, life-cycle and distribution. Considering the fact that mouse lemurs spend over half of their lives in sleeping sites [36], it can be expected that the differences in sleeping site ecology, including the different degrees of sociality and corresponding variations in allogrooming rates, will be reflected in different patterns of ectoparasitism. We expected a higher frequency of ectoparasites transmitted by host contact (lice and mites) in the more gregarious M. ravelobensis, while parasite removal via allogrooming may reduce the frequency of temporary ectoparasites (ticks) in this species. Regarding sex, male mouse lemurs may be more susceptible to ectoparasite infestation than females due to the immunosuppressive properties of testosterone. Abiotic factors can also be expected to have a notable impact on ectoparasite infestations, in particular on temporary ectoparasites that only spend a limited time on the host and are more susceptible to environmental factors. While temperatures at the study site seem favorable year-round, precipitation and humidity are subjected to extreme variations in northwestern Madagascar and thus probably affect off-host ectoparasite survival and development. We therefore predicted a higher abundance of temporary ectoparasites during the hot and humid rainy season. Detailed analyses of the study populations’ body mass changes were included as a proxy of body condition and as such, as an indicator of environmental challenges, i.e. nutritional stress. Increasing food scarcity over the course of the dry season was predicted to impact host condition, rendering mouse lemurs more susceptible to parasitic infections. Overall, this study gives a comprehensive picture of the ectoparasite communities of M. murinus and M. ravelobensis, including a report on two mite species formerly not described in mouse lemurs, and a detailed description of a putative new Haemaphysalis species.


Study site

The study was conducted in the Ankarafantsika National Park, which is located in northwestern Madagascar, about 120 km southeast of Mahajanga. The climate in the dry deciduous forests of this region is characterized by a hot rainy season (November-April) and a relatively cooler dry season (May-October) (Fig. 1). Between April and November 2015 and from March to May 2016, 78 free ranging M. murinus (36 females, 42 males) and 100 M. ravelobensis (55 females, 45 males) were trapped and sampled in a designated mapped forest area of 30.6 ha called the Jardin Botanique A (JBA, 16°19'S, 46°48'E.).

Fig. 1
figure 1

Climatic factors at the Ankarafantsika National Park (Ampijoroa Forest Station), Madagascar. a Precipitation in mm (Durrell Wildlife Preservation Fund, personal communication). b Temperature in °C (red line) and relative humidity in % (blue area) (Dr Hiroki Sato, Kyoto University, personal communication). For temperature and humidity, the monthly averages of hourly measurements are plotted

The rainy season preceding the first field period had an exceptionally high total precipitation of 3688.6 mm; from November 2015 to April 2016 total rainfall was 1529 mm (Durrell Wildlife Preservation Fund, personal communication). Average yearly precipitation at the study site is 1562.5 mm [37]. Mean daily temperature during the study period varied between 17.57 °C (03.08.2015) and 30.05 °C (17.11.2015) (Dr Hiroki Sato, Kyoto University, personal communication).

Mouse lemur trapping, weighing and sampling for ectoparasites

Mouse lemurs were trapped for 6 nights per month using Sherman live traps (Sherman Traps, Inc., Tallahassee, FL, USA). Ninety traps were installed in the late afternoon at each intersection of the rectangular trail system and baited with small pieces of banana. Traps were controlled in the early morning, or after about five hours in the offspring rearing season (March and April), respectively. Captured animals were individually marked subcutaneously with a small transponder (Trovan ID-100; Telinject®, Römerberg, Germany) that allows lifelong identification. Mouse lemurs were measured, weighed and sexed according to established methods [38] and macroscopically examined for ectoparasites. All animals were scanned systematically for ectoparasites with particularly thorough investigation of the head, ears and inner thighs at each capture. Collected arthropods were stored in 90% ethanol. Captured mouse lemurs were also checked for their reproductive status, with females being classified as “inactive” (no morphological changes), “cyclic” (reddening, swelling or opening of the vulva), “pregnant” (diagnosed by abdominal palpation and weight gain) or “lactating” (morphological changes in mammary glands, milk secretion), and males grouped in “testis large” (palpable testicles with a total width > 6 mm) or “testis small” (no testes palpable).

Morphological and genetic identification of ectoparasites

Morphological identification

Upon return to Germany, all collected ectoparasite samples were investigated microscopically and 38 specimens [7 mites (3 Laelaptidae, 4 Trombiculidae), 11 lice, 20 ticks] were embedded in polyvinyl-lactophenol for further morphological measurements. Microscopic images and measurements were taken using a stereomicroscope (Stemi SV II, Zeiss, Jena, Germany) or Axiophote microscope (Carl Zeiss MicroImaging, Jena, Germany) equipped with a Colorview IIIu Camera, using cell^B Image Acquisition Software (version 3.1; Olympus Soft Imaging Solutions, Hamburg, Germany). Specimens damaged in relevant features were excluded from morphological measurements of the respective characteristic, leading to unequal sample sizes. Species identification was based on morphological characteristics if possible (ticks: [39,40,41,42,43]; lice: [44,45,46]; mites: [47,48,49,50,51]) and was complemented by an additional genetic analysis of a subset of samples.

Genetic genus/species identification

Six lice (4 from M. murinus, 2 from M. ravelobensis), 8 ticks (3 from M. murinus, 5 from M. ravelobensis) and 2 mites (1 Laelaptidae, 1 Trombiculidae, both from M. murinus) were used for genetic analyses. DNA was extracted from ticks individually homogenized with polystyrene pistils (Roth) using the DirectPCR® Lysis Reagent Cell (PEQLAB Biotechnology GmbH, Erlangen, Germany) following the manufacturer’s instructions. For selected tick specimens, a 760 bp fragment of the cytochrome c oxidase subunit 1 gene (cox1) was amplified using primers Cox1F und Cox1R [52] in a 25 μl reaction mixture containing 18.5 μl double-distilled water, 0.5 μl dNTPs (10 mM each), 1 μl for/rev primer (10 μM each), 2.5 μl 10× buffer, 0.5 μl Taq polymerase (5 Prime, Hilden, Germany) and 1 μl DNA template. Thermocycling conditions were as follows: 95 °C for 5 min followed by 40 cycles at 95 °C for 30 s, 55 °C for 1 min and 72 °C for 1 min, and final extension at 72 °C for 5 min. For a tick specimen a 240 bp fragment, and for lice specimens a 209 bp fragment of the 18S rRNA gene was amplified using primers Ns1 and Ns2a [53] in a reaction setup corresponding to the recipe used for tick specimens. Thermocycling included an initial denaturation at 95 °C for 3 min, followed by 10 cycles at 95 °C for 30 s, 40 °C for 1 min and 72 °C for 1 min, and subsequently 40 cycles at 94 °C for 40 s, 48 °C for 1 min and 72 °C for 1 min, and final extension at 72 °C for 5 min. For two lice samples, additional cox1 sequences were amplified using primers L6625 and H7005 following the protocol of Light & Reed [54] but with adjustment of the elongation temperature to 72 °C. For the two mite samples, a 535 bp or 739 bp fragment of the 18S rRNA gene, respectively, was amplified using primers 18Sfw and rev960 [55] in a reaction setup analogous to that for lice and tick specimens. Thermocycling conditions were: 94 °C for 3 min followed by 40 cycles at 94 °C for 1 min, 50 °C for 1 min and 72 °C for 1 min and final extension at 72 °C for 10 min. Amplified PCR products were loaded onto 1.5% agarose gels and visualized bands of the expected size were excised and purified using the Wizard® PCR Preps DNA Purification System (Promega GmbH, Mannheim, Germany). PCR products were Sanger-sequenced at the Seqlab Sequence Laboratories (Göttingen, Germany) or GATC Biotech (Cologne, Germany). For 18S rRNA gene fragments of lice and tick specimens, additional sequencing primers (13+a and 13-a [53]) were used. Obtained nucleotide sequences were blasted against published sequences in NCBI GenBank and aligned using Clone Manager Professional Edition 9 (Scientific and Educational Software, Denver, CO, USA). Sequences were submitted to the GenBank database under the accession numbers MG132088-MG13294 and MG983747-MG983749.

Phylogenetic analyses

Phylogenetic analyses were performed for mite specimens as these could not be identified to the genus/species level by morphological characteristics or BLAST sequence comparison. The phylogenetic tree was constructed using the Maximum Likelihood method (Tamura-Nei model [56]) in MEGA7 software [57]. Bootstrap analyses [58] were performed with 1000 replicates.

Data analyses

Taxon-specific presence-absence data were analyzed on the basis of all individual capture events by fitting generalized linear mixed effects models (GLMMs) with logit-link and binomial assumption for ticks, lice and both mite species, with the following fixed effects (predictive variables): species (M. murinus, M. ravelobensis), sex (male, female), seasonality (rainy season, dry season), reproductive status (females: inactive, cyclic, pregnant, lactating; males: testis large, testis small), age (juvenile, adult), weight and the temporal factors month and year (subsumed in seasons). When the different sampling time-points were included in statistical models on a monthly basis as influencing factors, parameters proved to be inestimable, leading to abstruse estimates and standard deviations. Sampling months were therefore grouped into seasons as follows: “late rainy season”, March until end of April; “early dry season”, first of May until July 15th; “late dry season”, July 16th until end of October; “early rainy season”, November. Repeated measurements were accounted for by including the grouping factor “animal ID” as a random-effect term. The influence of the study year was tested by comparing April-May 2015 to April-May 2016 as these were the only months sampled in both years. If no significant difference was determined (as was the case for tick infestation), data of both years was pooled by month for subsequent analysis, providing a larger dataset for these months. In case of lice and mites with significant differences between study years, the temporal factor was categorized as season-year, e.g. late rainy season 2015. Data from April 2015 had to be excluded from the GLMM for lice [leading to a drop out of 21 (1.6%) observations and a drop out of 3 individuals that were not captured again in later seasons], as the highly irregular distribution made it otherwise impossible to calculate a reliable model. Potential predictive variables were first tested one by one and successively added to the model, if influences were significant and/or improved the final model, based on the Akaike information criterion (AIC). The factor reproductive status, with the attributes “inactive”, “cyclic”, “pregnant” and “lactating” for females, and “testis large” or “testis small” for males, was tested separately in the final model, as the opposite sex is inherently excluded when the reproductive attributes are added to the model. Different models were compared via likelihood ratio tests (LRT). The predictive variable season was subjected to post-hoc analysis, computing all pairwise differences between seasons (in analogy to Tukey’s test) based on the parameters of the fitted GLMM , if identified as significant in the overall model. Statistics were performed in R version 3.1.2 (R Core Team 2014) using the packages lme4 [59] and multcomp [60].

The animals’ body mass was analyzed as a response variable in a linear mixed effects model, including the fixed effects sex, species and their interaction. Juveniles and pregnant females were excluded from this analysis as their expected increase in body mass may obscure the weight development of the adult study population. Furthermore, the seasonal changes of weights were modelled as fixed effects with mean weight differences between seasons (early dry season, late dry season, early rainy season, late rainy season) and regression terms for mean change of weight per day within season, where regression slopes were allowed to differ between seasons. To account for repeated measures from the same individuals, random effects for differences between individuals, as well as differences between seasons within the same individuals were included, and finally a continuous autoregressive correlation structure (cAR(1)) was assumed for the residuals. A comparison of different random effect models based on AICc showed that model fit could not be improved by additionally assuming random slopes between individual or between seasons within individuals. The model was fitted using package nlme_3.1-128 [61], AICc was computed using package MuMIn_1.15.6 [62]. Based on the model fit the following post-hoc comparisons were performed (package multcomp [60]) including adjustments for multiple comparisons: pairwise differences of mean weights at the beginning of seasons were compared between seasons (in analogy to Tukey test), and regression slopes for weight change within seasons estimated and tested against a slope of 0. Subsets for M. murinus and M. ravelobensis were additionally analyzed separately for seasonal weight changes in the same way.


A total of 78 M. murinus (36 females, 42 males) and 100 M. ravelobensis (55 females, 45 males) were trapped and sampled for ectoparasites with high recapture rates leading to an overall sample size of 1306 separate capture events. The majority of animals (73.74%) contributed more than one data point to the final dataset. Individuals of both mouse lemur species were found to be infested with ticks, lice and two species of mites.

Ticks and description of Haemaphysalis sp. “microcebi”

A total of 170 ticks were detected on captured mouse lemurs. Twenty-three tick larvae were recovered from 16 mouse lemurs (10 M. murinus, 6 M. ravelobensis) captured in the early months of the dry season (May, June and July 2015 and May 2016). Nymphs represented the majority of ticks (n = 145, 85.29%) infesting M. murinus (n = 73) and M. ravelobensis (n = 72) and were present from June to November 2015 with an infestation peak in August (Fig. 2). Only two adult male ticks were collected from two M. murinus in March and April 2016, and no adult female ticks were found on either of the two mouse lemurs. The GLMM revealed a significant influence of season and mouse lemur host species on tick infestation (Table 1). The highest tick incidence was recorded in the late dry season and the risk of infection was significantly higher for M. murinus. No significant differences were found between sexes and neither age nor reproductive status had a significant influence on tick infestation.

Fig. 2
figure 2

Monthly tick frequency for all M. murinus and M. ravelobensis captures. Tick-positive captures are shown in dark blue for M. murinus (n = 71) and dark brown for M. ravelobensis (n = 68), tick-negative captures are in light blue for M. murinus (n = 461) and light brown for M. ravelobensis (n = 705). Bar widths indicate sample size for the sampling month(s) and numbers indicate respective positive/negative captures

Table 1 Results of generalized linear mixed models (GLMM, logit-link, binomial assumption), and subsequent pairwise comparisons between seasons, respectively, for Haemaphysalis sp. “microcebi”, Lemurpediculus sp., Trombiculidae gen. sp. and Laelaptidae gen. sp.

Collected specimens were identified as haemaphysaline ticks and morphologically resembled the original description of Haemaphysalis lemuris by Hoogstraal [39]. Comparison of a 240 bp fragment of the 18S rRNA gene (GenBank: MG983749) showed 100% identity with H. punctata (GenBank: Z74478), H. longicornis (GenBank: JQ346680), H. concinna (GenBank: KC511630), H. sulcata (GenBank: JX573126), H. flava (GenBank: JX573120) and H. formosensis (GenBank: JX573121), confirming the classification in the genus Haemaphysalis. However, even though comparison of the obtained 760 bp cox1 fragments (GenBank: MG132088-MG132092) showed 98 or 97% amino acid identity with H. lemuris sequences (GenBank: AFR33744 and AFR33745), substantial differences were observed regarding the respective nucleotide sequences, showing only 85% identity (GenBank: JX470177 and JX470178). This divergence suggests the presence of a separate species (hereinafter referred to as Haemaphysalis sp. “microcebi”).

Adult males and nymphs of Haemaphysalis sp. “microcebi” (Fig. 3) morphologically conform to the description of H. lemuris, with marked festoons, a triangular rounded spur on all coxae, flanked by a lateral bristle and a blunt spur on trochanter I to IV. Palpi are triangular with a convex basal margin and the hypostome shows a dentition pattern of 3/3 in male adults and 2/2 in nymphs, distinguishing the collected specimens from the morphologically very similar H. simplex. The two male adult specimens have a total length of 1753 and 1760 μm, respectively, with the scutum measuring 1251 and 1328 μm in length and 772 and 894 μm in width. The basis capituli is about half as long as wide (length: 112 and 123 μm, width: 229 and 238 μm). The hypostome measures 131 and 173 μm.

Fig. 3
figure 3

Different developmental stages of Haemaphysalis sp. “microcebi”. a Larva. b Nymph. c Adult male

A total of 113 nymphs were measured with a mean total length of 1245 μm (range: 974–1808 μm). Total nymph length, unlike the other measures, did not correspond to a normal distribution, probably due to different feeding durations at the time of sample collection and consequently different levels of abdominal enlargement of collected ticks. The oval scutum measures on average 340 ± 26 μm in length (range: 282–388 μm; n = 64) and 500 ± 31 μm in width (range: 412–561 μm; n = 64), the basis capituli is 74 ± 15 μm long (range: 41–107 μm; n = 69) and 161 ± 13 μm wide (range: 119–190 μm; n = 72) and mean hypostome length is 114 ± 19 μm (range: 74–154 μm; n = 72). In the 23 recovered larvae of Haemaphysalis sp. “microcebi”, festoons are less pronounced, coxal spurs are sometimes missing or indistinct and dentition is 2/2 (Fig. 2). The average total length of larvae is 745 μm (range: 576–1172 μm; n = 20) and, as in nymphs, total length is not distributed normally. The mean scutal length is 189 ± 20 μm (range: 166–228 μm; n = 10), mean width 321 ± 17 μm (range: 289–347 μm; n = 9). The basis capituli measures on average 53 ± 8 μm in length (range: 44–68 μm; n = 13) and 102 ± 13 μm in width (range: 84–121 μm; n = 12), the hypostome is on average 74 ± 19 μm long (range: 43–108 μm; n = 13). Comparative measurements of the scutum, basis capituli, hypostome and length from tips of palpi to posterior scutal margin of Haemaphysalis sp. “microcebi” and 12 further Malagasy Haemaphysalis species are provided in Table 2.

Table 2 Descriptive measurements (in mm) of Haemaphysalis sp. “microcebi” and 12 further haemaphysaline species currently described in Madagascar. Developmental stages missing in this table have not yet been described


Based on morphological characteristics, collected lice specimens from both mouse lemur species were identified as Lemurpediculus sp., showing a strong resemblance with Lemurpediculus verruculosus, originally described by Ward [44] and previously reported as parasites of Microcebus rufus [45]. Comparison of six 209-bp 18S rRNA sequences (4 from specimens ex M. murinus and 2 from specimens ex M. ravelobensis) with two published L. verruculosus sequences (GenBank: HM171410 and HM171409), showed a 100% identity, confirming the genus classification, but additional sequencing of fragments of the cytochrome c oxidase subunit 1 gene (GenBank: MG983747 and MG983748) revealed substantial differences to published L. verruculosus sequences (GenBank: HM171448 and HM171447). Collected specimens furthermore show variations in morphological characteristics within and between species, as well as to Lemurpediculus madagascariensis, a recently described new sucking louse species from M. murinus hosts of the Ankarafantsika National Park [46]. Lice collected in this study will therefore be conservatively addressed as Lemurpediculus sp.

Temporal parameters (month and year) influenced lice infestation significantly (Fig. 4). The risk of lice infestation significantly increased from the early dry to the early rainy season 2015 (P < 0.001), decreased towards the late rainy season 2016 (P < 0.001) and rose again until the end of the study period (P = 0.02) (Table 1). Lemur host species also proved to be of significant influence, with M. ravelobensis being significantly more often infected than M. murinus (P < 0.001). Host age did not have a significant influence on lice infestation. However, the presence of large testis during the period of reproductive activity from July to November, signaling hormonal activity, was associated with a higher likelihood of lice infestation (P = 0.009), although host sex as such did not significantly influence the lice infestation risk (Table 1).

Fig. 4
figure 4

Monthly lice frequency for M. murinus and M. ravelobensis. Lice positive captures are shown in dark blue for M. murinus (n = 112) and dark brown for M. ravelobensis (n = 369), lice negative captures are in light blue for M. murinus (n = 419) and light brown for M. ravelobensis (n = 404). Bar widths indicate sample size for the sampling month(s) and numbers indicate respective positive/negative captures


Two different species of mites (Trombiculidae gen. sp. and Laelaptidae gen. sp.) were collected from M. murinus and M. ravelobensis (Fig. 5). Trombiculidae gen. sp. were isolated from scrapings of scurfy, crusty skin alterations, particularly around the eyes and snout, and morphologically identified as chigger larvae. Sequence comparison of a 535-bp 18S rRNA gene fragment with published sequences revealed 98% identity with Eutrombicula splendens (GenBank: KP325057), confirming classification in the family Trombiculidae (Fig. 6). Characteristic skin conditions caused by larvae of Trombiculidae gen. sp. were significantly more often observed in M. murinus. Furthermore, significant differences were apparent between the different sampling seasons and years (Table 1). The risk of Trombiculidae infestation was higher in the dry than in the rainy season (P < 0.001) and higher in 2016 than in 2015 (P < 0.001). Neither host sex, nor reproductive status had a significant effect on Trombiculidae infestations.

Fig. 5
figure 5

Mites found on Microcebus spp. a Characteristic accumulation of Trombiculidae gen. sp. near the eyes (shown is a male M. murinus host). b Microscopic view of Trombiculidae gen. sp. c Microscopic view of an adult female Laelaptidae gen. sp. individual (contains an egg)

Fig. 6
figure 6

Phylogenetic tree of eight prostigmatic mites based on partial 18S rRNA gene sequences using the Maximum Likelihood method. The percentage of replicate trees in which the associated species clustered together in the bootstrap test (1000 replicates) is shown next to the branches. The sequence of the trombiculid mite of the present study is framed in red

The second mite species was only observed on 19 sampling occasions and significantly more often in M. murinus (n = 17) than in M. ravelobensis (n = 2) (P = 0.001) (Table 1). Genetic analysis of a 739-bp 18S rRNA gene fragment placed the collected specimens in the mite family Laelaptidae, showing 99% identity with Androlaelaps madagascariensis (GenBank: FJ911849) (Fig. 7), but morphological characteristics did not match any of the species previously described in Madagascar. No significant influence on Laelaptidae gen. sp. infestations was found for host sex. Regarding seasonal differences, the frequency of Laelaptidae gen. sp. occurrence was too low to perform reliable statistical analyses.

Fig. 7
figure 7

Phylogenetic tree of eight dermanyssoid mites based on partial 18S rRNA gene sequences using the maximum likelihood method. The percentage of replicate trees in which the associated species clustered together in the bootstrap test (1000 replicates) is shown next to the branches. The sequence of the laelaptid mite of the present study is framed in red. The sequence of Proarctacarus oregonensis was used as an outgroup

Body mass

A mean decrease of 5.24 ± 0.8 g in body mass was observed in adult mouse lemurs (n = 153) between the early and the late dry season. From the early rainy season 2015 to the late rainy season 2016, body mass increased by an average of 7.54 ± 0.8 g (Fig. 8, Table 3). Both variations proved to be significant (P < 0.001). Body mass showed a statistically significant decreasing tendency of 0.071 ± 0.013 g/day (i.e. an average loss of 1 g every 14 days) within the early dry season 2015, while this pattern was reversed over the course of the late dry season with a mean daily weight gain of 0.028 ± 0.007 g. A statistically significant difference was observed between the two study species (P = 0.0286), with M. ravelobensis (n = 90) being generally slightly heavier than M. murinus (n = 63), but no sex-specific differences were found. Separate analyses of body mass variations for each species revealed more pronounced changes between as well as within seasons in M. ravelobensis than M. murinus (Fig. 8, Additional file 1: Table S1).

Fig. 8
figure 8

Longitudinal changes in body mass for adult, non-pregnant M. murinus and M. ravelobensis over the course of the study period. Data from April 2015 were not available

Table 3 Results of the linear-mixed effects model, including post-hoc results of simultaneous tests for general linear hypotheses for body mass differences between and within seasons


A number of studies have investigated ectoparasites of Malagasy primates and have found lemurs hosting ticks (Ixodes lemuris, Haemaphysalis lemuris and H. simplex), mites (e.g. Psoroptidae, Laelaptidae), lice (sucking lice: Lemurpediculus spp., Phthirpediculus sp.; chewing lice: Trichophilopterus babakotophilus), endemic hippoboscid flies (Allobosca crassipes and Parabosca alata) and one introduced flea species (Echidnophaga gallinacean) (for the Cheirogaleidae summarized in Zohdy et al. [63]). In this study, individuals of Microcebus murinus and M. ravelobensis were infested with a haemaphysaline tick species (Haemaphysalis sp. “microcebi”), lice species (Lemurpediculus sp.) and two mite species belonging to the families of Trombiculidae and Laelaptidae. Ectoparasite infestation was influenced by temporal (sampling month and year) and potentially socioecological factors, since species differences in ectoparasite infestation might be due to divergences in sociality and the choice of sleeping sites. The findings for the different ectoparasite taxa are discussed in succession.


A great effort was undertaken by Harry Hoogstraal in the middle of the last century to characterize the haemaphysaline fauna of Madagascar. The original descriptions of H. elongata and H. simplex [64], H. obtusa [65] and H. hoodi madagascariensis [66] were complemented by the description of nine new species (H. anoplos, H. eupleres, H. fossae, H. lemuris, H. nesomys, H. simplicima, H. subelongata, H. theilerae and H. tiptoni) [39,40,41,42,43]. More recent studies [20,21,22, 67] identified collected tick specimens based on these descriptions and complementary cox1 gene sequences were generated for H. lemuris by Blanco et al. [68]. Assuming a correct classification in this previous study, our collected tick specimens showed distinct genetic differences (only 85% nucleotide identity with published H. lemuris sequences obtained from a M. rufus host), even though morphological characteristics visualized by light microscopy resembled the description of H. lemuris. Recently, a new species of the genus Ixodes, I. inopinatus, has been described, that can be differentiated from the similar I. ricinus only by combination of critical characteristics [69]. Similar subtle differences may be present in H. lemuris and the tick specimens collected in this study. Taking into account that the adult tick is considered the diagnostic stage, i.e. identification to species level is best achieved with adults [70], and that we only collected two adult male specimens, further sample collection including adult females will be necessary to delineate a new species and to describe it properly. Based on genetic sequence comparison of ticks collected in the present study, we consider Haemaphysalis sp. “microcebi” a putative new species. Our results emphasize the limitations of mere morphological differentiation of arthropod species and highlight the informative value of supplementary molecular genetic analyses, as demonstrated for I. inopinatus [69]. However, genetic comparison was only based on cox1 sequences as other genetic data, e.g. 18S rRNA gene sequences, are not available for H. lemuris. Thus, generation or release of additional sequences is desirable to assess genetic relationships more reliably.

The seasonal distribution of the different developmental stages of Haemaphysalis sp. “microcebi” can be explained by a univoltine life-cycle, i.e. only one generation of ticks per year, as proposed for H. lemuris [71]. Haemaphysalis spp. are known to be three-host ticks, needing a suitable new host for each developmental stage. Larvae may infest mouse lemurs in the early dry season (May to July) and develop into nymphs which can be found feeding on mouse lemurs into the rainy season. Adult haemaphysaline ticks may infest larger-bodied hosts, such as larger lemurs, tenrecs and introduced species, in the rainy season. However, the detection of two adult male ticks in our study suggests a modification for Haemaphysalis sp. “microcebi” with respect to the proposed life-cycle model for H. lemuris [71] by adding mouse lemurs as potential hosts also for adult ticks in the rainy season. Detection of adult haemaphysaline ticks on Lepilemur edwardsi [72] in the rainy season supports the predicted univoltine life-cycle and implies a vector potential for disease transmission between endemic lemur species.

Tick infestation is shaped on the one hand by the chance to encounter questing ticks and on the other hand by the host’s ability to effectively dispose of encountered parasites. Microcebus murinus and M. ravelobensis are both known to descend to the forest floor while foraging [28] and are thus equally exposed to questing ticks, which are usually found less than one meter above ground [73]. Tick encounters may be lower during the rainy season when other food sources, such as fruits and nectar in the higher forest layers, become available, reducing the need to descend to the floor [29]. The peak in tick infestation in the dry season and the decrease in the rainy season in our study is consistent with such seasonal changes in the feeding ecology of the two mouse lemur species.

Disposal of arthropods can be achieved by means of self-grooming or allogrooming. Lemurs have a particular tooth arrangement in the lower jaw, with finely spaced incisors and canine teeth facing forward, forming a toothcomb and thus providing an effective tool for grooming [74]. The vast majority of ticks in our study, however, were found attached to the animals’ ears, a part of the body that cannot be reached by teeth for self-grooming. The higher degree of sociality at the sleeping site of M. ravelobensis, and corresponding higher allogrooming rates, can contribute to tick removal and might explain the significantly lower infestation rate in this host species. The same positive effects of sociality on parasite removal were expected for female M. murinus, who are known to sleep in groups, but no significant difference was detected between the sexes. Exemplary sleeping site data of ten female M. murinus (27.78% of all caught female M. murinus) revealed that during our study, in contrast to previous findings [33], female M. murinus were found predominantly sleeping solitarily (unpublished results). If these findings represent the overall sleeping patterns of female M. murinus in the studied population during our research period, this could well explain the species differences observed in tick infestation in this study.


Sucking lice are obligate, permanent ectoparasites, which have evolved special morphological adaptations to their life on the mammalian host, such as tibio-tarsal claws for attachment to the hair and piercing mouthparts to penetrate the skin and feed directly from the blood vessel [75]. Being entirely dependent on the vertebrate host for survival, sucking lice have a very intimate host-parasite relationship and depend on direct body contact for transmission from one individual to another, as the time they can spend off a host is limited. This may be the underlying cause for the higher incidence and more rapid spread of lice in the group-sleeping M. ravelobensis as observed in this study. The intimate host-parasite relationship makes sucking lice also more susceptible to varying conditions of the host. Zohdy et al. [76] registered an increase in the louse population prior to the breeding period of the host M. rufus in eastern Madagascar, suggesting that reproduction of L. verruculosus may be triggered by an increase of host sex hormones in the imbibed blood. Frequent social interactions during the mating season increase transmission possibilities for sucking lice and the synchronization of reproductive activity may thus prove favorable for the parasite. We also observed an increase in lice infestation together with the onset of testis development, starting in July. However, we would not ascribe this phenomenon solely to the influence of sex hormones. In sheep, it is very well known that animals under stress and in poor body condition carry the heaviest lice infestations [77]. For the mouse lemurs in the Ankarafantsika National Park, the dry season constitutes a period of food scarcity and corresponding nutritional stress, which was reflected in a significant decrease in body weight of our study population. The availability of high quality food resources such as fruits, flowers and nectar, declines over the course of the dry season, until an increase in flowering is again observed in September [28, 29]. The observed variations in body mass correspond to the seasonal changes in the availability of high-quality food resources. Thus, it seems likely that the increase in lice infestations is due to the additive effects of internal (hormonal activity, mating season) and external stressors (nutritional stress). Since weight loss was more prominent in M. ravelobensis, whereas reproductive activity was observed for both studied host species equally, external factors like food abundance, i.e. nutritive stress, and social factors like sleeping-group composition/body contact may be the main parameters influencing lice infestation dynamics of M. murinus and M. ravelobensis.

Feeding on several different hosts makes lice also potential vectors for disease transmission. Sucking lice have been identified as vectors for pathogens such as poxvirus in pigs [78], Mycoplasma in rats and mice [70] or Borrelia recurrentis causing epidemic relapsing fever in humans [79]. Also, parasites may be transmitted via sucking lice as shown for the seal louse Echinophthirius horridus that has been identified as an intermediate host for microfilariae of the seal heartworm Acanthocheilonema spirocauda (formerly called Dipetalonema spirocauda) [80]. As ectoparasites of M. murinus and M. ravelobensis, Lemurpediculus sp. may play a role in the transmission of blood-borne pathogens within one species as well as between the two Microcebus species. Apart from this potential role as a vector, sucking lice can also have a harmful effect on the host by inducing anemia due to blood loss that may result in weakness or stunted growth, especially in young animals. There is a need for additional investigations for a more precise taxonomic classification of the collected sucking lice specimens. A comparative study, including morphological and genetic analysis, may help to complement the picture of interrelations between sucking lice and mouse lemurs.


This study is the first report of chigger mites (family Trombiculidae) in a lemur species. Trombiculid mites occur throughout the world and more than 3000 species have been identified [81]; however, little is known about the chigger fauna of Madagascar. Thus, the collected specimens, isolated from skin scrapings of M. murinus and M. ravelobensis, could not be identified to the species level, but genetic analysis confirmed assignment to the family Trombiculidae. In most chigger species, the larval stage, which is the only parasitic stage of this arthropod, feeding on lymph or tissue fluid from an animal’s skin, shows large seasonal fluctuations. While temperature has been identified as the limiting factor in temperate regions, the amount of precipitation seems to be of greater influence on chigger mite abundance in tropical areas [82]. In the present study, only two incidences of skin alterations caused by trombiculid mites were observed in September 2015, and no trombiculid activity was registered in October and November 2015, when relative humidity was below 55%. These observations support the influence of humidity on chiggers’ development. Chigger mite infestations were significantly more often encountered in the dry season, but the overall low frequency of Trombiculidae gen. sp. on both mouse lemur hosts did not allow a more detailed statistical analysis, that may enable differentiation between early and late dry season or correlation with climatic parameters. Low numbers of chigger mite infestations observed in the hot and humid month of April 2015 and March 2016 could be attributed to the lower sample size (April 15, n = 15; March 16, n = 22), as the high food abundance in the forest at the end of the rainy season had a negative impact on trapping success. The results for these months should therefore be interpreted cautiously.

Many chigger species show a preference to a certain area of the host’s body. For the collected Trombiculidae gen. sp. the predilection site was the face, especially around the eyes and the lateral snout, where the animals are not able to groom themselves by means of their toothcomb. Skin alterations due to trombiculid larvae were significantly more often observed in M. murinus. As discussed above regarding tick infestations, the higher degree of sociality at the sleeping site of M. ravelobensis which should coincide with higher allogrooming rates, may have increased disposal of trombiculid mites.

The second mite species collected from M. murinus and M. ravelobensis in this study could again not be identified to species level; however, genetic analyses assigned the collected specimens to the family Laelaptidae. Laelapid mites have been described as facultative or obligate parasites in nests of mammals and Androlaelaps mites, a genus of lealaptid mites known as parasites of Malagasy lemurs, are characterized as nidiculous, polyphagous opportunists with varying degrees of parasitic feeding [83]. This matches our findings of laelapid mites occurring only occasionally (n = 19) and with the exception of two incidences exclusively on M. murinus. The frequent use of tree holes as daytime sleeping sites by this host species presents an ideal setting to maintain the mites’ life-cycle. The mouse lemurs’ sleeping site provides a rich food supply, such as scabs and excretions, and the animal itself facilitates dispersal to different sleeping sites. The parasitism by laelapid mites in mouse lemurs may, however, be underestimated, given that these nidiculous parasites only spend a limited time on the host and the detection rate on the body of the mouse lemurs does therefore not necessarily reflect the situation at the host’s sleeping site. Invasive sampling of the sleeping sites would be necessary to obtain a more comprehensive picture on Laelaptidae gen. sp. prevalence. However, we decided against this approach to avoid disturbance of the study habitat and following impairment of long-term data collection.


The two mouse lemur species M. murinus and M. ravelobensis were found to host haemaphysaline ticks, lice and mites in the Ankarafantsika National Park of northwestern Madagascar. The probability of ectoparasite infestation was influenced by temporal (month, year) parameters, and by the host species, which could potentially be attributed to differences in the socioecology of the two host species. The results of this longitudinal study give a more comprehensive picture of the complex dynamics between environment and host-parasite interactions. The seasonal variations in ectoparasite prevalence need to be considered when interpreting ectoparasite data of a particular period in future studies. This is particularly relevant, as Madagascar is known for extreme climatic variations and unpredictable weather conditions between and within seasons and years [84] and environmental stressors therefore need to be evaluated thoroughly. The detection of the same ectoparasite species in two closely related sympatric hosts indicates a potential cross-species pathway for pathogen transmission. While ectoparasites themselves may have a negative effect on individuals through irritation, impairment of the natural barrier function of the skin and anemia due to blood-feeding, they may also represent potential vectors for disease transmission between individuals. Further studies will be needed to investigate possible vector-borne pathogens circulating in the studied M. murinus and M. ravelobensis populations, which might also pose a risk to other endemic species as well as humans and livestock.


  1. Lack D. The natural regulation of animal numbers. Oxford: The Clarendon Press; 1954.

    Google Scholar 

  2. Pedersen AB, Greives TJ. The interaction of parasites and resources cause crashes in a wild mouse population. J Anim Ecol. 2008;77:370–7.

    Article  PubMed  Google Scholar 

  3. Scott ME. The impact of infection and disease on animal populations: implications for conservation biology. Conserv Biol. 1988;2:40–56.

    Article  Google Scholar 

  4. Marcogliese DJ, Pietrock M. Combined effects of parasites and contaminants on animal health: parasites do matter. Trends Parasitol. 2011;27:123–30.

    Article  PubMed  Google Scholar 

  5. Pedersen AB, Davies TJ. Cross-species pathogen transmission and disease emergence in primates. EcoHealth. 2009;6:496–508.

    Article  PubMed  Google Scholar 

  6. Van Oosten A, Heylen D, Matthysen E. Host specificity of a bird-specialised endophilic ectoparasite, the tree-hole tick Ixodes arboricola. Parasitol Res. 2014;113:4397–405.

    Article  PubMed  CAS  Google Scholar 

  7. Rifkin JL, Nunn CL, Garamszegi LZ. Do animals living in larger groups experience greater parasitism? A meta-analysis. Am Nat. 2012;180:70–82.

    Article  PubMed  Google Scholar 

  8. Mooring MS, Hart BL. Animal grouping for protection from parasites: selfish herd and encounter-dilution effects. Behaviour. 1992;123:173–93.

    Article  Google Scholar 

  9. Akinyi MY, Tung J, Jeneby M, Patel NB, Altmann J, Alberts SC. Role of grooming in reducing tick load in wild baboons (Papio cynocephalus). Anim Behav. 2013;85:559–68.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Roberts ML, Buchanan KL, Evans M. Testing the immunocompetence handicap hypothesis: a review of the evidence. Anim Behav. 2004;68:227–39.

    Article  Google Scholar 

  11. Perez-Orella C, Schulte-Hostedde AI. Effects of sex and body size on ectoparasite loads in the northern flying squirrel (Glaucomys sabrinus). Can J Zool. 2005;83:1381.

    Article  Google Scholar 

  12. Rothschild M, Ford B. Breeding of the rabbit flea (Spilopsyllus cuniculi (Dale)) controlled by the reproductive hormones of the host. Nature. 1964;201:103–4.

    Article  Google Scholar 

  13. Kakuda H, Shiraishi S, Uchida TA. Seasonal fluctuations of populations and effects of temperatures on development and growth in the tick, Haemaphysalis flava. J Fac Agric Kyushu Univ. 1990;35:17–26.

    Google Scholar 

  14. Heath A. The temperature and humidity preferences of Haemaphysalis longicornis, Ixodes holocyclus and Rhipicephalus sanguineus (Ixodidae): studies on engorged larvae. Int J Parasitol. 1981;11:169–75.

    Article  PubMed  CAS  Google Scholar 

  15. Dutton CJ, Junge RE, Louis EE. Biomedical evaluation of free-ranging red ruffed lemurs (Varecia rubra) within the Masoala National Park, Madagascar. J Zoo Wildl Med. 2008;39:76–85.

    Article  PubMed  Google Scholar 

  16. Loudon JE, Sauther ML, Fish KD, Hunter-Ishikawa M, Jack IAY. One reserve, three primates: applying a holistic approach to understand the interconnections among ring-tailed lemurs (Lemur catta), Verreaux’s sifaka (Propithecus verreauxi), and humans (Homo sapiens) at Beza Mahafaly Special Reserve, Madagascar. Ecol Environ Anthropol. 2006;2:54–74.

    Google Scholar 

  17. Junge RE, Louis EE. Biomedical evaluation of two sympatric lemur species (Propithecus verreauxi deckeni and Eulemur fulvus rufus) in Tsiombokibo Classified Forest, Madagascar. J Zoo Wildl Med. 2005;36:581–9.

    Article  PubMed  Google Scholar 

  18. Junge RE, Louis EE. Biomedical evaluation of black lemurs (Eulemur macaco macaco) in Lokobe Reserve, Madagascar. J Zoo Wildl Med. 2007;38:67–76.

    Article  PubMed  Google Scholar 

  19. Dutton CJ, Junge RE, Louis EE. Biomedical evaluation of free-ranging ring-tailed lemurs (Lemur catta) in Tsimanampetsotsa Strict Nature Reserve, Madagascar. J Zoo Wildl Med. 2003;34:16–24.20.

    Article  PubMed  Google Scholar 

  20. Takahata Y, Kawamoto Y, Hirai H, Miyamoto N, Koyama N, Kitaoka S, Suzuki H. Ticks found among the wild ringtailed lemurs at the Berenty Reserve, Madagascar. Afr Study Monogr. 1998;19:217–22.

    Google Scholar 

  21. Junge RE, Louis EE. Medical evaluation of free-ranging primates in Betampona Reserve, Madagascar. Lemur News. 2002;7:23–5.

    Google Scholar 

  22. Klompen H, Junge RE, Williams CV. Ectoparasites of Propithecus diadema (Primates: Indriidae) with notes on unusual attachment site selection by Haemaphysalis lemuris (Parasitiformes: Ixodidae). J Med Entomol. 2015;52:315–319.

  23. Hotaling S, Foley ME, Lawrence NM, Bocanegra J, Blanco MB, Rasoloarison R, et al. Species discovery and validation in a cryptic radiation of endangered primates: coalescent-based species delimitation in Madagascar’s mouse lemurs. Mol Ecol. 2016;25:2029–45.

    Article  PubMed  CAS  Google Scholar 

  24. Rasoloarison RM, Weisrock DW, Yoder AD, Rakotondravony D, Kappeler PM. Two new species of mouse lemurs (Cheirogaleidae: Microcebus) from eastern Madagascar. Int J Primatol. 2013;34:455–69.

    Article  Google Scholar 

  25. Radespiel U, Ratsimbazafy JH, Rasoloharijaona S, Raveloson H, Andriaholinirina N, Rakotondravony R, et al. First indications of a highland specialist among mouse lemurs (Microcebus spp.) and evidence for a new mouse lemur species from eastern Madagascar. Primates. 2012;53:157–70.

    Article  PubMed  Google Scholar 

  26. Zimmermann E, Radespiel U. Species concepts, diversity, and evolution in primates: lessons to be learned from mouse lemurs. Evol Anthropol. 2014;23:11–4.

    Article  PubMed  Google Scholar 

  27. Zimmermann E, Cepok S, Rakotoarison N, Radespiel U. Sympatric mouse lemurs in north-west Madagascar: a new rufous mouse lemur species (Microcebus ravelobensis). Folia Primatol. 1998;69:106–14.

    Article  PubMed  CAS  Google Scholar 

  28. Radespiel U, Reimann W, Rahelinirina M, Zimmermann E. Feeding ecology of sympatric mouse lemur species in northwestern Madagascar. Int J Primatol. 2006;27:311–21.

    Article  Google Scholar 

  29. Thorén S, Quietzsch F, Schwochow D, Sehen L, Meusel C, Meares K, Radespiel U. Seasonal changes in feeding ecology and activity patterns of two sympatric mouse lemur species, the gray mouse lemur (Microcebus murinus) and the golden-brown mouse lemur (M. ravelobensis), in northwestern Madagascar. Int J Primatol. 2011;32:566–86.

    Article  Google Scholar 

  30. Rendigs A, Radespiel U, Wrogemann D, Zimmermann E. Relationship between microhabitat structure and distribution of mouse lemurs (Microcebus spp.) in northwestern Madagascar. Int J Primatol. 2003;24:47–64.

    Article  Google Scholar 

  31. Radespiel U. Sociality in the gray mouse lemur (Microcebus murinus) in northwestern Madagascar. Am J Primatol. 2000;51:21–40.

    Article  PubMed  CAS  Google Scholar 

  32. Randrianambinina B, Rakotondravony D, Radespiel U, Zimmermann E. Seasonal changes in general activity, body mass and reproduction of two small nocturnal primates: a comparison of the golden brown mouse lemur (Microcebus ravelobensis) in Northwestern Madagascar and the brown mouse lemur (Microcebus rufus) in Eastern Madagascar. Primates. 2003;44:321–31.

    Article  PubMed  Google Scholar 

  33. Radespiel U, Cepok S, Zietemann V, Zimmermann E. Sex-specific usage patterns of sleeping sites in grey mouse lemurs (Microcebus murinus) in northwestern Madagascar. Am J Primatol. 1998;46:77–84.

    Article  PubMed  CAS  Google Scholar 

  34. Radespiel U, Ehresmann P, Zimmermann E. Species-specific usage of sleeping sites in two sympatric mouse lemur species (Microcebus murinus and M. ravelobensis) in northwestern Madagascar. Am J Primatol. 2003;59:139–51.

    Article  PubMed  Google Scholar 

  35. Radespiel U, Jurić M, Zimmermann E. Sociogenetic structures, dispersal and the risk of inbreeding in a small nocturnal lemur, the golden-brown mouse lemur (Microcebus ravelobensis). Behaviour. 2009;146:607–28.

  36. McNamara P, Barton RA, Nunn CL. Evolution of Sleep: Phylogenetic and Functional Perspectives. Cambridge: Cambridge University Press; 2010.

  37. Global species. Myers Enterprises II. 2009–2017. Accessed 30 June 2018.

  38. Hafen T, Neveu H, Rumpler Y, Wilden I, Zimmermann E. Acoustically dimorphic advertisement calls separate morphologically and genetically homogenous populations of the grey mouse lemur (Microcebus murinus). Folia Primatol. 1998;69:342–56.

    Article  PubMed  Google Scholar 

  39. Hoogstraal H. Ticks (Ixodoidea) of the Malagasy faunal region (excepting the Seychelles): their origins and host-relationships; with descriptions of five new Haemaphysalis species. Bull Mus Comp Zool Harv. 1953;111:37–113.

    Google Scholar 

  40. Hoogstraal H, Camicas J-L. Haemaphysalis (Rhipistoma) eupleres (Ixodoidea: Ixodidae), a parasite of the Madagascar falanouc (mongoose): new data and male identity. J Parasitol. 1977;63:1099–102.

    Article  PubMed  CAS  Google Scholar 

  41. Hoogstraal H, Kohls GM, Trapido H. Haemaphysalis (Rhipistoma) eupleres sp. n. from a Madagascar carnivore and definition of the subgenus Rhipistoma Koch (resurrected) (Ixodoidea, Ixodidae). J Parasitol. 1965;51:997–1000.

    Article  PubMed  CAS  Google Scholar 

  42. Hoogstraal H, Uilenberg G, Klein J-M. Haemaphysalis (Rhipistoma) anoplos sp. n., a spurless tick of the elongata group (Ixodoidea, Ixodidae) parasitizing Nesomys rufus Peters (Rodentia) in Madagascar. J Parasitol. 1967;53:1103–5.

    Article  PubMed  CAS  Google Scholar 

  43. Hoogstraal H, Uilenberg G, Klein J-M. Haemaphysalis (Dermaphysalis) nesomys subgen. et sp. n. (Ixodoidea, Ixodidae), a leathery parasite of Nesomys rufus Peters (Rodentia) in Madagascar. J Parasitol. 1966;52:1199–202.

    Article  PubMed  CAS  Google Scholar 

  44. Ward RA. Description of a new species of Anoplura (Lemurphthirus verruculosus) from a Madagascar lemur. Entomol News. 1951;62:190–2.

    Google Scholar 

  45. Durden LA, Zohdy S, Laakkonen J. Lice and ticks of the eastern rufous mouse lemur, Microcebus rufus, with descriptions of the male and third instar nymph of Lemurpediculus verruculosus (Phthiraptera: Anoplura). J Parasitol. 2010;96:874–8.

    Article  PubMed  Google Scholar 

  46. Durden LA, Kessler SE, Radespiel U, Zimmermann E, Hasiniaina AF, Zohdy S. A new species of sucking louse (Phthiraptera: Anoplura: Polyplacidae) from the gray mouse lemur, Microcebus murinus (Primates: Cheirogaleidae), in Madagascar. J Med Entomol. 2018;55:910–4.

    Article  PubMed  Google Scholar 

  47. Wohltmann A, du Preez L, Rödel M-O, Köhler J, Vences M. Endoparasitic mites of the genus Endotrombicula Ewing, 1931 (Acari: Prostigmata: Parasitengona: Trombiculidae) from African and Madagascan anurans, with description of a new species. Folia Parasitol. 2007;54:225–35.

    Article  PubMed  Google Scholar 

  48. Tipton VJ. Zygolaelaps madagascariensis (Acari: Laelaptidae) a new genus of mites from Madagascar. J Parasitol. 1957;43:367–70.

    Article  PubMed  CAS  Google Scholar 

  49. Dowling AP, Bochkov AV, Oconnor BM. Revision of the genus Andreacarus (Acari: Laelapidae) with description of seven new species and a new genus for Australian species formerly placed in Andreacarus. J Med Entomol. 2007;44:405–21.

    Article  PubMed  Google Scholar 

  50. Steckolnikov AA, Fain A. A new genus and four new species of chigger mites (Acari Trombiculidae) from Madagascar. Belg J Entomol. 2004;6:337–52.

    Google Scholar 

  51. Domrow R, Taufflieb R. A second species of Aetholaelaps from a Malagasy lemur (Acarina, Laelapidae). Acarologia. 1963;5:526–9.

    Google Scholar 

  52. Chitimia L, Lin R, Cosoroaba I, Wu X, Song H, Yuan Z, Zhu X. Genetic characterization of ticks from southwestern Romania by sequences of mitochondrial cox1 and nad5 genes. Exp Appl Acarol. 2010;52:305–11.

    Article  PubMed  Google Scholar 

  53. Barker SC, Whiting M, Johnson KP, Murrell A. Phylogeny of the lice (Insecta, Phthiraptera) inferred from small subunit rRNA. Zool Scr. 2003;32:407–14.

    Article  Google Scholar 

  54. Light JE, Reed DL. Multigene analysis of phylogenetic relationships and divergence times of primate sucking lice (Phthiraptera: Anoplura). Mol Phylogenet Evol. 2009;50:376–90.

    Article  PubMed  CAS  Google Scholar 

  55. Dabert M, Witalinski W, Kazmierski A, Olszanowski Z, Dabert J. Molecular phylogeny of acariform mites (Acari, Arachnida): strong conflict between phylogenetic signal and long-branch attraction artifacts. Mol Phylogenet Evol. 2010;56:222–41.

    Article  PubMed  Google Scholar 

  56. Tamura K, Nei M. Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Mol Biol Evol. 1993;10:512–26.

    PubMed  CAS  Google Scholar 

  57. Tamura K, Dudley J, Nei M, Kumar S. MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. Mol Biol Evol. 2007;24:1596–9.

    Article  PubMed  CAS  Google Scholar 

  58. Felsenstein J. Confidence limits on phylogenies: an approach using the bootstrap. Evolution. 1985;39:783–91.

    Article  PubMed  Google Scholar 

  59. Bates D, Maechler M, Bolker B, Walker S. lme4: Linear mixed-effects models using Eigen and S4. R package version; 2014. p. 1. Accessed 30 June 2018

    Google Scholar 

  60. Hothorn T, Bretz F, Westfall P. Simultaneous inference in general parametric models. Biom J. 2008;50:346–63.

    Article  PubMed  Google Scholar 

  61. Pinheiro J, Bates D, DebRoy S, Sarkar D, R Core Team. nlme: linear and nonlinear mixed effects models. R package version 3; 2014. p. 1–117. Accessed 30 June 2018.

    Google Scholar 

  62. Barton K. MuMIn: multi-Model Inference. R package version 1.15.6. 2016. Accessed 30 June 2018.

  63. Zohdy S, Durden LA. A review of ectoparasites in the Cheirogaleidae. In: Lehman SM, Radespiel U, Zimmermann E, editors. The Dwarf and Mouse Lemurs of Madagascar: Biology, Behavior and Conservation Biogeography of the Cheirogaleidae. Cambridge: Cambridge University Press; 2016. p. 220–31.

    Chapter  Google Scholar 

  64. Neumann G. Revision de la famille des Ixodides. (4e memoire). Mém Soc Zool Fr. 1901;14:249–372.

    Google Scholar 

  65. Dönitz FKW. Die Zecken Südafrikas. In: Schultze L, editor. Zoologische und anthropologische Ergebnisse einer Forschungsreise im westlichen und Zentralen Südafrika ausgeführt in den Jahren 1903–1905. Denkschr med - naturw Ges Jena, vol. 16; 1910. p. 398–494.

    Google Scholar 

  66. Colas-Belcour J, Millot J. Contribution à l’étude des Isodidés de Madagascar. Sur une variété nouvelle de Haemaphysalis hoodi. Parasitisme humain par un Boophilus. Bull Soc Path Exot. 1948;41:384–8.

    Google Scholar 

  67. Rodriguez IA, Rasoazanabary E, Godfrey LR. Multiple ectoparasites infest Microcebus griseorufus at Beza Mahafaly Special Reserve, Madagascar. Madag Conserv Dev. 2012;7:45–8.

    Google Scholar 

  68. Blanco MB, Elfawal MA, Durden LA, Beati L, Xu G, Godfrey LR, Rich SM. Genetic diversity of ixodid ticks parasitizing eastern mouse and dwarf lemurs in Madagascar, with descriptions of the larva, nymph, and male of Ixodes lemuris (Acari: Ixodidae). J Parasitol. 2013;99:11–8.

    Article  PubMed  CAS  Google Scholar 

  69. Estrada-Peña A, Nava S, Petney T. Description of all the stages of Ixodes inopinatus n. sp. (Acari: Ixodidae). Ticks Tick Borne Dis. 2014;5:734–43.

    Article  PubMed  Google Scholar 

  70. Andrews RH, Chilton NB, Beveridge I, Spratt D, Mayrhofer G. Genetic markers for the identification of three Australian tick species at various stages in their life cycles. J Parasitol. 1992;2:366–8.

    Article  Google Scholar 

  71. Rodriguez IA, Rasoazanabary E, Godfrey LR. Seasonal variation in the abundance and distribution of ticks that parasitize Microcebus griseorufus at the Beza Mahafaly Special Reserve, Madagascar. Int J Parasitol Parasites Wildl. 2015;4:408–13.

    Article  PubMed  PubMed Central  Google Scholar 

  72. Hokan M, Strube C, Radespiel U, Zimmermann E. Sleeping site ecology, but not sex, affect ecto-and hemoparasite risk, in sympatric, arboreal primates (Avahi occidentalis and Lepilemur edwardsi). Front Zool. 2017;14:44–56.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  73. Tsunoda T, Tatsuzawa S. Questing height of nymphs of the bush tick, Haemaphysalis longicornis, and its closely related species, H mageshimaensis: correlation with body size of the host. Parasitol. 2004;128:503–9.

    Article  CAS  Google Scholar 

  74. Eaglen RH. Toothcomb homology and toothcomb function in extant strepsirhines. Int J Primatol. 1980;1:275–86.

    Article  Google Scholar 

  75. Light JE, Smith VS, Allen JM, Durden LA, Reed DL. Evolutionary history of mammalian sucking lice (Phthiraptera: Anoplura). BMC Evol Biol. 2010;10:292–306.

    Article  PubMed  PubMed Central  Google Scholar 

  76. Zohdy S, Kemp AD, Durden LA, Wright PC, Jernvall J. Mapping the social network: tracking lice in a wild primate (Microcebus rufus) population to infer social contacts and vector potential. BMC Ecol. 2012;12:1–11.

    Article  Google Scholar 

  77. Sertse T, Wossene A. A study on ectoparasites of sheep and goats in eastern part of Amhara region, northeast Ethiopia. Small Ruminant Res. 2007;69:62–7.

    Article  Google Scholar 

  78. Mullen GR, Durden LA. Medical and Veterinary Entomology. 2nd ed. Amsterdam: Academic Press; 2009.

    Google Scholar 

  79. Roux V, Raoult D. Body lice as tools for diagnosis and surveillance of reemerging diseases. J Clin Microbiol. 1999;37:596–9.

    PubMed  PubMed Central  CAS  Google Scholar 

  80. Geraci J, Fortin J, Aubin DS, Hicks B. The seal louse, Echinophthirius horridus: an intermediate host of the seal heartworm, Dipetalonema spirocauda (Nematoda). Can J Zool. 1981;59:1457–9.

    Article  Google Scholar 

  81. Goff ML, Loomis RB, Welbourn WC, Wrenn WJ. A glossary of chigger terminology (Acari: Trombiculidae). J Med Entomol. 1982;19:221–38.

    Article  PubMed  CAS  Google Scholar 

  82. Sasa M. Biology of chiggers. Annu Rev Entomol. 1961;6:221–44.

    Article  Google Scholar 

  83. Radovsky FJ. The evolution of parasitism and the distribution of some dermanyssoid mites (Mesostigmata) on vertebrate hosts. In: Houck MA, editor. Mites: Ecological and Evolutionary Analyses of Life-history Patterns. New York: Springer; 1994. p. 186–217.

  84. Dewar RE, Richard AF. Evolution in the hypervariable environment of Madagascar. Proc Natl Acad Sci USA. 2007;104:13723–7.

Download references


This study was conducted under the Accord de Collaboration between the Institute of Zoology, Hanover, the University of Antananarivo and l’Association Nationale pour la Gestion des Aires Protégées [ANGAP, now Madagascar National Parks (MNP)] signed July 22nd, 2014. We would like to thank the Malagasy government, Ministère De L’Environnement et des Forêts and MNP for their permission to work in the Ankarafantsika National Park and are grateful to our long-term cooperation partners Solofonirina Rasoloharijaona, Blanchard Randrianambinina and Romule Rakotondravony from the University of Mahajanga for supporting our field work in Madagascar. We thank Djacoba Herrimann Tehindrazanarivelo, Eva Helene Kleine, Mona Zimmermann, Lotte Caecilia Striewe and Paul Tsiverizado for assistance during sampling and data collection in the field and Sabine Händel for technical assistance during ectoparasite analysis. The Durrell Wildlife Preservation Trust and Dr Hiroki Sato from Kyoto University are acknowledged for providing the climate data.


The field study received funding from the Primate Conservation Inc. (research grant PCI# 1299), the German Academic Exchange Service (DAAD, travel grant no. 57212311) and the Gesellschaft für Primatologie (GfP, Christian-Vogel Fond, financial support for personal equipment and field assistants).

Availability of data and materials

The data supporting the conclusions of this article are included within the article and its additional file. The newly generated nucleotide sequences were submitted to the GenBank database under the accession numbers MG132088-MG132094 and MG983747-MG983749.

Author information

Authors and Affiliations



AK collected samples, performed laboratory analyses and drafted the manuscript. EZ initiated the study and guided the zoological part in Madagascar. EZ, CS, AK and UR contributed to the design of the study. CS supervised the parasitological examinations and AS participated in genetic analyses and drafting the manuscript. FS and UR supported statistical analyses. All authors participated in data analysis and interpretation and read and approved the final manuscript.

Corresponding author

Correspondence to Christina Strube.

Ethics declarations

Ethics approval

The field research was authorized by the Ministére de l’Environment, des Eaux et Forêts Malgache [Autorisation de recherche no. 063/15/MEEMEF/SG/DGF/DCB.SAP/SCB du 12/03/2015, Autorisation de recherche no. 34/16/MEEMEF/SG/DGF/DAPT/SCBT.Re (Renouvellement de l’Aut no. 210/15 du 27/08/2015)]. All animal handling and sampling procedures complied with the code of veterinary ethics and the German Protection of Animals Act and conformed to the accepted principles of animal welfare in experimental science and the principles defined in the European Convention for the Protection of Vertebrate Animals used for Experimental and Other Scientific Purposes. The fieldwork, furthermore, met the ethical guidelines for the treatment of primates of the Gesellschaft für Primatologie (GfP) and International Primatological Society (IPS) and accorded to the legal requirements formulated by the Malagasy authorities.

Consent for publication

Not applicable

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Additional file

Additional file 1:

Table S1. Post-hoc results of simultaneous tests for general linear hypotheses for body mass differences between and within seasons for M. murinus and M. ravelobensis. (DOCX 25 kb)

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Klein, A., Zimmermann, E., Radespiel, U. et al. Ectoparasite communities of small-bodied Malagasy primates: seasonal and socioecological influences on tick, mite and lice infestation of Microcebus murinus and M. ravelobensis in northwestern Madagascar. Parasites Vectors 11, 459 (2018).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: