- Open Access
Epidemiological traits of the malaria-like parasite Polychromophilus murinus in the Daubenton’s bat Myotis daubentonii
© Witsenburg et al.; licensee BioMed Central. 2014
- Received: 18 June 2014
- Accepted: 24 November 2014
- Published: 9 December 2014
The great diversity of bat haemosporidians is being uncovered with the help of molecular tools. Yet most of these studies provide only snapshots in time of the parasites discovered. Polychromophilus murinus, a malaria-like blood parasite, specialised on temperate-zone bats is a species that is being ‘rediscovered’. This study describes the infection dynamics over time and between host sex and age classes.
For three years we followed the members of three breeding colonies of Myotis daubentonii in Western Switzerland and screened them for the prevalence and parasitemia of P. murinus using both molecular tools and traditional microscopy. In order to identify more susceptible classes of hosts, we measured, sexed and aged all individuals. During one year, we additionally measured body temperature and haematocrit values.
Juvenile bats demonstrated much higher parasitemia than any other age class sampled, suggesting that first exposure to the parasite is very early in life during which infections are also at their most intense. Moreover, in subadults there was a clear negative correlation between body condition and intensity of infection, whereas a weak positive correlation was observed in adults. Neither body temperature, nor haematocrit, two proxies used for pathology, could be linked to intensities of infection.
If both weaker condition and younger age are associated with higher infection intensity, then the highest selection pressure exerted by P. murinus should be at the juvenile stage. Confusion over the identities and nomenclature of malarial-like parasites requires that molecular barcodes are coupled to accurate morphological descriptions.
Bats are the hosts to a large array of blood parasites (e.g. Bartonella, piroplasms, trypanosomes and microfillaria). In particular, bats are host to a unique collection of Haemosporida (Apicomplexa). Besides Plasmodium spp. and the rarer Hepatocystis spp., which infect several orders of Mammalia, bats host at least two unique genera not found outside the Chiroptera , Nycteria and Polychromophilus, plus two additional genera known from a single record (Dionisia and Biguetellia). The diversity of haemosporidian parasites of bats suggests, together with a recent phylogeny , that the Chiroptera might have been the original host of all mammalian Haemosporida.
Naturally, this has sparked renewed interest in bat haemosporidians, and Polychromophilus spp. have seen a particular rise in attention. The increasing ease and efficiency of molecular techniques has facilitated the detection of these parasites, enabling studies on its prevalence ,, phylogenetic origins  and the discovery of new species . However its development in a host population both through time and between host classes and other ecological measures are lacking, keeping large parts of its biology still a mystery. The aim of the current study is to describe these parameters for a temperate-zone member of the Polychromophilus genus, P. murinus. Its type host is Vespertilio murinus, but an important reservoir species seems to be Myotis daubentonii, the Daubenton’s bat, a common bat species spread across the Palearctic ,,.
Though its epidemiology is practically unknown, the life cycle of P. murinus is surprisingly well described, both in the host as well as the vector. Exoerythrocytic schizogony initially takes place in several organs, but finally develops inside the Kupffer cells of the liver ,. The gametocytes are the only stages invading erythrocytes and these are taken up by the bat fly Nycteribia kolenatii (Nycteribiidae: Diptera). Here sexual reproduction takes place, after which an oocyst develops sporozoites on the gut wall .
The distribution of P. murinus has been documented in very few studies but since it has been observed in Italy, Switzerland and Great Britain ,, it is likely that P. murinus has established itself in populations of M. daubentonii across Europe. In contrast, we have little idea about the prevalence variation over time, as well as the development of infection over the summer season. The aim of the current study was therefore to determine these epidemiological parameters in M. daubentonii at a local site. Secondly, by observing the susceptibility of each host age and sex class, the most likely source of the epidemic can be identified, which provides clues how the infection is maintained at this site. We will use both molecular methods, for parasite detection, and microscopy, for visual confirmation and assessment of the intensity of infection.
By definition, a parasite should have a negative effect on the host’s fitness. The direct effects of an infection with a haemosporidian parasite can be very severe ,, but may depend heavily on both the parasite and host species . The only attempt at studying the physiological effects of P. murinus on bats failed when the artificially inoculated heterospecific host appeared unsusceptible to infection . The attempt to infect a human with P. murinus by injecting infected bat blood failed as well; though the test subject did develop a fever, this was probably caused by other pathogens introduced by the injection . Our aim here is not to perform a clinical experiment, but to explore possible effects of P. murinus infection using two physiological characteristics that can be used as proxies for pathology: haematocrit for anaemia and body temperature for fever.
Myotis daubentonii were captured during the seasons of 2010, 2011 and 2012 on the University of Lausanne campus, near Lake Geneva in Switzerland. The bats originated from three breeding colonies located in the forest on campus and were caught using a harp trap positioned over the Sorge stream at dusk. While highly pregnant and lactating females were immediately released upon capture, all other bats were used for sampling. Each bat was ringed to prevent resampling. The age of the bat, either ‘adult’ or ‘subadult’ was determined by the presence of a dark spot on the lower lip, which fades after 1-2 years. Each bat’s forearm length (to the nearest 0.1 mm) and weight (to the nearest 0.1 gram) were measured. We used the residuals from an OLS regression of body mass on forearm length as a measure of body condition . In 2012, the haematocrit value (see below) and body temperature were also measured. Captured bats were immediately removed from the trap and body temperature was measured by inserting a lubricated probe into the rectum (RET-3 animal rectal probe and BAT-12 microprobe thermometer, Physitemp, Clifton, USA).
Blood was obtained by puncturing the uropatagial vein with a 0.5 mm gauge needle (Neolus). Between 5 and 30 μL of blood were collected using either microvettes with EDTA (Sarstedt; seasons 2010/2011) or heparinized glass microcapillary tubes (Marcel Blanc & Cie; season 2012). Samples were stored at -20°C until molecular analysis. Haematocrit was measured by centrifuging the microcapillary tubes containing fresh blood for 7 minutes at 12,800 rpm. The haematocrit value was calculated by dividing the length of the red blood cell column by the total length (measured to the nearest 0.1 mm).
After blood sampling, haemostatic cotton was applied to the punctured vein until bleeding ceased. All bats were captured under the licenses #1317 and #1656, authorized by the Cantonal Veterinarian Service of Vaud, Switzerland.
Blood parasite observation
From each blood sample, one drop of fresh blood was applied to a microscope object glass to make a thin smear. Slides were subsequently dried and immediately submerged in 100% methanol for fixation. Finally, a 5% Giemsa-stain was applied for one hour to stain the cells. Slides were inspected with a light microscope at 600× and 1000× magnification. Polychromophilus murinus gametocytes were identified following Garnham  and Landau et al.. Of a subset of gametocytes we noted the sex, counted manually the number of pigment granules and measured the dimensions of cells and nuclei.
The relative abundance of P. murinus gametocytes in the blood was estimated by scoring the number of P. murinus gametocytes observed in each smear at 600× magnification for 15 minutes. This measure, from now on referred to as parasitemia, should give an idea of the intensity of infection.
DNA was extracted using the Blood and Tissue spin column kit (Qiagen, CA), following the manufacturer’s tissue protocol, with an overnight digestion and eluted in 2 * 50 μL. To control for contamination, a negative control was always included during the extraction process. The infection status of the bat host was determined by detecting the presence of a 705 bp fragment of the mitochondrial cytochrome b gene (cytb) of the parasite following a nested PCR protocol. Primers, reagent concentrations and thermal profiles can be found in Megali et al. . Amplified fragments were run on a 1.5% agarose gel and visualised under UV light. For every eight samples tested, a negative control was included in the amplification protocol. Each sample was tested in two independent tests. Samples with ambiguous results were tested again in duplicate. Samples remaining ambiguous were discarded from the data set.
A previous study at this site had demonstrated that the local M. daubentonii bats were exclusively infected by P. murinus and that this parasite population consisted of seven, almost identical cytb haplotypes . The aim of our current study was not to describe the parasite molecularly. However, to confirm these previous findings, as well as our microscopic observations, we had a subset of the PCR positive samples purified and sequenced by a commercial agent (Microsynth, Switzerland) using both the forward and reverse primers of the nested reactions.
Factors influencing P. murinus prevalence, as assessed by the nested PCR protocol, were identified by logistic regression. The original model included the variables sex, age, body length and condition, as well as year and date, the latter variable expressed as standardized days since April 1st. Interactions were included based on their biological relevance: year x date, date x condition, sex x condition and age x condition. Terms were removed by backward selection, based on AIC and non-significant residual deviances until a minimal adequate model was found.
Since the parasitemia data was zero-inflated and showed signs of overdispersion, a zero-inflated (i.e. ‘mixed’) negative binomial approach (ZINB) was implemented using the pscl package for R . To identify factors that influence P. murinus parasitemia in wild M. daubentonii hosts, this model considers the overly abundant zeros to come from two different processes, i.e. ‘false zeros’, caused either by poor observations or individuals that did not encounter the parasite, and ‘true zeros’, resulting from the covariates being unfavorable for the parasite . For both the false-zero portion of the model, which attempts to discriminate between the two types of zeros, and the count portion, the same host-related covariates were used as for the previously described logistic regression of infection status. However, the variable date was also included in its squared form after graphical inspection of the data. A backward selection procedure was adopted wherein a term was dropped from either the false-zero or count portion of the model until no further decrease in AICc was observed. Each progressive model was tested for a significant change in log likelihood compared to its predecessor .
Juveniles were collected only in September and October of 2012. These are fledged young-of-the-year, that can be recognized by the incomplete ossification of their finger joints. Because of their age, it is not recommended to capture them earlier in the season and they were therefore not included in the previously described analyses. A comparison between juveniles and the other two age classes was therefore done separately. An F-value was obtained by performing an ANOVA on parasitemia by age class, with date as a covariate. This F-value was compared to a null distribution obtained by randomizing age 999 times.
The effects of parasitemia on bat hematocrit values and body temperatures were tested by linear regression. To linearize the relationship, parasitemia was log(x + 0.5) transformed. As female mammals can have lower hematocrit levels  and higher body temperatures , sex was included as a cofactor in each analysis.
All statistical analyses were calculated using R ver. 3.0.1 .
Morphometric measurements taken of the gametocytes, in μm
Mean ± S.D.
Mean ± S.D.
6.69 – 8.29
7.45 ± 0.38
7.29 – 8.64
8.01 ± 0.44
5.50 – 7.84
6.97 ± 0.52
5.45 – 8.05
7.10 ± 0.72
1.58 – 2.56
2.12 ± 0.23
3.08 – 5.95
4.66 ± 0.67
1.34 – 2.10
1.7 ± 0.21
2.15 – 4.78
3.29 ± 0.63
Number of pigment granules
20.30 ± 4.52
12 - 27
19.3 ± 5.54
The female macro- and male microgametocytes are easily distinguished, with the macrogametocyte having a compact, round, well-bordered nucleus in a dense cytoplasm. In contrast, the often more oval-shaped microgametocyte has a much lighter coloured cytoplasm with a diffuse, ill-defined and randomly shaped nucleus, which is considered a clear characteristic of P. murinus. Due to its irregular shape, measuring the male nucleus width in a consistent way was challenging and the values should again be taken with caution (Table 1).
Of the 212 M. daubentonii tested, 157 (74.1%) were PCR positive for the cytb fragment. Of the 186 individuals of which also the blood smear had been searched for parasites, 58 (31.1%) were positive. 80 individuals were negative by microscopic analysis but positive by PCR and 48 were negative according to both methods. All nine successfully sequenced cytb fragments had a 100% identity with P. murinus, six were identical with haplotype 1 (Genbank Accession HM055583) and the three remaining with haplotype 2 (Genbank Accession HM055584; following ).
Estimates of the parameters and their significance for the logistic regression of prevalence
Date x year (2011)
Date x year (2012)
Estimates of the parasitemia statistical model parameters and their significance for the model
Count model μ
Date x condition
Age x condition
False zero model π
Polychromophilus murinus reached its highest abundances in juvenile M. daubentonii, which have to carry the heaviest burden of infection. However, no direct physiological effect of infection was found. Furthermore, the zero-inflated model showed that across the whole season parasitemia was much higher in subadults than adults. This suggests that with age, bats are better able to cope with the infection.
Previous work has shown that the primary exposure to a haemosporidian parasite causes much higher parasitemia in hosts than any further encounters . Our study demonstrated much higher parasite abundances in juveniles than other age classes, supporting this observation. Bat ectoparasites synchronise their reproduction with their hosts . After female bats have given birth, the ectoparasites move in mass onto the pups , introducing blood parasites to the neonates at a very early stage of development. The primary exposure to the haemosporidian parasite causes extreme high levels of parasitemia, which in turn increases the probability of establishing an infection in the abundant newly emerged bat flies. As bat flies are long lived and can overwinter , this in itself might suffice to maintain the P. murinus infection.
The bat’s body condition was linked to the chance of being infected and it correlated with the progression of infection as well as the maximum intensity of the infection. Notably, the effect of host body condition on the parasite intensity depended on the age of the host, for which several non-mutually exclusive processes might be responsible. Subadults with larger fat storages could be better equipped to mount a costly immune response , though no direct relation was found in the Brazilian free-tailed bat Tadarida brasiliensis. In M. daubentonii body condition increases with maturation . The strong decline of parasitemia with condition seen in subadults might therefore actually represent maturing individuals which at the same time learn to cope with infection.
However, in adults, the relationship between condition and parasitemia is slightly positive. Heavier adults might be trading off mass against immunity, though it is unclear why this would only affect adults . Like other bat ectoparasites , the vector N. kolenatii is attracted to hosts in higher body condition ; these bats might therefore be more often exposed to new infections, which causes a slight increase in parasitemia. It might also be a sampling artefact: perhaps for bats with similar levels of infection, only those in good condition can tolerate it enough to go foraging at night when we caught them. Lastly, the positive correlation might be caused by pregnant females, which are relatively heavy for their size and also immunosuppressed . Though highly gravid females were never sampled, females in earlier stages of gestation are more difficult to recognize and might therefore be present in the data set.
It is worth noting, that in our statistical analyses we have considered a bat’s body condition as one of the causes predicting the likelihood of infection and its intensity. Yet, in contrast to date or age, the reverse is just as likely. Mounting an immune response requires energy which should reduce fat reserves . Loss of body mass might therefore very well be a symptom of infection with P. murinus. Only experimental infections under controlled conditions could resolve this question of cause and effect.
Apart from possible weight loss, we found no other sign of pathology. Bats showed no signs of fever; however, whether or not fever is applied by heterotherms is debated . The lack of anaemia on the other hand might be because of the biology of P. murinus. Unlike Plasmodium spp., Polychromophilus spp. have no asexual multiplication in the blood. The number of erythrocytes destroyed during an infection should therefore be much lower compared to other malaria species.
Over the three years we found an average infection rate of 74.1% which is the same rate as Megali et al. found at the same site in 2009 using the same screening method. Prevalence was not stable throughout the season, but this pattern seemed different each year suggesting either random emergent fluctuations prevalence or the influence of (unmeasured) climatic variables.
Prevalence was much higher based on PCR than based on the microscopy results. It is well established that nested PCR is more sensitive than pure visual control, though the two methods can approach each other in efficacy . The proportion of ‘false zeros’ determined by the ZINB model did not correspond to the number of bats tested negative by PCR. When all PCR-negative individuals were removed from the parasitemia analysis, zero-inflation was still an issue. The false zeroes were therefore not only caused by hosts that had not encountered the parasite, but also ‘bad observations’. In our case, the ZINB found no factor influencing the appearance of false zeroes, indicating that this rate of zero detection was unbiased across the categories of hosts. In contrast with this, the actual probability of being infected, as demonstrated by the logistic regression, depends mainly on time of season and the host’s condition.
The rise of molecular techniques in parasitology also inadvertently meant a decline of light microscopy , not only to describe new parasite species or lineages (but see: ), but also to determine parasite prevalence and abundance. Although PCR and qPCR are undeniably much more efficient approaches for analysing hundreds of blood samples at a time, some pitfalls are associated with the use of molecular techniques. Primers may be unsuitable for the parasite present  or only dead-end stages, injected by the vector, are detected , leading to the false conclusions that the host is uninfected or infected respectively. In this study we used PCR methods to scan for infections. Our main findings, however, stem from our results produced by microscopical investigation.
The currently available species descriptions for P. murinus are either not very exhaustive  or contradictory; Landau et al., for example, would sometimes describe the P. murinus gametocytes as of the type malariae, yet in other publications as of the type falciparum, whereas Garnham describes it as of type vivax. Here we tried to provide some quantitative measures with our morphological description of P. murinus to link the morphospecies to the available genetic sequences. With the current confusing species descriptions available, a proper redescription would be welcome. However, for a complete description it is essential to have access to the schizonts, which can be sampled by dissection. Such complete redescriptions coupled to sound genetic bar codes is needed to resolve the presently confused state of taxonomy among malarial-like parasites.
Juvenile M. daubentonii clearly carried the highest P. murinus parasite loads. Furthermore, bat host condition was strongly correlated to the infection intensity. If both weaker condition and younger age are associated with a more intense infection, then the highest selection pressure exerted by P. murinus should be on the juvenile M. daubentonii. Weak young are pruned from the population and any surviving bats will have developed a tolerance against further infections with P. murinus. This could explain both the absence of any pathological symptoms in adults as well as the ability of the parasite to remain present in bat populations throughout the year.
The authors would like to thank all those who helped catching bats in the field, in particular Ludovic Dutoit and Laura Clément. We are also grateful to Laura for DNA sequencing of the samples. Jérôme Goudet gave helpful statistical advice. We thank the Centre de Coordination Ouest pour l'Etude et la Protection des Chauves-souris in Geneva for logistic support. We thank Tania Jenkins, Karen McCoy, Nadir Alvarez and an anonymous reviewer for helpful comments on earlier drafts of this paper. This study has been supported by grants no 31003A-120479 and 31003A-138187 by the Swiss National Science Foundation.
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