9 Feb 2017: Demanche C, Deville M, Michaux J, Barriel V, Pinçon C, et al. (2017) Correction: What Do Pneumocystis Organisms Tell Us about the Phylogeography of Their Hosts? The Case of the Woodmouse Apodemus sylvaticus in Continental Europe and Western Mediterranean Islands. PLOS ONE 12(2): e0171282. https://doi.org/10.1371/journal.pone.0171282 View correction
Pneumocystis fungi represent a highly diversified biological group with numerous species, which display a strong host-specificity suggesting a long co-speciation process. In the present study, the presence and genetic diversity of Pneumocystis organisms was investigated in 203 lung samples from woodmice (Apodemus sylvaticus) collected on western continental Europe and Mediterranean islands. The presence of Pneumocystis DNA was assessed by nested PCR at both large and small mitochondrial subunit (mtLSU and mtSSU) rRNA loci. Direct sequencing of nested PCR products demonstrated a very high variability among woodmouse-derived Pneumocystis organisms with a total number of 30 distinct combined mtLSU and mtSSU sequence types. However, the genetic divergence among these sequence types was very low (up to 3.87%) and the presence of several Pneumocystis species within Apodemus sylvaticus was considered unlikely. The analysis of the genetic structure of woodmouse-derived Pneumocystis revealed two distinct groups. The first one comprised Pneumocystis from woodmice collected in continental Spain, France and Balearic islands. The second one included Pneumocystis from woodmice collected in continental Italy, Corsica and Sicily. These two genetic groups were in accordance with the two lineages currently described within the host species Apodemus sylvaticus. Pneumocystis organisms are emerging as powerful tools for phylogeographic studies in mammals.
Citation: Demanche C, Deville M, Michaux J, Barriel V, Pinçon C, Aliouat-Denis CM, et al. (2015) What Do Pneumocystis Organisms Tell Us about the Phylogeography of Their Hosts? The Case of the Woodmouse Apodemus sylvaticus in Continental Europe and Western Mediterranean Islands. PLoS ONE 10(4): e0120839. https://doi.org/10.1371/journal.pone.0120839
Academic Editor: Nadir Alvarez, University of Lausanne, SWITZERLAND
Received: October 28, 2013; Accepted: February 11, 2015; Published: April 1, 2015
Copyright: © 2015 Demanche et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Funding: This work was supported by the French Ministry of Research (www.enseignementsup-recherche.gouv.fr) (EA4547 Lille Nord de France University and Lille Pasteur Institute) and by the French Institute of Biodiversity (IFB) (www.biodiversite-sbstta.org) in the framework of “Insularité et Parasitisme: diversité parasitaire et écologie évolutive des populations de rongeurs insulaires”. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: Christophe Noel has been employed by Geneius laboratories since September 2008 as Head of Research and Development department. The author's collaboration to the work presented in the manuscript bares no link to any products in development or marketed products, testing or protocols that Geneius Laboratories uses. Therefore no competing interests exist and contribution to the work by the author does not alter the authors' adherence to PLOS ONE policies on sharing data and materials.
Phylogeography is a field of research, which studies the principles and processes determining the geographical distribution of genetic lineages. Quite frequently, parasites provide an additional source of information and can better reconstruct the common history of hosts and parasites . For this reason, some parasites have been recently used as phylogeographic markers [1–7]. As an example, host associations of Spinturnicid mites likely result from a complex interaction between the phylogenetic history of the bat hosts and the behaviour and the ecology of both parasites and hosts . Moreover, Spinturnicid mites seem to be a biological tag to reveal the former presence of a nowadays locally extinct bat host species . Similarly, studies on the co-divergence between A. sylvaticus and the parasitic nematode Heligmosomoides polygyrus [2, 8] demonstrated a general association between the parasite genetic structure and the host evolutionary history.
Pneumocystis organisms are opportunistic fungi that infect the lungs of a wide range of mammalian species, including humans [9–11]. These atypical fungi are considered to be highly diversified with numerous species [12–14] which display a strong host specificity [10–11, 14–19]. Many molecular studies suggest the existence of a co-speciation process occurring between Pneumocystis organisms and their corresponding hosts [10–11, 14, 18, 20–21]. Consistently, in primate-derived Pneumocystis organisms, specific DNA sequence divergence among Pneumocystis species was correlated with the phylogeny of their specific hosts [10, 21, 22]. Similar observations were noticed at the Pneumocystis infra-specific level for the migrating bat Tadarida brasiliensis where Pneumocystis strain polymorphism could be used as a phylogeographic tool to track natural host populations [18–19].
The woodmouse (Apodemus sylvaticus, Rodentia, Muridae) is a common forest dweller, and has been present throughout Europe for at least 3 million years . Apodemus sylvaticus is one of the most intensively studied species in the genus. The phylogeographic history of this species in Europe and in the Middle East is well known, proposing an original pattern of postglacial colonization where the Iberian and southern France refuge populations colonized almost all European regions [23–24].
In the present study, we detected and characterised Pneumocystis organisms in woodmice from western continental Europe and Mediterranean islands. Questions regarding host and parasite co-divergence as well as comparative phylogeography were specifically addressed. Our objective was to assess whether Pneumocystis organisms can be used as phylogeographic markers for rodents, in addition to previous studies on parasites of Apodemus and in order to demonstrate that Pneumocystis is a promising biological tag for mammalian hosts.
Materials and Methods
All animal experiments were performed according to the directive 2010/63/EEC on the Protection of Animals Used for Experimental and Other Scientific Purposes. The animal work also complied with the French law (nu 2012–10 dated 05/01/2012 and 2013–118 dated 01/02/2013). The rodents, Apodemus sylvaticus, were captured using Sherman traps from July until October, 2001. The trapping locations in which woodmice were collected are described in Fig. 1. The study of woodmice did not require to be approved by an ethical committee (European directives 86–609 CEE and 2010/63/EEC). This species is not protected, and no experiment was performed on living animals. No permit approval was needed as this species was trapped outside any preserved areas (national parks or natural reserves). Oral authorization was received from land owners to get trapping authorization on their property (forests or land shrubs). The rodents were euthanized by vertebrate dislocation immediately after capture in agreement with the legislation and the ethical recommendations (2010/63/EEC annexe IV) (see also protocol available on http://www.ceropath.org/references/rodent_protocols_book). All experimental protocols involving animals were carried out by qualified staff (agreement number: 59–350070, accreditation number of the Lille Pasteur Institute: A59107, accreditation number of the Center of Biology and Management of the Populations (CBGP) for wild and inbred animal manipulations: A34-1691). This study is part of a project entitled « Insularité et Parasitisme: diversité parasitaire et écologie évolutive des populations de rongeurs insulaires » supported by the French Institute of Biodiversity.
Samples are designated according to the location in which they were collected. The number of examined field mice is indicated between brackets. Spa, Montseny (42); Pyr, the Pyrenees (15); Mon, Montpellier (21); Cal, Calabria (39); Mal, Mallorca (25); Min, Minorca (14); Sic, Sicily (32); Por, Porquerolles (10); Cor, Corsica (5). The thick lines correspond to the main European biogeographic barriers: the Pyrenees (west) and the Alps (east). Sample locations are shown by circles.
Woodmice were trapped on islands and mainland areas in western Europe (Fig. 1). Mainland areas included Calabria (Italy), Montseny (Spain), Montpellier and the Pyrenees (France). The Mediterranean islands were Mallorca and Minorca (Spain), Corsica and Porquerolles (France), and Sicily (Italy). These Apodemus samples are conserved in the collection of the Conservation Genetics Unit of the University of Liège (currator J.R. Michaux). All organs and viscera were dissected following capture. The lungs were immediately excised and stored at -20°C until analysis. A total number of 203 woodmice lung samples were collected.
DNA extraction from lung tissue samples was performed using DNeasy tissue kit (Qiagen, Courtaboeuf, France) following the manufacturer procedure with some modifications. Lysis of lung tissue was done overnight in an incubator at 56°C with permanent rotation. In order to concentrate Pneumocystis DNA, the column was re-hydrated with 100 μl of elution AE buffer instead of 200 μl. Extracted DNA was stored at -20°C prior to amplification. A negative control was systematically included in each series of DNA extraction.
Detection of Pneumocystis organisms by nested PCR
Pneumocystis DNA was detected in pulmonary samples by nested PCR at the mitochondrial large subunit (mtLSU) rRNA and the mitochondrial small subunit (mtSSU) rRNA genes.
At the mtLSU rRNA locus, the first round of nested PCR consisted of 30 cycles and was performed using the external primer set PH/PE . Each cycle consisted of 3 steps: denaturation for 30s at 94°C, annealing for 1 min at 50°C, and extension for 1 min at 72°C. Five percent (vol/vol) of the amplified product from the first PCR round was used as starting matrix in the second round of PCR. The second PCR round consisted of 30 cycles and was performed using the internal primer set PX/PZ . Each cycle consisted of 3 steps: denaturation for 30s at 94°C, annealing for 1 min at 55°C, and extension for 2 min at 72°C.
At the mtSSU rRNA locus, the first round of nested PCR consisted of 40 cycles and was performed using the external primer set pAZ112-10F-R1 / pAZ112-10R-R1 . Each cycle consisted of 3 steps: denaturation for 30 s at 94°C, annealing for 1 min at 55°C, and extension for 1 min at 65°C. Five percent (vol/vol) of the amplified product from the first round of PCR was used as starting matrix in the second round. The second round of nested PCR consisted of 40 cycles and was performed using the internal primer set pAZ112-13-R1 / pAZ112-14-R1 . Each cycle consisted of 3 steps: denaturation for 30 s at 94°C, annealing for 1 min at 52°C, and extension for 1 min at 65°C for 10 cycles; and denaturation for 30 s at 94°C, annealing for 1 min at 63°C, and extension for 1 min at 65°C for 30 cycles.
Negative controls were included in each experiment, in both DNA extraction and PCR amplification. When non-specific bands were detected, amplification products of expected size (about 250–300 pb) were extracted from a 2% agarose gel (run in Tris-borate-EDTA buffer) using a PCR purification kit (QIAEX II Gel Extraction Kit, Qiagen, Courtabœuf, France). Purified products were sent for sequencing to GenoScreen (Pasteur campus, Genopole of Lille, France). When a unique band of expected size was present, amplified products were directly sent for purification and sequencing to GenoScreen. Sequencing from both ends using sets of internal primers was performed on an automated DNA sequencer (3730XL DNA Analyser, Applied Biosystems). Not all the positive samples were sequenced; representative positive samples were randomly chosen to be sequenced.
Nucleotide sequence accession numbers
Pneumocystis mtLSU rDNA or mtSSU rDNA sequences obtained in this study were deposited in GenBank under accession numbers KF411466, KF384955 to KF385004, and KF384913 to KF384954.
Statistical analyses were performed using SAS (SAS v9, SAS Institute). Variables are described as counts (proportions). A Mc Nemar test was performed to assess the agreement between detection of Pneumocystis DNA using mtLSU and mtSSU rRNA. Pneumocystis infection was investigated using a two-way analysis of variance with country and insularity as crossed fixed-effect factors, analyzed with a generalized linear mixed model approach (proc GLIMMIX). Models were built with a binomial error distribution and the logit link function. Two-sided p-values<0.05 were deemed to be statistically significant.
The mtLSU and mtSSU rRNA gene sequences described in this study were concatenated and initially aligned with homologous sequences of Pneumocystis from the mouse Mus musculus (P. murina GenBank accession numbers AF257179 and KF384954, respectively) and from the squirrel Sciureus aestuans (GenBank accession numbers KF411466 and KF384953, respectively) using CLUSTAL X v1.63b . The sequence alignment was then refined by visual optimization using Se-Al v2.0a11  respecting the four criteria defined by Barriel : (1) minimize the number of mutations, which means substitution and insertion-deletion events, and prefer substitution to insertion-deletion; (2) favour transitions to transversions because they are more frequent; (3) minimize the number of sites affected by mutation; (4) minimize the number of phylogenetic implications. All analyses were performed using sequences from P. murina and Pneumocystis of the squirrel S. aestuans as outgroups. Once the alignment was finalised, the insertion-deletion events were coded as “id” to exploit their phylogenetic information, independently of their size, following the procedure of Barriel . This procedure is particularly useful for complex zones with complex insertions/deletions with substitutions. This strategy requires the introduction of three new character states in the matrix: “i” (insertion), “d” (deletion) and question marks “?” as missing data.
Maximum parsimony (MP) analysis was conducted using Phylogenetic Analysis Using Parcimony Program (PAUP) v4.0b9 . A MP tree was inferred using a heuristic search of 1,000 random additions of sequences with TBR (tree bisection reconnection) branch-swapping. All sites were equally weighed, gaps were scored as missing (the ID code was included in the matrix, so gaps were taken into account).
In a second step, the positions corresponding to missing data in some sequences were removed from the original alignment. Maximum likelihood (ML) analysis of sequences was carried out with PHYML v3.0  using the GTR (general time reversible) + Γ (gamma distribution of rates with four rate categories) + I (proportion of invariant sites) model. The appropriate model of sequence evolution was selected using the program jModelTest2 . Bootstrap values (BVs) were obtained from 1,000 pseudo-replicates. Bayesian analysis was also performed with the program MrBAYES v3.1  on the same data set using the same model and Bayesian Posterior Probabilities (BPPs) were calculated using a Markov Chain Monte Carlo (MCMC) sampling approach . The starting tree was random, and four simultaneous Markov chains were run in duplicates for 2 million generations with burn-in values set at 10,000 generations (based on empirical values of stabilizing likelihoods). Trees were sampled every 100 generations (the other settings being set to default). Distance matrices and bootstrap sampling (1,000 pseudo-replicates) were subsequently generated by using Seqboot and Dnadist combination (Phylip v.3.69) with the Jukes Cantor model. Matrices were analysed using BioNJ  and consensus tree computed with Consense (Phylip v.3.69). Alignments of mtLSU and mtSSU rRNA gene sequences utilised in the various analyses are available upon request to the corresponding author.
A minimum spanning network was constructed using the MINSPNET algorithm available in the ARLEQUIN 2.0 program . The genetic divergences (GD) between sample groups were estimated using a distance analysis (K2P, mega program). The nucleotide (π) and haplotype (h) diversities were estimated using the DNA sequence polymorphism (DnaSP) version 5 program .
Detection of Pneumocystis DNA in woodmice lungs
A sample was considered to be positive for the presence of Pneumocystis DNA when a specific band was amplified by PCR at the expected size either at the mtLSU or mtSSU rRNA locus or at both loci (Table 1). Pneumocystis DNA was detected in 189 out of 203 woodmice lung samples examined (93.1%). Amplifications at both mtSSU and mtLSU rDNA were positive for the same individual in 38 animals (Table 1).
Potential influence of country and insularity versus mainland in Pneumocystis carriage
No significant statistical association could be established between the presence of Pneumocystis DNA and the country of origin of animals (p = 0.79) (Table 2). No interaction was observed between country and insularity (p = 0.85). However, the frequency of Pneumocystis DNA detection was significantly higher in woodmice from continent than in insular woodmice (p = 0.02). The probability of picking a Pneumocystis-infected woodmouse was 6-fold higher on the continent than on islands (Table 2).
Direct sequencing of nested PCR products demonstrated a very high variability among woodmice-derived Pneumocystis sequences. A total number of 32 distinct mtLSU sequence types and 13 distinct mtSSU sequence types were detected. Sequences at the mtLSU rRNA locus seemed to be more variable than those at the mtSSU rRNA locus (Table 1). After combining mtLSU and mtSSU sequences, 30 distinct sequence types were generated (Tables 1 and 3). Phylogenetic analyses were then carried out using the concatenated sequence dataset. A total number of 555 bp (360 bp and 195 bp from mtSSUrRNA and mtLSUrRNA loci, respectively) was selected in the subsequent phylogenetic analyses. The initial alignment included 32 taxa (2 outgroups and 30 taxa ingroups), 555 characters and 513 common sites. After coding the insertion-deletion events , the final alignment with the ID code included 32 taxa and 584 characters.
Most of the combined sequences corresponded to specific geographical areas (Tables 1; Fig. 2). Three combined Pneumocystis sequence types were detected in the woodmice from the Pyrenees (France). Similarly, unique Pneumocystis sequence types were characterized in the woodmice captured in the Spanish islands of Mallorca (2 sequence types) and Minorca (2 sequence types). As for Sicilian woodmice, 7 distinct Pneumocystis sequence types were detected. For Montpellier (France), we detected 4 specific Pneumocystis sequence types; another sequence type (Mon5, Table 1) was common with 2 other ones isolated in woodmice from Montseny (Spain, Spa19) and Porquerolles (France, Por15). Among the 3 specific Pneumocystis sequence-types found in the woodmice from Calabria (Italy), one Pneumocystis sequence was common with that found in a woodmouse from Corsica (France). In addition, 2 unique Pneumocystis sequence-types were detected in the corsican woodmice (Table 1).
NJ, MP, ML and MB are inferred from the combined mitochondrial small subunit (mtSSU) and large subunit (mtLSU) rRNA sequences. The percentages displayed above the branches are the frequencies with which a given branch appeared in 1,000 bootstrap replications in NJ/MP/ML/MB analyses respectively. *Bootstrap values below 50% are depicted by a star.
The total genetic divergence among the studied localities (Table 3) delineated 2 groups of combined sequence types. The first one, named the Western European clade, comprised Pneumocystis from woodmice collected in continental Spain (Montseny), France and Balearic islands (range of genetic divergence: 0% to 0.2%). The second one, named the Italo-Corsican clade, included Pneumocystis from woodmice collected in continental Italy (Calabria), Corsica and Sicily (range of genetic divergence: 0% to 0.3%). The genetic divergence existing between the Western-European and Italo-Corsican clades ranged from 0.8% to 1.4% and is higher than the genetic divergence existing within each clade (Table 3).
When comparing the genetic diversity values of Pneumocystis isolated from woodmice captured on islands versus those from host populations originating from mainland, a trend toward the loss of Pneumocystis genetic diversity was noticed. Indeed, the nucleotide diversity tends to decrease (π) in the Pneumocystis sequences isolated from insular host populations except for Sicily (8 individuals and 8 sequences types) and Minorca (2 individuals and 2 sequences types) (Table 4). With regard to both Pneumocystis groups (Fig. 2 and 3), the sole insular Pneumocystis population that seemed to display levels of genetic divergence (GD) and mean nucleotide diversity (π) that were comparable to those assessed in population from continental Italy (Calabria) was isolated from Sicilian rodents. All other Pneumocystis populations from Mediterranean islands were characterised by lower values of GD and π than mainland source populations except for Minorca (Table 4).
Geographic origins (see Table 1 and Fig. 1) are indicated: Spa, Montseny; Pyr, the Pyrenees; Mon, Montpellier; Cal, Calabria; Mal, Mallorca; Min, Minorca; Sic, Sicily; Por, Porquerolles; Cor, Corsica. Numbers correspond to the mutational steps observed between haplotypes.
The Pneumocystis continental populations from Calabria, Montpellier and the Pyrenees displayed the highest levels of π except for Montseny (Table 4).
The matrix of 584 characters included 440 constant characters, 95 variable parsimony-uninformative characters and 49 parsimony-informative characters. The analysis yielded 31 738 equally parsimonious trees (length = 213 steps, CI = 0.761 and RI = 0.748).
The analysis of the genetic structure of woodmice-derived Pneumocystis revealed two distinct groups (Fig. 2). The Pneumocystis clade from Italy and Corsica was well individualized in the phylogenetic analyses (NJ, MP, ML, MB) and it was supported by bootstrap values higher than 80%. A small subgroup corresponding to most of the Pneumocystis sequences isolated from woodmice trapped in Sicily (Sc3, Sc8, Sc9, Sc13 and Sc16), was weakly or well supported by bootstrap values depending on the various analyses applied (Fig. 2).
Pneumocystis sequence types from Western European woodmice (Porquerolles and mainland France, Balearic Islands and mainland Spain) always met outside of the Italo-Corsican clade and consequently constituted a second group of Pneumocystis that was not well supported by bootstrap values and was not monophyletic (Fig. 2). The relationships existing inside this group remain unclear with the exception of 2 Pneumocystis sequence types isolated from 2 woodmice trapped in Montpellier (Mon23 and Mon4) (Fig. 2).
The minimum spanning network displayed 24 haplotypes of Pneumocystis clearly distributed in 2 major clades defined above and separated from each other by a genetic distance of 5 mutational steps (Fig. 3). However, two other clades seemed to appear, each constituted by only one Pneumocystis haplotype isolated from 2 woodmice trapped in Montpellier (Mon23 and Mon4). These Pneumocystis types were clearly divergent from the others. For the 2 major clades, the first one comprised Pneumocystis haplotypes resulting from woodmice from Sicily, Calabria and Corsica (clade 1). The second group included Pneumocystis haplotypes from woodmice from Spain, Montpelier, Mallorca and Minorca as well as the Pyrenees (Western European clade 2). Within clade 2, almost all haplotypes were connected together in a star-like topology. Pneumocystis isolated from woodmice captured in Spain, Montpellier, Porquerolles and the Pyrenees (Spa19, Mon5, Por15, Spa4 and Pyr14) were grouped into the same haplotype. Another Pneumocystis sequence-type isolated from woodmice sampled in Spain fell into another haplotype shared with a sample from Minorca (Spa3 and Mn33).
The topology of the Italo-Corsican clade (clade 1) is more heterogeneous than in the Western European clade. We note the proximity between the Pneumocystis from the woodmice from Corsica, Calabria and Sicily, but also 2 haplotypes shared by Pneumocystis from Calabrian and Corsican woodmice (Fig. 3). On the other hand, Sicilian woodmice possessed their own Pneumocystis haplotypes and did not share them with the Corsican or Calabrian woodmice (Fig. 3).
Prevalence of Pneumocystis in Apodemus sylvaticus
Previous studies using nested PCR reported important differences in Pneumocystis prevalence between mammal species of the same zoological group such as primates or rodents. Prevalence of Pneumocystis reached 26.5% in captive primates  and 33.6% in healthy macaques maintained in partial release . In micromammals collected in France, Pneumocystis prevalence reached 68.0% when molecular techniques were applied . In Thailand, 57.7% of wild rats harboured Pneumocystis . Pneumocystis was found in rodents of the genus Apodemus in several European and Japanese regions, with rates of prevalence ranging from 0 to 43% .
The prevalence reported in the present study (93.1%) was much higher than previously cited values. This result may be explained both by the efficiency of molecular amplification used for Pneumocystis detection in our study, and by the gregarious behaviour of A. sylvaticus  as crowding favours the transmission of Pneumocystis by aerial route [19, 39, 44]. The Pneumocystis transmission is influenced by the interactions between mammals and the structuring of mammalian society [19, 39]. Consequently, Pneumocystis can be considered as a marker of social structuring of mammals.
Potential influence of insularity versus continent
The prevalence of Pneumocystis colonization was significantly higher in woodmice from continent than in the ones from islands. This finding is not in accordance with previous study . Indeed, the prevalence and intensity of parasitism are often higher in insular than in mainland populations for parasites that are directly transmitted from host-to-host. This high insularity prevalence is in relation with the low parasite species richness in insular host populations. A study found that there was a significant influence of insularity on the decrease in parasite species richness of A. sylvaticus , which can be explained by the decrease of mammal diversity .
Another study on H. polygyrus and its host A. sylvaticus highlighted the “island syndrome” in this parasitic nematode species with a loss of genetic diversity following territory colonization . Our results tend to support this observation (Table 4). In the first clade (Western European Pneumocystis woodmice), the Majorcan Pneumocystis population displayed a significant loss of genetic diversity (GD = 0.1%; π = 0.0011). Even if nucleotidic diversity of the Minorcan Pneumocystis population appeared to be higher than the diversity of the Spanish population (mainland origin), both were yet lower than those of Montpellier and the Pyrenees. Moreover, Nieberding et al.  observed in the case of Minorcan H. polygyrus that the GD and π values were intermediate when compared to those from Spain and Majorcan populations. The lower values of GD and π of Pneumocystis Spanish populations seem to reflect past genetic bottlenecks or recent population expansion from a small number of founder individuals.
In the case of the second clade (Calabria, Sicily and Corsica), we observed the same tendency of decrease in Pneumocystis genetic and nucleotidic diversity in islands, except for Sicily, thus confirming the results obtained previously for A. sylvaticus and its nematode parasite H. polygyrus [23, 48].
The results of the present work support the hypothesis that the Pneumocystis Balearic populations originated from South-Western Europe and the Italian region was the continental source for Pneumocystis Sicilian and Corsican populations as well as for its host A. sylvaticus and other parasites like H. polygyrus .
Genetic diversity of Pneumocystis from Apodemus sylvaticus
Several studies reported Pneumocystis sequence types from various host species. The genetic divergence ranged from 7.5% to 28.2% according to the used locus, i.e. mtLSU rRNA or mtSSU rRNA, and the host species examined [10, 13, 19]. The genetic divergence among Pneumocystis organisms from A. sylvaticus was very low (lower than 3.87% of divergence) and strongly suggested that a single Pneumocystis species is present in the woodmouse. The phylogenetic analysis of Pneumocystis sequences was in accordance with the host specificity concept of Pneumocystis [14–15, 17]. A first investigation about primate-derived Pneumocystis organisms demonstrated that Pneumocystis phylogeny mirrors its host phylogeny, suggesting long-range functional and genetic adaptation process leading to cospeciation . Pneumocystis organisms may have evolved together with their hosts. The low genetic divergence in woodmice-derived Pneumocystis organisms is in connection with the geographical place where the rodents were captured.
A phylogenetic tree for A. sylvaticus was first provided by Michaux et al. [23, 49–50]. According to this analysis, two groups of populations can be distinguished: a first group comprises woodmice from France, Spain as well as Balearic Islands (Western European group); the second group includes woodmice from the Balkans, Italy and Sicily. The phylogenetic study inferred from Pneumocystis sequences detected in woodmice showed the same tendency of grouping (Fig. 2). Particularly, Pneumocystis from woodmice in Italy, Corsica and Sicily were clustered in the same monophyletic group. In contrast, the other Western European populations of Pneumocystis appeared less structured. Concerning the Mediterranean islands, our results pointed out a close relationship of the Porquerolles and Mallorca islands with the continental French and Spanish Pneumocystis populations. In contrast, Corsican Pneumocystis appeared strongly associated to the Italian and Sicilian Pneumocystis populations (Fig. 2 and 3). Michaux et al.  demonstrated that A. sylvaticus underwent a significant bottleneck during Quaternary glaciations, finding refugia in the Iberian Peninsula and the Italo-Balkan areas. While the Iberian populations later spread throughout the rest of Europe, the Italo-Balkan populations remained trapped by surrounding mountains and did not contribute to the genetic constitution of central and north European populations. The results of the study suggest co-divergence: the population structure of woodmice-related Pneumocystis is in agreement with the evolutionary history of A. sylvaticus. Pneumocystis organisms were likely carried by their specific host during their migration and evolution.
In a recent study, using a nematode parasite as phylogeographic marker, Callejon et al.  underlined two clear-cut geographical and genetic lineages of the nematode Trichuris muris isolated from different Muridae hosts, including A. sylvaticus, in Europe: one lineage was widespread from Northern Spain (Catalonia) to Denmark (Western European region), while the second one colonized the Eastern European region (Croatia, Rumania, and Turkey) . The geographic repartition of Pneumocystis sequences is thus in accordance with the historical processes of Apodemus speciation described and emphasized by the parasite population evolution.
A focus on the last clade, comprising woodmice from the Balkans, Italy and Sicily, pointed out a division into two subclades showing a large and robust differentiation . Animals from Sicily displayed a higher level of nucleotide diversity than animals from Balkans and continental Italy . Nieberding et al.  established the phylogeographical pattern of the European nematode H. polygyrus, and, like its woodmouse host, the Italo-Balkan lineage comprised a Sicilian subclade. Moreover, Nieberding et al.  reported that the southern Italian region is the continental source for Sicilian populations of H. polygyrus as well as for its host A. sylvaticus. In the present study, the phylogenetic tree and the minimum spanning network showed a comparable trend to the grouping of woodmice-related Pneumocystis in this Sicilian clade, even if some relations remain unclear. Sicilian Pneumocystis population displayed levels of GD and π that were comparable to Calabrian source populations. Moreover, many more haplotypes were found in Sicilian Pneumocystis than fungi from other regions as depicted by the network analysis. This suggests a more heterogeneous distribution of Sicilian Pneumocystis and thus, a more stable population less subjected to a recent expansion. These results tend to confirm the hypothesis in which Sicily would be a ‘hotspot’ of genetic diversity for woodmice and its associated parasites .
Pneumocystis spp as proxies
Pneumocystis is widely present in ecosystems . Surveys in domestic, synanthropic or wild mammalian species showed that mammals harbor one or several host-specific Pneumocystis species or strains [10–11, 14, 18–19, 21, 41]. Similarly, woodmice harbor many host-specific Pneumocystis strains apparently related with host infra-specific variants. In addition, Pneumocystis polymorphism seems to be related with woodmice geographical distribution.
Some uncertainties remain in the Pneumocystis life cycle. Particularly, a question is unanswered: are Pneumocystis organisms able to survive or multiply in the environment? A recent study reports that the social or behavioural factors may influence transmission of Pneumocystis within the colonies of bat species, while the environmental factors do not seem to have an impact on the carriage rate of Pneumocystis . The strong host-species specificity and co-divergence do not support the hypothesis of an environmental reservoir [2, 6, 10–11, 13]. This rather suggests that Pneumocystis may only survive very ephemerally in the environment, and that the infection travels from host-to-host via the airborne route, while the crowding of mammals favours fungal transmission. Pneumocystis could be used as a tool to study the social structuring and phylogeny of their hosts.
Pneumocystis organisms are not only specific of hosts [2–3, 5–6, 8, 52–54], but they co-diverge with their hosts [2–3, 13] and it differs within the same host species according to the geographical place [10–11].
This double feature of Pneumocystis organisms, host and site specificities, constitutes a promising tool to unveil the phylogeny or the phylogeography for many mammalian hosts.
Pneumocystis species seem to be good candidates for phylogenetic and phylogeographic studies in Apodemus sylvaticus. Indeed, the prevalence of Pneumocystis carriage in A. sylvaticus is higher (93.1%) than that reported for other parasites like the nematode Heligmosomoides polygyrus also studied in A. sylvaticus. Thus, Pneumocystis organisms constitute an easily accessible marker. Furthermore, we determined host and parasite co-divergence. In woodmice-derived Pneumocystis, specific DNA sequence divergence among Pneumocystis genotypes was correlated with the geographic location of their specific hosts. The analysis of Pneumocystis genetic diversity confirmed the evolutionary history of A. sylvaticus in Europe. Furthermore, Sicily was confirmed to be a hotspot of intraspecific biodiversity not only at the level of the hosts but also of their parasites. Pneumocystis species and genotypes are emerging as powerful tools to conduct phylogeographic studies in mammals.
S1 Table. Divergence matrix of Pneumocystis combined mtLSU rDNA and mtSSU rDNA sequences amplified from 30 woodmice, two rodents (P. murina from mouse Mus musculus and Pneumocystis from squirrel Sciureus aestuans).
S1 Fig. Alignement of the Pneumocystis combined mtSSU rDNA and mtLSU rDNA sequences amplified from 30 woodmice, two other rodents (P. murina from mouse Mus musculus and Pneumocystis from squirrel Sciureus aestuans).
S2 Fig. NJ tree depicting relationships between Pneumocystis organisms isolated from A. sylvaticus of different trapping locations.
NJ is inferred from the combined mitochondrial small subunit (mtSSU) and large subunit (mtLSU) rRNA sequences. The percentages displayed above the branches are the frequencies with which a given branch appeared in 1,000 bootstrap replications.
S3 Fig. ML phylogenetic tree depicting relationships between Pneumocystis organisms isolated from A. sylvaticus of different trapping locations.
ML is inferred from the combined mitochondrial small subunit (mtSSU) and large subunit (mtLSU) rRNA sequences. The percentages displayed above the branches are the frequencies with which a given branch appeared in 1,000 bootstrap replications.
S4 Fig. MB phylogenetic tree depicting relationships between Pneumocystis organisms isolated from A. sylvaticus of different trapping locations.
MB are inferred from the combined mitochondrial small subunit (mtSSU) and large subunit (mtLSU) rRNA sequences. The percentages displayed above the branches are the frequencies with which a given branch appeared in 1,000 bootstrap replications.
S5 Fig. MP phylogenetic tree depicting relationships between Pneumocystis organisms isolated from A. sylvaticus of different trapping locations.
MP is inferred from the combined mitochondrial small subunit (mtSSU) and large subunit (mtLSU) rRNA sequences. The percentages displayed above the branches are the frequencies with which a given branch appeared in 1,000 bootstrap replications. *Bootstrap values below 50% are reported.
Conceived and designed the experiments: CD JM SM MD JG. Performed the experiments: CD JM SM MD JG MP EMA. Analyzed the data: CD JM SM MD JG VB CN EV ED CP. Contributed reagents/materials/analysis tools: CD JM SM MD JG. Wrote the paper: CD JM SM MD JG CMAD ED.
- 1. Nieberding CM, Olivieri I. Parasites: proxies for host genealogy and ecology? Trends Ecol Evol. 2007; 22(3): 156–65. pmid:17157954
- 2. Nieberding C, Morand S, Libois R, Michaux JR. A parasite reveals cryptic phylogeographic history of its host. Proc Biol Sci. 2004; 271(1557): 2559–68. pmid:15615681
- 3. Nieberding CM, Durette-Desset MC, Vanderpoorten A, Casanova JC, Ribas A, Deffontaine V, et al. Geography and host biogeography matter for understanding the phylogeography of a parasite. Mol Phylogenet Evol. 2008; 47(2): 538–54. pmid:18346916
- 4. Taylor ML, Chávez-Tapia CB, Rojas-Martínez A, del Rocio Reyes-Montes M, del Valle MB, Zúñiga G. Geographical distribution of genetic polymorphism of the pathogen Histoplasma capsulatum isolated from infected bats, captured in a central zone of Mexico. FEMS Immunol Med Microbiol. 2005; 45(3): 451–8. pmid:16061361
- 5. Criscione CD, Cooper B, Blouin MS. Parasite genotypes identify source populations of migratory fish more accurately than fish genotypes. Ecology. 2006; 87: 823–828. pmid:16676525
- 6. Bruyndonckx N, Dubey S, Ruedi M, Christe P. Molecular cophylogenetic relationships between European bats and their ectoparasitic mites (Acari, Spinturnicidae). Mol Phylogenet Evol. 2009; 51(2): 227–37. pmid:19236931
- 7. Bruyndonckx N, Biollaz F, Dubey S, Goudet J, Christe P. Mites as biological tags of their hosts. Mol Ecol. 2010; 19(13): 2770–8. pmid:20546134
- 8. Nieberding C, Libois R, Douady CJ, Morand S, Michaux JR. Phylogeography of a nematode (Heligmosomoides polygyrus) in the western Palearctic region: persistence of northern cryptic populations during ice ages? Mol Ecol. 2005; 14(3): 765–79. pmid:15723668
- 9. Dei-Cas E. Pneumocystis infections: the iceberg? Medical Mycology. 2000; 38: 23–32. pmid:11204150
- 10. Demanche C, Berthelemy M, Petit T, Polack B, Wakefield AE, Dei-Cas E, et al. Phylogeny of Pneumocystis carinii from 18 primate species confirms host specificity and suggests co-evolution. Journal of Clinical Microbiology. 2001; 39: 2126–2133. pmid:11376046
- 11. Guillot J, Demanche C, Hugot JP, Berthelemy M, Wakefield AE, Dei-Cas E, et al. Parallel phylogenies of Pneumocystis species and their mammalian hosts. J Euk Microbiol. 2001; Suppl: 133–115. pmid:11906025
- 12. Dei-Cas E, Cailliez JC. Pneumocystis carinii. Editorial. FEMS Immunol Med Microbiol. 1998; 22: 1–4. pmid:9792055
- 13. Dei-Cas E, Chabé M, Moukhlis R, Durand-Joly I, Aliouat EM, Stringer JR, et al. Pneumocystis oryctolagi sp. nov. an uncultured fungus causing pneumonia in rabbits at weaning: review of current knowledge and description if a new taxon on genotypic, phylogenetic and phenotypic bases. FEMS Microbiology Review. 2006; 30: 853–871. pmid:17064284
- 14. Aliouat-Denis CM, Chabé M, Demanche C, Aliouat EM, Viscogliosi E, Guillot J, et al. Pneumocystis species, co-evolution and pathogenic power. Infection, Genetics and Evolution. 2008; 8: 708–26. pmid:18565802
- 15. Aliouat EM, Mazars E, Dei-Cas E, Delcourt P, Billault P, Camus D. Pneumocystis cross infection experiments using SCID mice and nude rats as recipient hosts showed strong host specificity. J Eukaryot Microbiol. 1994; 41: S71.
- 16. Durand-Joly I, Aliouat EM, Recourt C, Guyot K, Francois N, Wauquier M, et al. Pneumocystis carinii f. sp. hominis is not infectious for SCID mice. J Clin Microbiol. 2002; 40: 1862–1865. pmid:11980979
- 17. Dei-Cas E, Mazars E, Aliouat EM, Nevez G, Cailliez JC, Camus D. The host-specificity of Pneumocystis carinii. J Mycol Med. 1998b; 8: 1–6.
- 18. Derouiche S, Deville M, Taylor ML, Akbar H, Guillot J, Pottier M, et al. Pneumocystis as phylogeographic markers? Memórias Instituto Oswaldo Cruz. 2009; 104: 112–117.
- 19. Akbar H, Pinçon C, Aliouat CM, Derouiche S, Taylor ML, Pottier M, et al. Characterizing Pneumocystis in the lungs of bats: understanding Pneumocystis Evolution and Spread of Pneumocystis organisms in mammal populations. Appl Environ Microbiol. 2012; 78(22): 8122–36. pmid:23001662
- 20. Palmer RJ, Settnes OP, Lodal J, Wakefield AE. Population structure of rat-derived Pneumocystis carinii in Danish wild rats. Appl Environ Microbiol. 2000; 66: 4954–4961. pmid:11055949
- 21. Hugot JP, Demanche C, Barriel V, Dei-Cas E, Guillot J. Phylogenetic systematics and evolution of primates-derived Pneumocystis based on mitochondrial and DNA sequences comparison. Systematic Biology. 2003 52: 735–744. pmid:14668114
- 22. Guillot J, Demanche C, Norris K, Wildschutte H, Wanert F, Tataine S, et al. Phylogenetic relationship among Pneumocystis from Asian macaques inferred from mitochondrial rRNA sequences. Mol Phylogenet Evol. 2004; 31: 988–996. pmid:15120396
- 23. Michaux JR, Magnanou E, Paradis E, Nieberding C, Libois R. Mitochondrial phylogeography of the Woodmouse (Apodemus sylvaticus) in the Western Paleartic region. Molecular Ecology. 2003; 12: 685–90. pmid:12675824
- 24. Dubey S, Michaux J, Brünner H, Hutterer R, Vogel P. False phylogenies on wood mice due to cryptic cytochrome-b pseudogene. Molecular Phylogenetics and Evolution. 2009; 50: 633–641. pmid:19126432
- 25. Wakefield AE. DNA sequences identical to Pneumocystis carinii f. sp. carinii and Pneumocystis carinii f. sp. hominis in samples of air spora. J Clin Microbiol. 1996; 34: 1754–9. pmid:8784583
- 26. Tsolaki AG, Beckers P, Wakefield AE. Pre-AIDS Era Isolates of Pneumocystis carinii f. sp. hominis: High Genotypic Similarity with Contemporary Isolates. J Clin Microbiol. 1998; 36: 90–93. pmid:9431927
- 27. Thompson JD. The Clustal X windows interface: flexible strategies for multiple sequence alignment aides by quality analysis tools. Nucleic Acids Res. 1997; 25: 4876–82. pmid:9396791
- 28. Rambaut A. Se-Al: Sequence alignment editor, version 1.0 alpha 1. 1996; Univ. Oxford, Oxford, U.K.
- 29. Barriel V. Molecular phylogenies and how to code insertion/deletion events. C R Acad Sci III. 1994; 317: 693–701. pmid:7882153
- 30. Swofford DL. PAUP*. Phylogenetic Analysis Using Parsimony (* and other methods). Version 4. 2003; Sinauer Associates, Sunderland, Massachusetts.
- 31. Guindon S, Lethiec F, Duroux P, Gascuel O. PHYML Online—a web server for fast maximum likelihood-based phylogenetic inference. Nucl Acids Res. 2005; 33(Web Server issue): W557–9. pmid:15980534
- 32. Darriba D, Taboada GL, Doallo R, Posada D. jModelTest 2: more models, new heuristics and parallel computing. Nature Methods. 2012; 9: 772. pmid:22847109
- 33. Huelsenbeck JP, Ronquist F. MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics. 2001; 17: 754–5. pmid:11524383
- 34. Green PJ. Reversible jump Markov chain Monte Carlo computation and Bayesian model determination. Biometrika. 1995; 8: 711–732.
- 35. Gascuel O. BIONJ: an improved version of the NJ algorithm based on a simple model of sequence data. Molecular Biology and Evolution. 1997; 14: 685–695. pmid:9254330
- 36. Schneider S, Roessli D, Excoffier L. Arlequin: a software for population genetics data analysis. User manual ver 2.000. Genetics and Biometry Lab, Dept. of Anthropology, University of Geneva, Geneva. 2000.
- 37. Librado P, Rozas J. DnaSP v5: A software for comprehensive analysis of DNA polymorphism data. Bioinformatics. 2009; 25: 1451–1452. pmid:19346325
- 38. Demanche C, Petit T, Moisson P, Ollivet F, Rigoulet J, Chermette R, et al. Assessment of Pneumocystis species carriage in captive primates. Veterinary Record. 2003; 152: 811–813. pmid:12862172
- 39. Demanche C, Wanert F, Barthélemy M, Mathieu J, Durand-Joly I, Dei-Cas E, et al. Molecular and serological evidence of Pneumocystis circulation in a social organization of healthy macaques (Macaca fascicularis). Microbiology. 2005; 151: 3117–3125. pmid:16151222
- 40. Mazars E, Guyot K, Fourmaintraux S, Renaud F, Petavy F, Camus D, et al. Detection of Pneumocystis in European wild animals. J Eukaryot Microbiol. 1997; 44: 39S. pmid:9508427
- 41. Chabé M, Herbreteau V, Hugot JP, Bouzard N, Deruyter L, Morand S, et al. Pneumocystis carinii and Pneumocystis wakefieldiae in wild Rattus norvegicus trapped in Thailand. J Euk Microbiol. 2010; 57: 213–217. pmid:20113380
- 42. Laakkonen J. Pneumocystis carinii in wildlife. Inter J Par. 1998; 28: 241–252.
- 43. Michaux J, Goüy de Bellocq J, Sara M, Morand S. Body size increase in insular rodent populations: a role for predators? Global Ecology and Biogeography. 2002; 11: 427–436.
- 44. Dumoulin A, Mazars E, Seguy N, Gargallo-Viola D, Vargas S, Cailliez JC, et al. Transmission of Pneumocystis carinii disease from immuno-competent contacts of infected hosts to susceptible hosts. Eur J Clin Microbiol Infect Dis. 2000; 19: 671–678. pmid:11057500
- 45. Fromont E, Morvilliers L, Artois M, Pontier D. Parasite richness and abundance in insular and mainland feral cats: insularity or density? Parasitology. 2001; 123: 143–151. pmid:11510679
- 46. Goüy de Bellocq J, Morand S, Feliu C. Patterns of parasites species richness of Western Palaeartic micro-mammals: island effects. Ecography. 2002; 25: 173–183.
- 47. Sara M, Morand S. Island incidence and mainland population density: mammals from Mediterranean islands. Diversity and Distributions. 2002; 8: 1–10.
- 48. Nieberding C, Morrand S, Libois R, Michaux JR. Parasites and the island syndrome: the colonization of the western Mediterranean islands by Heligmosomoides polygyrus (Dujardin, 1845). J Biogeogr. 2006; 33: 1212–1222.
- 49. Michaux JR, Libois R, Paradis E, Filippucci MG. Phylogeographic history of the yellow-necked fieldmouse (Apodemus flavicollis) in Europe and in the Near and Middle East. Mol Phylogenet Evol. 2004; 32(3): 788–98. pmid:15288056
- 50. Michaux JR, Libois R, Filippucci MG. So close and so different: comparative phylogeography of two small mammal species, the yellow-necked fieldmouse (Apodemus flavicollis) and the woodmouse (Apodemus sylvaticus) in the Western Palearctic region. Heredity (Edinb). 2005; 94(1): 52–63. pmid:15329664
- 51. Callejón R, de Rojas M, Nieberding C, Foronda P, Feliú C, Guevara D, et al. Molecular evolution of Trichuris muris isolated from different Muridae hosts in Europe. Parasitol Res. 2010; 107: 631–41. pmid:20473527
- 52. Cushion MT, Keely SP, Stringer JR. Molecular and phenotypic description of Pneumocystis wakefieldiae sp. nov., a new species in rats. Mycologia. 2004; 96(3): 429–38. pmid:21148866
- 53. Gigliotti F, Harmsen AG, Haidaris PJ. Pneumocystis carinii is not universally transmissible between mammalian species. Infect Immun. 1993; 61: 2886–2890. pmid:8514391
- 54. Keely SP, Fischer JM, Cushion MT, Stringer JR. Phylogenetic identification of Pneumocystis murina sp. nov., a new species in laboratory mice. Microbiol. 2004; 150: 1153–1165.