Introduction
Malaria parasites (order Haemosporida) infect birds, squamates, chelonians and several groups of mammals, including humans, and are transmitted by different groups of haematophagous dipterans (Garnham, Reference Garnham1966). The human-infecting parasite species belong to the genus Plasmodium, which is only one out of at least 15 genera that together comprise over 500 haemosporidian species. Parasites of this diverse group differ in host specificities, adaptations and their life cycles (Garnham, Reference Garnham1966). For instance, all haemosporidian genera, except Plasmodium, lack the distinct replication phase inside red blood cells, which is the exclusive cause of clinical symptoms of malaria. Therefore, studying the diversity and evolution of the entire haemosporidian parasite group will contribute to our understanding of the important malaria disease in humans (Galen et al., Reference Galen, Borner, Martinsen, Schaer, Austin, West and Perkins2018).
Parasites of the haemosporidian genus Polychromophilus are transmitted by ectoparasitic highly specialized nycteribiid flies and have exclusively been described in bats (Dionisi, Reference Dionisi1898; Garnham, Reference Garnham1966, Reference Garnham1973; Witsenburg et al., Reference Witsenburg, Salamin and Christe2012). Polychromophilus presents the only haemosporidian taxon that infects mammalian hosts in tropical as well as in temperate climate zones. These parasites are common in bats in Europe and in the tropical regions of Africa, Asia, Australia and South America (e.g. Garnham, Reference Garnham1966; Perkins and Schaer, Reference Perkins and Schaer2016). Even though Polychromophilus parasites are widespread and common, only five morphospecies have been formally described to date. Polychromophilus murinus has been mainly reported in bats of the family Vespertilionidae and Polychromophilus melanipherus in bats of the family Miniopteridae (e.g. Garnham, Reference Garnham1966; Gardner and Molyneux, Reference Gardner and Molyneux1988). The species Polychromophilus corradetti and Polychromophilus adami have been described from African Miniopterus species (Landau et al., Reference Landau, Rosin, Miltgen, Hugot, Leger, Beveridge and Baccam1980). The description of Polychromophilus deanei from Myotis nigricans (Vespertilionidae) in Brazil, and three other records of Polychromophilus from bats in Brazil and Southern USA provided evidence of chiropteran haemosporidian parasites in the New World (Wood, Reference Wood1952; Deane and Deane, Reference Deane and Deane1961; Garnham et al., Reference Garnham, Lainson and Shaw1971; Foster, Reference Foster1979). Several phylogenetic studies have confirmed that P. murinus and P. melanipherus comprise distinct species (e.g. Megali et al., Reference Megali, Yannic and Christe2011; Witsenburg et al., Reference Witsenburg, Salamin and Christe2012), the latter possibly representing a species complex (Duval et al., Reference Duval, Mejean, Maganga, Makanga, Mangama Koumba, Peirce, Ariey and Bourgarel2012). In molecular phylogenies, sequences from Polychromophilus of M. nigricans from Panama, which might represent P. deanei, group closely with P. murinus parasite sequences (Borner et al., Reference Borner, Pick, Thiede, Kolawole, Kingsley, Schulze, Cottontail, Wellinghausen, Schmidt-Chanasit, Bruchhaus and Burmester2016). The remaining two morphospecies have not been included in phylogenetic analyses yet, however Polychromophilus sequences sampled from the African Miniopterus host species of P. corradetti and P. adami grouped within the P. melanipherus clade (Duval et al., Reference Duval, Mejean, Maganga, Makanga, Mangama Koumba, Peirce, Ariey and Bourgarel2012; Rosskopf et al., Reference Rosskopf, Held, Gmeiner, Mordmüller, Matsiégui, Eckerle, Weber, Matuschewski and Schaer2019).
Very few studies have focused on morphological or molecular investigations of Polychromophilus parasites in Asia. Two morphological studies described Polychromophilus from hipposiderid bat species in Thailand and Malaysia (Eyles et al., Reference Eyles, Dunn and Liat1962; Landau et al., Reference Landau, Baccam, Ratanaworabhan, Yenbutra, Boulard and Chabaud1984). One molecular study published a Polychromophilus sequence from the vespertilionid bat Kerivoula hardwickii in Cambodia and a recent study published two short cytochrome b sequences for P. murinus and P. melanipherus from Myotis siligorensis (Vespertilionidae) and Taphozous melanopogon (Emballonuridae) in Thailand (Duval et al., Reference Duval, Robert, Csorba, Hassanin, Randrianarivelojosia, Walston, Nhim, Goodman and Ariey2007; Arnuphapprasert et al., Reference Arnuphapprasert, Riana, Ngamprasertwong, Wangthongchaicharoen, Soisook, Thanee, Bhodhibundit and Kaewthamasorn2020). Here, data are presented from molecular investigations of Polychromophilus infections in the lesser Asiatic yellow bat (Scotophilus kuhlii) in Thailand that were originally reported as unidentified haemosporidian parasites in a preliminary morphological study on white blood cell counts of S. kuhlii (Chumnandee and Pha-obnga, Reference Chumnandee and Pha-obnga2018) and add important information to the phylogeny of these neglected parasites.
Materials and methods
Bats were captured in April 2018 in the Muang district in the Nakhon Phanom province in Thailand (17°24′38.92″N and 104°46′42.82″E) using standard mist nets. A total of 44 bats were captured from the same colony. Standard morphological measurements were taken for each bat and the identification keys of Duengkae (Reference Duengkae2007) and Srinivasulu et al. (Reference Srinivasulu, Srinivasulu and Venkateshwarlu2010) were used for species identification. Bats were kept individually in cotton bags. Blood sampling followed approved animal care protocols and comprised 0.6–1.0% body mass of blood (e.g. 6–19 μL g−1) per bat (e.g. Predict One Health Consortium, 2013). The blood samples were used to prepare two thin blood smears and to preserve blood on DNA FTA cards. Bats were released at the capture side, once they had fully recovered. The thin blood smears were fixed and stained with Wright-Giemsa (following Paksuz et al., Reference Paksuz, Paksuz and Ozkan2009). Slides were thoroughly scanned by light microscopy with a magnification of ×1000 using oil immersion. The morphology of the blood stages of the parasites was compared to original species descriptions. Parasitaemia was calculated as the percentage of parasite-infected erythrocytes in the total number of erythrocytes (total number of parasites/products of mean number of erythrocytes per field × number of counted fields). The mean number of erythrocytes per field was determined by counting three fields and the number of parasites was recorded in 50 fields (fields with comparable erythrocyte density).
Whole genomic DNA was extracted from blood dots on DNA FTA cards using the DNeasy extraction kit (Qiagen). Two mitochondrial genes of the bats were amplified and sequenced to verify the morphological taxonomic identification of the bats (cytochrome b, cytb and part of the NADH dehydrogenase subunit 1, ND1) (Table S1). Sequences were compared to references in GenBank using the NCBI BLAST tool (e.g. Johnson et al., Reference Johnson, Zaretskaya, Raytselis, Merezhuk, McGinnis and Madden2008). Four genes from the three genomes of the parasites were amplified, the mitochondrial cytochrome b (cytb) and cytochrome oxidase I (cox1), the nuclear elongation factor 2 (EF2) and the apicoplast caseinolytic protease (clpC) using established protocols and primers (e.g. Martinsen et al., Reference Martinsen, Perkins and Schall2008; Schaer et al., Reference Schaer, Perkins, Decher, Leendertz, Fahr, Weber and Matuschewski2013) (Table S1; see Fig. S1 for primer locations). PCR products were sequenced in both directions and run on an ABI-373 sequencer (accession numbers listed in Table S2). The sequence data were combined with corresponding gene sequences of representatives of the major haemosporidian taxa that were obtained from GenBank (Table S2). Phylogenetic analysis of the concatenated dataset (total of 2793 bp: 978 bp of cytb, 957 bp of cox1, 483 bp of clpC, 375 bp of EF2) was carried out with PartitionFinder v.2 (Lanfear et al., Reference Lanfear, Frandsen, Wright, Senfeld and Calcott2017) and MrBayes v3.2.7 (Ronquist et al., Reference Ronquist, Teslenko, van der Mark, Ayres, Darling, Höhna, Larget, Liu, Suchard and Huelsenbeck2012) via the CIPRES Portal (Miller et al., Reference Miller, Pfeiffer and Schwartz2010) (Table S3). Bayesian inference methods were carried out with two runs of four chains (heated = 3, cold = 1, temperature = 0.01) each for 10 million generations. The first 25% of trees were discarded as burn-in. Tracer v1.6 was used to evaluate the mixing and convergence of runs and effective sample sizes (EES > 500) (Rambaut et al., Reference Rambaut, Suchard, Xie and Drummond2014). Trees were visualized with FigTree v1.4.4.
Results
The survey of haemosporidian parasites in a colony of S. kuhlii bats identified Polychromophilus infections in five out of 44 bat individuals (prevalence = 11%). This is the first host record for the vespertilionid bat genus Scotophilus and for the species S. kuhlii for infections with Polychromophilus parasites. The morphological bat species identifications were confirmed with molecular barcoding. The whole mitochondrial cytochrome b was sequenced, which featured a 99.7% nucleotide identity with the S. kuhlii reference sequences (e.g. EU750921) in GenBank. In addition, 928 bp of the mitochondrial NADH dehydrogenase subunit 1 were sequenced and nucleotide identity with an S. kuhlii reference sequence (AB079818) was 98.9% (accession numbers listed in Table S3).
The blood stages of Polychromophilus parasites are limited to gametocytes and the morphology corresponds to the description of Polychromophilus parasites of vespertilionid hosts. In Giemsa-stained blood smears, the immature parasites feature a pale cytoplasm and the nucleus is located peripherally and stains purple (Fig. 1A a). When mature, the gametocytes fill the host cell completely and cause a slight enlargement of the erythrocyte. Fine hemozoin pigment grains are scattered in the cytoplasm, a characteristic that is attributed to P. murinus (Fig. 1A b–f). In marked contrast, the pigment of P. melanipherus is much larger and coarse-grained. The male microgametocytes feature a light pink-stained cytoplasm (Fig. 1A b–c), whereas the female macrogametocytes stain purple-blue (Fig. 1A d–f), both exhibiting a small distinct pink-staining nucleus that is placed eccentrically. The morphology of the gametocyte stages did not allow a clear assignment to any described morphospecies.
Fig. 1. (A) Representative Giemsa-stained micrographs of gametocyte blood stages of Polychromophilus parasites from Scotophilus kuhlii in Thailand (a, c–d from bat sample CC-33; b, f from bat sample CC-28). Size bars = 5 μm, magnification = 1000×. (a) Immature gametocyte with pale cytoplasm and a peripheral purple nucleus. (b–f) Mature gametocytes that entirely occupy and slightly enlarge the host erythrocytes. The malaria pigment hemozoin is visible as fine dark grains scattered throughout the cytoplasm. (b–c) Male microgametocytes with the cytoplasm in a characteristic light pink colour and the small nucleus in a slightly darker pink. (d–f) Female macrogametocytes with a purple-blue cytoplasm and small nuclei in pink. (B) Parasitaemia in %. Parasitaemia values in the five infected S. kuhlii ranged between 0.01 and 0.1% (prevalence of 11%, 5/44 S. kuhlii infected). Inserted photograph of S. kuhlii.
The mean Polychromophilus gametocytaemia in the blood smear-positive samples was 0.05% (minimum of 0.01% and maximum of 0.1%) (Fig. 1B).
Sanger sequencing revealed that the parasite cytb nucleotide sequences were identical, while we noted that the cox1 sequences in one out of five samples differed by one base. Hence, the five S. kuhlii individuals were infected with one cytochrome b haplotype and two cytochrome oxidase 1 haplotypes of the same Polychromophilus species.
The three-genome phylogeny of Polychromophilus in the context of the major haemosporidian parasite clades recovered the Polychromophilus parasites (Fig. 2, highlighted in orange) as sister clade to a group that contains the lizard and bird Plasmodium species (highlighted in yellow), confirming previous studies that showed a distant relationship of Polychromophilus parasites to Plasmodium and Hepatocystis of mammalian hosts (highlighted in grey) (Fig. 2). Together, they group with the Plasmodium species of ungulates (Fig. 2, highlighted in blue). All Polychromophilus sequences group into one monophyletic clade (posterior probability of 1) that contains two main subclades. The first distinct subclade comprises all sequences of P. melanipherus of Miniopterus bat hosts (and one parasite sequence of a Taphozous bat host) and the second subclade exclusively includes sequences of Polychromophilus parasites of vespertilionid (and one rhinolophid) bat species, confirming a clear separation of parasites of miniopterid and vespertilionid hosts. The second subclade contains P. murinus sequences from bats in Europe, Madagascar and Thailand and one sequence that is basal to P. murinus, a sample from M. nigricans from Panama. The placement of the sample from K. hardwickii from Cambodia could not be resolved. The other subclade that is separated from the ‘P. murinus’ clade contains the sequences of Polychromophilus of S. kuhlii from Thailand (Fig. 2, highlighted in green) and two parasite samples from Pipistrellus aff. grandidieri and Laephotis capensis from Guinea.
Fig. 2. Bayesian analysis of Polychromophilus parasites (highlighted in orange) and selected haemosporidian taxa. Posterior probability values are given. The concatenated phylogeny was conducted via analysis of four genes, the mitochondrial cytochrome b and cytochrome oxidase I, the nuclear elongation factor 2, and the apicoplast caseinolytic protease. Note that the placement of Polychromophilus parasites as sister clade to a group that contains the lizard and bird Plasmodium species (highlighted in yellow) instead of the ungulate Plasmodium species (highlighted in blue) (as confirmed in Galen et al., Reference Galen, Borner, Martinsen, Schaer, Austin, West and Perkins2018) can be partly attributed to missing clpC and EF2 sequences in Polychromophilus reference samples. The monophyletic clade (posterior probability of 1) of Polychromophilus parasites comprises two distinctive subclades. One subclade includes all Polychromophilus melanipherus sequences isolated from Miniopterus bats. A second subclade encompasses all sequences of Polychromophilus parasites isolated from vespertilionid bats, including Polychromophilus murinus and Polychromophilus sp. The ‘Vespertilionidae’ subclade is again divided into two groups, one contains all ‘P. murinus’ sequences and the other distinct group comprises the sequences of this study, Polychromophilus sequences of Scotophilus kuhlii from Thailand (samples highlighted in green), and two Polychromophilus sequences isolated from Pipistrellus aff. grandidieri and Laephotis capensis (as Neoromicia capensis) in Guinea (Schaer et al., Reference Schaer, Perkins, Decher, Leendertz, Fahr, Weber and Matuschewski2013). The phylogenetic placement of the Guinean Polychromophilus and of the Polychromophilus parasites of Scotophilus kuhlii bats as distinct from the P. melanipherus and P. murinus could indicate that they present separate species.
Discussion
This study provides the first information on haemosporidian parasites in the bat species S. kuhlii in Thailand. The morphology of the blood stages and the phylogenetic analysis identify the parasites as belonging to the genus Polychromophilus. The infections featured low overall parasitaemias as reported from other Polychromophilus infections (e.g. Rosskopf et al., Reference Rosskopf, Held, Gmeiner, Mordmüller, Matsiégui, Eckerle, Weber, Matuschewski and Schaer2019). The three-genome phylogeny confirms a clear separation of Polychromophilus parasites of Miniopterus bat species and of vespertilionid bat species, the latter including the parasites of S. kuhlii. The phylogenetic analysis recovered the Polychromophilus parasites as sister clade to a group that contains the lizard and bird Plasmodium species, as shown before (Witsenburg et al., Reference Witsenburg, Salamin and Christe2012). However, the most comprehensive phylogeny based on multiple nuclear markers clearly placed Polychromophilus as sister clade to the ungulate Plasmodium species (Galen et al., Reference Galen, Borner, Martinsen, Schaer, Austin, West and Perkins2018). Thus, the placement of Polychromophilus as sister to the avian/lizard Plasmodium species in our analysis can likely be attributed to the unavailability of cox1, clpC and EF2 sequences for the majority of the Polychromophilus references that were included in the analysis (Tables S2 and S3). Genes display different rates and patterns of evolution and analysing genes of the parasites’ three genomes for robust phylogenies of haemosporidian parasites has been established (e.g. Martinsen et al., Reference Martinsen, Perkins and Schall2008). However, many phylogenetic studies are still limited to the analysis of (rather short) cytochrome b sequences.
To date, only four studies have reported Polychromophilus parasites from Asian bats. Eyles et al. (Reference Eyles, Dunn and Liat1962) reported Polychromophilus parasites in the bat species Hipposideros bicolor in Malaysia and described the gametocytes as oval in shape, with clear-cut borders and that the parasites only partially occupy the host erythrocytes (Eyles et al., Reference Eyles, Dunn and Liat1962). Another morphological study described Polychromophilus from Hipposideros larvatus in Thailand (as Biguetiella minuta which was considered as a vicariant form of Bioccala, a subgenus of Polychromophilus) (Landau et al., Reference Landau, Baccam, Ratanaworabhan, Yenbutra, Boulard and Chabaud1984). The gametocytes of the latter were also described as not filling the host cell. Thus, the gametocytes of Polychromophilus from hipposiderid hosts differ from the morphology of the mature gametocytes observed in the current study that fill the entire host cells and even slightly enlarge the erythrocytes. The only study that reported Polychromophilus from a vespertilionid bat species in Asia is that of Duval et al. (Reference Duval, Robert, Csorba, Hassanin, Randrianarivelojosia, Walston, Nhim, Goodman and Ariey2007) that found K. hardwickii in Cambodia infected with Polychromophilus sp. (Duval et al., Reference Duval, Robert, Csorba, Hassanin, Randrianarivelojosia, Walston, Nhim, Goodman and Ariey2007). In our phylogenetic analysis, the nucleotide sequence of Polychromophilus of K. hardwickii is separated from Polychromophilus of S. kuhlii. Therefore, we assume that the Polychromophilus parasites of S. kuhlii in Thailand do not represent the parasites detected in Asian hipposiderid hosts nor the Polychromophilus parasite reported from K. hardwickii in Cambodia. The phylogenetic analyses resulted in the placement of Polychromophilus of S. kuhlii outside the P. melanipherus and P. murinus clades, which also contain the two recently reported Polychromophilus parasites from Thailand (Arnuphapprasert et al., Reference Arnuphapprasert, Riana, Ngamprasertwong, Wangthongchaicharoen, Soisook, Thanee, Bhodhibundit and Kaewthamasorn2020). The Polychromophilus parasites of S. kuhlii form a group with the Guinean Polychromophilus parasites that have been suggested to represent a distinct species (Schaer et al., Reference Schaer, Perkins, Decher, Leendertz, Fahr, Weber and Matuschewski2013; Rosskopf et al., Reference Rosskopf, Held, Gmeiner, Mordmüller, Matsiégui, Eckerle, Weber, Matuschewski and Schaer2019). Within this group, the Polychromophilus parasites of S. kuhlii are clearly separated from the Guinean samples (posterior probability = 1) and might therefore also present a distinct species.
Future morphological studies that investigate the tissue stages and molecular studies of additional Polychromophilus parasites of Asian bats are needed to reassess this assumption. The host species S. kuhlii is widely distributed in South Asia, southern China and Southeast Asia and is found in primary and secondary habitats, both in rural and urban areas and might represent a species complex (Trujillo et al., Reference Trujillo, Patton, Schlitter and Bickham2009; Srinivasulu and Srinivasulu, Reference Srinivasulu and Srinivasulu2019). Systematic sampling of S. kuhlii across its distribution range and of other potential vespertilionid bat host species will add important information on the host specificity, the prevalence and nycteribiid vectors of Polychromophilus parasites in Asia.
Data
Nucleotide sequence data reported in this paper are available in the GenBank database under accession nos. MT750305-MT750321.
Supplementary material
The supplementary material for this article can be found at https://doi.org/10.1017/S003118202000222X.
Acknowledgements
We thank the Tobacco Authority of Thailand, Nakhon Phanom province for the permission to collect samples from bats.
Author contributions
C.C. and J.S. conceived and designed the study. J.S. and O.W. performed phylogenetic analysis. All authors conducted data gathering and wrote the article.
Financial support
This work was supported by the Research and Development Institute of Nakhon Phanom University. J.S. is funded by an individual research grant from the German Research Foundation (DFG; project number 437846632).
Conflict of interest
None.
Ethical standards
The Institutional Animal Care and Use Committee of Nakhon Phanom University (project code B1) reviewed and officially approved this survey (date 13.07.2017). Sampling followed approved animal care protocols (e.g. Predict One Health Consortium, 2013). The authors assert that all procedures contributing to this work comply with the ethical standards of the national and institutional guides on the care and use of animals.
Open access
