- Open Access
Multiple host-switching of Haemosporidia parasites in bats
© Duval et al; licensee BioMed Central Ltd. 2007
- Received: 02 November 2007
- Accepted: 29 November 2007
- Published: 29 November 2007
There have been reported cases of host-switching in avian and lizard species of Plasmodium (Apicomplexa, Haemosporidia), as well as in those infecting different primate species. However, no evidence has previously been found for host-swapping between wild birds and mammals.
This paper presents the results of the sampling of blood parasites of wild-captured bats from Madagascar and Cambodia. The presence of Haemosporidia infection in these animals is confirmed and cytochrome b gene sequences were used to construct a phylogenetic analysis.
Results reveal at least three different and independent Haemosporidia evolutionary histories in three different bat lineages from Madagascar and Cambodia.
Phylogenetic analysis strongly suggests multiple host-switching of Haemosporidia parasites in bats with those from avian and primate hosts.
- Bayesian Posterior Probability
- Blood Parasite
- Host Shift
- Human Malaria Parasite
Plasmodium falciparum (Apicomplexa, Haemosporidia), the most dangerous of human malaria parasites, is responsible for at least one million deaths a year . It has been suggested that its exceptional virulence, compared to the three other species of human Plasmodium, is due to its relatively recent host-shift from birds to humans and the short period for the latter to adapt to the parasite . Given the heavy burden of P. falciparum on human populations around the tropics , there is a critical need to better understand the origin and evolution of this parasite and related organisms. Plasmodium falciparum belongs to a group that also infects a considerable range of birds, squamates, crocodilians, chelonians and non-human mammals . These parasites are known to be virulent, invasive pathogens in a variety of wild animals and contribute to the parasite burden of natural populations, including several threatened species . Host switching by these parasites could be the trigger for emerging virulent diseases [6–8].
Madagascar and Cambodia are two biodiversity "hot spots" . The faunas of these areas, which are, in evolutionary terms, distant from one another, provide an attractive system for characterizing haemosporidian parasite species [10, 11] and for evaluating host-parasite co-evolution and exchange. Madagascar was part to the Gondwana continent and was separated 160 million and 90 million years ago from Africa and from India, respectively; whereas, Cambodia originated from the Laurasia continent.
The paper presents the result of the screening of over 500 bats belonging to seven families from different field sites in Madagascar and Cambodia. Haemosporidia parasites were isolated in the bat families, Hipposideridae, Vespertilionidae and Megadermatidae. Molecular sequences of bat haemosporidian parasites were not previously available. Herein, the phylogenetic analyses with cytochrome b mitochondrial gene sequences illustrate the first documented example of a cross-class host-switching of haemosporidian parasites between birds and mammals.
Field sites and sample collection
Screened material was obtained in Madagascar and Cambodia. In Madagascar, specimens were obtained at eight different field sites in the provinces of Mahajanga, Toliara and Antananarivo. The fieldwork was conducted between November 2001 and late 2004, in collaboration with the Institut Pasteur de Madagascar and WWF-Madagascar. In Cambodia, two field sites were sampled in the provinces of Kampot and Mondolkiri between December 2004 and May 2006, in collaboration with the Institut Pasteur du Cambodia and Wildlife Conservation Society. The field research was conducted with local and national permits from the Direction des Eaux et Forêts of Madagascar and the Ministry of Agriculture, Forestry and Fisheries in Cambodia. A total of 530 bats, belonging to seven families (Pteropodidae, Rhinolophidae, Hipposideridae, Megadermatidae, Emballonuridae, Vespertilionidae, and Molossidae) were trapped in the wild. A small sample of blood was obtained and the host was released without injury or in some cases retained as a voucher specimen.
Thin blood smears were made for each animal. They were fixed in methanol and stained by incubation with 10% Giemsa for 10 minutes. The smears were examined by microscopy for haemosporidian parasites. Parasites isolated from bats were referred to as Haemosporidia sp. Positive blood smears were catalogued in the Département 'Régulations, Développement et Diversité Moléculaire', Muséum National d'Histoire Naturelle, Paris, France.
DNA extraction and amplification
DNA was extracted from blood samples using the phenol/chloroform technique . The 709 bp cytochrome b fragments were amplified using PCR and nested-PCR. The PCR reaction was carried out in a total volume of 25 μl under the following condition: 1 μl of each of the primers: PLAS 1 (5'-GAGAATTATGGAGTGGATGGTG-3') and PLAS 2 (5'-GTGGTAATTGACATCCWATCC-3'), 1 mM of each dNTP, 1 U of Taq polymerase (Solis), 3 mM MgCl2. The PCR conditions were: 5 min at 94°C, 30 sec at 94°C, 30 sec at 55°C and 1 min 30 sec at 72°C for 40 cycles and a final 10 min extension at 72°C. The nested-PCR was carried out using 1 μl of the PCR products and performed with the following primers: PLAS 3 (5'-GGTGTTTYAGATAYATGCAYGC-3') and PLAS 4 (5'-CATCCWATCCATARTAWAGCATAG-3'). The conditions were: 5 min at 94°C, 30 sec at 94°C, 30 sec at 55°C, 1 min 30 sec at 72°C for 40 cycles and a final 10 min extension at 72°C. The PCR products were sequenced using PLAS3 and PLAS4 primers by Macrogen (Korea). All of these primers were designed by the research group. They are specific to haemosporidian parasites and do not amplify others Apicomplexa parasites or host DNA. Relevant sequences were selected for the phylogenetic analysis. There are numerous avian parasite sequences available and some representative sequences were chosen based on geographical localizations.
The nucleotide sequences (709 bp) were translated into amino acid sequences to minimize homoplasy due to saturation of synonymous mutations since some taxa have diverged over hundreds of millions years. The sequences were aligned using CLUSTAL W . Reference sequences of at least 219 amino acids without ambiguous positions were retrieved from GenBank. In the case of identical sequences in amino acids, only one sequence for the analysis was kept. Maximum Likelihood (ML) was performed using Phyml  and Parsimony analysis (P) was performed using Phylip package (version 3.62) . Nodal robustness was evaluated by non-parametric bootstrap (100 replicates). Bayesian analyses were conducted with MrBayes V3.1 software  using gamma distribution, 1 000 000 generations (average standard deviation of split sequences is below 0.01), with tree sampling every 100 generations and a burn-in of 2500 trees. The aim of the study was to analyse Haemosporidia phylogeny, so Theileria annulata, Babesia gibsoni and Toxoplasma gondii which belong to the phylum Apicomplexa but are non-haemosporidian parasites were choose as out-groups. The phylogenetic study was run using cytochrome b sequences. This is the most abundant marker in GenBank for a variety of haemosporidian parasites and widely used in phylogenetic studies because reference sequences from other genes are lacking.
Prevalence of Haemosporidia infection in bats from Madagascar
n infected (%)
Prevalence of Haemosporidia infection in bats from Cambodia
n infected (%)
Parasite taxa used in this study with host name, geographic location and GenBank accession number of the sequences used for the phylogenetic analysis
GenBank accession number
Old world monkeys
Old world monkeys
India and southeast Asia
Old world monkeys
Tropical and subtropical regions
Tropics of Africa and Asia
Tropical and subtropical regions
Congo and Cameroon
Plasmodium sp. 2
Plasmodium sp. 1
Wide range Bird
Plasmodium sp. 47
Plasmodium sp. 49
Plasmodium sp. 50
Haemosporidia (FMNH 172853)
Haemosporidia (FMNH 172862)
Haemosporidia (FMNH 172918)
Haemosporidia (FMNH 175810)
Haemoproteus sp. 1
Haemoproteus sp. 2
Haemoproteus sp. 3
The mitochondrial genome is more conserved in apicomplexan parasites  than in others metazoan eukaryotes. Cytochrome b gene is, therefore, a good marker to establish phylogenetic relationships between parasites that diverged several millions years ago .
The presence of a major division within haemosporidian parasites separating mammal and sauropsid hosts, suggests that parasites of these two vertebrate groups evolved separately. In the mammalian clade of parasites, except for P. falciparum, all primate Plasmodium species share a common ancestor, although host shifts occurred during the course of primate speciation. Indeed, wild primate populations are potential reservoirs for human malaria parasites and host shifts have occurred in Southeast Asia with, for example, Plasmodium knowlesi, which usually infect macaques, afflicting humans . Recently evidence on the origin of P. vivax as a macaque monkey malaria parasite in Southeast Asia has been proposed [7, 21]. In addition, Plasmodium simium and Plasmodium brasilianum, two species infecting South American platyrrhini primates, are genetically indistinguishable from P. vivax and P. malariae, respectively, and may have been associated with a human-platyrrhini host-switch [8, 21]. Further, haemosporidian parasite isolated from Hipposideros larvatus clusters with a baboon Hepatocystis. This association between bat and primate parasites has been previously proposed based on mitochondrial data, where a Hepatocystis species isolated from a bat (Cynopterus brachyotis, Family Pteropodidae) clusters with this baboon Hepatocystis . Needless to say, this result is not congruent with mammal phylogeny  and suggests a host switch from primates to bats.
In the sauropsid clade, the evolutionary history of Plasmodium that infects birds and lizards is not resolved. The parasite phylogeny clearly does not fit with the host phylogeny. Plasmodium parasites from birds and lizards are known to show little host specificity . Previous conclusions support that infrequent and unpredictable host shifts have occurred in the parasite-host sauropsid system . Surprisingly, the Haemosporidia isolated from Megaderma spasma in Cambodia falls within the sauropsid Plasmodium clade. However, phylogenetic relationships between the parasites of Megaderma and sauropsids are not completely resolved.
Furthermore, closely related haemosporidian parasites isolated from Myotis goudoti and Miniopterus manavi, two endemic Malagasy bat species and the haemosporidian parasite from the Cambodian Kerivoula hardwickii, all of which are placed in the family Vespertilionidae, fall within the sauropsid Plasmodium clade. This result clearly does not fit with vertebrate phylogeny and supports host switching from birds to bats. The haemosporidian vespertilionid parasites from Madagascar and Cambodia are monophyletic, which suggest that the host switching took place in the early evolutionary history of these bats and was followed by subsequent radiation and co-speciation. This is the first report showing host switching in haemosporidian parasites between birds and mammals (bats).
After rodents, bats are the largest order of mammals (at least 1,100 species, more than 20% of extant mammal species). The Chiroptera are very diverse and they are distributed almost worldwide and have extremely diverse life history traits and morphology. Based on recent molecular work, they are classified into four super-families that apparently diversified in different areas during the early Eocene as a "Big Bang" radiation  coincident with the peak of Tertiary insect diversity . In developing echolocation and different flight strategies, the ancestors of modern bats colonized various ecological niches , where birds and their associated blood parasites are thought to have been present, thus favoring host switching from birds to bats. Furthermore, Myotis goudoti and Miniopterus manavi often share common day roost sites in tree hollows, caves and rock shelters , which expose considerable numbers of densely packed individuals to the same potential blood parasite vectors.
The introduction of the 7 new genetic sequences from chiropteran hemoparasites does not alter the deep branching of P. falciparum within the mammalian clade [4, 17]. This result does not support a recent parasite transfer from birds to Homo sapiens, which has been used to explain the pathogenicity of P. falciparum in humans. Rather, the nearly exponential recent growth in human populations may have acted on P. falciparum selection patterns . However, the sequence data from blood parasites isolated from bats provide further insights into the possible evolutionary pathway of human malaria parasites. Those results show that P. falciparum has a different and independent evolutionary history than other human malaria parasites. This is consistent with recent studies providing genetic evidence that the four human parasites did not emerge from the same geographical region . Based on clear evidence presented herein of host switching between birds and bats, it is difficult to reject the hypothesis that P. falciparum has a non-primate origin. It may have emerged in humans associated with an ancient host switching and, as such, it could be one of the oldest "emerging" diseases in humans.
We thank Genevieve Milon and Richard E. L. Paul for support and advices.
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