Multiple host-switching of Haemosporidia parasites in bats

  • Linda Duval1, 2Email author,

    Affiliated with

    • Vincent Robert1, 3,

      Affiliated with

      • Gabor Csorba4,

        Affiliated with

        • Alexandre Hassanin1,

          Affiliated with

          • Milijaona Randrianarivelojosia5,

            Affiliated with

            • Joe Walston6,

              Affiliated with

              • Thy Nhim7, 8,

                Affiliated with

                • Steve M Goodman9, 10 and

                  Affiliated with

                  • Frédéric Ariey2

                    Affiliated with

                    Malaria Journal20076:157

                    DOI: 10.1186/1475-2875-6-157

                    Received: 02 November 2007

                    Accepted: 29 November 2007

                    Published: 29 November 2007

                    Abstract

                    Background

                    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.

                    Methods

                    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

                    Results reveal at least three different and independent Haemosporidia evolutionary histories in three different bat lineages from Madagascar and Cambodia.

                    Conclusion

                    Phylogenetic analysis strongly suggests multiple host-switching of Haemosporidia parasites in bats with those from avian and primate hosts.

                    Background

                    Plasmodium falciparum (Apicomplexa, Haemosporidia), the most dangerous of human malaria parasites, is responsible for at least one million deaths a year [1]. 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 [2]. Given the heavy burden of P. falciparum on human populations around the tropics [3], 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 [4]. 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 [5]. Host switching by these parasites could be the trigger for emerging virulent diseases [68].

                    Madagascar and Cambodia are two biodiversity "hot spots" [9]. 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.

                    Methods

                    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.

                    Microscopic examination

                    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 [12]. 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.

                    Phylogenetic analyses

                    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 [13]. 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 [14] and Parsimony analysis (P) was performed using Phylip package (version 3.62) [15]. Nodal robustness was evaluated by non-parametric bootstrap (100 replicates). Bayesian analyses were conducted with MrBayes V3.1 software [16] 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.

                    Results

                    530 blood samples were collected in Madagascar and in Cambodia belonging to seven families of bats. Haemosporidian infections were identified in three families: Hipposideridae, Vespertilionidae and Megadermatidae (Table 1 and Table 2). All the cytochrome b sequences that were isolated from these bats were previously unpublished and the parasite taxa, the host names, the collection localities and the GenBank accession numbers are given in Table 3. The three phylogenetic methods used, Parsimony (P), Maximum Likelihood (ML) and Bayesian analyses produced the same tree topology. The phylogeny is presented in Figure 1.
                    Table 1

                    Prevalence of Haemosporidia infection in bats from Madagascar

                    Species

                    Family

                    n sampled

                    n infected (%)

                    Eidolon dupreanum*

                    Pteropodidae

                    3

                    0

                    Rousettus madagascariensis*

                    Pteropodidae

                    33

                    0

                    Hipposideros commersoni

                    Hipposideridae

                    23

                    0

                    Triaenops furculus*

                    Hipposideridae

                    28

                    1 (4)

                    Triaenops rufus*

                    Hipposideridae

                    41

                    0

                    Emballonura tiavato*

                    Emballonuridae

                    2

                    0

                    Miniopterus gleni

                    Vespertilionidae

                    13

                    3 (23)

                    Myotis goudoti

                    Vespertilionidae

                    68

                    16 (24)

                    Miniopterus manavi*

                    Vespertilionidae

                    129

                    49 (38)

                    Chaerephon sp.*

                    Molossidae

                    1

                    0

                    Mormoproteus jugularis*

                    Molossidae

                    25

                    0

                    Otomops madagascariensis*

                    Molossidae

                    23

                    0

                    Chaerephon leucogaster*

                    Molossidae

                    9

                    0

                    Mops leucostigma

                    Molossidae

                    42

                    0

                    Total

                    440

                    69

                    * endemic species

                    Table 2

                    Prevalence of Haemosporidia infection in bats from Cambodia

                    Species

                    Family

                    n sampled

                    n infected (%)

                    Rhinolophus acuminatus

                    Rhinolophidae

                    3

                    0

                    Rhinolophus borneensis

                    Rhinolophidae

                    3

                    0

                    Rhinolophus malayanus

                    Rhinolophidae

                    1

                    0

                    Rhinolophus shameli

                    Rhinolophidae

                    2

                    0

                    Rhinolophus sp.

                    Rhinolophidae

                    1

                    0

                    Hipposideros armiger

                    Hipposideridae

                    2

                    0

                    Hipposideros larvatus

                    Hipposideridae

                    13

                    1 (8)

                    Hipposideros pomona

                    Hipposideridae

                    1

                    0

                    Megaderma spasma

                    Megadermatidae

                    5

                    4 (80)

                    Taphozous melanopogon

                    Emballonuridae

                    19

                    0

                    Glischropus sp.

                    Vespertilionidae

                    3

                    0

                    Murina cyclotis

                    Vespertilionidae

                    4

                    0

                    Murina tubinaris

                    Vespertilionidae

                    6

                    0

                    Myotis muricola

                    Vespertilionidae

                    1

                    0

                    Kerivoula hardwickii

                    Vespertilionidae

                    10

                    2 (20)

                    Kerivoula papillosa

                    Vespertilionidae

                    4

                    0

                    Tylonycteris robustula

                    Vespertilionidae

                    7

                    0

                    Chaerephon plicatus

                    Molossidae

                    5

                    0

                    Total

                    90

                    7

                    Table 3

                    Parasite taxa used in this study with host name, geographic location and GenBank accession number of the sequences used for the phylogenetic analysis

                    Parasites

                    Host

                    Geographic locality

                    GenBank accession number

                    Plasmodium falciparum

                    Homo sapiens

                    Tropical regions

                    AY069605

                    Plasmodium gonderi

                    Old world monkeys

                    Central Africa

                    AF069622

                    Plasmodium inui

                    Old world monkeys

                    India and southeast Asia

                    AF069617

                    Plasmodium knowlesi

                    Old world monkeys

                    Malaysia

                    AF069621

                    Plasmodium malariae

                    Homo sapiens

                    Tropical and subtropical regions

                    AF069624

                    Plasmodium ovale

                    Homo sapiens

                    Tropics of Africa and Asia

                    AF069625

                    Plasmodium vivax

                    Homo sapiens

                    Tropical and subtropical regions

                    AF069619

                    Hepatocystis sp.

                    Papio sp.

                    Ethiopia

                    AF069626

                    Plasmodium sp.

                    Mandrillus leucophaeus

                    Gabon

                    AF069623

                    Plasmodium atheruri

                    Atherurus africanus

                    Congo and Cameroon

                    AY099054

                    Plasmodium berghei

                    Grammomys surdaster

                    Central Africa

                    AF099049

                    Plasmodium chabaudi

                    Thamnomys rutilans

                    Central Africa

                    AF099050

                    Plasmodium vinckei

                    Grammomys surdaster

                    Congo

                    AY099052

                    Plasmodium elongatum

                    Passer domesticus

                    North America

                    AF069611

                    Plasmodium gallinaceum

                    Gallus gallus

                    Vietnam

                    DQ212189

                    Plasmodium relictum

                    Zeneida macroura

                    North America

                    AY099032

                    Plasmodium sp. 2

                    Ninox scutulata

                    Singapore

                    AY099035

                    Plasmodium sp. 1

                    Acrocephalus arundinaceus

                    Japan

                    AY099044

                    Plasmodium juxtanucleare

                    Gallus gallus

                    Asia

                    AB250415

                    Plasmodium cathemerium

                    Wide range Bird

                    Wallacean zones

                    AY377128

                    Plasmodium sp. 47

                    Agelaius phoeniceus

                    North America

                    AF465547

                    Plasmodium sp. 49

                    Zonotrichia leucophrys

                    North America

                    AF465549

                    Plasmodium sp. 50

                    Andropadus latirostris

                    Cameroon

                    AF465550

                    Plasmodium floridense

                    Anolis oculatus

                    Dominica

                    AY099059

                    Plasmodium mexicanum

                    Sceloporus occidentalis

                    California

                    AY099060

                    Plasmodium chiricahuae

                    Sceloporus jarrovi

                    Arizona

                    AY099061

                    Haemosporidia (FMNH 172853)

                    Miniopterus manavi

                    Madagascar

                    AY762070*

                    Haemosporidia (FMNH 172862)

                    Miniopterus manavi

                    Madagascar

                    AY762071*

                    Haemosporidia (FMNH 172918)

                    Miniopterus manavi

                    Madagascar

                    AY762074*

                    Haemosporidia (FMNH 175810)

                    Myotis goudoti

                    Madagascar

                    AY762075*

                    Haemosporidia (C285)

                    Kerivoula hardwickii

                    Cambodia

                    EF179354*

                    Haemosporidia (C289)

                    Megaderma spasma

                    Cambodia

                    EF179355*

                    Haemosporidia (C272)

                    Hipposideros larvatus

                    Cambodia

                    EF179356*

                    Haemoproteus majoris

                    Parus caeruleus

                    Sweden

                    AY099045

                    Haemoproteus sylvae

                    Acrocephalus arundinaceus

                    Sweden

                    AY099040

                    Haemoproteus sp. 1

                    Phylloscopus occipitalis

                    India

                    AY099043

                    Haemoproteus sp. 2

                    Phylloscopus occipitalis

                    India

                    AY099043

                    Haemoproteus sp. 3

                    Acrocephalus scirpaceus

                    Spain

                    AY099046

                    Leucocytozoon toddi

                    Accipiter francesii

                    Madagascar

                    AY684973

                    Toxoplasma gondii

                      

                    AF023246

                    Theileria annulata

                      

                    M63015

                    Babesia gibsoni

                      

                    AB215096

                    FMNH: Field Museum of Natural History

                    C: Cambodia

                    * Previously unpublished sequences

                    http://static-content.springer.com/image/art%3A10.1186%2F1475-2875-6-157/MediaObjects/12936_2007_Article_462_Fig1_HTML.jpg
                    Figure 1

                    Phylogeny of Haemosporidia inferred from cytochrome b amino acid sequences. Value above branches are Bayesian posterior probabilities [16] (value less then 0.5 not shown), below are bootstrap percentage obtained by maximum likelihood [14] (left of the slash, values under 50% not shown). In red are the previously unpublished bat sequences. See Tables 1 and 2 for sampling details. H. = Haemoproteus, L. = Leucocytozoon and P. = Plasmodium.

                    The results show the existence of two clades within Haemosporidia, separating mammal and sauropsid hosts (birds and lizards) (1.00 Bayesian posterior probabilities, 99 and 100 for ML and P respectively bootstrap support). In the first clade, the four malaria parasites afflicting humans, Plasmodium malariae, Plasmodium ovale Plasmodium vivax and P. falciparum form a polyphyletic group [17]. Rodent Plasmodium are the sister group and P. falciparum still exhibits a deep branch. Interestingly, parasite isolated from the bat Hipposideros larvatus (Family Hipposideridae) (Figures 2 and 3) clusters with a Hepatocystis parasite obtained from a baboon (Papio s p.) and falls within the Plasmodium primate group (Bayesian posterior probabilities of 1.00 and bootstrap support of 99 and 96 for ML and P, respectively).
                    http://static-content.springer.com/image/art%3A10.1186%2F1475-2875-6-157/MediaObjects/12936_2007_Article_462_Fig2_HTML.jpg
                    Figure 2

                    Haemosporidian parasite isolated from Hipposideros larvatus (C 272).

                    http://static-content.springer.com/image/art%3A10.1186%2F1475-2875-6-157/MediaObjects/12936_2007_Article_462_Fig3_HTML.jpg
                    Figure 3

                    Haemosporidian parasite isolated from Hipposideros larvatus (C 272).

                    In the second clade, between two clades of Plasmodium, are Leucocytozoon and Haemoproteus, two genera infecting only sauropsid hosts, and are close sister taxa of bird and lizard Plasmodium [18]. This renders the genus Plasmodium polyphyletic. Unexpectedly, the haemosporidian parasite isolated from the bat Megaderma spasma (Family Megadermatidae) (Figure 4) is included within the sauropsid Plasmodium clade. However, the bootstrap value is low (Bayesian posterior probabilities of 0.62). Remarkably, haemosporidian parasites isolated from the Malagasy endemic bats Myotis goudoti and Miniopterus manavi and the parasite isolated from the widespread Asiatic bat Kerivoula hardwickii (Figure 5) form a monophyletic cluster and fall within the sauropsid Plasmodium clade. All these bats are classically placed in the Family Vespertilionidae. This result is well support with 0.75 Bayesian posterior probabilities and 75 ML bootstrap.
                    http://static-content.springer.com/image/art%3A10.1186%2F1475-2875-6-157/MediaObjects/12936_2007_Article_462_Fig4_HTML.jpg
                    Figure 4

                    Haemosporidian parasites isolated from Megaderma spasma (C 289).

                    http://static-content.springer.com/image/art%3A10.1186%2F1475-2875-6-157/MediaObjects/12936_2007_Article_462_Fig5_HTML.jpg
                    Figure 5

                    Haemosporidian parasite isolated from Kerivoula hardwickii (C 285).

                    Discussion

                    The mitochondrial genome is more conserved in apicomplexan parasites [19] 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 [18].

                    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 [8] and host shifts have occurred in Southeast Asia with, for example, Plasmodium knowlesi, which usually infect macaques, afflicting humans [20]. 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 [4]. Needless to say, this result is not congruent with mammal phylogeny [22] 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 [23]. Previous conclusions support that infrequent and unpredictable host shifts have occurred in the parasite-host sauropsid system [24]. 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 [25] coincident with the peak of Tertiary insect diversity [26]. In developing echolocation and different flight strategies, the ancestors of modern bats colonized various ecological niches [27], 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 [28], which expose considerable numbers of densely packed individuals to the same potential blood parasite vectors.

                    Conclusion

                    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 [29]. 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 [30]. 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.

                    Declarations

                    Acknowledgements

                    We thank Genevieve Milon and Richard E. L. Paul for support and advices.

                    Authors’ Affiliations

                    (1)
                    Muséum National d'Histoire Naturelle, USM 504 et UMR 5202
                    (2)
                    Unité Epidémiologie moléculaire, Institut Pasteur du Cambodge
                    (3)
                    Institut de Recherche pour le Développement
                    (4)
                    Department of Zoology, Hungarian Natural History Museum
                    (5)
                    Unité Paludisme, Institut Pasteur de Madagascar
                    (6)
                    Cambodia Program, Wildlife Conservation Society
                    (7)
                    Department of Forestry and Wildlife, Phnom Tamao Zoo and Wildlife Rescue Center
                    (8)
                    Care for Confiscated Wild Life, WildAid
                    (9)
                    Field Museum of Natural History
                    (10)
                    WWF

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                    © Duval et al. 2007

                    This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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