Phylogeny of haemosporidian blood parasites revealed by a multi-gene approach

被引:81
作者
Borner, Janus [1 ]
Pick, Christian [1 ]
Thiede, Jenny [1 ]
Kolawole, Olatunji Matthew [2 ]
Kingsley, Manchang Tanyi [3 ]
Schulze, Jana [1 ]
Cottontail, Veronika M. [4 ]
Wellinghausen, Nele [5 ]
Schmidt-Chanasit, Jonas [6 ]
Bruchhaus, Iris [6 ]
Burmester, Thorsten [1 ]
机构
[1] Univ Hamburg, Inst Zool, D-20146 Hamburg, Germany
[2] Univ Ilorin, Fac Life Sci, Dept Microbiol, Ilorin, Kwara State, Nigeria
[3] Wakwa Reg Ctr, Vet Res Lab, Inst Agr Res Dev, Ngaoundere, Cameroon
[4] Univ Ulm, Inst Expt Ecol, D-89069 Ulm, Germany
[5] Gaertner & Colleagues Lab, D-88212 Ravensburg, Germany
[6] Bernhard Nocht Inst Trop Med, D-20359 Hamburg, Germany
关键词
Alveolata; Apicomplexa; Haemosporida; Malaria; Parasitology; MALARIA PARASITES; CYTOCHROME-B; GENOME SEQUENCE; PLASMODIUM; EVOLUTION; GENERA; BIRDS; POLYCHROMOPHILUS; DIVERSITY; SELECTION;
D O I
10.1016/j.ympev.2015.09.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The apicomplexan order Haemosporida is a clade of unicellular blood parasites that infect a variety of reptilian, avian and mammalian hosts. Among them are the agents of human malaria, parasites of the genus Plasmodium, which pose a major threat to human health. Illuminating the evolutionary history of Haemosporida may help us in understanding their enormous biological diversity, as well as tracing the multiple host switches and associated acquisitions of novel life-history traits. However, the deep-level phylogenetic relationships among major haemosporidian clades have remained enigmatic because the datasets employed in phylogenetic analyses were severely limited in either gene coverage or taxon sampling. Using a PCR-based approach that employs a novel set of primers, we sequenced fragments of 21 nuclear genes from seven haemosporidian parasites of the genera Leucocytozoon, Haemoproteus, Parahaemoproteus, Polychromophilus and Plasmodium. After addition of genomic data from 25 apicomplexan species, the unreduced alignment comprised 20,580 bp from 32 species. Phylogenetic analyses were performed based on nucleotide, codon and amino acid data employing Bayesian inference, maximum likelihood and maximum parsimony. All analyses resulted in highly congruent topologies. We found consistent support for a basal position of Leucogtozoon within Haemosporida. In contrast to all previous studies, we recovered a sister group relationship between the genera Polychromophilus and Plasmodium. Within Plasmodium, the sauropsid and mammal-infecting lineages were recovered as sister clades. Support for these relationships was high in nearly all trees, revealing a novel phylogeny of Haemosporida, which is robust to the choice of the outgroup and the method of tree inference. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:221 / 231
页数:11
相关论文
共 55 条
  • [11] Plasmodium knowlesi malaria in humans is widely distributed and potentially life threatening
    Cox-Singh, Janet
    Davis, Timothy M. E.
    Lee, Kim-Sung
    Shamsul, Sunita S. G.
    Matusop, Asmad
    Ratnam, Shanmuga
    Rahman, Hasan A.
    Conway, David J.
    Singh, Balbir
    [J]. CLINICAL INFECTIOUS DISEASES, 2008, 46 (02) : 165 - 171
  • [12] Saturation and base composition bias explain phylogenomic conflict in Plasmodium
    Davalos, Liliana A.
    Perkins, Susan L.
    [J]. GENOMICS, 2008, 91 (05) : 433 - 442
  • [13] Bayesian Phylogenetics with BEAUti and the BEAST 1.7
    Drummond, Alexei J.
    Suchard, Marc A.
    Xie, Dong
    Rambaut, Andrew
    [J]. MOLECULAR BIOLOGY AND EVOLUTION, 2012, 29 (08) : 1969 - 1973
  • [14] Multiple host-switching of Haemosporidia parasites in bats
    Duval, Linda
    Robert, Vincent
    Csorba, Gabor
    Hassanin, Alexandre
    Randrianarivelojosia, Milijaona
    Walston, Joe
    Nhim, Thy
    Goodman, Steve M.
    Ariey, Frederic
    [J]. MALARIA JOURNAL, 2007, 6 (1)
  • [15] ESCALANTE AA, 1995, MOL BIOL EVOL, V12, P616
  • [16] The evolution of primate malaria parasites based on the gene encoding cytochrome b from the linear mitochondrial genome
    Escalante, AA
    Freeland, DE
    Collins, WE
    Lal, AA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (14) : 8124 - 8129
  • [17] Felsenstein J., 2004, Phylip (phylogeny inference package) version 3.6
  • [18] Genome sequence of the human malaria parasite Plasmodium falciparum
    Gardner, MJ
    Hall, N
    Fung, E
    White, O
    Berriman, M
    Hyman, RW
    Carlton, JM
    Pain, A
    Nelson, KE
    Bowman, S
    Paulsen, IT
    James, K
    Eisen, JA
    Rutherford, K
    Salzberg, SL
    Craig, A
    Kyes, S
    Chan, MS
    Nene, V
    Shallom, SJ
    Suh, B
    Peterson, J
    Angiuoli, S
    Pertea, M
    Allen, J
    Selengut, J
    Haft, D
    Mather, MW
    Vaidya, AB
    Martin, DMA
    Fairlamb, AH
    Fraunholz, MJ
    Roos, DS
    Ralph, SA
    McFadden, GI
    Cummings, LM
    Subramanian, GM
    Mungall, C
    Venter, JC
    Carucci, DJ
    Hoffman, SL
    Newbold, C
    Davis, RW
    Fraser, CM
    Barrell, B
    [J]. NATURE, 2002, 419 (6906) : 498 - 511
  • [19] GARNHAM P. C. C., 1964, ANN SOC BELG MED TROP, V44, P267
  • [20] Garnham PCC, 1966, MALARIA PARASITES OT