Multiple radiations of spiny mice (Rodentia: Acomys) in dry open habitats of Afro-Arabia: evidence from a multi-locus phylogeny.


Journal

BMC evolutionary biology
ISSN: 1471-2148
Titre abrégé: BMC Evol Biol
Pays: England
ID NLM: 100966975

Informations de publication

Date de publication:
04 03 2019
Historique:
received: 16 05 2018
accepted: 01 02 2019
entrez: 6 3 2019
pubmed: 6 3 2019
medline: 10 7 2019
Statut: epublish

Résumé

Spiny mice of the genus Acomys are distributed mainly in dry open habitats in Africa and the Middle East, and they are widely used as model taxa for various biological disciplines (e.g. ecology, physiology and evolutionary biology). Despite their importance, large distribution and abundance in local communities, the phylogeny and the species limits in the genus are poorly resolved, and this is especially true for sub-Saharan taxa. The main aims of this study are (1) to reconstruct phylogenetic relationships of Acomys based on the largest available multilocus dataset (700 genotyped individuals from 282 localities), (2) to identify the main biogeographical divides in the distribution of Acomys diversity in dry open habitats in Afro-Arabia, (3) to reconstruct the historical biogeography of the genus, and finally (4) to estimate the species richness of the genus by application of the phylogenetic species concept. The multilocus phylogeny based on four genetic markers shows presence of five major groups of Acomys called here subspinosus, spinosissimus, russatus, wilsoni and cahirinus groups. Three of these major groups (spinosissimus, wilsoni and cahirinus) are further sub-structured to phylogenetic lineages with predominantly parapatric distributions. Combination of alternative species delimitation methods suggests the existence of 26 molecular operational taxonomic units (MOTUs), potentially corresponding to separate species. The highest genetic diversity was found in Eastern Africa. The origin of the genus Acomys is dated to late Miocene (ca. 8.7 Ma), when the first split occurred between spiny mice of eastern (Somali-Masai) and south-eastern (Zambezian) savannas. Further diversification, mostly in Plio-Pleistocene, and the current distribution of Acomys were influenced by the interplay of global climatic factors (e.g., Messinian salinity crisis, intensification of Northern Hemisphere glaciation) with local geomorphology (mountain chains, aridity belts, water bodies). Combination of divergence dating, species distribution modelling and historical biogeography analysis suggests repeated "out-of-East-Africa" dispersal events into western Africa, the Mediterranean region and Arabia. The genus Acomys is very suitable model for historical phylogeographic and biogeographic reconstructions of dry non-forested environments in Afro-Arabia. We provide the most thorough phylogenetic reconstruction of the genus and identify major factors that influenced its evolutionary history since the late Miocene. We also highlight the urgent need of integrative taxonomic revision of east African taxa.

Sections du résumé

BACKGROUND
Spiny mice of the genus Acomys are distributed mainly in dry open habitats in Africa and the Middle East, and they are widely used as model taxa for various biological disciplines (e.g. ecology, physiology and evolutionary biology). Despite their importance, large distribution and abundance in local communities, the phylogeny and the species limits in the genus are poorly resolved, and this is especially true for sub-Saharan taxa. The main aims of this study are (1) to reconstruct phylogenetic relationships of Acomys based on the largest available multilocus dataset (700 genotyped individuals from 282 localities), (2) to identify the main biogeographical divides in the distribution of Acomys diversity in dry open habitats in Afro-Arabia, (3) to reconstruct the historical biogeography of the genus, and finally (4) to estimate the species richness of the genus by application of the phylogenetic species concept.
RESULTS
The multilocus phylogeny based on four genetic markers shows presence of five major groups of Acomys called here subspinosus, spinosissimus, russatus, wilsoni and cahirinus groups. Three of these major groups (spinosissimus, wilsoni and cahirinus) are further sub-structured to phylogenetic lineages with predominantly parapatric distributions. Combination of alternative species delimitation methods suggests the existence of 26 molecular operational taxonomic units (MOTUs), potentially corresponding to separate species. The highest genetic diversity was found in Eastern Africa. The origin of the genus Acomys is dated to late Miocene (ca. 8.7 Ma), when the first split occurred between spiny mice of eastern (Somali-Masai) and south-eastern (Zambezian) savannas. Further diversification, mostly in Plio-Pleistocene, and the current distribution of Acomys were influenced by the interplay of global climatic factors (e.g., Messinian salinity crisis, intensification of Northern Hemisphere glaciation) with local geomorphology (mountain chains, aridity belts, water bodies). Combination of divergence dating, species distribution modelling and historical biogeography analysis suggests repeated "out-of-East-Africa" dispersal events into western Africa, the Mediterranean region and Arabia.
CONCLUSIONS
The genus Acomys is very suitable model for historical phylogeographic and biogeographic reconstructions of dry non-forested environments in Afro-Arabia. We provide the most thorough phylogenetic reconstruction of the genus and identify major factors that influenced its evolutionary history since the late Miocene. We also highlight the urgent need of integrative taxonomic revision of east African taxa.

Identifiants

pubmed: 30832573
doi: 10.1186/s12862-019-1380-9
pii: 10.1186/s12862-019-1380-9
pmc: PMC6399835
doi:

Substances chimiques

DNA, Mitochondrial 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

69

Références

Syst Biol. 2014 Nov;63(6):951-70
pubmed: 25123369
Mol Phylogenet Evol. 2018 Jan;118:64-74
pubmed: 28919506
Nature. 2000 Jan 13;403(6766):188-92
pubmed: 10646602
Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3433-6
pubmed: 8475093
Mol Ecol. 2015 Oct;24(20):5248-66
pubmed: 26340076
Science. 2006 Mar 24;311(5768):1751-3
pubmed: 16556838
Genet Mol Res. 2006 Jul 31;5(3):466-74
pubmed: 17117361
Syst Biol. 2003 Oct;52(5):665-73
pubmed: 14530133
Mol Ecol Resour. 2011 Jan;11(1):154-7
pubmed: 21429114
Proc Natl Acad Sci U S A. 2017 Feb 14;114(7):1607-1612
pubmed: 28137871
Mol Ecol. 2012 Apr;21(8):1864-77
pubmed: 21883587
Bioinformatics. 2017 Jun 1;33(11):1630-1638
pubmed: 28108445
Mol Ecol. 2010 Nov;19(21):4783-99
pubmed: 20958815
Biol Rev Camb Philos Soc. 2014 Feb;89(1):215-31
pubmed: 23848599
Curr Biol. 2016 Sep 26;26(18):2543-2549
pubmed: 27618261
J Am Assoc Lab Anim Sci. 2016 Jan;55(1):9-17
pubmed: 26817973
J Math Biol. 2017 Jan;74(1-2):447-467
pubmed: 27287395
Mol Ecol. 2013 Sep;22(17):4369-83
pubmed: 23855767
PLoS One. 2013 Nov 01;8(11):e77815
pubmed: 24223730
Proc Natl Acad Sci U S A. 2014 Jan 21;111(3):1043-8
pubmed: 24402169
Bioinformatics. 2014 May 1;30(9):1312-3
pubmed: 24451623
PLoS Biol. 2006 May;4(5):e88
pubmed: 16683862
PLoS One. 2017 Aug 15;12(8):e0181026
pubmed: 28809924
J Comp Physiol B. 2005 Apr;175(3):193-200
pubmed: 15742195
J Hum Evol. 2007 Nov;53(5):487-503
pubmed: 17935755
BMC Evol Biol. 2008 Jan 29;8:32
pubmed: 18230151
Nature. 2004 May 20;429(6989):263-7
pubmed: 15152244
Mitochondrial DNA A DNA Mapp Seq Anal. 2016;27(1):397-400
pubmed: 24660908
Science. 2013 Jan 4;339(6115):74-8
pubmed: 23258408
PLoS Comput Biol. 2014 Apr 10;10(4):e1003537
pubmed: 24722319
Bioinformatics. 2015 Apr 1;31(7):991-8
pubmed: 25422051
Mol Ecol. 2012 Aug;21(15):3656-70
pubmed: 22702960
BMC Biol. 2008 Dec 16;6:54
pubmed: 19087283
Dokl Biol Sci. 2011 Sep-Oct;440:335-9
pubmed: 22134826
Mol Phylogenet Evol. 1992 Jun;1(2):148-60
pubmed: 1342928
Am J Phys Anthropol. 2010 May;142(1):125-36
pubmed: 19918986
J Therm Biol. 2001 Apr;26(2):139-142
pubmed: 11163930
Bioinformatics. 2012 Jun 15;28(12):1647-9
pubmed: 22543367
J Mammal. 2006 Aug 1;87(4):643-662
pubmed: 19890476
Syst Biol. 2012 May;61(3):539-42
pubmed: 22357727
Syst Biol. 2004 Feb;53(1):47-67
pubmed: 14965900
Syst Biol. 2008 Feb;57(1):4-14
pubmed: 18253896
Comp Cytogenet. 2011 Dec 22;5(5):423-31
pubmed: 24260646
Behav Processes. 1999 Aug;47(1):1-10
pubmed: 24896688
BMC Bioinformatics. 2011 Jan 03;12:1
pubmed: 21199577
Mol Phylogenet Evol. 2001 Jan;18(1):37-46
pubmed: 11161740
Bioinformatics. 2013 Nov 15;29(22):2869-76
pubmed: 23990417
Nature. 2012 Sep 27;489(7417):561-5
pubmed: 23018966
Bioinformatics. 2010 May 15;26(10):1372-3
pubmed: 20228129
Mol Phylogenet Evol. 1998 Jun;9(3):560-6
pubmed: 9668005
J Theor Biol. 2008 Aug 21;253(4):769-78
pubmed: 18538793
Proc Natl Acad Sci U S A. 2003 Jul 8;100(14):8325-30
pubmed: 12821774
Mol Phylogenet Evol. 1998 Aug;10(1):104-17
pubmed: 9751921
BMC Evol Biol. 2014 Dec 14;14:256
pubmed: 25496476
PLoS One. 2017 Aug 16;12(8):e0183070
pubmed: 28813483
Mol Phylogenet Evol. 2018 Nov;128:98-111
pubmed: 30030180
Mol Phylogenet Evol. 2018 Jan;118:75-87
pubmed: 28963084
Mol Biol Evol. 2012 Jun;29(6):1695-701
pubmed: 22319168
Syst Biol. 2008 Feb;57(1):76-85
pubmed: 18275003
J Hum Evol. 2007 Nov;53(5):443-64
pubmed: 17915289
Philos Trans R Soc Lond B Biol Sci. 1998 Jan 29;353(1365):159-70; discussion 170-1
pubmed: 9507562
Heredity (Edinb). 2001 Apr;86(Pt 4):420-30
pubmed: 11520342
BMC Evol Biol. 2015 Apr 23;15:71
pubmed: 25900417
BMC Biol. 2007 Dec 21;5:57
pubmed: 18154651
Nucleic Acids Res. 2004 Mar 19;32(5):1792-7
pubmed: 15034147
Trends Ecol Evol. 2004 Dec;19(12):639-44
pubmed: 16701326

Auteurs

T Aghová (T)

Institute of Vertebrate Biology of the Czech Academy of Sciences, 603 65, Brno, Czech Republic. tatiana.aghova@gmail.com.
Department of Zoology, National Museum, 115 79, Prague, Czech Republic. tatiana.aghova@gmail.com.

K Palupčíková (K)

Department of Zoology, Faculty of Science, Charles University, 128 44, Prague, Czech Republic.

R Šumbera (R)

Department of Zoology, Faculty of Science, University of South Bohemia, 370 05, České Budějovice, Czech Republic.

D Frynta (D)

Department of Zoology, Faculty of Science, Charles University, 128 44, Prague, Czech Republic.

L A Lavrenchenko (LA)

A. N. Severtsov Institute of Ecology and Evolution RAS, 119071, Moscow, Russia.

Y Meheretu (Y)

Department of Biology and Institute of Mountain Research and Development, Mekelle University, P.O. Box 3102, Mekelle, Tigray, Ethiopia.

J Sádlová (J)

Department of Parasitology, Faculty of Science, Charles University, 128 44, Prague, Czech Republic.

J Votýpka (J)

Department of Parasitology, Faculty of Science, Charles University, 128 44, Prague, Czech Republic.
Institute of Parasitology, Biology Centre of the Czech Academy of Sciences, 370 05, České Budějovice, Czech Republic.

J S Mbau (JS)

Department of Land Resource Management and Agricultural Technology, College of Agriculture and Veterinary Sciences, University of Nairobi, Nairobi, Kenya.

D Modrý (D)

Institute of Parasitology, Biology Centre of the Czech Academy of Sciences, 370 05, České Budějovice, Czech Republic.
Department of Pathology and Parasitology, Faculty of Veterinary Medicine, University of Veterinary and Pharmaceutical Sciences, 612 42, Brno, Czech Republic.

J Bryja (J)

Institute of Vertebrate Biology of the Czech Academy of Sciences, 603 65, Brno, Czech Republic.
Department of Botany and Zoology, Faculty of Science, Masaryk University, 602 00, Brno, Czech Republic.

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