Literature DB >> 33366892

The complete mitochondrial genome of the meerkat (Suricata suricatta) and its phylogenetic relationship with other feliform species.

Lorena Derežanin1, Jörns Fickel1, Daniel Förster1.   

Abstract

The meerkat, Suricata suricatta, is a highly social member of the mongoose family (Herpestidae) and the only extant species of the genus Suricata. We present the first complete mitochondrial genome of the meerkat, assembled with a seed-and-extend algorithm using three closely related species as references. Phylogenetic analyses using 22 mitochondrial genome sequences confirm the position of meerkat within the Herpestidae family and the Feliformia, a suborder of Carnivora, with high support values. This position is in good agreement with formerly conducted studies based on a small number of mitochondrial and nuclear gene fragments. Our complete mitochondrial genome represents a valuable resource for further phylogenetic studies, especially of the underrepresented members of the Herpestidae family.
© 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  Feliformia; Herpestidae; Mitogenome; Suricata suricatta; phylogenetics

Year:  2020        PMID: 33366892      PMCID: PMC7748773          DOI: 10.1080/23802359.2020.1726221

Source DB:  PubMed          Journal:  Mitochondrial DNA B Resour        ISSN: 2380-2359            Impact factor:   0.658


The meerkat (Suricata suricatta) is a small carnivoran species occurring in southwestern Angola, Namibia, Botswana, and South Africa (Macdonald 2013). It is a member of the mongoose family (Herpestidae) and the only extant species of the genus Suricata. Meerkats are widespread in arid habitats such as shrubland but are absent from true deserts and mountainous areas (Macdonald 2013). They feed mostly on invertebrates and are highly social. Population densities are influenced by rainfall and predation and fluctuate considerably across meerkats’ range (Clutton-Brock et al. 1999). Still, current populations appear stable and the IUCN assessment for the species is ‘least concern’. A tissue sample (muscle) was obtained from a captive male from Poznan Zoo (52°24′03.2″N, 16°59′50.3″E), collected during necropsy conducted at the Leibniz Institute for Zoo and Wildlife Research, Berlin, Germany, where it is permanently stored in the IZW DNA Archive with the sample ID: 303_18. We extracted genomic DNA using the QIAGEN Blood & Cell Culture DNA kit following the manufacturer’s instructions. An Illumina TrueSeq DNA PCR-free library was built with an average insert size of 550 bp and was sequenced (PE 150) on the Illumina HiSeq. We performed adapter clipping and quality trimming of raw reads with TrimGalore v.0.6.4 (https://github.com/FelixKrueger/TrimGalore). The complete circular mitogenome was assembled using NOVOPlasty v.3.7 (Dierckxsens, Mardulyn and Smits, 2017). Three independent runs were performed, each employing a different mitochondrial reference sequence: Herpestes javanicus (GenBank: KY117548.1), Herpestes brachyurus hosei (GenBank: KY117547.1), and Mungotictis decemlineata (GenBank: NC_027828.1). The meerkat assemblies generated using the three different references were identical. We mapped 85,754 properly paired reads to mitogenome with Bowtie2 v.2.3.5.1 (Langmead and Salzberg 2012) and called consensus sequence with a minimum read coverage of 30× and a 100% base call threshold in Geneious v.9.0.5 (Kearse et al. 2012). The resultant circular sequence, 16,914 bp in length (GenBank Accession number: MN854374), was annotated using MITOS (Bernt et al. 2013). The complete mitogenome consists of a control region and a conserved set of 37 genes including 13 protein-coding genes with their expected open reading frames, 22 tRNA and 2 rRNA genes typical of vertebrate mitochondrial genomes. Lengths of protein-coding genes in the meerkat mitogenome were the same as in published mitogenomes of other herpestid species. We performed multiple sequence alignment with 21 representatives of the order Carnivora using MAFFT v.7.407 (Katoh and Standley, 2013), with gray wolf (C. lupus) used as an outgroup. The control region (1508 bp) was excluded from further analysis. The maximum-likelihood tree was constructed using RAxML v.8.2.9 (Stamatakis 2014) applying GTR + G+I as the substitution model, as determined using PartitionFinder v.2.1.1 (Lanfear et al. 2012, 2017). Our phylogenetic analysis supports the placement of the meerkat within the Herpestidae family, forming a sister clade to genus Herpestes with high confidence (100%) based on 1000 bootstrap replicates (Figure 1). This is in concordance with previously published analyses derived from a limited number of mitochondrial and nuclear genes (Patou et al. 2009).
Figure 1.

The phylogenetic relationship of Suricata suricatta with genus Herpestes and other clades within Feliformia inferred from maximum-likelihood analysis based on mitogenome sequences (alignment length = 15,406 bp). Numbers on branches represent bootstrap values. NCBI GenBank accession numbers are given in parentheses.

The phylogenetic relationship of Suricata suricatta with genus Herpestes and other clades within Feliformia inferred from maximum-likelihood analysis based on mitogenome sequences (alignment length = 15,406 bp). Numbers on branches represent bootstrap values. NCBI GenBank accession numbers are given in parentheses.
  9 in total

1.  Partitionfinder: combined selection of partitioning schemes and substitution models for phylogenetic analyses.

Authors:  Robert Lanfear; Brett Calcott; Simon Y W Ho; Stephane Guindon
Journal:  Mol Biol Evol       Date:  2012-01-20       Impact factor: 16.240

2.  PartitionFinder 2: New Methods for Selecting Partitioned Models of Evolution for Molecular and Morphological Phylogenetic Analyses.

Authors:  Robert Lanfear; Paul B Frandsen; April M Wright; Tereza Senfeld; Brett Calcott
Journal:  Mol Biol Evol       Date:  2017-03-01       Impact factor: 16.240

3.  Fast gapped-read alignment with Bowtie 2.

Authors:  Ben Langmead; Steven L Salzberg
Journal:  Nat Methods       Date:  2012-03-04       Impact factor: 28.547

4.  MAFFT multiple sequence alignment software version 7: improvements in performance and usability.

Authors:  Kazutaka Katoh; Daron M Standley
Journal:  Mol Biol Evol       Date:  2013-01-16       Impact factor: 16.240

5.  MITOS: improved de novo metazoan mitochondrial genome annotation.

Authors:  Matthias Bernt; Alexander Donath; Frank Jühling; Fabian Externbrink; Catherine Florentz; Guido Fritzsch; Joern Pütz; Martin Middendorf; Peter F Stadler
Journal:  Mol Phylogenet Evol       Date:  2012-09-07       Impact factor: 4.286

6.  Molecular phylogeny of the Herpestidae (Mammalia, Carnivora) with a special emphasis on the Asian Herpestes.

Authors:  Marie-Lilith Patou; Patricia A McLenachan; Craig G Morley; Arnaud Couloux; Andrew P Jennings; Géraldine Veron
Journal:  Mol Phylogenet Evol       Date:  2009-06-09       Impact factor: 4.286

7.  Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data.

Authors:  Matthew Kearse; Richard Moir; Amy Wilson; Steven Stones-Havas; Matthew Cheung; Shane Sturrock; Simon Buxton; Alex Cooper; Sidney Markowitz; Chris Duran; Tobias Thierer; Bruce Ashton; Peter Meintjes; Alexei Drummond
Journal:  Bioinformatics       Date:  2012-04-27       Impact factor: 6.937

8.  RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies.

Authors:  Alexandros Stamatakis
Journal:  Bioinformatics       Date:  2014-01-21       Impact factor: 6.937

9.  NOVOPlasty: de novo assembly of organelle genomes from whole genome data.

Authors:  Nicolas Dierckxsens; Patrick Mardulyn; Guillaume Smits
Journal:  Nucleic Acids Res       Date:  2017-02-28       Impact factor: 16.971

  9 in total

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