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Mitogenome Announcement

The complete mitochondrial genome of Tachysurus virgatus (Oshima 1926) (Siluriformes: Bagridae) and its phylogenetic status

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Pages 3019-3020 | Received 23 Jun 2020, Accepted 11 Jul 2020, Published online: 28 Jul 2020

Abstract

Tachysurus virgatus (Oshima 1926) is a small and benthic Bagridae species that resides in the Southern China and Viet Nam. Currently, limited published genetic information has hindered our understanding of this species. In the current study, the complete mitochondrial genome of T. virgatus was determined using next generation sequencing, which was 16,524 base pairs (bp) in length and identical to most genomes of bony fishes. Phylogenetic analyses supported four clades (I, II, III, and IV) occurring in the family Bagridae and T. virgatus formed an independent clade that was sister to the clades I and II.

Tachysurus virgatus (Oshima 1926), a catfish species within the family Bagridae, is a small and benthic species that mainly resides in the Southern China and Viet Nam (Chu et al. Citation1999; www.fishbase.org). This species seems to be likely neglected due to its low economic value. To date, thus, rare genetic analyses have been conducted for this species, which limits our understanding of this species, particularly in genetic aspects. In this study, we determine the whole mitochondrial genome of T. virgatus for the first time using next generation sequencing technology.

The sample of T. virgatus was captured during December in 2019 at Zhaoqing (23.041N, 112.467E) city, Guangdong Province, China, which locates in the middle and lower Xijiang River. The specimen (voucher number: TWW2019001) was stored in the fish collection of Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences. A bit of muscle tissues were preserved in anhydrous ethanol for DNA extraction. Total genomic DNA was extracted from muscle tissues using a Genomic DNA Isolation Kit (QiaGene, Hilden, Germany). The Illumina MiSeq platform was used to sequence the complete mitochondrial genome (Illumina Inc, San Diego, CA). We assembled the raw sequence reads into contigs using SPAdes 3.9.0 (Bankevich et al. Citation2012). Lastly, the complete mitochondrial genome was produced with the contigs using SOAPdenovo (Luo et al. Citation2012).

The complete mitogenome sequence of T. virgatus (GenBank no.: MT647840) is 16,524 base pairs (bp) in length and includes 13 protein-coding genes, two rRNA genes, 22 tRNA genes, and a control region. The structural organization and gene order were identical to other typical teleosts. The complete mitogenome of T. virgatus and 29 additional mitogenomes including 27 Bagridae species and two outgroups belonging to the family Siluridae were aligned using MUSCLE (Edgar Citation2004). Valid names of each species were proofread using Fishbase (www.fishbase.org). All 13 protein-coding genes were chosen by eye to combine into a single sequence for phylogenetic analyses. Bayesian inference was used for phylogenetic analyses using the optimal nucleotide substitution model (GTR + I+G), which inferred from MRMODELTEST version 2.3 (Nylander Citation2004). The BI analyses were performed in MrBayes 3.1.2 (Ronquist and Huelsenbeck Citation2003). The analyses of 20 million generations were run and sampled every 1000 generations, with the first 25% discarded as burn-in. Furthermore, neighbor-joining tree based on Kimura’s two-parameter (Kimura Citation1980) was implemented in MEGA 6.0 (Tamura et al. Citation2013) using 1000 bootstrap replicates to assess the branch support.

Both Bayesian tree and neighbor-joining tree yielded four well supported major clades with high supported values (clades I, II, III, and IV; ). Both clades I and II consisted of species from genera Pelteobagrus and Tachysurus, implying taxonomic problems occurring in these two genera. Tachysurus virgatus formed an independent clade (clade III) and was sister to the clades I and II (). From the above, we suggest that more work on morphological traits and phylogenetic inferences should be combined together to better understand the relationships among Bagridae species.

Figure 1. Phylogenetic tree based on Bayesian inference showing the relationships among 28 Bagridae species based on 13 protein-coding genes. Values on branches indicate Bayesian posterior probabilities and bootstrap values from a neighbor-joining analyses.

Figure 1. Phylogenetic tree based on Bayesian inference showing the relationships among 28 Bagridae species based on 13 protein-coding genes. Values on branches indicate Bayesian posterior probabilities and bootstrap values from a neighbor-joining analyses.

Ethical approval

Experiments were performed in accordance with the recommendations of the Ethics Committee of Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences. These policies were enacted according to the Chinese Association for the Laboratory Animal Sciences and the Institutional Animal Care and Use Committee (IACUC) protocols.

Data accessibility statement

The data that support the findings of this study are openly available in GenBank of NCBI at http://www.ncbi.nlm.nih.gov, reference number MT647840.

Disclosure statement

All authors declare that they have no conflict of interest.

Additional information

Funding

This work was supported by National Key R&D Program of China [2018YFD0900902] and Project of Innovation Team of Survey and Assessment of the Pearl River Fishery Resources [2020TD-10 and 2020ZJTD-04].

References

  • Bankevich A, Nurk S, Antipov D, Gurevich AA, Dvorkin M, Kulikov AS, Lesin VM, Nikolenko SI, Pham S, Prjibelski AD, et al. 2012. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol. 19(5):455–477.
  • Chu X, Zheng B, Dai D. 1999. Fauna Sinica, Class Teleostei, Siluriformes. Beijing: Scientific Press.
  • Edgar RC. 2004. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 32(5):1792–1797.
  • Kimura M. 1980. A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J Mol Evol. 16(2):111–120.
  • Luo R, Liu B, Xie Y, Li Z, Huang W, Yuan J, He G, Chen Y, Pan Q, Liu Y, et al. 2012. SOAPdenovo2: an empirically improved memory-efficient short-read de novo assembler. Gigascience. 1(1):18.
  • Nylander J. 2004. MrModeltest v2. Program distributed by the author. Evolutionary Biology Centre, Uppsala University.
  • Ronquist F, Huelsenbeck JP. 2003. MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 19(12):1572–1574.
  • Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. 2013. MEGA6: molecular evolutionary genetics analysis version 6.0. Mol Biol Evol. 30(12):2725–2729.