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. 2017 Jun 1;2(1):341–343. doi: 10.1080/23802359.2017.1334519

Complete mitochondrial genome of the Chihuil sea catfish Bagre panamensis (Siluriformes: Ariidae)

Jorge S Ramírez-Pérez a, Nancy C Saavedra-Sotelo b,, Raúl Llera-Herrera c, Quetzalli Yasu Abadía-Chanona a
PMCID: PMC7800565  PMID: 33473821

Abstract

The chihuil sea catfish (Bagre panamensis) is endemic of the Eastern Pacific and is a species of fishery importance in the Mexican Pacific. The complete mitochondrial genome of Bagre panamensis has been assembled from Illumina sequencing data. The circular genome was 16,714 bp in lengh, and consist of 13 protein-coding, two ribosomal RNAs (rRNAs), and 22 transfer RNA (tRNA) genes. Base composition is 30.8% A, 26.6% T, 28.2% C, and 14.4% G, and 42.6% GC content. Protein-coding genes present two start codon (ATG and GTG) and eight stop codon (TAA, TCT, CCT, TTA, CAT, AAT, ATT, and TAG). The control region possesses the highest A + T (64.4%) and lowest G + C content (35.6%) among all mitochondrial regions. These data would contribute to the evolutionary studies of related taxa.

Keywords: Sea catfish, Bagre panamensis, mitogenome, Illumina


The Ariidae familie (Order: Siluriformes) is widely distributed in world tropical shelves, includes 150–200 species approx. of which one third is endemic to American coasts (Betancur-R et al. 2007; Marceniuk & Menezes 2007). The Ariidae familie present a monophyletic ancestry, well-supported by morphological and molecular traits (Diogo 2004; Kailola 2004; Sullivan et al. 2006; Betancur-R et al. 2007); however, the systematics of its species is complex and there are many problems on its nomenclatural (Marceniuk & Menezes 2007). The ariids are predominantly marine species of which the chihuil catfish (Bagre panamensis) is endemic of the Eastern Pacific, it is distributed from southern California to northern Peru including Gulf of California and Galapagos Islands (Cooke 1992; Allen & Robertson 1994). Bagre panamensis is a demersal fish that habitat in muddy bottoms near to shore (177 m depth approx.), estuaries and mangroves (Cooke 1992).

In this study, we determined the complete mitochondrial genome of B. panamensis for first time. One specimen was collected from artisanal fishery Sinaloa, Mexico (23°28′32.5″N - 106°37′28.2″W). DNA was extracted from fresh muscle tissue using the Wizard® Genomic DNA Purification kit (Promega, Madison, WI). A genomic DNA library was constructed with the Kapa DNA library preparation kit (Kapa Biosystems, Wilmington, MA) using multiplex index, and the library was then sequenced alongside other barcoded libraries using a single lane (2 × 125 paired-end reads) in a MiSeq platform (Illumina, San Diego, CA). Reads were pre-processed using Trimmomatic v0.33 (Bolger et al. 2014) for trim low-quality ends (Q score <20), residual adapters and remove reads shorter than 100 bases. The obtained sequences were demultiplexed, and the recovered reads were analysed for quality control with FastQC v0.10.1 (Babraham Institute, Cambridge, UK) (Andrews 2011). 21′391,977 pair of high-quality reads (Q score >25) were recovered. The complete mitochondrion genome was obtained using MITObim v1.7 (Hahn et al. 2013), using the giant catfish mitogenome Netuma thalassina (GenBank accession number: KU986659.1) as a reference. The final assembly was annotated using MitoAnnotator pipeline (Iwasaki et al. 2013).

The mitogenome of B. panamensis (GenBank accession number KY930718) has a length of 16,673 bp with a base composition of A 38.8%, T 26.6%, C 28.2%, and G 14.4% (42.6% of GC content). The mitogenome contains all typical genes of vertebrate: 13 protein-coding genes, 22 transference RNA genes, two ribosomal RNAs, and one control region or d-loop (Figure 1). Almost all protein-coding genes initiated by typical ATG codon, except for the COX1 gene initiated by the GTC. For the stop codon, almost all genes presented TAA or CCT, the rest used a different one (Table 1). The control region (D-loop) is 1080 bp in length which was located between the tRNA-Pro and tRNA-Phe; it had the highest A + T content of 64.4% and lowest G + C content (35%) among all mitochondrial regions.

Figure 1.

Figure 1.

Maximum-likelihood (ML) phylogenetic tree of Bagre panamensis and the other 11 species of 8 families using Clarias fuscus and Heteropneustes fossilis as an outgroup. Number above each node indicates the ML bootstrap support values. In parenthesis the access numbers from NCBI database.

Table 1.

Annotation of the complete mitochondrial genome of Bagre panamensis.

Gene name Location (bp) Length (bp) Start codon Stop codon
tRNA-Phe 1–70 70    
12SrRNA 71–1030 960    
tRNA-Val 1031–1102 72    
16SrRNA 1103–2778 1676    
tRNA-Leu 2779–2853 75    
NAD1 2854–3825 972 ATG TAA
tRNA-Ile 3826–3897 72    
tRNA-Gln 3898–3968 71    
tRNA-Met 3969–4038 70    
NAD2 4039–5080 1042 ATG TCT
tRNA-Trp 5081–5153 73    
tRNA-Ala 5154–5222 69    
tRNA-Asn 5223–5295 73    
tRNA-Cys 5296–5362 67    
tRNA-Tyr 5363–5432 70    
COX1 5433–6983 1551 GTG TAA
tRNA-Ser 6984–7054 71    
tRNA-Asp 7055–7123 69    
COX2 7124–7814 691 ATG CCT
tRNA-Lys 7815–7888 74    
ATP8 7889–8056 168 ATG TAA
ATP6 8057–8739 683 ATG TTA
COX3 8740–9523 784 ATG CAT
tRNA-Gly 9524–9596 73    
NAD3 9597–9945 349 ATG AAT
tRNA-Arg 9946–10,016 71    
NAD4L 10,017–10,313 297 ATG TAA
NAD4 10,314–11,694 1381 ATG ATT
tRNA-His 11,695–11,764 70    
tRNA-Ser 11,765–11,831 67    
tRNA-Leu 11,832–11,904 73    
NAD5 11,905–13,731 1827 ATG TAA
NAD6 13,732–14,244 513 ATG TAG
tRNA-Glu 14,245–14,313 69    
CYTB 14,314–15,451 1138 ATG CCT
tRNA-Thr 15,452–15,523 72    
tRNA-Pro 15,524–15,593 70    
D-loop 15,594–16,673 1080    

To validate the phylogenetic position of B. panamensis, we used MEGA6 (Tamura et al. 2013) to construct a maximum-likelihood tree (500 boostrap replicates) containing complete mtDNA of the other 11 species (Figure 1). The phylogenetic position of B. panamensis was closely clustered with Netuma thalassina and Ariopsis seemanni, the three species belong to Ariidae family which are considered new world catfishes.

Acknowledgments

We are grateful to Paul Mendivil and Juan Antonio Maldonado for their help in field and lab. NCSS and RLH were benefited for an economic support through the program Cátedras CONACYT (No.: 2137 and 3285, respectively).

Disclosure statement

The authors report no conflicts of interest. They alone are responsible for the content and writing of the manuscript.

References

  1. Allen GR, Robertson DR.. 1994. Fishes of the tropical eastern Pacific. Honolulu, USA: University of Hawaii Press. [Google Scholar]
  2. Andrews S. 2011. FastQC high throughput sequence QC report v.0.10.1. Babraham Bioinformatics. [Google Scholar]
  3. Betancur-R R, Arturo AP, Bermingham E, Cooke R.. 2007. Systematics and biogeography of New World sea catfishes (Siluriformes: Ariidae) as inferred from mitochondrial, nuclear, and morphological evidence. Mol Phylogenet Evol. 45:339–357. [DOI] [PubMed] [Google Scholar]
  4. Bolger AM, Lohse M, Usadel B.. 2014. Trimmomatic: a flexible trimmer for illumina sequence data. Bioinformatics. 30:2114–2120. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cooke R. 1992. Prehistoric nearshore and littoral fishing in the eastern tropical Pacific: an ichthyological evaluation. J World Prehist. 6:1–49. [Google Scholar]
  6. Diogo R. 2004. Muscles versus bones: catfishes as a case study for a discussion on the relative contribution of myological and osteological features in phylogenetic reconstructions. Anim Biol. 54:373–391. [Google Scholar]
  7. Hahn C, Bachmann L, Chevreux B.. 2013. Reconstructing mitochondrial genomes directly from genomic next-generation sequencing reads-a baiting and iterative mapping approach. Nucleic Acids Res. 41:e129. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Iwasaki W, Fukunaga T, Isagozawa R, Yamada K, Maeda Y, Satoh TP, Mabuchi K, Takeshima H, Miya M, Nishida M.. 2013. MitoFish and MitoAnnotator: a mitochondrial genome database of fish with an accurate and automatic annotation pipeline. Mol Biol Evol. 30:2531–2540. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Kailola PJ. 2004. Phylogenetic Exploration of the Catfish Family Ariidae (Otophysi: Siluriformes). Beagle: Records of the Museums and Art galleries of the Northem territory. 87–166p. [Google Scholar]
  10. Marceniuk AP, Menezes NA.. 2007. Systematics of the family Ariidae (Ostariophysi, Siluriformes), with a redefinition of the genera. Zootaxa. 1416:1–126. [Google Scholar]
  11. Sullivan JP, Lundberg JG, Hardman M.. 2006. A phylogenetic analysis of the major groups of catfishes (Teleostei: Siluriformes) using rag1 and rag2 nuclear gene sequences. Mol Phylogenet Evol. 41:636–662. [DOI] [PubMed] [Google Scholar]
  12. Tamura K, Stecher G, Peterson D, Filipski A, Kumar S.. 2013. MEGA6: molecular evolutionary genetics analysis version 6.0. Mol Biol Evol. 30:2725–2729. [DOI] [PMC free article] [PubMed] [Google Scholar]

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