667
Views
0
CrossRef citations to date
0
Altmetric
Mitogenome Announcement

The complete mitochondrial genome of the Asian pitviper Gloydius changdaoensis (Squamata, Viperidae)

, , , &
Pages 3276-3277 | Received 13 Jul 2020, Accepted 01 Aug 2020, Published online: 01 Sep 2020

Abstract

Asian pitviper Gloydius changdaoensis is a coastal species, distributed in Shandong province, China. In this study, we successfully sequenced the mitochondrial genome of one individual of G. changdaoensis. The complete mitochondrial genome is circular molecular with 17,224 bp, containing an origin of light-strand replication (OL), two non-coding control regions (CRs), and 37 classical genes of vertebrate, which contain 13 protein-coding genes (PCGs), 2 ribosomal RNA genes, and 22 transfer RNA genes. A Bayesian phylogenetic tree using the complete mitochondrial genomes of all viper species available showed a consistent result with previous studies.

Gloydius Hoge & Romano-Hoge, 1981 is a genus of venomous pitviper endemic to Asia. The specimens from Shandong peninsula, China, are considered by Li (Citation1999) and Zhao (Citation2006) that should be treated as a synonym or a subspecies of G. saxatilis, named G. s. changdaoensis. Based on the comparison of both mitochondrial gene fragments and morphology, Shi et al. (Citation2016) stated that G.s.changdaoensis separated from G. saxatilis, and raised a valid species. However, the taxonomic status of this species is still controversial and undefined (Uetz et al. Citation2020).

In October 2018, a specimen (QY1213) of G. changdaoensis was collected from the type locality of Daheishan Island (37°58′N, 120°35′E), Changdao county, Shandong province, China, and used for sequencing of a complete mitogenome. Its liver tissue was fixed with 95% ethanol and stored at −20 °C in the herpetological collection, Chengdu Institute of Biology, Chinese Academy of Sciences. A small amount of liver tissue was shipped to Tsingke (Chengdu, China) for genomic extraction and 150-base-pair paired-end library construction; sequencing was performed on an Illumina HiSeq 2000 platform. De novo assembly of clean reads was performed using SPAdes v3.11.0 (Bankevich et al. Citation2012). Genes were annotated with the MITOS web server (Bernt et al. Citation2013), and then submitted to GenBank (accession no. MT731652). All sampling activities were conducted in accordance with the Guidelines of Animal Ethics published by the Chengdu Institute of Biology.

The complete length of the mitochondrial genomes (mitogenomes) of G. changdaoensis was 17,224 bp, containing an origin of light-strand replication (OL), two non-coding control regions (CRs), and 37 classical genes of vertebrate, which were 13 protein-coding genes (PCGs), two ribosomal RNA genes, and 22 transfer RNA genes. The base-pair composition was biased toward A and T with a 58.3% of A + T content on average (A 32.4%, C 28.7%, G 13.0%, and T 25.9%). The primary of the genes in the mitogenomes of G. changdaoensis were located on the heavy strand (H-strand) with except of one PCG (ND6) and eight tRNA genes (tRNA-Gln, Ala, Asn, Cys, Tyr, SerUCN, Glu, and Pro). In 13 PCGs, the shortest was ATP8 gene (150 bp) and the longest was ND5 gene (1788 bp). Most PCGs initiated with ATG except for COX1 with GTG, and ND1 and ND3 with ATA. Inverse, only five PCGs ended with complete stop codons, TAA (ATP8, ATP6, ND4L, ND5, and Cyt b), AGA (COX1), and AGG (ND6), and the other six genes ended with an incomplete stop codon, TTA (ND1, ND2, COX2, COX3, ND3, and ND4). The length of tRNA genes varied from 52 to 75 bp.

The concatenated PCGs were used to construct the Bayesian phylogenetic tree of G. changdaoensis and other 16 vipers. Bayesian phylogenetic tree indicated that all Gloydius were closely related to Crotalinae which were distributed in the America (PP 1.00) (). Subsequently, all pit vipers of Gloydius appeared no less than two major phyletic lineages (PP 1.00). The taxa of G. changdaoensis was a sister relationship with a clade which was formed by G. shedaoensis, G. saxatilis, and G. intermedius (PP 1.00). It is evident that G. changdaoensis was a monophyly that was separated from G. saxatilis and G. intermedius.

Figure 1. A majority-rule consensus tree inferred from Bayesian inference using MrBayes v.3.2.2 (Ronquist et al. Citation2012) with GTR + I+G substitution model that was selected by MrModelTest 2.3 under Akaike information criteria (Ronquist et al. Citation2012), based on the concatenated PCGs of 19 vipers of Crotalinae and one Colubridae taxa which were chosen as outgroup (Xu et al. Citation2016). DNA sequences were aligned in MEGA 7 (Kumar et al. Citation2016). Node numbers show Bayesian posterior probabilities. Branch lengths represent means of the posterior distribution. GenBank accession numbers were given with species names.

Figure 1. A majority-rule consensus tree inferred from Bayesian inference using MrBayes v.3.2.2 (Ronquist et al. Citation2012) with GTR + I+G substitution model that was selected by MrModelTest 2.3 under Akaike information criteria (Ronquist et al. Citation2012), based on the concatenated PCGs of 19 vipers of Crotalinae and one Colubridae taxa which were chosen as outgroup (Xu et al. Citation2016). DNA sequences were aligned in MEGA 7 (Kumar et al. Citation2016). Node numbers show Bayesian posterior probabilities. Branch lengths represent means of the posterior distribution. GenBank accession numbers were given with species names.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Data availability statement

The data that support the findings of this study are openly available in “NCBI” at https://www.ncbi.nlm.nih.gov/, reference number MT731652.

Additional information

Funding

This work was supported by the National Natural Science Foundation of China [Grant No. 31672270 to WYY], Special Fund for Youth Scholars on Taxonomy, the Chinese Academy of Sciences [Grant No. ZSBR-014 to CB], Sichuan Science and Technology Plan Project [Grant No. 2019JDKP0016 to WYY], and Scientific Research Foundation of Yibin University [Grant No. 2019JDKP0016 to WYY].

References

  • Bankevich A, Nurk S, Antipov D, Gurevich A, Dvorkin M, Kulikov AS, Lesin V, Nikolenko S, Pham S, Prjibelski A, et al. 2012. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J Comput Biol. 19(5):455–477.
  • Bernt M, Donath A, Jühling F, Externbrink F, Florentz C, Fritzsch G, Pütz J, Middendorf M, Stadler PF. 2013. MITOS: improved de novo metazoan mitochondrial genome annotation. Mol Phylogenet Evol. 69(2):313–319.
  • Kumar S, Stecher G, Tamura K. 2016. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol. 33(7):1870–1874.
  • Li J. 1999. Infraspecific classification of two species of Gloydius (Serpentes: Crotalinae). Zool Syst. 24(4):454–460.
  • Ronquist F, Teslenko M, Van Der Mark P, Ayres DL, Darling A, Höhna S, Larget B, Liu L, Suchard MA, Huelsenbeck JP. 2012. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst Biol. 61(3):539–542.
  • Shi J, Yang D, Zhang W, Qi S, Li P, Ding L. 2016. Distribution and infraspecies taxonomy of Gloydius halys–Gloydius intermedius complex China (Serpentes: Crotalinae). Chin J Zool. 51(5):777–798.
  • Uetz P, Freed P, Hošek J. 2020. The reptile database; [accessed 2019 Nov 9]. http://www.reptile-database.org
  • Xu C, Zhao S, Li C, Dou H. 2016. The complete mitochondrial genome of Gloydius intermedius (Squamata: Viperidae: Crotalinae) from China. Mitochondrial DNA Part A. 27(4):2373–2374.
  • Zhao EM. 2006. Snakes of China. Hefei: Anhui Science and Technology Publishing House.