Abstract
The complete mitochondrial genome of the deep sea amphipod Eurythenes magellanicus was determined in this paper. This molecular was 14,988 bp in length, and contained the typical 13 protein coding genes (PCGs), 22 transfer RNAs (tRNAs), two ribosomal RNAs (rRNAs) and one control region (CR). The gene order of E. magellanicus was identical to that from E. maldoror, a deep sea amphipod inhabiting in a deeper habitat than E. magellanicus. A maximum-likelihood tree based on the 13 PCGs from 25 amphipods indicated that E. magellanicus and E. maldoror were closely related and the origin of deep sea amphipods was not monophyletic.
Keywords: Amphipod, deep sea, mitochondrial genome
The lysianassoid amphipods in genus Eurythenes are bathymetrically and geographically widespread in the ocean (Thurston 1990). They are one of the most abundant samples handily obtained by the bait trapper from the deep sea and have been used for many aspects of scientific researches including species diversity (Havermans et al. 2013), feed habits (Hargrave et al. 1995; Janßen et al. 2000), and life history characterization (Thurston and Bett 1995). However, several species in Eurythenes were overlooked so that they had been regarded as one taxa named Eurythenes gryllus (Bowman and Manning 1972; Ingram and Hessler 1987; Ichiro and Kentaro 1998; Janßen et al. 2000). In 2013, the differentiation of these cryptic species in the “Eurythenes gryllus complex” was confirmed with both morphological and molecular evidences (Havermans et al. 2013; Eustace et al. 2016) and the genus Eurythenes was classified into at least 15 species-level lineages (Havermans et al. 2013; Eustace et al. 2016; Havermans 2016). The depth could be the major factor resulting in their speciation (Eustace et al. 2016).
Eurythenes magellanicus represents one of the abyssal-major clades in Eurythenes. Most of E. magellanicus inhabits around 4400 m (Eustace et al. 2016), whereas two individuals have been collected at the bathyal depth of 1300 –1400 m (Havermans 2016; Narahara-Nakano et al. 2018). A total of four E. magellanicus specimens were collected at the depth of 1048 m (110°27.522'E 17°31.337'N) in the South China Sea in May 2019 by the baited trapper installed on our “Feng-huang” Lander, which consolidated the distribution of E. magellanicus in the bathyal ranges was not occasional. The samples were deposited in the specimen room of the protein research lab of the Institute of Deep-sea Science and Engineering, Chinese Academy of Sciences (accession no. Nanhai-20190523FH22-AMP1 to Nanhai-20190523FH22-AMP4). Here, the complete mitochondrial genome of E. magellanicus was determined. It would be helpful for the future phylogenetic study, especially for the Eurythenes group, within which there could still be a high diversity of cryptic species (Havermans 2016).
DNA extraction, high-throughput sequencing, sequence assembly, and gene annotation followed our previous procedures (Li, Zeng, et al. 2019; Li, Song, et al. 2019). The phylogenetic tree was constructed using the PhyloSuite1.1.15 pipeline (Zhang et al. 2019). The maximum-likelihood phylogeny was inferred using IQ-TREE 1.6.8. (Nguyen et al. 2017). mtZOA + F + I + G4 model was selected as recommended by the built-in ModelFinder module in IQ-tree (Chernomor et al. 2016).
The complete mitochondrial genome of E. magellanicus was 14,988 bp in length (NCBI accession no. MN688221) and had a typical component of 13 PCGs, 22 tRNAs, 2 rRNAs and a control region. The gene arrangement of E. magellanicus was identical to that of Eurythenes maldoror (accession no. NC036429), which was the only available mitochondrial genome from Eurythenes before the present study. Considering E. maldoror was a deep sea amphipod mainly distributed at the abyssal depth from 4000 m to 6000 m [11], the differentiation in Eurythenes caused by the depth stratification seemed to have no influence on the mitochondrial gene order.
Our constructed phylogeny indicated that E. magellanicus clustered with E. maldoror. These two Eurythenes species were grouped with the hadal amphipod Hirondellea gigas and the shallow water Onisimus nanseni in the Arctic. They belonged to the superfamily Lysianassoidea (Figure 1). Other superfamilies (Alicellidea and Dexaminoidea) also included taxa from the deep sea environment (Figure 1), therefore, the divergency for the deep sea adaptation happened multiple times during the evolution of Amphipoda.
Figure 1.
Phylogenetic tree based on the 13 protein coding genes of the mitochondrial genomes from Eurythenes magellanicus and other 24 amphipods in Amphipoda. Bootstraps values were shown at each node, Genbank numbers were after the species names. * indicated the samples were from the deep sea environment.
Funding Statement
This study was supported by the National Key Research and Development Program of China (Grant no. 2016YFC0302504); the National Key Research and Development Program of China (Grant no. 2018YFC0309804); the National Key Research and Development Program of China (Grant no. 2016YFC0304905).
Disclosure statement
The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.
References
- Bowman TE, Manning RB. 1972. Two Arctic bathyal crustaceans: the shrimp Bythocaris cryonesus new species, and the amphipod Eurythenes gryllus, with in situ photographs from Ice Island T-3. Crustaceana. 23(2):187–201. [Google Scholar]
- Chernomor O, von Haeseler A, Minh BQ. 2016. Terrace aware data structure for phylogenomic inference from supermatrices. Syst Biol. 65(6):997–1008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eustace RM, Ritchie H, Kilgallen NM, Piertney SB, Jamieson AJ. 2016. Morphological and ontogenetic stratification of abyssal and hadal Eurythenes gryllus sensu lato (Amphipoda: Lysianassoidea) from the Peru–Chile Trench. Deep Sea Res I Oceanogr Res Pap. 109:91–98. [Google Scholar]
- Hargrave BT, Phillips GA, Prouse NJ, Cranford PJ. 1995. Rapid digestion and assimilation of bait by the deep-sea amphipod Eurythenes gryllus. Deep Sea Res I Oceanogr Res Pap. 42(11–12):1905–1921. [Google Scholar]
- Havermans C. 2015. Contribution to the systematics of the genus Eurythenes SI Smith in Scudder, 1882 (Crustacea: Amphipoda: Lysianassoidea: Eurytheneidae). Zootaxa. 3971(1):1–80. [Google Scholar]
- Havermans C. 2016. Have we so far only seen the tip of the iceberg? Exploring species diversity and distribution of the giant amphipod Eurythenes. Biodiversity. 17(1–2):12–25. [Google Scholar]
- Havermans C, Sonet G, d’Udekem d’Acoz C, Nagy ZT, Martin P, Brix S, Riehl T, Agrawal S, Held C. 2013. Genetic and morphological divergences in the cosmopolitan deep-sea amphipod Eurythenes gryllus reveal a diverse abyss and a bipolar species. PLoS One. 8(9):e74218. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ichiro T, Kentaro W. 1998. Respiration rate and swimming speed of the necrophagous amphipod Eurythenes gryllus from Antarctic deep waters. Mar Ecol Prog Ser. 163:285–288. [Google Scholar]
- Ingram CL, Hessler RR. 1987. Population biology of the deep-sea amphipod Eurythenes gryllus: inferences from instar analyses. Deep Sea Res A Oceanogr Res Pap. 34(12):1889–1910. [Google Scholar]
- Janßen F, Treude T, Witte U. 2000. Scavenger assemblages under differing trophic conditions: a case study in the deep Arabian Sea. Deep Sea Res II Top Stud Oceanogr. 47(14):2999–3026. [Google Scholar]
- Li JY, Zeng C, Yan GY, He LS. 2019. Characterization of the mitochondrial genome of an ancient amphipod Halice sp. MT-2017 (Pardaliscidae) from 10,908 m in the Mariana Trench. Sci Rep. 9(1):2610. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Li JY, Song ZL, Yan GY, He LS. 2019. The complete mitochondrial genome of the largest amphipod, Alicella gigantea: insight into its phylogenetic relationships and deep sea adaptive characters. Int J Biol Macromol. 141:570–577. [DOI] [PubMed] [Google Scholar]
- Narahara-Nakano Y, Nakano T, Tomikawa K. 2018. Deep-sea amphipod genus Eurythenes from Japan, with a description of a new Eurythenes species from off Hokkaido (Crustacea: Amphipoda: Lysianassoidea). Mar Biodivers. 48(1):603–620. [Google Scholar]
- Nguyen, et al. 2014. IQ-TREE: A Fast and Effective Stochastic Algorithm for Estimating Maximum-Likelihood Phylogenies. Molecular Biology and Evolution, 32(1):268–274. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nguyen LT, Schmidt HA, von Haeseler A, Minh BQ. 2015. IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol Biol Evol. 32(1):268–274. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thurston M.H. 1990. Abyssal necrophagous amphipods (Crustacea: Amphipoda) in the northeast and tropical Atlantic Ocean. Prog Oceanogr. 24(1–4):257–274. [Google Scholar]
- Thurston MH, Bett BJ. 1995. Hatchling size and aspects of biology in the deep-sea amphipod genus Eurythenes (Crustacea: Amphipoda). Int Revue Ges Hydrobiol Hydrogr. 80(2):201–216. [Google Scholar]
- Thurston MH, Petrillo M, Della Croce N. 2002. Population structure of the necrophagous amphipod Eurythenes gryllus (Amphipoda: Gammaridea) from the Atacama Trench (south-east Pacific Ocean). J Mar Biol Assoc. 82(2):205–211. [Google Scholar]
- Zhang D, Gao F, Jakovlić I, Zou H, Zhang J, Li WX, Wang GT. 2019. PhyloSuite: an integrated and scalable desktop platform for streamlined molecular sequence data management and evolutionary phylogenetics studies. Mol Ecol Resour. 0:1–8. [DOI] [PubMed] [Google Scholar]

