Abstract
Sturgeons are ancient fish, with 27 species distributed in the Northern Hemisphere. This review first touches upon the significance of sturgeons in the context of their biological, ecological, and economic importance, highlighting their status as “living fossils” and the challenges they face in genomic research due to their diverse chromosome numbers. This review then discusses how omics technologies (genomics, transcriptomics, proteomics, and metabolomics) have been used in sturgeon research, which so far has only been done on Acipenser species. It focuses on metabolomics as a way to better understand how sturgeons work and how they react to their environment. Specific studies in sturgeon metabolomics are cited, showing how metabolomics has been used to investigate various aspects of sturgeon biology, such as growth, reproduction, stress responses, and nutrition. These studies demonstrate the potential of metabolomics in improving sturgeon aquaculture practices and conservation efforts. Overall, the review suggests that metabolomics, as a relatively new scientific tool, has the potential to enhance our understanding of sturgeon biology and aid in their conservation and sustainable aquaculture, contributing to global food security efforts.
Avoid common mistakes on your manuscript.
Introduction
There are 27 species of sturgeons, all with ray-finned bodies but not neopterygian bodies. They are in the family Acipenseridae, which is in the class Actinopterygii, subclass Chondrostei, and order Acipenseriformes (Fricke et al. 2023), and has paraphyletic intergenic clades (Luo et al. 2019; Nedoluzhko et al. 2020; Shen et al. 2020). Their natural populations of 25 extant species in the wild (Froese and Pauly 2023; IUCN 2023) are distributed in riverine, lacustrine, estuarine, and coastal waters of the Northern Hemisphere (Pikitch et al. 2005), with non-native populations in South America (Avigliano et al. 2023). They are a remarkable evolutionary relic, earning the designation of “living fossils” by Charles Darwin (1859, p. 107). Positioned at the phylogenetic base of ray-finned fishes, sturgeons, with their archaic forms and ganoid scales, appear “frozen in time” (Du et al. 2020). Teleosts of neopterygian ray-finned fish went through three to four rounds of whole-genome duplications (Pasquier et al. 2016), but sturgeons only went through two rounds, kee** their primitive traits (Cheng et al. 2019; Du et al. 2020; Zhang et al. 2021).
Despite their unique biological characteristics, sturgeons present challenges for genome analyses due to diverse chromosome aneuploidy (Havelka et al. 2011). Studies have found that the number of chromosomes in different sturgeon species varies a lot. They range from 112 for the shovelnose sturgeon (Scaphirhynchus platorynchus) (Ohno et al. 1969) to 372 ± 6 for the shortnose sturgeon (Acipenser brevirostrum) (Fontana et al. 2008), 437 for the cultured Siberian sturgeon (A. baerii) (Havelka et al. 2016), and even 520 for the artificial octoploid Russian sturgeon (A. gueldenstaedtii) (Lebeda et al. 2020). These findings make it harder to do genomic engineering. Whole-genome sequencing has been done with only two sturgeon species (A. ruthenus and A. sinensis) (Cheng et al. 2019; Du et al. 2020; Wang et al. 2023a, b) and one paddlefish (Polyodon spathula) of the sturgeon-related family Polyodontidae (the order Acipenseriformes) (Zhang et al. 2021), besides complete mitochondrial genomes of Atlantic, Gulf, and European sturgeons (A. oxyrinchus oxyrinchus, A. o. desotoi, and A. sturio) (Liu et al. Data availability is not applicable to this article as no new data were created or analyzed in this study. Abed-Elmdoust A, Farahmand H, Mojazi-Amiri B, Rafiee G, Rahimi R (2017) Metabolic changes in droplet vitrified semen of wild endangered Persian sturgeon Acipenser persicus (Borodin, 1997). Cryobiology 76:111–118. https://doi.org/10.1016/j.cryobiol.2017.03.008 Abed-Elmdoust A, Rahimi R, Farahmand H, Amiri BM, Mirvaghefi A, Rafiee G (2019) Droplet vitrification versus straw cryopreservation for spermatozoa banking in Persian sturgeon (Acipenser persicus) from metabolite point of view. Theriogenology 129:110–115. https://doi.org/10.1016/j.theriogenology.2019.02.031 Albayrak G, Sengör G, Yörük E (2014) Characterization of GnRH, ILGFRI and AR genes in sturgeon’s genomics. Isr J Aquac-Bamidgeh 66:957 Alfaro AC, Young T (2018) Showcasing metabolomic applications in aquaculture: a review. Rev Aquacult 10:135–152. https://doi.org/10.1111/raq.12152 Avigliano E, Leisen M, Duquenoy C, Liotta J, Volpedo A (2023) Siberian and Russian sturgeon natal origin in South America: fish farm or established population? Austral Ecol 48:1121–1131. https://doi.org/10.1111/aec.13346 Boccaletto P, Siddique M-A-M, Cosson J (2018) Proteomics: a valuable approach to elucidate spermatozoa post–testicular maturation in the endangered Acipenseridae family. Anim Reprod Sci 192:18–27. https://doi.org/10.1016/j.anireprosci.2018.03.033 Boscari E, Barmintseva A, Pujolar JM, Doukakis P, Mugue N, Congiu L (2014) Species and hybrid identification of sturgeon caviar: a new molecular approach to detect illegal trade. Mol Ecol Resour 14:489–498. https://doi.org/10.1111/1755-0998.12203 Boscari E, Vitulo N, Ludwig A, Caruso C, Mugue NS, Suciu R, Onara DF, Papetti C, Marino IAM, Zane L, Congiu L (2017) Fast genetic identification of the Beluga sturgeon and its sought-after caviar to stem illegal trade. Food Control 75:145–152. https://doi.org/10.1016/j.foodcont.2016.11.039 Boscari E, Marino IAM, Caruso C, Gessner J, Lari M, Mugue N, Barmintseva A, Suciu R, Onara D, Zane L, Congiu L (2021) Defining criteria for the reintroduction of locally extinct populations based on contemporary and ancient genetic diversity: the case of the Adriatic Beluga sturgeon (Huso huso). Divers Distrib 27:816–827. https://doi.org/10.1111/ddi.13230 Boscari E, Vidotto M, Martini D, Papetti C, Ogden R, Congiu L (2015) Microsatellites from the genome and the transcriptome of the tetraploid Adriatic sturgeon, Acipenser naccarii (Bonaparte, 1836) and cross-species applicability to the diploid beluga sturgeon, Huso huso (Linnaeus, 1758). J Appl Ichthyol 31:977–983. https://doi.org/10.1111/jai.12906 Burcea A, Popa G-O, Florescu IE, Maereanu M, Dudu A, Georgescu SE, Costache M (2018) Expression characterization of six genes possibly involved in gonad development for stellate sturgeon individuals (Acipenser stellatus, Pallas 1771). Int J Genomics 2018:7835637. https://doi.org/10.1155/2018/7835637 Cai W-Q, Chen Y-W, Dong X-P, Shi Y-G, Wei J-L, Liu F-J (2021) Protein oxidation analysis based on comparative proteomic of Russian sturgeon (Acipenser gueldenstaedti) after sous-vide cooking. Food Control 121:107594. https://doi.org/10.1016/j.foodcont.2020.107594 Chandra G, Fopp-Bayat D (2021) Trends in aquaculture and conservation of sturgeons: a review of molecular and cytogenetic tools. Rev Aquacult 13:119–137. https://doi.org/10.1111/raq.12466 Chen Y, Wu X, Lai J, Liu Y, Song M, Li F, Gong Q (2023) Integrated biochemical, transcriptomic and metabolomic analyses provide insight into heat stress response in Yangtze sturgeon (Acipenser dabryanus). Ecotoxicol Environ Saf 249:114366. https://doi.org/10.1016/j.ecoenv.2022.114366 Cheng P, Huang Y, Du H, Li C, Lv Y, Ruan R, Ye H, Bian C, You X, Xu J, Liang X, Shi Q, Wei Q (2019) Draft genome and complete Hox-cluster characterization of the sterlet (Acipenser ruthenus). Front Genet 10:776. https://doi.org/10.3389/fgene.2019.00776 CITES (2001) CITES World - Official Newsletter of the Parties, Issue Number 8, December 2001, CITES (Convention on International Trade in Endangered Species of Wild Fauna and Flora), Geneva. https://cites.org/sites/default/files/eng/news/world/8.pdf. Accessed 2024–03–08 Darwin CR (1859) On the origin of species by means of natural selection, or the preservation of favoured races in the struggle for life (1st edn). John Murray, London, p 107. https://doi.org/10.5962/bhl.title.162283 Degani G, Nevo Sarel M, Hajouj A, Hurvitz A, Veksler-Lublinsky I, Meerson A (2022) Whole-genome inter-sex variation in Russian sturgeon (Acipenser gueldenstaedtii). Int J Mol Sci 23:9469. https://doi.org/10.3390/ijms23169469 Diez-Simon C, Mumm R, Hall RD (2019) Mass spectrometry-based metabolomics of volatiles as a new tool for understanding aroma and flavour chemistry in processed food products. Metabolomics 15(3). https://doi.org/10.1007/s11306-019-1493-6 Doukakis P, Pikitch EK, Rothschild A, DeSalle R, Amato G, Kolokotronis S-O (2012) Testing the effectiveness of an international conservation agreement: marketplace forensics and CITES caviar trade regulation. PLoS ONE 7:e40907. https://doi.org/10.1371/journal.pone.0040907 Du H, He S, Leng X, Liang X, Tan Q, Wei Q, Wu J, Zhou H (2019) Integrated metabolomic and transcriptomic analyses suggest that high dietary lipid levels facilitate ovary development through the enhanced arachidonic acid metabolism, cholesterol biosynthesis and steroid hormone synthesis in Chinese sturgeon (Acipenser sinensis). Brit J Nutr 122:1230–1241. https://doi.org/10.1017/S0007114519002010 Du K, Stöck M, Kneitz S, Klopp S, Woltering JM, Adolfi MC et al (2020) The sterlet sturgeon genome sequence and the mechanisms of segmental rediploidization. Nat Ecol Evol 4:841–852. https://doi.org/10.1038/s41559-020-1166-x Fiehn O (2002) Metabolomics - the link between genotypes and phenotypes. Plant Mol Biol 48:155–171. https://doi.org/10.1023/A:1013713905833 Fontana F, Congiu L, Mudrak VA, Quattro JM, Smith TIJ, Ware K, Doroshov SI (2008) Evidence of hexaploid karyotype in shortnose sturgeon. Genome 51:113–119. https://doi.org/10.1139/G07-112 Fricke R, Eschmeyer WN, Van der Laan R (eds) (2023) Eschmeyer’s catalog of fishes: genera, species, references, California Academy of Sciences, San Francisco. http://researcharchive.calacademy.org/research/ichthyology/catalog/fishcatmain.asp. Accessed 2023–12–23 Froese R, Pauly D (eds) (2023) FishBase, Kiel. https://fishbase.mnhn.fr/search.php. Accessed 2024–03–08 Hajirezaee S, Mirvaghefi A, Farahmand H, Agh N (2017) NMR-based metabolomic study on the toxicological effects of pesticide, diazinon on adaptation to sea water by endangered Persian sturgeon, Acipenser persicus fingerlings. Chemosphere 185:213–226. https://doi.org/10.1016/j.chemosphere.2017.07.016 Hajirezaee S, Mirvaghefi AR, Farahmand H, Agh N (2018) A metabolic approach to understanding adaptation to sea water by endangered Persian sturgeon, Acipenser persicus fingerlings. Aquacult Res 49:341–351. https://doi.org/10.1111/are.13464 Havelka M, Kašpar V, Hulák M, Flajšhans M (2011) Sturgeon genetics and cytogenetics: a review related to ploidy levels and interspecific hybridization. Folia Zool 60:93–103. https://doi.org/10.25225/fozo.v60.i2.a3.2011 Havelka M, Bytyutskyy D, Symonová R, Ráb P, Flajšhans M (2016) The second highest chromosome count among vertebrates is observed in cultured sturgeon and is associated with genome plasticity. Genet Sel Evol 48:12. https://doi.org/10.1186/s12711-016-0194-0 Heude C, Elbayed K, Jezequel T, Fanuel M, Lugan R, Heintz D, Benoit P, Piotto M (2016) Metabolic characterization of caviar specimens by 1H NMR spectroscopy: towards caviar authenticity and integrity. Food Anal Method 9:3428–3438. https://doi.org/10.1007/s12161-016-0540-4 Höhne C, Prokopov D, Kuhl H, Du K, Klopp C, Wuertz S, Trifonov V, Stöck M (2021) The immune system of sturgeons and paddlefish (Acipenseriformes): a review with new data from a chromosome-scale sturgeon genome. Rev Aquac 13:1709–1729. https://doi.org/10.1111/raq.12542 Huete-Pérez JA, Quezada F (2013) Genomic approaches in marine biodiversity and aquaculture. Biol Res 46:353–361. https://doi.org/10.4067/S0716-97602013000400007 IUCN (2023) The IUCN Red List of Threatened Species. Version 2023–1, International Union for Conservation of Nature and Natural Resources, Cambridge. https://www.iucnredlist.org. Accessed 2024–03–08. Jacob M, Lopata AL, Dasouki M, Rahman AMA (2019) Metabolomics toward personalized medicine. Mass Spectrom Rev 38:221–238. https://doi.org/10.1002/mas.21548 Jiang D-D, Shen S-K, Yu W-T, Bu Q-Y, Ding Z-W, Fu J-J (2023) Insights into peptide profiling of sturgeon myofibrillar proteins with low temperature vacuum heating. J Sci Food Agric 103(6):2858–2866. https://doi.org/10.1002/jsfa.12437 Keyvanshokooh S, Gharaei A (2010) A review of sex determination and searches for sex-specific markers in sturgeon. Aquac Res 41:e1–e7. https://doi.org/10.1111/j.1365-2109.2009.02463.x Keyvanshokooh S, Vaziri B (2008) Proteome analysis of Persian sturgeon (Acipenser persicus) ova. Anim Reprod Sci 109(1):287–297. https://doi.org/10.1016/j.anireprosci.2007.10.008 Keyvanshokooh S, Kalbassi M-R, Hosseinkhani S, Vaziri B (2009) Comparative proteomics analysis of male and female Persian sturgeon (Acipenser persicus) gonads. Anim Reprod Sci 111(2):361–368. https://doi.org/10.1016/j.anireprosci.2008.03.005 Keyvanshokooh S, Vaziri B, Gharaei A, Mahboudi F, Esmaili-Sari A, Shahriari-Moghadam M (2009) Proteome modifications of juvenile beluga (Huso huso) brain as an effect of dietary methylmercury. Comp Biochem Physiol Part D: Genomics Proteomics 4(4):243–248. https://doi.org/10.1016/j.cbd.2009.01.002 Kodzik N, Ciereszko A, Szczepkowski M, Karol H, Judycka S, Malinowska A, Świderska B, Dietrich M-A (2023) Comprehensive proteomic characterization and functional annotation of Siberian sturgeon seminal plasma proteins. Aquaculture 568:739326. https://doi.org/10.1016/j.aquaculture.2023.739326 Kodzik N, Ciereszko A, Szczepkowska B, Malinowska A, Dietrich M-A (2024) Comparative proteomic analysis of the ovarian fluid and eggs of Siberian sturgeon. BMC Genomics 25(1):451. https://doi.org/10.1186/s12864-024-10309-y Koyama H, Okamoto S, Watanabe N, Hoshino N, Jimbo M, Yasumoto K, Watabe S (2015) Dynamic changes in the accumulation of metabolites in brackish water clam Corbicula japonica associated with alternation of salinity. Comp Biochem Physiol B 181:59–70. https://doi.org/10.1016/j.cbpb.2014.11.007 Kuo C-H, Ballantyne R, Huang P-L, Ding S, Hong M-C, Lin T-Y, Wu F-C, Xu Z-Y, Chiu K, Chen B, Liu C-H (2022) Sarcodia suae modulates the immunity and disease resistance of white shrimp Litopenaeus vannamei against Vibrio alginolyticus via the purine metabolism and phenylalanine metabolism. Fish Shellfish Immun 127:766–777. https://doi.org/10.1016/j.fsi.2022.07.011 Lasalle A, Norbis W, Vizziano-Cantonnet D (2021) Sex identification of morphologically-undifferentiated Siberian sturgeon with statistical analysis of gene expression patterns. J Appl Ichthyol 37:835–846. https://doi.org/10.1111/jai.14268 Lazzari B, Mariani V, Malinverni R, Caprera A, Giuffra E (2008) A comparative gene index for the white sturgeon Acipenser transmontanus. Mar Genom 1:15–21. https://doi.org/10.1016/j.margen.2008.04.002 Lebeda I, Ráb P, Majtánová Z, Flajšhans M (2020) Artificial whole genome duplication in paleopolyploid sturgeons yields highest documented chromosome number in vertebrates. Sci Rep 10:19705. https://doi.org/10.1038/s41598-020-76680-4 Li P, Hulak M, Rodina M, Sulc M, Li Z-H, Linhart O (2010) Comparative protein profiles: potential molecular markers from spermatozoa of Acipenseriformes (Chondrostei, Pisces). Comp Biochem Physiol Part D: Genomics Proteomics 5(4):302–307. https://doi.org/10.1016/j.cbd.2010.08.003 Li P, Guo W, Yue H, Li C, Du H, Qiao X, Liu Z, Zhou Q, Wei Q (2017) Variability in the protein profiles in spermatozoa of two sturgeon species. PLoS ONE 12(10):e0186003. https://doi.org/10.1371/journal.pone.0186003 Li X, **e W, Bai F, Wang J, Zhou X, Gao R, Xu X, Zhao Y (2022) Influence of thermal processing on flavor and sensory profile of sturgeon meat. Food Chem 374:131689. https://doi.org/10.1016/j.foodchem.2021.131689 Lin C-Y, Huang L-H, Deng D-F, Lee S-H, Liang H-J, Hung SSO (2019) Metabolic adaptation to feed restriction on the green sturgeon (Acipenser medirostris) fingerlings. Sci Total Environ 684:78–88. https://doi.org/10.1016/j.scitotenv.2019.05.044 Liu X, Du H, **ao K, Hu Y, Liu J, Zhao X (2017) The complete mitochondrial genome of the hybrid sturgeon of Huso dauricus (♀) × Acipenser schrenckii (♂). Mitochondrial DNA B: Resour 2:11–12. https://doi.org/10.1080/23802359.2016.1275838 Liu F-J, Shen S-K, Chen Y-W, Dong X-P, Han J-R, **e H-J, Ding Z-W (2022) Quantitative proteomics reveals the relationship between protein changes and off-flavor in Russian sturgeon (Acipenser gueldenstaedti) fillets treated with low temperature vacuum heating. Food Chem 370:131371. https://doi.org/10.1016/j.foodchem.2021.131371 Lobanov VP, Pate J, Joyce J (2023) Sturgeon and paddlefish: review of research on broodstock and early life stage management. Aquac Fish, in press.https://doi.org/10.1016/j.aaf.2023.04.001 Lulijwa R, Alfaro AC, Young T (2022) Metabolomics in salmonid aquaculture research: applications and future perspectives. Rev Aquac 14(2):547–577. https://doi.org/10.1111/raq.12612 Luo D, Li Y, Zhao Q, Zhao L, Ludwig A, Peng Z (2019) Highly resolved phylogenetic relationships within order Acipenseriformes according to novel nuclear markers. Genes (Basel) 10:38. https://doi.org/10.3390/2Fgenes10010038 Lv W, ** S, Wang N, Cao D, ** X, Zhang Y (2021) Identification of important proteins from the gonads and pituitary involved in the gonad development of Amur sturgeon, Acipenser schrenckii, regulated by GnRH-a treatment by iTRAQ-based analysis. Comp Biochem Physiol Part D: Genomics Proteomics 39:100831. https://doi.org/10.1016/j.cbd.2021.100831 Ma J, Zhang T, Zhuang P, Zhang LZ, Liu T (2011) Annotation and analysis of expressed sequence tags (ESTs) from Chinese sturgeon (Acipenser sinensis) pituitary cDNA library. Mar Genom 4:173–179. https://doi.org/10.1016/j.margen.2011.04.002 Meng D, Wei Q, Takagi Y, Dai Z, Zhang Y (2023) Structural Properties and Biological Activities of Collagens from Four Main Processing By-Products (Skin Fin Cartilage Notochord) of Sturgeon (Acipenser gueldenstaedti). Waste and Biomass Valorization 14(12):3987–4002. https://doi.org/10.1007/s12649-023-02107-6 Mugue N, Terekhanova N, Afanasyev S, Krasnov A (2019) Transcriptome sequencing of hybrid bester sturgeon: responses to poly (I:C) in the context of comparative immunogenomics. Fish Shellfish Immunol 93:888–894. https://doi.org/10.1016/j.fsi.2019.08.038 Murphy A-E, Stokesbury M-J-W, Easy R-H (2020) Exploring epidermal mucus protease activity as an indicator of stress in Atlantic sturgeon (Acipenser oxyrinchus oxyrhinchus). J Fish Biol 97(5):1354–1362. https://doi.org/10.1111/jfb.14489 Nedoluzhko AV, Sharko FS, Tsygankova SV, Boulygina ES, Barmans’ve AE, Krasivskaya AA, Ibragimova AS, Gruzdeva NM, Rastorguev SM, Mugue NS (2020) Molecular phylogeny of one extinct and two critically endangered Central Asian sturgeon species (genus Pseudoscaphirhynchus) based on their mitochondrial genomes. Sci Rep 10:722. https://doi.org/10.1038/2Fs41598-020-57581-y Niksirat H, Andersson L, Golpour A, Chupani L, James P (2017) Quantification of egg proteome changes during fertilization in sterlet Acipenser ruthenus. Biochem Biophys Res Commun 490(2):189–193. https://doi.org/10.1016/j.bbrc.2017.06.019 Ogden R, Gharbi K, Mugue N, Martinsohn J, Senn H, Davey JW, Pourkazemi M, McEwing R, Eland C, Vidotto M, Sergeev A, Congiu L (2013) Sturgeon conservation genomics: SNP discovery and validation using RAD sequencing. Mol Ecol 22:3112–3123. https://doi.org/10.1111/mec.12234 Ohno S, Muramoto J, Stenius C, Christian L, Kittrell WA, Atkin NB (1969) Microchromosomes in holocephalian, chondrostean and holostean fishes. Chromosoma 26:35–40. https://doi.org/10.1007/BF00319498 Panagiotopoulou H, Marzecki K, Gawor J, Kuhl H, Koper M, Weglenski P, Fajkowska M, Szczepkowski M, Baca M, Gessner J, Płecha M, Rzepkowska M (2023) Extensive search of genetic sex markers in Siberian (Acipenser baerii) and Atlantic (A. oxyrinchus) sturgeons. Aquaculture 573:739517. https://doi.org/10.1016/j.aquaculture.2023.739517 Pasquier J, Cabau C, Nguyen T, Jouanno E, Severac D, Braasch I et al (2016) Gene evolution and gene expression after whole genome duplication in fish: the PhyloFish database. BMC Genomics 17:368. https://doi.org/10.1186/s12864-016-2709-z Pikitch EK, Doukakis P, Lauck L, Chakrabarty P, Erickson DL (2005) Status, trends and management of sturgeon and paddlefish fisheries. Fish Fish 6:233–265. https://doi.org/10.1111/j.1467-2979.2005.00190.x Popović D, Baca M, Panagiotopoulou H (2016) Complete mitochondrial genome sequences of Atlantic sturgeon, Acipenser oxyrinchus oxyrinchus, Gulf sturgeon, A. o. desotoi and European sturgeon A. sturio (Acipenseriformes: Acipenseridae) obtained through next generation sequencing. Mitochondrial DNA 27:2549–2551. https://doi.org/10.3109/19401736.2015.1038799 Qian X, Ba Y, Zhuang Q, Zhong G (2013) RNA-Seq technology and its application in fish transcriptomics. OMICS 18:98–110. https://doi.org/10.1089/omi.2013.0110 Qiu S, Cai Y, Yao H, Lin C, **e Y, Tang S, Zhang A (2023) Small molecule metabolites: discovery of biomarkers and therapeutic targets. Sig Transduct Target Ther 8:132. https://doi.org/10.1038/s41392-023-01399-3 Rahimi R, Farahmand H, Mirvaghefi A, Rafiee G, Abed-Elmdoust A (2019) 1H NMR metabolic profiling of the cryopreserved spermatozoa of the wild endangered Persian sturgeon (Acipenser persicus) with the use of beta-cyclodextrin as an external cryoprotectant. Fish Physiol Biochem 45:1029–1040. https://doi.org/10.1007/s10695-019-00615-8 Roques S, Deborde C, Richard N, Skiba‐Cassy S, Moing A, Fauconneau B (2020) Metabolomics and fish nutrition: a review in the context of sustainable feed development. Rev Aquac 12(1):261–282. https://doi.org/10.1111/raq.12316 Ruan R, Feng T, Li Y, Yue H, Ye H, Du H, Liu Q, Ruan J, Li C, Wei Q (2021) Screening and identification of female-specific DNA sequences in octaploid sturgeon using comparative genomics with high-throughput sequencing. Genomics 113:4237–4244. https://doi.org/10.1016/j.ygeno.2021.11.012 Salimi Khorshidi N, Salati A-P, Keyvanshokooh S (2021) The effects of bisphenol A on liver proteome and mucus vitellogenin in comparison to plasma as a non-invasive biomarker in immature Siberian sturgeons (Acipenser baerii). Comp Biochem Physiol Part D: Genomics Proteomics 38:100795. https://doi.org/10.1016/j.cbd.2021.100795 Sato Y, Nishida M (2010) Teleost fish with specific genome duplication as unique models of vertebrate evolution. Environ Biol Fishes 88:169–188. https://doi.org/10.1007/s10641-010-9628-7 Shaliutina A, Hulak M, Li P, Sulc M, Dzyuba B, Linhart O (2013) Comparison of protein fractions in seminal plasma from multiple sperm collections in sterlet (Acipenser ruthenus). Reprod Domest Anim 48(1):156–159. https://doi.org/10.1111/j.1439-0531.2012.02118.x Shen Y, Yang N, Liu Z, Chen Q, Li Y (2020) Phylogenetic perspective on the relationships and evolutionary history of the Acipenseriformes. Genomics 112:3511–3517. https://doi.org/10.1016/j.ygeno.2020.02.017 Shen S, Liu F, Chen Y, **e H, Hu H, Ren S, Ding Z, Bu Q (2022) Insight into the molecular mechanism of texture improvement of sturgeon fillets treated by low temperature vacuum heating technology using label-free quantitative proteomics. Food Res Int 157:111251. https://doi.org/10.1016/j.foodres.2022.111251 Silvestre F, Linares-Casenave J, Doroshov S-I, Kültz D (2010) A proteomic analysis of green and white sturgeon larvae exposed to heat stress and selenium. Sci Total Environ 408(16):3176–3188. https://doi.org/10.1016/j.scitotenv.2010.04.005 Soto E, Coleman D, Yazdi Z, Purcell SL, Camus A, Fast MD (2021) Analysis of the white sturgeon (Acipenser transmontanus) immune response during immunostimulation and Veronaea botryosa infection. Comp Biochem Physiol Part D Genomics Proteomics 40:100879. https://doi.org/10.1016/j.cbd.2021.100879 Stundl J, Martik ML, Chen D, Raja DA, Franěk R, Pospisilova A, Pšenička M, Metscher BD, Braasch I, Haitina T, Cerny R, Ahlberg PE, Bronner ME (2023) Ancient vertebrate dermal armor evolved from trunk neural crest. Proce Natl Acad Sci USA 120:e2221120120. https://doi.org/10.1073/pnas.2221120120 Tang D, Deng D, Zhang S, Yuan H, Wenbing Z, Xu Q, Wei Q (2019) Similarity analysis of the immune-related genes from Chinese sturgeon (Acipenser sinensis) and Dabry’s sturgeon (Acipenser dabryanus). Turk J Fish Aquat Sci 19:865–871. https://doi.org/10.4194/1303-2712-v19_10_06 Taylor J, King R, ltmann T, Fiehn O (2002) Application of metabolomics to plant genotype discrimination using statistics and machine learning. Bioinformatics 18 supple_2:S241-S248. https://doi.org/10.1093/bioinformatics/18.suppl_2.s241 Trifonov VA, Romanenko SS, Beklemisheva VR, Biltueva LS, Makunin AI, Lemskaya NA, Kulemzina AI, Stanyon R, Graphodatsky AS (2016) Evolutionary plasticity of Acipenseriform genomes. Chromosoma 125:661–668. https://doi.org/10.1007/s00412-016-0609-2 Tripathy PS, Khatei A, Parhi J (2021) Omics in aquaculture. In: Pandey PK, Parhi J (eds) Advances in fisheries biotechnology, Springer, Singapore, pp 83–94. https://doi.org/10.1007/978-981-16-3215-0_5 Vailati-Riboni M, Palombo V, Loor JJ (2017) What are omics sciences? In Ametaj BN (ed) Periparturient diseases of dairy cows, Springer, Cham, pp 1–7. https://doi.org/10.1007/978-3-319-43033-1_1 Verdegem M, Buschmann AH, Latt UW, Dalsgaard AJT, Lovatelli A (2023) The contribution of aquaculture systems to global aquaculture production. J World Aquacult Soc 54:206–250. https://doi.org/10.1111/jwas.12963 Viegas CSB, Simes DC, Laizé V, Williamson MK, Price PA, Cancela ML (2008) Gla-rich protein (GRP), a new vitamin K-dependent protein identified from sturgeon cartilage and highly conserved in vertebrates. J Biol Chem 283:36655–36664. https://doi.org/10.1074/jbc.M802761200 Wang C, Zhao Z, Lu S, Liu Y, Han S, Jiang H, Yang Y, Liu H (2023b) Physiological, nutritional and transcriptomic responses of sturgeon (Acipenser schrenckii) to complete substitution of fishmeal with cottonseed protein concentrate in aquafeed. Biology 12:490. https://doi.org/10.3390/biology12040490 Wang B, Wu B, Liu X, Hu Y, Ming Y, Bai M, et al. (2023a) Whole genome sequencing reveals autooctoploidy in the Chinese sturgeon and its evolutionary trajectories. Genom Proteom Bioinformat 2023: qzad002. https://doi.org/10.1093/gpbjnl/qzad002 Wenk M (2005) The emerging field of lipidomics. Nat Rev Drug Discov 4:594–610. https://doi.org/10.1038/nrd1776 Whitaker JM, Price LE, Boase JC, Bernatchez L, Welsh AB (2020) Detecting fine-scale population structure in the age of genomics: a case study of lake sturgeon in the Great Lakes. Fish Rese 230:105646. https://doi.org/10.1016/j.fishres.2020.105646 Wu J, Li J, Du H, Ruan R, Luo J, Qiao X, Liu Z, Liu Y, Xu Q, Yu T, Wei Q (2022) Transcriptome and lipidomics profiling of F2 generation female Chinese sturgeon (Acipenser sinensis) in response to different arachidonic acid diets. Aquac Rep 23:101020. https://doi.org/10.1016/j.aqrep.2022.101020 Youneszadeh-Fashalami M, Salati A-P, Keyvanshokooh S (2018) Comparison of proteomic profiles in the ovary of Sterlet sturgeon (Acipenser ruthenus) during vitellogenic stages. Comp Biochem Physiol Part D: Genomics Proteomics 27:23–29. https://doi.org/10.1016/j.cbd.2018.04.006 Yue H, Wu J, Fu P, Ruan R, Ye H, Hu B, Chen X, Li C (2022) Effect of glutamine supplementation against soybean meal-induced growth retardation, hepatic metabolomics and transcriptome alterations in hybrid sturgeon Acipenser baerii ♀ × A. schrenckii ♂. Aquac Rep 24:101158. https://doi.org/10.1016/j.aqrep.2022.101158 Zhang H, Wu J, Wang C, Ruan R, Li Y, Bian C, You X, Shi C, Han K, Xu J, Shi Q, Wei Q (2021) The American paddlefish genome provides novel insights into chromosomal evolution and bone mineralization in early vertebrates. Mol Biol Evol 38:1595–1607. https://doi.org/10.1093/molbev/msaa326 Zhang Y, Liu C, Liu J, Liu X, Tu Z, Zheng Y, Xu J, Fan H, Wang Y, Hu M (2022) Multi-omics reveals response mechanism of liver metabolism of hybrid sturgeon under ship noise stress. Sci Total Environ 851:158348. https://doi.org/10.1016/j.scitotenv.2022.158348 Zhou X, Ding Y, Wang Y (2012) Proteomics: present and future in fish, shellfish and seafood. Rev Aquacult 4:11–20. https://doi.org/10.1111/j.1753-5131.2012.01058.x Zhou M, Zhang D, Long X, Chen W, Jiang W, Chen P, Tan Q (2023) Biochemical compositions and transcriptome analysis reveal dynamic changes of embryonic development and nutrition metabolism in Chinese sturgeon (Acipenser sinensis). Aquaculture 577:740003. https://doi.org/10.1016/j.aquaculture.2023.740003 Zhu Y, Wu J, Leng X, Du H, Wu J, He S, Luo J, Liang X, Liu H, Wei Q, Tan Q (2020) Metabolomics and gene expressions revealed the metabolic changes of lipid and amino acids and the related energetic mechanism in response to ovary development of Chinese sturgeon (Acipenser sinensis). PLoS ONE 15:e0235043. https://doi.org/10.1371/journal.pone.0235043 Open Access funding provided by Hiroshima University. Part of this study was supported by JSPS KAKENHI No. 21K05782. Qi Liu: collection and analysis of relevant publications, and writing—original draft preparation. Takeshi Naganuma: conceptualization and planning of the review article, and writing—review and editing, supervision. The authors declare no competing interests. Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. Liu, Q., Naganuma, T. Metabolomics in sturgeon research: a mini-review.
Fish Physiol Biochem (2024). https://doi.org/10.1007/s10695-024-01377-8 Received: Accepted: Published: DOI: https://doi.org/10.1007/s10695-024-01377-8Data availability
References
Funding
Author information
Authors and Affiliations
Contributions
Corresponding author
Ethics declarations
Competing interests
Additional information
Publisher's Note
Rights and permissions
About this article
Cite this article
Keywords