Genetic diversity, variation, and structure of two populations of bigfn reef squid (Sepioteuthis lessoniana d’Orbigny) in Con Dao and Phu Quoc islands, Vietnam
Abstract Background Bigfn squid is one of the economically important seafood resources in Vietnam’s fsheries and the waters around Con Dao and Phu Quoc islands are two major fshing grounds where this species has been actively exploited. The start codon targeted polymorphism (SCoT) and CAAT box–de...
Đã lưu trong:
Những tác giả chính: | , , , |
---|---|
Định dạng: | Journal article |
Ngôn ngữ: | English |
Được phát hành: |
Springer
2023
|
Những chủ đề: | |
Truy cập trực tuyến: | https://scholar.dlu.edu.vn/handle/123456789/3244 https://doi.org/10.1186/s43141-023-00573-y |
Các nhãn: |
Thêm thẻ
Không có thẻ, Là người đầu tiên thẻ bản ghi này!
|
Thư viện lưu trữ: | Thư viện Trường Đại học Đà Lạt |
---|
id |
oai:scholar.dlu.edu.vn:123456789-3244 |
---|---|
record_format |
dspace |
institution |
Thư viện Trường Đại học Đà Lạt |
collection |
Thư viện số |
language |
English |
topic |
Bigfin reef squid SCoT CBDP COI Genetic diversity |
spellingShingle |
Bigfin reef squid SCoT CBDP COI Genetic diversity Lê, Ngọc Triệu Nguyễn, Văn Kết Thái, Thạch Bích Nguyễn, Văn Long Genetic diversity, variation, and structure of two populations of bigfn reef squid (Sepioteuthis lessoniana d’Orbigny) in Con Dao and Phu Quoc islands, Vietnam |
description |
Abstract
Background Bigfn squid is one of the economically important seafood resources in Vietnam’s fsheries
and the waters around Con Dao and Phu Quoc islands are two major fshing grounds where this species has been actively exploited. The start codon targeted polymorphism (SCoT) and CAAT box–derived polymorphism (CBDP) techniques were used to generate DNA fngerprinting data to analyze the genetic diversity, variation, and structure of the two populations in the waters surrounding Phu Quoc and Con Dao islands together with mitochondrial cytochrome C oxidase subunit I (COI) gene sequence data.
Results Con Dao population possessed a higher diversity [expected heterozygosity (He) = 0.2254, Shannon index (I) = 0.3459, percentage of polymorphic bands (PPB) = 80.14%, nucleotide diversity (π) = 0.0336, haplotype diversity (h) = 0.910 with 16 haplotypes] than Phu Quoc population (He = 0.1854, I = 0.2873, PPB = 70.38%, π = 0.0246, h = 0.838 with 14 haplotypes). The genetic diversity at species level in the investigated region was at level of He = 0.2169, I = 0.3399, PPB = 86.41, π = 0.0289, and h = 0.892 with 24 haplotypes. Based on DNA fngerprinting data, the pair wise genetic similarity coefcients among individuals of the Con Dao population were lower (average of 0.7977) than the Phu Quoc population (average of 0.8316). Based on mitochondrial COI data, the pairwise genetic distances among individuals of the Con Dao population were higher (average of 0.0361) than the Phu Quoc population
(average of 0.0263). Gene diferentiation (GST) between two investigated populations was 0.0316 and 0.0310 lead ing to the genetic distance was 0.0573 and 0.0213 and the gene fow between them was Nm = 8.2209 and 11.4700 migrants per generation among populations based on DNA fngerprinting and based on COI gene sequence data, respectively. Genetic variation within individuals of both populations (WP) played the key role in total genetic varia tion at species level in surveyed region.
Conclusions For the bigfn reef squid species in the surveyed region, the Con Dao population had the higher
genetic diversity than the Phu Quoc population, between them existed a low to moderate genetic diferentiation and a genetic exchange via gene fow. The DNA fngerprinting data better revealed the genetic diferentiation
between the two surveyed populations while the mitochondrial COI gene sequence data could show the phylo genetic relationship among the surveyed individuals and the other from the sea regions in Southeast Asia. Based on the results obtained, fsheries management strategies are suggested toward the conservation and sustainable exploitation of this species. |
format |
Journal article |
author |
Lê, Ngọc Triệu Nguyễn, Văn Kết Thái, Thạch Bích Nguyễn, Văn Long |
author_facet |
Lê, Ngọc Triệu Nguyễn, Văn Kết Thái, Thạch Bích Nguyễn, Văn Long |
author_sort |
Lê, Ngọc Triệu |
title |
Genetic diversity, variation, and structure of two populations of bigfn reef squid (Sepioteuthis lessoniana d’Orbigny) in Con Dao and Phu Quoc islands, Vietnam |
title_short |
Genetic diversity, variation, and structure of two populations of bigfn reef squid (Sepioteuthis lessoniana d’Orbigny) in Con Dao and Phu Quoc islands, Vietnam |
title_full |
Genetic diversity, variation, and structure of two populations of bigfn reef squid (Sepioteuthis lessoniana d’Orbigny) in Con Dao and Phu Quoc islands, Vietnam |
title_fullStr |
Genetic diversity, variation, and structure of two populations of bigfn reef squid (Sepioteuthis lessoniana d’Orbigny) in Con Dao and Phu Quoc islands, Vietnam |
title_full_unstemmed |
Genetic diversity, variation, and structure of two populations of bigfn reef squid (Sepioteuthis lessoniana d’Orbigny) in Con Dao and Phu Quoc islands, Vietnam |
title_sort |
genetic diversity, variation, and structure of two populations of bigfn reef squid (sepioteuthis lessoniana d’orbigny) in con dao and phu quoc islands, vietnam |
publisher |
Springer |
publishDate |
2023 |
url |
https://scholar.dlu.edu.vn/handle/123456789/3244 https://doi.org/10.1186/s43141-023-00573-y |
_version_ |
1785973331086802944 |
spelling |
oai:scholar.dlu.edu.vn:123456789-32442023-12-21T04:01:11Z Genetic diversity, variation, and structure of two populations of bigfn reef squid (Sepioteuthis lessoniana d’Orbigny) in Con Dao and Phu Quoc islands, Vietnam Lê, Ngọc Triệu Nguyễn, Văn Kết Thái, Thạch Bích Nguyễn, Văn Long Bigfin reef squid SCoT CBDP COI Genetic diversity Abstract Background Bigfn squid is one of the economically important seafood resources in Vietnam’s fsheries and the waters around Con Dao and Phu Quoc islands are two major fshing grounds where this species has been actively exploited. The start codon targeted polymorphism (SCoT) and CAAT box–derived polymorphism (CBDP) techniques were used to generate DNA fngerprinting data to analyze the genetic diversity, variation, and structure of the two populations in the waters surrounding Phu Quoc and Con Dao islands together with mitochondrial cytochrome C oxidase subunit I (COI) gene sequence data. Results Con Dao population possessed a higher diversity [expected heterozygosity (He) = 0.2254, Shannon index (I) = 0.3459, percentage of polymorphic bands (PPB) = 80.14%, nucleotide diversity (π) = 0.0336, haplotype diversity (h) = 0.910 with 16 haplotypes] than Phu Quoc population (He = 0.1854, I = 0.2873, PPB = 70.38%, π = 0.0246, h = 0.838 with 14 haplotypes). The genetic diversity at species level in the investigated region was at level of He = 0.2169, I = 0.3399, PPB = 86.41, π = 0.0289, and h = 0.892 with 24 haplotypes. Based on DNA fngerprinting data, the pair wise genetic similarity coefcients among individuals of the Con Dao population were lower (average of 0.7977) than the Phu Quoc population (average of 0.8316). Based on mitochondrial COI data, the pairwise genetic distances among individuals of the Con Dao population were higher (average of 0.0361) than the Phu Quoc population (average of 0.0263). Gene diferentiation (GST) between two investigated populations was 0.0316 and 0.0310 lead ing to the genetic distance was 0.0573 and 0.0213 and the gene fow between them was Nm = 8.2209 and 11.4700 migrants per generation among populations based on DNA fngerprinting and based on COI gene sequence data, respectively. Genetic variation within individuals of both populations (WP) played the key role in total genetic varia tion at species level in surveyed region. Conclusions For the bigfn reef squid species in the surveyed region, the Con Dao population had the higher genetic diversity than the Phu Quoc population, between them existed a low to moderate genetic diferentiation and a genetic exchange via gene fow. The DNA fngerprinting data better revealed the genetic diferentiation between the two surveyed populations while the mitochondrial COI gene sequence data could show the phylo genetic relationship among the surveyed individuals and the other from the sea regions in Southeast Asia. Based on the results obtained, fsheries management strategies are suggested toward the conservation and sustainable exploitation of this species. (2023) 21 116 1-13 2023-12-21T04:01:09Z 2023-12-21T04:01:09Z 2023-11 Journal article Bài báo đăng trên tạp chí thuộc ISI, bao gồm book chapter https://scholar.dlu.edu.vn/handle/123456789/3244 https://doi.org/10.1186/s43141-023-00573-y en Journal of Genetic Engineering and Biotechnology 1. Jereb P, Vecchione M, Roper CFE (2010) Family Loliginidae. In P. Jereb & CFE Roper, eds. Cephalopods of the world. An annotated and illustrated catalogue of species known to date. Volume 2. Myopsid and Oegopsid Squids. FAO Species Catalogue for Fishery Purposes. Rome, FAO 2(4): 38–117. 2. Duc NX, Duong TM, Thuy LD (1983) Species composition and exploited production of squid resources in the South Vietnam sea. Journal of Biology 1(2). 3. Aoki M, Imai H, Naruse T, Ikeda Y (2008) Low genetic diversity of oval squid, Sepioteuthis cf. lessoniana (Cephalopoda: Loliginidae), in Japanese waters inferred from a mitochondrial DNA non - coding region. Pacific Science 62: 403–411. 4. Cheng SH, Anderson FE, Bergman AM, Mahardika GN, Muchlisin ZA, Dang BT, Calumpong HP, Mohamed KS, Sasikumar G, Venkatesan V, Barber PH (2013) Molecular evidence for co - occurring cryptic lineages within the Sepioteuthis cf. lessoniana species complex in the Indian and Indo - West Pacific Oceans. Hydrobiologia 725(1): 165–188. 5. Young RE, Harman RF (1988) “Larva”, “paralarva” and “subadult” in cephalopod terminology. Malacologia 29: 201–208. 6. Zeidberg L, Hamner W (2002) Distribution of squid paralarvae, Loligo opalescens (Cephalopoda: Myopsida), in the Southern California Bight in the three years following the 1997 - 1998 El Niño. Marine Biology 141: 111–122. https://doi.org/10.1007/s00227-002-0813-x. 7. Pecl GT, Jackson GD (2007) The potential impacts of climate change on inshore squid: biology, ecology and fisheries. Reviews in Fish Biology and Fisheries 18(4): 373–385. 8. Edwards AJ (2020) Impact of climatic change on coral reefs, mangroves, and tropical seagrass ecosystems. Doeke Eisma (Eds), Climate Change: Impact on Coastal Habitation. Lewis Publishers, Boca Raton: 209–234. 9. Teixeira JC, Huber CD (2021) The inflated significance of neutral genetic diversity in conservation genetics. Proc Natl Acad Sci USA, 118(10). 10. Spielman D, Brook BW, Frankham R (2004) Most species are not driven to extinction before genetic factors impact them. Proc. Natl. Acad. Sci. USA. 101: 15261–15264. 11. Markert JA, Champlin DM, Gutjahr-Gobell R., Grear, J. S., Kuhn, A., McGreevy, T. J., Roth, A., Bagley, M. J. and Nacci, D. E. (2010) Population genetic diversity and fitness in multiple environments. BMC Evol. Biol. 10(1). doi:10.1186/1471-2148-10-205. 12. Pratoomchat B, Natsukari Y, Miki I, Chalermwat K (2001) Allozyme determination of genetic diversity in Japanese and Thai populations of oval squid (Sepioteuthis lessoniana Lesson, 1830). La mer 39: 133–139. 13. Tomano S, Ahmad – Syazni K, Ueta Y, Ohara K, Umino T (2013) Eleven Novel Polymorphic Microsatellite Loci for Oval Squid Sepioteuthis Lessoniana (Shiro - Ika Type). International Journal of Molecular 14: 19971–19975. 14. Zheng XD, Zuo ZR, Su XJ, Li Q (2012) Isolation and characterization of 24 polymorphic microsatellite loci in Sepioteuthis lessoniana. Genetics and Molecular Research, 11(4): 3961–3965. 15. Serra IA, Procaccini G, Intrieri MC, Migliaccio M, Mazzuca S, Innocenti AM (2007) Comparison of ISSR and SSR markers for analysis of genetic diversity in the seagrass Posidonia oceanica. Mar. Ecol. Prog. Ser. 338: 71–79. 16. Trieu LN, Bich TT, Ket NV (2022) Population genetic Diversity of Camellia Dilinhensis on the Di Linh plateau of Vietnam revealed by ISSR and SCoT markers. Dalat University Journal of Science 12(3): 43–55. 17. Borowsky RL (2001) Estimating Nucleotide Diversity from Random Amplified Polymorphic DNA and Amplified Fragment Length Polymorphism Data. Mol. Phylogenet. Evol. 18(1): 143–148. 18. Collard BCY, Mackill DJ (2008) Start Codon Targeted (SCoT) Polymorphism: A Simple, Novel DNA Marker Technique for Geneerating Genee - Targeted Markers in Plants. Plant Molecular Biology Reporter 27(1): 86 – 93. 19. 18. Singh AK, Rana MK, Singh S, Kumar S, Kumar R, Singh R (2013) CAAT box - derived polymorphism (CBDP): a novel promoter - targeted molecular marker for plants. Journal of Plant Biochem. Biotechnol 23(2): 175–183. 20. Zeinab AM, Mohammad A (2017) Using Start Codon Targeted (SCoT) polymorphism for Genetic Diversity Analysis of three Red Sea fishes (Family: Carangidae). IOSR Journal of Pharmacy and Biological Sciences 12(1): 50–56. 21. 20. Ali HAA (2020) Potential of Start Codon Targeted (SCoT) Markers and SDS-PAGE to Estimate Genetic Diversity and Relationships among Three Gastropods Species from The Mediterranean Sea, Port Said, Egypt. Egyptian Journal of Aquatic Biology & Fisheries 24(7): 133–143. 22. Ali HAA, Hala EA, Osama AA, Mohamed K (2020) Genetic Relationship Between Two Species of Genus Dicentrarchus Based on SCoT Markers and SDS – PAGE. Egypt. J. Aquat. Biol. Fish. 24(7): 393–402. 23. Romier C, Cocchiarella F, Mantovani R, Moras D (2002) The NF-YB/NF-YC Structure Gives Insight into DNA Binding and Transcription Regulation by CCAAT Factor NF-Y. Journal of Biological Chemistry 278(2): 1336–1345. doi:10.1074/jbc.m209635200. 24. Doyle JJ and Doyle JL (1987) A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochemical Bulletin 19: 11–15. 25. Adamkewicz SL, Harasewych MG (1996) Systematics and biogeography of the geneus Donax (Bivalvia: Donacidae) in eastern North America. American Malacological Bulletin 13(1): 97–103. 26. Weising K, Nybom H, Wolff K, Kahl G (2005). DNA fingerprinting in plants: Principles, methods, and applications (2nd ed.). CRCPress, Taylor & Francis Group. https://doi.org/10.1201/9781420040043. 27. Folmer O, Black M, Hoeh W, Lutz R, Vrijenhoek R (1994) DNA primers for amplification of mitochondrial cytochrome c oxidase subunit 1 from diverse metazoan invertebrates. Mol. Marine Biol. Biotechnol. 3: 294–299. 28. Kim DW, Yoo WG, Park HC, Yoo HS, Kang DW, Jin SD, Min HK, Paek WK, Lim J (2012) DNA barcoding of fish, insects, and shellfish in Korea. Genomics & informatics 10: 206 - 211. 29. Williams JGK, Kubelik AR, Livak KJ, Rafalski JA, Tingey SV (1990) DNA polymorphisms amplified by arbitrary primers are useful as genetic markers. Nucleic Acids Research 18: 6531–6535. 30. Carling MD, Brumfield RT (2007) Gene Sampling Strategies for Multi-Locus Population Estimates of Genetic Diversity. PLoS ONE 2, e160. 31. Yeh FC, Yang R, Boyle TJ, Ye Z, Xiyan JM (2000) PopGene32, Microsoft windows-based freeware for population genetic analysis, version 1.32. Molecular Biology and Biotechnology Centre: University of Alberta, Edmonton, Canada. 32. Rohlf FJ (2004) NTSYSpc numerical taxonomy and multivariate analysis system version 2.1 - User guide. Applied Biostatistics Inc. 33. Peakall R, Smouse PE (2012) GenAlEx 6.5: genetic analysis in Excel. Population genetic software for teaching and research – an update. Bioinformatics 28: 2537–2539. 34. Excoffier L, Lischer HEL (2010) Arlequin suite ver. 3.5: a new series of programs to perform population genetics analyses under Linux and Windows. Mol. Ecol. Resour. 10: 564–567. 35. Rozas J, Ferrer – Mata A, Sánchez – DelBarrio JC, Guirao – Rico S, Librado P, Ramos – Onsins SE, Sánchez – Gracia A (2017) DnaSP 6: DNA sequence polymorphism analysis of large data sets. Mol. Biol. Evol. 34: 3299–3302. 36. 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. 37. Felsenstein J (1985) Confidence limits on phylogenies: An approach using the bootstrap. Evol. 39: 783–791. 38. Mingting L, Jun W, Dongxiao W, Arnold LG, Song Y, Paola MR, Guoqing J (2019) Exploring the Importance of the Mindoro -Sibutu Pathway to the Upper - Layer Circulation of the South China Sea and the Indonesian Throughflow. JGR Oceans 124(7): 5054–5066. https://doi.org/10.1029/2018JC014910. 39. de Vicente MC, López C, Fulton T (2004) Genetic Diversity Analysis with Molecular Marker Data: Learning Module. International Plant Genetic Resources Institute (IPGRI), Rome, Italy. 40. Joana RF (2005) Molecular ecology. John Wiley & Sons Ltd., The Atrium, Southern Gate, Chichester, West Sussex PO19 8SQ, England. Springer Iran |