DOI QR코드

DOI QR Code

Analysis of genetic differentiation and population structure of the Korean-peninsula-endemic genus, Semisulcospira, using mitochondrial markers

  • Eun-Mi Kim (Biotechnology Research Division, National Institute of Fisheries Science) ;
  • Yeon Jung Park (National Fishery Products Quality Management Service) ;
  • Hye Min Lee (Biotechnology Research Division, National Institute of Fisheries Science) ;
  • Eun Soo Noh (Biotechnology Research Division, National Institute of Fisheries Science) ;
  • Jung-Ha Kang (West Sea Fisheries Research Institute, National Institute of Fisheries Science) ;
  • Bo-Hye Nam (Biotechnology Research Division, National Institute of Fisheries Science) ;
  • Young-Ok Kim (Biotechnology Research Division, National Institute of Fisheries Science) ;
  • Tae-Jin Choi (Department of Microbiology, Pukyoung National University)
  • Received : 2022.08.10
  • Accepted : 2022.10.12
  • Published : 2022.12.31

Abstract

The genus Semisulcospira is an economically and ecologically valuable freshwater resource. Among the species, Semisulcospira coreana, Semisulcospira forticosta and Semisulcospira tegulata are endemic to the Korean peninsula and Semisulcospira gottschei is widespread in Asia. Therefore, maintenance and conservation of wild populations of these snails are important. We investigated the genetic diversity and population structure of Semisulcospira based on the mitochondrial cytochrome c oxidase subunit I (COI), NADH dehydrogenase subunit 4 (ND4), and combined mitochondrial DNA (COI + ND4) sequences. All four species and various genetic makers showed a high level of haplotype diversity and a low level of nucleotide diversity. In addition, Fu's Fs and Tajima's D neutrality tests were performed to assess the variation in size among populations. Neutrality tests of the four species yielded negative Fu's Fs and Tajima's D values, except for populations with one haplotype. The minimum spanning network indicated a common haplotype for populations of S. coreana, S. tegulata and S. gottschei, whereas S. forticosta had a rare haplotype. Also, genetic differences and gene flows between populations were assessed by analysis of molecular variance and using the pairwise fixation index. Our findings provided insight into the degree of preservation of the species' genetic diversity and could be utilized to enhance the management of endemic species.

Keywords

Acknowledgement

This work was supported by grant from the National Institute of Fisheries Science (R2022044, R2022045).

References

  1. An HS, Lee JW, Dong CM. Population genetic structure of Korean pen shell (Atrina pectinata) in Korea inferred from microsatellite marker analysis. Genes Genomics. 2012;34:681-8. https://doi.org/10.1007/s13258-012-0091-z
  2. Anderson S. Area and endemism. Q Rev Biol. 1994;69:451-71. https://doi.org/10.1086/418743
  3. Arnaud S, Monteforte M, Galtier N, Bonhomme F, Blanc F. Population structure and genetic variability of pearl oyster Pinctada mazatlanica along Pacific coasts from Mexico to Panama. Conserv Genet. 2000;1:299-308. https://doi.org/10.1023/A:1011575722481
  4. Bae HG, Suk HY. Population genetic structure and colonization history of short ninespine sticklebacks (Pungitius kaibarae). Ecol Evol. 2015;5:3075-89. https://doi.org/10.1002/ece3.1594
  5. Bouckaert R, Heled J, Kuhnert D, Vaughan T, Wu CH, Xie D, et al. BEAST 2: a software platform for Bayesian evolutionary analysis. PLOS Comput Biol. 2014;10:e1003537.
  6. Chen CA, Ablan MCA, McManus JW, Bell JD, Tuan VS, Cabanban AS, et al. Population structure and genetic variability of six bar wrasse (Thallasoma hardwicki) in northern South China Sea revealed by mitochondrial control region sequences. Mar Biotechnol. 2004;6:312-26.  https://doi.org/10.1007/s10126-003-0028-2
  7. Chiu YW, Bor H, Kuo PH, Hsu KC, Tan MS, Wang WK, et al. Origins of Semisulcospira libertina (gastropoda: semisulcospiridae) in Taiwan. Mitochondrial DNA A DNA Mapp Seq Anal. 2017;28:518-25.
  8. Chiu YW, Bor H, Tan MS, Lin HD, Jean CT. Phylogeography and genetic differentiation among populations of the moon turban snail Lunella granulata Gmelin, 1791 (Gastropoda: Turbinidae). Int J Mol Sci. 2013;14:9062-79. https://doi.org/10.3390/ijms14059062
  9. Cho MY, Won KM, Han HJ, Kim HJ, Jee BY, Kim SR, et al. Currant status of detection of aquatic animal pathogens in cultured juveniles for stock enhancement from 2009 to 2012. The Korean Society of Fish Pathology. 2013;26:99-110.
  10. De Jong MA, Wahlberg N, Van Eijk M, Brakefield PM, Zwaan BJ. Mitochondrial DNA signature for range-wide populations of Bicyclus anynana suggests a rapid expansion from recent refugia. PLOS ONE. 2011;6:e21385.
  11. Doosey MH, Bart HL Jr, Saitoh K, Miya M. Phylogenetic relationships of catostomid fishes (Actinopterygii: Cypriniformes) based on mitochondrial ND4/ND5 gene sequences. Mol Phylogenetics Evol. 2010;54:1028-34. https://doi.org/10.1016/j.ympev.2009.06.006
  12. Drummond AJ, Rambaut A, Shapiro B, Pybus OG. Bayesian coalescent inference of past population dynamics from molecular sequences. Mol Biol Evol. 2005;22:1185-92. https://doi.org/10.1093/molbev/msi103
  13. Dunham RA. Aquaculture and fisheries biotechnology: genetic approaches. Wallingford: CABI; 2004.
  14. Fu YX. Statistical tests of neutrality of mutations against population growth, hitchhiking and background selection. Genetics. 1997;147:915-25. https://doi.org/10.1093/genetics/147.2.915
  15. Grant WAS, Bowen BW. Shallow population histories in deep evolutionary lineages of marine fishes: insights from sardines and anchovies and lessons for conservation. J Hered. 1998;89:415-26. https://doi.org/10.1093/jhered/89.5.415
  16. Gu QH, Cheng QQ, Li XJ, Zhou CJ. Novel polymorphic microsatellite markers for Bellamya and their application in population genetics of three species. Genet Mol Res. 2015;14:15201-12. https://doi.org/10.4238/2015.November.25.8
  17. Hillis DM, Mable BK, Moritz C. Applications of molecular systematics: the state of the field and a look to the future. In: Hillis DM, Moritz C, Mable BK, editors. Molecular systematics. Sunderland, MA: Sinauer Associates; 1996. p. 515-43.
  18. Holland BS, Cowie RH. A geographic mosaic of passive dispersal: population structure in the endemic Hawaiian amber snail Succinea caduca (Mighels, 1845). Mol Ecol. 2007;16:2422-35. https://doi.org/10.1111/j.1365-294X.2007.03246.x
  19. Jacquemyn H, Honnay O, Galbusera P, Roldan-Ruiz I. Genetic structure of the forest herb Primula elatior in a changing landscape. Mol Ecol. 2004;13:211-9. https://doi.org/10.1046/j.1365-294X.2003.02033.x
  20. Jang SJ, Ko MH, Kwan Y, Won YJ. Population genetic structure of the Korean endemic species, Iksookimia pacifica (Pisces: Cobitidae) distributed in northeast Korea. Korean J Environ Ecol. 2017;31:461-71. https://doi.org/10.13047/KJEE.2017.31.5.461
  21. Jung Y, Park GM, Park J, Kim JJ, Min DY, Chung PR. Allozyme variability in three species of genus Semisulcospira (Prosobranchia: Pleuroceridae). Korean J Malacol. 1999;15:13-20.
  22. Kang JH, Yu KH, Kim SK, Park JY, Kim BS, An CM. Species identification and genetic structure of Octopus minor from Korea and China on the basis of partial sequences of mitochondrial cytochrome oxidase I. Korean J Malacol. 2010;26:285-90.
  23. Katsares V, Tsiora A, Galinou-Mitsoudi S, Imsiridou A. Genetic structure of the endangered species Pinna nobilis (Mollusca: Bivalvia) inferred from mtDNA sequences. Biologia. 2008;63:412-7. https://doi.org/10.2478/s11756-008-0061-8
  24. Khosravi R, Malekian M, Hemami MR, Silva TL, Brito JC. Low genetic diversity in the vulnerable Goitred Gazelle, Gazella subgutturosa (Cetartiodactyla: Bovidae), in Iran: potential genetic consequence of recent population declines. Zool Middle East. 2019;65:104-15.
  25. Kim DH, Bang IC, Lee WO, Baek JM. Reproductive ecology of the freshwater melania snail, Semisulcospira coreana (v. Martens) in Bukhan river. Korean J Malacol. 2012;28:175-85. https://doi.org/10.9710/kjm.2012.28.2.175
  26. Kim WJ, Kim DH, Lee JS, Bang IC, Lee WO, Jung H. Systematic relationships of Korean freshwater snails of Semisulcospira, Koreanomelania, and Koreoleptoxis (Cerithiodiea; Pleuroceridae) revealed by mitochondrial cytochrome oxidase I sequences. Korean J Malacol. 2010;26:275-83.
  27. Kohler F. Rampant taxonomic incongruence in a mitochondrial phylogeny of Semisulcospira freshwater snails from Japan (Cerithioidea: Semisulcospiridae). J Molluscan Stud. 2016;82:268-81. https://doi.org/10.1093/mollus/eyv057
  28. Lynch M. Evolution of the mutation rate. Trends Genet. 2010; 26:345-352. https://doi.org/10.1016/j.tig.2010.05.003
  29. Matsumoto M. Phylogenetic analysis of the subclass Pteriomorphia (Bivalvia) from mtDNA COI sequences. Mol Phylogenet Evol. 2003;27:429-40. https://doi.org/10.1016/S1055-7903(03)00013-7
  30. McGlashan DJ, Hughes JM. Reconciling patterns of genetic variation with stream structure, earth history and biology in the Australian freshwater fish Craterocephalus stercusmuscarum (Atherinidae). Mol Ecol. 2000;9:1737-51. https://doi.org/10.1046/j.1365-294x.2000.01054.x
  31. Nehemia A, Ngendu Y, Kochzius M. Genetic population structure of the mangrove snails Littoraria subvittata and L. pallescens in the Western Indian Ocean. J Exp Mar Biol Ecol. 2019;514-515:27-33. https://doi.org/10.1016/j.jembe.2019.03.005
  32. Nguyen LT, Schmidt HA, von Haeseler A, Minh BQ. IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol Biol Evol. 2015;32:268-74. https://doi.org/10.1093/molbev/msu300
  33. Pan B, Wang Z, He X. Studies on assemblage characteristics of macrozoobenthos in the West River. Acta Hydrobiol Sin. 2011;35:851-6.
  34. Park YJ, Lee MN, Kang JH, Park JY, Noh JK, Choi TJ, et al. Population genetic structure of Semisulcospira gottschei: simultaneous examination of mtDNA and microsatellite markers. Mol Biol Rep. 2021;48:97-104. https://doi.org/10.1007/s11033-020-05821-9
  35. Pfenninger M, Salinger M, Haun T, Feldmeyer B. Factors and processes shaping the population structure and distribution of genetic variation across the species range of the freshwater snail Radix balthica (Pulmonata, Basommatophora). BMC Evol Biol. 2011;11:135.
  36. Puvanasundram P, Esa YB, Rahim KAA, Nurul Amin SM. Phylogeography and population structure of Tenualosa toli inferred from Cytochrome b mitochondrial DNA fragment. J Environ Biol. 2018;39:895-906. https://doi.org/10.22438/jeb/39/5(SI)/26
  37. Rambaut A, Drummond AJ, Xie D, Baele G, Suchard MA. Posterior summarization in Bayesian phylogenetics using Tracer 1.7. Syst Biol. 2018;67:901-4. https://doi.org/10.1093/sysbio/syy032
  38. Regnier C, Fontaine B, Bouchet P. Not knowing, not recording, not listing: numerous unnoticed mollusk extinctions. Conserv Biol. 2009;23:1214-21. https://doi.org/10.1111/j.1523-1739.2009.01245.x
  39. Strayer DL, Dudgeon D. Freshwater biodiversity conservation: recent progress and future challenges. J North Am Benthol Soc. 2010;29:344-58. https://doi.org/10.1899/08-171.1
  40. Strong EE, Whelan NV. Assessing the diversity of Western North American Juga (Semisulcospiridae, Gastropoda). Mol Phylogenet Evol. 2019;136:87-103. https://doi.org/10.1016/j.ympev.2019.04.009
  41. Ward RD, Zemlak TS, Innes BH, Last PR, Hebert PDN. DNA barcoding Australia's fish species. Philos Trans R Soc Lond B Biol Sci. 2005;360:1847-57. https://doi.org/10.1098/rstb.2005.1716
  42. Wright S. The interpretation of population structure by F-statistics with special regard to systems of mating. Evolution. 1965;19:395-420. https://doi.org/10.2307/2406450
  43. Zein-Eddine R, Djuikwo-Teukeng FF, Dar Y, Dreyfuss G, Van den Broeck F. Population genetics of the Schistosoma snail host Bulinus truncatus in Egypt. Acta Trop. 2017;172:36-43. https://doi.org/10.1016/j.actatropica.2017.04.002