{"title":"16S rRNA基因在印度尼西亚北苏门答腊和亚齐红树林生态系统中的应用","authors":"Hatika Hairani, Rizka Amelia, Ipanna Enggar Susetya, Arida Susilowati, Yuntha Bimantara, Tadashi Kajita, Mohammad Basyuni","doi":"10.20473/jipk.v15i1.36686","DOIUrl":null,"url":null,"abstract":"Highlight Research\n\nThe genetic diversity of fish and shrimp from mangrove habitats was relatively substantial, with a heterozygosity of 0.926 and the exception of Langsa samples.\nAMOVA revealed that the diversity among individuals in the populations were higher compared to those within individuals.\nDNA barcode in mangroves is useful in developing mangrove conservation and restoration initiatives\n\n \nAbstract\nFish and shrimp are among the species that are vulnerable to high level of disturbance in mangrove ecosystem. This study aimed to investigate the implementation of 16S rRNA gene for fish and shrimp barcoding in mangrove ecosystems in North Sumatra and Aceh, Indonesia. 50 samples fresh fish and shrimp were collected from five mangrove ecosystems in North Sumatra, namely Belawan, Lubuk Kertang, Percut Sei Tuan, and Pulau Sembilan and Langsa of Aceh for DNA extraction process. The research was divided into four activities: sample collection, DNA isolation, PCR amplification, and data analysis. DNA was extracted using kit extraction (kit Reliaprep gDNA Tissue Miniprep System) and with PCR amplification. Genetic parameters were analyzed using Gen Alex 6.51 software and the relationship between sites was examined using the MVSP 3.22. The genetic diversity of fish and shrimp from mangrove habitats was relatively substantial, according to the findings, with a heterozygosity of 0.926, with the exception of Langsa samples, which were only identified in subclass A1. Genetic relationship between sites revealed that all samples clustered into two branches and were randomly dispersed within each site. This work confirmed the 16S rRNA gene worked for fish and shrimp barcoding in mangrove ecosystems, North Sumatra and Aceh, Indonesia and our findings are expected to be useful in developing mangrove conservation and restoration initiatives.","PeriodicalId":17760,"journal":{"name":"Jurnal Ilmiah Perikanan dan Kelautan","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Implementation of 16S rRNA Gene for Fish and Shrimp Barcoding in Mangrove Ecosystems in North Sumatra and Aceh, Indonesia\",\"authors\":\"Hatika Hairani, Rizka Amelia, Ipanna Enggar Susetya, Arida Susilowati, Yuntha Bimantara, Tadashi Kajita, Mohammad Basyuni\",\"doi\":\"10.20473/jipk.v15i1.36686\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Highlight Research\\n\\nThe genetic diversity of fish and shrimp from mangrove habitats was relatively substantial, with a heterozygosity of 0.926 and the exception of Langsa samples.\\nAMOVA revealed that the diversity among individuals in the populations were higher compared to those within individuals.\\nDNA barcode in mangroves is useful in developing mangrove conservation and restoration initiatives\\n\\n \\nAbstract\\nFish and shrimp are among the species that are vulnerable to high level of disturbance in mangrove ecosystem. This study aimed to investigate the implementation of 16S rRNA gene for fish and shrimp barcoding in mangrove ecosystems in North Sumatra and Aceh, Indonesia. 50 samples fresh fish and shrimp were collected from five mangrove ecosystems in North Sumatra, namely Belawan, Lubuk Kertang, Percut Sei Tuan, and Pulau Sembilan and Langsa of Aceh for DNA extraction process. The research was divided into four activities: sample collection, DNA isolation, PCR amplification, and data analysis. DNA was extracted using kit extraction (kit Reliaprep gDNA Tissue Miniprep System) and with PCR amplification. Genetic parameters were analyzed using Gen Alex 6.51 software and the relationship between sites was examined using the MVSP 3.22. The genetic diversity of fish and shrimp from mangrove habitats was relatively substantial, according to the findings, with a heterozygosity of 0.926, with the exception of Langsa samples, which were only identified in subclass A1. Genetic relationship between sites revealed that all samples clustered into two branches and were randomly dispersed within each site. This work confirmed the 16S rRNA gene worked for fish and shrimp barcoding in mangrove ecosystems, North Sumatra and Aceh, Indonesia and our findings are expected to be useful in developing mangrove conservation and restoration initiatives.\",\"PeriodicalId\":17760,\"journal\":{\"name\":\"Jurnal Ilmiah Perikanan dan Kelautan\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Jurnal Ilmiah Perikanan dan Kelautan\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.20473/jipk.v15i1.36686\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Agricultural and Biological Sciences\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Jurnal Ilmiah Perikanan dan Kelautan","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20473/jipk.v15i1.36686","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
引用次数: 0
摘要
亮点研究红树林生境鱼虾的遗传多样性相对较大,杂合度为0.926,Langsa样本除外。AMOVA显示,与个体内部相比,种群中个体之间的多样性更高。红树林中的DNA条形码有助于制定红树林保护和恢复计划摘要鱼类和虾是红树林生态系统中易受高度干扰的物种之一。本研究旨在调查16S rRNA基因在印度尼西亚北苏门答腊和亚齐红树林生态系统中的应用。从北苏门答腊的五个红树林生态系统,即Belawan、Lubuk Kertang、Perct Sei Tuan以及亚齐的Pulau Sembilan和Langsa,采集了50份鲜鱼和虾样本进行DNA提取。该研究分为四项活动:样本采集、DNA分离、PCR扩增和数据分析。使用试剂盒提取(试剂盒Reliaprep gDNA Tissue Miniprep System)和PCR扩增提取DNA。使用Gen Alex 6.51软件分析遗传参数,并使用MVSP 3.22检查位点之间的关系。根据研究结果,红树林栖息地的鱼类和虾的遗传多样性相对较大,杂合度为0.926,但Langsa样本除外,它们仅在A1亚类中被鉴定。位点之间的遗传关系表明,所有样本都聚集成两个分支,并随机分布在每个位点内。这项工作证实了16S rRNA基因在印度尼西亚北苏门答腊和亚齐的红树林生态系统中对鱼虾条形码起作用,我们的发现有望对制定红树林保护和恢复计划有用。
Implementation of 16S rRNA Gene for Fish and Shrimp Barcoding in Mangrove Ecosystems in North Sumatra and Aceh, Indonesia
Highlight Research
The genetic diversity of fish and shrimp from mangrove habitats was relatively substantial, with a heterozygosity of 0.926 and the exception of Langsa samples.
AMOVA revealed that the diversity among individuals in the populations were higher compared to those within individuals.
DNA barcode in mangroves is useful in developing mangrove conservation and restoration initiatives
Abstract
Fish and shrimp are among the species that are vulnerable to high level of disturbance in mangrove ecosystem. This study aimed to investigate the implementation of 16S rRNA gene for fish and shrimp barcoding in mangrove ecosystems in North Sumatra and Aceh, Indonesia. 50 samples fresh fish and shrimp were collected from five mangrove ecosystems in North Sumatra, namely Belawan, Lubuk Kertang, Percut Sei Tuan, and Pulau Sembilan and Langsa of Aceh for DNA extraction process. The research was divided into four activities: sample collection, DNA isolation, PCR amplification, and data analysis. DNA was extracted using kit extraction (kit Reliaprep gDNA Tissue Miniprep System) and with PCR amplification. Genetic parameters were analyzed using Gen Alex 6.51 software and the relationship between sites was examined using the MVSP 3.22. The genetic diversity of fish and shrimp from mangrove habitats was relatively substantial, according to the findings, with a heterozygosity of 0.926, with the exception of Langsa samples, which were only identified in subclass A1. Genetic relationship between sites revealed that all samples clustered into two branches and were randomly dispersed within each site. This work confirmed the 16S rRNA gene worked for fish and shrimp barcoding in mangrove ecosystems, North Sumatra and Aceh, Indonesia and our findings are expected to be useful in developing mangrove conservation and restoration initiatives.