Development and Testing of Species-Specific Primers for Detecting the Presence of the Northern Pacific Sea Star (Asterias amurensis) from Environmental DNA
The starfish Asterias amurensis , a well-known predator of molluscan species in intertidal ecosystems, has caused substantial ecological and economic losses in North China such as offshore Qingdao. Effective monitoring and prevention measures are urged to minimize its negative impacts. Compared with...
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creator | Yang, Chenhu Du, Yanzhen Zeng, Xiaoqi Ni, Gang |
description | The starfish
Asterias amurensis
, a well-known predator of molluscan species in intertidal ecosystems, has caused substantial ecological and economic losses in North China such as offshore Qingdao. Effective monitoring and prevention measures are urged to minimize its negative impacts. Compared with traditional biomonitoring methods, environmental DNA technology has emerged as a powerful and cost-efficient tool for inferring species’ presence and abundance. In this study, we developed a pair of species-specific primers (i.e.,
Ast-F
and
Ast-R
) for the
A. amurensis
mitochondrial
COI
gene and tested its utility in amplifying and quantifying the DNA fragments from environmental samples under both laboratory and field conditions. The results of controlled water tank experiments demonstrated that the amount of eDNA released by
A. amurensis
was positively related to its biomass; after the removal of the starfish, the eDNA degraded significantly in 24 h and remained detectable for 8 days. The number of eDNA copies enriched tended to increase with smaller pore size of filter membrane and larger volume of filtered water. For field tests, we confirmed the validation of our approach in six locations in Qingdao by filtering 1000 ml water per sample with a 0.45-µm pore size filtration. All the amplification products generated a single and bright band via gel electrophoresis, and the quantitative PCR results unveiled significant differences in eDNA copies. This study provided an eDNA-based approach for investigating the distribution and biomass of
A. amurensis
, which may help to formulate early warning and management strategies in coastal Qingdao and other regions. |
doi_str_mv | 10.1007/s10126-024-10292-1 |
format | Article |
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Asterias amurensis
, a well-known predator of molluscan species in intertidal ecosystems, has caused substantial ecological and economic losses in North China such as offshore Qingdao. Effective monitoring and prevention measures are urged to minimize its negative impacts. Compared with traditional biomonitoring methods, environmental DNA technology has emerged as a powerful and cost-efficient tool for inferring species’ presence and abundance. In this study, we developed a pair of species-specific primers (i.e.,
Ast-F
and
Ast-R
) for the
A. amurensis
mitochondrial
COI
gene and tested its utility in amplifying and quantifying the DNA fragments from environmental samples under both laboratory and field conditions. The results of controlled water tank experiments demonstrated that the amount of eDNA released by
A. amurensis
was positively related to its biomass; after the removal of the starfish, the eDNA degraded significantly in 24 h and remained detectable for 8 days. The number of eDNA copies enriched tended to increase with smaller pore size of filter membrane and larger volume of filtered water. For field tests, we confirmed the validation of our approach in six locations in Qingdao by filtering 1000 ml water per sample with a 0.45-µm pore size filtration. All the amplification products generated a single and bright band via gel electrophoresis, and the quantitative PCR results unveiled significant differences in eDNA copies. This study provided an eDNA-based approach for investigating the distribution and biomass of
A. amurensis
, which may help to formulate early warning and management strategies in coastal Qingdao and other regions.</description><identifier>ISSN: 1436-2228</identifier><identifier>EISSN: 1436-2236</identifier><identifier>DOI: 10.1007/s10126-024-10292-1</identifier><identifier>PMID: 38341825</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Amplification ; Asterias ; Asterias amurensis ; Biomass ; Biomedical and Life Sciences ; Biomonitoring ; Coastal management ; COI protein ; cost effectiveness ; Deoxyribonucleic acid ; DNA ; Economic impact ; Electrophoresis ; Engineering ; Environmental DNA ; environmental monitoring ; Field tests ; filtration ; Freshwater & Marine Ecology ; Gel electrophoresis ; Gels ; genes ; Life Sciences ; littoral zone ; Microbiology ; mitochondria ; Mollusks ; Nucleotide sequence ; Offshore ; Pore size ; porosity ; Predators ; Primers ; quantitative polymerase chain reaction ; species ; Water purification ; Water tanks ; Zoology</subject><ispartof>Marine biotechnology (New York, N.Y.), 2024-04, Vol.26 (2), p.215-222</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c359t-a94b31daa14cf38ffaaf01ca71ab1206b85258f5bc46d39aa37a3de468d043583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10126-024-10292-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10126-024-10292-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38341825$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Chenhu</creatorcontrib><creatorcontrib>Du, Yanzhen</creatorcontrib><creatorcontrib>Zeng, Xiaoqi</creatorcontrib><creatorcontrib>Ni, Gang</creatorcontrib><title>Development and Testing of Species-Specific Primers for Detecting the Presence of the Northern Pacific Sea Star (Asterias amurensis) from Environmental DNA</title><title>Marine biotechnology (New York, N.Y.)</title><addtitle>Mar Biotechnol</addtitle><addtitle>Mar Biotechnol (NY)</addtitle><description>The starfish
Asterias amurensis
, a well-known predator of molluscan species in intertidal ecosystems, has caused substantial ecological and economic losses in North China such as offshore Qingdao. Effective monitoring and prevention measures are urged to minimize its negative impacts. Compared with traditional biomonitoring methods, environmental DNA technology has emerged as a powerful and cost-efficient tool for inferring species’ presence and abundance. In this study, we developed a pair of species-specific primers (i.e.,
Ast-F
and
Ast-R
) for the
A. amurensis
mitochondrial
COI
gene and tested its utility in amplifying and quantifying the DNA fragments from environmental samples under both laboratory and field conditions. The results of controlled water tank experiments demonstrated that the amount of eDNA released by
A. amurensis
was positively related to its biomass; after the removal of the starfish, the eDNA degraded significantly in 24 h and remained detectable for 8 days. The number of eDNA copies enriched tended to increase with smaller pore size of filter membrane and larger volume of filtered water. For field tests, we confirmed the validation of our approach in six locations in Qingdao by filtering 1000 ml water per sample with a 0.45-µm pore size filtration. All the amplification products generated a single and bright band via gel electrophoresis, and the quantitative PCR results unveiled significant differences in eDNA copies. This study provided an eDNA-based approach for investigating the distribution and biomass of
A. amurensis
, which may help to formulate early warning and management strategies in coastal Qingdao and other regions.</description><subject>Amplification</subject><subject>Asterias</subject><subject>Asterias amurensis</subject><subject>Biomass</subject><subject>Biomedical and Life Sciences</subject><subject>Biomonitoring</subject><subject>Coastal management</subject><subject>COI protein</subject><subject>cost effectiveness</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Economic impact</subject><subject>Electrophoresis</subject><subject>Engineering</subject><subject>Environmental DNA</subject><subject>environmental monitoring</subject><subject>Field tests</subject><subject>filtration</subject><subject>Freshwater & Marine Ecology</subject><subject>Gel electrophoresis</subject><subject>Gels</subject><subject>genes</subject><subject>Life Sciences</subject><subject>littoral zone</subject><subject>Microbiology</subject><subject>mitochondria</subject><subject>Mollusks</subject><subject>Nucleotide sequence</subject><subject>Offshore</subject><subject>Pore size</subject><subject>porosity</subject><subject>Predators</subject><subject>Primers</subject><subject>quantitative polymerase chain reaction</subject><subject>species</subject><subject>Water purification</subject><subject>Water tanks</subject><subject>Zoology</subject><issn>1436-2228</issn><issn>1436-2236</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1TAQhSMEoqXwAiyQJTZlEfBv4iyvesuPVJVKt6ytiTMuqRL7YieV-iy8LM5NKRILWI2t-c4Zj09RvGb0PaO0_pAYZbwqKZclo7zhJXtSHDMpqpJzUT19PHN9VLxI6ZZmUS3o8-JIaCGZ5uq4-LnFOxzCfkQ_EfAducY09f6GBEd2e7Q9pvJQXW_JVexHjIm4EMkWJ7QHcvqOuYMJvcVFttwvQ8wlenIFq3SHQHYTRHK6SRPGHhKBcY7oU5_eERfDSM79XR-DX14CA9lebl4WzxwMCV891JPi28fz67PP5cXXT1_ONhelFaqZSmhkK1gHwKR1QjsH4CizUDNoGadVqxVX2qnWyqoTDYCoQXQoK91RKZQWJ8Xp6ruP4cec9zdjnywOA3gMczKCKVExpTT_L5pTUFJLKqqMvv0LvQ1z9HkRI6hUom4asczmK2VjSCmiM_v8yRDvDaNmSdmsKZucsjmkbFgWvXmwntsRu0fJ71gzIFYg5Za_wfhn9j9sfwGW1rLX</recordid><startdate>20240401</startdate><enddate>20240401</enddate><creator>Yang, Chenhu</creator><creator>Du, Yanzhen</creator><creator>Zeng, Xiaoqi</creator><creator>Ni, Gang</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7TN</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H98</scope><scope>H99</scope><scope>K9.</scope><scope>L.F</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20240401</creationdate><title>Development and Testing of Species-Specific Primers for Detecting the Presence of the Northern Pacific Sea Star (Asterias amurensis) from Environmental DNA</title><author>Yang, Chenhu ; Du, Yanzhen ; Zeng, Xiaoqi ; Ni, Gang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-a94b31daa14cf38ffaaf01ca71ab1206b85258f5bc46d39aa37a3de468d043583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Amplification</topic><topic>Asterias</topic><topic>Asterias amurensis</topic><topic>Biomass</topic><topic>Biomedical and Life Sciences</topic><topic>Biomonitoring</topic><topic>Coastal management</topic><topic>COI protein</topic><topic>cost effectiveness</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Economic impact</topic><topic>Electrophoresis</topic><topic>Engineering</topic><topic>Environmental DNA</topic><topic>environmental monitoring</topic><topic>Field tests</topic><topic>filtration</topic><topic>Freshwater & Marine Ecology</topic><topic>Gel electrophoresis</topic><topic>Gels</topic><topic>genes</topic><topic>Life Sciences</topic><topic>littoral zone</topic><topic>Microbiology</topic><topic>mitochondria</topic><topic>Mollusks</topic><topic>Nucleotide sequence</topic><topic>Offshore</topic><topic>Pore size</topic><topic>porosity</topic><topic>Predators</topic><topic>Primers</topic><topic>quantitative polymerase chain reaction</topic><topic>species</topic><topic>Water purification</topic><topic>Water tanks</topic><topic>Zoology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Chenhu</creatorcontrib><creatorcontrib>Du, Yanzhen</creatorcontrib><creatorcontrib>Zeng, Xiaoqi</creatorcontrib><creatorcontrib>Ni, Gang</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Oceanic Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Marine biotechnology (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Chenhu</au><au>Du, Yanzhen</au><au>Zeng, Xiaoqi</au><au>Ni, Gang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development and Testing of Species-Specific Primers for Detecting the Presence of the Northern Pacific Sea Star (Asterias amurensis) from Environmental DNA</atitle><jtitle>Marine biotechnology (New York, N.Y.)</jtitle><stitle>Mar Biotechnol</stitle><addtitle>Mar Biotechnol (NY)</addtitle><date>2024-04-01</date><risdate>2024</risdate><volume>26</volume><issue>2</issue><spage>215</spage><epage>222</epage><pages>215-222</pages><issn>1436-2228</issn><eissn>1436-2236</eissn><abstract>The starfish
Asterias amurensis
, a well-known predator of molluscan species in intertidal ecosystems, has caused substantial ecological and economic losses in North China such as offshore Qingdao. Effective monitoring and prevention measures are urged to minimize its negative impacts. Compared with traditional biomonitoring methods, environmental DNA technology has emerged as a powerful and cost-efficient tool for inferring species’ presence and abundance. In this study, we developed a pair of species-specific primers (i.e.,
Ast-F
and
Ast-R
) for the
A. amurensis
mitochondrial
COI
gene and tested its utility in amplifying and quantifying the DNA fragments from environmental samples under both laboratory and field conditions. The results of controlled water tank experiments demonstrated that the amount of eDNA released by
A. amurensis
was positively related to its biomass; after the removal of the starfish, the eDNA degraded significantly in 24 h and remained detectable for 8 days. The number of eDNA copies enriched tended to increase with smaller pore size of filter membrane and larger volume of filtered water. For field tests, we confirmed the validation of our approach in six locations in Qingdao by filtering 1000 ml water per sample with a 0.45-µm pore size filtration. All the amplification products generated a single and bright band via gel electrophoresis, and the quantitative PCR results unveiled significant differences in eDNA copies. This study provided an eDNA-based approach for investigating the distribution and biomass of
A. amurensis
, which may help to formulate early warning and management strategies in coastal Qingdao and other regions.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>38341825</pmid><doi>10.1007/s10126-024-10292-1</doi><tpages>8</tpages></addata></record> |
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subjects | Amplification Asterias Asterias amurensis Biomass Biomedical and Life Sciences Biomonitoring Coastal management COI protein cost effectiveness Deoxyribonucleic acid DNA Economic impact Electrophoresis Engineering Environmental DNA environmental monitoring Field tests filtration Freshwater & Marine Ecology Gel electrophoresis Gels genes Life Sciences littoral zone Microbiology mitochondria Mollusks Nucleotide sequence Offshore Pore size porosity Predators Primers quantitative polymerase chain reaction species Water purification Water tanks Zoology |
title | Development and Testing of Species-Specific Primers for Detecting the Presence of the Northern Pacific Sea Star (Asterias amurensis) from Environmental DNA |
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