Combination of restriction endonuclease digestion with the ΔΔCt method in real-time PCR to monitor etoxazole resistance allele frequency in the two-spotted spider mite
Monitoring resistance allele frequency at the early stage of resistance development is important for the successful acaricide resistance management. Etoxazole is a mite growth inhibitor to which resistance is conferred by an amino acid substitution in the chitin synthase 1 (CHS1; I1017F) in T. urtic...
Gespeichert in:
Veröffentlicht in: | Pesticide biochemistry and physiology 2017-06, Vol.139, p.1-8 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 8 |
---|---|
container_issue | |
container_start_page | 1 |
container_title | Pesticide biochemistry and physiology |
container_volume | 139 |
creator | Osakabe, Masahiro Imamura, Tsuyoshi Nakano, Ryohei Kamikawa, Satoshi Tadatsu, Misono Kunimoto, Yoshinori Doi, Makoto |
description | Monitoring resistance allele frequency at the early stage of resistance development is important for the successful acaricide resistance management. Etoxazole is a mite growth inhibitor to which resistance is conferred by an amino acid substitution in the chitin synthase 1 (CHS1; I1017F) in T. urticae. If the susceptible allele can be specifically digested by restriction endonuclease, the ΔΔCt method using real-time PCR for genomic DNA (RED-ΔΔCt method) may be available for monitoring the resistance allele frequency. We tested whether the etoxazole resistance allele frequency in a pooled sample was accurately measured by the RED-ΔΔCt method and validated whether the resistance variant frequency was correlated with etoxazole resistance phenotype in a bioassay. Finally, we performed a pilot test using field populations. Strong linearity of the measures by the RED-ΔΔCt method with practical resistance allele frequencies; resistance allele frequency in the range between 0.5% to at least 0.75% was strictly represented. The strong linear relationship between hatchability of haploid male eggs after the etoxazole treatments (phenotype) and resistance allele frequencies in their mothers provided direct evidence that I1017F is a primary resistance factor to etoxazole in the strains used for experiments. The pilot test revealed a significant correlation between egg hatchability (including both diploid female eggs and haploid male eggs) and estimators in field populations. Consequently, we concluded that the RED-ΔΔCt method is a powerful tool for monitoring a resistance allele in a pooled sample.
[Display omitted]
•“The RED-ΔΔCt method” to monitor etoxazole-resistance allele frequency was developed in the two-spotted spider mite.•The resistant variant at ≥0.5% in a pooled DNA sample was accurately measured.•The resistance variant frequency was practically correlated with resistant phenotype in a bioassay.•The RED-ΔΔCt method is a powerful tool for monitoring rare resistance alleles. |
doi_str_mv | 10.1016/j.pestbp.2017.04.003 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1908432609</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0048357517300950</els_id><sourcerecordid>1908432609</sourcerecordid><originalsourceid>FETCH-LOGICAL-c362t-2ebdcef0d48e7d9ab3b889c2bc7eed6e484087b361e492eb27a95b58484b03a63</originalsourceid><addsrcrecordid>eNp9kU1u1TAUhS0Eoo_CDhDykEnCTeIk9gQJRVCQKoEQjC3_3PD8lMTB9qO06-gm2EzXhMMrDBlZPj7nXNsfIc8rKCuouleHcsWY9FrWUPUlsBKgeUB2FYi2EKIRD8kOgPGiafv2jDyJ8QAAgoF4TM5q3opWVN2O_Br8rN2ikvML9SMNuTM482eLi_XL0UyoIlLrvuWjTb5yaU_THund7d3tkOiMae8tdUsOq6lIbkb6afhMk6ezX1zygWLyP9WNn3DrdzGpxSBV04RZGQN-P-JirreGrTZd-SKuPiW0NK7OYqCzS_iUPBrVFPHZ_XpOvr57-2V4X1x-vPgwvLksTNPVqahRW4MjWMaxt0LpRnMuTK1Nj2g7ZJwB73XTVchENte9Eq1uedY1NKprzsnLU-8afL5YTHJ20eA0qQX9McpKAGdN3YHIVnaymuBjDDjKNbhZhWtZgdwgyYM8QZIbJAlMZkg59uJ-wlHPaP-F_lLJhtcnA-Z3_nAYZDQufxFaF9Akab37_4Tf-1KrPw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1908432609</pqid></control><display><type>article</type><title>Combination of restriction endonuclease digestion with the ΔΔCt method in real-time PCR to monitor etoxazole resistance allele frequency in the two-spotted spider mite</title><source>Elsevier ScienceDirect Journals Complete - AutoHoldings</source><source>MEDLINE</source><creator>Osakabe, Masahiro ; Imamura, Tsuyoshi ; Nakano, Ryohei ; Kamikawa, Satoshi ; Tadatsu, Misono ; Kunimoto, Yoshinori ; Doi, Makoto</creator><creatorcontrib>Osakabe, Masahiro ; Imamura, Tsuyoshi ; Nakano, Ryohei ; Kamikawa, Satoshi ; Tadatsu, Misono ; Kunimoto, Yoshinori ; Doi, Makoto</creatorcontrib><description>Monitoring resistance allele frequency at the early stage of resistance development is important for the successful acaricide resistance management. Etoxazole is a mite growth inhibitor to which resistance is conferred by an amino acid substitution in the chitin synthase 1 (CHS1; I1017F) in T. urticae. If the susceptible allele can be specifically digested by restriction endonuclease, the ΔΔCt method using real-time PCR for genomic DNA (RED-ΔΔCt method) may be available for monitoring the resistance allele frequency. We tested whether the etoxazole resistance allele frequency in a pooled sample was accurately measured by the RED-ΔΔCt method and validated whether the resistance variant frequency was correlated with etoxazole resistance phenotype in a bioassay. Finally, we performed a pilot test using field populations. Strong linearity of the measures by the RED-ΔΔCt method with practical resistance allele frequencies; resistance allele frequency in the range between 0.5% to at least 0.75% was strictly represented. The strong linear relationship between hatchability of haploid male eggs after the etoxazole treatments (phenotype) and resistance allele frequencies in their mothers provided direct evidence that I1017F is a primary resistance factor to etoxazole in the strains used for experiments. The pilot test revealed a significant correlation between egg hatchability (including both diploid female eggs and haploid male eggs) and estimators in field populations. Consequently, we concluded that the RED-ΔΔCt method is a powerful tool for monitoring a resistance allele in a pooled sample.
[Display omitted]
•“The RED-ΔΔCt method” to monitor etoxazole-resistance allele frequency was developed in the two-spotted spider mite.•The resistant variant at ≥0.5% in a pooled DNA sample was accurately measured.•The resistance variant frequency was practically correlated with resistant phenotype in a bioassay.•The RED-ΔΔCt method is a powerful tool for monitoring rare resistance alleles.</description><identifier>ISSN: 0048-3575</identifier><identifier>EISSN: 1095-9939</identifier><identifier>DOI: 10.1016/j.pestbp.2017.04.003</identifier><identifier>PMID: 28595916</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Acari ; Acaricide resistance ; Animals ; Chitin synthase 1 ; CHS1 ; DNA Restriction Enzymes - metabolism ; Drug Resistance - genetics ; Female ; Gene Frequency - drug effects ; Male ; Oxazoles - pharmacology ; qPCR ; Real-Time Polymerase Chain Reaction - methods ; Tetranychidae ; Tetranychidae - drug effects ; Tetranychidae - genetics ; Tetranychus urticae</subject><ispartof>Pesticide biochemistry and physiology, 2017-06, Vol.139, p.1-8</ispartof><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-2ebdcef0d48e7d9ab3b889c2bc7eed6e484087b361e492eb27a95b58484b03a63</citedby><cites>FETCH-LOGICAL-c362t-2ebdcef0d48e7d9ab3b889c2bc7eed6e484087b361e492eb27a95b58484b03a63</cites><orcidid>0000-0002-2246-3431</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.pestbp.2017.04.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27907,27908,45978</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28595916$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Osakabe, Masahiro</creatorcontrib><creatorcontrib>Imamura, Tsuyoshi</creatorcontrib><creatorcontrib>Nakano, Ryohei</creatorcontrib><creatorcontrib>Kamikawa, Satoshi</creatorcontrib><creatorcontrib>Tadatsu, Misono</creatorcontrib><creatorcontrib>Kunimoto, Yoshinori</creatorcontrib><creatorcontrib>Doi, Makoto</creatorcontrib><title>Combination of restriction endonuclease digestion with the ΔΔCt method in real-time PCR to monitor etoxazole resistance allele frequency in the two-spotted spider mite</title><title>Pesticide biochemistry and physiology</title><addtitle>Pestic Biochem Physiol</addtitle><description>Monitoring resistance allele frequency at the early stage of resistance development is important for the successful acaricide resistance management. Etoxazole is a mite growth inhibitor to which resistance is conferred by an amino acid substitution in the chitin synthase 1 (CHS1; I1017F) in T. urticae. If the susceptible allele can be specifically digested by restriction endonuclease, the ΔΔCt method using real-time PCR for genomic DNA (RED-ΔΔCt method) may be available for monitoring the resistance allele frequency. We tested whether the etoxazole resistance allele frequency in a pooled sample was accurately measured by the RED-ΔΔCt method and validated whether the resistance variant frequency was correlated with etoxazole resistance phenotype in a bioassay. Finally, we performed a pilot test using field populations. Strong linearity of the measures by the RED-ΔΔCt method with practical resistance allele frequencies; resistance allele frequency in the range between 0.5% to at least 0.75% was strictly represented. The strong linear relationship between hatchability of haploid male eggs after the etoxazole treatments (phenotype) and resistance allele frequencies in their mothers provided direct evidence that I1017F is a primary resistance factor to etoxazole in the strains used for experiments. The pilot test revealed a significant correlation between egg hatchability (including both diploid female eggs and haploid male eggs) and estimators in field populations. Consequently, we concluded that the RED-ΔΔCt method is a powerful tool for monitoring a resistance allele in a pooled sample.
[Display omitted]
•“The RED-ΔΔCt method” to monitor etoxazole-resistance allele frequency was developed in the two-spotted spider mite.•The resistant variant at ≥0.5% in a pooled DNA sample was accurately measured.•The resistance variant frequency was practically correlated with resistant phenotype in a bioassay.•The RED-ΔΔCt method is a powerful tool for monitoring rare resistance alleles.</description><subject>Acari</subject><subject>Acaricide resistance</subject><subject>Animals</subject><subject>Chitin synthase 1</subject><subject>CHS1</subject><subject>DNA Restriction Enzymes - metabolism</subject><subject>Drug Resistance - genetics</subject><subject>Female</subject><subject>Gene Frequency - drug effects</subject><subject>Male</subject><subject>Oxazoles - pharmacology</subject><subject>qPCR</subject><subject>Real-Time Polymerase Chain Reaction - methods</subject><subject>Tetranychidae</subject><subject>Tetranychidae - drug effects</subject><subject>Tetranychidae - genetics</subject><subject>Tetranychus urticae</subject><issn>0048-3575</issn><issn>1095-9939</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1u1TAUhS0Eoo_CDhDykEnCTeIk9gQJRVCQKoEQjC3_3PD8lMTB9qO06-gm2EzXhMMrDBlZPj7nXNsfIc8rKCuouleHcsWY9FrWUPUlsBKgeUB2FYi2EKIRD8kOgPGiafv2jDyJ8QAAgoF4TM5q3opWVN2O_Br8rN2ikvML9SMNuTM482eLi_XL0UyoIlLrvuWjTb5yaU_THund7d3tkOiMae8tdUsOq6lIbkb6afhMk6ezX1zygWLyP9WNn3DrdzGpxSBV04RZGQN-P-JirreGrTZd-SKuPiW0NK7OYqCzS_iUPBrVFPHZ_XpOvr57-2V4X1x-vPgwvLksTNPVqahRW4MjWMaxt0LpRnMuTK1Nj2g7ZJwB73XTVchENte9Eq1uedY1NKprzsnLU-8afL5YTHJ20eA0qQX9McpKAGdN3YHIVnaymuBjDDjKNbhZhWtZgdwgyYM8QZIbJAlMZkg59uJ-wlHPaP-F_lLJhtcnA-Z3_nAYZDQufxFaF9Akab37_4Tf-1KrPw</recordid><startdate>201706</startdate><enddate>201706</enddate><creator>Osakabe, Masahiro</creator><creator>Imamura, Tsuyoshi</creator><creator>Nakano, Ryohei</creator><creator>Kamikawa, Satoshi</creator><creator>Tadatsu, Misono</creator><creator>Kunimoto, Yoshinori</creator><creator>Doi, Makoto</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2246-3431</orcidid></search><sort><creationdate>201706</creationdate><title>Combination of restriction endonuclease digestion with the ΔΔCt method in real-time PCR to monitor etoxazole resistance allele frequency in the two-spotted spider mite</title><author>Osakabe, Masahiro ; Imamura, Tsuyoshi ; Nakano, Ryohei ; Kamikawa, Satoshi ; Tadatsu, Misono ; Kunimoto, Yoshinori ; Doi, Makoto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-2ebdcef0d48e7d9ab3b889c2bc7eed6e484087b361e492eb27a95b58484b03a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acari</topic><topic>Acaricide resistance</topic><topic>Animals</topic><topic>Chitin synthase 1</topic><topic>CHS1</topic><topic>DNA Restriction Enzymes - metabolism</topic><topic>Drug Resistance - genetics</topic><topic>Female</topic><topic>Gene Frequency - drug effects</topic><topic>Male</topic><topic>Oxazoles - pharmacology</topic><topic>qPCR</topic><topic>Real-Time Polymerase Chain Reaction - methods</topic><topic>Tetranychidae</topic><topic>Tetranychidae - drug effects</topic><topic>Tetranychidae - genetics</topic><topic>Tetranychus urticae</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Osakabe, Masahiro</creatorcontrib><creatorcontrib>Imamura, Tsuyoshi</creatorcontrib><creatorcontrib>Nakano, Ryohei</creatorcontrib><creatorcontrib>Kamikawa, Satoshi</creatorcontrib><creatorcontrib>Tadatsu, Misono</creatorcontrib><creatorcontrib>Kunimoto, Yoshinori</creatorcontrib><creatorcontrib>Doi, Makoto</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pesticide biochemistry and physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Osakabe, Masahiro</au><au>Imamura, Tsuyoshi</au><au>Nakano, Ryohei</au><au>Kamikawa, Satoshi</au><au>Tadatsu, Misono</au><au>Kunimoto, Yoshinori</au><au>Doi, Makoto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combination of restriction endonuclease digestion with the ΔΔCt method in real-time PCR to monitor etoxazole resistance allele frequency in the two-spotted spider mite</atitle><jtitle>Pesticide biochemistry and physiology</jtitle><addtitle>Pestic Biochem Physiol</addtitle><date>2017-06</date><risdate>2017</risdate><volume>139</volume><spage>1</spage><epage>8</epage><pages>1-8</pages><issn>0048-3575</issn><eissn>1095-9939</eissn><abstract>Monitoring resistance allele frequency at the early stage of resistance development is important for the successful acaricide resistance management. Etoxazole is a mite growth inhibitor to which resistance is conferred by an amino acid substitution in the chitin synthase 1 (CHS1; I1017F) in T. urticae. If the susceptible allele can be specifically digested by restriction endonuclease, the ΔΔCt method using real-time PCR for genomic DNA (RED-ΔΔCt method) may be available for monitoring the resistance allele frequency. We tested whether the etoxazole resistance allele frequency in a pooled sample was accurately measured by the RED-ΔΔCt method and validated whether the resistance variant frequency was correlated with etoxazole resistance phenotype in a bioassay. Finally, we performed a pilot test using field populations. Strong linearity of the measures by the RED-ΔΔCt method with practical resistance allele frequencies; resistance allele frequency in the range between 0.5% to at least 0.75% was strictly represented. The strong linear relationship between hatchability of haploid male eggs after the etoxazole treatments (phenotype) and resistance allele frequencies in their mothers provided direct evidence that I1017F is a primary resistance factor to etoxazole in the strains used for experiments. The pilot test revealed a significant correlation between egg hatchability (including both diploid female eggs and haploid male eggs) and estimators in field populations. Consequently, we concluded that the RED-ΔΔCt method is a powerful tool for monitoring a resistance allele in a pooled sample.
[Display omitted]
•“The RED-ΔΔCt method” to monitor etoxazole-resistance allele frequency was developed in the two-spotted spider mite.•The resistant variant at ≥0.5% in a pooled DNA sample was accurately measured.•The resistance variant frequency was practically correlated with resistant phenotype in a bioassay.•The RED-ΔΔCt method is a powerful tool for monitoring rare resistance alleles.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28595916</pmid><doi>10.1016/j.pestbp.2017.04.003</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-2246-3431</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0048-3575 |
ispartof | Pesticide biochemistry and physiology, 2017-06, Vol.139, p.1-8 |
issn | 0048-3575 1095-9939 |
language | eng |
recordid | cdi_proquest_miscellaneous_1908432609 |
source | Elsevier ScienceDirect Journals Complete - AutoHoldings; MEDLINE |
subjects | Acari Acaricide resistance Animals Chitin synthase 1 CHS1 DNA Restriction Enzymes - metabolism Drug Resistance - genetics Female Gene Frequency - drug effects Male Oxazoles - pharmacology qPCR Real-Time Polymerase Chain Reaction - methods Tetranychidae Tetranychidae - drug effects Tetranychidae - genetics Tetranychus urticae |
title | Combination of restriction endonuclease digestion with the ΔΔCt method in real-time PCR to monitor etoxazole resistance allele frequency in the two-spotted spider mite |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T07%3A53%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Combination%20of%20restriction%20endonuclease%20digestion%20with%20the%20%CE%94%CE%94Ct%20method%20in%20real-time%20PCR%20to%20monitor%20etoxazole%20resistance%20allele%20frequency%20in%20the%20two-spotted%20spider%20mite&rft.jtitle=Pesticide%20biochemistry%20and%20physiology&rft.au=Osakabe,%20Masahiro&rft.date=2017-06&rft.volume=139&rft.spage=1&rft.epage=8&rft.pages=1-8&rft.issn=0048-3575&rft.eissn=1095-9939&rft_id=info:doi/10.1016/j.pestbp.2017.04.003&rft_dat=%3Cproquest_cross%3E1908432609%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1908432609&rft_id=info:pmid/28595916&rft_els_id=S0048357517300950&rfr_iscdi=true |