Molecular characterization of an NADPH cytochrome P450 reductase from Bemisia tabaci Q: Potential involvement in susceptibility to imidacloprid

NADPH cytochrome P450 reductase (CPR) is an integral component of cytochrome P450-mediated biological reactions, such as the metabolism of xenobiotics, including insecticides. CPR has been reported to be associated with insecticide tolerance in several insects. However, the biochemical characteristi...

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Veröffentlicht in:Pesticide biochemistry and physiology 2020-01, Vol.162 (C), p.29-35
Hauptverfasser: He, Chao, Liang, Jinjin, Liu, Shaonan, Zeng, Yang, Wang, Shaoli, Wu, Qingjun, Xie, Wen, Zhang, Youjun
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container_end_page 35
container_issue C
container_start_page 29
container_title Pesticide biochemistry and physiology
container_volume 162
creator He, Chao
Liang, Jinjin
Liu, Shaonan
Zeng, Yang
Wang, Shaoli
Wu, Qingjun
Xie, Wen
Zhang, Youjun
description NADPH cytochrome P450 reductase (CPR) is an integral component of cytochrome P450-mediated biological reactions, such as the metabolism of xenobiotics, including insecticides. CPR has been reported to be associated with insecticide tolerance in several insects. However, the biochemical characteristics and biological function of CPR in Bemisia tabaci Q (BtCPR) remain undefined. In this study, BtCPR was cloned, and bioinformatic analysis showed that BtCPR is a transmembrane protein with a molecular weight (MW) of 76.73 kDa and contains conserved binding domains (FMN, FAD, and NADPH). Tissue- and developmental stage-dependent expression indicated that the highest expression levels of BtCPR occurred in head tissue and in male adults. Transcripts of BtCPR in the field B. tabaci Q strain were 1.62-fold higher than those of the laboratory B. tabaci Q strain. In both field and laboratory adults, the susceptibility of BtCPR-knockdown B. tabaci Q to imidacloprid substantially increased compared to that of the B. tabaci Q control group. Furthermore, the heterologous expression of BtCPR in Sf9 cells exhibited catalytic activity for cytochrome c reduction, following Michaelis-Menten kinetics. Sf9 cells overexpressing BtCPR had greater viability than the control cells when treated with imidacloprid. The results suggest that BtCPR could affect the susceptibility of B. tabaci Q to imidacloprid and could also be considered a novel target for pest control. [Display omitted] •Full-length cDNA of BtCPR gene were cloned and characterized in Bemisia tabaci Q•In both field and laboratory adults, the susceptibility of BtCPR-knockdown B. tabaci Q to imidacloprid substantially increased compared to that of the B. tabaci Q control group.•Heterologous expression of BtCPR in Sf9 cells exhibited catalytic activity for cytochrome c reduction and had greater viability than the control cells when treated with imidacloprid
doi_str_mv 10.1016/j.pestbp.2019.07.018
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CPR has been reported to be associated with insecticide tolerance in several insects. However, the biochemical characteristics and biological function of CPR in Bemisia tabaci Q (BtCPR) remain undefined. In this study, BtCPR was cloned, and bioinformatic analysis showed that BtCPR is a transmembrane protein with a molecular weight (MW) of 76.73 kDa and contains conserved binding domains (FMN, FAD, and NADPH). Tissue- and developmental stage-dependent expression indicated that the highest expression levels of BtCPR occurred in head tissue and in male adults. Transcripts of BtCPR in the field B. tabaci Q strain were 1.62-fold higher than those of the laboratory B. tabaci Q strain. In both field and laboratory adults, the susceptibility of BtCPR-knockdown B. tabaci Q to imidacloprid substantially increased compared to that of the B. tabaci Q control group. Furthermore, the heterologous expression of BtCPR in Sf9 cells exhibited catalytic activity for cytochrome c reduction, following Michaelis-Menten kinetics. Sf9 cells overexpressing BtCPR had greater viability than the control cells when treated with imidacloprid. The results suggest that BtCPR could affect the susceptibility of B. tabaci Q to imidacloprid and could also be considered a novel target for pest control. [Display omitted] •Full-length cDNA of BtCPR gene were cloned and characterized in Bemisia tabaci Q•In both field and laboratory adults, the susceptibility of BtCPR-knockdown B. tabaci Q to imidacloprid substantially increased compared to that of the B. tabaci Q control group.•Heterologous expression of BtCPR in Sf9 cells exhibited catalytic activity for cytochrome c reduction and had greater viability than the control cells when treated with imidacloprid</description><identifier>ISSN: 0048-3575</identifier><identifier>EISSN: 1095-9939</identifier><identifier>DOI: 10.1016/j.pestbp.2019.07.018</identifier><identifier>PMID: 31836051</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Bemisia tabaci ; CPR ; Cytochrome P-450 Enzyme System ; Hemiptera ; Imidacloprid ; Imidazoles ; Insecticide Resistance ; Insecticides ; Male ; NADPH-Ferrihemoprotein Reductase ; Neonicotinoids ; Nitro Compounds ; RNAi</subject><ispartof>Pesticide biochemistry and physiology, 2020-01, Vol.162 (C), p.29-35</ispartof><rights>2019 Elsevier Inc.</rights><rights>Copyright © 2019 Elsevier Inc. 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CPR has been reported to be associated with insecticide tolerance in several insects. However, the biochemical characteristics and biological function of CPR in Bemisia tabaci Q (BtCPR) remain undefined. In this study, BtCPR was cloned, and bioinformatic analysis showed that BtCPR is a transmembrane protein with a molecular weight (MW) of 76.73 kDa and contains conserved binding domains (FMN, FAD, and NADPH). Tissue- and developmental stage-dependent expression indicated that the highest expression levels of BtCPR occurred in head tissue and in male adults. Transcripts of BtCPR in the field B. tabaci Q strain were 1.62-fold higher than those of the laboratory B. tabaci Q strain. In both field and laboratory adults, the susceptibility of BtCPR-knockdown B. tabaci Q to imidacloprid substantially increased compared to that of the B. tabaci Q control group. Furthermore, the heterologous expression of BtCPR in Sf9 cells exhibited catalytic activity for cytochrome c reduction, following Michaelis-Menten kinetics. Sf9 cells overexpressing BtCPR had greater viability than the control cells when treated with imidacloprid. The results suggest that BtCPR could affect the susceptibility of B. tabaci Q to imidacloprid and could also be considered a novel target for pest control. [Display omitted] •Full-length cDNA of BtCPR gene were cloned and characterized in Bemisia tabaci Q•In both field and laboratory adults, the susceptibility of BtCPR-knockdown B. tabaci Q to imidacloprid substantially increased compared to that of the B. tabaci Q control group.•Heterologous expression of BtCPR in Sf9 cells exhibited catalytic activity for cytochrome c reduction and had greater viability than the control cells when treated with imidacloprid</description><subject>Animals</subject><subject>Bemisia tabaci</subject><subject>CPR</subject><subject>Cytochrome P-450 Enzyme System</subject><subject>Hemiptera</subject><subject>Imidacloprid</subject><subject>Imidazoles</subject><subject>Insecticide Resistance</subject><subject>Insecticides</subject><subject>Male</subject><subject>NADPH-Ferrihemoprotein Reductase</subject><subject>Neonicotinoids</subject><subject>Nitro Compounds</subject><subject>RNAi</subject><issn>0048-3575</issn><issn>1095-9939</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcuO1SAYgInROMfRNzCGuHLTCqWU4sJkHC9jMuox0TWh9CeHk7Z0gJ7k-BK-sjQdXbriku-_fgg9p6SkhDavj-UMMXVzWREqSyJKQtsHaEeJ5IWUTD5EO0LqtmBc8Av0JMYjIUTWRD5GF4y2rCGc7tDvL34Asww6YHPQQZsEwf3SyfkJe4v1hL9evd_fYHNO3hyCHwHva05wgH4xSUfANn_idzC66DROutPG4e9v8N4nmJLTA3bTyQ8nGPMz33FcooE5uc4NLp1x8tiNrtdm8HNw_VP0yOohwrP78xL9_Pjhx_VNcfvt0-frq9vC1IynQvKecwZQWa6FbSyvqsp0UnOwFRWiZ6QVuuuFENqIxtpaNB2nrQCmG84rxi7Ryy2vj8mpaFwCczB-msAkRZu2qvkKvdqgOfi7JW9b5SkNDIOewC9R5TyNlC1jJKP1hprgYwxgVZ5m1OGsKFGrL3VUmy-1-lJEqOwrh724r7B0I_T_gv4KysDbDYC8jJODsPYKk4HehbXV3rv_V_gDJTOqLg</recordid><startdate>202001</startdate><enddate>202001</enddate><creator>He, Chao</creator><creator>Liang, Jinjin</creator><creator>Liu, Shaonan</creator><creator>Zeng, Yang</creator><creator>Wang, Shaoli</creator><creator>Wu, Qingjun</creator><creator>Xie, Wen</creator><creator>Zhang, Youjun</creator><general>Elsevier Inc</general><general>Elsevier</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><scope>OTOTI</scope></search><sort><creationdate>202001</creationdate><title>Molecular characterization of an NADPH cytochrome P450 reductase from Bemisia tabaci Q: Potential involvement in susceptibility to imidacloprid</title><author>He, Chao ; Liang, Jinjin ; Liu, Shaonan ; Zeng, Yang ; Wang, Shaoli ; Wu, Qingjun ; Xie, Wen ; Zhang, Youjun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-95d553ee2f5a7f6f5222cb9a5ef2177d3087abd777ac76ff476b5187e3a655233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Bemisia tabaci</topic><topic>CPR</topic><topic>Cytochrome P-450 Enzyme System</topic><topic>Hemiptera</topic><topic>Imidacloprid</topic><topic>Imidazoles</topic><topic>Insecticide Resistance</topic><topic>Insecticides</topic><topic>Male</topic><topic>NADPH-Ferrihemoprotein Reductase</topic><topic>Neonicotinoids</topic><topic>Nitro Compounds</topic><topic>RNAi</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>He, Chao</creatorcontrib><creatorcontrib>Liang, Jinjin</creatorcontrib><creatorcontrib>Liu, Shaonan</creatorcontrib><creatorcontrib>Zeng, Yang</creatorcontrib><creatorcontrib>Wang, Shaoli</creatorcontrib><creatorcontrib>Wu, Qingjun</creatorcontrib><creatorcontrib>Xie, Wen</creatorcontrib><creatorcontrib>Zhang, Youjun</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><collection>OSTI.GOV</collection><jtitle>Pesticide biochemistry and physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>He, Chao</au><au>Liang, Jinjin</au><au>Liu, Shaonan</au><au>Zeng, Yang</au><au>Wang, Shaoli</au><au>Wu, Qingjun</au><au>Xie, Wen</au><au>Zhang, Youjun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular characterization of an NADPH cytochrome P450 reductase from Bemisia tabaci Q: Potential involvement in susceptibility to imidacloprid</atitle><jtitle>Pesticide biochemistry and physiology</jtitle><addtitle>Pestic Biochem Physiol</addtitle><date>2020-01</date><risdate>2020</risdate><volume>162</volume><issue>C</issue><spage>29</spage><epage>35</epage><pages>29-35</pages><issn>0048-3575</issn><eissn>1095-9939</eissn><abstract>NADPH cytochrome P450 reductase (CPR) is an integral component of cytochrome P450-mediated biological reactions, such as the metabolism of xenobiotics, including insecticides. CPR has been reported to be associated with insecticide tolerance in several insects. However, the biochemical characteristics and biological function of CPR in Bemisia tabaci Q (BtCPR) remain undefined. In this study, BtCPR was cloned, and bioinformatic analysis showed that BtCPR is a transmembrane protein with a molecular weight (MW) of 76.73 kDa and contains conserved binding domains (FMN, FAD, and NADPH). Tissue- and developmental stage-dependent expression indicated that the highest expression levels of BtCPR occurred in head tissue and in male adults. Transcripts of BtCPR in the field B. tabaci Q strain were 1.62-fold higher than those of the laboratory B. tabaci Q strain. In both field and laboratory adults, the susceptibility of BtCPR-knockdown B. tabaci Q to imidacloprid substantially increased compared to that of the B. tabaci Q control group. Furthermore, the heterologous expression of BtCPR in Sf9 cells exhibited catalytic activity for cytochrome c reduction, following Michaelis-Menten kinetics. Sf9 cells overexpressing BtCPR had greater viability than the control cells when treated with imidacloprid. The results suggest that BtCPR could affect the susceptibility of B. tabaci Q to imidacloprid and could also be considered a novel target for pest control. [Display omitted] •Full-length cDNA of BtCPR gene were cloned and characterized in Bemisia tabaci Q•In both field and laboratory adults, the susceptibility of BtCPR-knockdown B. tabaci Q to imidacloprid substantially increased compared to that of the B. tabaci Q control group.•Heterologous expression of BtCPR in Sf9 cells exhibited catalytic activity for cytochrome c reduction and had greater viability than the control cells when treated with imidacloprid</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>31836051</pmid><doi>10.1016/j.pestbp.2019.07.018</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Bemisia tabaci
CPR
Cytochrome P-450 Enzyme System
Hemiptera
Imidacloprid
Imidazoles
Insecticide Resistance
Insecticides
Male
NADPH-Ferrihemoprotein Reductase
Neonicotinoids
Nitro Compounds
RNAi
title Molecular characterization of an NADPH cytochrome P450 reductase from Bemisia tabaci Q: Potential involvement in susceptibility to imidacloprid
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