RNAi induced knockdown of a cadherin-like protein (EF531715) does not affect toxicity of Cry34/35Ab1 or Cry3Aa to Diabrotica virgifera virgifera larvae (Coleoptera: Chrysomelidae)

The western corn rootworm (WCR), Diabrotica virgifera virgifera LeConte, is an important maize pest throughout most of the U.S. Corn Belt. Bacillus thuringiensis (Bt) insecticidal proteins including modified Cry3Aa and Cry34/35Ab1 have been expressed in transgenic maize to protect against WCR feedin...

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Veröffentlicht in:Insect biochemistry and molecular biology 2016-08, Vol.75, p.117-124
Hauptverfasser: Tan, Sek Yee, Rangasamy, Murugesan, Wang, Haichuan, Vélez, Ana María, Hasler, James, McCaskill, David, Xu, Tao, Chen, Hong, Jurzenski, Jessica, Kelker, Matthew, Xu, Xiaoping, Narva, Kenneth, Siegfried, Blair D.
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container_issue
container_start_page 117
container_title Insect biochemistry and molecular biology
container_volume 75
creator Tan, Sek Yee
Rangasamy, Murugesan
Wang, Haichuan
Vélez, Ana María
Hasler, James
McCaskill, David
Xu, Tao
Chen, Hong
Jurzenski, Jessica
Kelker, Matthew
Xu, Xiaoping
Narva, Kenneth
Siegfried, Blair D.
description The western corn rootworm (WCR), Diabrotica virgifera virgifera LeConte, is an important maize pest throughout most of the U.S. Corn Belt. Bacillus thuringiensis (Bt) insecticidal proteins including modified Cry3Aa and Cry34/35Ab1 have been expressed in transgenic maize to protect against WCR feeding damage. To date, there is limited information regarding the WCR midgut target sites for these proteins. In this study, we examined whether a cadherin-like gene from Diabrotica virgifera virgifera (DvvCad; GenBank accession # EF531715) associated with WCR larval midgut tissue is necessary for Cry3Aa or Cry34/35Ab1 toxicity. Experiments were designed to examine the sensitivity of WCR to trypsin activated Cry3Aa and Cry34/35Ab1 after oral feeding of the DvvCad dsRNA to knockdown gene expression. Quantitative real-time PCR confirmed that DvvCad mRNA transcript levels were reduced in larvae treated with cadherin dsRNA. Relative cadherin expression by immunoblot analysis and nano-liquid chromatography - mass spectrometry (nanoLC-MS) of WCR neonate brush border membrane vesicle (BBMV) preparations exposed to DvvCad dsRNA confirmed reduced cadherin expression when compared to BBMV from untreated larvae. However, the larval mortality and growth inhibition of WCR neonates exposed to cadherin dsRNA for two days followed by feeding exposure to either Cry3Aa or Cry34/35Ab1 for four days was not significantly different to that observed in insects exposed to either Cry3Aa or Cry34/35Ab1 alone. In combination, these results suggest that cadherin is unlikely to be involved in the toxicity of Cry3Aa or Cry34/35Ab1 to WCR. [Display omitted] •A cadherin gene from western corn rootworms was used as a template to synthesize dsRNA.•Feeding of cadherin dsRNA resulted in reduced gene expression and protein abundance at 3 and 6 days.•Exposure of dsRNA treated larvae to Bt proteins, was used to measure the role of cadherin in Cry3Aa and Cry34/35Ab1 toxicity.•Knockdown of the cadherin gene did not affect toxicity of either protein.•These results indicate that the rootworm cadherin is not involved in toxicity of these proteins.
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Bacillus thuringiensis (Bt) insecticidal proteins including modified Cry3Aa and Cry34/35Ab1 have been expressed in transgenic maize to protect against WCR feeding damage. To date, there is limited information regarding the WCR midgut target sites for these proteins. In this study, we examined whether a cadherin-like gene from Diabrotica virgifera virgifera (DvvCad; GenBank accession # EF531715) associated with WCR larval midgut tissue is necessary for Cry3Aa or Cry34/35Ab1 toxicity. Experiments were designed to examine the sensitivity of WCR to trypsin activated Cry3Aa and Cry34/35Ab1 after oral feeding of the DvvCad dsRNA to knockdown gene expression. Quantitative real-time PCR confirmed that DvvCad mRNA transcript levels were reduced in larvae treated with cadherin dsRNA. Relative cadherin expression by immunoblot analysis and nano-liquid chromatography - mass spectrometry (nanoLC-MS) of WCR neonate brush border membrane vesicle (BBMV) preparations exposed to DvvCad dsRNA confirmed reduced cadherin expression when compared to BBMV from untreated larvae. However, the larval mortality and growth inhibition of WCR neonates exposed to cadherin dsRNA for two days followed by feeding exposure to either Cry3Aa or Cry34/35Ab1 for four days was not significantly different to that observed in insects exposed to either Cry3Aa or Cry34/35Ab1 alone. In combination, these results suggest that cadherin is unlikely to be involved in the toxicity of Cry3Aa or Cry34/35Ab1 to WCR. [Display omitted] •A cadherin gene from western corn rootworms was used as a template to synthesize dsRNA.•Feeding of cadherin dsRNA resulted in reduced gene expression and protein abundance at 3 and 6 days.•Exposure of dsRNA treated larvae to Bt proteins, was used to measure the role of cadherin in Cry3Aa and Cry34/35Ab1 toxicity.•Knockdown of the cadherin gene did not affect toxicity of either protein.•These results indicate that the rootworm cadherin is not involved in toxicity of these proteins.</description><identifier>ISSN: 0965-1748</identifier><identifier>EISSN: 1879-0240</identifier><identifier>DOI: 10.1016/j.ibmb.2016.06.006</identifier><identifier>PMID: 27334721</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Bacillus thuringiensis ; Bacillus thuringiensis - genetics ; Bacterial Proteins - pharmacology ; Cadherin ; Cadherins - genetics ; Cadherins - metabolism ; Chrysomelidae ; Coleoptera ; Coleoptera - drug effects ; Coleoptera - genetics ; Coleoptera - growth &amp; development ; Coleoptera - metabolism ; Cry34/35Ab1 ; Cry34Ab1 ; Cry35Ab1 ; Cry3Aa ; Diabrotica virgifera virgifera ; Endotoxins - pharmacology ; Hemolysin Proteins - pharmacology ; Insect Proteins - genetics ; Insect Proteins - metabolism ; Insecticide Resistance ; Insecticides - pharmacology ; Larva - drug effects ; Larva - genetics ; Larva - growth &amp; development ; Larva - metabolism ; Plants, Genetically Modified - chemistry ; Real-Time Polymerase Chain Reaction ; RNA Interference ; RNAi ; Zea mays ; Zea mays - chemistry</subject><ispartof>Insect biochemistry and molecular biology, 2016-08, Vol.75, p.117-124</ispartof><rights>2016 Elsevier Ltd</rights><rights>Copyright © 2016 Elsevier Ltd. 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Bacillus thuringiensis (Bt) insecticidal proteins including modified Cry3Aa and Cry34/35Ab1 have been expressed in transgenic maize to protect against WCR feeding damage. To date, there is limited information regarding the WCR midgut target sites for these proteins. In this study, we examined whether a cadherin-like gene from Diabrotica virgifera virgifera (DvvCad; GenBank accession # EF531715) associated with WCR larval midgut tissue is necessary for Cry3Aa or Cry34/35Ab1 toxicity. Experiments were designed to examine the sensitivity of WCR to trypsin activated Cry3Aa and Cry34/35Ab1 after oral feeding of the DvvCad dsRNA to knockdown gene expression. Quantitative real-time PCR confirmed that DvvCad mRNA transcript levels were reduced in larvae treated with cadherin dsRNA. Relative cadherin expression by immunoblot analysis and nano-liquid chromatography - mass spectrometry (nanoLC-MS) of WCR neonate brush border membrane vesicle (BBMV) preparations exposed to DvvCad dsRNA confirmed reduced cadherin expression when compared to BBMV from untreated larvae. However, the larval mortality and growth inhibition of WCR neonates exposed to cadherin dsRNA for two days followed by feeding exposure to either Cry3Aa or Cry34/35Ab1 for four days was not significantly different to that observed in insects exposed to either Cry3Aa or Cry34/35Ab1 alone. In combination, these results suggest that cadherin is unlikely to be involved in the toxicity of Cry3Aa or Cry34/35Ab1 to WCR. 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development</topic><topic>Larva - metabolism</topic><topic>Plants, Genetically Modified - chemistry</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>RNA Interference</topic><topic>RNAi</topic><topic>Zea mays</topic><topic>Zea mays - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tan, Sek Yee</creatorcontrib><creatorcontrib>Rangasamy, Murugesan</creatorcontrib><creatorcontrib>Wang, Haichuan</creatorcontrib><creatorcontrib>Vélez, Ana María</creatorcontrib><creatorcontrib>Hasler, James</creatorcontrib><creatorcontrib>McCaskill, David</creatorcontrib><creatorcontrib>Xu, Tao</creatorcontrib><creatorcontrib>Chen, Hong</creatorcontrib><creatorcontrib>Jurzenski, Jessica</creatorcontrib><creatorcontrib>Kelker, Matthew</creatorcontrib><creatorcontrib>Xu, Xiaoping</creatorcontrib><creatorcontrib>Narva, Kenneth</creatorcontrib><creatorcontrib>Siegfried, Blair D.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><jtitle>Insect biochemistry and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tan, Sek Yee</au><au>Rangasamy, Murugesan</au><au>Wang, Haichuan</au><au>Vélez, Ana María</au><au>Hasler, James</au><au>McCaskill, David</au><au>Xu, Tao</au><au>Chen, Hong</au><au>Jurzenski, Jessica</au><au>Kelker, Matthew</au><au>Xu, Xiaoping</au><au>Narva, Kenneth</au><au>Siegfried, Blair D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>RNAi induced knockdown of a cadherin-like protein (EF531715) does not affect toxicity of Cry34/35Ab1 or Cry3Aa to Diabrotica virgifera virgifera larvae (Coleoptera: Chrysomelidae)</atitle><jtitle>Insect biochemistry and molecular biology</jtitle><addtitle>Insect Biochem Mol Biol</addtitle><date>2016-08</date><risdate>2016</risdate><volume>75</volume><spage>117</spage><epage>124</epage><pages>117-124</pages><issn>0965-1748</issn><eissn>1879-0240</eissn><abstract>The western corn rootworm (WCR), Diabrotica virgifera virgifera LeConte, is an important maize pest throughout most of the U.S. Corn Belt. Bacillus thuringiensis (Bt) insecticidal proteins including modified Cry3Aa and Cry34/35Ab1 have been expressed in transgenic maize to protect against WCR feeding damage. To date, there is limited information regarding the WCR midgut target sites for these proteins. In this study, we examined whether a cadherin-like gene from Diabrotica virgifera virgifera (DvvCad; GenBank accession # EF531715) associated with WCR larval midgut tissue is necessary for Cry3Aa or Cry34/35Ab1 toxicity. Experiments were designed to examine the sensitivity of WCR to trypsin activated Cry3Aa and Cry34/35Ab1 after oral feeding of the DvvCad dsRNA to knockdown gene expression. Quantitative real-time PCR confirmed that DvvCad mRNA transcript levels were reduced in larvae treated with cadherin dsRNA. Relative cadherin expression by immunoblot analysis and nano-liquid chromatography - mass spectrometry (nanoLC-MS) of WCR neonate brush border membrane vesicle (BBMV) preparations exposed to DvvCad dsRNA confirmed reduced cadherin expression when compared to BBMV from untreated larvae. However, the larval mortality and growth inhibition of WCR neonates exposed to cadherin dsRNA for two days followed by feeding exposure to either Cry3Aa or Cry34/35Ab1 for four days was not significantly different to that observed in insects exposed to either Cry3Aa or Cry34/35Ab1 alone. In combination, these results suggest that cadherin is unlikely to be involved in the toxicity of Cry3Aa or Cry34/35Ab1 to WCR. [Display omitted] •A cadherin gene from western corn rootworms was used as a template to synthesize dsRNA.•Feeding of cadherin dsRNA resulted in reduced gene expression and protein abundance at 3 and 6 days.•Exposure of dsRNA treated larvae to Bt proteins, was used to measure the role of cadherin in Cry3Aa and Cry34/35Ab1 toxicity.•Knockdown of the cadherin gene did not affect toxicity of either protein.•These results indicate that the rootworm cadherin is not involved in toxicity of these proteins.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>27334721</pmid><doi>10.1016/j.ibmb.2016.06.006</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Bacillus thuringiensis
Bacillus thuringiensis - genetics
Bacterial Proteins - pharmacology
Cadherin
Cadherins - genetics
Cadherins - metabolism
Chrysomelidae
Coleoptera
Coleoptera - drug effects
Coleoptera - genetics
Coleoptera - growth & development
Coleoptera - metabolism
Cry34/35Ab1
Cry34Ab1
Cry35Ab1
Cry3Aa
Diabrotica virgifera virgifera
Endotoxins - pharmacology
Hemolysin Proteins - pharmacology
Insect Proteins - genetics
Insect Proteins - metabolism
Insecticide Resistance
Insecticides - pharmacology
Larva - drug effects
Larva - genetics
Larva - growth & development
Larva - metabolism
Plants, Genetically Modified - chemistry
Real-Time Polymerase Chain Reaction
RNA Interference
RNAi
Zea mays
Zea mays - chemistry
title RNAi induced knockdown of a cadherin-like protein (EF531715) does not affect toxicity of Cry34/35Ab1 or Cry3Aa to Diabrotica virgifera virgifera larvae (Coleoptera: Chrysomelidae)
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