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Organisme vivant modifié (LMO)
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BCH-LMO-SCBD-14992-10   |   PDF   |   Imprimer   |  
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Décisions sur l’OVM Évaluations des risques  
published: 12 juin 2006 last updated: 13 juil. 2026
Identité de l’organisme vivant modifié
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VIPCOT™ Cotton
EN
COT102
Oui
SYN-IR1Ø2-7
The cotton (Gossypium hirsutum) was modified for resistance against lepidopteran insect pests. The LM cotton was also modified to express a selectable marker during transformation. To achieve lepidopteran resistance, the cotton expresses Bacillus thuringiensis vegetative insecticidal protein 3Aa (Vip3Aa), which causes gut paralysis and lysis of epithelium cells of feeding larvae. Vip3Aa is a vegetative insecticidal protein that binds to specific midgut receptors distinct from those recognized by Cry proteins and disrupts the integrity of epithelial cell membranes. For the selection marker, the cotton expresses Escherichia coli hygromycin-B phosphotransferase is also expressed.
EN
Le terme « organisme récepteur » désigne un organisme (non modifié ou déjà modifié) ayant fait l'objet d'une modification génétique, tandis que les « organismes parentaux » désignent les organismes impliqués dans un croisement ou une fusion cellulaire pour générer un organisme modifié.
Cultivar: Coker 312
EN
Caractéristiques du processus de modification
pCOT-1
EN
  • Transgénèse par agrobacterium
Certains de ces éléments génétiques peuvent être présents sous forme de fragments ou sous forme tronquée. Veuillez consulter les notes ci-dessous, s’il y a lieu.
  • BCH-GENE-SCBD-14991-8 Hygromycin B phosphotransferase gene | Escherichia coli (ECOLX)
    Séquence codante de protéines | Résistance aux antibiotiques (Hygromycine),Gènes marqueurs et gènes rapporteurs sélectables
  • BCH-GENE-SCBD-14990-5 Vegetative insecticidal protein 3A | Bacillus thuringiensis (Bt, Bacillus, BACTU)
    Séquence codante de protéines | Résistance aux maladies et aux parasites (Insectes, Chenille tisseuse (papillons et mites))
  • BCH-GENE-SCBD-104517-2 Actin 2 promoter | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Promoteur
  • BCH-GENE-SCBD-100269-8 Nopaline Synthase Gene Terminator | Agrobacterium tumefaciens (Agrobacterium)
    Terminateur
  • BCH-GENE-SCBD-101874-2 Ubiquitin gene 3 promoter | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Promoteur
Information on the inserted DNA sequences
The transforming plasmid pCOT-1 carried a transfer DNA comprising two gene cassettes: Escherichia coli hygromycin B phosphotransferase (hph) and Bacillus thuringiensis vegetative insecticidal protein 3A (vip3Aa).

(1) Transcription of hph is under control of the Arabidopsis thaliana ubiquitin 3 promoter and the Agrobacterium tumefaciens nopaline synthase (nos) terminator. The gene cassette is present in the counterclockwise orientation.

(2) The expression of Bacillus thuringiensis vip3Aa is under transcriptional control of the A. thaliana actin 2 promoter and the nos terminator.

Note
  • The coding sequence of the vip3Aa was optimized for expression in plant cells.
  • Transcription is expected to occur at elevated levels due to the constitutive nature of the promoters.
  • Southern blot analysis indicated the incorporation of a single copy of the transgene cassettes without the integration of the vector backbone sequences.
  • Western blot analysis confirmed the expression of the proteins. 
EN
Caractéristiques de l’OVM
FR
  • Nourriture pour les animaux
  • Fibre / textile
  • Nourriture
Méthode(s) de détection
Southern blot analysis of the genomic DNA from COT102 revealed the incorporation of single intact copies of the vip3Aa and hph genes, along with intact copies of their respective regulatory sequences. Results of these analyses also demonstrated that none of the vector backbone sequences, including the streptomycin adenyltransferase (aadA) gene, were incorporated into the genomic DNA.
EN
Informations supplémentaires
The cotton line COT102 was engineered to resist attack from Lepidopteran insect pests such as the cotton bollworm (Helicoverpa zea), tobacco budworm (Heliothis virescens), pink bollworm (Pectinophora gossypiella), fall armyworm (Spodoptera frugiperd), beet armyworm (Spodoptera exigua), soybean looper (Pseudoplusia includens), cabbage looper (Trichoplusia ni), and cotton leaf perforator (Bucculatrix thurberiella).

This insect resistance is conferred by the vip3Aa gene, originally isolated from the common soil bacterium Bacillus thuringiensis strain AB88. The vip3Aa gene produces the insect control protein VIP3A in the plant tissues. VIP3A is a member of a class of recently discovered insecticidal proteins: VIP (vegetative insecticidal proteins) proteins are expressed by the bacterium during the vegetative stage, as well as during sporulation, the stage at which the delta-endotoxins (i.e., Cry proteins) are expressed. 

VIP proteins have an insecticidal mode of action similar to that of the delta-endotoxins: the ingestion by targeted insects leads to feeding cessation, loss of gut peristalsis, insect paralysis, and death. As with Cry proteins, VIP proteins also possess an active proteolytic core, which is activated by insect gut proteases, and binds to specific sites localized on the midgut lining of susceptible insect species. However, the VIP3A protein targets different molecules (i.e., receptors) in the mid-gut lining, and the binding results in the formation of ion channels distinct from those formed by delta endotoxins, such as Cry1Ab. 

VIP proteins are not expected to affect other invertebrate and vertebrate organisms, including beneficial arthropods, birds and mammals. Only lepidopteran insect species possess VIP binding sites on the surface of their gut epithelia, therefore, livestock animals and humans are not susceptible to these proteins. Also, since only lepidopteran insect species are targeted by the VIP proteins, species of other insect orders, including beneficial and pest species, are not expected to be affected by this insecticidal protein. 
EN
Les fichiers qui font référence à ce document Montré dans la recherche
Type de fichier Champs Fichier(s) :
Organisme vivant modifié Organisme récepteur ou organismes parentaux 19
Décision de pays ou tout autre communication Identification de l'OVM 12
Évaluation des risques générée par un processus de réglementation Organisme(s) vivant(s) modifié(s) 10
Laboratoire pour la détection et d'identification des OVM OVM(s) détectable(s) par le laboratoire 1
Évaluations des risques générées par un processus indépendant ou non réglementaire Organisme(s) vivant(s) modifié(s) 1