Brussels, Belgium
July 14, 2005
The European Food Safety Authority Journal (2005) 252, 1-23
Summary of the Opinion
This document provides an
opinion of the Scientific Panel on Genetically Modified
Organisms (GMO Panel) of the European Food Safety Authority
(EFSA) on genetically modified maize MON 863 x MON 810 (Unique
Identifier MON-ØØ863-5 x MON-ØØ81Ø-6).
In the past, EFSA was requested to deliver its opinion on two
questions raised by the Commission related to applications for
the placing on the market of MON 863 x MON 810 maize under the
Novel Food Regulation (EC) No 258/97 for food uses and under the
Directive 2001/18/EC on the deliberate release of genetically
modified organisms (GMOs) into the environment for feed uses,
import and processing.
In its opinions of 2 April 2004, the Panel concluded that it was
acceptable to use data for the single insert lines MON 863 and
MON 810 in support of the safety assessment of MON 863 x MON 810
maize, in addition to the data package provided for MON 863 x
MON 810 maize. However, the Panel was divided over the need for
confirmatory data for the risk assessment of MON 863 x MON 810
maize, in particular the need for an additional 90 day rat study
with MON 863 x MON 810 maize. Therefore, the Panel could not
reach agreement on the safety evaluation of MON 863 x MON 810
maize. To resolve this issue, EFSA decided to request the study
in question from the applicant in order to allow the Panel to
finalise its evaluation.
After receipt of the full data package on the 90 days rat study,
EFSA referred the issue back to the GMO Panel and asked the
Panel to conclude the risk assessment of MON 863 x MON 810
maize.
Due to changes in the EU legislation, the applicant had to
introduce an application under Regulation (EC) No 1829/2003 to
replace the application under Regulation (EC) No 258/97 and
decided to include in the scope both food and feed uses
(reference EFSA GMO DE 2004 03). Import and processing are still
covered by the scope of the notification under Directive 2001/18
(reference C/DE/02/9).
In delivering the present opinion the Panel considered the
different applications regarding MON 863 x MON 810 maize, the
information concerning the single insert lines MON 863 and MON
810, the additional information provided by the applicant and
the specific questions and concerns, raised by the Member
States. Although an overall single risk assessment has been
made, for regulatory reasons, opinions for the application under
Regulation (EC) No 1829/2003 and the notification under
Directive 2001/18/EC are issued separately.
MON 863 x MON 810 maize was assessed with reference to the
intended uses and the appropriate principles described in the
guidance document of the Scientific Panel on Genetically
Modified Organisms for the risk assessment of genetically
modified plants and derived food and feed. The scientific
assessment included molecular characterisation of the inserted
DNA and expression of target proteins. A comparative analysis of
agronomic traits and composition was undertaken and the safety
of the new proteins and the whole food/feed was evaluated with
respect to toxicity and allergenicity. Both a nutritional and an
environmental assessment, including monitoring plans, were
undertaken.
MON 863 maize was developed to provide protection against
certain coleopteran pests, principally corn rootworm (Diabrotica
spp.) by the introduction of a variant Bacillus thuringiensis
cry3Bb1 gene expressing an insecticidal protein. MON 863 has
received an EFSA opinion in favour of its authorisation. MON 810
maize produces the protein Cry1Ab, which confers protection
against certain lepidopteran insect pests (Ostrinia nubilalis
and Sesamia spp.). MON 810 was approved under Directive
90/220/EEC by Commission Decision 98/294/EC. The use of food and
food ingredients from MON 810 maize was notified in 1997 under
Regulation (EC) No 258/97.
MON 863 x MON 810 maize was produced by crosses between maize
inbred lines containing MON 863 and MON 810 events to combine
the rootworm resistance trait in MON 863 with the trait present
in MON 810 protecting against lepidopteran pests.
Molecular analysis of the DNA inserts present in MON 863 x MON
810 maize confirmed that the insert structures of the single
events were retained.
Cry3Bb1 and Cry1Ab protein levels in kernels of MON 863 x MON
810 maize were higher than in the individual MON 863 and MON 810
lines. However, the ranges were broad and there were overlaps
between the levels of Cry proteins expressed in the MON 863 and
MON 810 parents and in MON 863 x MON 810 maize. The Panel
concludes that these data do not raise safety concerns.
The safety and the allergenic risk of the Cry3Bb1, Cry1Ab and
NptII proteins have previously been assessed in the single
events for which positive opinions were issued.
Feeding studies conducted on broilers with MON 863 x MON 810
maize showed no adverse effects. The Panel considers that the
nutritional properties of this maize would be no different from
those of conventional maize.
The results of the 90 day sub chronic rodent study do not
indicate adverse effects from consumption of MON 863 x MON 810
maize and the Panel concludes that there are no concerns over
its safety.
The application EFSA GMO DE 2004 03 concerns food and feed uses.
There is therefore no requirement for scientific information on
possible environmental effects associated with the cultivation
of the maize lines. The GMO Panel agrees that unintended
environmental effects due to the establishment and spread of GM
maize will not be different from that of traditionally bred
maize. The Panel concludes that the amounts of Cry toxin being
distributed in the environment would be very low, minimizing the
possibility for exposure of potentially sensitive non target
organisms. The monitoring plan provided by the applicant is in
line with the intended uses for the GMO.
In conclusion, the Panel considers that the information
available for MON 863 x MON 810 maize addresses the outstanding
questions raised by the Member States and considers that it will
not have adverse effects on human and animal health or the
environment in the context of its proposed use.
Opinion in PDF format:
http://www.efsa.eu.int/science/gmo/gmo_opinions/1031/gmo_opinion_ej252_mon863x810_2_en1.pdf
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