scholarly journals Safety evaluation of the food enzyme xylanase from the genetically modified Aspergillus luchuensis Inui strain RF7398

EFSA Journal ◽  
2020 ◽  
Vol 18 (1) ◽  
Author(s):  
◽  
Vittorio Silano ◽  
José Manuel Barat Baviera ◽  
Claudia Bolognesi ◽  
Pier Sandro Cocconcelli ◽  
...  
EFSA Journal ◽  
2021 ◽  
Vol 19 (4) ◽  
Author(s):  
◽  
Claude Lambré ◽  
José Manuel Barat Baviera ◽  
Claudia Bolognesi ◽  
Pier Sandro Cocconcelli ◽  
...  

EFSA Journal ◽  
2020 ◽  
Vol 18 (11) ◽  
Author(s):  
◽  
Vittorio Silano ◽  
José Manuel Barat Baviera ◽  
Claudia Bolognesi ◽  
Pier Sandro Cocconcelli ◽  
...  

EFSA Journal ◽  
2020 ◽  
Vol 18 (1) ◽  
Author(s):  
◽  
Vittorio Silano ◽  
José Manuel Barat Baviera ◽  
Claudia Bolognesi ◽  
Pier Sandro Cocconcelli ◽  
...  

EFSA Journal ◽  
2019 ◽  
Vol 17 (11) ◽  
Author(s):  
◽  
Vittorio Silano ◽  
José Manuel Barat Baviera ◽  
Claudia Bolognesi ◽  
Pier Sandro Cocconcelli ◽  
...  

2019 ◽  
Vol 20 (6) ◽  
pp. 1472 ◽  
Author(s):  
Isabelle Gabriëls ◽  
Lucia Vergauwen ◽  
Marthe De Boevre ◽  
Stefan Van Dongen ◽  
Ronny Blust ◽  
...  

In Europe, the toxicological safety of genetically modified (GM) crops is routinely evaluated using rodent feeding trials, originally designed for testing oral toxicity of chemical compounds. We aimed to develop and optimize methods for advancing the use of zebrafish feeding trials for the safety evaluation of GM crops, using maize as a case study. In a first step, we evaluated the effect of different maize substitution levels. Our results demonstrate the need for preliminary testing to assess potential feed component-related effects on the overall nutritional balance. Next, since a potential effect of a GM crop should ideally be interpreted relative to the natural response variation (i.e., the range of biological values that is considered normal for a particular endpoint) in order to assess the toxicological relevance, we established natural response variation datasets for various zebrafish endpoints. We applied equivalence testing to calculate threshold equivalence limits (ELs) based on the natural response variation as a method for quantifying the range within which a GM crop and its control are considered equivalent. Finally, our results illustrate that the use of commercial control diets (CCDs) and null segregant (NS) controls (helpful for assessing potential effects of the transformation process) would be valuable additions to GM safety assessment strategies.


EFSA Journal ◽  
2018 ◽  
Vol 16 (5) ◽  
Author(s):  
◽  
Vittorio Silano ◽  
Claudia Bolognesi ◽  
Laurence Castle ◽  
Kevin Chipman ◽  
...  

EFSA Journal ◽  
2018 ◽  
Vol 16 (11) ◽  
Author(s):  
◽  
Vittorio Silano ◽  
José Manuel Barat Baviera ◽  
Claudia Bolognesi ◽  
Beat Johannes Brüschweiler ◽  
...  

2002 ◽  
Vol 61 (1) ◽  
pp. 25-29 ◽  
Author(s):  
I. R. Rowland

In contrast to the situation in the USA, where a wide range of genetically modified (GM) foods is available, in Europe very few GM products have been approved for marketing as foods, and there is widespread public concern about their safety and environmental impact. The marketing of a GM crop for food use in Europe falls under the EC novel foods regulations, and applications require the submission of an extensive dossier of information. The safety evaluation of GM foods presents considerable problems both in the conduct and interpretation of experimental studies, because conventional toxicity tests used in the evaluation of simple chemicals may not be appropriate for whole foods. To rationalise the safety evaluation process and to circumvent the difficulties in toxicological assessment of food materials, the concept of substantial equivalence has been developed. The concept is that if it can be demonstrated that the novel food is essentially similar to its conventional counterpart in terms of critical nutritional or anutritional components, then it is likely to be no more or less toxic than the latter. The possible introduction of unintended effects by the genetic modification process is particularly problematic for the safety evaluation process. The new genomic and post-genomic techniques are potentially valuable in the safety evaluation of GM foods, although they are as yet in their infancy.


EFSA Journal ◽  
2021 ◽  
Vol 19 (5) ◽  
Author(s):  
◽  
Claude Lambré ◽  
José Manuel Barat Baviera ◽  
Claudia Bolognesi ◽  
Pier Sandro Cocconcelli ◽  
...  

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