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Workshop PMEM

Post Market Monitoring: Legal Framework in Brazil and First Results (Contribution to the 4th International Workshop on PMEM of Genetically Modified Plants, Quedlinburg)

Monitoring von GVO in Brasilien: gesetzliche Vorgaben und erste Erfahrungen (Beitrag zum 4. internationalen Workshop zum Anbaubegleitenden Monitoring von gentechnisch veränderten Pflanzen, Quedlinburg)

Marcia A. Melo1, Ederson A. Kido2 and Paulo P. Andrade3
Institute
Federal University of Campina Grande, Laboratory of Molecular Biology, CSTR/UFCG, Av. Universitária s/n, 58708-110, Patos, PB, Brazil1
Federal University of Pernambuco, Laboratory of Molecular Genetics, CCB/UFPE, Av. Moraes Rego s/n, 50670-901, Recife, PE, Brazil2
National Technical Commission for Biosafety (CTNBio), Setor Policial Sul-SPO Área 5 Quadra 3 Bloco B, 70610-200, Brasília, DF, Brazil3

Journal für Kulturpflanzen, 63 (7). S. 226–231, 2011, ISSN 0027-7479, DOI: 10.5073/JfK.2011.07.04, Verlag Eugen Ulmer KG, Stuttgart

Correspondence
Prof. Dr. Marcia Almeida de Melo, Federal University of Campina Grande, Laboratory of Molecular Biology, CSTR/UFCG, Av. Universitária s/n, 58708-110, Patos, PB, Brazil, E-Mail: marcia.melo@pq.cnpq.br
Accepted
2 May 2011

Abstract

Brazil is presently (2010) the second largest producer of genetically modified (GM) crops. The legal framework to support both research activities and the commercial release of Genetically Modified Organisms (GMOs) is, however, very recent, as the Biosafety Law dates back from 2005. After the indispensable risk analysis, done by National Technical Commission for Biosafety (CTNBio), a GM plant can be approved for commercial release. Nevertheless, as stated in the Normative Resolution Nr. 5 (NR-5), of 2008, the post-market monitoring is mandatory. However, the first GM crop in Brazil, the herbicide tolerant soybean, was harvested in 2005. The CTNBio then asked for a monitoring plan and the applicant designed a complex study focused on case-specific monitoring. After four years the detailed field studies proved that no harm derived from this crop. The costs, nevertheless, were enormous. In June 2010, 21 GM plants were already approved for commercial release in Brazil, corresponding to different events in soybean (6), cotton (8) and maize (9). Single and stacked events tolerant to herbicides or insect-resistant are presently been planted. If, for each single event and for the stacks, a laborious post market monitoring plan were to be executed, the total costs would be unbearably high. The applicant is legally and financially responsible for the monitoring in Brazil. It is also responsible to produce an adequate monitoring plan. Since the NR-5 rules are far from being clear, the applicants either proposed an elabo­rated plan for case-specific monitoring or, conversely, submitted a very simple plan, targeting some potential adverse effect that can be more easily evaluated in commercial fields. It is not clearly stated either in the Biosafety Law or in the NR-5 that monitoring should be split in case-specific monitoring and general surveillance, as adopted in Europe. If case-specific monitoring plans are difficult to design, a sensible suggestion for the general surveillance was not yet achieved. Never­theless, the info-concentrating Brazilian Biosafety Infor­mation System may be a valuable source for the general surveillance, once it starts to operate. The general surveillance is presently either not contemplated in the monito­ring plans or only minimally treated. It is important to keep in mind that the applicants are responsible to produce most of the data, even for the general surveillance, and this can be extremely difficult in a scenario where many different events are cultivated, frequently in neighbouring fields. A conceptual framework for post market monitoring must therefore be established following a dia­log with all stakeholders. CTNBio is aware of these challenges and has already started to adjust the NR-5 to better guide the applicants in their writing of monitoring plans.

Key words: Genetically modified organism (GMO), transgenic crops, post market monitoring, Brazil, CTNBio, regulations on GMO

Zusammenfassung

Brasilien war 2010 der zweitgrößte Anbauer von gentechnisch veränderten Pflanzen. Die rechtliche Basis für die Forschung und kommerzielle Freisetzung von gentechnisch veränderten Organismen geht zurück auf das Jahr 2005. Nach der notwendigen Risikobewertung durch die nationale Technische Kommission für Biologische Sicherheit (CTNBio), kann eine Genehmigung für die kommerzielle Verwertung einer gentechnisch veränderten Pflanze erteilt werden. Allerdings erfordert die Normregel Nr. 5 (NR-5) aus dem Jahre 2008 ein begleitendes Monitoring. Allerdings wurde bereits im Jahre 2005 die erste transgene Pflanze, eine Herbizid-tolerante Sojabohne, in Brasilien angebaut. CTNBio forderte die Ausarbeitung eines Monitoringplanes, dem die Antragsteller mit einem komplexen, fallspezifisch fokussierten Monitoringdesign nachkamen. Nach vier Jahren detaillierter Feldstudien konnten keine Schäden durch den Anbau der transgenen Pflanzen nachgewiesen werden. Der Kostenaufwand war jedoch enorm. Im Juni 2010 waren bereits 23 gentechnisch veränderte Pflanzen mit verschiedenen transgenen Merkmalen für die kommer­zielle Nutzung in Brasilien zugelassen: Soja (6 Zulassungen), Baumwolle (8) und Mais (9). Einzelne oder gekoppelte Merkmale für Herbizidtoleranz und Insektenresistenz werden derzeit genutzt. Müsste für jedes einzelne Merkmal oder gekoppelte Merkmale ein eigenständiges Monitoringprogramm durchgeführt werden, wären die Kosten praktisch untragbar. Die Antragsteller sind nach brasilianischem Recht für die Planung und Durchführung des Monitoring verantwortlich. Da die Normregel Nr. 5 keine klaren Vorgaben macht, reichen die Antragsteller entweder sehr detaillierte, fallspezifisch orientierte oder sehr einfache, allgemeine Monitoringpläne ein, die sich auf einfach nachzuweisende, mögliche Effekte im kommerziellen Anbau beziehen. Im Gegensatz zum euro­päischen Recht unterscheidet weder das brasilianische Biosicherheitsgesetz noch Normregel Nr. 5 ein fallspezi­fisches Monitoring und eine Allgemeine Beobachtung. Sollte ein fallspezifischer Monitoringplan schwer herzuleiten sein, gibt es keine verbindlichen Vorgaben für eine Allgemeine Beobachtung. Hier kann ein zukünftiges brasilianisches Informationssystem für Biosicherheit wertvolle Unterstützung bieten. Derzeit jedoch ist eine Allgemeine Beobachtung gar nicht oder nur sehr begrenzt in den Monitoringplänen vorgesehen. Es ist zu beachten, dass die Antragsteller in jedem Fall für das Monitoring verantwortlich bleiben. Dies kann jedoch bei zunehmendem Anbau transgener Pflanzen mit verschiedenen (ähnlichen), einzelnen oder gekoppelten Merkmalen auf benachbarten Feldern zu großen Schwierigkeiten bei der Interpretation der einzelnen Monitoringdaten führen. Deshalb ist es notwendig, eine breit angelegte und mit verschiedenen Interessengruppen kommunizierte Monitoringstrategie zu entwickeln. CTNBio ist sich dieser Herausforderungen bewusst und hat in einem ersten Schritt die Normregel Nr. 5 überarbeitet, um den Antragstellern klarere Vorgaben für den Entwurf von Monitoringplänen zu bieten.

Stichwörter: Gentechnisch veränderte Organismen (GVO), GVO-Monitoring, Brasilien, CTNBio, Gentechnikrecht

Introduction

Brazil is presently (2010) the second largest producer of GM crops (James, 2009). However, until 2005 there was a lack of legal framework to support both research activi­ties and the commercial release of GMOs (Capalbo et al., 2003; Fontes, 2003). After the approval for commercial release of Roundup Ready® soybeans by the National Technical Commission for Biosafety (CTNBio), back in 1998, a long and sterile debate extended for more than 6 years, until the approval by the National Congress of the new Biosafety Law in March 2005, authorizing the first harvest of the transgenic soybean. During these years, as observed by Reis et al. (2006), discussions were centred in non-scientific issues or, sometimes, on misquoted scientific data. Other purely scientific activities, as laboratory experiments and field trials were largely prohibited.

This scenario has radically changed in 2005, by the decree of law nr. 11.105 nicknamed Biosafety Law (Naves and Freire de Sá, 2005; Tanus Job, 2008), which provides for safety norms and inspection mechanisms for the construction, culture, production, manipulation, transportation, transfer, import, export, storage, research, marke­ting, environmental release and discharge of genetically modified organisms – GMOs and their by-products, among other measures. After the indispensable risk analysis, a GM plant can be approved for commercial release. However, as stated in the CTNBio Normative Resolution nr. 5, of 2008, the post-market monitoring is mandatory, as it is elsewhere (CFIA, 2000; EFSA, 2006). Here we present the Brazilian experience and the uncertainties on monitoring, acutely felt by the members of the National Technical Commission for Biosafety (CTNBio), as well as by the other stakeholders.

Legal framework and commercial releases

The commercial release of Genetically Modified Organisms (GMO) and their derivatives must comply with the rules of NR-5, of 2008 (available at http://www.ctnbio.gov.br/index.php/content/view/12857.html). Its Article 10 obliges the applicant, following approval for commercial release of a GMO by its internal biosafety commission, to submit to CTNBio a monitoring plan, according to the Annex I of the resolution (see Table 1). However, the first GM crop in Brazil, the herbicide-tolerant Roundup Ready® soybean, was harvested in 2005. The CTNBio specifically asked for the monitoring of commercial production areas of soybean cultivars derived from the authorized breeding line GTS 40-3-2 for a period of five years, with the objective to deve­lop compared studies about the plant species, insects and microorganisms present in the fields (Communication n. 54/1998, available at http://www.ctnbio.gov.br/index.php/content/view/220.html). As the preliminary risk analysis did not point to any relevant risk for the envi­ronment or health, CTNBio issued a rather broad requirement for case-specific monitoring, solely focused on poten­tial environmental risks. As a consequence, the applicant designed a complex case-specific monitoring. After four years the detailed field studies produced a huge amount of data and decisively proved that no harm derived from this crop. The costs, taken by the applicant, as elsewhere (Paulauskas et al., 2008), were nevertheless enormous. A general surveillance system was not required by CTNBio nor proposed by the applicant.

Table 1. Genetically modified crops approved for commercial use in Brazil

Crop

Gene(s)

Trait(s)

Applicant

Approval
in Brazil
(year)

 

Countries where the events were also approved

Corn

Pat

Glufosinate tolerance

Bayer

2007

 

AR, AU, BR. CA, CH, EU, JP,
KO, ME, PH, SA, TW, US

pat, cry1Ab

Glufosinate tolerance,
resistance to lepidopterans

Syngenta

2007

 

AR, AU, BR. CA, CH, CO, EU,
JP, KO, ME, PH, RU, SA, SZ,
TW, UK, US, UY

Cry1Ab

Resistance to lepidopterans

Monsanto

2007

 

AR, AU, BR. CA, CH, CO, EU, JP, KO, ME, PH, SA, SZ,TW, US, UY

Cp4-epsps

Glyphosate tolerance

Monsanto

2008

 

AR, AU, BR. CA, CH, CO, ES, EU, JP, KO, ME, PH, SA, TW, US

Epsps

Glyphosate tolerance

Syngenta

2008

 

AR, AU, BR. CA, CH, EU, JP, KO, ME, PH, RU, SA, TW, US

pat, cry1Fa2

Glufosinate tolerance,
resistance to lepidopterans

Dow

2008

 

AR, AU, BR. CA, CH, CO, ES, EU, JP, KO, ME, PH, SA, TW, US

pat, epsps,
cry1Ab

Glufosinate and glyphosate tolerance, resistance to lepidopterans

Syngenta

2009

 

BR, CA, JP. KO, ME, PH

Cp4-epsps, cry1Ab

Glyphosate tolerance,
resistance to lepidopterans

Monsanto

2009

 

AR, BR, CA, ES, EU, JP, KO, ME, PH, SA, TW

Vip3Aa20

Resistance to lepidopterans

Syngenta

2009

 

AU, BR, CA, JP, ME, PH, TW, US

Cry1A.105

Resistance to lepidopterans

Monsanto

2009

 

AU, BR, CA, CO, EU, JP, KO,
PH, TW, US

pat, cp4-epsps, cry1Fa2

Glufosinate and glyphosate tolerance, resistance to lepidopterans

Dow

2009

 

AR, BR, CA, EU, JP, KO, ME, PH

Cotton

Cry1Ac

Resistance to lepidopterans

Monsanto

2005

 

AR, AU, BR, CA, CH, CO, EU,
IN, JP, KO, ME, PH, SA, US

pat

Glufosinate tolerance

Bayer

2008

 

AU, BR, CA, CH, EU, JP, KO,
ME, US

cp4-epsps

Glyphosate tolerance

Monsanto

2008

 

AR, AU, BR, CA, CH, CO, EU,
JP, KO, ME, PH, SA, US

pat, cry1F

Glufosinate tolerance,
resistance to lepidopterans

Dow

2009

 

BR, CA, JP, ME, US

cry1Ac, cry2Ab

Resistance to lepidopterans

Monsanto

2009

 

AU, BF, BR, CA, CH, EU, IN, JP,
KO, ME, PH, SA, US

cry1Ac, cp4-epsps

Glyphosate tolerance,
resistance to lepidopterans

Monsanto

2009

 

AR, AU, BR, CO, EU, JA, KO,
ME, PH, SA

Soybean

cp4-epsps

Glyphosate tolerance

Monsanto

1998

 

AR, AU, BR, CA, CH, CO, CZ,
EU, JP, KO, ME, PA, PH, RU,
SA, SZ,TW, UK, US, UY

csr1-2

Imidazolinone tolerance

BASF/
Embrapa Soja

2009

 

BR

pat

Glufosinate tolerance

Bayer

2010

 

BR, CA, JP, ME, US

pat

Glufosinate tolerance

Bayer

2010

 

AU, BR, CA, CH, EU, JP, KO,
ME, PH, TW, SA, US

Source: CTNBio website (http://www.ctnbio.gov.br/index.php/content/view/14785.html); CERA GMO database (http://cera-gmc.org).AR = Argentine, AU = Australia, BF = Burkina Faso, BR = Brazil. CA = Canada, CH = China, CO = Colombia, CZ = Czech Republic, ES = El Salvador, EU = European Union, IN = India, JP = Japan, KO = Korea, ME = Mexico, PA = Paraguay, PH = Philippines, RU = Russia, SA = South Africa, SZ = Switzerland, TW = Taiwan, UK = United Kingdom, US = United States, UY = Uruguay

In May 2010 a query at the CERA and CTNBio databases returned 21 results for Brazil, corresponding to different events in soybean (4), cotton (6) and maize (11) (Table 1). Single and stacked events tolerant to herbicides or insect-resistant are presently been planted for all three crops. If, for each single event and for the stacks, a laborious post market monitoring plan were to be executed, the total costs would be unbearably high. The applicant, i.e. the seed company in the case of the three common crops, is legally responsible for the monitoring in Brazil. It is also responsible to produce an adequate monitoring plan. However, since the rules in Annex I are far from being clear (cf. Table 2 for a summary of requests), the applicants either propose an elaborated plan for case-specific monitoring or, conversely, submit a very simple plan, targeting some potential adverse effect that can be more easily evaluated in commercial fields.

Table 2. Post Market Monitoring requirements to the applicants in Brazil. Essential information was extracted from Annex I of Normative Resolution n.5.

Document

Monitoring plan

Upon delivering the application for
commercial release

Objective

To oversee the effects resulting from
commercial release of a GMO on the
environment and human and animal health.

Case-specific monitoring and general
surveillance

Follow up

Supervisory agencies and entities

Agencies at the Ministries of Health and Environment, the Ministry of Agriculture
and CTNBio (Law n° 11.105, of 24 March 2005,
art. 16, § 1)

Reports

Yearly

For at least 5 years

Some considerations on the monitoring plan format and on its implementation

Monitoring is also a responsibility of some Brazilian fede­ral agencies, as stated in the Biosafety Law. Registration and inspection agencies and entities under the Ministry of Health, the Ministry of Agriculture, Cattle Raising and Supply and the Ministry for the Environment and the Ministry for Aquaculture are responsible for, among other duties, “keeping updated information in the Biosafety Infor­mation Systems (SIB)”. The SIB is, therefore, the orga­nization, affiliated to the Ministry of Science and Technology, that receives, organizes and shares information on monitoring. However, it is not yet operational and therefore monitoring results are sent to and analyzed by CTNBio.

Nineteen monitoring plans have been submitted to CTN­Bio. Even for the same crop and similar transgenic traits the set of proposed actions differed widely. Table 3 summarizes six proposed plans for insect-resistant corn and cotton and for herbicide-tolerant soybeans. Clearly some plans are oversized, as the prior risk analyses did not identify relevant risks either for the environment or for human or animal health. On the other hand, no clear actions were delineated for a general surveillance, and only undemanding initiatives were suggested, either focused on crop traits or in official health reports.

Table 3. Synopsis of contrasting monitoring plans submitted to CTNBio. A follow up of crop traits. In some cases an education program were also suggested

Trait

First Application

Second Application

Insect-resistant cotton

Monitoring of target insects
Protein degradability in soil
Soil chemical parameters
Soil physical parameters
Gene flow to conventional crop
Stover degradability
Soil microbial diversity
Diversity of micorrhiza fungi
Diversity of soil arthropods
Non-target arthropods (visual)
Non-target arthropods (traps)
Aquatic NTO
Bioaccumulation in NTO
Human and animal health

Monitoring of target insects
Protein degradability in soil
Resistance among target insects

Insect-resistant corn

Monitoring of target insects
Protein degradability in soil
Soil chemical parameters
Soil microbial diversity
Gene flow to conventional crop
Diversity of soil arthropods
Non-target arthropods
Aquatic NTO
Bioaccumulation in NTO
Human and animal health

Resistance among target insects

Herbicide-tolerant soybean

Weed population (incl. diaspores)
Resistant weeds
Soil chemical parameters
Soil physical parameters
Herbicide-degrading microorganisms
Human and animal health

Weed population
Resistant weeds

NTO = Non-target organism

It is not clearly stated neither in the Biosafety Law nor in the NR-5 that monitoring should be split in case-specific monitoring and general surveillance, as adopted in Europe. If case-specific monitoring plans are difficult to design, a sensible suggestion for the general surveillance was not yet achieved. Nevertheless, the info-concentrating SIB may be a valuable source for the general surveillance, once it starts to operate.

Concluding remarks

Due to the lack of clear information about how to produce an adequate monitoring plan, applicants either tended to unnecessarily enlarge the monitoring scope or shorten it to a few objectives. The general surveillance is not contemplated in the monitoring plans or minimally treated. It is important to keep in mind that the applicants are responsible to produce most of the data, even for the general surveillance, as well as bear the costs, and this can be extremely difficult in a realistic scenario where many different events are cultivated, frequently in neighbouring fields.

Sanvido et al. (2005) established the conceptual framework for a post market monitoring plan, composed of case-specific monitoring (CSM) and general surveillance, focused on anticipated effects of a specific GM plant and on unanticipated effects on general safeguard subjects, such as natural resources, respectively. CSM follows a conceptual line which is also used by CTNBio and by the applicants in Brazil. Since trying to detect the unexpec­ted is an inherent challenge, the authors suggested that general surveillance should concentrate on environmental subjects needed to be preserved. However, since the term environment is unspecific, there is a further need for defining specific safeguard subjects, which will be the focus of general surveillance. This is by itself also a challenge and the regulatory agency, as well as applicants, must keep an enlightening dialog as to better reach this goal. The proposed conceptual framework could be of assistance to the different stakeholders, when asses­sing GM plants during commercialization.

The EuropaBio suggestions for general surveillance, namely a farmer questionnaire and a network of surveillance systems, which are not GM crop focused (Wandelt et al., – The EuropaBio approach to general surveillance for cultivation of GM crops. Available from Nature Precedings <http://dx.doi.org/10.1038/npre.2010.4451.1> (2010)), are interesting and could be implemented in Brazil, but some difficulties can be anticipated: farmers may be unable to meaningfully answer the questions and the network has a very restricted number of potential participants in Brazil.

Moreover, integrating data from different sources may also be challenging. Reuter et al. (2010) developed the structure for an Information System for Monitoring GMO (ISMO) combining three interrelated components: a knowledge database on relevant information to GMO monitoring and on scientific hypotheses on cause-effects; a monitoring database with monitoring data and metadata, linked with data from other monitoring programs which are relevant for GMO-related questions; and a database covering administrative and procedural data. As stated by the authors, neither national nor international approaches to an ISMO exist yet.

CTNBio is aware of these challenges and has already started to adjust the NR-5 to better guide the applicants in their writing of monitoring plans.

References

Capalbo, D.M., A. Hilbeck, D. Andow, A. Snow, B. Ba Bong, F.H. Wan, E.M. Fontes, E. Onyango Osir, G.P. Fitt, J. Johnston, J. Songa, K.L. Heong, A.N. Birch, 2003: Brazil and the development of inter­national scientific biosafety testing guidelines for transgenic crops. J. Invertebr. Pathol. 83(2), 104-106.

CFIA (Canadian Food Inspection Agency), 2000: Regulatory Directive Dir94-08: Assessment Criteria for Determining Environmental Safety of Plants With Novel Traits. Canada, 24 pp. Available at http://www.inspection.gc.ca/english/plaveg/bio/dir/dir9408e.shtml.

EFSA, 2006: Opinion of the Scientific Panel on Genetically Modified Organisms on the Post Market Environmental Monitoring (PMEM) of genetically modified plants. EFSA J. 319, 1-27.

Fontes, E.M.G., 2003: Legal and regulatory concerns about transgenic plants in Brazil. J. Invert. Pathol. 83(2), 100-103.

James, C., 2009: Global Status of Commercialized Biotech/GM Crops: 2009. ISAAA Brief No. 41. ISAAA, Ithaca, NY.

Paulauskas, A., G. Jodinskas, D. Lygis, M. Jodinskiene, 2008: GMO Monitoring System in Lithuania. J. Verbr. Lebensm. 3 (Suppl. 2), 32-36.

Reuter, H., U. Middelhoff, F. Graef, R. Verhoeven, T. Batz, M. Weis, G. Schmidt, W. Schröder, B. Breckling, 2010: Information system for monitoring environmental impacts of genetically modified orga­nisms. Environ. Sci. Pollut. Res. (publ. online 23 April 2010). DOI 10.1007/s11356-010-0334-y.

Sanvido, O., F. Widmer, M. Winzeler, F. Bigler, 2005: A conceptual framework for the design of environmental post-market monito­ring of genetically modified plants. Environ. Biosafety Res. 4, 13-27.

Tanus Job, B.M., 2008: The previous risk treatment of the transgenic crops in the Brazilian biosafety regulatory system. Law Hum Genome Rev. 28,159-174.

Wandelt, C., E. Alcalde, K. Hayter, G. Legris, B.J. Patterson, B. Tinland, P. Windels, 2010: The EuropaBio approach to general surveillance for cultivation of GM crops. Available from Nature Precedings <http://dx.doi.org/10.1038/npre.2010.4451.1>.


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