SUMMARY STATEMENT OF THE ASILOMAR CONFERENCE ON RECOMBINANT DNA NOLECULES™ * Summary statement of the report submitted to the Assembly of Life Sciences of the National. Academy of Sciences and approved by its Executive Committee on 20 May 1975. NOTICE: The project which is the subject of this report was approved by the Governing Board of the National Research Council, acting in behalf of the National Academy of Sciences. Such. approval reflects the Board's judgment that the project is of national importance and appropriate with respect to both the purposes ahd resources of the National Research Council. The members of the committee selected to undertake this project and prepare this report were chosen for recognized scholarly competence and with due consideration for the balance of dis- ciplines appropriate to the project. Responsibi lity for the detailed aspects of this report rests with that committee. Each report issuing from a study committee of the National Research Council is reviewed by an independent group of qualified individuals according to procedures established and monitored by the Report Review Committee of the National Academy of Sciences. Distribution of the report is approved, by the President of the Academy, upon satisfactory completion of the review process. ORGANIZING COMMITTEE FOR THE INTERNATIONAL CONFERENCE ON RECOMBINANT DNA MOLECULES Paul Berg, Chatrman Professor of Biochemistry Department of Biochemistry Stanford University Medical Center Stanford, California David Baltimore American Cancer Society Professor of Microbiology Center for Cancer Research Massachusetts Institute of Technology Cambridge, Massachusetts Sydney Brenner Member, Scientific Staff of the Medical Research Council of the United Kingdom Cambridge, England Richard 0. Roblin III Professor of Microbiology and Molecular Genetics Harvard Medical School and Assistant Bacteriologist, Infectious Disease Unit Massachusetts General Hospital Boston, Massachusetts Maxine F, Singer Head, Rucleic Acid Enzymolooy Section Laboratory of Biochemistry National Cancer Institute National Institutes of Health Bethesda Maryland National Academy of Sciences-National Research Council Staff: Artemis P. Simopoulos Executive Secretary Division of Medical Sciences “Assembly of Life Sciences Elena 0. Nightingale Resident-Fellow Division of Hedical Sciences Assembly of Life Sciences Supported by the National Institutes of Health (Contract NO1-0D-5-2103) and the National Science Foundation ( Grant GBMS75-05293) Requests for reprints should be addressed to: Division of Medical] Sciences Assenbly of Life Sciences National Academy of Sciences 2101 Constitution Avenue, N.W, Washington, D.C. 20418 Summary Statement of the Asilomar Conference on Recombinant DNA Molecules Introduction and General Conclusions ¢ This meeting was organized to review scientific progress in research on recombinant DNA molecules and to discuss appropriate ways ‘to deal with the potential biohazards of this work. Impressive scientific achievements ‘have already been made in this field and these techniques have a remarkable potential for furthering our understanding of fundamental biochemical processes in pro- and eukaryotic cells. The use of recombinant DNA methodology - promises ‘to revolutionize the practice of molecular biology. While there has as yet been no practical application of the new techniques, there is everv reason to believe that they will have significant practical utility in the future. Of particular concern te the participants at the meeting was the issue of whether the pause in certain aspects of research in this area, called for by the Committee on Recombinant BNA Holecules of the National Academy -of Sciences, U.S.A. in the letter published in July, 1974, should end; and, if so, how the scientific work could be under taken with minimal ‘risks to workers in laboratories, to the public at large and to the animal and plant species sharing our ecosystems.. _. The new techniques, which permit combination of genetic information from very “different organisms, place us in an area of biology with many unknowns. Even in the present, more limited conduct of research in this field, the evaluation of potential biohazards has proved to be extremely Il. difficult. It is this ignorance that has compelled us to conclude that it would be wise to exercise considerable caution in performing this research. Nevertheless, the participants at the Conference agreed that most of the work on construction of recombinant DNA molecules should proceed provided that appropriate safeguards, principally biological and physical” barriers adequate to contain the newly created organisms, are employed. Moreover, “the standards of protection should be greater at the beginning and modified as improvements in the methodology occur and assessments of the risks change. Furthermore, it-was agreed that there are certain experiments in which the potential risks are of such a serious nature that they ought not. to be done with presently available containment facilities. In the longer term serious problems may arise in the large scale annlication of this methodoloay in industry, medicine and agriculture. But it was also recognized that future research and expervence may show that many of the potential bio- hazards are less serious and/or less probable than we now suspect. Principles Guiding the Recommendations and Conclusions _ Though our assessments of the risks involved with each of the various lines of research on recombinant DNA molecules may differ, few, if any, believe that this methodology is free from any risk. Reasonable principles for dealing with these potential risks are: 1) that containment be made an essential consideration in the experimental design and, 2) that the effectiveness of the containment should match, as ciosely as-possible, the estima ted risk. Consequently, whatever scale of risks is agreed upon, there should be a commensura te scale of containment. Estimating the “risks will be difficult and intuitive at first but this will improve as we acquire additional knowledge; at each stage we shall have to match the potential risk with an appropriate level of containment. Experiments -requiring large scale operations would seem to be riskier than equivalent experiments done on a small scale and, therefore, require more stringent containment procedures. “The use of cloning vehicles or vectors (plasmids, phages) and bacterial hosts with a restricted capacity to multiply outside of the laboratory would reduce the potential biohazard of a particular experiment. Thus, the ways in which potential biohazards and different levels of containment are “matched may vary from time to time particularly as the containment technology is improved. The means for assessing and balancing risks with appropriate levels of containment wil] need to be reexamined from time to time. Hopefully, through both formal and informal channels of information within and between the nations of the world, the way - in which potential biohazards and levels of containment are matched would be consistent. Containment of potentially bioliazardous agents can be achieved in several ways. The most significant contribution to limiting the spread of the recombinant DNAs, is the use of biological barriers. These barriers are of two types: 1) fastidious bacterial hosts unable “to survive in natural environments, and 2) non-transmissible and equally fastidious vectors (plasmids, bacteriophages or other viruses) able to grow only in specified hosts. “Physical containment, ex- emplified by the use of suitable hoods, or where applicable, limited Ill, - . -accessS or negative pressure laboratories, provides an additional factor of safety. Particularly important is strict adherence to good micro- biological practices which, to a large measure can Limit the .escape of organisms from the experimental situation, and thereby increase the safety of the operation. Consequently, education and training of all personnel involved in the experiments is essefitial to the effec- tiveness of all containment measures. In practice these different | means of containment will complement one another and documented substantial improvements in the ability to restrict the growth of bacterial hosts and vectors could permit modifications of the complementary physical containment requirements. — Stringent physical containment and rigorous laboratory procedures can reduce but not eliminate the possibility of spreading potentially hazardous agents. Therefore, investigators relying upon "disarmed" hosts and vectors for additional safety must rigorously test the effectiveness of these agents before accepting their validity as biological barriers. Specific Recommendations for Matching Types of Containment with Types of Experiments No classification of experiments as to risk and no set of containment procedures can anticipate all situations. Given our present uncer tain- ties about the hazards, the parameters proposed here are broadly con- ceived and meant to provide provisional guidelines for investigators and agencies concerned with research on recombinant DNAs. However, each investigator bears a responsibility for determining whether, in his particular case, special circumstances warrant a higher level of containment than is suggested here. A. Types of Containment 1. Minimal Risk: This type of containment is intended for experiments in which the biohazards may be accurately assessed and are expected to be minimal. Such containment can be achieved by following the operating procedures recommended for clinical micro- biological laboratories. Essential features of such facilities are no drinking, eating or smoking in the laboratory, wearing laboratory coats in the work area, the use of cotton-plugged pipettes or prefer- ably mechanical pipetting devices and prompt disinfection of con- taminated materials. 2. Low Risk: This level of containment is appropriate for experiments which generate novel biotypes but where the available information indicates that the recombinant DHA cannot alter appreciably the ecological behavior of the recipient species, increase significantly its pathogenicity, or prevent effective treatment of any resulting infections. The key features of this containment (in addition to the minimal procedures mentioned above) are a prohibition on mouth pipetting, access limited to laboratory personnel, and the use of biological safety cabinets for procedures likely to produce aerosols (e.g., blending and sonication). Though existing vectors may be used in conjunction with low risk procedures, safer vectors and hosts should be adopted as they become available. 3. Moderate Risk: Such containment facilities are intended for experiments in which there is a probability of generating an agent with a significant potential for pathogenicity or ecological disruption, The principle features of this level of containment, in addition to those of the two preceding classes, are that transfer operations should be carried out-in biological safety cabinets (e.g., laminar flow hoods), gloves should be worn during the handling of infectious materials, vacuum lines must be protected by filters and negative pressure should be maintained in the limited access laboratories. Moreover, experiments posing a moderate risk must be done only with vectors and hosts that have an appreciably impaired capacity to multiply outside of the laboratory. 4, High Risk: This level of containment is intended tor experiments atha n antnritea AF tha eu wen nat wt we we a Sn which tha natontial Far arnlnaaicoel dicruntian ar n @ae one e wee wee rv wee we ee oe — ae ee ft a awe ~ mee hee wy . I fort be atcal runtio: modified organism could be severe and thereby pose a serious biohazard to laboratory personnel or the public. The main features of this type of facility, which was designed to contain highly infectious microbiological agents, are its isolation from other areas by air locks, a negative pressure environment, a requirement for clothing changes and showers for entering _ personnel and laboratories fitted with treatment systems to inactivate or remove biological agents that may be contaminants in exhaust air, liquid and solid wastes. Al} persons occupying these areas should wear protective laboratory clothing and shower at each exit from the containment facility. The handling of agents should be confined to biological safety cabinets in which the exhaust air is incinerated or passed through Hepa filters. High risk containment includes, beside the physical and procedural features described above, the use of rigorously tested vectors and hosts whose growth can be confined to the laboratory. B. Types of Experiments Accurate es tima tes of the risks associated with different types of experiments are difficult to obtain because of our ignorance-of the probability that the anticipated dangers will manifest themselves. Nevertheless, experiments involving the construction and propaga- tion of recombinant DNA molecules using DNAs from 1) prokaryotes, bacteriophages and other plasmids, 2) animal viruses, and 3) eukaryotes have been characterized as minimal, low, moderate and high risks to guide investigators in their choice of the appropriate containment. These designations should be viewed as interim assignments which will need to be revised-upward or downward in the light of future experience. The recombinant DNA molecules themselves, as distinct from cells carrying them, may be infectious to bacteria or higher organisms. DNA preparations from these experiments, particularly in large quan- tities, should be chemically inactivated before disposal. 1. Prokaryotes, bacteriophages and bacterial plasmids: Where the construction of recombinant DNA molecules and their prop- agation involves prokaryotic agents that are known to exchange genetic information naturally, the experiments can be performed in minimal risk containment facilities. Where such experiments pose a potential hazard, more stringent containment may be warranted, Experiments involving the creation and propagation of recombinant DNA molecules from DNAs of species that ordinarily do not exchange genetic information, generate novel biotypes. Because such experiments may pose biohazards greater than those associated with the original organisms, they should be performed, at least, in low risk contain- ‘ment facilities. If the experiments involve either pathogenic organ- isms, or genetic determinants that may increase the pathogenicity of the recipient species, or if the transferred DNA can confer upon the recipient organisms new metabolic activities not native to these ~ species and thereby modify its relationship with the environment, then ‘moderate or high risk containment should be used. Experiments extending the range of resistance of established human, pathogens to therapeutically useful antibiotics or disinfectants should be undertaken only under moderate or high risk containment | depending upon the virulence of the organism involved. ?, Animal Viruses: Experiments involving linkage of viral genomes or genome segments to prokaryotic vectors and their propaga tion an prokaryotic cells snould be performed only with vector-host systems having demonstrably restricted growth capabilities outside the laboratory and with moderate risk containment facilities. Rigorously purified and characterized segments of non-oncogenic viral ee of the dem- onstrably non-transforming regions of oncogenic: viral DNAs can be attached to presently existing vectors and propagated in moderate risk containment - facilities; as safer vector-hos t systems become available such experiments may be performed in low risk facilities. Experiments designed to introduce or propagate DNA from non-viral or other low risk agents in animal cells should use only low risk ‘animal DNAs as vectors (e.g., viral, mitochondrial) and manipulations should be confined to moderate risk containment facilities. 3. Eukaryotes: The risks associated with joining random fragments of eukaryote DNA to prokaryotic DNA vectors and the prop- agation of these recombinant DNAs in prokaryotic hosts are the most difficult to assess. A priori, the DNA from warm-blooded vertebrates is more likely to contain. tryptic viral genomes potentially pathogenic for many than.is the DNA from other eukaryotes. Consequently, attempts to clone segments of DRA from such animal and particularly primate genomes should be performed only with vector-host systems having demonstrably restricted growth capabilities outside the laboratory and in a moderate risk containment facility. Until clonea segments of warm-blooded ver tebrate DNA are completely characterized, they should continue to be maintained in the mi aK madawnatn visk contoinmont a aa a ed os ocw laboratories; when such cloned segments are characterized, they may be propagated as suggested above for purified segments of virus genomes. Unless the organism makes a product known to be dangerous (e.g., toxin, virus), recombinant DNAs from cold- blooded vertebrates and all other lower eukaryotes can be constructed and propagated with the safest vector-host system available in low risk containment Facilities. Purified DNA from any source that performs known functions and can be judged to be non-toxic, may be cloned with currently available vectors in low risk containment facilities. (Toxic here includes potentially oncogenic products or substances that might perturb normal metabolism if produced in an animal or plant by a resident microorganism. ) TV. 10. 4. Experiments to be Deferred: There are feasible experiments which present such serious dangers that their performance should not be undertaken at this time with the currently available vector-host systems and the presently available containment éapability. These in- ‘clude the cloning of recombinant DNAs derived from highly pathogenic organisms (i.e., Class III, IV, V etiologic agents as classified by the United Stated Department of Health, Education and Welfare), DNA containing toxin genes and large scale experiments (more than 10 liters of culture) using recombinant DNAs that are able to make products potent- “dally harmful to man, animals or plants. ~ Implementation In many countries steps are already being taken by national bodies to formulate codes of practice for the. conduct of experiments with &nown or potential biohazard. * Until these are established, we urge individual scientists to use the proposals in this document as a guide. ‘In addition, there are some recommendations which could be immediately and directly ‘implemented by the scientific community. A. Development of Safer Vectors and Hosts An important and encouraging accomplishment of the meeting was the realization that special bacteria and vectors can be constructed genetically, which have a restricted capacity to multiply outside the laboratory, and * Advisory Board for the Research Councils. Report of the Working Party on the Experimental Manipulation of the Genetic Composition of Micro-Organisms. Presented to Parliament by the Secretary of State for Education. and Science by Command of Her Majesty January 1975. London: Her Majesty's Stationery Office, 1975, 23pp. oe + . National Institutes of Health Recombinant DNA Molecule Program Advisory Committee 11. that the use of these organisms could enhance the safety of recombinant DNA experiments by many orders of magnitude. Experiments along these lines are presently in progress and in the near future, variants of 4 bacteriophage, non-transmissible plasmids and special strains of E£. colt will become available. An of these vectors could reduce the potential biohazards by very large factors and improve the methodology as well. Other vector-host systems, particularly modified strains of Bacillus subtilis and their relevant bacteriophages and plasmids, may also be useful for particular purposes. Quite possibly safe and suitable vectors may be found for eukaryotic hosts such 7 yeast and readily cultured plant and animal cells. There is likely to be a continuous development in this area and the participants at the meeting agreed that improved vector-hest systems which reduce the biohazards of recombinant DNA research will be made freely available to all interested investigators. B. Laboratory Procedures It is the clear responsibility of the principal investigator to inform the staff of the laboratory of the potential hazards of such experiments, before they are initiated. Free and open discussion is necessary so that — each individual participating in the experiment fully understands the nature of the experiment and any risk that might be involved. All workers must be properly trained in the containment procedures that are designed to control the hazard, including emergency actions in the event of a hazard. It is also recommended that appropriate health surveillance of all personnel, including serological monitoring, be conducted periodically. v. 12. C. Education and Reassessment Research in this area will develop very quickly and the methods will be applied to many different biological problems. At any given time it is impossible to foresee the entire range of all potential experiments and make judgments on them. Therefore, it is essential to undertake a contin- uing reassessment of the problems in the light of new scientific knowledge. . This could be achieved by a series of annual workshops and meetings, some of which should beat the international level. There should also be courses to train individuals in the relevant methods since it is likely that the work will be taken up by laboratories which may not have had extensive experience in this area. High priority should also be given to research that could improve and evaluate the containment effectiveness of new and existing vector-host systems. New Knowledge This document represents our first assessment of the potential bic- hazards in the light of current knowledge. However, little is known about the survival of laboratory strains. of bacteria and bacteriophages in different ecological niches in the outside world. Even less is known about whether -recombinant DNA molecules will enhance or depress the survival of their vectors and hosts in nature. These questions are fundamental to the testing of any new organism that may be constructed. Research in this area needs to be undertaken and should be given high priority. In general, however, molecular biologists who may construct DNA recombinant molecules do not ‘undertake these experiments and it will be necessary to facilitate collaborative 13. research between them and groups skilled in the study of bacterial “infection or ecological microbiology. Work should also be undertaken which would enable us to monitor the escape or dissemination of cloning vehicles and their hosts. Nothing is known about the potential infectivity in higher organisms of phages or bacteria containing segments of eukaryotic DNA and very little about the infectivity of the DNA molecules themselves. Genetic trans- formation of bacteria does occur in animals suggesting that recombinant DNA molecules can retain their biological potency in this environment. There are many questions in this area, the answers to which are essential for our assessment of the biohazards of experiments with recombinant DNA molecules. It will be necessary to ensure that this work will be planned and carried out; and it will be particulerly important to have this in- formation before large scale applications of the use of recombinant DNA molecules is attempted.