Experiments Subject to the USG DURC-PEPP Policy
Category 1 Experiments (Section 4.1.2 of the USG DURC-PEPP Policy)
Research within the scope of Category 1 are those experimental outcomes with a biological agent or toxin outlined in the USG DURC-PEPP Policy that are reasonably anticipated to:
- Increase transmissibility of a pathogen within or between host species;
- Increase the virulence of a pathogen or convey virulence to a non-pathogen;
- Increase the stability of a pathogen or toxin in the environment, or increase the ability to disseminate a pathogen or toxin;
- Alter the host range or tropism of a pathogen or toxin;
- Decrease the ability for a human or veterinary pathogen or toxin to be detected using standard diagnostic or analytical methods;
- Increase resistance of a pathogen or toxin to clinical and/or veterinary prophylactic or therapeutic interventions;
- Alter a human or veterinary pathogen or toxin to disrupt the effectiveness of preexisting immunity, via immunization or natural infection, against the pathogen or toxin; or
- Enhance the susceptibility of a host population to a pathogen or toxin.
Category 2 Experiments
Research within the scope of Category 2 are those experimental outcomes or actions with a pathogen outlined in the USG DURC-PEPP Policy that are reasonably anticipated to:
- Enhance transmissibility of the pathogen in humans;
- Enhance the virulence of the pathogen in humans;
- Enhance the immune evasion of the pathogen in humans such as by modifying the pathogen to disrupt the effectiveness of pre-existing immunity via immunization or natural infection;
- Generate, use, reconstitute, or transfer an eradicated or extinct PPP, or a previously identified PEPP.