Biological indicator for determining the efficacy of an oxidative sterilization process and methods of use

A biological indicator for determining the efficacy of an oxidative sterilization process, said biological indicator comprising, in a single container:

• a set of microbial spores;
• at least one fluorescent sensor protein;
• and
• a culture medium,
• wherein the at least one fluorescent sensor protein is capable of yielding an optically detectable signal when the at least one fluorescent sensor protein is not in a denatured state due to the oxidative sterilization process, the at least one fluorescent protein being further capable of yielding a different optically detectable signal when the at least one sensor protein is in a denatured state after the oxidative sterilization process, said difference being independent of a catalytic activity of the at least one fluorescent sensor protein and the culture medium being brought into contact with the set of microbial spores,
• wherein said culture medium is capable of inducing growth of any viable microbial life present after the oxidative sterilization process,
• wherein said culture medium comprises a colorimetric component being capable of undergoing an optically detectable color shift in the presence of microbial growth, and
• wherein the fluorescent sensor protein is a chimeric protein comprising a non-fluorescent protein selected from lysozyme, amylase, lipase, pepsin, glucosidase, phosphatase, galactosidase, chymotrypsin and lipase and a fluorescent protein selected from the group comprising green fluorescent proteins (Green Fluorescent Protein wild type GFPwt, Enhanced Green Fluorescent Protein EGFP, Super Folder Green Fluorescent Protein SFGFP, Emerald, Aequorea Victoria jellyfish Green Fluorescent Protein avGFP, T-Saphire), blue fluorescent proteins (Sirius, Azurite, Enhanced Blue Fluorescent Protein EBFP, Enhanced Blue Fluorescent Protein 2 EBFP2, mKalama1, Enhanced Tagged Green Fluorescent Protein TagGFP), cyan fluorescent proteins (Enhanced Cyan Fluorescent Protein ECFP, Cerulean, CyPet, mTurquoise2, Super Cyan Fluorescent Protein SCFP), yellow fluorescent proteins (Yellow Fluorescent Protein YFP, Citrine, Venus, YPet, Super Yellow Fluorescent Protein SYFP, Topaz, mAmetrina), red fluorescent proteins (tdTomato, mPlum, DsRed, mCherry, mStrawberry, mRaspberry, mRuby) and orange fluorescent proteins (mOrange, monomeric Kusabira Orange mKO and mOrange2).

A method of determining the efficacy of an oxidative sterilization process, by means of a self-contained biological indicator, wherein said biological indicator comprises, in a single container,

• wherein the at least one fluorescent sensor protein is capable of yielding an optically detectable signal when the at least one fluorescent sensor protein is not in a denatured state due to the oxidative sterilization process, the at least one fluorescent protein being further capable of yielding a different optically detectable signal when the at least one sensor protein is in a denatured state after the oxidative sterilization process, said difference being independent of a catalytic activity of the at least one fluorescent sensor protein and the culture medium being brought into contact with the set of microbial spores,
• wherein said culture medium is capable of inducing growth of any viable microbial life present after the oxidative sterilization process,
• wherein said culture medium comprises a colorimetric component being capable of undergoing an optically detectable color shift in the presence of microbial growth,
• wherein denaturation of the fluorescent sensor protein is correlated with death of the microbial spores, a decrease in the optically detectable signal being indicative of a successful sterilization process,
• wherein said fluorescent sensor protein is exogenous from said microbial spores and said decrease is detectable instantaneously after the sterilization process, and
• wherein the method comprises the steps of:
• a) placing the biological indicator along with a target material to be sterilized within a sterilizer,
• b) carrying out an oxidative sterilization process,
• c) placing the biological indicator in an incubator,
• d) screening the biological indicator for immediate detectable changes in fluorescence intensity, while incubating the biological indicator in the incubator,
• e) determining the efficacy of the oxidative sterilization process based on the screening carried out during step d),
• f) extending the incubation of the biological indicator obtained in step d)
• g) screening the incubated biological indicators obtained in step e) for an optically detectable color change, and
• h) determining the efficacy of the oxidative sterilization process, according to optically detectable changes obtained in step g).