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PCR Prevalence of Murine Opportunistic Microbes and their Mitigation by Using Vaporized Hydrogen Peroxide
Natalie H Ragland1, Emily L Miedel2, Robert W Engelman2
1Department of Comparative Medicine, H Lee Moffitt Cancer Center and Research Institute, University of South Florida, Tampa, Florida, USA. nragland@usf.edu.
Abstract:
Exposing immunodeficient mice to opportunistic microbes introduces risks of data variability, morbidity, mortality, and the invalidation of studies involving unique human reagents, including the loss of primary human hematopoietic cells, patient-derived xenografts, and experimental therapeutics. The prevalence of 15 opportunistic microbes in a murine research facility was determined by yearlong PCR-based murine and IVC equipment surveillance comprising 1738 specimens. Of the 8 microbes detected, 3 organisms- Staphylococcus xylosus, Proteus mirabilis, and Pasteurella pneumotropica biotype Heyl-were most prevalent in both murine and IVC exhaust plenum specimens. Overall, the 8 detectable microbes were more readily PCR-detectable in IVC exhaust airways than in murine specimens, supporting the utility of PCR testing of IVC exhaust airways as a component of immunodeficient murine health surveillance. Vaporized hydrogen peroxide (VHP) exposure of IVC equipment left unassembled (that is, in a 'static-open' configuration) did not eliminate PCR detectable evidence of microbes. In contrast, VHP exposure of IVC equipment assembled 'active-closed' eliminated PCR-detectable evidence of all microbes. Ensuring data integrity and maintaining a topographically complex immunodeficient murine research environment is facilitated by knowing the prevalent opportunistic microbes to be monitored and by implementing a PCR-validated method of facility decontamination that mitigates opportunistic microbes and the risk of invalidation of studies involving immunodeficient mice.
Insights
Opportunistic microbes in research facilities pose risks to immunodeficient mice studies. PCR surveillance of IVC exhaust and proper decontamination are key to ensuring data integrity and preventing study invalidation.
Area of Science:
- Microbiology
- Immunology
- Laboratory Animal Science
Background:
- Immunodeficient mice are crucial for research but susceptible to opportunistic microbes.
- Microbial contamination can lead to data variability, morbidity, mortality, and loss of valuable research materials.
- Effective health surveillance and decontamination are vital for reliable results in immunodeficient mouse models.
Purpose of the Study:
- To determine the prevalence of opportunistic microbes in a murine research facility.
- To evaluate the efficacy of PCR testing in IVC (individually ventilated cage) exhaust for health surveillance.
- To assess the effectiveness of vaporized hydrogen peroxide (VHP) decontamination methods.
Main Methods:
- Yearlong PCR-based surveillance of 1738 specimens from mice and IVC equipment.
- Detection of 8 out of 15 targeted opportunistic microbes.
- Testing VHP decontamination on static-open and active-closed IVC configurations.
Main Results:
- Staphylococcus xylosus, Proteus mirabilis, and Pasteurella pneumotropica were most prevalent.
- Microbes were more readily detected in IVC exhaust airways than in murine specimens.
- VHP decontamination was effective only when IVC equipment was assembled in the 'active-closed' configuration.
Conclusions:
- PCR testing of IVC exhaust is a valuable tool for immunodeficient mouse health surveillance.
- Effective decontamination requires specific protocols, such as VHP on assembled IVC equipment.
- Monitoring prevalent opportunistic microbes and implementing validated decontamination mitigates risks to research integrity.
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