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Pathogen Inactivating Properties and Increased Sensitivity in Molecular Diagnostics by PAXgene,a Novel Non-Crosslinking Tissue Fixative
Authors:Martina Loibner  Walter Buzina  Christian Viertler  Daniel Groelz  Anja Hausleitner  Gintare Siaulyte  Iris Kufferath  Bettina K?lli  Kurt Zatloukal
Institution:1. Christian Doppler Laboratory for Biospecimen Research and Biobanking Technologies, Institute of Pathology, Medical University Graz, Graz, Austria;2. Medical University Graz, Institute of Pathology, Graz, Austria;3. Medical University Graz, Institute of Hygiene, Microbiology and Environmental Medicine, Graz, Austria;4. Qiagen GmbH, Research and Development, Hilden, Germany;5. LKH Hospital Weiz, Laboratory of Medical Department, Weiz, Austria;University of Torino, ITALY
Abstract:

Background

Requirements on tissue fixatives are getting more demanding as molecular analysis becomes increasingly relevant for routine diagnostics. Buffered formaldehyde in pathology laboratories for tissue fixation is known to cause chemical modifications of biomolecules which affect molecular testing. A novel non-crosslinking tissue preservation technology, PAXgene Tissue (PAXgene), was developed to preserve the integrity of nucleic acids in a comparable way to cryopreservation and also to preserve morphological features comparable to those of formalin fixed samples.

Methods

Because of the excellent preservation of biomolecules by PAXgene we investigated its pathogen inactivation ability and biosafety in comparison to formalin by in-vitro testing of bacteria, human relevant fungi and human cytomegalovirus (CMV). Guidelines for testing disinfectants served as reference for inactivation assays. Furthermore, we tested the properties of PAXgene for detection of pathogens by PCR based assays.

Results

All microorganisms tested were similarly inactivated by PAXgene and formalin except Clostridium sporogenes, which remained viable in seven out of ten assays after PAXgene treatment and in three out of ten assays after formalin fixation. The findings suggest that similar biosafety measures can be applied for PAXgene and formalin fixed samples. Detection of pathogens in PCR-based diagnostics using two CMV assays resulted in a reduction of four to ten quantification cycles of PAXgene treated samples which is a remarkable increase of sensitivity.

Conclusion

PAXgene fixation might be superior to formalin fixation when molecular diagnostics and highly sensitive detection of pathogens is required in parallel to morphology assessment.
Keywords:
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