Microbial occurrence in liquid nitrogen storage tanks: a challenge for cryobanking?

• Published in: Applied microbiology and biotechnology Vol. 105; no. 20; pp. 7635 - 7650
• Main Authors: Bajerski, Felizitas, Nagel, Manuela, Overmann, Joerg
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01-10-2021; Springer; Springer Nature B.V
• Subjects: Biobanks; Biological materials; Biomedical and Life Sciences; Biotechnology; Cell culture; Contaminants; Contamination; Cryopreservation; Crystals; Culture; Culture collections; Distribution; Freezers; Gases; Gene banks; Humans; Ice; Ice crystals; Ice formation; Life Sciences; Liquid nitrogen; Medical materials; Microbial contamination; Microbial Genetics and Genomics; Microbiology; Microbiomes; Microorganisms; Mini-Review; Nitrogen; Physiological aspects; Quality management; Risk assessment; Spreadsheets; Storage containers; Storage tanks; Temperature; Vapor phases; Very Low Frequencies; Germany; Safe storage; Biobanking; Risk/quality management; Cryopreservation; Bioarchive; Biorepository; Microbial contamination; Cryoconservation; Cryobank
• ISSN: 0175-7598; 1432-0614
• DOI: 10.1007/s00253-021-11531-4

Modern biobanks maintain valuable living materials for medical diagnostics, reproduction medicine, and conservation purposes. To guarantee high quality during long-term storage and to avoid metabolic activities, cryostorage is often conducted in the N
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vapour phase or in liquid nitrogen (LN) at temperatures below − 150 °C. One potential risk of cryostorage is microbial cross contamination in the LN storage tanks. The current review summarises data on the occurrence of microorganisms that may compromise the safety and quality of biological materials during long-term storage. We assess the potential for the microbial contamination of LN in storage tanks holding different biological materials based on the detection by culture-based and molecular approaches. The samples themselves, the LN, the human microbiome, and the surrounding environment are possible routes of contamination and can cause cross contaminations via the LN phase. In general, the results showed that LN is typically not the source of major contaminations and only a few studies provided evidence for a risk of microbial cross contamination. So far, culture-based and culture-independent techniques detected only low amounts of microbial cells, indicating that cross contamination may occur at a very low frequency. To further minimise the potential risk of microbial cross contaminations, we recommend reducing the formation of ice crystals in cryotanks that can entrap environmental microorganisms and using sealed or second sample packing. A short survey demonstrated the awareness for microbial contaminations of storage containers among different culture collections. Although most participants consider the risk of cross contaminations in LN storage tanks as low, they prevent potential contaminations by using sealed devices and − 150 °C freezers. It is concluded that the overall risk for cross contaminations in biobanks is relatively low when following standard operating procedures (SOPs). We evaluated the potential sources in detail and summarised our results in a risk assessment spreadsheet which can be used for the quality management of biobanks.
Key points
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Identification of potential contaminants and their sources in LN storage tanks.
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Recommendations to reduce this risk of LN storage tank contamination.
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Development of a risk assessment spreadsheet to support quality management.