Pulido Barriga M Fabiola, Randolph James W J, Glassman Sydney I
Department of Microbiology and Plant Pathology, University of California-Riverside, Riverside, California, USA.
Department of Ecology and Evolutionary Biology, University of California, Irvine, California, USA.
mSphere. 2025 Jan 28;10(1):e0060324. doi: 10.1128/msphere.00603-24. Epub 2024 Dec 20.
Advances in technology have facilitated extensive sample collection to explore microbiomes across diverse systems, leading to a growing reliance on ultracold freezers for storing both samples and extracted DNA. However, freezer malfunctions can jeopardize data integrity. To evaluate the impact of an unexpected -80°C freezer failure and the recoverability of thawed soil samples, we extracted DNA and compared it to long-term DNA stored at -20°C and original 16S and ITS2 sequencing data collected before the malfunction. Using Illumina MiSeq, we assessed how the freezer failure and long-term storage influenced the resilience of bacterial or fungal richness or community composition and our ability to accurately determine experimental treatment effects. Our results reveal substantial resilience in fungal richness and both bacterial and fungal beta-diversity to soil sample thawing and extended frozen DNA storage. This resilience facilitated biological inferences that closely mirrored those observed in the original study. Notably, fungi exhibited greater resilience to short-term thawing compared to bacteria, which showed sensitivity to both thawing and long-term freezing. Moreover, taxonomic composition analysis revealed the persistence of dominant microbial taxa under thawing and prolonged freezing, suggesting that dominant microbes remain viable for tracking across temporal studies. In conclusion, our study highlights that beta-diversity is more robust than alpha-diversity and fungi are more resilient to freezer failure than bacteria. Furthermore, our findings underscore the effectiveness of soil storage at -80°C compared to storage of extracted DNA at -20°C, despite potential freezer failures, as the most robust method for long-term storage in microbiome studies.
Microbiome studies heavily rely on ultracold freezers for sample storage. Unfortunately, these freezers are prone to frequent malfunctions, resulting in the loss of invaluable samples at laboratories worldwide. Such losses can halt research progress due to potential issues with sample reliability. Our research demonstrates that not all is lost when an unforeseen freezer failure occurs. Samples can still be reliably used to assess treatment effects, which is particularly important for long-term temporal studies where samples cannot be readily obtained again.
技术进步推动了广泛的样本采集,以探索不同系统中的微生物群落,这使得越来越依赖超低温冰箱来存储样本和提取的DNA。然而,冰箱故障可能会危及数据完整性。为了评估意外的-80°C冰箱故障的影响以及解冻后的土壤样本的可恢复性,我们提取了DNA,并将其与储存在-20°C的长期DNA以及故障发生前收集的原始16S和ITS2测序数据进行比较。使用Illumina MiSeq,我们评估了冰箱故障和长期储存如何影响细菌或真菌丰富度的恢复力或群落组成,以及我们准确确定实验处理效果的能力。我们的结果表明,真菌丰富度以及细菌和真菌的β多样性对土壤样本解冻和延长的冷冻DNA储存具有显著的恢复力。这种恢复力有助于进行生物学推断,这些推断与原始研究中观察到的推断非常相似。值得注意的是,与细菌相比,真菌对短期解冻表现出更大的恢复力,细菌对解冻和长期冷冻都很敏感。此外,分类组成分析表明,优势微生物类群在解冻和长期冷冻下持续存在,这表明优势微生物在跨时间研究中仍可追踪。总之,我们的研究强调,β多样性比α多样性更稳健,并且真菌比细菌对冰箱故障更具恢复力。此外,我们的研究结果强调了在微生物组研究中,与将提取的DNA储存在-20°C相比,尽管可能存在冰箱故障,但将土壤储存在-80°C是长期储存的最稳健方法。
微生物组研究严重依赖超低温冰箱进行样本储存。不幸的是,这些冰箱容易频繁出现故障,导致全球实验室中宝贵样本的丢失。由于样本可靠性方面的潜在问题,此类损失可能会阻碍研究进展。我们的研究表明,当发生意外的冰箱故障时,并非一切都已失去。样本仍然可以可靠地用于评估处理效果,这对于无法轻易再次获得样本的长期时间研究尤为重要。