Keeping it cool: Soil sample cold pack storage and DNA shipment up to 1 month does not impact metabarcoding results

Citation

Delavaux, C.S., Bever, J.D., Karppinen, E.M., Bainard, L.D. (2020). Keeping it cool: Soil sample cold pack storage and DNA shipment up to 1 month does not impact metabarcoding results. Ecology and Evolution, [online] 10(11), 4652-4664. http://dx.doi.org/10.1002/ece3.6219

Plain language summary

With advances in molecular biology tools such as DNA sequencing, it is now possible to identify the majority of microorganisms. Although these tools give us tremendous power and open many doors to answer important questions, we must understand how we process samples may impact our results and interpretations. In this study, we aimed to determine how four different soil storage methods (room temperature, cooler with ice packs, flash freezing with liquid nitrogen, and liquid preservation) and the impact of sample thaw time affect the DNA sequencing and abundance of fungi and bacteria in the samples. Overall, we found that storage using standard cold packs with subsequent storage at −20°C is little different than immediate storage in liquid nitrogen, suggesting that the historical and current method is adequate. We also found evidence that storage at room temperature or with aid of a chemical solution can lead to changes in microbial abundance and community composition and we advise against these storage methods for DNA-based analyses. Finally, based on our study, researchers working abroad or in remote areas can be confident that for at least 1 month, thawing extracted DNA will not impact their results. We hope that this work will help researchers working with soil bacteria and fungi make informed decisions about soil storage and transport to ensure repeatability and accuracy of results and interpretations.

Abstract

With the advances of sequencing tools, the fields of environmental microbiology and soil ecology have been transformed. Today, the unculturable majority of soil microbes can be sequenced. Although these tools give us tremendous power and open many doors to answer important questions, we must understand how sample processing may impact our results and interpretations. Here, we test the impacts of four soil storage methods on downstream amplicon metabarcoding and qPCR analyses for fungi and bacteria. We further investigate the impact of thaw time on extracted DNA to determine a safe length of time during which this can occur with minimal impact on study results. Overall, we find that storage using standard cold packs with subsequent storage at −20°C is little different than immediate storage in liquid nitrogen, suggesting that the historical and current method is adequate. We further find evidence that storage at room temperature or with aid of RNAlater can lead to changes in community composition and in the case of RNAlater, lower gene copies. We therefore advise against these storage methods for metabarcoding analyses. Finally, we show that over 1 month, DNA extract thaw time does not impact diversity or qPCR metrics. We hope that this work will help researchers working with soil bacteria and fungi make informed decisions about soil storage and transport to ensure repeatability and accuracy of results and interpretations.