Janssen Kathrin, Low Shook Ling, Wang Yan, Mu Qi-Yong, Bierbaum Gabriele, Gee Carole T
Institute of Medical Microbiology, Immunology and Parasitology, University Clinic of Bonn, Rheinische Friedrich-Wilhelms-University Bonn, Venusberg-Campus 1 53127 Bonn Germany.
Institute of Geosciences, Division of Paleontology Rheinische Friedrich-Wilhelms-University Bonn, Nussallee 8 53115 Bonn Germany.
Appl Plant Sci. 2021 Aug 28;9(8):e11444. doi: 10.1002/aps3.11444. eCollection 2021 Aug.
Within a broader study on leaf fossilization in freshwater environments, a long-term study on the development and microbiome composition of biofilms on the foliage of aquatic plants has been initiated to understand how microbes and biofilms contribute to leaf decay and preservation. Here, water lily leaves are employed as a study model to investigate the relationship between bacterial microbiomes, biodegradation, and fossilization. We compare four DNA extraction kits to reduce biases in interpretation and to identify the most suitable kit for the extraction of DNA from bacteria associated with biofilms on decaying water lily leaves for 16S rRNA amplicon analysis.
We extracted surface-associated DNA from leaves in early stages of decay at two water depth levels using four commercially available kits to identify the most suitable protocol for bacterial extraction, applying a mock microbial community standard to enable a reliable comparison of the kits.
Kit 4, the FastDNA Spin Kit for Soil, resulted in high DNA concentrations with better quality and yielded the most accurate depiction of the mock community. Comparison of the leaves at two water depths showed no significant differences in community composition.
The success of Kit 4 may be attributed to its use of bead beating with a homogenizer, which was more efficient in the lysis of Gram-positive bacteria than the manual vortexing protocols used by the other kits. Our results show that microbial composition on leaves during early decay remains comparable and may change only in later stages of decomposition.
在一项关于淡水环境中叶化石形成的更广泛研究中,已启动一项关于水生植物叶片上生物膜的发育和微生物群落组成的长期研究,以了解微生物和生物膜如何促进叶片腐烂和保存。在此,睡莲叶片被用作研究模型,以研究细菌微生物群落、生物降解和化石形成之间的关系。我们比较了四种DNA提取试剂盒,以减少解释偏差,并确定最适合从腐烂睡莲叶片上与生物膜相关的细菌中提取DNA用于16S rRNA扩增子分析的试剂盒。
我们使用四种市售试剂盒从两个水深水平处于腐烂早期的叶片中提取表面相关DNA,以确定最适合细菌提取的方案,并应用模拟微生物群落标准来可靠地比较这些试剂盒。
试剂盒4,即土壤快速DNA提取试剂盒,产生了高浓度且质量更好的DNA,并对模拟群落进行了最准确的描述。两个水深的叶片群落组成比较显示没有显著差异。
试剂盒4的成功可能归因于其使用均质器进行珠磨,这在裂解革兰氏阳性细菌方面比其他试剂盒使用的手动涡旋方案更有效。我们的结果表明,叶片在早期腐烂期间的微生物组成保持可比,并且可能仅在分解后期发生变化。