Elucidating biofilm diversity on water lily leaves through 16S rRNA amplicon analysis: Comparison of four DNA extraction kits

被引:3
|
作者
Janssen, Kathrin [1 ]
Low, Shook Ling [2 ]
Wang, Yan [3 ]
Mu, Qi-Yong [3 ]
Bierbaum, Gabriele [1 ]
Gee, Carole T. [2 ,4 ]
机构
[1] Rheinische Friedrich Wilhelms Univ Bonn, Univ Clin Bonn, Inst Med Microbiol Immunol & Parasitol, Venusberg Campus 1, D-53127 Bonn, Germany
[2] Rheinische Friedrich Wilhelms Univ Bonn, Inst Geosci, Div Paleontol, Nussallee 8, D-53115 Bonn, Germany
[3] Chinese Acad Sci, CAS Key Lab Trop Forest Ecol, Xishuangbanna Trop Bot Garden, Mengla 666303, Peoples R China
[4] Huntington Bot Gardens, 1151 Oxford Rd, San Marino, CA 91108 USA
来源
APPLICATIONS IN PLANT SCIENCES | 2021年 / 9卷 / 08期
关键词
bacterial DNA sequencing; environmental microbiomics; leaf fossilization; leaf microbiome; Nymphaea; plant taphonomy; SP-NOV; BACTERIAL; IDENTIFICATION; FOSSILIZATION; DECAY; AMPLIFICATION; CONTAMINATION; PRESERVATION; COMMUNITIES; MICROBIOME;
D O I
10.1002/aps3.11444
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Premise 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. Methods We extracted surface-associated DNA from Nymphaea 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. Results 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. Discussion 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.
引用
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页数:15
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