Elucidating biofilm diversity on water lily leaves through 16S rRNA amplicon analysis: Comparison of four DNA extraction kits
Abstract 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....
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doaj-546eb17a9f574f03b3572dfac3c1355a2021-09-06T05:44:27ZengWileyApplications in Plant Sciences2168-04502021-08-0198n/an/a10.1002/aps3.11444Elucidating biofilm diversity on water lily leaves through 16S rRNA amplicon analysis: Comparison of four DNA extraction kitsKathrin Janssen0Shook Ling Low1Yan Wang2Qi‐Yong Mu3Gabriele Bierbaum4Carole T. Gee5Institute of Medical Microbiology, Immunology and Parasitology, University Clinic of Bonn, Rheinische Friedrich‐Wilhelms‐University Bonn, Venusberg‐Campus 1 53127 Bonn GermanyInstitute of Geosciences, Division of Paleontology Rheinische Friedrich‐Wilhelms‐University Bonn, Nussallee 8 53115 Bonn GermanyCAS Key Laboratory of Tropical Forest Ecology, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences Mengla 666303 ChinaCAS Key Laboratory of Tropical Forest Ecology, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences Mengla 666303 ChinaInstitute of Medical Microbiology, Immunology and Parasitology, University Clinic of Bonn, Rheinische Friedrich‐Wilhelms‐University Bonn, Venusberg‐Campus 1 53127 Bonn GermanyInstitute of Geosciences, Division of Paleontology Rheinische Friedrich‐Wilhelms‐University Bonn, Nussallee 8 53115 Bonn GermanyAbstract 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.https://doi.org/10.1002/aps3.11444bacterial DNA sequencingenvironmental microbiomicsleaf fossilizationleaf microbiomeNymphaeaplant taphonomy |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kathrin Janssen Shook Ling Low Yan Wang Qi‐Yong Mu Gabriele Bierbaum Carole T. Gee |
spellingShingle |
Kathrin Janssen Shook Ling Low Yan Wang Qi‐Yong Mu Gabriele Bierbaum Carole T. Gee Elucidating biofilm diversity on water lily leaves through 16S rRNA amplicon analysis: Comparison of four DNA extraction kits Applications in Plant Sciences bacterial DNA sequencing environmental microbiomics leaf fossilization leaf microbiome Nymphaea plant taphonomy |
author_facet |
Kathrin Janssen Shook Ling Low Yan Wang Qi‐Yong Mu Gabriele Bierbaum Carole T. Gee |
author_sort |
Kathrin Janssen |
title |
Elucidating biofilm diversity on water lily leaves through 16S rRNA amplicon analysis: Comparison of four DNA extraction kits |
title_short |
Elucidating biofilm diversity on water lily leaves through 16S rRNA amplicon analysis: Comparison of four DNA extraction kits |
title_full |
Elucidating biofilm diversity on water lily leaves through 16S rRNA amplicon analysis: Comparison of four DNA extraction kits |
title_fullStr |
Elucidating biofilm diversity on water lily leaves through 16S rRNA amplicon analysis: Comparison of four DNA extraction kits |
title_full_unstemmed |
Elucidating biofilm diversity on water lily leaves through 16S rRNA amplicon analysis: Comparison of four DNA extraction kits |
title_sort |
elucidating biofilm diversity on water lily leaves through 16s rrna amplicon analysis: comparison of four dna extraction kits |
publisher |
Wiley |
series |
Applications in Plant Sciences |
issn |
2168-0450 |
publishDate |
2021-08-01 |
description |
Abstract 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. |
topic |
bacterial DNA sequencing environmental microbiomics leaf fossilization leaf microbiome Nymphaea plant taphonomy |
url |
https://doi.org/10.1002/aps3.11444 |
work_keys_str_mv |
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