Soil pretreatment and fast cell lysis for direct polymerase chain reaction from forest soils for terminal restriction fragment length polymorphism analysis of fungal communities

Bibliographic Details
Title: Soil pretreatment and fast cell lysis for direct polymerase chain reaction from forest soils for terminal restriction fragment length polymorphism analysis of fungal communities
Authors: Cheng, Fei, Hou, Lin, Woeste, Keith, Shang, Zhengchun, Peng, Xiaobang, Zhao, Peng, Zhang, Shuoxin
Source: Brazilian Journal of Microbiology. December 2016 47(4)
Publisher Information: Sociedade Brasileira de Microbiologia, 2016.
Publication Year: 2016
Subject Terms: Cell lysis, DNA extraction method, DNA purity, Terminal restriction fragment length polymorphism, Fungal community
More Details: Humic substances in soil DNA samples can influence the assessment of microbial diversity and community composition. Using multiple steps during or after cell lysis adds expenses, is time-consuming, and causes DNA loss. A pretreatment of soil samples and a single step DNA extraction may improve experimental results. In order to optimize a protocol for obtaining high purity DNA from soil microbiota, five prewashing agents were compared in terms of their efficiency and effectiveness in removing soil contaminants. Residual contaminants were precipitated by adding 0.6 mL of 0.5 M CaCl2. Four cell lysis methods were applied to test their compatibility with the pretreatment (prewashing + Ca2+ flocculation) and to ultimately identify the optimal cell lysis method for analyzing fungal communities in forest soils. The results showed that pretreatment with TNP + Triton X-100 + skim milk (100 mM Tris, 100 mM Na4P2O7, 1% polyvinylpyrrolidone, 100 mM NaCl, 0.05% Triton X-100, 4% skim milk, pH 10.0) removed most soil humic contaminants. When the pretreatment was combined with Ca2+ flocculation, the purity of all soil DNA samples was further improved. DNA samples obtained by the fast glass bead-beating method (MethodFGB) had the highest purity. The resulting DNA was successfully used, without further purification steps, as a template for polymerase chain reaction targeting fungal internal transcribed spacer regions. The results obtained by terminal restriction fragment length polymorphism analysis indicated that the MethodFGB revealed greater fungal diversity and more distinctive community structure compared with the other methods tested. Our study provides a protocol for fungal cell lysis in soil, which is fast, convenient, and effective for analyzing fungal communities in forest soils.
Document Type: article
File Description: text/html
Language: English
ISSN: 1517-8382
DOI: 10.1016/j.bjm.2016.06.007
Access URL: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822016000400817
Rights: info:eu-repo/semantics/openAccess
Accession Number: edssci.S1517.83822016000400817
Database: SciELO
More Details
ISSN:15178382
DOI:10.1016/j.bjm.2016.06.007
Published in:Brazilian Journal of Microbiology
Language:English