The ability of terminal restriction fragment (T-RFLP or TRF) profiles of 165 rRNA genes to provide useful information about the relative diversity of complex microbial communities was investigated by comparison with other methods. Four soil communities representing two pinyon rhizosphere and two between-tree (interspace) soil environments were compared by analysis of 16S rRNA gene clone libraries and culture collections (Dunbar et al., Appl. Environ. Microbiol. 65:1662-1669, 1998) and by analysis of 16S rDNA TRF profiles of community DNA. The TRF method was able to differentiate the four communities in a manner consistent with previous comparisons of the communities by analysis of 16S rDNA clone libraries. TRF profiles were not useful for calculating and comparing traditional community richness or evenness values among the four soil environments. Statistics calculated from RsaI, NhaI, HaeIII, and MspI profiles of each community were inconsistent, and the combined data were not significantly different between samples. The detection sensitivity of the method was tested. In standard PCRs, a seeded population comprising 0.1 to 1% of the total community could be detected. The combined results demonstrate that TRF analysis is an excellent method for rapidly comparing the relationships between bacterial communities in environmental samples. However, for highly complex communities, the method appears unable to provide classical measures of relative community diversity.
机构:
Hong Kong Univ Sci & Technol, Dept Biol, Kowloon, Hong Kong, Peoples R ChinaHong Kong Univ Sci & Technol, Dept Biol, Kowloon, Hong Kong, Peoples R China
Wu, M
Song, LS
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Hong Kong Univ Sci & Technol, Dept Biol, Kowloon, Hong Kong, Peoples R ChinaHong Kong Univ Sci & Technol, Dept Biol, Kowloon, Hong Kong, Peoples R China
Song, LS
Ren, JP
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Hong Kong Univ Sci & Technol, Dept Biol, Kowloon, Hong Kong, Peoples R ChinaHong Kong Univ Sci & Technol, Dept Biol, Kowloon, Hong Kong, Peoples R China
Ren, JP
Kan, JJ
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Hong Kong Univ Sci & Technol, Dept Biol, Kowloon, Hong Kong, Peoples R ChinaHong Kong Univ Sci & Technol, Dept Biol, Kowloon, Hong Kong, Peoples R China
Kan, JJ
Qian, PY
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Hong Kong Univ Sci & Technol, Dept Biol, Kowloon, Hong Kong, Peoples R ChinaHong Kong Univ Sci & Technol, Dept Biol, Kowloon, Hong Kong, Peoples R China
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Univ So Calif, Dept Biol Sci, Geomicrobiol Grp, Los Angeles, CA 90089 USAUniv So Calif, Dept Biol Sci, Geomicrobiol Grp, Los Angeles, CA 90089 USA
Orcutt, Beth
Bailey, Brad
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Univ Calif San Diego, Scripps Inst Oceanog, Inst Geophys & Planetary Phys, La Jolla, CA 92037 USAUniv So Calif, Dept Biol Sci, Geomicrobiol Grp, Los Angeles, CA 90089 USA
Bailey, Brad
Staudigel, Hubert
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Univ Calif San Diego, Scripps Inst Oceanog, Inst Geophys & Planetary Phys, La Jolla, CA 92037 USAUniv So Calif, Dept Biol Sci, Geomicrobiol Grp, Los Angeles, CA 90089 USA
Staudigel, Hubert
Tebo, Bradley M.
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Oregon Hlth & Sci Univ, Div Environm & Biomol Syst, Beaverton, OR 97006 USAUniv So Calif, Dept Biol Sci, Geomicrobiol Grp, Los Angeles, CA 90089 USA
Tebo, Bradley M.
Edwards, Katrina J.
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Univ So Calif, Dept Biol Sci, Geomicrobiol Grp, Los Angeles, CA 90089 USAUniv So Calif, Dept Biol Sci, Geomicrobiol Grp, Los Angeles, CA 90089 USA
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Texas A&M Univ, Dept Small Anim Clin Sci, Coll Vet Med & Biomed Sci, Gastrointestinal Lab, College Stn, TX 77843 USATexas A&M Univ, Dept Small Anim Clin Sci, Coll Vet Med & Biomed Sci, Gastrointestinal Lab, College Stn, TX 77843 USA
Ritchie, Lauren E.
Steiner, Joerg M.
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Texas A&M Univ, Dept Small Anim Clin Sci, Coll Vet Med & Biomed Sci, Gastrointestinal Lab, College Stn, TX 77843 USATexas A&M Univ, Dept Small Anim Clin Sci, Coll Vet Med & Biomed Sci, Gastrointestinal Lab, College Stn, TX 77843 USA
Steiner, Joerg M.
Suchodolski, Jan S.
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Texas A&M Univ, Dept Small Anim Clin Sci, Coll Vet Med & Biomed Sci, Gastrointestinal Lab, College Stn, TX 77843 USATexas A&M Univ, Dept Small Anim Clin Sci, Coll Vet Med & Biomed Sci, Gastrointestinal Lab, College Stn, TX 77843 USA