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Microbiology Research - Academic Journals

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Table 3. Advantages and disadvantages of common fingerprinting methods used in the analysis of soil microbial communities.<br />

Methods Advantages Disadvantages References<br />

DGGE∗/TGGE<br />

SSCP<br />

T-RFLP<br />

Provides full sequences that can be subject to further<br />

analysis technically; obtain an overview of the dominant<br />

species<br />

Provides full sequences that can be subject to further<br />

analysis technically; obtain an overview of the dominant<br />

species<br />

Technically simple and reproducible; high discrimination<br />

power (number of types/analysis);<br />

ARDRA Technically simple and convenient<br />

LH-PCR/ARISA<br />

FISH<br />

PLFA<br />

Microarrays<br />

Technically simple; replicate profiles are highly<br />

reproducible; it can quickly evaluate community changes<br />

Direct analysis without extraction of nucleic acid;<br />

generally quantitative;<br />

No bias due to PCR; cover whole communities across<br />

kingdoms; quantitative description of the community<br />

No bias due to PCR; simultaneously analyze about ten<br />

thousand samples; high sample throughput expensive<br />

equipment parallel analysis of different parameters<br />

16SrDNA library Technically simple, can evaluate the community overall<br />

∗See text for the explanation of abbreviations.<br />

Only short sequences < 400 bp can be analyzed;<br />

DNA fragments of different species might have<br />

similar electrophoretic mobility<br />

Only short sequences < 200 bp can be analyzed<br />

Loss of some variability (sequences not cleaved or<br />

cleaved near to primer); low phylogenetic<br />

specificity of terminal restriction sites;<br />

Affected by PCR biases and the choice of the<br />

enzyme;<br />

Low discrimination power; amplicon distributions<br />

are sometimes difficult to resolve with the current<br />

software; one amplicon can represent more than<br />

one taxon<br />

Low fluorescent intensity cannot be detected; its<br />

rRNA sequence must be known (if the probe has<br />

not yet been published);<br />

Low taxonomic separation limited to community<br />

composition analysis; not a good choice as a<br />

standard alone method<br />

Detects only sequences corresponding to probes;<br />

detection limit lower than in PCR-based methods;<br />

impossible discover a new species;<br />

Only detected the absence or exist between to<br />

samples; PCR biases; selected clone numbers<br />

Wang et al. 5083<br />

Sanz and Köchling (2007),<br />

Muyzer et al. (1993) and<br />

Nannipieri et al. (2003).<br />

Lee et al. (1996), Dohrmann and<br />

Tebbe (2004) and Sanz and<br />

Köchling (2007).<br />

Liu et al. (1997) and Nannipieri<br />

et al. (2003).<br />

Ranjard et al. (2000).<br />

Fisher and Triplett (1999) and<br />

Mills et al. (2007).<br />

Dahllof (2002) and Sanz and<br />

Köchling (2007).<br />

Findlay et al. (1989) and Sanz<br />

and Köchling (2007).<br />

Shalon et al. (1996) and Ranjard<br />

et al. (2000).<br />

Li et al. (2007).<br />

Forestry University (500017) and Ornamental Plant and Horticulture key lab of Yunnan Province, Southwest Forestry University (000703).

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