Author/Authors :
Liles، نويسنده , , Mark R. and Turkmen، نويسنده , , Ozgur and Manske، نويسنده , , Brian F. and Zhang، نويسنده , , Mingzi and Rouillard، نويسنده , , Jean-Marie and George، نويسنده , , Isabelle and Balser، نويسنده , , Teri and Billor، نويسنده , , Nedret and Goodman، نويسنده , , Robert M.، نويسنده ,
Abstract :
We designed an oligonucleotide microarray using probe sequences based upon a phylogenetic analysis of 16S rRNA genes recovered from members of the bacterial division Acidobacteria. A total of 42,194 oligonucleotide probes targeting members of the Acidobacteria division at multiple phylogenetic levels were included on a high-density microarray. Positive control hybridizations revealed a linear relationship between hybridization signal and template concentration, and a substantial decrease in non-specific hybridization was achieved through the addition of 2.5 M betaine to the hybridization buffer. A mean hybridization signal value was calculated for each Acidobacteria lineage, with the resultant lineage-specific hybridization data revealing strong predictive value for the positive control hybridizations. The Acidobacteria phylochip was then used to evaluate Acidobacteria rRNA genes from a Wisconsin soil and within a soil clay fraction. The Acidobacteria hybridization profile revealed the predominance of Acidobacteria subdivisions four and six, and also suggested a decrease in the abundance of subdivision six relative to subdivision four in the soil clay fraction. The change in relative abundance of these subdivisions in a soil clay fraction was supported by data from quantitative PCR. These results support the utility of a phylogenetic microarray in revealing changes in microbial population-level distributions in a complex soil microbial assemblage.
Keywords :
16S rRNA , Acidobacteria , Microarray , Phylogeny , PhyloChip , clay