Specific PCR assays were used to amplify the 16S rRNA genes of the Desulfob
acteriaceae and the Desulfovibrionaceae from extracted environmental DNA fr
om rice roots. 16S rDNA-based community patterns of the Desulfobacteriaceae
were generated via terminal restriction fragment length polymorphism analy
sis from rice roots and compared with bulk soil. The molecular fingerprints
showed no significant difference between rice roots and bulk soil. but cha
nges during the vegetation period. 16S rDNA clone libraries and sequencing
showed that the predominant terminal restriction fragments represented dist
inct phylogenetic groups. The 16S rDNA clone sequences of the Desulfobacter
iaceae fell in the phylogenetic radiation of Desulfonema and Desulfosarcina
or grouped within the Desulfohabdus-Syntrophobacter assemblage. Three of t
he latter sequences were closely affiliated with the MPN isolate EZ-2C2 fro
m rice roots. All Desulfovibrionaceae 16S rDNA clone sequences, with one ex
ception. were affiliated with the MPN isolate FI-7b from rice roots. The cl
ustering of the clone sequences and the close phylogenetic affiliation with
isolates from MPN enrichments from the same habitat in two cases indicated
that these sequence clusters may represent predominant Gram-negative sulfa
te reducers on rice roots. Quantification of the bacterial abundances was a
ccomplished by rRNA dot blot hybridization. In total the Gram-negative sulf
ate reducers accounted for approximately 2-3% of the total rRNA content. Th
e relative rRNA abundance of the Desulfobacteriaceae was, at 1.4%, higher t
han that of the Desulfovibrionaceae crf (0.5%). (C) 2001 Federation of Euro
pean Microbiological Societies. Published by Elsevier Science B.V. All righ
ts reserved.