During the last two decades, an increasing number of novel sulfate-reducing bacteria (SRB) have been isolated from a wide variety of environments such as fresh to saline and hypersaline waters or sediments, either from surface or subsurface habitats (Voordouw, 1995;Widdel & Bak, 1992). Among them, strains of the genus Desulfovibrio are the most commonly isolated. Subsequently, a great number of novel Desulfovibrio species has been described during the last 10 years. Recently, several strains of SRB were isolated from a subsurface aquifer water sample. Among them, strain B7-43 T was phylogenetically related, although distantly, to a large cluster of Desulfovibrio species. Considering its very low similarity to the closest existing species of the genus Desulfovibrio (less than 90 % 16S rRNA gene sequence similarity), strain B7-43 T could possibly be described as a representative of a new genus of SRB. However, due to its phylogenetic position within the large Desulfovibrio cluster and its physiological traits, which are similar to those of most Desulfovibrio species, it is proposed that strain B7-43 T should be classified in the genus Desulfovibrio. Therefore, because of its phylogenetic distance to the most closely related validly published members of the genus and its differing physiological traits, strain B7-43 T is proposed as a representative of a novel species, Desulfovibrio putealis sp. nov.Strain B7-43 T was isolated from a sample of deep subsurface water from the Paris Basin, France. Samples of formation water were aseptically collected at the wellhead under anoxic conditions as described previously (Basso et al., 2004). The total number of bacteria in a water sample (counted after staining with acridine orange) was 3610 4 cells ml
21. Handling and enrichment cultures of sulfate-reducers were accomplished as described previously (Magot et al., 1992). The final salinity of the culture media was adjusted by addition of NaCl (1 g l
21) to mimic in situ conditions. Incubations were carried out at 30 u C, corresponding to the in situ temperature in the aquifer. Enrichment cultures were obtained by serial dilutions in Hungate tubes. The last positive tube was used for isolation by streaking on solid medium in Petri dishes under anaerobic conditions. Colonies obtained after 2 weeks incubation were picked and their isolation was repeated twice. The purity of strains was checked by phase-contrast microscopy. Strain B7-43 T was selected for detailed investigation. It was composed of vibrioid cells that were actively motile with a single polar flagellum. The cells were generally 2?3-4?1 mm in length and 0?7 mm wide. Cells occurred either singly or in pairs and stained Gram-negative.To obtain a picture of the physiological properties of strain B7-43 T , the following tests were carried out: utilization of carbon and energy sources, utilization of a variety of Abbreviation: SRB, sulfate-reducing bacteria (-um).