Two bacterial strains, designated BBH5 and BBH7 T , were isolated from a deep-sea sediment sample collected from the Chagos Trench of the Indian Ocean (116 069 S 726 319 E). Based on their 16S rRNA gene sequence similarity (99.9 %), level of DNA-DNA relatedness (93 %) and a number of similar phenotypic characteristics, the two strains are identified as representing the same species. Their phylogenetically nearest neighbours, based on 16S rRNA gene sequence similarity values (97.9-98.4 %), were identified as Brevibacterium iodinum, Brevibacterium epidermidis, Brevibacterium linens and Brevibacterium permense. However, strains BBH5 and BBH7T could be distinguished from the above four species by a number of phenotypic characteristics, and levels of DNA-DNA relatedness between the two new isolates and these Brevibacterium species were 35-42 %. Therefore, strains BBH5 and BBH7 T are considered to represent a novel species of the genus Brevibacterium, for which the name Brevibacterium oceani sp. nov. is proposed. The type strain is BBH7 T (5LMG 23457 T 5IAM 15353 T ).The genus Brevibacterium was first described by Breed (1953) with Brevibacterium linens as type species; the description was emended by Collins et al. (1980). Species of the genus Brevibacterium exhibit a rod-coccus cell cycle, are aerobic, possess meso-diaminopimelic acid in the peptidoglycan and have MK-8(H 2 ) as the major respiratory menaquinone, diphosphatidylglycerol, phosphatidylglycerol, dimannosidediacylglycerol and phosphatidylinositol as major polar lipids and anteiso-and iso-branched fatty acids as major cellular fatty acids (Collins et al., 1980;Jones & Keddie, 1986;Heyrman et al., 2004). Brevibacterium species have been isolated from diverse habitats such as milk products, clinical specimens, soil, sediment, brown algae, paintings and foot lesions of fowl (Wauters et al., 2004;Lee, 2006;Gavrish et al., 2004;Ivanova et al., 2004;Heyrman et al., 2004;Pascual & Collins, 1999). Here we describe two Brevibacterium-like strains, BBH5 and BBH7 T , isolated from a sediment sample collected at a water depth of 5904 m (from a 50-70-cm section of a deep sediment core of 4.6 m, approximately 50 000 years old) from the Chagos Trench in the Indian Ocean (11 u 069 S 72 u 319 E) (Raghukumar et al., 2004).Deep-sea sediment samples were collected as described by Raghukumar et al. (2004). Approximately 1.0 g of the sediment was suspended in 10 ml 2 % NaCl and vortexed for 1 min and the suspension was then allowed to settle for 2 min. Next, 100 ml of the top aqueous layer was spread on a plate of yeast extract/peptone (YP) agar (per litre distilled water: 5 g yeast extract, 10 g peptone, 30 g NaCl, 15 g agar) and incubated at 15 u C for 15 days. The number of colonyforming units per gram of sediment ranged from 4.4610 3 to 7.6610 3 . A total of 21 pale-orange-coloured colonies were purified and subjected to total protein analysis via SDS-PAGE (Laemmli, 1970). All 21 isolates showed similar protein banding patterns and were assumed to be representatives of a sin...