Phylogenetic diversity of bacteria associated with the marine sponge Rhopaloeides odorabile

被引:266
作者
Webster, NS
Wilson, KJ
Blackall, LL
Hill, RT
机构
[1] Univ Maryland, Ctr Marine Biotechnol, Baltimore, MD 21202 USA
[2] Australian Inst Marine Sci, Townsville, Qld 4810, Australia
[3] Univ Queensland, Dept Microbiol & Parasitol, St Lucia, Qld 4067, Australia
关键词
D O I
10.1128/AEM.67.1.434-444.2001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Molecular techniques were employed to document the microbial diversity associated with the marine sponge Rhopaloeides odorabile. The phylogenetic affiliation of sponge-associated bacteria was assessed by 16S rRNA sequencing of cloned DNA fragments. Fluorescence in situ hybridization (FISH) was used to confirm the presence of the predominant groups indicated by 16S rDNA analysis. The community structure was extremely diverse with representatives of the Actinobacteria, low-G+C gram-positive bacteria, the beta- and gamma -subdivisions of the Proteobacteria, Cytophaga/Flavobacterium, green sulfur bacteria, green nonsulfur bacteria, planctomycetes, and other sequence types with no known close relatives. FISH probes revealed the spatial location of these bacteria within the sponge tissue, in some cases suggesting possible symbiotic functions. The high proportion of 16S rRNA sequences derived from novel actinomycetes is good evidence for the presence of an indigenous marine actinomycete assemblage in R. odorabile. High microbial diversity was inferred from low duplication of clones in a library with 70 representatives. Determining the phylogenetic affiliation of sponge-associated microorganisms by 16S rRNA analysis facilitated the rational selection of culture media and isolation conditions to target specific groups of well-represented bacteria for laboratory culture. Novel media incorporating sponge extracts were used to isolate bacteria not previously recovered from this sponge.
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页码:434 / 444
页数:11
相关论文
共 51 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   FLUORESCENT-OLIGONUCLEOTIDE PROBING OF WHOLE CELLS FOR DETERMINATIVE, PHYLOGENETIC, AND ENVIRONMENTAL-STUDIES IN MICROBIOLOGY [J].
AMANN, RI ;
KRUMHOLZ, L ;
STAHL, DA .
JOURNAL OF BACTERIOLOGY, 1990, 172 (02) :762-770
[3]  
BELL AH, 1998, MEM QUEENSL MUS, V44, P51
[4]   BROMINATED ACETYLENIC FATTY-ACIDS FROM XESTOSPONGIA SP, A MARINE SPONGE-BACTERIA ASSOCIATION [J].
BRANTLEY, SE ;
MOLINSKI, TF ;
PRESTON, CM ;
DELONG, EF .
TETRAHEDRON, 1995, 51 (28) :7667-7672
[5]   Lutoside: An acyl-1-(acyl-6'-mannobiosyl)-3-glycerol isolated from the sponge-associated bacterium Micrococcus luteus [J].
BultelPonce, V ;
Debitus, C ;
Blond, A ;
Cerceau, C ;
Guyot, M .
TETRAHEDRON LETTERS, 1997, 38 (33) :5805-5808
[6]  
Burja Adam M., 1999, Memoirs of the Queensland Museum, V44, P63
[7]   Phylogenetic diversity of archaea and bacteria in a deep subsurface paleosol [J].
Chandler, DP ;
Brockman, FJ ;
Bailey, TJ ;
Fredrickson, JK .
MICROBIAL ECOLOGY, 1998, 36 (01) :37-50
[8]  
Chun J., 1995, THESIS U NEWCASTLE T
[9]   Taxonomy and biotransformation activities of some deep-sea actinomycetes [J].
Colquhoun, JA ;
Heald, SC ;
Li, L ;
Tamaoka, J ;
Kato, C ;
Horikoshi, K ;
Bull, AT .
EXTREMOPHILES, 1998, 2 (03) :269-277
[10]   LINTENOLIDES, NEW PENTACYCLIC BIOACTIVE SESTERTERPENES FROM THE CARIBBEAN SPONGE CACOSPONGIA CF LINTEIFORMIS [J].
CONTE, MR ;
FATTORUSSO, E ;
LANZOTTI, V ;
MAGNO, S ;
MAYOL, L .
TETRAHEDRON, 1994, 50 (03) :849-856