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Change of Sponge(Axinella sp.)-Associated Bacterial Community during the Cultivation with Hexabromobenzene
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 Title & Authors
Change of Sponge(Axinella sp.)-Associated Bacterial Community during the Cultivation with Hexabromobenzene
Seo, Hyun-Seok; Yang, Sung-Hyun; Bae, Seung Seob; Lee, Jung-Hyun; Kwon, Kae Kyoung;
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Bacteria associated with marine sponges seemed to be concerned in halogenation/dehalogenation process of natural compounds. In the present study, the effect of hexabromobenzene (HBB) on the community structure of bacteria associated with a marine sponge Axinella sp. from Chuuk State under anaerobic condition was investigated. Regardless of 100 ppm HBB, most of detected microorganisms displayed high similarity with clones reported from coral or sponges. Amongst, Desulfovibrio marinisediminis like clones were dominant. Clones affiliated with Lentisphaerae and Fusibacter paucivorans (Clostridia) were detected at the conditions without HBB but clones affiliated with Vallitalea guaymasensis (Clostridia) increased its proportion with HBB. From these results and previous reports clones affiliated with D. marinisediminis and V. guaymasensis seemed to be concerned in halogenation/dehalogenation process.
dehalogenation;sponge;bacteria;Desulfovibrio marinisediminis;Vallitalea guaymasensis;
 Cited by
Ahn, Y-B., Rhee, S-K., Fennell, D. E., Kerkhof, L.J., Hentschel, U. and Haggblom, M. M. 2003. Reductive dehalogenation of brominated phenolic compounds by microorganisms associated with the marine sponge Aplysina aerophoba. Appl Environ Microbiol. 69, 4159-4166. crossref(new window)

Bowman JP and McCuaig RD. 2003. Biodiversity, community structural shifts, and biogeography of prokaryotes within Antarctic continental shelf sediment. Appl Environ Microbiol. 69, 2463-2483. crossref(new window)

Boyle, A.W., Phelps, C.D. and Young, L.Y. 1999. Isolation from estuarine sediments of a Desulfovibrio strain which can grow on lactate coupled to the reductive dehalogenation of 2,4, 6-tribromophenol. Appl. Environ. Microbiol. 65, 1133-1140.

Bruchajzer, E., Frydrych, B, and Szymanska, J. A. 2004. Effect of repeated administration of hexabromobenzene and 1,2,4,5-tetrabromo- benzene on the levels of selected cytochromes in rat liver. Int J Occup Med Environ Health. 17, 347-353

Felsenstein, J. 1985. Confidence limits on phylogenies: an approach using the bootstrap. Evolution. 39, 783-791. crossref(new window)

Felsenstein, J. 1993. PHYLIP: Phylogeny inference package version 3.5c. University of Washington, USA.

Franken, S. M., Rozeboom, H. J., Kalk, K. H. and Dijkstra, B. W. 1991. Crystal structure of haloackane dehalogenase: an enzyme to detoxify halogenated alkanes. The EMBO Journal. 10, 1297-1302.

Gauthier, L. T., Potter, D., Hebert, C. E, and Letcher, R. J. 2009. Temporal trends and spatial distribution of non-polybrominated diphenyl ether flame retardants in the eggs of colonial populations of Great Lakes Herring Gulls. Environ. Sci. Technol. 43, 312-317. crossref(new window)

Janssen, D. B., Pries, F., VAN DER Ploeg, J., Kazemier, B., Terpstra, P. and Witholt, B. 1989. Cloning of 1.2-dichlorethane degradation genes of Xanthobacter autotrophicus GJ10 and expression and sequencing of the dhlA Gene. J. Bacteriol. 171, 6791-6799. crossref(new window)

Jukes, T. H. and Cantor, C. R. 1969. Evolution of protein molecules. In Mammalian Protein Metabolism, vol. 3, pp.21-32. Edited by H. N. Munro. New York: Academic Press.

Kemp, P. F., and Aller, J. Y. 2004. Bacterial diversity in aquatic and other environments: what 16S rDNA libraries can tell us. FEMS Microbiol. Ecol. 47, 161-177. crossref(new window)

Lakhal, R., Pradel, N., Postec, A., Hamdi, M., Ollivier, B., Godfroy, A., and Fardeau, M.L. 2013. Characterization of Vallitalea guaymasensis gen. nov., sp. nov., a novel marine bacterium, isolated from sediments of Guaymas basin. Int. J. Syst. Evol. Microbiol. 63, 3019-3023. crossref(new window)

Lopez, J., A. Ledger, C. Peterson, K. Sfanos, D. Harmody, S. Pomponi, and P. McCarthy. 2006. Molecular census and comparison of cultured and uncultured microbial symbiont diversity from an ancient metazoan host, phylum Porifera, abstr. 6.15. Abstr. 5th Int. Symbiosis Soc. Congr., Vienna, Austria, 4 to 10 August 2006.

Mohamed, N.M., Enticknap, J.J., Lohr, J.E., McIntosh, S.M. and Hill, R.T. 2008. Changes in bacterial communities of the marine sponge Mycale laxissima on transfer into aquaculture. Appl. Environ. Microbiol. 74, 1209-1222. crossref(new window)

Ravot, G., Magot, M., Fardeau, M.L., Patel, B.K., Thomas, P., Garcia, J.L., and Ollivier, B. 1999. Fusibacter paucivorans gen. nov., sp. nov., an anaerobic, thiosulfate-reducing bacterium from an oil-producing well. Int. J. Syst. Bacteriol. 49, 1141-1147. crossref(new window)

Rohwer, F., Breitbart, M., Jara, J., Azam, F., and Knowlton, N. 2001. Diversity of bacteria associated with the Caribbean coral Montastraea franksi. Coral Reefs 20, 85-91. crossref(new window)

Saitou, N. and Nei, M. 1987. The neighborjoining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol. 4, 406-425.

Schloss, P. D., and Handelsman, J. 2005. Introducing DOTUR, a computer program for defining operational taxonomic units and estimating species richness. Appl. Environ. Microbiol. 71, 1501-1506. crossref(new window)

Schmitz, F. J. and Gopichand, Y. 1978. (7E, $13\xi$, 15Z)-14,16-dibromo-7,13,15-hexadecatrien-5ynoic acid. A novel dibromo acetylenic acid from the marine sponge Xestospongia muta. Tetrahedron Lett. 19, 3637-3640. crossref(new window)

Sekar, R., Kaczmarsky, L.T. and Richardson, L.L. 2008. Microbial community composition of black band disease on the coral host Siderastrea siderea from three regions of the wider Caribbean. Mar. Ecol. Prog. Ser. 362, 85-98. crossref(new window)

Sinkko, H., Lukkari, K., Jama, A.S., Sihvonen, L.M., Sivonen, K., Leivuori, M., Rantanen, M., Paulin, L., and Lyra. C. 2011. Phosphorus chemistry and bacterial community composition interact in brackish sediments receiving agricultural discharges. PLoS One 6, e21555. crossref(new window)

Sunagawa, S., DeSantis, T.Z., Piceno, Y.M., Brodie, E.L., DeSalvo, M.K., Voolstra, C.R., Weil, E., Andersen, G.L. and Medina, M. 2009. Bacterial diversity and White Plague Disease-associated community changes in the Caribbean coral Montastraea faveolata. ISME J 3, 512-521. crossref(new window)

Szymanska, J.A, and Piotrowski, J.K. 2000. Hepatotoxicity of monobromobenzene and hexabromobenzene: effects of repeated dosage in rats. Chemosphere. 41, 1689-1696. crossref(new window)

Takii, S., Hanada, S., Hase, Y., Tamaki, H., Uyeno, Y., Sekiguchi, Y. and Matsuura, K. 2008. Desulfovibrio marinisediminis sp. nov., a novel sulfate-reducing bacterium isolated from coastal marine sediment via enrichment with Casamino acids. Int. J. Syst. Evol. Microbiol. 58, 2433-2438. crossref(new window)

Watanabe, I., Kashimoto, T, and Tatsukawa, R. 1986. Confirmation of the presence of the flame retardant decabromobiphenylether in river sediment from Osaka, Japan. Bull. Environ. Contam. Toxico. 36, 839-842. crossref(new window)

Yamaguchi, Y., Kawano, M, and Tatsukawa, R. 1986. Tissue distribution and excretion of hexabromobenzene (HBB) and hexachlorobenzene (HCB) administered to rats. Chemosphere. 15, 453-459. crossref(new window)

Yamaguchi, Y., Kawano, M, and Tatsukawa, R. 1988. Hexabromobenzene and its debrominated compounds in human adipose tissues of Japan. Chemosphere 17, 703-707. crossref(new window)

Zitko, V., and Hutzinger, O. 1976. Uptake of Chloro- and Bromobiphenyls, Hexachloro- and Hexabromobenzene by Fish. Bullet. Environ. Contam. & Toxicol. 16, 665-673. crossref(new window)