全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Diversity of Bacterial Photosymbionts in Lubomirskiidae Sponges from Lake Baikal

DOI: 10.1155/2014/152097

Full-Text   Cite this paper   Add to My Lib

Abstract:

Sponges are permanent benthos residents which establish complex associations with a variety of microorganisms that raise interest in the nature of sponge-symbionts interactions. A molecular approach, based on the identification of the 16S rRNA and ribulose-1,5-bisphosphate carboxylase/oxygenase large subunit genes, was applied to investigate diversity and phylogeny of bacterial phototrophs associated with four species of Lubomirskiidae in Lake Baikal. The phylogeny inferred from both genes showed three main clusters of Synechococcus associated with Baikalian sponges. One of the clusters belonged to the cosmopolitan Synechococcus rubescens group and the two other were not related to any of the assigned phylogenetic groups but placed as sister clusters to S. rubescens. These results expanded the understanding of freshwater sponge-associated photoautotroph diversity and suggested that the three phylogenetic groups of Synechococcus are common photosynthetic symbionts in Lubomirskiidae sponges. 1. Introduction Sponges are an important component of the marine and freshwater benthos ecosystems that establish associations with a great diversity of unicellular and multicellular organisms [1]. At the photosynthetic zone, sponges can benefit from phototrophic symbionts which fix carbon using the Calvin-Benson cycle and provide products of photosynthesis to the host [2–4]. Photosynthetic symbionts are prevalent in marine sponges of coastal regions worldwide where they contribute significantly to net primary production [5, 6]. From one-third to more than half of the sponges of tropical and temperate regions harbor a high level of photosynthetic symbionts [7, 8]. In Lake Baikal, sponges are necessary components of the benthos and ubiquitous on rocky grounds in the littoral zone. Sponges from the endemic family Lubomirskiidae are widely distributed in Lake Baikal and often harbor photosynthetic symbionts. From 14 described species of Lubomirskiidae [9], there are three common species among which photosynthetic Lubomirskia baicalensis (L. baicalensis) and Baikalospongia bacillifera (B. bacillifera) are widely distributed in the photic zone of Lake Baikal. In contrast to marine sponges, there is not a lot of data on photosynthetic symbionts of freshwater sponges, although associations with unicellular green algae, including Chlorella spp., Choricystis minor, yellow-green algae, and Chloroflexi have been shown in cosmopolitan sponges [4, 10–13] and cyanobacterial sequences detected in L. baicalensis [14]. Nevertheless, the identification and diversity of

References

[1]  C. R. Wilkinson, “Microbial associations in sponges. I. Ecology, physiology and microbial populations of coral reef sponges,” Marine Biology, vol. 49, no. 2, pp. 161–167, 1978.
[2]  C. R. Wilkinson and J. Vacelet, “Transplantation of marine sponges to different conditions of light and current,” Journal of Experimental Marine Biology and Ecology, vol. 37, no. 1, pp. 91–104, 1979.
[3]  T. M. Frost and C. E. Williamson, “In situ determination of the effect of symbiotic algae on the growth of the freshwater sponge Spongilla lacustris,” Journal of Ecology, vol. 61, pp. 1361–1370, 1980.
[4]  A. A. Venn, J. E. Loram, and A. E. Douglas, “Photosynthetic symbioses in animals,” Journal of Experimental Botany, vol. 59, no. 5, pp. 1069–1080, 2008.
[5]  C. R. Wilkinson, “Net primary productivity in coral reef sponges,” Science, vol. 219, no. 4583, pp. 410–412, 1983.
[6]  K. M. Usher, “The ecology and phylogeny of cyanobacterial symbionts in sponges,” Marine Ecology, vol. 29, no. 2, pp. 178–192, 2008.
[7]  P. M. Erwin and R. W. Thacker, “Incidence and identity of photosynthetic symbionts in Caribbean coral reef sponge assemblages,” Journal of the Marine Biological Association of the United Kingdom, vol. 87, no. 6, pp. 1683–1692, 2007.
[8]  M.-L. Lemloh, J. Fromont, F. Brümmer, and K. M. Usher, “Diversity and abundance of photosynthetic sponges in temperate Western Australia,” BMC Ecology, vol. 9, article 4, 2009.
[9]  S. M. Efremova, “New genus and new sponge species of the family Lubomirskiidae Rezvoy, 1936,” in Index of Animal Species Inhabiting Lake Baikal and Its Catchment Area, vol. 1, book 2, pp. 1261–1278, Nauka, Novosibirsk, Russia, 2004.
[10]  C. R. Wilkinson, “Nutrient translocation from green algal symbionts to the freshwater sponge Ephydatia fluviatilis,” Hydrobiologia, vol. 75, no. 3, pp. 241–250, 1980.
[11]  T. M. Frost, L. E. Graham, J. E. Elias, M. J. Haase, D. W. Kretchmer, and J. A. Kranzfelder, “A yellow-green algal symbiont in the freshwater sponge, Corvomeyenia everetti: convergent evolution of symbiotic associations,” Freshwater Biology, vol. 38, no. 2, pp. 395–399, 1997.
[12]  C. Gernert, F. O. Gl?ckner, G. Krohne, and U. Hentschel, “Microbial diversity of the freshwater sponge Spongilla lacustris,” Microbial Ecology, vol. 50, no. 2, pp. 206–212, 2005.
[13]  S. Handa, M. Nakahara, H. Tsubota, H. Deguchi, Y. Masuda, and T. Nakano, “Choricystis minor (Trebouxiophyceae, Chlorophyta) as a symbiont of several species of freshwater sponge,” Hikobia, vol. 14, no. 4, pp. 365–373, 2006.
[14]  O. V. Kaliuzhnaia, A. A. Krivich, and V. B. Itskovich, “Diversity of 16S rRNA genes in metagenomic community of the freshwater sponge Lubomirskia baicalensis,” Genetika, vol. 48, no. 8, pp. 1003–1006, 2012 (Russian).
[15]  H. E. Elsaied, H. Kimura, and T. Naganuma, “Composition of archaeal, bacterial, and eukaryal RuBisCO genotypes in three Western Pacific arc hydrothermal vent systems,” Extremophiles, vol. 11, no. 1, pp. 191–202, 2007.
[16]  H. Elsaied and T. Naganuma, “Phylogenetic diversity of ribulose-1,5-bisphosphate carboxylase/oxygenase large-subunit genes from deep-sea microorganisms,” Applied and Environmental Microbiology, vol. 67, no. 4, pp. 1751–1765, 2001.
[17]  L. Steindler, D. Huchon, A. Avni, and M. Ilan, “16S rRNA phylogeny of sponge-associated cyanobacteria,” Applied and Environmental Microbiology, vol. 71, no. 7, pp. 4127–4131, 2005.
[18]  U. Hentschel, J. Hopke, M. Horn et al., “Molecular evidence for a uniform microbial community in sponges from different oceans,” Applied and Environmental Microbiology, vol. 68, no. 9, pp. 4431–4440, 2002.
[19]  R. L. Simister, P. Deines, E. S. Botté, N. S. Webster, and M. W. Taylor, “Sponge-specific clusters revisited: a comprehensive phylogeny of sponge-associated microorganisms,” Environmental Microbiology, vol. 14, no. 2, pp. 517–524, 2012.
[20]  N. D. Crosbie, M. P?ckl, and T. Weisse, “Dispersal and phylogenetic diversity of nonmarine picocyanobacteria, inferred from 16S rRNA gene and cpcBA-intergenic spacer sequence analyses,” Applied and Environmental Microbiology, vol. 69, no. 9, pp. 5716–5721, 2003.
[21]  T. Pommier, B. Canb?ck, L. Riemann et al., “Global patterns of diversity and community structure in marine bacterioplankton,” Molecular Ecology, vol. 16, no. 4, pp. 867–880, 2007.
[22]  P. D. Rezvoi, “Freshwater sponges of the USSR,” in The Fauna of the USSR, D. P. Rezvoi, Ed., vol. 2, pp. 21–41, Academy of Sciences, Moscow, Russia, 1936.
[23]  S. M. Efremova, “Porifera,” in An Annotated List of the Fauna of Lake Baikal and Its Catchment Area, O. A. Timoshkin, Ed., vol. 1, pp. 177–190, Nauka, Novosibirsk, Russia, 2001, (Russian).
[24]  M. Bergmann and R. H. Peters, “A simple reflectance method for the measurement of particulate pigment in lake water and its application to Phosphorus-Chlorophyll-Seston Relationships,” Canadian Journal of Fisheries and Aquatic Sciences, vol. 37, pp. 111–114, 1980.
[25]  D. J. Webb, B. K. Burnison, A. M. Trimbee, and E. E. Prepas, “Comparison of chlorophyll a extractions with ethanol and dimethyl sulfoxide/acetone, and a concern about spectrophotometric phaeopigment correction,” Canadian Journal of Fisheries and Aquatic Sciences, vol. 49, pp. 2331–2336, 1992.
[26]  U. Nübel, F. Garcia-Pichel, and G. Muyzer, “PCR primers to amplify 16S rRNA genes from cyanobacteria,” Applied and Environmental Microbiology, vol. 63, no. 8, pp. 3327–3332, 1997.
[27]  E. S. Wright, L. S. Yilmaz, and D. R. Noguera, “DECIPHER, a search-based approach to chimera identification for 16S rRNA sequences,” Applied and Environmental Microbiology, vol. 78, no. 3, pp. 717–725, 2012.
[28]  T. A. Hall, “BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT,” Nucleic Acids Symposium Series, vol. 41, pp. 95–98, 1999.
[29]  F. Ronquist, M. Teslenko, P. van der Mark et al., “Mrbayes 3.2: efficient bayesian phylogenetic inference and model choice across a large model space,” Systematic Biology, vol. 61, no. 3, pp. 539–542, 2012.
[30]  K. Tamura, D. Peterson, N. Peterson, G. Stecher, M. Nei, and S. Kumar, “MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods,” Molecular Biology and Evolution, vol. 28, no. 10, pp. 2731–2739, 2011.
[31]  M. Kimura, “A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences,” Journal of Molecular Evolution, vol. 16, no. 2, pp. 111–120, 1980.

Full-Text

Contact Us

[email protected]

QQ:3279437679

WhatsApp +8615387084133