Cite this paper:
LUO Congqiang, YI Chunlong, NI Leyi, GUO Longgen. Fish-mediated changes in bacterioplankton community composition: an in situ mesocosm experiment[J]. Journal of Oceanology and Limnology, 2018, 36(2): 341-350

Fish-mediated changes in bacterioplankton community composition: an in situ mesocosm experiment

LUO Congqiang1,2, YI Chunlong1, NI Leyi1, GUO Longgen1
1 Donghu Experimental Station of Lake Ecosystems, State Key Laboratory of Freshwater Ecology and Biotechnology of China, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China;
2 Collaborative Innovation Center for Efficient and Health Production of Fisheries in Hunan Province, Key Laboratory of Health Aquaculture and Product Processing in Dongting Lake Area of Hunan Province, Hunan University of Arts and Science, Changde 415000, China
Abstract:
We characterized variations in bacterioplankton community composition (BCC) in mesocosms subject to three different treatments. Two groups contained fish (group one:Cyprinus carpio; group two:Hypophthalmichthys molitrix); and group three, the untreated mesocosm, was the control. Samples were taken seven times over a 49-d period, and BCC was analyzed by PCR-denaturing gradient gel electrophoresis (DGGE) and real-time quantitative PCR (qPCR). Results revealed that introduction of C. carpio and H. molitrix had a remarkable impact on the composition of bacterioplankton communities, and the BCC was significantly different between each treatment. Sequencing of DGGE bands revealed that the bacterioplankton community in the different treatment groups was consistent at a taxonomic level, but differed in its abundance. H. molitrix promoted the richness of Alphaproteobacteria and Actinobacteria, while more bands affiliated to Cyanobacteria were detected in C. carpio mesocosms. The redundancy analysis (RDA) result demonstrated that the BCC was closely related to the bottom-up (total phosphorus, chlorophyll a, phytoplankton biomass) and top-down forces (biomass of copepods and cladocera) in C. carpio and control mesocosms, respectively. We found no evidence for top-down regulation of BCC by zooplankton in H. molitrix mesocosms, while grazing by protozoa (heterotrophic nanoflagellates, ciliates) became the major way to regulate BCC. Total bacterioplankton abundances were significantly higher in C. carpio mesocosms because of high nutrient concentration and suspended solids. Our study provided insights into the relationship between fish and bacterioplankton at species level, leading to a deep understanding of the function of the microbial loop and the aquatic ecosystem.
Key words:    bacterioplankton community composition (BCC)|PCR-DGGE|qPCR|analysis of similarities (ANOSIM)|redundancy analysis (RDA)   
Received: 2016-10-11   Revised:
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References:
Baines S B, Pace M L. 1991. The production of dissolved organic matter by phytoplankton and its importance to bacteria:patterns across marine and freshwater systems.Limnol. Oceangr., 36(6):1 078-1 090.
Chen X X, Wang K, Guo A N, Dong Z Y, Zhao Q F, Qian J, Zhang D M. 2016. Excess phosphate loading shifts bacterioplankton community composition in oligotrophic coastal water microcosms over time. J. Exp. Mar. Biol.Ecol., 483:139-146.
Chrzanowski T H, Sterner R W, Elser J J. 1995. Nutrient enrichment and nutrient regeneration stimulate bacterioplankton growth. Microb. Ecol., 29(3):221-230.
Cole J J, Findlay S, Pace M L. 1988. Bacterial production in fresh and saltwater ecosystems:a cross-system overview.Mar. Ecol. Prog. Ser., 43:1-10.
do Rêgo Monteiro Starling F L. 1993. Control of eutrophication by silver carp (Hypophthalmichthys molitrix) in the tropical Paranoá Reservoir (Brasília, Brazil):a mesocosm experiment. Hydrobiologia, 257(3):143-152.
Fromin N, Hamelin J, Tarnawski S, Roesti D, JourdainMiserez K, Forestier N, Teyssier-Cuvelle S, Gillet F, Aragno M, Rossi P. 2002. Statistical analysis of denaturing gel electrophoresis (DGE) fingerprinting patterns.Environ. Microbiol., 4(11):634-643.
Greenberg A E, Clesceri L S, Eaton A D. 1992. Standard Methods for the Examination of Water and Wastewater. 18th edn. American Public Health Association, Washington D.C.
Holmquist L, Kjelleberg S. 1993. Changes in viability, respiratory activity and morphology of the marine Vibrio sp. strain S14 during starvation of individual nutrients and subsequent recovery. FEMS Microbiol. Ecol., 12(4):215-223.
Jürgens K, Jeppesen E. 2000. The impact of metazooplankton on the structure of the microbial food web in a shallow, hypertrophic lake. J. Plankton Res., 22(6):1 047-1 070.
Jürgens K, Matz C. 2002. Predation as a shaping force for the phenotypic and genotypic composition of planktonic bacteria. Antonie van Leeuwenhoek, 81(1-4):413-434.
Jürgens K, Pernthaler J, Schalla S, Amann R. 1999.Morphological and compositional changes in a planktonic bacterial community in response to enhanced protozoan grazing. Appl. Environ. Microbiol., 65(3):1 241-1 250.
Kisand V, Zingel P. 2000. Dominance of ciliate grazing on bacteria during spring in a shallow eutrophic lake. Aquat.Microb. Ecol., 22(2):135-142.
Langenheder S, Jürgens K. 2001. Regulation of bacterial biomass and community structure by metazoan and protozoan predation. Limnol. Oceanogr., 46(1):121-134.
Li M, Penner G B, Hernandez-Sanabria E, Oba M, Guan L L. 2009. Effects of sampling location and time, and host animal on assessment of bacterial diversity and fermentation parameters in the bovine rumen. J. Appl.Microbiol., 107(6):1 924-1 934.
Lindh M V, Lefébure R, Degerman R, Lundin D, Andersson A, Pinhassi J. 2015. Consequences of increased terrestrial dissolved organic matter and temperature on bacterioplankton community composition during a Baltic Sea mesocosm experiment. AMBIO, 44(S3):402-412.
Mátyás K, Oldal I, Korponai J, Tátrai I, Paulovits G. 2003.Indirect effect of different fish communities on nutrient chlorophyll relationship in shallow hypertrophic water quality reservoirs. Hydrobiologia, 504(1-3):231-239.
Muyzer G, de Waal E C, Uitterlinden A G. 1993. Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reactionamplified genes coding for 16S rRNA. Appl. Environ.Microbiol., 59(3):695-700.
Niu Y, Shen H, Chen J, Xie P, Yang X, Tao M, Ma Z M, Qi M. 2011. Phytoplankton community succession shaping bacterioplankton community composition in Lake Taihu, China. Water Res., 45(14):4 169-4 182.
Niu Y, Yu H, Jiang X. 2015. Within-lake heterogeneity of environmental factors structuring bacterial community composition in Lake Dongting, China. World J. Microbiol.Biotechnol., 31(11):1 683-1 689.
Pinhassi J, Sala M M, Havskum H, Peters F, Guadayol Ò, Malits A, Marrasé C. 2004. Changes in bacterioplankton composition under different phytoplankton regimens.Appl. Environ. Microbiol., 70(11):6 753-6 766.
Roozen F C J M, Lürling M, Vlek H, Van Der Pouw Kraan E A J, Ibelings B W, Scheffer M. 2007. Resuspension of algal cells by benthivorous fish boosts phytoplankton biomass and alters community structure in shallow lakes.Freshwater Biol., 52(6):977-987.
Saarenheimo J, Aalto S L, Syväranta J, Devlin S P, Tiirola M, Jones R I. 2016. Bacterial community response to changes in a tri-trophic cascade during a whole-lake fish manipulation. Ecology, 97(3):684-693.
Wang S Q, Zhu L, Li Q, Li G B, Li L, Song L R, Gan N Q. 2015. Distribution and population dynamics of potential anatoxin-a-producing cyanobacteria in Lake Dianchi, China. Harmful Algae, 48:63-68.
Wu Q L, Zwart G, Wu J F, Kamst-van Agterveld M P, Liu S J, Hahn M W. 2007. Submersed macrophytes play a key role in structuring bacterioplankton community composition in the large, shallow, subtropical Taihu Lake, China.Environ. Microbiol., 9(11):2 765-2 774.
Zöllner E, Santer B, Boersma M, Hoppe H G, Jürgens K. 2003.Cascading predation effects of Daphnia and copepods on microbial food web components. Freshwater Biol., 48(12):2 174-2 193.
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