» Articles » PMID: 25144467

Bacterial Community Composition of Size-fractioned Aggregates Within the Phycosphere of Cyanobacterial Blooms in a Eutrophic Freshwater Lake

Overview
Journal PLoS One
Date 2014 Aug 22
PMID 25144467
Citations 47
Authors
Affiliations
Soon will be listed here.
Abstract

Bacterial community composition of different sized aggregates within the Microcystis cyanobacterial phycosphere were determined during summer and fall in Lake Taihu, a eutrophic lake in eastern China. Bloom samples taken in August and September represent healthy bloom biomass, whereas samples from October represent decomposing bloom biomass. To improve our understanding of the complex interior structure in the phycosphere, bloom samples were separated into large (>100 µm), medium (10-100 µm) and small (0.2-10 µm) size aggregates. Species richness and library coverage indicated that pyrosequencing recovered a large bacterial diversity. The community of each size aggregate was highly organized, indicating highly specific conditions within the Microcystis phycosphere. While the communities of medium and small-size aggregates clustered together in August and September samples, large- and medium-size aggregate communities in the October sample were grouped together and distinct from small-size aggregate community. Pronounced changes in the absolute and relative percentages of the dominant genus from the two most important phyla Proteobacteria and Bacteroidetes were observed among the various size aggregates. Bacterial species on large and small-size aggregates likely have the ability to degrade high and low molecular weight compounds, respectively. Thus, there exists a spatial differentiation of bacterial taxa within the phycosphere, possibly operating in sequence and synergy to catalyze the turnover of complex organic matters.

Citing Articles

Unprecedented toxic blooms of Microcystis spp. in 2019 in the Chowan River, North Carolina.

Pierce E, Valera M, Vander Borgh M, Wiltsie D, Fensin E, Godwin C Harmful Algae. 2024; 140:102747.

PMID: 39613371 PMC: 11647567. DOI: 10.1016/j.hal.2024.102747.


Diversity and networking of uni-cyanobacterial cultures and associated heterotrophic bacteria from the benthic microbial mat of a desert hydrothermal spring.

Lassoued K, Mahjoubi M, Asimakis E, Bel Mokhtar N, Stathopoulou P, Ben Hamouda R FEMS Microbiol Ecol. 2024; 100(12).

PMID: 39557663 PMC: 11650863. DOI: 10.1093/femsec/fiae148.


Variation in resource competition traits among strains is affected by their microbiomes.

Baker D, Godwin C, Khanam M, Burtner A, Dick G, Denef V mLife. 2024; 2(4):401-415.

PMID: 38818269 PMC: 10989160. DOI: 10.1002/mlf2.12094.


Aerobic anoxygenic phototrophs play important roles in nutrient cycling within cyanobacterial Microcystis bloom microbiomes.

Cai H, McLimans C, Jiang H, Chen F, Krumholz L, Hambright K Microbiome. 2024; 12(1):88.

PMID: 38741135 PMC: 11089705. DOI: 10.1186/s40168-024-01801-4.


Oxic methane production from methylphosphonate in a large oligotrophic lake: limitation by substrate and organic carbon supply.

Peoples L, Dore J, Bilbrey E, Vick-Majors T, Ranieri J, Evans K Appl Environ Microbiol. 2023; 89(12):e0109723.

PMID: 38032216 PMC: 10734540. DOI: 10.1128/aem.01097-23.


References
1.
Grossart H, Levold F, Allgaier M, Simon M, Brinkhoff T . Marine diatom species harbour distinct bacterial communities. Environ Microbiol. 2005; 7(6):860-73. DOI: 10.1111/j.1462-2920.2005.00759.x. View

2.
Marzorati M, Wittebolle L, Boon N, Daffonchio D, Verstraete W . How to get more out of molecular fingerprints: practical tools for microbial ecology. Environ Microbiol. 2008; 10(6):1571-81. DOI: 10.1111/j.1462-2920.2008.01572.x. View

3.
Jasti S, Sieracki M, Poulton N, Giewat M, Rooney-Varga J . Phylogenetic diversity and specificity of bacteria closely associated with Alexandrium spp. and other phytoplankton. Appl Environ Microbiol. 2005; 71(7):3483-94. PMC: 1169014. DOI: 10.1128/AEM.71.7.3483-3494.2005. View

4.
Davidov Y, Jurkevitch E . Diversity and evolution of Bdellovibrio-and-like organisms (BALOs), reclassification of Bacteriovorax starrii as Peredibacter starrii gen. nov., comb. nov., and description of the Bacteriovorax-Peredibacter clade as Bacteriovoracaceae fam. nov. Int J Syst Evol Microbiol. 2004; 54(Pt 5):1439-1452. DOI: 10.1099/ijs.0.02978-0. View

5.
Carey C, Ibelings B, Hoffmann E, Hamilton D, Brookes J . Eco-physiological adaptations that favour freshwater cyanobacteria in a changing climate. Water Res. 2012; 46(5):1394-407. DOI: 10.1016/j.watres.2011.12.016. View