Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
Add more filters










Database
Language
Publication year range
1.
Environ Microbiol ; 17(5): 1574-85, 2015 May.
Article in English | MEDLINE | ID: mdl-25088527

ABSTRACT

Enhanced biological phosphorus removal (EBPR) is an important industrial wastewater treatment process mediated by polyphosphate-accumulating organisms (PAOs). Members of the genus Candidatus Accumulibacter are one of the most extensively studied PAO as they are commonly enriched in lab-scale EBPR reactors. Members of different Accumulibacter clades are often enriched through changes in reactor process conditions; however, the two currently sequenced Accumulibacter genomes show extensive metabolic similarity. Here, we expand our understanding of Accumulibacter genomic diversity through recovery of eight population genomes using deep metagenomics, including seven from phylogenetic clades with no previously sequenced representative. Comparative genomic analysis revealed a core of shared genes involved primarily in carbon and phosphorus metabolism; however, each Accumulibacter genome also encoded a substantial number of unique genes (> 700 genes). A major difference between the Accumulibacter clades was the type of nitrate reductase encoded and the capacity to perform subsequent steps in denitrification. The Accumulibacter clade IIF genomes also contained acetaldehyde dehydrogenase that may allow ethanol to be used as carbon source. These differences in metabolism between Accumulibacter genomes provide a molecular basis for niche differentiation observed in lab-scale reactors and may offer new opportunities for process optimization.


Subject(s)
Betaproteobacteria/genetics , Betaproteobacteria/metabolism , Wastewater/chemistry , Water Purification/methods , Aldehyde Oxidoreductases/genetics , Betaproteobacteria/enzymology , Bioreactors , Carbon/metabolism , Denitrification/genetics , Denitrification/physiology , Ethanol/metabolism , Genetic Variation/genetics , Metagenomics , Nitrate Reductase/genetics , Nitrogen Fixation/physiology , Phosphorus/metabolism , Phylogeny , Polymorphism, Single Nucleotide , Polyphosphates/metabolism
2.
Environ Technol ; 34(5-8): 695-701, 2013.
Article in English | MEDLINE | ID: mdl-23837320

ABSTRACT

Coal seam gas (CSG) is being touted as a transition fuel as the world moves towards low-carbon economies. However, the development of CSG reserves will generate enormous volumes of saline water. In this work, we investigate the potential of using this saline water to support mass algae production. Water and brine from a CSG water treatment facility (1.6 and 11.6 g total dissolved solids per litre (TDS L(-1)) respectively) were inoculated with algal biomass from freshwater and seawater environments and supplemented with nutrients in open, fed-batch reactors. Significant algal growth was recorded, with maximum specific growth rates in CSG water and CSG brine of 0.20 +/- 0.05 d(-1) and 0.26 +/- 0.04 d(-1) respectively. These maximum specific growth rates were equal to or greater than specific growth rates in deionized water and seawater diluted to the same salinity. However, algal growth lag time in CSG brine was between 7 and 9 times longer than in other waters. Microscopy and terminal-restriction fragment length polymorphism (T-RFLP) were used to monitor community structure in the reactors. The same few algal species dominated all of the reactors, except for the CSG brine reactor at day 15. This result indicates that conditions in CSG brine select for different species of algae compared to seawater of the same salinity and other waters tested. The findings suggest that mass algae production in CSG water is feasible but algae community composition may be a function of CSG water chemistry. This has implications for the downstream use of algae.


Subject(s)
Batch Cell Culture Techniques/methods , Bioreactors/microbiology , Eukaryota/physiology , Microbial Consortia/physiology , Sodium Chloride/metabolism , Water Microbiology , Cell Proliferation , Coal , Coculture Techniques/methods , Computer Simulation , Gases , Models, Biological
3.
FEMS Microbiol Lett ; 315(1): 17-22, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21133989

ABSTRACT

The 2009-2010 influenza pandemic saw many people treated with antivirals and antibiotics. High proportions of both classes of drugs are excreted and enter wastewater treatment plants (WWTPs) in biologically active forms. To date, there has been no study into the potential for influenza pandemic-scale pharmaceutical use to disrupt WWTP function. Furthermore, there is currently little indication as to whether WWTP microbial consortia can degrade antiviral neuraminidase inhibitors when exposed to pandemic-scale doses. In this study, we exposed an aerobic granular sludge sequencing batch reactor, operated for enhanced biological phosphorus removal (EBPR), to a simulated influenza-pandemic dosing of antibiotics and antivirals for 8 weeks. We monitored the removal of the active form of Tamiflu(®), oseltamivir carboxylate (OC), bacterial community structure, granule structure and changes in EBPR and nitrification performance. There was little removal of OC by sludge and no evidence that the activated sludge community adapted to degrade OC. There was evidence of changes to the bacterial community structure and disruption to EBPR and nitrification during and after high-OC dosing. This work highlights the potential for the antiviral contamination of receiving waters and indicates the risk of destabilizing WWTP microbial consortia as a result of high concentrations of bioactive pharmaceuticals during an influenza pandemic.


Subject(s)
Antiviral Agents/metabolism , Bacteria/metabolism , Oseltamivir/analogs & derivatives , Sewage/chemistry , Sewage/microbiology , Water Pollutants, Chemical/metabolism , Anti-Bacterial Agents/metabolism , Antiviral Agents/analysis , Bacteria/chemistry , Biodegradation, Environmental , Bioreactors , Microbial Consortia , Models, Biological , Oseltamivir/analysis , Oseltamivir/metabolism , Pandemics , Particle Size , Phosphorus/metabolism , Waste Disposal, Fluid/methods , Water Pollutants, Chemical/analysis , Water Purification
4.
FEMS Microbiol Ecol ; 74(3): 631-42, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20883494

ABSTRACT

Bacteria are known to play important roles in biogeochemical cycles and biotechnology processes, but little is known about the influence of bacteriophage on these processes. A major impediment to the study of host-bacteriophage interactions is that the bacteria and their bacteriophage are often not available in a pure culture. In this study, we detected an unexpected decline in the phosphorus-removal performance of a granular laboratory-scale wastewater treatment reactor. Investigations by FISH, transmission electron microscopy and proteomics led us to hypothesize that a bacteriophage infection of the uncultured Candidatus 'Accumulibacter phosphatis' was responsible for the decline in performance. Further experiments demonstrated that the addition of a putative bacteriophage-rich supernatant, obtained from the previous failed reactor to phosphorus-removal reactors, caused a decrease in the abundance of Accumulibacter in both granular and floccular activated sludges. This coincided with increases in bacteriophage-like particles and declining phosphorus-removal performance. The granular sludge did not recover after the attack, but the floccular sludge regained Accumulibacter numbers and phosphorus-removal performance. These findings suggest that bacteriophage may play a significant role in determining the structure and function of bacterial communities in activated sludges.


Subject(s)
Bacteriophages/growth & development , Betaproteobacteria/virology , Phosphorus/metabolism , Sewage/microbiology , Sewage/virology , Betaproteobacteria/metabolism , Bioreactors , In Situ Hybridization, Fluorescence , Microscopy, Electron, Transmission , Proteomics , Waste Disposal, Fluid
5.
Microb Ecol ; 60(4): 873-84, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20512486

ABSTRACT

A key interest of microbial ecology is to understand the role of environmental heterogeneity in shaping bacterial diversity and fitness. However, quantifying relevant selection pressures and their effects is challenging due to the number of parameters that must be considered and the multiple scales over which they act. In the current study, a model system was employed to investigate the effects of a spatially heterogeneous mercuric ion (Hg(2+)) selection pressure on a population comprising Hg-sensitive and Hg-resistant pseudomonads. The Hg-sensitive bacteria were Pseudomonas fluorescens SBW25::rfp and Hg-resistant bacteria were P. fluorescens SBW25 carrying a gfp-labelled, Hg resistance plasmid. In the absence of Hg, the plasmid confers a considerable fitness cost on the host, with µ(max) for plasmid-carrying cells relative to plasmid-free cells of only 0.66. Two image analysis techniques were developed to investigate the structure that developed in biofilms about foci of Hg (cellulose fibres imbued with HgCl(2)). Both techniques indicated selection for the resistant phenotype occurred only in small areas of approximately 178-353 µm (manually defined contour region analysis) or 275-350 µm (daime analysis) from foci. Hg also elicited toxic effects that reduced the growth of both Hg-sensitive and Hg-resistant bacteria up to 250 µm from foci. Selection for the Hg resistance phenotype was therefore highly localised when Hg was spatially heterogeneous. As such, for this model system, we define here the spatial scale over which selection operates. The ability to quantify changes in the strength of selection for particular phenotypes over sub-millimetre scales is useful for understanding the scale over which environmental variables affect bacterial populations.


Subject(s)
Bacteriological Techniques/methods , Ecosystem , Mercury/pharmacology , Pseudomonas fluorescens/genetics , Selection, Genetic , Drug Resistance, Bacterial , Mercury/metabolism , Models, Biological , Plasmids/genetics , Pseudomonas fluorescens/drug effects , Pseudomonas fluorescens/growth & development
6.
FEMS Microbiol Ecol ; 66(1): 3-13, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18507680

ABSTRACT

Plasmid-mediated horizontal gene transfer influences bacterial community structure and evolution. However, an understanding of the forces which dictate the fate of plasmids in bacterial populations remains elusive. This is in part due to the enormous diversity of plasmids, in terms of size, structure, transmission, evolutionary history and accessory phenotypes, coupled with the lack of a standard theoretical framework within which to investigate them. This review discusses how ecological factors, such as spatial structure and temporal fluctuations, shape both the population dynamics and the physical features of plasmids. Novel data indicate that larger plasmids are more likely to be harboured by hosts in complex environments. Plasmid size may therefore be determined by environmentally mediated fitness trade-offs. As the correlation between replicon size and complexity of environment is similar for plasmids and chromosomes, plasmids could be used as tractable tools to investigate the influence of ecological factors on chromosomes. Parallels are drawn between plasmids and bacterial facultative symbionts, including the evolution of some members of both groups to a more obligate relationship with their host. The similarity between the influences of ecological factors on plasmids and bacterial symbionts suggests that it may be appropriate to study plasmids within a classical ecological framework.


Subject(s)
Bacteria/genetics , Ecology , Plasmids/genetics , Evolution, Molecular , Gene Transfer, Horizontal , Genetic Variation , Population Dynamics , Replicon , Symbiosis
7.
Appl Environ Microbiol ; 74(10): 3189-97, 2008 May.
Article in English | MEDLINE | ID: mdl-18378654

ABSTRACT

Environmental conditions under which fitness tradeoffs of plasmid carriage are balanced to facilitate plasmid persistence remain elusive. Periodic selection for plasmid-encoded traits due to the spatial and temporal variation typical in most natural environments (such as soil particles, plant leaf and root surfaces, gut linings, and the skin) may play a role. However, quantification of selection pressures and their effects is difficult at a scale relevant to the bacterium in situ. The present work describes a novel experimental system for such fine-scale quantification, with conditions designed to mimic the mosaic of spatially variable selection pressures present in natural surface environments. The effects of uniform and spatially heterogeneous mercuric chloride (HgCl(2)) on the dynamics of a model community of plasmid-carrying, mercury-resistant (Hg(r)) and plasmid-free, mercury-sensitive (Hg(s)) pseudomonads were compared. Hg resulted in an increase in the surface area occupied by, and therefore an increase in the fitness of, Hg(r) bacteria relative to Hg(s) bacteria. Uniform and heterogeneous Hg distributions were demonstrated to result in different community structures by epifluorescence microscopy, with heterogeneous Hg producing spatially variable selection landscapes. The effects of heterogeneous Hg were only apparent at scales of a few hundred micrometers, emphasizing the importance of using appropriate analysis methods to detect effects of environmental heterogeneity on community dynamics. Heterogeneous Hg resulted in negative frequency-dependent selection for Hg(r) cells, suggesting that sporadic selection may facilitate the discontinuous distribution of plasmids through host populations in complex, structured environments.


Subject(s)
Drug Resistance, Bacterial/genetics , Mercuric Chloride/toxicity , Plasmids , Pseudomonas/growth & development , Pseudomonas/genetics , Pseudomonas/drug effects , Selection, Genetic
SELECTION OF CITATIONS
SEARCH DETAIL
...