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To examine the potential impact of invasive dreissenid mussels on in situ populations of phytoplankton and nutrients in western Lake Erie, we combined mussel population estimates from a 2018 survey, results from mussel excretion, grazing, and in situ growth experiments, along with nutrient measurements on collected lake water. We calculated the proportion of the water column filtered per day, based on both clearance rates from grazing experiments and mussel biomass. In most cases the water column was filtered less than once per day. Based on mussel densities from nearby survey sites, we found that mussels could be expected to clear less than 5% of phytoplankton from the water column each day. We combined measurements of nitrogen and phosphorus excretion by mussels with survey densities and found that concentrations of nitrogen and phosphorus from excretion were much less than the ambient inorganic nitrogen and phosphorus measured throughout the season. Despite the modest potential impact that we measured, spatial variability in mussel density and temporal variability in nutrients and seston suggest that more substantial impact likely occurs in some conditions. Lastly, we used a mass balance approach to compare flows of nitrogen and phosphorus attributable to mussel assimilation, growth, and excretion. The proportion of assimilated nitrogen (0.01-0.21) and phosphorus (0.007-0.08) due to growth changed markedly throughout the season, but the excretion rate sometimes exceeded the apparent assimilation rate. These differences in growth:assimilation suggest changes in food quantity or quality, fluctuations in growth rates over time, or other physiological effects can lead to short-term imbalance in nutrient cycling by mussels, which could lead to locally important impacts on phytoplankton and algal blooms. Moreover, this work underscores the importance of mapping mussel densities at fine spatial scales and across interannual variation. [ABSTRACT FROM AUTHOR]

We measured Quagga Mussel grazing-induced changes in seston concentration in 20-L laboratory mesocosms containing lake water, during May-October, as part of a study to investigate the present role of mussel feeding and nutrient excretion in affecting phytoplankton composition. A variety of measuring methodologies including size-fractionated chlorophyll (< 2, 2-20, and >20 µm), phytoplankton groups by FluoroProbe, cyanobacterial genera by 16S rRNA gene sequencing, and particulate C, N, and P gave us different insights into seasonal phytoplankton dynamics and mussel selective feeding and assimilation. High clearance rates and/or high assimilation rates were seen during late May-early July across all size categories, with high rates seen particularly in cryptophytes and diatoms as revealed by FluoroProbe. Starting in late July cyanophytes dominated the phytoplankton and feeding rate on them was generally zero or low. Sequencing analyses suggested that there was a diverse cyanobacterial community present, with Microcystis, contrary to expectation, dominating only in late June. Cyanobium was the dominant genera at most times during summer-fall, and as expected, Microcystis was rejected by mussels relative to other cyanobacteria. Planktothrix, dominant in spring, was readily ingested as well as Anabaena in late June. We show that a combination of methods is helpful to make progress in understanding plankton succession and grazing. These methods were important adjuncts to microscopic analysis (Carrick et al, this issue). Our results support the hypothesis that dreissenid mussels, when abundant, can affect seasonal succession of phytoplankton shifting composition to cyanobacteria and even changes within the cyanobacterial community; however, impacts are likely modest now due low mussel biomass (Carter et al., this issue). Assimilation of C, N, and P was generally high, which is important for mussel population maintenance. [ABSTRACT FROM AUTHOR]

Herein we provide experimental evidence for the effects invasive mussels (Dreissena) grazing can exert on a natural assemblage of plankton that included both hetero- and photo-trophic components in western Lake Erie. Five mussel feeding experiments were performed seasonally in 2018 (May, June, July August, October). Pre- and post-grazing samples were collected from seven 20-L mesocosms (3 control, 4 mussel), and analyzed using microscope cell counts. Results from our experiments showed that Dreissena were active grazers of plankton on all dates, with significant correspondence between mussel clearance rates measured using microscopy versus size-specific chlorophyll and FluoroProbe based estimates (Spearman rank correlation, r = 0.45, and r = 0.48, respectively, p < 0.05). Clearance rates (ml mg-1 h-1) were variable among taxonomic groups and seemed to track the abundance of ambient plankton assemblage (range 1.70 to 25.00, mean ± SE 11.70 ± 1.33). Dreissena grazed consistently on nano-sized hetero- and phototrophic plankton that constituted key trophic linkages in the Lake Erie foodweb. The most actively grazed plankton were phototrophic cryptophytes (Rhodomonas minuta, Cryptomonas spp.), centric diatoms (Cyclotella sp. and Discotella spp.), and non-pigmented chrysomonads (Chromulina sp., Ochromonas sp.). Conversely, clearance rates were low for cyanobacteria (e.g. Microcystis), dinoflagellates (Gymnodinium varians), and some colonial chlorophytes (Desmodesmus, Pediastrum); these plankton groups occurred during specific temporal windows (one-way ANOVA, p < 0.05). Our results indicate the potential mussel grazing can suppress typical, non-harmful plankton species in the nanoplankton size range, thereby favoring the occurrence of less-edible, larger cyanobacteria and chlorophyte species in western Lake Erie. [ABSTRACT FROM AUTHOR]

Recent mieroarray experiments suggested that Burkholderia xenovorans LB400, a potent polychlorinated biphenyl (PCB)-degrading bacterium, utilizes up to three apparently redundant benzoate pathways and a [C.sub.1] metabolic pathway during biphenyl and benzoate metabolism. To better characterize the roles of these pathways, we performed quantitative proteome profiling of cells grown on succinate, benzoate, or biphenyl and harvested during either mid-logarithmic growth or the transition between the logarithmic and stationary growth phases. The Bph enzymes, catabolizing biphenyl, were ~16-fold more abundant in biphenyl- versus succinate-grown cells. Moreover, the upper and lower bph pathways were independently regulated. Expression of each benzoate pathway depended on growth substrate and phase. Proteins specifying catabolism via benzoate dihydroxylation and catechol ortho-cleavage (ben-cat pathway) were approximately an order of magnitude more abundant in benzoate- versus biphenyl-grown cells at the same growth phase. The chromosomal copy of the benzoyl-coenzyme A (CoA) ([box.sub.c]) pathway was also expressed during growth on biphenyl: [box.sub.c] proteins were approximately twice as abundant as Ben and Cat proteins under these conditions. By contrast, proteins of the megaplasmid copy of the benzoyl-CoA ([box.sub.M]) pathway were only detected in transition-phase benzoate-grown cells. Other proteins detected at increased levels in benzoate- and biphenyl-grown cells included general stress response proteins potentially induced by reactive oxygen species formed during aerobic aromatic catabolism. Finally, [C.sub.1] metabolic enzymes were present in biphenyl-grown cells during transition phase. This study provides insights into the physiological roles and integration of apparently redundant catabolic pathways in large-genome bacteria and establishes a basis for investigating the PCB-degrading abilities of this strain.

The whole-genome expression patterns were investigated when Burkholderia xenovorans LB400 was grown on biphenyl or benzoate and it was compared to the patterns when the organism was grown on succinate. The microarray results were validated by using the data for a subset of genes measured by quantitative reverse transcription PCR (Q-RT-PCR).

A study is conducted on the role of genetics and genomics in the transcriptomic and proteomic analyses of Burkholderia xenovorans LB400, which is a potent polychlorinated biphenyl (PCB) degrader. It is seen that the absence of wild-type LB400 degrader made the Benzoate-catabolic pathways preferentially active under reduced oxygen tension.