Application of the mixture design to decolourise effluent textile wastewater using continuous stirred bed reactor

Important pollutants in textile effluents are mainly recalcitrant organics, colours, toxicants and inhibitory compounds, surfactants, chlorinated compounds (AOX), pH and salts. An aerobic system using a continuous stirred bed reactor (SBR) was continuously operated at constant temperature and fed with textile wastewater (pH 7 and total chemical oxygen demand (COD) 1 700 mg/ℓ).This report is focused on the decolourisation treatment of effluent by a bacterial consortium (Sphingomonas paucimobilis, Bacillus sp. and filamentous bacteria). The influence of the different mixtures of 3 strains on the decolourisation of effluent (cell density fixed at OD600 = 1) was studied using an equilateral triangle diagram and mixture experimental design to assess colour and COD removal during species evolution. With the aid of analysis software (Minitab 14.0), the formulation of pure culture was optimised for several responses and the best formulation obtained. The results suggested that the highest predictable specific decolourisation rate and chemical oxygen demand (COD) were 86.72% and 75.06%, respectively. Regression coefficients between the variables and the responses of decolourisation and COD removal were, respectively, R2 = 72.48% and 54.28%, which indicated excellent evaluation of experimental data by the polynomial regression model. UV-visible analysis confirmed biodegradation of effluent.Keywords: textile wastewater, bacterial decolourisation, response surface, mixture design, SB

Les Aeromonas mobiles : quelle évolution spatiale et temporelle dans un effluent urbain et en milieu marin côtier ?

L'analyse bactériologique des eaux de surface dans un effluent urbain et en milieu marin côtier montre une contamination saisonnière mais fréquente de ces eaux par les Aeromonas mobiles. L'évolution spatiale et temporelle des abondances de ces bactéries, en relation avec certains facteurs environnementaux, a été étudiée pendant un an dans le rejet final épuré et dans les eaux marines réceptacles de l'effluent. Ces bactéries présentent, dans les eaux lagunaires, des évolutions saisonnières identiques à celles des coliformes fécaux avec des densités élevées en période froide (moyenne : 29·106 UFC/100 mL) et faibles en période chaude (moyenne : 6·106 UFC/100 mL). L'abattement des abondances d'Aeromonas se trouve corrélé à une forte irradiation et à une faible turbidité.Le déversement des eaux de la station d'épuration dans les eaux marines côtières de la région n'induit pas globalement de modifications de la forme de comportement des bactéries témoins de contamination fécale. À l'opposé, l'évolution des abondances des Aeromonas spp. mobiles s'inverse pour devenir maximale en période chaude (moyenne : 56 CFU/100 mL pour S3) et minimale en période froide (moyenne : 5 CFU/100 mL pour S3). La salinité paraît responsable de la déstabilisation des séquences saisonnières des Aeromonas et de leur réduction à des concentrations non détectables dans les volumes d'eaux analysés.La présence de ces bactéries dans les effluents épurés, parfois à des concentrations supérieures à celles des coliformes fécaux, pose un problème d'intérêt sanitaire et montre clairement que les bactéries témoins de contamination fécale ne peuvent pas être prédictives de la présence ou de l'absence d'Aeromonas et, par conséquent, ne peuvent pas être considérées comme un bon indicateur de pollution.Bacteriological analyse of surface water in an urban effluent and in coastal marine environment showed a seasonal contamination of this water by motile Aeromonas. Spatial and seasonal changes of Aeromonas abundances were studied, in relation to several environmental factors, in the purified effluent and in seawater.The motile Aeromonas spp. and the fecal coliform distributions in the sewage treatment effluent showed the same seasonal cycles with a maximum occuring in winter (mean: 29·106 UFC/100 ml) and a minimum in summer (mean of 6·106 UFC/100 mL). The abatement of Aeromonas abundances was correlated with a strong irradiation and a low turbidity.In the coastal marine water, there was an inversion of the motile Aeromonas spp. cycle in comparison with that of fecal coliforms, with high levels in hot periods (mean: 56 CFU/100 mL for S3) and low levels in cold periods (mean of 5 CFU/100 mL for S3). Salinity appeared responsible for the destabilisation of the seasonal sequences of Aeromonas and their reduction with non detectable concentrations in water analysed volumes.The presence of these bacteria in the purified effluent, sometimes with concentrations higher than those of the fecal coliforms, poses a problem of health hazard and clearly show that fecal contamination bacteria cannot be predictive for the presence or the absence of Aeromonas and, consequently, cannot be considered as good indicators of pollution

Virulence properties and random amplification of polymorphic DNA (RAPD) fingerprinting of Candida albicans isolates obtained from Monastir dental hospital, Tunisia

Genotypic and phenotypic characterization as well as studies on the virulence factors of Candida albicans isolates obtained from oral cavity of patients was carried out using random amplified polymorphic DNA (RAPD) fingerprinting and epithelial cells adherence assay, respectively. RAPD patterns revealed the presence of 13 C. albicans genotypes separated into two clusters at 75% ofsimilarity when they were combined. Results also showed the presence of haemolytic protease activity as virulence factors with 88% of the C. albicans strains been able to adhere to Caco-2 cells and only 64% to Hep-2. RAPD-polymerase chain reaction (PCR) is a molecular tool used to differentiate the isolates into various genotypes based on their virulence properties.Key words: Candida albicans, stomatitis, random amplified polymorphic DNA, Hep-2, Caco-2 cells

The cientificWorldJOURNAL Research Article Removal of Triphenylmethane Dyes by Bacterial Consortium

A new consortium of four bacterial isolates (Agrobacterium radiobacter; Bacillus spp.; Sphingomonas paucimobilis, and Aeromonas hydrophila)-(CM-4) was used to degrade and to decolorize triphenylmethane dyes. All bacteria were isolated from activated sludge extracted from a wastewater treatment station of a dyeing industry plant. Individual bacterial isolates exhibited a remarkable colorremoval capability against crystal violet (50 mg/L) and malachite green (50 mg/L) dyes within 24 h. Interestingly, the microbial consortium CM-4 shows a high decolorizing percentage for crystal violet and malachite green, respectively, 91% and 99% within 2 h. The rate of chemical oxygen demand (COD) removal increases after 24 h, reaching 61.5% and 84.2% for crystal violet and malachite green, respectively. UV-Visible absorption spectra, FTIR analysis and the inspection of bacterial cells growth indicated that color removal by the CM-4 was due to biodegradation. Evaluation of mutagenicity by using Salmonella typhimurium test strains, TA98 and TA100 studies revealed that the degradation of crystal violet and malachite green by CM-4 did not lead to mutagenic products. Altogether, these results demonstrated the usefulness of the bacterial consortium in the treatment of the textile dyes

Seawater salt-trapped Pseudomonas aeruginosa survives for years and gets primed for salinity tolerance

Background In nature, microorganisms have to adapt to long-term stressful conditions often with growth limitations. However, little is known about the evolution of the adaptability of new bacteria to such environments. Pseudomonas aeruginosa, an opportunistic pathogen, after natural evaporation of seawater, was shown to be trapped in laboratory-grown halite crystals and to remain viable after entrapment for years. However, how this bacterium persists and survives in such hypersaline conditions is not understood. Results In this study, we aimed to understand the basis of survival, and to characterise the physiological changes required to develop salt tolerance using P. aeruginosa as a model. Several clones of P. aeruginosa were rescued after 14 years in naturally evaporated marine salt crystals. Incubation of samples in nutrient-rich broth allowed re-growth and subsequent plating yielded observable colonies. Whole genome sequencing of the P. aeruginosa isolates confirmed the recovery of the original strain. The re-grown strains, however, showed a new phenotype consisting of an enhanced growth in growing salt concentration compared to the ancestor strain. The intracellular accumulation of K+ was elicited by high concentration of Na+ in the external medium to maintain the homeostasis. Whole transcriptomic analysis by microarray indicated that 78 genes had differential expression between the parental strain and its derivative clones. Sixty-one transcripts were up-regulated, while 17 were down-regulated. Based on a collection of single-gene knockout mutants and gene ontology analysis, we suggest that the adaptive response in P. aeruginosa to hyper-salinity relies on multiple gene product interactions. Conclusions The individual gene contributions build up the observed phenotype, but do not ease the identification of salinity-related metabolic pathways. The long-term inclusion of P. aeruginosa in salt crystals primes the bacteria, mediating a readjustment of the bacterial physiology to growth in higher salt concentrations. Our findings provide a starting point to understand how P. aeruginosa, a relevant environmental and pathogenic bacterium, survives to long-term salt stress

Detection of macrolide and disinfectant resistance genes in clinical Staphylococcus aureus and coagulase-negative staphylococci

<p>Abstract</p> <p>Background</p> <p><it>Staphylococcus aureus </it>and Coagulase-negative staphylococci (CoNS) are a major source of infections associated with indwelling medical devices. Many antiseptic agents are used in hygienic handwash to prevent nosocomial infections by Staphylococci. Our aim was to determine the antibiotic susceptibility and resistance to quaternary ammonium compound of 46 <it>S. aureus </it>strains and 71 CoNS.</p> <p>Methods</p> <p><it>S. aureus </it>(n = 46) isolated from auricular infection and CoNS (n = 71), 22 of the strains isolated from dialysis fluids and 49 of the strains isolated from needles cultures were investigated. Erythromycin resistance genes (<it>erm</it>A, <it>erm</it>B, <it>erm</it>C, <it>msr</it>A and <it>mef</it>) were analysed by multiplex PCR and disinfectant-resistant genes (<it>qac</it>A, <it>qac</it>B, and <it>qac</it>C) were studied by PCR-RFLP.</p> <p>Results</p> <p>The frequency of erythromycin resistance genes in <it>S. aureus </it>was: <it>erm</it>A+ 7.7%, <it>erm</it>B+ 13.7%, <it>erm</it>C+ 6% and <it>msr</it>A+ 10.2%. In addition, the number of positive isolates in CoNS was respectively <it>erm</it>A+ (9.4%), <it>erm</it>B+ (11.1%), <it>erm</it>C+ (27.4%), and <it>msr</it>A+ (41%). The MIC analyses revealed that 88 isolates (74%) were resistant to quaternary ammonium compound-based disinfectant benzalkonium chloride (BC). 56% of the BC-resistant staphylococcus isolates have at least one of the three resistant disinfectants genes (<it>qac</it>A, <it>qac</it>B and <it>qac</it>C). Nine strains (7.7%) among the CoNS species and two <it>S. aureus </it>strains (2%) harboured the three-<it>qac </it>genes. In addition, the <it>qac</it>C were detected in 41 strains.</p> <p>Conclusions</p> <p>Multi-resistant strains towards macrolide and disinfectant were recorded. The investigation of antibiotics and antiseptic-resistant CoNS may provide crucial information on the control of nosocomial infections.</p

Antibacterial activity of Thymoquinone, an active principle of Nigella sativa and its potency to prevent bacterial biofilm formation

<p>Abstract</p> <p>Background</p> <p>Thymoquinone is an active principle of <it>Nigella sativa </it>seed known as "Habbah Al-Sauda" in Arabic countries and "Sinouj" in Tunisia. Bacterial biofilms tend to exhibit significant tolerance to antimicrobials drugs during infections.</p> <p>Methods</p> <p>The antibacterial activity of Thymoquinone (TQ) and its biofilm inhibition potencies were investigated on 11 human pathogenic bacteria. The growth and development of the biofilm were assessed using the crystal violet (CV) and the 2, 3-bis [2-methyloxy-4-nitro-5-sulfophenyl]-2H-tetrazolium-5-carboxanilide (XTT) reduction assay.</p> <p>Results</p> <p>TQ exhibited a significant bactericidal activity against the majority of the tested bacteria (MICs values ranged from 8 to 32 μg/ml) especially Gram positive cocci (<it>Staphylococcus aureus </it>ATCC 25923 and <it>Staphylococcus epidermidis </it>CIP 106510). Crystal violet assay demonstrated that the minimum biofilm inhibition concentration (BIC50) was reached with 22 and 60 μg/ml for <it>Staphylococcus aureus </it>ATCC 25923 and <it>Staphylococcus epidermidis </it>CIP 106510 respectively. In addition our data revealed that cells oxidative activity was influenced by TQ supplementation. In the same way, TQ prevented cell adhesion to glass slides surface.</p> <p>Conclusion</p> <p>The ability of TQ to prevent biofilm formation warrants further investigation to explore its use as bioactive substances with antibiofilm potential.</p

Resuscitation of eleven-year VBNC Citrobacter

Citrobacter freundii strain WA1 was stressed by incubation in seawater microcosms for eleven years. After two years of starvation, no culturable strain was observed. Incubation of samples in nutrient-rich broth medium not supplemented with growth factors, however, allowed resuscitation of VBNC cells so that subsequent plating yielded observable colonies for significantly extended periods of time. Recovery of VBNC Citrobacter freundii was obtained by incubation in nutrient broth even after eleven years of starvation. To see whether the samples contained the same strain of Citrobacter freundii inoculated 11 years ago. The complete 16S rRNA gene was PCR amplified and sequenced from initial, stressed and revived strains of Citrobacter freundii strain WA1.The 16S rRNA gene sequences from eleven-year stressed strains were homologous with a high degree of similarity to the GenBank reference strain and were identical to each other