RESUMEN
Enterococcus spp. from two poultry farms and proximate surface and ground water sites in an area of intensive poultry production were tested for resistance to 16 clinical antibiotics. Resistance patterns were compared to assess trends and possible correlations for specific antimicrobials and levels of resistance. Enterococci were detected at all 12 surface water sites and three of 28 ground water sites. Resistance to lincomycin, tetracycline, penicillin and ciprofloxacin in poultry litter isolates was high (80.3%, 65.3%, 61.1% and 49.6%, respectively). Resistance in the surface water to the same antibiotics was 87.1%, 24.1%, 7.6% and 12.9%, respectively. Overall, 86% of litter isolates, 58% of surface water isolates and 100% of ground water isolates were resistant to more than one antibiotic. Fifty-four different resistance patterns were recognised in isolates obtained from litter and environmental samples and several E. faecium and E. faecalis isolates from litter and environment samples shared the same resistance pattern. Multiple antibiotic resistant (MAR) indices calculated to assess health risks due to the presence of resistant enterococci suggested an increased presence of antibiotics in surface water, likely from poultry sources as no other wastewater contributions in the area were documented.
Asunto(s)
Crianza de Animales Domésticos , Antibacterianos/farmacología , Farmacorresistencia Bacteriana Múltiple , Enterococcus/efectos de los fármacos , Aves de Corral , Animales , Enterococcus/aislamiento & purificación , Monitoreo del Ambiente , Pruebas de Sensibilidad Microbiana , Contaminantes del Suelo/aislamiento & purificación , Contaminantes del Agua/aislamiento & purificaciónRESUMEN
Genetic relatedness of enterococci from poultry litter to enterococci from nearby surface water and groundwater in the Lower Fraser Valley regions of British Columbia, Canada was determined. A new automated BOX-PCR and Pulsed-Field Gel Electrophoresis (PFGE) were used to subtype enterococcal isolates from broiler and layer litter and surface and groundwater. All surface water samples (n = 12) were positive for enterococci, as were 11% (3/28) of groundwater samples. Enterococcus faecium (n = 90) was isolated from all sources, while Enterococcus faecalis (n = 59) was isolated from all sources except layer litter. The majority of E. faecalis originated from broiler litter (28/59; 47.5%) while the majority of E. faecium were isolated from layer litter (29/90; 32.2%). E. faecalis grouped primarily by source using BOX-PCR. Isolates from water samples were dispersed more frequently among PFGE groups containing isolates from poultry litter. E. faecium strains were genetically diverse as overall clustering was independent of source by both molecular methods. Subgroups of E. faecium isolates based upon source (layer litter) were present in BOX-PCR groups. Three individual E. faecalis groups and two individual E. faecium groups were 100% similar using BOX-PCR; only one instance of 100% similarity among isolates using PFGE was observed. Although enterococci from litter and water sources were grouped together using BOX-PCR and PFGE, isolates originating from water could not be definitively identified as originating from poultry litter. Automation of BOX-PCR amplicon separation and visualization increased the reproducibility and standardization of subtyping using this procedure.
Asunto(s)
Electroforesis en Gel de Campo Pulsado/métodos , Enterococcus/clasificación , Heces/microbiología , Agua Dulce/microbiología , Reacción en Cadena de la Polimerasa/métodos , Aves de Corral , Crianza de Animales Domésticos , Animales , Técnicas de Tipificación Bacteriana , Colombia Británica , Análisis por Conglomerados , Enterococcus/genética , Enterococcus/aislamiento & purificación , Enterococcus faecalis/clasificación , Enterococcus faecalis/genética , Enterococcus faecalis/aislamiento & purificación , Enterococcus faecium/clasificación , Enterococcus faecium/genética , Enterococcus faecium/aislamiento & purificación , Monitoreo del Ambiente/métodos , Variación Genética , Reproducibilidad de los Resultados , Sensibilidad y EspecificidadRESUMEN
The effects of agricultural activities on stream water quality were assessed by nitrogen analysis, further investigated by gas chromatography mass spectrometry (GC-MS) sterol analysis (including chemometric analysis), and characterized by bacterial source tracking (BST). Surface water samples were collected from five sites, throughout the agriculturally-influenced Nathan Creek watershed, British Columbia, Canada and a nearby control site between October 2005 and March 2006. From a total of 48 samples, Canadian Water Quality Guidelines were exceeded nineteen times for nitrate (NO3-; guideline value: 2.94 mg/L N) and four times for un-ionized ammonia (NH3; guideline value 0.019 mg/L N). Gas chromatography mass spectrometry single ion monitoring (GC-MS SIM) analysis of 18 sterols showed that five fecal sterols (coprostanol, episoprostanol, cholesterol, cholestanol, desmosterol) were detected at all sites except the control site (where only cholesterol, cholestanol and desmosterol were detected). Three phytosterols (campesterol, stigmasterol and ß-sitosterol) were also detected at all sites while the hormone estrone was present at one site on two occasions at concentrations of 0.01 and 0.04 µg/L. Chemometric analysis (principal component analysis and cluster analysis) grouped sites based on their similarities in sterol composition. Analysis of ten sterol ratios (seven for identifying human fecal contamination and four for differentiating sources of fecal contamination) showed multiple instances of human and animal contamination for every site but the control site. Application of a Bacteroides-BST method confirmed contamination from ruminant animals, pigs and dogs in varying combinations at all impact sites. Together, these results confirmed the impact of agricultural activities on the Nathan Creek watershed and support a need for better land management practices to protect water quality and aquatic life.
Asunto(s)
Bacteroides/aislamiento & purificación , Monitoreo del Ambiente/métodos , Nitrógeno/aislamiento & purificación , Esteroles/aislamiento & purificación , Microbiología del Agua , Contaminación del Agua/análisis , Calidad del Agua/normas , Animales , Colombia Británica , Análisis por Conglomerados , Humanos , Límite de Detección , Ganado , Análisis de Componente Principal , Ríos/química , Ríos/microbiología , Propiedades de SuperficieRESUMEN
Pharmaceuticals are emerging contaminants with potential risks to the environment and human health. A liquid chromatography-tandem mass spectrometry (LC-MS-MS) method was developed for determination of the antimicrobials virginiamycin, monensin, salinomycin, narasin and nicarbazin in poultry litter and soil. This method involves methanol extraction and clean-up of extracts through glass microfibre filters, introduction of the extracts and separation of compounds on a Zorbax Eclipse XDB C8 column, and compound detection in a Quattro Micro Micromass spectrometer. For litter samples, Method Detection Limits ranged from 0.1-0.6 microg Kg(-1), while Limits of Quantitation (LOQs) were 2, 1, 0.4, 1 and 2 microg Kg(-1) for virginiamycin, monensin, salinomycin, narasin and nicarbazin, respectively. For soil samples calculated LOQs were 2, 3, 1, 1, and 1 microg Kg(-1) for virginiamycin, monensin, salinomycin, narasin and nicarbazin, respectively. Application of the LC-MS-MS method for detection of veterinary pharmaceuticals in litter collected from commercial poultry farms showed that compounds were present at concentrations ranging from 10-11,000 microg Kg(-1).
Asunto(s)
Fraccionamiento Químico/métodos , Estiércol/análisis , Aves de Corral , Suelo/análisis , Drogas Veterinarias/análisis , Animales , Cromatografía Líquida de Alta Presión/métodos , Vidrio/química , Humanos , Límite de Detección , Metanol/química , Espectrometría de Masas en Tándem/métodosRESUMEN
A new approach to surface water analysis has been investigated in order to enhance the detection of different organic contaminants in Nathan Creek, British Columbia. Water samples from Nathan Creek were prepared by liquid/liquid extraction using dichloromethane (DCM) as an extraction solvent and analyzed by gas chromatography mass spectrometry method in scan mode (GC-MS scan). To increase sensitivity for pesticides detection, acquired scan data were further analyzed by Automated Mass Spectrometry Deconvolution and Identification Software (AMDIS) incorporated into the Agilent Deconvolution Reporting Software (DRS), which also includes mass spectral libraries for 567 pesticides. Extracts were reanalyzed by gas chromatography mass spectrometry single ion monitoring (GC-MS-SIM) to confirm and quantitate detected pesticides. Pesticides: atrazine, dimethoate, diazinone, metalaxyl, myclobutanil, napropamide, oxadiazon, propazine and simazine were detected at three sampling sites on the mainstream of the Nathan Creek. Results of the study are further discussed in terms of detectivity and identification level for each pesticide found. The proposed approach of monitoring pesticides in surface waters enables their detection and identification at trace levels.
Asunto(s)
Agua Dulce/química , Cromatografía de Gases y Espectrometría de Masas/normas , Residuos de Plaguicidas/análisis , Programas Informáticos , Contaminantes Químicos del Agua/análisis , Automatización , Sensibilidad y EspecificidadRESUMEN
A simple, very efficient method is presented for routine analysis of herbicide Krovar I (active components bromacil and diuron) in water and soil samples. Water samples were extracted by liquid-liquid extraction with dichloromethane (DCM) as extraction solvent. For soil samples two different extraction techniques were compared: microwave-assisted solvent extraction and a shaking technique using a platform shaker. Extracts were analyzed by high performance liquid chromatography using a water:methanol gradient. Liquid chromatography was coupled with atmospheric pressure chemical ionization mass spectrometry (LC-APCI-MS) for quantification of bromacil and diuron. Optimization of the APCI-MS was done by using standards in the flow injection analysis mode (FIA). Method detection limit for liquid samples for bromacil is 0.04 microg L(-1) and for diuron 0.03 microg L(-1). Method detection limit for soil samples is 0.01 microg g(-1) dry weight for both compounds. Results of analysis of field samples of water and soil are also presented.
Asunto(s)
Bromouracilo/análogos & derivados , Bromouracilo/análisis , Diurona/análisis , Monitoreo del Ambiente/métodos , Herbicidas/análisis , Contaminantes del Suelo/análisis , Contaminantes Químicos del Agua/análisis , Presión Atmosférica , Cromatografía de Gases , Cromatografía Liquida , Monitoreo del Ambiente/instrumentación , Espectrometría de Masas , Sensibilidad y EspecificidadRESUMEN
This study was conducted to describe the acute lethality and latent toxicity of didecyldimethylammonium chloride (DDAC) on early life stages of white sturgeon (Acipenser transmontanus). Fish responses to 0, 10, 50, 100, 250, 500 microg/L concentrations of DDAC were determined using a 96-h standard static renewal method for acute toxicity testing, with three replicates per concentration. Twenty fish per replicate were tested for 3, 11, and 42-d-old larvae, and 7 fish per replicate were tested for 78-d-old juveniles. Following exposure, survival and growth were evaluated in exposed fish raised in clean water for 2 weeks. The 96-h median lethal concentration (LC50) values for DDAC were 10.0 to 50.0, 58.5, and 99.7 microg/L for 3, 11, and 42-d-old larvae and 100 to 250 microg/L for 78-d-old juveniles. Significant decreases in larval growth and survival were noted at all tested concentrations and in all sturgeon age groups. Results of this study reveal age- and concentration-dependent responses to DDAC. Among the age groups tested, the 3-d-old larvae were the most sensitive group. Results also revealed that 96-h lethality testing alone is not adequate for determining the toxicity of DDAC to white sturgeon.