Impact of sludge residence time on the relative biodegradation and biosorption of sulfonamide antibiotics in activated sludge

Four sequencing batch reactors (SBR) are operated with sludge residence time （SRT）of 2, 8, 14, and 20 days to analyze the impact of SRT on removal of sulfanomide (5 μg/L). In batch experiments, three treatments (active biomass, inhibited biomass, and controls of no biomass) are performed in 100 mL batch reactors in triplicate that simulated one SBR cycle, and are investigated to distinguish biodegradation, biosorption, and volatilization losses, respectively. The results show that biomass removed an average 2.14±0.60 μg/g SS of sulfamethoxazole, 1.14±0.63 μg/g SS of sulfadiazine, 2.33±0.67 μg/g SS of sulfadimethoxine, 2.45±0.85 μg/gSS of sulfamerazine, with 63%, 83%, 35%, 55% of the removal respectively due to sorption. When SBRs (3 L total volume) are spiked continuously with 5 μg/L sulfamethoxazole for 60 days, 10%, 41%, 51%, 58% is removed with SRTs of 2d, 8d, 14d, 20d, respectively. Removal increased significantly with SRT, but the normalized mass removed per gram of biomass decreases. Growth of filamentous organisms with a 2-d SRT increases the sorption capacity of this sludge, although biodegradation is the dominant mechanism for removal. Higher biomass concentrations established by longer SRTs are more significant for biodegradation than species diversity, which do not vary with SRT. As wastewater treatment plants implement longer SRTs for nutrient removal, they will also achieve improved removal of some pharmaceuticals.     

Genotype and Environment Variation for Arabinoxylans in Hard Winter and Spring Wheats of the U.S. Pacific Northwest

The development of high‐quality wheat (Triticum aestivum L.) cultivars depends on a thorough understanding of the constituents of grain and their variation due to genetics and environment. Arabinoxylans (pentosans) are key constituents of wheat grain and have broad and far‐reaching influences on milling and baking quality. However, variation in arabinoxylans due to genotype and environment are not fully understood. In this study, 25 hard winter and 25 hard spring wheat commercial cultivars and advanced breeding lines developed from eight public and private breeding programs in the U.S. Pacific Northwest were analyzed for water‐extractable and total arabinoxylan contents (WE‐AX and total AX), and the proportion of total AX that was water‐extractable. Winter and spring genotypes were grown in three environments each. The results indicated that there were significant differences among both sets of hard wheat genotypes for WE‐AX, total AX, and proportion of total AX that was WE‐AX. The WE‐AX and total AX mean content ranges for the winter cultivars were 0.390–0.808 and 3.09–4.04%, respectively; and for the spring cultivars 0.476–0.919 and 3.94–4.70%, respectively. WE‐AX as a percentage of total AX was similar between the two genotype sets, 11.7–23.0%. Arabinoxylan fractions were generally not correlated with grain protein, test weight, and kernel hardness. The two highest correlations for winter wheats were between protein and total AX (r = –0.40) and test weight and percentage of total AX that were water‐extractable (r = 0.37) for winter wheats. Among spring wheats, single‐kernel characterization system hardness was negatively correlated with WE‐AX and proportion of total AX that was WE‐AX (r = –0.46 and –0.51, respectively). Although often significant, arabinoxylan fractions were usually not highly intercorrelated, indicating some independence of traits. Notable genotypes, being especially high or low for one or more arabinoxylan fraction and, thus, candidates for further genetic study and cross‐breeding, included Juniper, Eddy, and ORN980995 winter wheats, and Hollis, Alta Blanca, and WQL9HDALP spring wheats. Although the results indicate that arabinoxylan fractions of wheat grain can be highly influenced by environment, there is clear support for the existence of genetic differences, especially for WE‐AX and the proportion of total AX that is water‐extractable. As such, the manipulation of arabinoxylan content of wheat grain seems to be a reasonable breeding objective.     

Effects of human recombinant alpha-2b interferon and feline recombinant omega interferon on in vitro replication of feline herpesvirus-1

OBJECTIVE: To evaluate the effects of recombinant human interferon alpha-2b (rHuIFN-alpha2b) and recombinant feline interferon omega (rFeIFN-omega) on in vitro replication of feline herpesvirus (FHV)-1. SAMPLE POPULATION: Cultures of Crandell-Rees feline kidney (CRFK) cells. PROCEDURES: CRFK cells were treated with rFeIFN-omega or rHuIFN-alpha2b at concentrations ranging from 100 to 500,000 U/mL. Cultures were then inoculated with FHV-1. Constant concentrations of interferon products were maintained throughout the study. Reductions in the number and size of plaques were used as indicators of antiviral activity. Six plaque reduction assays were performed in duplicate. A 3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide assay was used to detect cytotoxic effects of interferon. A 1-way ANOVA and Dunnett test were used to determine significant differences. RESULTS: Treatment with rFeIFN-omega at various concentrations resulted in significant reductions in the number of plaques (100,000 U/mL, 54.7%; and 500,000 U/mL, 59.8%) and in plaque size (100,000 U/mL, 47.5%; 250,000 U/mL, 81.0%; and 500,000 U/mL; 70.5%). Treatment with various concentrations of rHuIFN-alpha2b resulted in a significant reduction in plaque size (100,000 U/mL, 56.0%; 250,000 U/mL, 75.7%; and 500,000 U/mL, 69.0%). None of the tested concentrations of interferon caused significant cellular toxicosis. CONCLUSIONS AND CLINICAL RELEVANCE: At some of the higher concentrations, the antiviral effect of rFeIFN-omega was greater than the antiviral effect of rHuIFN-alpha2b. Reduction in plaque size appeared to be a good indicator of the antiviral activity of interferon against FHV-1.     

Evaluation of gastrointestinal permeability and mucosal absorptive capacity in dogs with chronic enteropathy

OBJECTIVE: To assess intestinal mucosal function by measuring permeability and absorptive capacity in dogs with chronic enteropathy (CE) before and after treatment and to determine whether those variables were correlated with clinical disease activity or histologic scoring of intestinal biopsy specimens. ANIMALS: 29 dogs with CE. PROCEDURE: Dogs were designated as having dietresponsive CE or CE requiring glucorticoid treatment. Severity of clinical signs was assessed by calculating the canine inflammatory bowel disease activity index (CIBDAI). Histologic severity of intestinal infiltration was assessed before and after 4 weeks of treatment in the diet-responsive group and before and after 10 weeks of treatment in the glucocorticoid group. Gastrointestinal permeability and mucosal absorptive capacity were assessed by use of intragastric administration of a solution containing lactulose, rhamnose, xylose, 3-O-methylglucose, and sucrose. Urine was collected 6 hours after administration of the sugar solution to determine urinary lactulose-to-rhamnose (L:R), xylose-to-methylglucose (X:M), and sucrose-to-methylglucose (S:M) ratios. RESULTS: Median CIBDAI scores decreased significantly in both groups of dogs after treatment. However, the median histologic grade of intestinal biopsy specimens did not change with treatment in either group. There were no significant differences in L:R, X:M, or S:M ratios after treatment in either group and no significant correlations between L:R, X:M, or S:M ratios and CIBDAI or histologic scores. CONCLUSIONS AND CLINICAL RELEVANCE: Results of tests for intestinal permeability and mucosal absorptive capacity were not useful indicators of clinical disease activity as assessed by the CIBDAI or the sever ity of infiltration as indicated by histologic evaluation.     

Detection of Echinococcus granulosus coproantigens in faeces from naturally infected rural domestic dogs in south eastern Australia

OBJECTIVE: To investigate the occurrence of Echinococcus granulosus in rural domestic dogs in farming areas around Yass, New South Wales, and Mansfield and Whitfield, Victoria. DESIGN: Faeces were collected per-rectally from farm dogs voluntarily presented by their owners in four farming districts in New South Wales and two in Victoria. PROCEDURE: Faeces were collected in the field, an extract prepared from each sample and E granulosus coproantigens detected in an ELISA. Farmers were also questioned about their dog feeding and worming practices. RESULTS: Echinococcus granulosus coproantigens were detected in 99 of 344 dogs (29%) from 95 farms in south eastern New South Wales and 38 of 217 dogs (17.5%) from 43 farms in Victoria. Cross-reactions between E granulosus coproantigen trapping antibody and coproantigens in faeces from dogs monospecifically infected with other species of intestinal helminthes (Taenia ovis, T hydatigena, T pisiformis, Spirometra ericacei, Dipylidium caninum, hookworm, Toxocara canis, Trichuris vulpis) were not evident. Dietary and worming data revealed many owners fed raw meat and occasionally offal from domestic livestock and wildlife to their dogs and few owners wormed their dogs frequently enough to preclude the chance of patent E granulosus being present in their dogs. CONCLUSION: Echinococcus granulosus occurs commonly in rural dogs in south eastern Australia and an education program promoting the public health importance of responsible management of rural dogs is urgently needed.     

Evaluation of risk factors for Cryptococcus gattii infection in dogs and cats

OBJECTIVE: To determine risk factors associated with Cryptococcus gattii infection in dogs and cats residing on Vancouver Island in British Columbia, Canada. DESIGN: Matched case-control study. ANIMALS: 20 dogs and 29 cats with C gattii infection and matched controls. PROCEDURE: Dogs and cats with a confirmed or probable diagnosis of cryptococcosis resulting from infection with C gattii were enrolled by veterinarians, and owners completed a questionnaire designed to obtain information pertaining to potential risk factors for the disease. Owners of matched control animals were also interviewed. Odds ratios and 95% confidence intervals or paired t tests were calculated to determine significant associations. RESULTS: Animals were enrolled during 2 noncontiguous periods in August 2001 to February 2002 (8 dogs and 9 cats enrolled) and May to December 2003 (12 dogs and 20 cats enrolled). Risk factors significantly associated with development of cryptococcosis included residing within 10 km of a logging site or other area of commercial soil disturbance, above-average level of activity of the animal, travelling of the animal on Vancouver Island, hunting by the animal, and owners hiking or visiting a botanic garden. CONCLUSIONS AND CLINICAL RELEVANCE: Results indicated that dogs and cats that were active or that lived near a site of commercial environmental disturbance had a significantly increased risk of developing C gattii infection. Veterinarians should communicate these risks to owners in context because cryptococcosis was an uncommon disease in this population.     

Lactoferrin interaction with retinoid signaling: cell growth and apoptosis in mammary cells

Lactoferrin (Lf) is a multifunctional iron-binding protein that was first identified in mammary secretions, but is synthesized by most mammalian tissues. The protein has a signal sequence that dictates secretion; it also has a nuclear localization sequence that facilitates entry into the cell nucleus. The mechanism of the latter action is currently unknown, but is thought to occur via a Lf receptor. Lactoferrin content of mammary tissue and secretions varies with developmental state; it is synthesized in mammary tissue at high levels during both pregnancy and involution, and during mammary infections. Using fluorescent (FITC)-labeled holo-bLf, we show that bovine primary epithelial cells and MCF-7 breast cancer cells do not translocate the exogenously added Lf to the nucleus after culture in serum free media (SFM). However, the supplementation of SFM with 1 μM all-trans retinoic acid (atRA) caused breast cancer cells to gain the capacity to take up labeled bLf into the cell nucleus. Primary bovine mammary cells (MeBo) exhibited similar capacity in culture. This suggests that in addition to Lf, one or more components modulated by atRA, are necessary for nuclear translocation to occur. Transfection experiments with atRA treated MCF-7 cells containing retinoic acid response element reporter constructs showed that the extracellular application of lactoferrin alters reporter gene expression. Lactoferrin increased a DR5 luciferase response element in a dose-dependent manner only when atRA was applied. Immunocytochemical markers for the cell cycle (Ki67) and apoptotic events (Caspase-3 and PARP-85) showed that lactoferrin alters the atRA-induced phenotype, blocking apoptosis and maintaining cell cycle activity in both MCF-7 and MeBo cells in the presence of 1 μM atRA. We propose that nuclear lactoferrin interacts with retinoic acid signaling pathways in cells and alters/blocks the signals so that cells remain in the cell cycle and/or do not enter the apoptotic pathway.