4,893 research outputs found

    Genome sequences of 14 Firmicutes strains isolated from the human vagina

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    Research on vaginal infections is currently limited by a lack of available fully sequenced bacterial reference strains. Here, we present strains (now available through BEI Resources) and genome sequences for a set of 14 vaginal isolates from the phylum Firmicutes. These genome sequences provide a valuable resource for future research in understanding the role of Gram-positive bacteria in vaginal health and disease

    Genome sequences of 11 human vaginal Actinobacteria strains

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    The composition of the vaginal microbiota is an important health determinant. Several members of the phylum Actinobacteria have been implicated in bacterial vaginosis, a condition associated with many negative health outcomes. Here, we present 11 strains of vaginal Actinobacteria (now available through BEI Resources) along with draft genome sequences

    Genome sequences of nine gram-negative vaginal bacterial isolates

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    The vagina is home to a wide variety of bacteria that have great potential to impact human health. Here, we announce reference strains (now available through BEI Resources) and draft genome sequences for 9 Gram-negative vaginal isolates from the taxa Citrobacter, Klebsiella, Fusobacterium, Proteus, and Prevotella

    Establishing the Tolerability to Turkeys of Nonanoic Acid at Practical Levels of Use as a Feed Flavoring

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    Objective: Nonanoic acid (NA) is one of a series of straight-chain aliphatic alcohols, aldehydes, acids and their derivatives with a well-documented history of use as a synthetic flavoring in human food. As part of a safety evaluation of NA for use as a flavoring in animal feed, an experiment was conducted to evaluate the ability of turkeys to tolerate NA at levels relevant to practical feeding practices. Materials and Methods: A total of 594-day-old BUT Premium turkeys (300 males and 294 females) were allocated at random to 40 floor pens containing either 15 males or 13 to 15 females. Poults were fed one of 4 treatment diets in crumble (0 to 14 days) or pellet (15 to 59 days) form containing 0 (control), 100, 300 or 1000 mg NA/kg complete feed for 59 days. General health and performance were monitored for the duration of the study. At days 57 and 59 of age, blood samples were taken and birds were sacrificed and necropsied for histopathological examination of the digestive tract. Significant differences were considered at P ≤ 0.05 and near-significant trends at P ≤ 0.10. Results: NA had no effect on mortality (Pχ2 = 0.54), average daily feed intake (ADFI) (P = 0.11), average daily gain (ADG) (P = 0.12) or feed conversion ratio (FCR) (P = 0.45) in poults over the 56-day feeding period. No treatment-related effects on blood parameters or tissue pathology were observed. Conclusion: The results of the study support the safety and tolerance of NA to turkeys at dietary levels of up to 1000 mg/kg which will provide a considerable margin of safety compared to anticipated practical conditions of use as a feed flavoring.info:eu-repo/semantics/publishedVersio

    Vulnerability to alcohol operant-drinking behaviour: implications of environmental stim

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    Environmental stimuli, occurring early in life, shape the drinking trajectories and the psychopathological outcome of alcohol consumption in adult life. In particular, early perinatal procedures can permanently alter various patterns of drug use and behaviour in rat adulthood (Pryce CR, 2001). Early handling (EH) apparently is responsible for neurochemical and behavioural changes in adulthood, due to boosts in maternal care after daily reunion. It has been suggested that fostered maternal care, in the form of licking and grooming, is a key feature in determining neural changes and offspring fear responses and alter the reward/reinforcement pathway through epigenetic mechanisms that likely underlie remodeling in DA transmission (Francis, 2008, Francis et al., 2002). Such evidence is important, since fear together with stress, is thought to be related to vulnerability associated with drug abuse (Kreek and LaForge, 2007; Sinha and Li, 2007). Various studies on ethanol consumption and preference, showed less vulnerability to ethanol in adult male rats submitted to EH procedure (Ploj K, 2003). Based upon these findings, this study was aimed at examining the impact of brief early handling, 15-minute daily separations of litters from the dams during the first 2 weeks of life, on vulnerability to heavy drinking and dependence in adult male Wistar rats employed an operant self-administration procedure well known as a valid paradigm, highly predictive of drug-seeking and drug-taking behaviour in rats (Higgins et al., 1994). The operant-drinking behaviour protocol consisted of: 1) Training phase in which the animals learnt to self-administer EtOH 10% over 21 days; 2) Extinction phase during which reward delivery was suspended; 3) Deprivation period when ethanol self-administration was suspended for 7 days to achieve a forced abstinence; 4) Relapse phase, 7 days, to assess animal reinstatement for ethanol (Cacace, 2012). Our data revealed that EH procedure has a protective influence towards the onset and escalation of drug abuse, showing a reduction in addictive behaviour as displayed by a lower frequency of lever presses with respect to control group. These findings further corroborate the role of early life experiences on ethanol consumption in adulthood, highlighting that environmental influences may induce individual different responses to drug abuse

    Alcohol, Brain Derived Neurotrophic Factor and Obesity among People Living with HIV

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    Introduction In an expanding HAART era, obesity has become a health problem among persons living with HIV (PLWH). Whereas the rising level of obesity has been largely attributed to poor nutrition and exercise habits, differences in biological factors may explain why some individuals gain more weight than others. Thus, our main goal is to prospectively determine in PLWH whether plasma brain-derived neurotrophic factor (BDNF), and hazardous alcohol use (HAU), two overlooked but highly prevalent conditions among PLWH, correlate with an adverse anthropometric profile. Also to test whether these relationships varied in men and women Methods The Platelets mediating Alcohol and HIV Damage Study (PADS) is an ongoing multiethnic study of 400 PLWH receiving regular medical care in South Florida (37% females and 63% males). Semi-annual visits consisted of a medical exam, including anthropometrics to assess both general (body mass index: BMI) and central obesity (waist and hip circumferences). Participants also completed health history questionnaires, and provided a fasting blood sample to obtain BDNF and immune and biochemical assessments. Results A sizable proportion of participants met the National Institutes of Health definition of overweight (BMI = 25?29.9 kg/m2; 26%) and obese (BMI ? 30 kg/m2; 35%). Women were more likely to be obese than men (OR=4.9, 95% CI=2.9?8.2, p=0.0001). Compared to men, women also exhibited the highest mean plasma BDNF levels (9,959 ± 6,578 vs. 7,470 ± 6,068 pg/ml, p=0.0001). Additional analyses indicated that HAU, particularly heavy drinkers, had the smallest waist and hip circumferences if they were males, but the opposite if they were females. High BDNF levels were positively correlated with BMI. Linear regression analysis revealed that gender, BDNF, and HAU were the best predictors of BMI. Conclusion In summary, our findings offer novel insights into the relationships between BDNF, and alcohol use among overweight and obese PLWH. Our results also suggest that these relationships may be inherently different by gender

    An 18F-labeled poly(ADP-ribose) polymerase positron emission tomography imaging agent

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    Poly(ADP-ribose) polymerase (PARP) is involved in repair of DNA breaks and is over-expressed in a wide variety of tumors, making PARP an attractive biomarker for positron emission tomography (PET) and single photon emission computed tomography imaging. Consequently, over the past decade, there has been a drive to develop nuclear imaging agents targeting PARP. Here, we report the discovery of a PET tracer that is based on the potent PARP inhibitor olaparib (1). Our lead PET tracer candidate, [18F]20, was synthesized and evaluated as a potential PARP PET radiotracer in mice bearing subcutaneous glioblastoma xenografts using ex vivo biodistribution and PET−magnetic resonance imaging techniques. Results showed that [18F]20 could be produced in a good radioactivity yield and exhibited specific PARP binding allowing visualization of tumors overexpressing PARP. [18F]20 is therefore a potential candidate radiotracer for in vivo PARP PET imaging
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