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1.
Subst Use Misuse ; 49(7): 779-82, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24499464

ABSTRACT

BACKGROUND: This research provides an estimate of the frequency of company-sponsored alcohol brand-related sites on Facebook™. OBJECTIVES: We conducted a systematic overview of the extent of alcohol brand-related sites on Facebook™ in 2012. METHODS: We conducted a 2012 Facebook™ search for sites specifically related to 898 alcohol brands across 16 different alcoholic beverage types. Descriptive statistics were produced using Microsoft SQL Server. RESULTS: We identified 1,017 company-sponsored alcohol-brand related sites on Facebook™. CONCLUSIONS: Our study advances previous literature by providing a systematic overview of the extent of alcohol brand sites on Facebook™.


Subject(s)
Advertising/statistics & numerical data , Alcohol Drinking , Alcoholic Beverages , Internet/statistics & numerical data , Social Networking , Humans
2.
Proc Natl Acad Sci U S A ; 110(24): E2209-18, 2013 Jun 11.
Article in English | MEDLINE | ID: mdl-23716675

ABSTRACT

Microbial capsular antigens are effective vaccines but are chemically and immunologically diverse, resulting in a major barrier to their use against multiple pathogens. A ß-(1→6)-linked poly-N-acetyl-d-glucosamine (PNAG) surface capsule is synthesized by four proteins encoded in genetic loci designated intercellular adhesion in Staphylococcus aureus or polyglucosamine in selected Gram-negative bacterial pathogens. We report that many microbial pathogens lacking an identifiable intercellular adhesion or polyglucosamine locus produce PNAG, including Gram-positive, Gram-negative, and fungal pathogens, as well as protozoa, e.g., Trichomonas vaginalis, Plasmodium berghei, and sporozoites and blood-stage forms of Plasmodium falciparum. Natural antibody to PNAG is common in humans and animals and binds primarily to the highly acetylated glycoform of PNAG but is not protective against infection due to lack of deposition of complement opsonins. Polyclonal animal antibody raised to deacetylated glycoforms of PNAG and a fully human IgG1 monoclonal antibody that both bind to native and deacetylated glycoforms of PNAG mediated complement-dependent opsonic or bactericidal killing and protected mice against local and/or systemic infections by Streptococcus pyogenes, Streptococcus pneumoniae, Listeria monocytogenes, Neisseria meningitidis serogroup B, Candida albicans, and P. berghei ANKA, and against colonic pathology in a model of infectious colitis. PNAG is also a capsular polysaccharide for Neisseria gonorrhoeae and nontypable Hemophilus influenzae, and protects cells from environmental stress. Vaccination targeting PNAG could contribute to immunity against serious and diverse prokaryotic and eukaryotic pathogens, and the conserved production of PNAG suggests that it is a critical factor in microbial biology.


Subject(s)
Acetylglucosamine/immunology , Antibodies, Bacterial/immunology , Bacterial Infections/immunology , Malaria/immunology , Mycoses/immunology , Staphylococcus aureus/immunology , Animals , Antibodies, Bacterial/pharmacology , Antibodies, Monoclonal/immunology , Antibodies, Monoclonal/pharmacology , Bacterial Capsules/immunology , Bacterial Capsules/metabolism , Bacterial Infections/microbiology , Bacterial Infections/prevention & control , Fungi/immunology , Fungi/physiology , Gram-Negative Bacteria/immunology , Gram-Negative Bacteria/physiology , Gram-Positive Bacteria/immunology , Gram-Positive Bacteria/physiology , Host-Pathogen Interactions/drug effects , Host-Pathogen Interactions/immunology , Humans , Immunoglobulin G/immunology , Immunoglobulin G/pharmacology , Malaria/parasitology , Malaria/prevention & control , Mice , Mice, Inbred C57BL , Mycoses/microbiology , Mycoses/prevention & control , Opsonin Proteins/immunology , Plasmodium berghei/immunology , Plasmodium berghei/physiology , Protein Binding/immunology , Staphylococcus aureus/metabolism , Survival Analysis , Time Factors
3.
Alcohol Clin Exp Res ; 36(7): 1288-97, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22316218

ABSTRACT

BACKGROUND: There are no existing data on alcoholic beverage prices and ethanol (EtOH) content at the level of alcohol brand. A comprehensive understanding of alcohol prices and EtOH content at the brand level is essential for the development of effective public policy to reduce alcohol use among underage youth. The purpose of this study was to comprehensively assess alcoholic beverage prices and EtOH content at the brand level. METHODS: Using online alcohol price data from 15 control states and 164 online alcohol stores, we estimated the average alcohol price and percent alcohol by volume for 900 brands of alcohol, across 17 different alcoholic beverage types, in the United States in 2011. RESULTS: There is considerable variation in both brand-specific alcohol prices and EtOH content within most alcoholic beverage types. For many types of alcohol, the within-category variation between brands exceeds the variation in average price and EtOH content among the several alcoholic beverage types. Despite differences in average prices between alcoholic beverage types, in 12 of the 16 alcoholic beverage types, customers can purchase at least 1 brand of alcohol that is under $1 per ounce of EtOH. CONCLUSIONS: Relying on data or assumptions about alcohol prices and EtOH content at the level of alcoholic beverage type is insufficient for understanding and influencing youth drinking behavior. Surveillance of alcohol prices and EtOH content at the brand level should become a standard part of alcohol research.


Subject(s)
Alcoholic Beverages/economics , Commerce/economics , Ethanol/chemistry , Ethanol/economics , Marketing/economics , Commerce/trends , Databases, Factual/economics , Databases, Factual/trends , Humans , Marketing/trends , United States
4.
Mol Biochem Parasitol ; 175(1): 68-75, 2011 Jan.
Article in English | MEDLINE | ID: mdl-20888370

ABSTRACT

The Trypanosoma brucei flagellum controls motility and is crucial for cell polarity and division. Unique features of trypanosome motility suggest that flagellar beat regulation in this organism is unusual and worthy of study. The flagellar axoneme, required for motility, has a structure that is highly conserved among eukaryotes. Of the several dyneins in the axonemal inner arm complex, dynein f is thought to control flagellar waveform shape. A T. brucei gene predicted to encode the dynein f alpha heavy chain, TbDNAH10, was silenced using RNA interference in procyclic T. brucei cells. This resulted in immotile flagella, showing no movement except for occasional slight twitches at the tips. Cell growth slowed dramatically and cells were found in large clusters. Microscopic analysis of silenced cultures showed many cells with detached flagella, sometimes entangled between multiple cells. DAPI staining showed an increased frequency of mis-positioned kinetoplasts and multinucleate cells, suggesting that these cells experience disruption at an early cell cycle stage, probably secondary to the motility defect. TEM images showed apparently normal axonemes and no discernable defects in inner arm structure. This study demonstrates the use of RNAi as an effective method to study very large genes such as dynein heavy chains (HCs), and the immotility phenotype of these dynein knockdowns suggests that an intact inner arm is necessary for flagellar beating in T. brucei. Since analogous mutants in Chlamydomonas reinhardtii retain motility, this phenotype likely reflects differences in requirements for motility and/or dynein assembly between the two organisms and these comparative studies will help elucidate the mechanisms of flagellar beat regulation.


Subject(s)
Dyneins/antagonists & inhibitors , Flagella/physiology , Locomotion , RNA Interference , Trypanosoma brucei brucei/physiology , Cell Nucleus/ultrastructure , Dyneins/genetics , Flagella/genetics , Flagella/ultrastructure , Microscopy, Electron, Transmission , Organelles/ultrastructure , Protozoan Proteins/antagonists & inhibitors , Protozoan Proteins/genetics , Trypanosoma brucei brucei/genetics , Trypanosoma brucei brucei/ultrastructure
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