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            "title": "Three-dimensional structure of bacteriophage T4 baseplate",
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                {
                    "creatorType": "author",
                    "firstName": "Victor A.",
                    "lastName": "Kostyuchenko"
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                    "firstName": "Petr G.",
                    "lastName": "Leiman"
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                    "firstName": "Paul R.",
                    "lastName": "Chipman"
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                    "lastName": "Kanamaru"
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                    "lastName": "van Raaij"
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                    "lastName": "Arisaka"
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                    "firstName": "Vadim V.",
                    "lastName": "Mesyanzhinov"
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                    "lastName": "Rossmann"
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            "abstractNote": "The baseplate of bacteriophage T4 is a multiprotein molecular machine that controls host cell recognition, attachment, tail sheath contraction and viral DNA ejection. We report here the three-dimensional structure of the baseplate-tail tube complex determined to a resolution of 12 A by cryoelectron microscopy. The baseplate has a six-fold symmetric, dome-like structure approximately 520 A in diameter and approximately 270 A long, assembled around a central hub. A 940 A-long and 96 A-diameter tail tube, coaxial with the hub, is connected to the top of the baseplate. At the center of the dome is a needle-like structure that was previously identified as a cell puncturing device. We have identified the locations of six proteins with known atomic structures, and established the position and shape of several other baseplate proteins. The baseplate structure suggests a mechanism of baseplate triggering and structural transition during the initial stages of T4 infection.",
            "publicationTitle": "Nature Structural Biology",
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            "date": "Sep 2003",
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            "pages": "688-693",
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            "journalAbbreviation": "Nat. Struct. Biol.",
            "DOI": "10.1038/nsb970",
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            "extra": "PMID: 12923574",
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                    "tag": "Cryoelectron Microscopy",
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                {
                    "tag": "Protein Structure, Tertiary",
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            "itemType": "journalArticle",
            "title": "Strain Specific Phage Treatment for Staphylococcus aureus Infection Is Influenced by Host Immunity and Site of Infection",
            "creators": [
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                    "creatorType": "author",
                    "firstName": "Nathan B.",
                    "lastName": "Pincus"
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                {
                    "creatorType": "author",
                    "firstName": "Jensen D.",
                    "lastName": "Reckhow"
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                    "creatorType": "author",
                    "firstName": "Danial",
                    "lastName": "Saleem"
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                    "creatorType": "author",
                    "firstName": "Momodou L.",
                    "lastName": "Jammeh"
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                    "firstName": "Sandip K.",
                    "lastName": "Datta"
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                    "firstName": "Ian A.",
                    "lastName": "Myles"
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            "abstractNote": "The response to multi-drug resistant bacterial infections must be a global priority. While mounting resistance threatens to create what the World Health Organization has termed a \"post-antibiotic era\", the recent discovery that antibiotic use may adversely impact the microbiome adds further urgency to the need for new developmental approaches for anti-pathogen treatments. Methicillin-resistant Staphylococcus aureus (MRSA), in particular, has declared itself a serious threat within the United States and abroad. A potential solution to the problem of antibiotic resistance may not entail looking to the future for completely novel treatments, but instead looking into our history of bacteriophage therapy. This study aimed to test the efficacy, safety, and commercial viability of the use of phages to treat Staphylococcus aureus infections using the commercially available phage SATA-8505. We found that SATA-8505 effectively controls S. aureus growth and reduces bacterial viability both in vitro and in a skin infection mouse model. However, this killing effect was not observed when phage was cultured in the presence of human whole blood. SATA-8505 did not induce inflammatory responses in peripheral blood mononuclear cultures. However, phage did induce IFN gamma production in primary human keratinocyte cultures and induced inflammatory responses in our mouse models, particularly in a mouse model of chronic granulomatous disease. Our findings support the potential efficacy of phage therapy, although regulatory and market factors may limit its wider investigation and use.",
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            "extra": "PMID: 16188359",
            "tags": [
                {
                    "tag": "Animals",
                    "type": 1
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                {
                    "tag": "Bacteriophages",
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                {
                    "tag": "Body Weight",
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                    "type": 1
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            "title": "Phage inactivation of foodborne pathogens on cooked and raw meat",
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                    "firstName": "T.",
                    "lastName": "Bigwood"
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                    "lastName": "Hudson"
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                    "creatorType": "author",
                    "firstName": "C.",
                    "lastName": "Billington"
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                    "lastName": "Carey-Smith"
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                    "firstName": "J. A.",
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            "abstractNote": "Phages infecting Salmonella Typhimurium PT160 and Campylobacter jejuni were added at a low or high (10 or 104) multiplicity of infection (MOI) to either low or high (&lt;100 or 104 cm−2) densities of host bacteria inoculated onto raw and cooked beef, and incubated at 5 and 24 °C to simulate refrigerated and room temperature storage. Counts of host bacteria were made throughout the incubation period, with phages being counted at the first and last sampling times. Host inactivation was variable and depended on the incubation conditions and food type. Significant host inactivations of the order of 2–3 log10 cm−2 at 5 °C and &gt;5.9 log10 cm−2 at 24 °C were achieved compared to phage-free controls using the Salmonella phage under optimal conditions (high host cell density and MOI). These results alongside those already published indicate that phages may be useful in the control for foodborne pathogens.",
            "publicationTitle": "Food Microbiology",
            "publisher": "",
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            "date": "February 2008",
            "volume": "25",
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            "partTitle": "",
            "pages": "400-406",
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            "DOI": "10.1016/j.fm.2007.11.003",
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