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Immunostimulatory properties of the emerging pathogen Stenotrophomonas maltophilia.

Immunostimulatory properties of the emerging pathogen Stenotrophomonas maltophilia. Research Abstract Details 

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  • Immunostimulatory properties of the emerging pathogen Stenotrophomonas maltophilia. Abstract Text:

    valerie j watersValerie J Waters,marisa i Marisa I ,grace soongGrace Soong,sunil aminSunil Amin,robert k ernstRobert K Ernst,alice princeAlice Prince,

    Stenotrophomonas maltophilia is a multiple-antibiotic-resistant opportunistic pathogen that is being isolated with increasing frequency from patients with health-care-associated infections and especially from patients with cystic fibrosis (CF). While clinicians feel compelled to treat infections involving this organism, its potential for virulence is not well established. We evaluated the immunostimulatory properties and overall virulence of clinical isolates of S. maltophilia using the well-characterized opportunistic pathogen Pseudomonas aeruginosa PAO1 as a control. The properties of CF isolates were examined specifically to see if they have a common phenotype. The immunostimulatory properties of S. maltophilia were studied in vitro by stimulating airway epithelial and macrophage cell lines. A neonatal mouse model of pneumonia was used to determine the rates of pneumonia, bacteremia, and mortality, as well as the inflammatory response elicited by S. maltophilia infection. Respiratory and nonrespiratory S. maltophilia isolates were highly immunostimulatory and elicited significant interleukin-8 expression by airway epithelial cells, as well as tumor necrosis factor alpha (TNF-alpha) expression by macrophages. TNF-alpha signaling appears to be important in the pathogenesis of S. maltophilia infection as less than 20% of TNFR1 null mice (compared with 100% of wild-type mice) developed pneumonia and bacteremia following intranasal inoculation. The S. maltophilia isolates were weakly invasive, and low-level bacteremia with no mortality was observed. Despite the lack of invasiveness of S. maltophilia, the immunostimulatory properties of this organism and its induction of TNF-alpha expression specifically indicate that it is likely to contribute significantly to airway inflammation.

    Immunostimulatory properties of the emerging pathogen Stenotrophomonas maltophilia. Publishing Authors By Initials

    vj watersVJ Waters,mi MI ,g soongG Soong,s aminS Amin,rk ernstRK Ernst,a princeA Prince,

    For similar peptides: intercellular signaling peptides and proteins: cytokines: monokines: tumor necrosis factor-alpha research abstracts see: peptides: intercellular signaling peptides and proteins: cytokines: monokines: tumor necrosis factor-alpha research

    PUBMED ID PMID:

    MEDLINE DATE:

    Immunostimulatory properties of the emerging pathogen Stenotrophomonas maltophilia. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Infection and immunity

    VOLUME: 75

    Page Numbers: 1698-703

    Journal Abbreviation: Infect. Immun.

    ISSN: 0019-9567

    DAY: 12

    MONTH: 01

    YEAR: 2007

    Immunostimulatory properties of the emerging pathogen Stenotrophomonas maltophilia. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 246127

    Immunostimulatory properties of the emerging pathogen Stenotrophomonas maltophilia. Keywords Mesh Terms:

    KEYWORDS: Tumor Necrosis Factor-alpha

    MESH TERMS: biosynthesis

    Chemical & Substance for Abstract: Immunostimulatory properties of the emerging pathogen Stenotrophomonas maltophilia. Information

    Substance Name: Tumor Necrosis Factor-alpha

    Registry Number: 0

    Grant and Affiliation Information for Immunostimulatory properties of the emerging pathogen Stenotrophomonas maltophilia.

    AFFILIATION: College of Physicians and Surgeons, Columbia University, 650 W. 168th Street, BB 4-416, New York, NY 10032, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIDDK

    GRANT: R01 DK 36393

    ACRONYM: DK

    MEDLINETA: Infect Immun

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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