Abstract
Increases in the incidence and severity of community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) infections have spawned efforts to define unique virulence properties among prevalent strains. Panton-Valentine leukocidin (PVL), a pore-forming cytotoxin, has garnered attention because of its epidemiologic association with CA-MRSA. Using both the clinical isolate LAC, which is representative of the epidemic USA300 strain, and its isogenic PVL-negative strain in murine models of staphylococcal skin infection and pneumonia, we expanded upon recent studies by assessing the contribution of PVL in the genetic background of BALB/c mice. The data presented in this report support the observation that PVL does not contribute to the pathogenesis of staphylococcal infection of mice.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, N.I.H., Intramural
MeSH terms
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Animals
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Bacterial Toxins* / genetics
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Bacterial Toxins* / metabolism
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Community-Acquired Infections / microbiology
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Community-Acquired Infections / pathology*
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Disease Models, Animal
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Exotoxins* / genetics
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Exotoxins* / metabolism
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Female
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Humans
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Leukocidins* / genetics
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Leukocidins* / metabolism
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Methicillin Resistance*
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Mice
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Mice, Inbred BALB C
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Mutation
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Pneumonia, Staphylococcal / microbiology
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Pneumonia, Staphylococcal / mortality
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Pneumonia, Staphylococcal / pathology*
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Staphylococcal Skin Infections / microbiology
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Staphylococcal Skin Infections / pathology*
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Staphylococcus aureus / drug effects
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Staphylococcus aureus / genetics
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Staphylococcus aureus / isolation & purification
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Staphylococcus aureus / pathogenicity*
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Virulence
Substances
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Bacterial Toxins
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Exotoxins
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Leukocidins
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Panton-Valentine leukocidin