4.4 Article

Staphylococcus aureus Potentiates the Hemolytic Activity of Burkholderia cepacia Complex (Bcc) Bacteria

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CURRENT MICROBIOLOGY
卷 78, 期 5, 页码 1864-1870

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SPRINGER
DOI: 10.1007/s00284-021-02458-0

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资金

  1. 2019-20 Junior/Senior Intramural Grant [0357019]
  2. National Institute of Allergy and Infectious Diseases of the National Institutes of Health (NIH) [SC3GM125556, R01AI100560, R01AI063517, R01AI072219]
  3. Cleveland Department of Veterans Affairs from the Biomedical Laboratory Research & Development Service of the VA Office of Research and Development [1I01BX002872, 1I01BX001974]
  4. Geriatric Research Education and Clinical Center VISN 10
  5. Cystic Fibrosis Foundation [691309]
  6. CONICET

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Polymicrobial lung infections in individuals with Cystic Fibrosis are complex and can be caused by opportunistic pathogens like S. aureus, P. aeruginosa and Burkholderia cepacia complex. Interaction studies between S. aureus and Bcc reveal potential impact on the severity and outcomes of infections in CF patients.
Polymicrobial lung infections in individuals with Cystic Fibrosis (CF) contribute to the complexity of this disease and are a major cause of morbidity and mortality in the CF community. The microorganisms most commonly associated with severe airway infections in individuals with CF are the opportunistic pathogens S. aureus, P. aeruginosa and bacteria from the Burkholderia cepacia complex (Bcc), particularly B. cenocepacia and B. multivorans. Three Bcc strains, two S. aureus wild-type strains, and two derivative mutants were used to investigate the interplay between S. aureus and Bcc with a focus on the hemolytic activity of Bcc. Our results revealed that extracellular products from S. aureus potentiated the hemolysis of Bcc strains. Moreover, this effect was influenced by the composition of the medium in which S. aureus is grown. These findings contribute towards the understanding of the impact of interactions between S. aureus and Bcc and their possible implications in the context of co-infections by these pathogens in individuals with CF.

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