Analyze Diet
Applied and environmental microbiology1985; 50(5); 1315-1318; doi: 10.1128/aem.50.5.1315-1318.1985

Fibronectin enhances transfection of Staphylococcus aureus.

Abstract: The factor in normal sera primarily responsible for the enhancement of transfection (and transformation) of Staphylococcus aureus was identified as fibronectin. Serum samples which were depleted of fibronectin by affinity chromatography showed a marked decrease in enhancing activity. Fibronectin isolated from sera of several animal species demonstrated enhancing activity.
Publication Date: 1985-11-01 PubMed ID: 4091560PubMed Central: PMC238748DOI: 10.1128/aem.50.5.1315-1318.1985Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Research Support
  • U.S. Gov't
  • P.H.S.

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research discusses that fibronectin, a protein found in serum (the liquid part of blood), significantly increases the process of transfection in Staphylococcus aureus (a type of bacteria), with serum samples lacking fibronectin showing a notable decrease in enhancement activity. Further, fibronectin sourced from the serum of various animal species exhibited enhancing activity.

Introduction of the Study

  • The study primarily focuses on understanding the role of a serum protein, fibronectin, in enhancing the process of transfection and transformation in Staphylococcus aureus.
  • Staphylococcus aureus is a kind of bacteria that is known to cause various kinds of infections in humans and animals. Transfection is a process wherein the genetic material (like DNA) of one organism is introduced in the cell of another organism.
  • The researchers believe that fibronectin plays a crucial role in the successful implementation of the transfection process. This study aims to validate this hypothesis.

Methods Used in the Study

  • The researchers observed the serum samples that had a decreased amount of fibronectin. Affinity chromatography, a biochemical method, was utilized to deplete the serum samples of fibronectin.
  • The presence, quantity, and activity of fibronectin in the sera of several animal species were also observed, recorded, and analyzed. This was done to understand the role of fibronectin across different species.

Findings of the Study

  • The fibronectin-depleted serum samples were found to have a significant decrease in enhancing activity. This highlights that fibronectin is a significant factor in enhancing transfection in Staphylococcus aureus.
  • Fibronectin isolated from the serum of various animal species also demonstrated a clear enhancement in the transfection activity. This indicates that the enhancing property of fibronectin is consistent across different species and is not confined to just one.

Significance of the Research

  • The findings provide evidence for the role of fibronectin in the transfection process, offering a better understanding of Staphylococcus aureus, which could lead to advancements in research related to bacterial infections or transgenic studies.
  • This study could also provide insight into potential therapeutic applications. If the enhancement of transfection by fibronectin can be manipulated, scientists could develop methods for controlling or preventing infections caused by Staphylococcus aureus.
  • The research, moreover, illustrates the non-selective nature of fibronectin, affirming that its enhancing property is evident across various species. This can have great implications in fields like veterinary science, genetic science, and more.

Cite This Article

APA
Thompson NE, Bergdoll MS, Pattee PA. (1985). Fibronectin enhances transfection of Staphylococcus aureus. Appl Environ Microbiol, 50(5), 1315-1318. https://doi.org/10.1128/aem.50.5.1315-1318.1985

Publication

ISSN: 0099-2240
NlmUniqueID: 7605801
Country: United States
Language: English
Volume: 50
Issue: 5
Pages: 1315-1318

Researcher Affiliations

Thompson, N E
    Bergdoll, M S
      Pattee, P A

        MeSH Terms

        • Animals
        • Blood
        • Culture Media
        • Fibronectins / pharmacology
        • Horses
        • Humans
        • Rabbits
        • Species Specificity
        • Staphylococcus aureus / drug effects
        • Staphylococcus aureus / genetics
        • Transfection / drug effects

        Grant Funding

        • AI-06647 / NIAID NIH HHS

        References

        This article includes 20 references
        1. J Immunol. 1966 Dec;97(6):822-7
          pubmed: 4163007
        2. FEBS Lett. 1984 Mar 26;168(2):313-6
          pubmed: 6723955
        3. J Biol Chem. 1970 Nov 10;245(21):5728-36
          pubmed: 4097343
        4. J Bacteriol. 1973 Feb;113(2):576-85
          pubmed: 4266172
        5. J Bacteriol. 1974 Apr;118(1):155-64
          pubmed: 4274456
        6. J Bacteriol. 1977 Feb;129(2):778-88
          pubmed: 138674
        7. Int J Cancer. 1977 Jul 15;20(1):1-5
          pubmed: 903179
        8. Nature. 1978 Dec 14;276(5689):718-20
          pubmed: 732875
        9. Cell. 1979 Nov;18(3):649-57
          pubmed: 519752
        10. Infect Immun. 1980 Feb;27(2):532-41
          pubmed: 6445878
        11. Blood. 1980 Aug;56(2):145-58
          pubmed: 6994838
        12. Science. 1980 Aug 22;209(4459):927-9
          pubmed: 7403857
        13. Arch Pathol Lab Med. 1981 Aug;105(8):393-6
          pubmed: 6894844
        14. J Invest Dermatol. 1981 Aug;77(2):175-80
          pubmed: 7276612
        15. J Bacteriol. 1981 Oct;148(1):294-300
          pubmed: 6457025
        16. J Bacteriol. 1981 Oct;148(1):301-7
          pubmed: 6457027
        17. J Biol Chem. 1982 Dec 25;257(24):14788-94
          pubmed: 6294079
        18. Infect Immun. 1983 Feb;39(2):939-47
          pubmed: 6219953
        19. Biochim Biophys Acta. 1983 Oct 28;748(2):308-20
          pubmed: 6138099
        20. Nature. 1970 Aug 15;227(5259):680-5
          pubmed: 5432063