Effect of cold atmospheric plasma (CAP) on human adenoviruses is adenovirus type-dependent

PLoS One. 2018 Oct 26;13(10):e0202352. doi: 10.1371/journal.pone.0202352. eCollection 2018.

Abstract

More than 70 human adenovirus types were identified divided into 7 different species (A-G). Diseases caused by human adenoviruses are type-dependent and can range from mild to severe respiratory infections, gastrointestinal infections or eye infections such as epidemic keratoconjunctivitis. Unfortunately there is no specific anti-adenovirus therapy available. Here we addressed the question whether treatment with cold atmospheric plasma (CAP) for anti-adenoviral therapy such as virus-mediated ulcerations may be feasible. CAP has already been explored for the treatment of dermatological diseases such as chronic wounds. To investigate whether CAP is an effective antiviral tool, purified human adenovirus types derived from different human adenovirus species (HAdV -4, -5, -20, -35, -37, -50) tagged with luciferase were treated with defined dosages of plasma. The CAP treatment was varied by incrementally increasing the time span of CAP treatment. After CAP treatment, the virus containing solution was added to eukaryotic cells and the viral load was determined by measurement of luciferase expression levels. Through the plasma treatment the adenovirus driven luciferase expression directly correlating with adenovirus transduction efficiencies could be reduced for HAdV-5 and HAdV-37. Plasma treatment had no influence on adenovirus derived luciferase expression levels for HAdV-4 and HAdV-50 and it even had a positive effect on luciferase expression levels for HAdV-20 and HAdV-35. These results suggest that CAP has a type dependent effect on adenoviruses and that infectivity can be even increased for certain adenovirus types. Further studies should address the mechanisms behind this phenomenon. In summary we demonstrate that CAP may represent an interesting option for antiviral treatment in a virus type dependent manner.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenovirus Infections, Human / physiopathology
  • Adenovirus Infections, Human / therapy*
  • Adenovirus Infections, Human / virology
  • Adenoviruses, Human / pathogenicity
  • Adenoviruses, Human / radiation effects*
  • Conjunctivitis, Viral / physiopathology
  • Conjunctivitis, Viral / therapy*
  • Conjunctivitis, Viral / virology
  • DNA, Viral
  • Humans
  • Plasma Gases / therapeutic use*
  • Respiratory Tract Infections / therapy
  • Respiratory Tract Infections / virology
  • Viral Load / radiation effects
  • Virus Replication / radiation effects

Substances

  • DNA, Viral
  • Plasma Gases

Grants and funding

This research received funding from the internal grant program (PhD and Dr. rer. nat. Program Biomedicine) of the Faculty of Health at Witten/Herdecke University, Germany.