Is this project an undergraduate, graduate, or faculty project?

Undergraduate

group

What campus are you from?

Daytona Beach

Authors' Class Standing

Stefani Caspaso-Villanueva: Freshman Reilly Taylor: Freshman Ana Cruz: Senior Sebastian Tucker: Senior Alba Chavez: Faculty

Lead Presenter's Name

Stefani Caspaso-Villanueva

Faculty Mentor Name

Alba Chavez

Abstract

The emergence in antimicrobial resistance has become an increased problem as a consequence to human vulnerability to fungal infections. Human commensal microbes (those who in normal conditions do not cause any infection, including yeast) have become opportunistic pathogens when patients become immunocompromised. It has been previously reported that commensal yeast strains can become pathogenic when exposed to extreme environments, such as fluctuations in temperature, oxygen availability and microgravity; conditions that astronauts experience during space flight missions. As a consequence, strains that commonly do not cause disease then become a serious health concern. Moreover, the use of conventional antifungal drugs such as azoles and polyenes can lead to clinical failure and difficulties related to treating fungal infections, and combined with the time required to develop new drugs, we require urgent consideration of other therapeutic alternatives. Drug repurposing is a promising and fast solution that the scientific community can use with low cost and safety advantages. In the present study, we tested multiple NSAID (non steroidal, anti-inflammatory drugs) as potential candidates for antifungal activity. We tested the efficacy of Finasteride, Flufenamic acid, Quinacrine and Colistin against two yeast strains isolated from the International Space Station (Candida parapsilosis and Rhodotorula mucilaginosa) in an effort to decipher the best repurposing strategy to treat potential fungal infections.

Did this research project receive funding support from the Office of Undergraduate Research.

No

Share

COinS
 

Drug Repurposing in Mycology: Identification of Compounds as Potential Antifungals Against Yeast Strains Isolated From the International Space Station

The emergence in antimicrobial resistance has become an increased problem as a consequence to human vulnerability to fungal infections. Human commensal microbes (those who in normal conditions do not cause any infection, including yeast) have become opportunistic pathogens when patients become immunocompromised. It has been previously reported that commensal yeast strains can become pathogenic when exposed to extreme environments, such as fluctuations in temperature, oxygen availability and microgravity; conditions that astronauts experience during space flight missions. As a consequence, strains that commonly do not cause disease then become a serious health concern. Moreover, the use of conventional antifungal drugs such as azoles and polyenes can lead to clinical failure and difficulties related to treating fungal infections, and combined with the time required to develop new drugs, we require urgent consideration of other therapeutic alternatives. Drug repurposing is a promising and fast solution that the scientific community can use with low cost and safety advantages. In the present study, we tested multiple NSAID (non steroidal, anti-inflammatory drugs) as potential candidates for antifungal activity. We tested the efficacy of Finasteride, Flufenamic acid, Quinacrine and Colistin against two yeast strains isolated from the International Space Station (Candida parapsilosis and Rhodotorula mucilaginosa) in an effort to decipher the best repurposing strategy to treat potential fungal infections.

 

To view the content in your browser, please download Adobe Reader or, alternately,
you may Download the file to your hard drive.

NOTE: The latest versions of Adobe Reader do not support viewing PDF files within Firefox on Mac OS and if you are using a modern (Intel) Mac, there is no official plugin for viewing PDF files within the browser window.