Genetically Engineered Virus Nanofibers as an Efficient Vaccine for Preventing Fungal Infection.

Adv Healthc Mater

Department of Chemistry and Biochemistry, Stephenson Life Sciences Research Center, University of Oklahoma, 101 Stephenson Parkway, Norman, OK, 73019-5300, USA.

Published: April 2016

AI Article Synopsis

  • Candida albicans (CA) is a dangerous fungus mainly affecting immunocompromised patients, and preventing its infection remains challenging.
  • Researchers propose using filamentous phage, a harmless nanofiber virus, to display a peptide from secreted aspartyl proteinases 2 (Sap2) as a potential vaccine.
  • In mouse studies, this engineered virus significantly stimulated strong immune responses, enhancing survival rates in CA-infected mice, indicating its promise as a vaccine against fungal infections.

Article Abstract

Candida albicans (CA) is a kind of fungus that can cause high morbidity and mortality in immunocompromised patients. However, preventing CA infection in these patients is still a daunting challenge. Herein, inspired from the fact that immunization with secreted aspartyl proteinases 2 (Sap2) can prevent the infection, it is proposed to use filamentous phage, a human-safe virus nanofiber specifically infecting bacteria (≈900 nm long and 7 nm wide), to display an epitope peptide of Sap2 (EPS, with a sequence of Val-Lys-Tyr-Thr-Ser) on its side wall and thus serve as a vaccine for preventing CA infection. The engineered virus nanofibers and recombinant Sap2 (rSap2) are then separately used to immunize mice. The humoral and cellular immune responses in the immunized mice are evaluated. Surprisingly, the virus nanofibers significantly induce mice to produce strong immune response as rSap2 and generate antibodies that can bind Sap2 and CA to inhibit the CA infection. Consequently, immunization with the virus nanofibers in mice dramatically increases the survival rate of CA-infected mice. All these results, along with the fact that the virus nanofibers can be mass-produced by infecting bacteria cost-effectively, suggest that virus nanofibers displaying EPS can be a vaccine candidate against fungal infection.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828319PMC
http://dx.doi.org/10.1002/adhm.201500930DOI Listing

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