Pronounced therapeutic potential of oligonucleotides fixed on inorganic nanoparticles against highly pathogenic H5N1 influenza A virus in vivo

This study describes the effective attack of oligonucleotides on the viral genome of highly pathogenic H5N1 influenza A virus (IAV) in vivo using for the first time the new delivery system consisting of biocompatible low-toxic titanium dioxide nanoparticles and immobilized polylysine-containing oligonucleotides with the native (ODN) and partially modified (ODNm) internucleotide bonds. Intraperitoneal injection of the TiO2 center dot PL-ODN nanocomposite provided 65-70% survival of mice, while intraperitoneal or oral administration of TiO2 center dot PL-ODNm was somewhat more efficient (similar to 80% survival). The virus titer in the lung was reduced by two-three orders of magnitude. The nanocomposites are nontoxic to mice under the used conditions. TiO2 nanoparticles, unbound ODN, and the nanocomposite bearing the random oligonucleotide showed an insignificant protective effect, which indicates the ability of targeted oligonucleotides delivered in mice in the nanocomposites to site-specifically interact with complementary RNAs. The protection of oligonucleotides in nanocomposites by TiO2 nanoparticles and partial modification of the internucleotide bonds provides a continued presence of oligonucleotides in the body for the effective and specific action on the viral RNA. The proposed oligonucleotide delivery system can claim not only to effectively inhibit IAV genes but also to turn off other genes responsible for diseases caused by nucleic acids.

Automated summary

This study demonstrates the effective attack of oligonucleotides on the viral genome of highly pathogenic H5N1 influenza A virus in mice using TiO2 nanoparticles and oligonucleotide nanocomposites. The nanocomposites showed high survival rates and significant reduction in virus titers, suggesting targeted oligonucleotides delivered by the system can interact with complementary RNAs specifically. The proposed oligonucleotide delivery system not only effectively inhibits IAV genes but also has the potential to target genes responsible for diseases caused by nucleic acids.