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Dolzhikova, I.

Publications and source records attributed to Dolzhikova, I..

2 recordsLinked to original sources

Oral Administration of the carboxylic acid ester prodrug NHC SN_9 protects mice from lethal Orthopoxvirus challenge: Implications for the Treatment of Monkeypox

The global resurgence of monkeypox (Mpox) since 2022 has highlighted an urgent need for effective antiviral therapeutics against orthopoxvirus infections. While vaccines provide prophylactic protection, therapeutic options remain limited, particularly for immunocompromised individuals. Previously, we demonstrated potent antiviral activity of N4-hydroxycytidine (NHC) analogs against coronaviruses, including SARS-CoV-2. In the present study, we evaluated the antiviral efficacy of one such analog, NHC conjugate with phenylpropionic acid - SN_9, against orthopoxviruses using Vaccinia virus (VACV) as a model. SN_9 demonstrated superior in vitro antiviral activity compared with EIDD-2801 (molnupiravir), significantly inhibiting VACV replication. In vivo, oral administration of SN_9 provided substantial protection in murine models of orthopoxvirus infection, achieving 90% survival in a sublethal infection model and 70% survival in a lethal challenge model. Animals receiving treatment showed a reduction in disease severity and faster weight recovery. Given the high genetic and antigenic similarity among orthopoxviruses, including VACV, variola virus, and monkeypox virus (MPXV), these findings suggest that SN_9 represents a promising candidate for the treatment and prophylaxis of Mpox.

pathology↗

Characterization of a lethal Crimean-Congo hemorrhagic fever virus infection model in interferon-deficient mice for studies of virus pathogenicity and vaccine efficacy

Crimean-Congo hemorrhagic fever virus (CCHFV) is a highly pathogenic tick-borne virus causing severe human disease and representing a significant public health threat. The absence of licensed vaccines and specific antiviral therapies highlights the need for well-characterized experimental models suitable for studying viral pathogenicity and evaluating medical countermeasures. In this study, we established and characterized an integrated in vitro and in vivo platform for CCHFV research. Virus propagation was optimized by comparing Vero E6 and SW-13 cell lines. SW-13 cells supported efficient CCHFV replication resulting in pronounced virus-induced cytopathic effects, whereas no detectable cytopathic effects were observed in Vero E6 cells. Virus titers determined by cytopathic effect based endpoint dilution and antigen ELISA coincided, supporting the use of SW-13 cells for virus stock preparation. Using virus stocks generated in SW-13 cells, interferon-deficient mice were infected with different doses of CCHFV to assess dose-dependent pathogenicity. Infection resulted in severe disease and high mortality across all tested doses. Based on survival analysis, a dose of 10 TCID50 was selected for further characterization, which revealed progressive weight loss and high viral loads in peripheral organs. Overall, this study establishes a robust IFN knockout mouse model suitable for studying CCHFV pathogenicity, comparing viral genovariants, and evaluating vaccines, antiviral compounds, and neutralizing antibodies.

microbiology↗