Key result
LAVR-289 potently inhibited Marek's disease virus replication at nanomolar concentrations in avian cell cultures, leading to a marked reduction in virus-induced plaques with minimal cytotoxicity.
Why the study?
Antivirals targeting human herpesviruses have limited veterinary application due to poor bioavailability and toxicity, prompting evaluation of the novel analogue LAVR-289 against Marek's disease virus.
Does LAVR-289 inhibit Marek's disease virus replication in avian cell culture models?
Does LAVR-289 inhibit Marek's disease virus replication in avian cell culture models?
LAVR-289 demonstrates potent in vitro antiviral activity against Marek's disease virus with minimal cytotoxicity, suggesting potential as a veterinary antiviral.
Hypothesis-generating for LAVR-289 against MDV; leaves open in vivo efficacy, safety, and veterinary adoption.
Since the 1970s, numerous antivirals targeting human herpesviruses have been developed, yet their application in veterinary medicine remains limited due to poor bioavailability and significant toxicity in animals. Recently, LAVR-289, a novel acyclic nucleoside phosphonate analogue, has demonstrated broad-spectrum antiviral activity against various DNA viruses. In the present study, we investigated the antiviral potential of LAVR-289 against Marek's disease virus (MDV), an avian herpesvirus responsible for a fatal lymphoproliferative disease in chickens and substantial economic losses to the poultry industry. Using two different avian cell culture infection models, we showed that LAVR-289 potently inhibited MDV replication at nanomolar concentrations, leading to a marked reduction in both the number and size of virus-induced plaques. Importantly, LAVR-289 exhibited minimal cytotoxicity in the treated cell cultures. Further analyses also revealed that LAVR-289 was effective at both early and late stages of MDV infection, and its antiviral activity was maintained under oxygen levels close to physiological conditions. Taken together, these findings highlight LAVR-289 as a promising antiviral drug against MDV and potentially other avian DNA viruses.
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Styranec et al. (2026) studied Marek's disease virus (MDV) infection. LAVR-289 was evaluated on MDV replication (number and size of virus-induced plaques). LAVR-289 potently inhibited Marek's disease virus replication at nanomolar concentrations in avian cell cultures, leading to a marked reduction in virus-induced plaques with minimal cytotoxicity.
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