Key result
Treatment with 2'-C-methylcytidine protected 100% of SCID mice (15/15) against lethal FMD virus infection up to 14 days, whereas all 8 untreated mice developed acute disease and were euthanized.
Why the study?
Does 2'-C-methylcytidine protect SCID mice against lethal foot-and-mouth disease virus infection?
Does 2'-C-methylcytidine protect SCID mice against lethal foot-and-mouth disease virus infection?
Absolute Event Rate: 100% vs 0%
The nucleoside analogue 2'-C-methylcytidine protects SCID mice against lethal foot-and-mouth disease virus infection, demonstrating the potential of small molecules for FMD control.
Supports nucleoside analogues for FMD control; leaves open translation to livestock or field use.
Recent European contingency plans envisage emergency vaccination as an animal-friendly control strategy for foot-and-mouth disease (FMD). Anti-viral drugs may be used as an alternative or complementary measure. We here demonstrate that the nucleoside analogue 2'-C-methylcytidine (2'CMC) protects severe combined immunodeficient (SCID) mice against lethal FMD virus infection. In brief, SCID mice were inoculated with serotype A FMD virus and treated for five consecutive days with 2'CMC. All 15 treated mice remained healthy until the end of the study at 14 days post-infection (dpi). At that time, viral RNA was no longer detected in 13 of 15 treated mice. All eight untreated mice suffered from an acute generalized disease and were euthanized for ethical reasons on average at 4 dpi. These results illustrate the potential of small molecules to control FMD.
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Lefebvre et al. (2013) studied Foot-and-mouth disease (FMD) virus infection (n=23). 2'-C-methylcytidine (2'CMC) vs. untreated was evaluated on Remaining healthy until 14 days post-infection. Treatment with 2'-C-methylcytidine protected 100% of SCID mice (15/15) against lethal FMD virus infection up to 14 days, whereas all 8 untreated mice developed acute disease and were euthanized.
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