Abstract: Crimean Congo hemorrhagic fever is a tick born, highly contagious, viral illness with high mortality
rates in humans. There is no treatment for this viral disease at present. We recently reported that Crimean Congo
hemorrhagic fever virus nucleocapsid protein (CCHFV N protein) has two distinct RNA binding sites in the
stalk and head domains. The RNA binding site located in the head domain non-specifically binds to the single
strand RNA of viral or nonviral origin. However, the RNA binding site located in the stalk domain specifically
binds to the double strand panhandle structure formed by the base pairing of highly conserved and
complementary nucleotides at the 5’ and 3’ termini of the viral genome. Interestingly the viral mRNA 5’ UTR
also folds into a panhandle-like secondary structure, which is also specifically recognized by the stalk domain of
N protein. The interaction between N protein and viral mRNA 5’ UTR facilitates the translation of downstream
open reading frame (ORF). The majority of eukaryotic mRNA translation is m7G cap dependent and is initiated
by the assembly of eIF4F cap binding complex, composed of three initiation factors eIF4E, eIF4A and eIF4G.
Our preliminary data shows that N protein mediated translation strategy does not require the assembly of eIF4F
complex but the structural integrity of individual components of this complex is required for this viral
translation mechanism. This published data suggests that CHFV N protein highly likely lures the host translation
apparatus for the preferential translation of viral mRNA during the course of infection, to boost the translation of
viral mRNA in the infected cell. We will use multifaceted experimental avenues to test the hypothesis that
CCHFV N protein interacts with the components of eIF4F complex to selectively engage the 40S ribosomal
subunits on the viral mRNA 5’ UTR. Since ribosome loading on mRNA is a critical rate limiting step in
eukaryotic translation, CCHFV N protein likely helps the viral transcripts at this critical step by selectively
engaging the host cell ribosomes on viral mRNA 5’ UTR. This selective ribosome loading likely helps viral
transcripts by avoiding the competition from host cell transcripts for the same host translation machinery. We
will determine whether CCHFV N protein mediated translation strategy selectively facilitates the translation of
viral mRNA during the course of infection.