Kaposi's sarcoma- associated herpesvirus ubiquitin ligases downregulate cell surface expression of ι-selectin

Kaposi's sarcoma- associated herpesvirus (KSHV) is an oncogenic etiological factor for Kaposi's sarcoma and primary effusion lymphoma in immunocompromised patients. KSHV utilizes two immune evasion E3 ubiquitin ligases, namely K3 and K5, to downregulate the expression of antigen- presenting molecules and ligands of natural killer (NK) cells in the host cells through an ubiquitin- dependent endocytic mechanism. This allows the infected cells to evade surveillance and elimination by cytotoxic lymphocytes and NK cells. The number of host cell molecular substrates reported for these ubiquitin ligases is limited. The identification of novel substrates for these ligases will aid in elucidating the mechanism underlying immune evasion of KSHV. This study demonstrated that K5 downregulated the cell surface expression of iota- selectin, a C- type lectin- like adhesion receptor expressed in the lymphocytes. Tryptophan residue located at the centre of the E2- binding site in the K5 RINGv domain was essential to downregulate iota- selectin expression. Additionally, the lysine residues located at the cytoplasmic tail of iota-selectin were required for the K5- mediated downregulation of iota- selectin. K5 promoted the degradation of iota- selectin through polyubiquitination. These results suggest that K5 downregulates iota- selectin expression on the cell surface by promoting polyubiquitination and ubiquitin- dependent endocytosis, which indicated that iota- selectin is a novel substrate for K5. Additionally, K3 downregulated iota- selectin expression. The findings of this study will aid in the elucidation of a novel immune evasion mechanism in KSHV.

Automated summary

KSHV utilizes E3 ubiquitin ligases K3 and K5 to downregulate antigen-presenting molecules and NK cell ligands, evading cytotoxic lymphocytes and NK cells. This study revealed that K5 downregulates iota-selectin expression through ubiquitination-dependent endocytosis, indicating a novel immune evasion mechanism.