Chemokine-Binding Proteins Encoded by Parapoxvirus of Red Deer of New Zealand Display Evidence of Gene Duplication and Divergence of Ligand Specificity

• Published in: Frontiers in microbiology 2019-06, Vol.10, p.1421-1421
• Main Authors: Sharif, Saeed, Ueda, Norihito, Nakatani, Yoshio, Wise, Lyn M, Clifton, Sheree, Lateef, Zabeen, Mercer, Andrew A, Fleming, Stephen B
• Format: Article
• Language: English
• Subjects: cell migration; chemokine; chemokine-binding protein; Microbiology; parapoxvirus; parapoxvirus of red deer in New Zealand
• ISSN: 1664-302X; 1664-302X
• DOI: 10.3389/fmicb.2019.01421

Parapoxvirus of red deer in New Zealand (PVNZ) is a species of the genus that causes pustular dermatitis. We identified a cluster of genes in PVNZ that encode three unique chemokine-binding proteins (CBPs) namely ORF112.0, ORF112.3 and ORF112.6. Chemokines are a large family of molecules that direct cell trafficking to sites of inflammation and through lymphatic organs. The PVNZ-CBPs were analyzed by surface plasmon resonance against a broad spectrum of CXC, CC, XC and CX C chemokines and were found to differ in their specificity and binding affinity. ORF112.0 interacted with chemokines from the CXC, CC and XC classes of chemokines with nM affinities. The ORF112.3 showed a preference for CXC chemokines, while ORF112.6 showed pM affinity binding for CC chemokines. Structural modeling analysis showed alterations in the chemokine binding sites of the CBPs, although the core structure containing two ß-sheets and three α-helices being conserved with the other CBPs. Chemotaxis assays using neutrophils and monocytes revealed inhibitory impact of the CBPs on cell migration. Our results suggest that the PVNZ-CBPs are likely to have evolved through a process of gene duplication and divergence, and may have a role in suppressing inflammation and the anti-viral immune response.