Abstract

Jingmen viruses are newly described segmented flavi-like viruses that have a worldwide distribution in ticks and have been associated with febrile illnesses in humans. Computational analyses were used to predict that Jingmen flavi-like virus glycoproteins have structural features of class II viral fusion proteins, including an ectodomain consisting of beta-sheets and short alpha-helices, a fusion peptide with interfacial hydrophobicity and a three-domain architecture. Jingmen flavi-like virus glycoproteins have a sequence enriched in serine, threonine, and proline at the amino terminus, which is a feature of mucin-like domains. Several of the serines and threonines are predicted be modified by the addition of O-linked glycans. Some of the glycoproteins are predicted to have an additional mucin-like domain located prior to the transmembrane anchor, whereas others are predicted to have a stem consisting of two alpha-helices. The flavivirus envelope protein and Jingmen flavi-virus glycoproteins may have diverged from a common class II precursor glycoprotein with a mucin-like domain or domains acquired after divergence.

Highlights

  • The Flaviviridae family contains several important human and animal pathogens, including dengue, yellow fever, West Nile, hepatitis C, Zika, and bovine viral diarrhea viruses

  • Jingmen tick virus (JMTV) is a novel tick-borne segmented RNA virus containing genome segments derived from unsegmented viral ancestors [7]

  • The amino terminal end of VP1, the sole glycoprotein of certain Jingmen group viruses (JMTV, Mogiana tick virus (MGTV), AMTV, and others), bears sequence similarity to the N-terminus of VP1a, the longest of the two envelope proteins encoded by other Jingmen viruses (ALSV, Yanggou tick virus (YGTV) and others); VP1b is similar to the C-termini of VP1

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Summary

Introduction

The Flaviviridae family contains several important human and animal pathogens, including dengue, yellow fever, West Nile, hepatitis C, Zika, and bovine viral diarrhea viruses. The family is currently divided into four genera, Flavivirus, Hepacivirus, Pestivirus, and Pegivirus [1]. Members of the Flavivirus genus are capable of replicating in both insect and vertebrate hosts [2,3]. Hepaciviruses, pestiviruses, and pegiviruses were each considered until recently to be exclusively viruses of mammals [4,5]. All current members of the Flaviviridae have an unsegmented, single-stranded, positive-sense RNA genome of less than 13 kb. The genome is translated into a single polyprotein that is cleaved by host and viral proteases into structural and nonstructural (NS)

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