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. 2016 Feb 25;12(2):e1005390.
doi: 10.1371/journal.ppat.1005390. eCollection 2016 Feb.

Emerging Paramyxoviruses: Receptor Tropism and Zoonotic Potential

Affiliations

Emerging Paramyxoviruses: Receptor Tropism and Zoonotic Potential

Antra Zeltina et al. PLoS Pathog. .
No abstract available

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Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1
Maximum likelihood phylogenies of Paramyxoviridae L (A), F (B), and HN/H/G (C) protein sequences using MEGA6 (Molecular Evolutionary Genetics Analysis Version 6.0) [34], based on the LG+G+I+F model [35]. Scale bar indicates amino acid substitutions per site. Numbers at the nodes represent bootstrap values (1,000 replicates). Colored circles are used to indicate genera and empty black circles indicate viruses with varying positions between the L, F, and HN/H/G phylogenies. Uncategorized viruses awaiting taxonomic evaluation by the International Committee on Taxonomy of Viruses are marked with an asterisk. Virus names (abbreviations) and GenBank accession numbers are as follows: Mojiang virus (MojPV) NC_025352; Ghanaian bat henipavirus (GhV) HQ660129; Cedar virus (CedPV) NC_025351; Nipah virus (NiV) NC_002728; Hendra virus (HeV) NC_001906; Sendai virus (SeV) NC_001552; human parainfluenza virus 1 (hPIV1) NC_003461; human parainfluenza virus 3 (hPIV3) AY283063 (for HN) and NC_001796.2 (for L and F); bovine parainfluenza virus 3 (bPIV3) NC_002161; Tuhoko virus 1 (ThkPV1) NC_025410; Menangle virus (MenPV) NC_007620; Tioman virus (TioPV) NC_004074; parainfluenza virus 5 (PIV5) NC_006430; human parainfluenza virus 2 (hPIV2) NC_003443; porcine rubulavirus (PorPV) NC_009640; mumps virus (MuV) NC_002200; avian paramyxovirus 6 (APMV6) NC_003043; Newcastle disease virus (NDV) AF212323 (for HN) and NC_002617 (for L and F); canine distemper virus (CDV) AY386315; peste-des-petits-ruminants virus (PPRV) FJ905304; rinderpest virus (RPV) JN234010; measles virus (MeV) NC_001498; Mossman virus (MosPV) NC_005339; Nariva virus (NarPV) NC_017937.1; Beilong virus (BeiPV) NC_007803; Tailam virus (TaiPV) NC_025355; J paramyxovirus (JPV) NC_007454; Salem virus (SalPV) NC_025386; Fer-de-lance virus (FdlPV) NC_005084; Atlantic salmon paramyxovirus (AsaPV) NC_025360; Tupaia paramyxovirus (TupPV) NC_002199; feline morbillivirus (FmoPV) JQ411014.
Fig 2
Fig 2. Mapping sequence conservation onto henipavirus and morbillivirus attachment glycoproteins.
(A) Crystal structure of Ghanaian bat henipavirus attachment glycoprotein (GhV-G, PDB [Protein Data Bank] ID 4UF7) in complex with ephrinB2. EphrinB2 is shown as a yellow ribbon and GhV-G is shown in surface representation and colored according to sequence conservation with (left to right) HeV-G, NiV-G, CedPV-G, and MojPV-G. Sequence identical residues are colored red and similar residues pink. At the bottom of the panel are tables summarizing overall glycoprotein sequence identity (bottom right) and sequence similarity at the ephrin receptor-binding site (top left), with respect to GhV-G. (B) Crystal structure of measles virus hemagglutinin (MeV-H) in complex with nectin-4 cell surface receptor (PDB ID 4GJT), with the position of SLAM/F1 (green ribbon) receptor-binding shown (based upon structural overlay with the MeV-H-SLAM/F1 crystal structure; PDB ID 3ALZ). Nectin-4 and SLAM/F1 are shown as cyan and green ribbons, respectively. MeV-H is shown in surface representation and colored according to sequence conservation, as in panel A, with RPV-H, PPRV-H, CDV-H, FmoPV-H, and SalPV-G (left to right). At the bottom of the panel are tables summarizing overall glycoprotein sequence identity (bottom right) and sequence similarity at the nectin-4– (top) and SLAM/F1-binding sites (left), with respect to MeV-H. The tables are color-coded from dark gray (highly conserved) to white (variable).

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