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Figure 14
                                                                                                   Avian Paramyxoviruses |   109

                                                     APMV-8/white-fronted goose/Kazakhstan/92/2013
                                                   93
                                                 81   APMV-8/white-fronted goose/Kazakhstan/62/2013

                                               61      APMV-8/white-fronted goose/Kazakhstan/65/2013

                                              95   APMV-8/whooper swan/Kazakhstan/95/2013

                                      68
                                                      APMV-8/little stint/Kazakhstan/14/2013
                                                               APMV-8/wild bird/Mongolia/020/2012

                                            APMV-8/pintail/Wakuya/20/78

                                                               APMV-8/goose/Delaware/1053/76



                                      0.0050

          Figure 3.14  Phylogenetic analysis of APMV-8 strains. The evolutionary history was inferred based on the complete coding sequences of
          fusion gene of eight APMV-8 strains by using the Maximum Likelihood method based on the Kimura 2-parameter model (Kimura, 1980) in
          MEGA7 (Kumar et al., 2016).


          sequences of each of the four APMV-10 strains is 15,456 nt. The   APMV-14
          3′-leader and 5′-trailer regions are 55 nt and 296 nt, respectively.   APMV strain duck/Japan/11OG0352/2011 (11OG0352) was
          The genome contains six non-overlapping genes. The putative   isolated from a duck faeces in Northern Japan in 2011 during
          aa sequence of the F protein cleavage site of all four APMV-10   AIV surveillance (Thampaisarn  et  al., 2017). The complete
          strains contain dibasic residues, K-P-S-Q-RI. APMV-10 grows   genome of the virus is 15,444 nt and contains six genes. The
          in Vero and DF-1 cells only with the addition of trypsin. Phylo-  leader and trailer regions are 55 nt and 277 nt, respectively.
          genetic analysis showed that all four isolates grouped together,   The F protein cleavage site is T-R-E-G-KL which resembles
          and they are more closely related to APMV-2, -8, -15, and -20   a lentogenic strain of APMV-1. This is the only APMV which
          viruses at the aa sequence level (Miller et al., 2010; Goraichuk   contains a K residue at the –1 position, whereas all other APMV
          et al., 2017).                                        serotypes contain an R residue at this position. The significance
                                                                of the K residue at this position is unknown. In the absence of
          APMV-11                                               trypsin, strain 11OG0352 replicated in CEF cells but not in
          APMV-11    (AMAvV-11)     strain  common     snipe/   MDBK, MDCK, and Vero cells. Exogenous trypsin augmented
          France/100212/2010  (France/100212)  was  isolated  from   growth and syncytia formation in CEF cells. The virus showed
          a  live  common  snipe  (Gallinago gallinago)  in  France  during   low cross-reaction by HI test with APMV-6. Comparison of
          AIV active surveillance in 2010 (Briand et al., 2012). The   full genome sequences showed that APMV-5 is most closely
          genome  of  APMV-11  is  17,412 nt.  To  date,  this  is  the  largest   related to the APMV-14 strain 11OG0352 (51.4% nt identity)
          APMV  genome reported. The genome  organization is typical   and the latter differs most from APMV-3 and -4 (each with
          of other APMVs, with six genes encoding 8 different proteins.   42.7% nt identity). The virus showed very low cross-reactivity
          The APMV-11 differs from other APMV serotypes in that the   with APMV-6 by HI test (Thampaisarn et al., 2017). Strain
          V  protein  is  produced  from  the  unedited  mRNA  and  the  P   11OG0352 replicates only in chicken embryo fibroblast cells,
          protein is produced from an mRNA containing a two-G inser-  indicating that the virus is highly restrictive to avian species.
          tion (Briand et al., 2012) (Fig. 3.10). The F gene of APMV-11   This virus represents species AMAvV-14.
          strain France/100212 has two ORFs. A small ORF of 279 nt
          that encode a 92 aa hypothetical protein initiates upstream and   APMV-15
          overlaps with the second ORF. The second start codon (ATG)   A novel APMV strain Calidris fuscicollis/Brazil/RS-1177/2012
          appears to be optimized for protein translation and code for the   (RS-1177) was isolated from a migratory bird, white-rumped
          F protein of APMV-11. The significance of the upstream small   sandpiper (Calidris fuscicollis), during active AIV and NDV sur-
          ORF is not known. The putative cleavage site sequence of the   veillance in South Brazil in 2012 (Thomazelli et al., 2017). The
          F protein is S-G-T-K-RF. The leader and trailer regions are   virus was antigenically and genetically distinct from other APMV
          55 nt and 402 nt, respectively. The highest genomic nt identity   serotypes. The genome was 14,952 nt long, with six genes. The F
          (49.6%) is with APMV-2 strain Yucaipa. The only known strain   protein cleavage site contained two basic aa (V-P-K-E-RL), typi-
          France/100212 is the prototype strain for APMV-11.    cal of avirulent APMV-1 strains. Phylogenetic analysis indicated
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