| Autor: |
Young KT; Department of Pathology, College of Veterinary Medicine, University of Georgiagrid.213876.9, Athens, Georgia, USA., Stephens JQ; Department of Pathology, College of Veterinary Medicine, University of Georgiagrid.213876.9, Athens, Georgia, USA., Poulson RL; Department of Population Health, Southeastern Cooperative Wildlife Disease Study, University of Georgiagrid.213876.9, Athens, Georgia, USA., Stallknecht DE; Department of Population Health, Southeastern Cooperative Wildlife Disease Study, University of Georgiagrid.213876.9, Athens, Georgia, USA., Dimitrov KM; Department of Virology, Texas A&M University, College Station, Texas, USA., Butt SL; Department of Pathology, University of Agriculture Faisalabad, Faisalabad, Pakistan., Stanton JB; Department of Pathology, College of Veterinary Medicine, University of Georgiagrid.213876.9, Athens, Georgia, USA. |
| Abstrakt: |
Avian paramyxoviruses (APMVs) (subfamily Avulavirinae ) have been isolated from over 200 species of wild and domestic birds around the world. The International Committee on Taxonomy of Viruses (ICTV) currently defines 22 different APMV species, with Avian orthoavulavirus 1 (whose viruses are designated APMV-1) being the most frequently studied due to its economic burden to the poultry industry. Less is known about other APMV species, including limited knowledge on the genetic diversity in wild birds, and there is a paucity of public whole-genome sequences for APMV-2 to -22. The goal of this study was to use MinION sequencing to genetically characterize APMVs isolated from wild bird swab samples collected during 2016 to 2018 in the United States. Multiplexed MinION libraries were prepared using a random strand-switching approach using 37 egg-cultured, influenza-negative, hemagglutination-positive samples. Forty-one APMVs were detected, with 37 APMVs having complete polymerase coding sequences allowing for species identification using ICTV's current Paramyxoviridae phylogenetic methodology. APMV-1, -4, -6, and -8 viruses were classified, one putative novel species ( Avian orthoavulavirus 23 ) was identified from viruses isolated in this study, two putative new APMV species ( Avian metaavulavirus 24 and 27 ) were identified from viruses isolated in this study and from retrospective GenBank sequences, and two putative new APMV species ( Avian metaavulavirus 25 and 26 ) were identified solely from retrospective GenBank sequences. Furthermore, coinfections of APMVs were identified in four samples. The potential limitations of the branch length being the only species identification criterion and the potential benefit of a group pairwise distance analysis are discussed. IMPORTANCE Most species of APMVs are understudied and/or underreported, and many species were incidentally identified from asymptomatic wild birds; however, the disease significance of APMVs in wild birds is not fully determined. The rapid rise in high-throughput sequencing coupled with avian influenza surveillance programs have identified 12 different APMV species in the last decade and have challenged the resolution of classical serological methods to identify new viral species. Currently, ICTV's only criterion for Paramyxoviridae species classification is the requirement of a branch length of >0.03 using a phylogenetic tree constructed from polymerase (L) amino acid sequences. The results from this study identify one new APMV species, propose four additional new APMV species, and highlight that the criterion may have insufficient resolution for APMV species demarcation and that refinement or expansion of this criterion may need to be established for Paramyxoviridae species identification. |
