2022
DOI: 10.1128/aem.00466-22
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Putative Novel Avian Paramyxovirus (AMPV) and Reidentification of APMV-2 and APMV-6 to the Species Level Based on Wild Bird Surveillance (United States, 2016–2018)

Abstract: 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.

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Cited by 5 publications
(7 citation statements)
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“…Sequencing was controlled using MinKNOW v.21.06.0 (ONT) for 29 hours with default settings and hourly MUX scans. Post-sequencing analysis workflow followed the randomly primed, MinION-based sequencing as previously described (42,43). In brief, raw reads were basecalled, with the GPU version of Guppy v.6.1.3 (ONT) using the following command: guppybasecaller -i <input path> -s <save path> --flowcell <FLO-MIN106> --kit <SQK-LSK110> --device auto --calib_detect.…”
Section: Histopathologymentioning
confidence: 99%
“…Sequencing was controlled using MinKNOW v.21.06.0 (ONT) for 29 hours with default settings and hourly MUX scans. Post-sequencing analysis workflow followed the randomly primed, MinION-based sequencing as previously described (42,43). In brief, raw reads were basecalled, with the GPU version of Guppy v.6.1.3 (ONT) using the following command: guppybasecaller -i <input path> -s <save path> --flowcell <FLO-MIN106> --kit <SQK-LSK110> --device auto --calib_detect.…”
Section: Histopathologymentioning
confidence: 99%
“…Homogenized samples underwent viral enrichment ( 14 , 15 ). We extracted RNA by using Trizol LS Reagent (Thermo Fisher Scientific, https://www.thermofisher.com ) and prepared the cDNA library as previously described ( 16 , 17 )​, using manufacturer-suggested kits for ligation-based sequencing of amplicons (SQK-LSK110 with EXP-PBC096) and sequencing on a FLO-MIN106 R9.4.1 flow cell in a MinION Mk1B sequencing device (Oxford Nanopore Technologies, https://nanoporetech.com ). The postsequencing analysis workflow followed the randomly primed, MinION-based sequencing as previously described ( 16 , 17 ).…”
Section: Methodsmentioning
confidence: 99%
“…The first description of APMV-6 was isolated from a domestic duck in Hong Kong in 1977 [ 14 ]. APMV-6 can be characterized into two distinct subgroups based on both the antigenic serotype and genomic make-up; however, only 38 complete genomes have been sequenced prior to this study, so the actual diversity of this serotype in nature is unknown [ 14 , 16 ]. APMV-6 is genetically different from other APMV subtypes because it encodes a small hydrophobic (SH) protein.…”
Section: Introductionmentioning
confidence: 99%
“…Ukraine is a hot spot for the detection of avian diseases in wild bird populations because the geographical region spans three major flyways: East Africa and West Asia, Central Asia, and the Black and Mediterranean Seas. Similar to other RNA viruses (e.g., AIV), the introduction of APMV to naïve poultry populations is thought to be transmitted from wild migratory birds [ 6 , 7 , 9 , 11 , 16 ]. Horizontal transmission occurs through oropharyngeal and fecal secretions, thus resulting in a facile route of infection.…”
Section: Introductionmentioning
confidence: 99%