Detection and Genome Sequence Analysis of Avian Metapneumovirus Subtype A Viruses Circulating in Commercial Chicken Flocks in Mexico

• Published in: Veterinary sciences 2022-10, Vol.9 (10), p.579-579
• Main Authors: Kariithi, Henry M., Christy, Nancy, Decanini, Eduardo L., Lemiere, Stéphane, Volkening, Jeremy D., Afonso, Claudio L., Suarez, David L.
• Format: Article
• Language: English
• Subjects: Amino acids; aMPV; Avian metapneumovirus; Bioinformatics; chickens; cluster; de novo assembly; Epidemics; Farms; FTA card; genome; Genomes; Genotypes; Infections; Laboratories; Mexico; Next-generation sequencing; NGS; Nucleotide sequence; nucleotide sequences; nucleotides; Pathogens; Phylogeny; Polymerase chain reaction; Poultry; Proteins; Respiratory diseases; RNA polymerase; SEP rRT-PCR; Sequence analysis; Strains (organisms); Taxonomy; Vaccines; Viral infections; Viruses
• ISSN: 2306-7381; 2306-7381
• DOI: 10.3390/vetsci9100579

Avian metapneumoviruses (aMPV subtypes A-D) are respiratory and reproductive pathogens of poultry. Since aMPV-A was initially reported in Mexico in 2014, there have been no additional reports of its detection in the country. Using nontargeted next-generation sequencing (NGS) of FTA card-spotted respiratory samples from commercial chickens in Mexico, seven full genome sequences of aMPV-A (lengths of 13,288–13,381 nucleotides) were de novo assembled. Additionally, complete coding sequences of genes N (n = 2), P and M (n = 7 each), F and L (n = 1 each), M2 (n = 6), SH (n = 5) and G (n = 2) were reference-based assembled from another seven samples. The Mexican isolates phylogenetically group with, but in a distinct clade separate from, other aMPV-A strains. The genome and G-gene nt sequences of the Mexican aMPVs are closest to strain UK/8544/06 (97.22–97.47% and 95.07–95.83%, respectively). Various amino acid variations distinguish the Mexican isolates from each other, and other aMPV-A strains, most of which are in the G (n = 38), F (n = 12), and L (n = 19) proteins. Using our sequence data and publicly available aMPV-A data, we revised a previously published rRT-PCR test, which resulted in different cycling and amplification conditions for aMPV-A to make it more compatible with other commonly used rRT-PCR diagnostic cycling conditions. This is the first comprehensive sequence analysis of aMPVs in Mexico and demonstrates the value of nontargeted NGS to identify pathogens where targeted virus surveillance is likely not routinely performed.