Changes in the Transcriptome Profile in Young Chickens after Infection with LaSota Newcastle Disease Virus

• Published in: Vaccines (Basel) 2024-05, Vol.12 (6), p.592
• Main Authors: Lopes, Taina S B, Nankemann, Jannis, Breedlove, Cassandra, Pietruska, Andrea, Espejo, Raimundo, Cuadrado, Camila, Hauck, Ruediger
• Format: Article
• Language: English
• Subjects: Analysis; bioinformatics; Biomarkers; Birds; Chickens; Chicks; Design of experiments; Diagnosis; Epidemics; Gene expression; Gene regulation; Gene sequencing; Genes; Genetic aspects; Genetic transcription; Genomes; Health aspects; Human papillomavirus; Immune response; Immune system; Immunity; immunogenomics; Infections; Innate immunity; Juveniles; Newcastle disease; Ontology; Pathogens; pathway analysis; Poultry; Proteins; Ribonucleic acid; RNA; RNA viruses; Signal transduction; Specific pathogen free; Trade restrictions; Transcriptomes; vaccine; Vaccines; Viruses
• ISSN: 2076-393X; 2076-393X
• DOI: 10.3390/vaccines12060592

Understanding gene expression changes in chicks after vaccination against Newcastle Disease (ND) can reveal vaccine biomarkers. There are limited data on chicks' early immune response after ND vaccination. Two trials focused on this knowledge gap. In experiment one, 42 13-day-old specific-pathogen-free (SPF) chicks were used. Harderian glands (Hgs) and tracheas (Tcs) from five birds per group were sampled at 12, 24, and 48 h post-vaccination (hpv) to evaluate the gene transcription levels by RNA sequencing (RNA-seq) and RT-qPCR. The results of RNA-seq were compared by glmFTest, while results of RT-qPCR were compared by t-test. With RNA-seq, a significant up-regulation of interferon-related genes along with JAK-STAT signaling pathway regulation was observed in the Hgs at 24 hpv. None of the differentially expressed genes (DEGs) identified by RNA-seq were positive for RT-qPCR. Experiment 2 used 112 SPF and commercial chickens that were 1 day old and 14 days old. Only the commercial birds had maternal antibodies for Newcastle Disease virus (NDV). By RNA-seq, 20 core DEGs associated with innate immunity and viral genome replication inhibition were identified. Genes previously unlinked to NDV response, such as USP41, were identified. This research present genes with potential as immunity biomarkers for vaccines, yet further investigation is needed to correlate the core gene expression with viral shedding post-vaccination.