Enhanced protection through genotype-matched bivalent H9N2-Newcastle disease virus vaccination: Comparative efficacy against contemporary field strains in specific-pathogen-free chickens
Ahmed Abdelhalim , Nahed Yahia , Mehdi Elharrak , Halima Rhazi , Ahmed Hassan Soliman , Amal Turkistan , Hussien Ali Hussien , Ahmed A. Khalil
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引用次数: 0
Abstract
Newcastle Disease Virus (NDV) and Low Pathogenic Avian Influenza (LPAI H9N2) infections cause substantial economic losses in poultry production globally. Despite widespread vaccination, outbreaks persist due to antigenic mismatches between vaccine and circulating field strains, highlighting the need for improved vaccines with better genetic and antigenic matching. This study evaluated the efficacy of a novel bivalent inactivated vaccine (Aviline FLU H9 ND-K) containing genetically matched H9N2 (Saudi Arabian strain, G1 lineage B) and NDV (LaSota genotype II and genotype VII.1.1) strains against contemporary field isolates. The novel vaccine was compared to a commercial vaccine containing heterologous H9N2 (UAE origin, G1 lineage C) and NDV (Ulster strain, genotype II) antigens in a controlled challenge study. Seventy specific-pathogen-free (SPF) chickens were allocated to seven groups (n = 10/group) and vaccinated subcutaneously at 4 weeks of age. Four weeks post-vaccination, birds were challenged with either LPAI A/chicken/Egypt/SP3/2022 (H9N2) or NDV-B7-RLQP-CH-EG-12 (genotype VII). Clinical protection, antibody responses (hemagglutination inhibition), viral shedding (qRT-PCR), and cytokine expression interleukin-6 (IL-6), interferon-gamma (IFN-γ) were comprehensively assessed. Both vaccines conferred 100 % protection against clinical disease and mortality. However, the Aviline FLU H9 ND-K vaccine induced significantly higher antibody titers against both H9N2 (p < 0.001) and NDV (p < 0.05 at 7- and 14-days post-challenge). Viral shedding was substantially reduced in the genotype-matched vaccine groups, with H9N2 shedding eliminated by 7 post-challenge (dpc) with marked reduction by 5 dpc compared to 7 dpc with the commercial vaccine (p < 0.01). Similarly, NDV shedding ceased by 7 dpc in the Aviline FLU H9 ND-K group but persisted in the commercial vaccine group (p < 0.001). Pro-inflammatory cytokine expression was more effectively modulated in birds receiving the genotype-matched vaccine, with significantly lower IL-6 levels (p < 0.01) and higher IFN-γ expression (p < 0.05) compared to birds receiving the commercial vaccine. These findings demonstrate that the genotype-matched vaccine provides superior immunogenicity, enhanced viral clearance, and improved immunomodulatory effects, emphasizing the critical importance of antigenic matching in vaccine development for effective control of evolving avian pathogens. The potential impact on viral evolution and transmission dynamics within vaccinated populations warrants further investigation.
期刊介绍:
Veterinary Microbiology is concerned with microbial (bacterial, fungal, viral) diseases of domesticated vertebrate animals (livestock, companion animals, fur-bearing animals, game, poultry, fish) that supply food, other useful products or companionship. In addition, Microbial diseases of wild animals living in captivity, or as members of the feral fauna will also be considered if the infections are of interest because of their interrelation with humans (zoonoses) and/or domestic animals. Studies of antimicrobial resistance are also included, provided that the results represent a substantial advance in knowledge. Authors are strongly encouraged to read - prior to submission - the Editorials (''Scope or cope'' and ''Scope or cope II'') published previously in the journal. The Editors reserve the right to suggest submission to another journal for those papers which they feel would be more appropriate for consideration by that journal.
Original research papers of high quality and novelty on aspects of control, host response, molecular biology, pathogenesis, prevention, and treatment of microbial diseases of animals are published. Papers dealing primarily with immunology, epidemiology, molecular biology and antiviral or microbial agents will only be considered if they demonstrate a clear impact on a disease. Papers focusing solely on diagnostic techniques (such as another PCR protocol or ELISA) will not be published - focus should be on a microorganism and not on a particular technique. Papers only reporting microbial sequences, transcriptomics data, or proteomics data will not be considered unless the results represent a substantial advance in knowledge.
Drug trial papers will be considered if they have general application or significance. Papers on the identification of microorganisms will also be considered, but detailed taxonomic studies do not fall within the scope of the journal. Case reports will not be published, unless they have general application or contain novel aspects. Papers of geographically limited interest, which repeat what had been established elsewhere will not be considered. The readership of the journal is global.