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      Chimeric H5 influenza virus-like particle vaccine elicits broader cross-clade antibody responses in chickens than in ducks

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          Abstract

          Eurasian-lineage highly pathogenic avian influenza (HPAI) H5 viruses have spread throughout Asia, the Middle East, Europe, Africa, and most recently, North and South America. These viruses are independently evolving into genetically and antigenically divergent clades, and broad-spectrum vaccines protecting against these divergent clades are needed. In this study, we developed a chimeric virus-like particle (VLP) vaccine co-expressing hemagglutinins from two clades (clades 1 and 2.3.2.1) of HPAI H5 viruses and performed comparative cross-clade hemagglutination inhibition (HI) analysis in chickens and ducks. The chimeric VLP immunization induced a significantly broader spectrum of antibodies against various clades of HPAI H5 viruses than monovalent VLPs both in chickens and ducks. While the chimeric VLP led to broadened antibody responses in both species, significantly lower levels of HI antibodies were elicited in ducks than in chickens. Moreover, boost immunization failed to increase antibody responses in ducks regardless of the VLPs used, in contrast to chickens that showed significantly enhanced antibody responses upon boost immunization. These results suggest (1) the potential application of the chimeric VLP technology in poultry to help control HPAI H5 viruses by offering broader antibody responses against antigenically different strains and (2) possible obstacles in generating high levels of antibody responses against HPAI H5 viruses in ducks via vaccination, implying the need for advanced vaccination strategies for ducks.

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          Most cited references30

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          Avian influenza A (H5N1) infection in humans.

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            Gene splicing and mutagenesis by PCR-driven overlap extension.

            Extension of overlapping gene segments by PCR is a simple, versatile technique for site-directed mutagenesis and gene splicing. Initial PCRs generate overlapping gene segments that are then used as template DNA for another PCR to create a full-length product. Internal primers generate overlapping, complementary 3' ends on the intermediate segments and introduce nucleotide substitutions, insertions or deletions for site-directed mutagenesis, or for gene splicing, encode the nucleotides found at the junction of adjoining gene segments. Overlapping strands of these intermediate products hybridize at this 3' region in a subsequent PCR and are extended to generate the full-length product amplified by flanking primers that can include restriction enzyme sites for inserting the product into an expression vector for cloning purposes. The highly efficient generation of mutant or chimeric genes by this method can easily be accomplished with standard laboratory reagents in approximately 1 week.
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              Universal primer set for the full-length amplification of all influenza A viruses.

              To systematically identify and analyze the 15 HA and 9 NA subtypes of influenza A virus, we need reliable, simple methods that not only characterize partial sequences but analyze the entire influenza A genome. We designed primers based on the fact that the 15 and 21 terminal segment specific nucleotides of the genomic viral RNA are conserved between all influenza A viruses and unique for each segment. The primers designed for each segment contain influenza virus specific nucleotides at their 3'-end and non-influenza virus nucleotides at the 5'-end. With this set of primers, we were able to amplify all eight segments of N1, N2, N4, N5, and N8 subtypes. For N3, N6, N7, and N9 subtypes, the segment specific sequences of the neuraminidase genes are different. Therefore, we optimized the primer design to allow the amplification of those neuraminidase genes as well. The resultant primer set is suitable for all influenza A viruses to generate full-length cDNAs, to subtype viruses, to sequence their DNA, and to construct expression plasmids for reverse genetics systems.
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                Author and article information

                Contributors
                Journal
                Front Vet Sci
                Front Vet Sci
                Front. Vet. Sci.
                Frontiers in Veterinary Science
                Frontiers Media S.A.
                2297-1769
                15 June 2023
                2023
                : 10
                : 1158233
                Affiliations
                [1] 1College of Veterinary Medicine, Konkuk University , Seoul, South Korea
                [2] 2Department of Veterinary Medicine, Virginia-Maryland College of Veterinary Medicine, University of Maryland , College Park, MD, United States
                [3] 3Department of Pathobiology and Veterinary Sciences, University of Connecticut , Storrs, CT, United States
                [4] 4Department of Nutritional Sciences, University of Connecticut , Storrs, CT, United States
                [5] 5College of Veterinary Medicine, Kyungpook National University , Daegu, Republic of Korea
                [6] 6College of Medicine and Medical Research Institute, Chungbuk National University , Cheongju, Republic of Korea
                Author notes

                Edited by: Jasmina M. Luczo, CSIRO Australian Centre for Disease Preparedness, Australia

                Reviewed by: Semmannan Kalaiyarasu, ICAR-National Institute of High Security Animal Diseases (ICAR-NIHSAD), India; Ivette Nunez, Division of Clinical Research (NIAID/NIH), United States

                *Correspondence: Dong-Hun Lee, donghunlee@ 123456konkuk.ac.kr

                These authors have contributed equally to this work

                Article
                10.3389/fvets.2023.1158233
                10310301
                f62c541b-c6f4-41eb-9c04-239edafbd340
                Copyright © 2023 Park, Song, Chung, Choi, Kwon, Youk and Lee.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 03 February 2023
                : 31 May 2023
                Page count
                Figures: 5, Tables: 0, Equations: 0, References: 30, Pages: 8, Words: 5575
                Funding
                Funded by: Ministry of Agriculture, Food and Rural Affairs (MAFRA), doi 10.13039/501100003624;
                Award ID: 122057–2
                Funded by: Korea Institute of Planning and Evaluation for Technology in Food, Agriculture and Forestry (IPET)
                Categories
                Veterinary Science
                Original Research
                Custom metadata
                Veterinary Infectious Diseases

                highly pathogenic avian influenza virus,vaccine,virus like particle,insect cell,poultry,chicken,duck

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