<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang X</submitter><funding>Wanzhe Yuan</funding><pagination>920</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12474205</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(9)</volume><pubmed_abstract>The widespread prevalence of different serotypes of fowl adenoviruses (FAdVs) has led to diverse vaccine demands, especially for subunit vaccines targeting FAdV-4 and FAdV-11, which cause hydropericardium-hepatitis syndrome (HHS) and inclusion body hepatitis (IBH), respectively. Although the Fiber protein is known to elicit robust immune protection, further exploration is needed to enhance the production of cross-neutralizing antibodies. This study utilized structural prediction and homology modeling techniques, employing domain-swapping strategy to integrate neutralizing epitope-containing amino acid sequences (274-451aa and 364-543aa) into the shaft domain of the Fiber protein. Two novel chimeric proteins were recombinantly expressed and developed into subunit vaccines: Fiber-C4/D11 and </pubmed_abstract><journal>Veterinary sciences</journal><pubmed_title>A Novel Chimeric Fiber-C4/D11 Subunit Vaccine Induces Cross-Neutralizing Antibodies and Provides Better Protection Against Fowl Adenovirus (FAdV) Type 4 and Type 11 Than the Fiber-D11/C4 Subunit Vaccine.</pubmed_title><pmcid>PMC12474205</pmcid><funding_grant_id>2023YFD1802602</funding_grant_id><pubmed_authors>Qiao Y</pubmed_authors><pubmed_authors>Jiang W</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Zhao K</pubmed_authors><pubmed_authors>Lei B</pubmed_authors><pubmed_authors>Yuan W</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Novel Chimeric Fiber-C4/D11 Subunit Vaccine Induces Cross-Neutralizing Antibodies and Provides Better Protection Against Fowl Adenovirus (FAdV) Type 4 and Type 11 Than the Fiber-D11/C4 Subunit Vaccine.</name><description>The widespread prevalence of different serotypes of fowl adenoviruses (FAdVs) has led to diverse vaccine demands, especially for subunit vaccines targeting FAdV-4 and FAdV-11, which cause hydropericardium-hepatitis syndrome (HHS) and inclusion body hepatitis (IBH), respectively. Although the Fiber protein is known to elicit robust immune protection, further exploration is needed to enhance the production of cross-neutralizing antibodies. This study utilized structural prediction and homology modeling techniques, employing domain-swapping strategy to integrate neutralizing epitope-containing amino acid sequences (274-451aa and 364-543aa) into the shaft domain of the Fiber protein. Two novel chimeric proteins were recombinantly expressed and developed into subunit vaccines: Fiber-C4/D11 and </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-02T03:21:14.098Z</modification><creation>2026-05-02T03:11:50.274Z</creation></dates><accession>S-EPMC12474205</accession><cross_references><pubmed>41012845</pubmed><doi>10.3390/vetsci12090920</doi></cross_references></HashMap>