<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chugh S</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>NIAID NIH HHS</funding><funding>Michigan State University</funding><pagination>1031-1040</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9112674</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(5)</volume><pubmed_abstract>Bovine leukemia virus (BLV) is a C-type retrovirus of cattle that causes huge economic losses with high infection rates in the majority of countries worldwide. To develop an anti-BLV vaccine, we constructed a peptide conjugate using the envelope glycoprotein gp51-peptide epitope, a putative receptor-binding site. This highly antigenic peptide was covalently linked to a mutant bacteriophage carrier (mQβ) using two different linker strategies, isothiocyanate (NCS) and dinitrophenyl adipate. Both constructs elicited higher anti-BLV peptide IgG titers than the corresponding conjugate with keyhole limpet hemocyanin protein carrier (gold standard) in mice with the NCS linker strategy requiring less sample processing. The mQβ-gp51-peptide construct is the first BLV peptide-based vaccine candidate</pubmed_abstract><journal>ACS infectious diseases</journal><pubmed_title>Design and Synthesis of Bovine Leukemia Virus-Associated Peptide-Based Qβ Conjugate Eliciting Long-Lasting Neutralizing Antibodies in Mice.</pubmed_title><pmcid>PMC9112674</pmcid><funding_grant_id>R01 AI146210</funding_grant_id><funding_grant_id>R01AI146210</funding_grant_id><pubmed_authors>Yuzbasiyan-Gurkan V</pubmed_authors><pubmed_authors>Swenson C</pubmed_authors><pubmed_authors>Huang X</pubmed_authors><pubmed_authors>Chugh S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Design and Synthesis of Bovine Leukemia Virus-Associated Peptide-Based Qβ Conjugate Eliciting Long-Lasting Neutralizing Antibodies in Mice.</name><description>Bovine leukemia virus (BLV) is a C-type retrovirus of cattle that causes huge economic losses with high infection rates in the majority of countries worldwide. To develop an anti-BLV vaccine, we constructed a peptide conjugate using the envelope glycoprotein gp51-peptide epitope, a putative receptor-binding site. This highly antigenic peptide was covalently linked to a mutant bacteriophage carrier (mQβ) using two different linker strategies, isothiocyanate (NCS) and dinitrophenyl adipate. Both constructs elicited higher anti-BLV peptide IgG titers than the corresponding conjugate with keyhole limpet hemocyanin protein carrier (gold standard) in mice with the NCS linker strategy requiring less sample processing. The mQβ-gp51-peptide construct is the first BLV peptide-based vaccine candidate</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-05-29T16:22:58.382Z</modification><creation>2025-05-29T16:22:58.382Z</creation></dates><accession>S-EPMC9112674</accession><cross_references><pubmed>35482583</pubmed><doi>10.1021/acsinfecdis.2c00001</doi></cross_references></HashMap>