Human parainfluenza virus 3 vaccine candidates attenuated by codon-pair deoptimization are immunogenic and protective in hamsters.
Animals
Parainfluenza Virus 3, Human
/ immunology
Humans
Vaccines, Attenuated
/ immunology
Codon
/ genetics
Cricetinae
Virus Replication
Respirovirus Infections
/ immunology
Chlorocebus aethiops
Vero Cells
Open Reading Frames
/ genetics
Mesocricetus
Antibodies, Viral
/ immunology
Viral Vaccines
/ immunology
Viral Proteins
/ immunology
Parainfluenza Vaccines
/ immunology
codon pair deoptimization
human parainfluenza virus type 3
intranasal vaccine
live attenuated vaccine
parainfluenza virus vaccine
Journal
Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876
Informations de publication
Date de publication:
18 Jun 2024
18 Jun 2024
Historique:
medline:
11
6
2024
pubmed:
11
6
2024
entrez:
11
6
2024
Statut:
ppublish
Résumé
Human parainfluenza virus type 3 (HPIV3) is a major pediatric respiratory pathogen lacking available vaccines or antiviral drugs. We generated live-attenuated HPIV3 vaccine candidates by codon-pair deoptimization (CPD). HPIV3 open reading frames (ORFs) encoding the nucleoprotein (N), phosphoprotein (P), matrix (M), fusion (F), hemagglutinin-neuraminidase (HN), and polymerase (L) were modified singly or in combination to generate 12 viruses designated Min-N, Min-P, Min-M, Min-FHN, Min-L, Min-NP, Min-NPM, Min-NPL, Min-PM, Min-PFHN, Min-MFHN, and Min-PMFHN. CPD of N or L severely reduced growth in vitro and was not further evaluated. CPD of P or M was associated with increased and decreased interferon (IFN) response in vitro, respectively, but had little effect on virus replication. In Vero cells, CPD of F and HN delayed virus replication, but final titers were comparable to wild-type (wt) HPIV3. In human lung epithelial A549 cells, CPD F and HN induced a stronger IFN response, viral titers were reduced 100-fold, and the expression of F and HN proteins was significantly reduced without affecting N or P or the relative packaging of proteins into virions. Following intranasal infection in hamsters, replication in the nasal turbinates and lungs tended to be the most reduced for viruses bearing CPD F and HN, with maximum reductions of approximately 10-fold. Despite decreased in vivo replication (and lower expression of CPD F and HN in vitro), all viruses induced titers of serum HPIV3-neutralizing antibodies similar to wt and provided complete protection against HPIV3 challenge. In summary, CPD of HPIV3 yielded promising vaccine candidates suitable for further development.
Identifiants
pubmed: 38861603
doi: 10.1073/pnas.2316376121
doi:
Substances chimiques
Vaccines, Attenuated
0
Codon
0
Antibodies, Viral
0
Viral Vaccines
0
Viral Proteins
0
Parainfluenza Vaccines
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e2316376121Subventions
Organisme : HHS | NIH | NIAID | Division of Intramural Research (DIR, NIAID)
ID : ZIA AI000327-38
Déclaration de conflit d'intérêts
Competing interests statement:S.A., S. Mueller, P.L.C., U.J.B., and S. Munir are inventors on the provisional patent application number 63/580,772, entitled “Human parainfluenza virus immunogenic molecules” filed by the United States Department of Health and Human Services.