Epitope mapping and a candidate vaccine design from canine distemper virus

被引:0
作者
dos Santos, Camila Pereira [1 ]
Telles, Jerlane Tarcilia Gomes [1 ]
Guimaraes, Georgia de Freitas [1 ]
Gil, Laura Helena Vega Gonzales [2 ]
Vieira, Amanda Mota [1 ]
Pinheiro Junior, Jose Wilton [1 ]
Calzavara-Silva, Carlos Eduardo [3 ]
Maia, Rita de Cassia Carvalho [1 ]
机构
[1] Univ Fed Rural Pernambuco, Dept Vet Med, Recife, Brazil
[2] Aggeu Magalhaes Res Ctr, Dept Virol & Expt Therapy, Recife, Brazil
[3] Rene Rachou Inst Fiocruz Minas, Lab Cellular & Mol Immunol, Belo Horizonte, Brazil
关键词
CDV; ELISPOT; Hemagglutinin; Peptides; Vaccine; WILD-TYPE; ELISPOT; PROTEIN; PEPTIDE; GENE; DOGS;
D O I
10.5455/OVJ.2024.v14.i4.9
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background: Canine distemper (CD) is a worldwide spread disease that has been described in 12 families of mammals, especially in the Carnivora order, being better studied in domestic canines where vaccination represents the best means of control. CD is controlled by vaccination, but many cases of the disease still occur in vaccinated animals. Aim: The aim of this work was to study antigen-specific epitopes that can subsidize the development of a new vaccine approach. Methods: Mapping of T cell reactive epitopes for CD virus (CDV) was carried out through enzyme-linked immunospot assays using 119 overlapped synthetic peptides from the viral hemagglutinin protein, grouped in 22 pools forming a matrix to test the immune response of 32 animals. Results: Evaluations using the criteria established to identify reactive pools, demonstrated that 26 animals presented at least one reactive pool, that one pool was not reactive to any animal, and six pools were the most frequent among the reactive peptides. The crisscrossing of the most reactive pools in the matrix revealed nine peptides considered potential candidate epitopes for T cell stimulation against the CDV and those were used to design an in-silico protein, containing also predicted epitopes for B cell stimulation, and further analyzed using immune epitope databases to ensure protein quality and stability. Conclusion: The final in silico optimized protein presents characteristics that qualify it to be used to develop a new prototype epitope-based anti-CDV vaccine.
引用
收藏
页码:1019 / 1028
页数:10
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