Immunogenic Evaluation of Bivalent Vaccine Candidate against Enterohemorrhagic and Enterotoxigenic Escherichia coli.
Animals
Antibodies, Bacterial
/ blood
Antigens, Bacterial
/ genetics
Enterohemorrhagic Escherichia coli
/ physiology
Enterotoxigenic Escherichia coli
/ physiology
Enterotoxins
/ genetics
Escherichia coli Vaccines
/ immunology
Female
Humans
Immunization
Immunodominant Epitopes
/ genetics
Mice
Mice, Inbred BALB C
Recombinant Fusion Proteins
/ genetics
Vaccines, Subunit
Journal
Iranian journal of immunology : IJI
ISSN: 1735-367X
Titre abrégé: Iran J Immunol
Pays: Iran
ID NLM: 101282932
Informations de publication
Date de publication:
Sep 2019
Sep 2019
Historique:
entrez:
26
9
2019
pubmed:
26
9
2019
medline:
29
5
2020
Statut:
ppublish
Résumé
Caused by bacterial, viral, and parasitic pathogens, diarrhea is the second leading cause of death among children under five. Two strains of E. coli, namely Enterotoxigenic, ETEC and Enterohemorrhagic EHEC are the most important causes of this disease in developing countries. EHEC is a major causative agent of bloody diarrhea and hemorrhagic uremic syndrome, while ETEC is the most important cause of diarrhea in neonates and travelers. To evaluate the immunologic properties of a subunit vaccine candidate comprising the main immunogenic epitopes from these two bacterial strains. The construct comprised of LTB and CfaB antigens from ETEC, and Intimin and Stx2B antigens from EHEC, was designed, analyzed and synthesized using bioinformatics methods. The chimeric gene was sub-cloned in the expression vector and expressed in E. coli host. The purified chimera protein was injected subcutaneously into the experimental animals. The production of specific antibodies was confirmed by immunological methods, and the protection capacity was evaluated by the challenge of immunized mice with the pathogenic bacteria. Chimeric recombinant protein was able to increase IgG titer. Neutralization assay indicated that the antibodies generated against LtB moiety were able to neutralize ETEC toxin. In animal challenge study, all non-immune mice died within 3 days after the injection of toxin, but all immunized mice survived from Stx toxin. The immunity to both ETEC and EHEC bacteria is significant, and this structure can be considered as a candidate for vaccine production against these bacterial strains.
Sections du résumé
BACKGROUND
BACKGROUND
Caused by bacterial, viral, and parasitic pathogens, diarrhea is the second leading cause of death among children under five. Two strains of E. coli, namely Enterotoxigenic, ETEC and Enterohemorrhagic EHEC are the most important causes of this disease in developing countries. EHEC is a major causative agent of bloody diarrhea and hemorrhagic uremic syndrome, while ETEC is the most important cause of diarrhea in neonates and travelers.
OBJECTIVES
OBJECTIVE
To evaluate the immunologic properties of a subunit vaccine candidate comprising the main immunogenic epitopes from these two bacterial strains.
METHODS
METHODS
The construct comprised of LTB and CfaB antigens from ETEC, and Intimin and Stx2B antigens from EHEC, was designed, analyzed and synthesized using bioinformatics methods. The chimeric gene was sub-cloned in the expression vector and expressed in E. coli host. The purified chimera protein was injected subcutaneously into the experimental animals. The production of specific antibodies was confirmed by immunological methods, and the protection capacity was evaluated by the challenge of immunized mice with the pathogenic bacteria.
RESULTS
RESULTS
Chimeric recombinant protein was able to increase IgG titer. Neutralization assay indicated that the antibodies generated against LtB moiety were able to neutralize ETEC toxin. In animal challenge study, all non-immune mice died within 3 days after the injection of toxin, but all immunized mice survived from Stx toxin.
CONCLUSIONS
CONCLUSIONS
The immunity to both ETEC and EHEC bacteria is significant, and this structure can be considered as a candidate for vaccine production against these bacterial strains.
Identifiants
pubmed: 31552829
pii: 02
doi: 10.22034/IJI.2019.80271
doi:
Substances chimiques
Antibodies, Bacterial
0
Antigens, Bacterial
0
Enterotoxins
0
Escherichia coli Vaccines
0
Immunodominant Epitopes
0
Recombinant Fusion Proteins
0
Vaccines, Subunit
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM