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Protection efficacy of the Brucella abortus ghost vaccine candidate lysed by the N-terminal 24-amino acid fragment (GI24) of the 36-amino acid peptide PMAP-36 (porcine myeloid antimicrobial peptide 36) in murine modelsopen access

Authors
Kwon, Ae JeongMoon, Ja YoungKim, Won KyongKim, SukHur, Jin
Issue Date
Oct-2016
Publisher
JAPAN SOC VET SCI
Keywords
antimicrobial peptide; Brucella abortus; brucellosis; vaccination
Citation
JOURNAL OF VETERINARY MEDICAL SCIENCE, v.78, no.10, pp.1541 - 1548
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF VETERINARY MEDICAL SCIENCE
Volume
78
Number
10
Start Page
1541
End Page
1548
URI
https://scholarworks.bwise.kr/gnu/handle/sw.gnu/15238
DOI
10.1292/jvms.16-0036
ISSN
0916-7250
Abstract
Brucella abortus cells were lysed by the N-terminal 24-amino acid fragment (GI24) of the 36-amino acid peptide PMAP-36 (porcine myeloid antimicrobial peptide 36). Next, the protection efficacy of the lysed fragment as a vaccine candidate was evaluated. Group A mice were immunized with sterile PBS, group B mice were intraperitoneally (ip) immunized with 3 x 10(8) colony-forming units (CFUs) of B. abortus strain RB51, group C mice were immunized ip with 3 x 10(8) cells of the B. abortus vaccine candidate, and group D mice were orally immunized with 3 x 10(9) cells of the B. abortus vaccine candidate. Brucella lipopolysaccharide (LPS)-specific serum IgG titers were considerably higher in groups C and D than in group A. The levels of interleukin (IL)-4, IL-10, tumor necrosis factor alpha (TNF-alpha) and interferon gamma (IFN-gamma) were significantly higher in groups B-D than in group A. After an ip challenge with B. abortus 544, only group C mice showed a significant level of protection as compared to group A. Overall, these results show that ip immunization with a vaccine candidate lysed by GI24 can effectively protect mice from systemic infection with virulent B. abortus.
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