A nano particle vector comprised of poly lactic-co-glycolic acid and monophosphoryl lipid A and recombinant Mycobacterium avium subsp paratuberculosis peptides stimulate a pro-immune profile in bovine macrophages

Authors

C.D. Souza, Washington State University, PullmanFollow
John Bannantine, USDA ARS National Animal Disease CenterFollow
W.C. Brown, Washington State University, Pullman
M.G. Norton, Washington State University, Pullman
W.C. Davis, Washington State University, Pullman
J.K. Hwang, Washington State University, Pullman
P. Ziaei, Washington State University, Pullman
Gaber S. Abdellrazeq, Washington State University, Pullman & Alexandria University
M.V. Eren, Washington State University, Pullman
J.R. Deringer, Washington State University, Pullman
E. Laws, Washington State University, Pullman
M.C.D. Cardieri, Washington State University, Pullman

ORCID IDs

http://orcid.org/0000-0002-8677-911X

Document Type

Article

Date of this Version

2017

Citation

Journal of Applied Microbiology 123, 54--65

doi:10.1111/jam.13491

Comments

2017 The Society for Applied Microbiology

Abstract

Aims: We evaluated the potential of a nanoparticle (NP) delivery system to improve methods of delivery of candidate peptide-based vaccines for Paratuberculosis in cattle.

Methods and Results: Peptides derived from Mycobacterium avium subsp. paratuberculosis (Map), and the pro-inflammatory monophosphoryl lipid A (MPLA) were incorporated in polymeric NPs based on poly (D,L-lactide-co- glycolide) (PLGA). The PLGA/MPLA NPs carriers were incubated with macrophages to examine their effects on survival and function. PLGA/MPLA NPs, with and without Map antigens, are efficiently phagocytized by macrophages with no evidence of toxicity. PLGA/MPLA NP formulations did not alter the level of expression of MHC I or II molecules. Expression of TNFa and IL12p40 was increased in Map-loaded NPs. T-cell proliferation studies using a model peptide from Anaplasma marginale demonstrated that a CD4 T- cell recall response could be elicited with macrophages pulsed with the peptide encapsulated in the PLGA/MPLA NP.

Conclusions: These findings indicate PLGA/MPLA NPs can be used as a vehicle for delivery and testing of candidate peptide-based vaccines.

Significance and Impact of the Study: These results will assist on more in depth studies on PLGA NP delivery systems that may lead to the development of a peptide-based vaccine for cattle.