Pasteurella multocidainactivated with ferric chloride and adjuvanted with bacterial DNA is a potent and efficacious vaccine in Balb/c mice. Issue 9 (September 2018)

• Record Type: Journal Article
• Authors: Homayoon, Maryam; Tahamtan, Yahya; Kargar, Mohammad; Hosseini, Seyed Mohammad Hossein; Sepahy, Abbas Akhavan
• Is Part Of: Journal of medical microbiology. Volume 67:Issue 9(2018)
• Publication Date: 2018-09
• Subjects: Pasteurella multocida -- bacterial DNA -- ferric chloride -- adjuvant -- vaccine -- spleen culture; Medical microbiology -- Periodicals; 616.9041
• DOI: 10.1099/jmm.0.000794
• Languages: English
• ISSNs: 0022-2615

Abstract

Abstract : Purpose. : Pasteurella multocida ( P. multocida ) is a principal pathogen of domestic animals and an opportunistic pathogen of humans. It is the causative agent of pneumonia and haemorrhagic septicaemia in cattle, sheep and goats, fowl cholera in chickens and progressive atrophic rhinitis in swine. In this study, we investigated the humoral and cellular immune responses and protective immunity conferred by an iron‐inactivated vaccine with bacterial DNA (IIV+bDNA) as an adjuvant in mice. Methodology. : P. multocida was grown in BHI broth, inactivated with formalin and FeCl3 and adjuvanted with alum and bDNA. Mice were immunized with two whole‐cell inactivated vaccine doses 2 weeks apart. The animals were challenged 4 weeks after booster immunization. Immunogens (vaccines and bDNA) posed no safety problems when mice were injected subcutaneously (s/c) with these preparations. The serum antibody titres were tested by ELISA. At 28 days post immunization, cell‐mediated immunity responses were determined. The responses were measured by assay of IL‐6 and IL‐12 in lymphocyte spleen culture supernatants. Results. : ELISA results showed that the levels of antibodies in iron inactivated with bDNA adjuvant groups were higher than in the formalin inactivated with alum adjuvant vaccine group. The protection rate of IIV+bDNA adjuvant vaccine was superior to that of the other vaccines and it protected 100 % of the challenge group mice. Following immunization, bDNA promoted increased production of interleukins compared to the control groups. Conclusion. : These studies indicate that bDNA is effective as an immune adjuvant, and along with stimulatory bDNA represent promising new humoral and cellular immune enhancers for vaccination applications. In addition, this vaccine is able to provide long‐term protection against infection.