Mannheimia haemolytica together with
Pasteurella multocida represents a major bacterial causative agent of buffalo,
cattle, sheep and goat respiratory diseases, and it's one of the most important
causes for economic losses to these animals. Vaccination has proven to be the
most cost-effective strategy for controlling a wide range of infectious
diseases. The cross-protection between Pasteurella species has been
demonstrated. Commercially available vaccines were used to prevent infections
caused by P. multocida and M. haemolytica.
Thus, the aim of the present study was to evaluate the cross-protection
efficacy of two vaccines to protect mice against M. haemolytica, studying humoral immunity, using Enzyme-Linked
Immunosorbent Assay (ELISA), and conducting a challenge test. Forty-five mice
were divided into three equal groups; group one and two were inoculated 4μl
subcutaneously JOVAPAST® and 1μl of Al-kindi vaccines, respectively, while the
third group (control group) was inoculated with 0.5 ml PBS. Lethal Dose 50
(LD50) for M. haemolytica was
estimated as 2× 106 cfu/ml, and a challenge test was conducted by dropping 0.05
ml 2× 106 cfu/ml intranasally after three weeks of immunisation for the three
groups. The results of Enzyme-Linked Immunosorbent Assay showed a significant
increase of antibody titers at (P<0.01) in groups 1 and 2 after first- and
second-post immunisation, in comparison with the control group. Also, the
re-isolation of M. haemolytica from
lung tissue of all groups, after the challenge test, was positive with a
significant difference between the control and immunised group. The control
group was 4× 108 cfu ∕ml, which was higher than the immunised group one and
group two, which were 2.5×104 cfu∕ml and 3,5×105 cfu∕ml, respectively, after 24
hours of intranasal infection. In conclusion, the two commercial vaccines
showed good cross-protection efficacy against M. haemolytica, but the JOVAPAST® vaccine showed higher efficacy
than the Alkindi vaccine, as it contains two heterologous inactivated strains
and provides the basis for the production of a vaccine from the two pathogen of
local strains is recommended.
Author(s)
Details
Waffa A. Ahmed
Department of
Microbiology, College of Veterinary Medicine, University of Baghdad, Iraq.
Asmaa H. Abdullah
Department of
Microbiology, College of Veterinary Medicine, University of Baghdad, Iraq.
Ansam K. Mohammed
Department of
Microbiology, College of Veterinary Medicine, University of Baghdad, Iraq.
Roua J. Mohammed
Department of
Microbiology, College of Veterinary Medicine, University of Baghdad, Iraq.
Please
see the book here:- https://doi.org/10.9734/bpi/rpbs/v5/2612
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