Dominant serotype strains of a riemerella anatipestifer disease area and its application
A technology of Riemerella anatipestifer and Mergerella anatipestifer, applied in the directions of bacteria, antibacterial drugs, bacterial antigen components, etc., can solve the problems of easy generation of drug resistance, food safety, drug residues, etc., and achieve easy promotion and pertinence. Strong, virulent effect
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Embodiment 1
[0029]An epidemiological survey was carried out on Riemerella anatipestifer to obtain the dominant serotype of Riemerella anatipestifer, and then 126 strains of Riemerella anatipestifer isolated from different areas in Hubei Province were analyzed by culture characteristics, Morphological characteristics, biochemical characteristics, serotype identification, virulence test and immunogenicity test, and two dominant serotype strains with strong pathogenicity and good immunogenicity were screened. The specific preparation method is as follows:
[0030] 1. Source of disease materials: Tissues with typical lesions such as pericarditis, perihepatitis, and air sacculitis that were submitted or collected from duck farms in Xinzhou, Hubei, clinically with neurological symptoms, and autopsyed.
[0031] 2. Main reagents: Tryptic Soy Agar (TSA) and Tryptic Soy Broth (TSB) were purchased from Difco Company; MacConkey Agar was purchased from Hangzhou Microbial Reagent Co., Ltd.; calf serum ...
Embodiment 2
[0038] Example 2 Application of regional dominant serotype strains of Riemerella anatipestifer
[0039] Inoculate suitable culture medium with Riemerella anatipestifer RAHB-1 and Riemerella anatipestifer RAHB-2, harvest the culture, inactivate it with formaldehyde, add aluminum hydroxide glue and mix to make aluminum hydroxide glue seedling. It is used to prevent Riemerella anatipestifer, that is, duck serositis.
[0040] 1. Preparation of bacterial solution for vaccine production: Inoculate Riemerella anatipestifer RAHB-1 and Riemerella anatipestifer RAHB-2 into TSB containing 5% calf serum respectively, and culture on a shaker at 37°C for 24-48 hours , mixed at a volume ratio of 1:1 to obtain a mixed bacterial solution. Sampling for pure inspection and counting of live bacteria, according to "People's Republic of China Veterinary Pharmacopoeia (2010 Edition)" appendix 42 for pure inspection, should be pure. Count live bacteria according to Appendix 19 of "The Veterinary Ph...
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