Literature DB >> 9645317

Differentiating turkey postvaccination isolants of Pasteurella multocida using arbitrarily primed polymerase chain reaction.

B A Hopkins1, T H Huang, L D Olson.   

Abstract

The chromosomal DNA of 29 field isolants of Pasteurella multocida from commercial turkey farms in Missouri and the avirulent Clemson University (CU) and M-9 vaccine strains of P. multocida were tested using the arbitrarily primed polymerase chain reaction (AP-PCR) in combination with 32P-labeled deoxycytidine triphosphate (dCTP) and high-resolution gel electrophoresis. The 29 field isolants of P. multocida were isolated from outbreaks of fowl cholera in turkey flocks in which vaccination with the CU vaccine had been performed within 2 weeks of the isolation, and it was suspected that the outbreak could have been due to the use of the live CU vaccine. The results of this study showed that: 1) the use of the live CU vaccine can lead to the isolation of the vaccine strain if the outbreak occurs within 2 weeks of vaccination; 2) a higher proportion of field isolants collected during 1983 and 1984, when the usage of the CU vaccine strain was highest on Missouri turkey farms, had PCR-amplified product profiles similar or identical to those of the CU vaccine strain compared with the period between 1987 and 1992, when its use was less; and 3) there was no relationship between the PCR-amplified product profiles and the serotype.

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Year:  1998        PMID: 9645317

Source DB:  PubMed          Journal:  Avian Dis        ISSN: 0005-2086            Impact factor:   1.577


  7 in total

1.  Random amplified polymorphic DNA and amplified fragment length polymorphism analyses of Pasteurella multocida isolates from fatal fowl cholera infections.

Authors:  Brad S Huber; Darin V Allred; John C Carmen; David D Frame; David G Whiting; Jason R Cryan; Terry R Olson; Paul J Jackson; Karen Hill; Miriam T Laker; Richard A Robison
Journal:  J Clin Microbiol       Date:  2002-06       Impact factor: 5.948

2.  Acapsular Pasteurella multocida B:2 can stimulate protective immunity against pasteurellosis.

Authors:  J D Boyce; B Adler
Journal:  Infect Immun       Date:  2001-03       Impact factor: 3.441

3.  PlpE Epitopes of Pasteurella multocida Fusion Protein as Novel Subunit Vaccine Candidates.

Authors:  Saied Mostaan; Abbas Ghasemzadeh; Parastoo Ehsani; Soroush Sardari; Mohammad Ali Shokrgozar; Mohsen Abolhassani; Gholamreza Nikbakht Brujeni
Journal:  Adv Biomed Res       Date:  2020-08-28

Review 4.  Advances in diagnosis of respiratory diseases of small ruminants.

Authors:  Sandip Chakraborty; Amit Kumar; Ruchi Tiwari; Anu Rahal; Yash Malik; Kuldeep Dhama; Amar Pal; Minakshi Prasad
Journal:  Vet Med Int       Date:  2014-06-15

Review 5.  Spatial, Temporal, and Demographic Patterns in the Prevalence of Hemorrhagic Septicemia in 41 Countries in 2005-2019: A Systematic Analysis with Special Focus on the Potential Development of a New-Generation Vaccine.

Authors:  Reyad Almoheer; Mohd Effendy Abd Wahid; Hidayatul Aini Zakaria; Mohd Anuar Bin Jonet; Muhanna Mohammed Al-Shaibani; Adel Al-Gheethi; Siti Nor Khadijah Addis
Journal:  Vaccines (Basel)       Date:  2022-02-17

6.  Screening of 71 P. multocida proteins for protective efficacy in a fowl cholera infection model and characterization of the protective antigen PlpE.

Authors:  Tamás Hatfaludi; Keith Al-Hasani; Lan Gong; John D Boyce; Mark Ford; Ian W Wilkie; Noelene Quinsey; Michelle A Dunstone; David E Hoke; Ben Adler
Journal:  PLoS One       Date:  2012-07-05       Impact factor: 3.240

7.  In silico Analysis of Pasteurella multocida PlpE Protein Epitopes As Novel Subunit Vaccine Candidates.

Authors:  Saied Mostaan; Abbas Ghasemzadeh; Parastoo Ehsani; Soroush Sardari; Mohammad Ali Shokrgozar; Mohsen Abolhassani; Gholamreza Nikbakht Brujeni
Journal:  Iran Biomed J       Date:  2020-01-04
  7 in total

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