Faculty of Veterinary Science
The University of Sydney
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Research Projects - Cattle

  1. Dam mutants of S. typhimurium as modified live vaccines in calves
  2. Bovine Pink Eye
  3. Prevention and Treatment of Environmental Mastitis

Dam mutants of S. typhimurium as modified live vaccines in calves

 
Farm Animal Health Staff Associate Professor John House
National Collaborators Dr Keith Walker
Dr Michael Hornitzky
Elizabeth Macarthur Agricultural Institute (NSW DPI)
International Collaborators Dr Michael Mahan & Mr Doug Heihoff
University of California, Santa Barbara
BSc(Hons) Student

Ms Jenny Mohler

Summary Salmonellae are important pathogens of animals and man. They can cause food poisoning in humans upon consumption of contaminated meat and animal products. This proposal is based on our previous discovery that Salmonella typhimurium containing mutations in the dam gene that prevent DNA adenine methylase (dam) expression are virulent yet confer protective immunity as modified live vaccines in murine, avian, and calf models of typhoid fever. One of the principal challenges to the development of commercial livestock vaccines is that multiple Salmonella strains are often endemic on farms, and traditional vaccines normally elicit protection against a single strain. We have recently shown that dam mutant Salmonella confer cross-protective immunity to multiple Salmonella strains when used as modified live vaccines in murine and avian models of typhoid fever.

Specific aims include:

  • to determine if Salmonella dam mutant vaccines can confer cross-protective immunity against multiple Salmonella isolates in calves. A principal concern with all modified live vaccines is safety.
  • to introduce additional attenuating mutations (e.g., aroA) to reduce the virulence capacity of the Salmonella dam vaccine without compromising efficacy in calves.
  • to determine if Salmonella dam vaccines can be used as a platform for delivering passenger antigens to elicit protection against the cognate pathogen. We have chosen the Enterotoxogenic E. coli (ETEC) K99 fimbriae as a model passenger antigen since ETEC strains that express K99 fimbriae account for nearly all cases of ETEC infection in newborn calves and K99 fimbriae are a known immunogen that confers protective immunity against clinically relevant ETEC infections in calves and other species. The K99 fimbriae antigen from ETEC clinical isolates will be expressed in dam Salmonella. Vaccine efficacy will be assessed by elicitation of protective immunity against ETEC diarrheal disease in calves via passive colostral transfer of protective antibodies from vaccinated cows.
  • to develop safe and effective vaccines against Salmonella infection of cattle, and to demonstrate that this vaccine platform may be used to express cognate antigens from other pathogens thereby promoting the health and productivity of livestock, reducing Salmonella contamination of livestock, livestock-derived food products, and enhancing food safety.
Source of Funding United States Department of Agriculture
Project
Timeframe
Continuing

Bovine Pink Eye

 
Farm Animal Health Staff Associate Professor John House
National Collaborators 25 Veterinary Practices from around Australia
International Collaborators Dr John Angelos,
University of California, Davis
Masters Student Mr Craig McConnell
Summary Infectious bovine keratoconjunctivitis (IBK) is considered the most common ocular disease of cattle throughout the world. IBK is important both in terms of animal welfare and as a cause of lost production.

Despite the susceptibility of the causative bacterium Moraxella bovis, to a large number of antimicrobial compounds the treatment of affected cattle has many disadvantages and the prevention of IBK is therefore preferable. M. bovis virulence factors include the production of leukotoxin, protease, and β-hemolysin along with the presence of fimbriae on the bacterial cell surface that play a role in adherence. M. bovis fimbrial proteins act as immunogens and vaccination with isolated fimbriae stimulates bovine anti-fimbrial antibodies. However, strains of M. bovis are known to differ in their fimbrial antigens, with two types of fimbriae identified along with at least seven distinct serogroups of fimbriated M. bovis. Efficacious application of fimbrial based IBK vaccines requires production of a polyvalent vaccine targeting specific regional isolates.

The aims of this project are:

  • to conduct a survey of Moraxella bovis strains in Australia to determine the prevalence of different serotypes across the country
  • to determine which virulence attributes are common to most isolates
  • to design a pink eye vaccine applicable to prevention of bovine infectious keratoconjunctivitis in Australia.
Source of Funding Schering Plough Animal Health
Project Timeframe Completed - January 2006

Prevention and Treatment of Environmental Mastitis

 
Farm Animal Health Staff

Associate Professor John House

Masters Student Ms Lucy Shum
Summary

The prevalence of contagious mastitis in dairy cattle has dropped over the last 20 years. Environmental mastitis subsequently accounts for the largest proportion of intramammary infections and the associated losses in production. Surveys of mastitis conducted in Australia have reported that Streptococcus uberis is the most frequent environmental mastitis pathogen and suggest that coliform mastitis is relatively infrequent in Australian dairy cattle. These prevalence surveys have been conducted in Victoria and reflect the prevalence of disease in pasture fed dairy cattle.

Over the last 10 years there has been a steady and continuing trend toward intensification of the dairy industry with more farms providing supplementary feeding and some farms feeding total mixed rations similar to dairy production systems in Europe and the United States. Working with intensive dairy production systems in NSW we have observed a higher incidence of coliform mastitis than reported in Victorian surveys.

The objective of this study is to determine the prevalence of different mastitis pathogens on intensive dairies in NSW and to investigate the interaction between diet and environment on the major groups (coliforms and streptococci) of environmental pathogens.

Source of Funding Pfizer Animal Health
Project
Timeframe
January 2004 - December 2006