The University of Tennessee
Institute of Agriculture
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Mathew

 

Professor
Co-Director The University Of Tennessee
Food Safety Center of Excellence
59 McCord Hall
Phone: (865) 974-7260
FAX: 865-974-9043
Email: soliver@tennessee.edu

Research Appointment: 85%
Teaching Appointment: 15%

EDUCATION and TRAINING

B.S. 1976 North Carolina State University, Animal Science
M.S. 1978 The Ohio State University, Dairy Science
Ph.D. 1980 The Ohio State University, Dairy Science

RESEARCH INTERESTS

Mastitis in dairy cows is a complex multifactor disease and is likely the most costly disease affecting animal agriculture in the world. Mastitis differs from other animal diseases in that several diverse bacteria are capable of causing the disease. Control is extremely difficult due to diverse types and sources of mastitis pathogens coupled with a poor understanding of bacterial and host factors associated with the disease process. Mastitis caused by environmental pathogens such as Streptococcus uberis is particularly problematic because current methods of control are less effective, often ineffective, against pathogens that are ubiquitous in the dairy farm environment. Consequently, mastitis caused by environmental pathogens remains a serious problem in several herds, and can become a significant problem in dairies that have controlled the more common mastitis pathogens. Research conducted by Dr. Oliver has focused extensively on mastitis in dairy cows, particularly mastitis caused by environmental pathogens such as Streptococcus uberis. Objectives of Dr. Oliver's research are to: 1) characterize factors which affect resistance of the udder to mastitis, 2) characterize factors and mechanisms which permit mastitis pathogens to invade the udder and produce mastitis, 3) develop and evaluate techniques for the prevention and control of mastitis in dairy cows, and 4) characterize dairy food safety issues relevant to mastitis.

RESEARCH ON HEIFER MASTITIS: Dr. Oliver demonstrated that mastitis in pregnant heifers was much higher than previously thought. Many of these infections can persist for long periods, are associated with elevated somatic cell counts, and likely impair mammary development during gestation and affect milk production after calving. Collectively, results of studies on prevention and control of heifer mastitis by Dr. Oliver demonstrated that prepartum intramammary antibiotic infusion of heifer mammary glands a few weeks before calving is an effective procedure for eliminating many infections in heifers during late gestation and for reducing the prevalence of mastitis in heifers both during early lactation and throughout lactation. Prepartum antibiotic-treated heifers produced significantly more milk and had significantly lower somatic cell count scores than untreated control heifers. Prepartum antibiotic treatment to reduce mastitis in heifers during early lactation was economically beneficial. Prepartum antibiotic-treated heifers produced 531 kg more milk than heifers in the untreated control group. Multiplying this increase by a milk price of $0.408/kg yielded a $216.24 per-heifer increase in gross revenue. Subtracting the cost of treatment from gross revenue (including the cost of testing for antibiotic residues), the net revenue from the actual production increase amounted to $200.64 per heifer.

IDENTIFICATION AND CHARACTERIZATION OF STREPTOCOCCAL VIRULENCE FACTORS: RELATIONSHIP WITH IMMUNITY TO MASITITS IN DAIRY COWS:Relationship with Immunity to Mastitis in Dairy Cows: Another very active area of research in Dr. Oliver's laboratory is identification and characterization of streptococcal virulence factors and their relationship with immunity to mastitis. Nonantibiotic approaches for the prevention and control of environmental mastitis in dairy cows is an appealing concept. Studies aimed at development of new vaccines against mastitis pathogens that are refractory to current methods of mastitis control are likely to have huge payoffs in the future as use of antibiotics in the dairy industry come under greater scrutiny by federal regulatory agencies. Initial studies have focused primarily on Strep. uberis. In many dairy herds, Strep. uberis is responsible for a high proportion of clinical and subclinical mastitis in lactating cows, and is the predominate organism isolated from mammary glands during the nonlactating period. Strategies for controlling Strep. uberis mastitis are poorly defined and currently inadequate. Objectives focus on: 1) genotypic characterization of Strep. uberis; 2) phenotypic characterization of Strep. uberis with particular reference to bacterial cell surface components and factors involved in bacterial adherence and invasion; 3) development of a Strep. uberis experimental infection model to characterize the infection process, and to facilitate evaluation of new control strategies; and 4) evaluation of the immune response and efficacy of experimental vaccines for the prevention of Strep. uberis mastitis following immunization of dairy cows with novel streptococcal antigens. Dr. Oliver's research group has identified several potential Strep. uberis virulence factors. These include: hyaluronic acid capsule surrounding the bacterium; binding to extracellular matrix proteins such as laminin, collagen, and fibronectin; and bacterial synthesis and secretion of collagen-binding protein, lactoferrin-binding protein and M-like protein.

DNA FINGERPRINTING FOR RAPID & ACCURATE DETECTION OF PATHOGENS: Dr. Oliver's laboratory developed DNA fingerprinting techniques for identification of several mastitis pathogens including Streptococcus, Enterococcus, and Staphylococcus species. These procedures have been used to separate new from persistent intramammary infections by subtyping pathogens. The same subtype of Strep. uberis or Strep. dysgalactiae was detected from some mammary glands from one lactation to the next. DNA fingerprinting procedures developed in Dr. Oliver's laboratory have also been used as a tool to establish the role of horn flies in the transmission of Staph. aureus mastitis in heifers. A Staph. aureus strain with a characteristic DNA fingerprint pattern was used as a marker strain to determine if horn flies served as a vector in the transmission of Staph. aureus mastitis in heifers. When Staph. aureus colonized horn flies were allowed to feed on teats of uninfected dairy heifers, intramammary infection with the same Staph. aureus DNA fingerprint subtype resulted. This indicates that horn flies can transmit Staph. aureus to heifer teats if a sufficient source of organisms is present.

DNA fingerprinting techniques developed in Dr. Oliver's laboratory have also been useful in antimicrobial drug and vaccine efficacy studies when attempting to delineate new and persistent intramammary infections. DNA fingerprinting procedures are also being used as epidemiological tools to determine important on-farm sources of mastitis pathogens and foodborne pathogens. A grant proposal funded by the National Pork Board resulted in development of DNA-based methods for rapid and accurate detection of Salmonella cholerasuis and Salmonella typhimurium. Molecular profiles of foodborne pathogens are being evaluated in a study funded by the Food and Drug Administration to define their distribution within and among livestock production areas and to determine the environmental sources of specific subtypes in different geographic regions. This information will also be useful to track movement of specific subtypes from one geographical production region to another. The relatedness of foodborne pathogens isolated from dairy farms can be compared with existing national databases on human pathogens isolated from cases of foodborne illness or foodborne disease outbreaks.

INTERACTION OF MASTITIS & REPRODUCTIVE PREFORMANCE: Even cows from well-managed dairy herds utilizing the most recent and most effective mastitis control measures experience mastitis, especially during the 1st 90 days of lactation. Collaborative research with Dr. F. Neal Schrick of the Department of Animal Science at The University of Tennessee has shown that mastitis significantly impairs reproductive performance of dairy cows. Reproductive efficiency is of great concern to dairy producers because reduced reproductive performance is associated with a great monetary loss. These losses are in addition to costs associated with mastitis such as decreased milk production, altered milk composition, treatment costs, discarded milk, increased involuntary culling rate, etc.

We recently reported that Jersey cows with clinical and/or subclinical mastitis during early lactation exhibited a prolonged period until 1st service opportunity than cows with no clinical mastitis. Additionally, an increased number of days open and services/conception were observed in cows with clinical or subclinical mastitis between 1st service and establishment of pregnancy compared to cows not experiencing clinical mastitis or cows with clinical mastitis either before 1st service or after pregnancy was confirmed. We found no differences between effects of mastitis due to contagious or environmental pathogens on either days to 1st service, days open, or services/conception. Results suggest that clinical and subclinical mastitis during early lactation can have a profound effect on reproductive performance of dairy cows.

PREHARVEST FOOD SAFETY RESEARCH: Reports from the Center for Disease Control and Prevention, the Food and Drug Administration and USDA indicate that the risk of foodborne illness has increased markedly over the last 20 years. Today, nearly a quarter of the US population is at higher risk for foodborne illness. Costs associated with foodborne illnesses are exorbitant, estimated to range from $19 billion to $37 billion annually. The situation becomes even more problematic because of rapidly changing demographics, with an increasing number of elderly people and immunocompromised individuals who are more susceptible to foodborne pathogens. The threats are numerous and varied such as E. coli O157:H7 in meat and apple juice; Salmonella in eggs, on vegetables and on poultry; Vibrio in shellfish; Cyclospora and hepatitis A virus on fruit; and Cryptosporidium in drinking water. Much has changed in what we eat and where we eat. Americans are eating a greater variety of foods, particularly poultry, seafood and fresh fruit and vegetables. Americans are also eating more of their meals away from home. This food is purchased and consumed from grocery stores, restaurants, and in institutional settings such as schools, hospitals, nursing homes and day care centers. Consequently, as more people become involved in preparing our meals, the chance for foodborne illness increases dramatically.

In 1998, Dr. Oliver was instrumental in organizing a food safety initiative at The University of Tennessee Institute of Agriculture, which encompasses interdepartmental, multidisciplinary collaborations among researchers, extension personnel and allied personnel in the Agricultural Experiment Station, Agricultural Extension Service and the College of Veterinary Medicine. More recently, Dr. Oliver was primary author of a proposal to establish a Food Safety Center of Excellence at The University of Tennessee that was selected to receive $5 million dollars of University funding. He serves as Co-Director of The University of Tennessee Food Safety Center of Excellence.

The vision for The UT Food Safety Center of Excellence is to be the leader in the state, region, nation, and the world in the development and dissemination of science-based information on timely and relevant food safety issues and concerns that will minimize problems associated with foodborne illness; to significantly impact development of new technologies and economic development; and to enhance research funding, notoriety and prestige for the university. Research and development of educational materials by The UT Food Safety Center of Excellence will be consistent with priority areas defined by the National Food Safety Initiative. Goals are to develop and evaluate strategies to destroy or control foodborne pathogens and reduce the occurrence of foodborne illness; to identify mechanisms associated with development and transfer of antibiotic resistance in foodborne pathogens, and devise strategies that limit occurrence of antibiotic resistant bacteria in foods; to develop nonantibiotic approaches and other novel strategies, such as identification of disease resistant animals, for the prevention and control of diseases of food-producing animals that impact food quantity and quality; to develop strategies to reduce environmental contamination with foodborne pathogens during animal production and food processing through environmental management and risk assessment; and to develop, communicate and disseminate instructional food safety information to students (beginning in K-12), consumers, producers and processors of food products, and the food service industry in Tennessee and nationally.

The primary goal of pre-harvest food safety research conducted by Dr. Oliver's laboratory is to provide comprehensive information on the occurrence of Salmonella, Escherichia coli O157:H7, Listeria monocytogenes, Campylobacter jejuni, and other emerging pathogens on dairy farms under varying management conditions. This information is critical for implementation of on-farm foodborne pathogen reduction programs. A second objective is characterization of foodborne pathogens isolated from milk and dairy beef in a study funded by FDA. Molecular epidemiological patterns and antibiotic resistance patterns of foodborne pathogens isolated from bulk tank milk and from cull dairy cows are being delineated. This information will be useful to track movement of specific subtypes from one geographical production region to another. The relatedness of foodborne pathogens isolated from dairy farms can be compared with existing national databases on human pathogens isolated from cases of foodborne illness or foodborne disease outbreaks. A third area of interest is development of accurate and rapid methods for the detection of foodborne pathogens. A recent grant proposal funded by the National Pork Producers Council resulted in the development of a PCR-ELISA method for rapid and accurate detection of Salmonella serogroups A, B, C1, C2 and D with particular emphasis on Salmonella choleraesuis and Salmonella typhimurium.