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National Programs Food Safety, (animal and plant products)
National Program Annual Report:
FY 1999

Food Safety (animal & plant products)
National Program # 108 Annual Report
Fiscal year: 1999
Introduction
The ARS food safety research program significantly expanded in 1999 with a budget increase of $11.72 million, $7.3 million for preharvest research and $4.42 million for postharvest research. The funds were directed for research in the areas of: manure handling and distribution, risk assessment, antibiotic resistance, fungal toxins, zoonotic disease risk, pathogen control during slaughter and processing, pathogen control in fruits and vegetables, and antimicrobial resistance.

During fiscal year 1999, four new research programs were initiated: a molecular systematics and diagnostics program for parasites in foods and food animals; a food safety-engineering program at Purdue University, for the development of new technology and systems to detect and prevent chemical and microbial food contaminants; a food safety-remote sensing program with the Institute for Technology Development, Stennis Space Centre, specifically focused on the development of imaging technology on-line for the inspection of poultry products during processing; and a Food Safety Research Information Office at the USDA National Agricultural Library.

In fiscal year 1999, ARS held several workshops to help relate the research progress in the program to customer and stakeholder needs. The 11th Annual Aflatoxin Elimination Workshop held October, in St. Louis, Missouri updated the peanut, corn, cottonseed and tree nut industries on ARS supported research progress made to control aflatoxin in these commodities. ARS in conjunction with CSREES, held the Congressionally mandated National Conference on Food Safety Research, in November in Alexandria, Virginia. The purpose of the meeting was to assess the research needs of a variety of audiences, from federal regulatory agencies, producers, processing and handling companies, retailers, consumers and consumer agencies. The 19th Annual ARS-FSIS Research Program Planning Meeting held in December in Athens, Georgia, brought together ARS scientists and FSIS staff for a research progress update, and discussion of FSIS needs for meeting their regulatory responsibilities.

The National Program Staff conducted the ARS Food Safety National Program Program Planning Workshop in February 1999, at Wyndmoor, Pennsylvania, to identify specific program research priorities and objectives. A second National Planning Workshop to address the research needs of the Produce and Imported Foods Safety Initiative (PFSI) was held in May 1999, in Monterey, California. A 5-year Action Plan was developed from the Workshops and is available on the World Wide Web: www.nps.ars.usda.gov/programs/108/action plan. Research progress with regards to three of the National Program components, microbial pathogens, residues and toxic plants was documented in the 1999 Progress Report on Food Safety Research Conducted by ARS, provided both in hardcover form, and on the World Wide Web: www.nps.ars.usda.gov/programs/108/progress report.

Microbial Pathogens
Determining how to reduce microbial pathogens in food products, throughout food operations from farm to fork, is the most urgent food safety problem today. The major pathogens addressed were the bacterial pathogens Salmonella, Campylobacter, E. coli 0157:H7 and related EHEC, Shigella, Listeria, Yersinia, Aeromonas, Arcobacter, Vibrio and Clostridium; the parasites Cryptosporidium and Toxoplasma; and various viruses, hepatitis A Norwalk and Norwalk-like. Important new research programs were initiated in detection of parasites in foods, control of pathogens in animal manure, understanding and control of antibiotic and antimicrobial resistance, fruits and vegetables, on-line imaging, and biosensor technology.
Prevention of Salmonella in swine. Salmonella carried in the gut of swine can cause foodborne illness in humans due to consumption of contaminated meat products. ARS scientists have developed and patented a culture of normal intestinal bacteria from adult swine that can competitively exclude pathogenic bacteria in the pig gastrointestinal tract. The culture has been shown to significantly reduce levels of Salmonella in the gut of newborn and weaned pigs and significantly reduce the transmission of the pathogen between penmates. When used within the framework of current swine production practices, it should provide an effective tool to decrease Salmonella in pork products and help to further protect public health.

Early exposure of beef calves to E. coli O157:H7. ARS scientists demonstrated that most beef calves are exposed to E. coli O157:H7 even in relatively isolated range environments. This exposure occurs prior to weaning, shipping, and mixing with calves from diverse sources, circumstances which commonly contribute to exposure to infectious agents. Thus, in order to prevent calf infections with E. coli O157:H7, interventions must be implemented early in the life of the calf. This information will help target the timing of procedures to prevent infection of calves with this dangerous zoonotic pathogen.

Protection against Salmonella infections in broiler birds. During the first 7-14 days after hatch, poultry has an immune system that is functionally immature, with only limited capability to respond to pathogenic infections. Thus newly hatched chicks are extremely susceptible to infection with zoonotic pathogens such as Salmonella. ARS scientists demonstrated that administration of Salmonella enteritidis-immune lymphokines (SILK) to day-old chickens and turkeys, by routes routinely used by the industry for vaccines, conferred protection to the birds against localized enteric Salmonella infections, and hastened immune system development. Prophylactic administration of SILK can reduce the incidence of Salmonella in broiler birds and thus help to protect the public health.

Detection of Salmonella typhimurium DT-104 using a unique antibiotic resistance gene. Salmonella typhimurium DT-104 is a highly pathogenic, foodborne bacteria that is difficult and time-consuming to identify. ARS scientists discovered that DT-104 contains a unique gene, which they named St-flo, that confers resistance to the antibiotics chloramphenicol and florfenical. They developed a DNA-based detection system with nearly 100% sensitivity and specificity for detection of the St-flo gene, which allows identification of the pathogen in 2 days. Rapid detection of DT-104 is important to identify outbreaks, to identify individuals for treatment, and to protect the public health.

Color of cooked beef patties and the food safety risk. Previous USDA advice to consumers on cooking hamburgers was lack of pink/red color equaled done and safe. This advice however, may have been oversimplistic, since patties subjected to grilling may lose their red color (premature browning), but not yet have reached a temperature high enough to destroy pathogenic bacteria, such as E. coli O157:H7. To determine when color gives false information, ARS collaborated with the Food Safety Inspection Service to determine when premature browning occurs, by using meat stored frozen or nonfrozen, and thawed either in the refrigerator, at room temperature, or by microwave. The studies showed that thawed ground beef produced more brown color when cooked than patties cooked either fresh or rapidly thawed. The USDA now advises that cooked beef patty color is not a good indicator of safe food and that consumers should not eat ground beef patties that are pink or red in the middle unless a food thermometer has been used to verify cooked temperature.

Treating surfaces to resist pathogens. New methods are being devised to make inanimate surfaces in the processing areas more resistant to bacterial contamination. ARS scientists tested various methods of treating stainless steel, including sanding, grinding, polishing, and electrochemical, to determine which method best inhibited bacterial attachment. Stainless steel samples that had been electropolished showed the most significant reduction in bacterial attachment. This will aid manufacturers in designing and producing equipment that is not conducive to bacterial growth.

Rapid Test for E. coli O157:H7. The presence of pathogenic bacteria at any stage of food production, processing, and distribution must be determined quickly in order to allow proper treatment of the food before consumption by the general public. ARS scientists in cooperation with IGEN of Gaithersburg, Maryland, developed an immunomagnetic-electrochemiluminescent test for the detection of as few as a single E. coli O157:H7 bacterium in 25 grams of ground or unground beef. The inexpensive, user-friendly test can be conducted in less than 8 hours and is 100 times more sensitive than tests currently available. This test will allow detection and quantification of this important pathogen, thus ensuring a safe food supply and protecting public health.

Epidemiology of Salmonella and Campylobacter in broilers. Although the incidence of Salmonella and Campylobacter in broilers has been decreasing, further measures are needed to assure a safe food supply. ARS conducted a nationwide epidemiology study of Salmonella and Campylobacter in broilers to: identify the most importance sources of Campylobacter and Salmonella in the production environment, and determine intervention strategies that effectively reduce transmission and limit consumer exposure to Campylobacter and Salmonella. The results of this study has allowed development of a commercial scale trial that targets four control points to further reduce the levels of pathogens on poultry; these are hatching cabinet disinfection, consistent use of new paper pads for newly hatched chickens, competition exclusion, and litter treatment in the production house.

Rapid detection of antibiotic resistant Salmonella. Rapid methods are needed to identify multi-drug antibiotic resistant bacteria, such as, Salmonella typhimurium DT104 in food producing animals and their environment. ARS determined that the resistance to the antibiotics florfenical and chloramphincol are conferred by the flo gene. Presumptive identification of this multiresistance can now be made rapidly based on the presence of the gene and its resulting phenotype. This information will enhance the development of a rapid test kit to identify DT104 in a timely manner, and slow its spread to food products.

Using competitive exclusion for pathogens in swine. A competitive exclusion culture was developed to control Salmonella and other enteropathogens in swine. This culture significantly reduced mortality in baby and weaned pigs, and in addition significantly reduced mortality associated with pathogenic E. coli in very early-weaned pigs. The individual bacteria have been isolated and a recombined culture has been developed that has the same efficacy as the original culture. Specific identification of the bacterial components of such cultures is necessary to allow reproducibility of results and for FDA approvals.

Contamination of the Chesapeake Bay. ARS research to characterize the extent and distribution of Cryptosporidium parvum oocysts in Chesapeake Bay indicates that oysters from all monitoring sites are contaminated and contain viable oocysts. A real-time fluorescent-probe based PCR assay was developed for the detection of oocysts in less than two hours, with a detection limit of 5 to 100 oocysts depending on whether the water is clear or turbid. By detecting C. parvum ARS has shown that shellfish can be good indicators of fecal pollution of surface waters and that oysters pose a public health risk if eaten raw. Sequencing of the PCR products from some oysters indicates that the oocysts are C. parvum, bovine genotype. Utilizing PCR testing for detection of Cryptosporidium increases our ability to detect lighter infections and to differentiate species infectious for humans versus those noninfectious for humans and in some cases to determine the source of the fecal contamination.

Broiler transportation. Studies compared conventional solid to elevated wire mesh flooring during transport and holding of poultry broilers prior to slaughter. Results indicated that although broilers transported and held on solid flooring had noticeably dirtier breast feathers and higher coliform and E. coli counts prior to scalding and defeathering, bacteria recovery from external carcass rinses did not differ between the solid and wire flooring treatments after defeathering. The processing steps of immersion scalding and defeathering consistently lowered carcass bacteria counts and the incidence of Campylobacter-positive, but not Salmonella-positive carcasses.

Cold shock sensitizes pathogens in fruit juices. Research showed that a sensitizing cold treatment prior to thermal processing increased the effectiveness of the thermal process for the destruction of L. monocytogenes, E. coli O157:H7 and S. typhimurium in juices. The inducible and enhanced vulnerability to heat in model and food systems shows the potential for this approach to be used by the food industry as a practical and efficacious post-processing intervention strategy to eliminate these bacterial pathogens. Cold shock prior to pasteurization of fruit juices could provide an extra measure of safety and would also allow juice processors to reduce thermal processing requirements for pathogen control, while maintaining the fresh qualities of the juice.

Heat resistance of Listeria monocytogenes. Studies were performed to determine the heat treatment required to kill L. monocytogenes. The data was used to develop a mathematical model for determining the effects of environmental parameters on thermal resistance of the bacterium. Using this predictive model, food processors should be able to design thermal processes for the production of a safe food with extended shelf life without substantially adversely affecting the quality of the product.

New method for detecting E. coli in ground beef. A procedure to rapidly detect the E. coli in beef hamburger patties was developed. Streptavidin coated magnetic beads and biotin-labeled anti E. coli O157 antibodies were used to capture the bacteria, which were further immobilized on biotinylated nitrocellulose membrane sticks. The bacteria were further treated with fluorescein-labeled anti E. coli O157 antibodies and urease conjugated anti fluorescein antibody. Urease catalyzed production rate of NH3 from urea was then determined. The approach allows detection of E. coli O157:H7 at a level of ~1 CFU/g after a six-hour enrichment. The approach may be applied for field use, that is, sample collection from remote locations away from central laboratories, since the immobilized bacterial samples are stable for 48 h at 4C without significant changes in signal.

Color as an indicator of hamburger safety. ARS research resulted in the FSIS issuing a message to consumers that "consumers should not eat ground beef patties that are pink or red in the middle unless a food thermometer has been used to verify cooked temperature". Subsequent surveys indicate that most consumers either do not own a meat thermometer or if they own one, do not use it in cooking meat products. Thus, additional joint ARS-FSIS studies on premature brown color in cooked beef patties were conducted, focusing on:

(1) the use of outdoor gas grills as the cooking equipment and,

(2) temperature and color changes post-cooking and before consumption. Results indicated that internal color of patties prepared and cooked under these conditions is even less reliable as an indicator of food safety. A workshop held in Washington, DC in November 1998 resulted in the formation of a Food Temperature Indicator Association to conduct research and perform consumer affairs regarding temperature devices. Also several major retailers, for example, Giant food stores have initiated ground beef thermometer usage programs employing ARS-FSIS research findings on safe cooking of beef patties.

Apple decontamination. The efficacy of commercial brush washing equipment, used in conjunction with conventional and experimental washing and sanitizing agents, in decontaminating apples was investigated in a commercial cider mill operated in Placerville, California. Results indicated that brush washing in the presence or absence of washing and sanitizing agents did not significantly reduce the bacterial population on apples or in cider. Cider contamination probably resulted from the inability of such washing systems to inactivate or remove microorganisms in inaccessible calyx and stem areas of apples.

E. coli O157:H7 contamination of apples used for cider. Studies were conducted to determine whether areas of decay in grounder apples ("drops") may be a potential source of E. coli O157:H7 in apple cider made from such fruit. Wounds in fresh apples inoculated with this human pathogen and one of two decay fungi, Penicillium expansum or Glomerella cingulata indicated that the P. exapansum fungus was antagonistic to the bacteria. However, apple wounds containing G. cingulata and E. coli O157:H7, showed extensive bacterial growth. Since the extent of growth of E. coli O157:H7 in the presence of Glomerella would be sufficient to contaminate a large quantity of cider, these results clearly demonstrate the potential risk of using decayed apples for production of unpasteurized cider.

Decontamination of sprouts. Research on novel combination treatments for decontamination of alfalfa seeds was conducted, and several alternative treatments were realized. A combination of treatments using gamma irradiation followed by chemical sanitizing with 2% calcium hypochlorite yielded a 5 log reduction in the population of Salmonella on inoculated seeds, a reduction level that could not be achieved with the individual treatments alone. The efficacy of 20,000 ppm chlorine in sanitizing seed contaminated with E. coli O157:H7 was confirmed. Data generated on the use of 2% calcium hypochlorite was used in support of a successful joint USDA/industry petition to the EPA to allow use of this agent for sanitizing seed destined for sprouting. This technology is now widely used in the U.S. sprouting industry. The combination treatment strategy should enable sprout growers to achieve FDA goals with current technology if there are no unforeseen regulatory restrictions or economic constraints.

Chemical Residues
The objectives of the chemical residue program are to reduce the risks of chemical residues from animal drugs, food additives, herbicides and pesticides and environmental contaminants that are potentially present in foods. A major goal is to develop reliable, effective, accurate, user-friendly, cost-effective residue detection methodology that requires minimal amounts of organic solvents to detect these residues.
Immunoassays for rapid analysis of drug residues in food animal products. Modern agricultural practices rely heavily on the use of chemicals and veterinary drugs to maintain high levels of production as well as pest-free and disease-free products. However, chemical residues in meats, poultry, and feeds represent a serious food safety problem, since many chemicals are known to have adverse health effects in humans, such as the development of allergies. ARS scientists have developed several immunological-based tests to assay for a variety of drugs and chemicals, for example, the antibiotic Ceftiofur, the anticoccidial drug Halofuginone, the anticoccidiostat feed additive Salinomycin, the coccidiostat Monensin, the antibiotics sulfathiazole, sulfamethazine, and sulfadimethoxine, and the natural toxicants found in potatoes and tomatoes (alpha-soladine and alpha-tomatine). The immunoassays are designed in simple, inexpensive, noninstrumental kit form that requires no organic chemicals and has a sensitivity equal to the traditional chemical-based assays. These immunoassays will allow increased monitoring at all levels of food production to ensure that no residues are present or that residue levels are below the established tolerances for good health.

Detection of dioxins. ARS has developed a rapid, inexpensive immunoaffinity column (IAC) clean-up method for the detection of polychlorinated dibenzo-p-dioxins (PCDDs) and related compounds, from serum samples. Studies showed that several of the most toxic PCDDs bound to the IAC, and the congeners could be readily eluted before analysis by high resolution gas chromatography-high resolution mass spectrometry. Addition of a prewashing step before applying the sample, dramatically increased the recovery of 2,3,7,8-TCDD from 16% to 83%. Verification studies of samples provided by the CDC indicated that six dioxin and furan congeners were quantitated within the 95% confidence limits of the method at the part-per-quadrillion (ppq) level. This simpler technology will be of importance to regulatory agencies and other scientists for reducing the time and costs associated with dioxin analysis, presently $1000/sample.

Mycotoxins
The presence and potential for the presence of mycotoxins in crops is not only a direct food safety problem, but it threatens the competitiveness of U.S. agriculture in the world market. Major goals were to control aflatoxin in peanuts, corn, cottonseed, tree nuts and figs; fumonisins in corn; and deoxynivalenol in wheat and barley through an understanding of the biology of plant-fungus interactions and toxin production in the field.
Gene identified for the biosynthesis of the important fungal toxin fumonisin. Fumonisins are a family of structurally related toxins produced by molds in the genus Fusarium. The toxins are usually found on grains such as corn, and appear to affect a wide variety of different animals. The gene FUM-5 that is essential for the biosynthesis of fumonisins was recently identified, cloned and characterized by ARS scientists. This is the first gene for fumonisin to be identified and studied. By altering FUM-5, strains of the fungus that cannot make fumonisin can be identified and used as tools to develop potential biological control agents and to determine the role of fumonisins in the infection and disease processes in corn. Control of fumonisins, which are currently being more closely scrutinized by the Food and Drug Administration can help keep the food supply safe for consumers.

Automated system for detection and removal of pistachios contaminated with aflatoxin. Aflatoxins are a family of structurally related toxins produced by molds in the genus Aspergillus. The toxins are usually associated with tree nuts, peanuts, corn, and cottonseed and affect a wide variety of different animals, including humans. ARS scientists developed an automated system that identifies and removes aflatoxin containing pistachio nuts from packing house production lines. The high-speed processing software and hardware is linked to sorters equipped with digital image cameras, instead of conventional color sensors. The system allows highly accurate, real-time sorting of the nuts, reduces losses from sorting errors, ensures edibility, and increases marketability of the pistachio nuts especially in countries with stringent aflatoxin standards. Prototypes of the imaging system are currently being tested at a major pistachio processing plant in central California.

Toxicity studies of fumonisins help to establish regulatory guidance. Several diseases of farm animals are caused by toxic metabolites produced by Fusarium moniliforme associated with major crops, particularly corn. The Food and Drug Administration (FDA) is concerned about levels of the toxin, fumonisin B1, in grain and may issue regulatory guidance. ARS scientists directly contributed to the design and successful completion of chronic toxicity and carcinogenicity studies of fumonisin B1 in rats and mice, as well as teratology studies of the mycotoxin in rabbits and rats. These studies showed that fumonisin B1 is carcinogenic in rodents, provided target organ and dose-response data, and also showed that fumonisin is not teratogenic. The data is critical for completion of FDA risk assessments to protect the public health.

Marker strains of Aspergillus flavus facilitate crop resistance determination. Aflatoxins are natural poisons produced by two common fungi, Aspergillus flavus and Aspergillus parasiticus. These fungi invade crops such as, corn, peanuts, cotton and treenuts, and produce aflatoxins, thus making the crops unfit for sale under the existing regulatory guidelines. ARS scientists have developed marker strains of A. parasiticus to monitor the progression of aflatoxigenic fungi during invasion of corn and cotton and their ability to make toxin. These marker strains of the fungus allow the rapid screening of germplasm of the affected crops, both in the laboratory and in the field, to determine its resistance to funal invasion and toxin formation.

Disrupted fungal gene will help determine toxin biosynthesis pathway. The fungus Fusarium graminearum that causes Fusarium head scab also produces the toxin deoxynivalenol (DON), that is harmful to humans and animals that eat toxin contaminated food or feed. ARS scientists have cloned the TRI101 gene from Fusarium graminearum, and by gene disruption, identified its role in DON biosynthesis and toxin resistance. Mutant strains with a disrupted TRI101 gene will be useful as tools to identify additional toxin resistance genes in Fusarium and to determine the DON biosynthesis pathway, thus leading to effective control strategies.

Natural resistance to aflatoxin formation found in Tulare walnuts. Contamination of tree nuts by aflatoxins produced by the fungi, Aspergillus flavus and Aspergillus parasiticus, is a serious problem because of the potential threat to human health and the resulting stringent regulatory levels imposed for these toxins. The current US guideline set by the FDA is 20 ppb total aflatoxins, however, the European Community has instituted a standard of 2 ppb aflatoxin B1 and 4 ppb total aflatoxins. ARS research has demonstrated a significant difference in the ability of almonds and walnuts to support aflatoxin production, and there is further significant varietal difference within each crop. In these studies the Tulare variety of walnut completely suppressed aflatoxin production, which is the first example of a commercial variety of any susceptible crop plant that shows complete resistance to aflatoxin. This information suggests that selections of tree nut breeding lines for aflatoxin resistance can be effectively made.

Spatial reference of Aspergillus flavus fungal communities aids assessment of aflatoxin control strategy. Because an aflatoxin management strategy to modify the Aspergillus flavus community structure is being implemented over thousands of acres in Arizona, it is important to understand the spatial characteristics of communities of this fungal. Soil samples were collected statewide, and spatially referenced using GPS. These samples were used to characterize A. flavus communities statewide by both incidences of A. flavus S strain and by regional shifts in S strain incidence over time. This work provides the framework that to assist both the assessment and implementation of aflatoxin management programs based on reducing toxigenic A. flavus communities.

Toxic Plants
This program component seeks to minimize the exposure of animals and humans to natural toxins from poisonous plants.
Reduction of abortions in cattle caused by ingestion of Ponderosa Pine . Ponderosa Pine needles cause multimillion dollar losses to the cattle industry in widespread areas of the western ranges. ARS scientists recently identified the Ponderosa Pine needle toxin, isocupressic acid, as the causative agent of last trimester abortion/premature births and retained placenta in cattle. Studies showed that upon ingestion, isocupressic acid is metabolized to at least four major metabolites. Identifying when the pine needles are toxic and developing grazing strategies to reduce ingestion of toxic plants by cattle are crucial since programs have been unsuccessful in averting cattle to grazing green pine needles. This information will also allow enhanced utilization of western ranges for grazing by cattle.

Utilizing tall larkspur without toxic effects Larkspur (Delphinium spp.) is toxic to grazing cattle and causes serious losses to livestock producers in western ranges. ARS research established that toxic alkaloid levels in tall larkspur vary between species, locations and over the growing season, however, the alkaloids appear to be synthesized in the first 3-4 weeks of growth followed by dilution of concentrations as the plants continue to grow throughout the season. Understanding such patterns will help predict the potential toxicity of larkspur populations to susceptible grazing livestock.

Identification of low dose effects of locoweed will aid decisions on range management Locoweed (species of Astragalus and Oxytropis) is a major management problem for cattle ranchers since it causes abortion, weak calves at birth, and weight loss in the stocker-yearling herd. ARS research demonstrated that alkaline phosphatase and serum iron levels change very quickly (within 24 hours of initial exposure to swainsonine) and these changes occur prior to changes in other cellular damage markers. This indicates that swainsonine alters cellular metabolism and nutrient utilization, and that this may occur before tissue damage or clinical signs are present. This information will help ranchers make more informed management decisions on utilization of ranges.

 

Program Summary
   Program Direction
   Program Rationale
   Program Component Definitions
   Projected Outcomes

Action Plan
  Action Plan

Program Annual Reports
  FY 2003
  FY 2002
  FY 2001
  FY 2000
  FY 1999
  FY 1998


Project Information
   List of Projects in this Program
   List of Project Annual Reports in this program

Program Team
  Lindsay, James A
(co-leader)
  Robens, Jane F
(co-leader)
 
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