Potential for Infiltration, Survival, and Growth of Human Pathogens within Fruits and Vegetables
In the Federal Register of April 24, 1998 (63 FR 20450), FDA proposed to adopt regulations to ensure the safe and sanitary processing of fruit and vegetable juices through implementation of Hazard Analysis Critical Control Point (HACCP) systems. In addition, in the Federal Register of July 8, 1998 (63 FR 37030), FDA published a final rule requiring that juice products not specifically processed to destroy harmful bacteria (i.e., processed to achieve a 5-log reduction in the most resistant pathogen of public health concern) bear a warning statement informing consumers of the potential risk of foodborne illness associated with the product. In the HACCP proposal, the agency proposed to require that juice processors include in their HACCP plans control measures that will produce at least a 5-log reduction in the pertinent pathogen. Prior to the 1998 rulemakings, FDA had sought the advice of the National Advisory Committee on Microbiological Criteria for Foods (NACMCF). In response to FDA's request, NACMCF recommended the proposed 5-log performance standard in order to ensure the safety of juice.
Consistent with NACMCF recommendation, FDA has not proposed a specific intervention technology (e.g., pasteurization) to be used to meet the performance standard. Instead, the agency has proposed a flexible 5-log reduction standard that theoretically could be met for some fruit (e.g., citrus) through cumulative steps. In the April 1998 proposal, FDA stated that steps such as culling, washing, brushing, and sanitizing, followed by extraction processes that minimize contact with the peel, could be used cumulatively to attain the 5-log reduction as long as processors could validate bacterial reduction under their HACCP systems.
At the time of the proposal, FDA believed that such cumulative steps could be appropriate for juices produced from citrus fruit because pathogens were not reasonably likely to be found in the interior of such fruit (63 FR 20450, April 24, 1998). The agency also stated that the acidic nature of citrus fruits could further inactivate any pathogens that may be present in the fruit. However, comments to the proposed rule have questioned the assumption that pathogens are not likely to be found in the interior of citrus fruit. In addition, FDA conducted a search of the relevant published literature and has undertaken research. Both the literature and FDA research suggest that pathogens could be internalized into citrus fruit and survive once inside the fruit.
This background document summarizes the pertinent published and unpublished information. The information contained in this document was collected by conducting computer searches on relevant topics and contacting researchers who have done studies in related areas. These studies were categorized as shown in Table 1.
|Table 1. Studies conducted on the internalization, survival, or growth of|
microorganisms in produce and juice.
|Internalization of Microorganisms||Survival and Growth Of Microorganisms In Produce/Juice|
|Microorganism Type||Microorganism Type||Microorganism Type|
|Human Pathogen||Other||Human Pathogen||Other||Human Pathogen||Other|
|(a)Value represents the number of studies performed on a given subject.|
Internalization of Microorganisms into Fruits and Vegetables
Information is available regarding internalization of plant and human pathogens into fruits and vegetables generally. Specifically, research has been conducted regarding mechanisms by which microbes enter produce, the types of organisms that have been shown to gain entry, and the commodities for which microbial contamination is a potential problem.
Microorganisms have been shown to enter produce through various pathways available due to the natural structure of certain produce. Bacteria can enter leaves of plants through the stomata and enter fruit through the stem, stem scar, or calyx (Charkowski, 1999; Samish and Etinger-Tulczynska, 1963; Samish et al., 1963; Zhuang et al., 1995). Leben (1972) showed that bacteria can be found in more than 60 percent of the buds of field-grown commodities studied, including red clover, soybeans, cucumbers, turnips, and grapes. In this same study, large numbers of bacteria were associated with buds, flowers, and small pods on field soybean plants. Baldwin and Goodman (1963) found a high percentage of apple buds yielding a specific plant pathogen in midwinter, which suggested that the buds were infected the previous growing season. Seo and Frank (1999), using confocal scanning laser microscopy, showed that lettuce leaves dipped in a suspension of Escherichia coli O157:H7 absorbed the pathogen through the stomata and cut surfaces on the leaves.
Microorganisms may also enter fruits and vegetables through damage to the natural structure, such as punctures, wounds, cuts, and splits. These injuries can occur during maturation or during harvesting and processing. For example, citrus fruits may suffer rind damage and microbial penetration as a result of creasing during growing, which may result in splits during washing or packing; stem-end rot also facilitates microbial entry. In addition, pitting of the citrus rind can occur when fruit is exposed to temperatures below 0° C, and stem-end rind breakdown can occur as a result of aging (Ryall and Pentzer, 1982). Hill and Faville (1951) postulated that citrus on the tree could become infected by insect punctures, thorn injury, or hail damage, but noted that in order for microbes to reproduce and cause infection the injury would have to penetrate the juice sacs. Subsequently, Hill and Wenzel (1963) found that 35 percent of dropped and frost-damaged oranges had microholes too small for visual detection; half of the fruit having microholes was contaminated with microbes.
Almed et al. (1973) found that citrus fruits could be damaged in numerous ways during harvesting and that the damage provides opportunities for decay organisms to gain entrance to the fruit. Manually harvested fruits are subject to plugging (tearing off a portion of the peel around the stem end of the fruit during picking), while mechanically harvested fruit is more subject to splits, punctures, and bruises. Mechanical harvesting also results in an increased number of fruits with attached stems more than 1 cm long, which can puncture other fruits.
Ballinger and Nesbitt (1982) found that grapes with torn stem scars had 6 - 10 times more internal decay than grapes with dry stem scars. They noted that stem scars of muscadine grapes appear to be a prime site for entrance of plant pathogens. Carballo and coworkers (1994) found that bell peppers packaged in a packinghouse had more bruises than peppers packaged on field packing lines; however, the field-packed peppers had more abrasions. The authors noted that volume of open skin injuries (which were more numerous on field-packed fruit) was positively associated with greater tissue decay. Bartz and Showalter (1981) have demonstrated that tomatoes with fresh stem scars are more vulnerable to infiltration than tomatoes with old stem scars and also showed that green and pink tomatoes are more susceptible to water infiltration and became diseased earlier than did similarly treated red fruits. Sugar and Spotts (1993) showed that pears, when exposed to bruising and pressure for extended periods of time in the presence of spores of Phialophora malorum, do not become infected unless they also have puncture wounds.
Bacterial soft rot in fruits and vegetables may increase the likelihood of contamination of the fruit or vegetable with pathogens of concern. Wells and Butterfield (1997) demonstrated that Salmonella spp. was present in 18 - 20 percent of soft-rotted samples of vegetables, including sprouts, beans, broccoli, cantaloupe, carrots, lettuce, onions, peppers, potatoes, tomatoes and mixed vegetables. This is nearly double the rate (9 - 10 %) found on intact, healthy samples of the same vegetables. When vegetable disks were inoculated with Salmonella and co-inoculated with Salmonella and a soft rot bacterium, disks that were co-inoculated contained approximately 10 times the number of Salmonella as the disks that contained only Salmonella. Many studies (Robbs et al., 1996; Sherman and Allen, 1983; Segall et al., 1977; Bartz and Kelman, 1986; Lund and Kelman; 1977) have shown that vegetables such as celery, potatoes, peppers, and tomatoes are particularly susceptible to bacterial soft rot. Studies have shown that packinghouse procedures such as fluming and dump tanks can increase the incidence of soft rot (Segall et al., 1977; Lund and Kelman, 1977), while chemical treatments, including chlorination of water, appear to reduce the incidence of soft rot (Sherman and Allen, 1983; Bartz and Kelman, 1986).
Insects, birds, and dust can act as vectors for plant and human pathogens, especially after fruits and vegetables have been injured (Beuchat, 1996). Houseflies have been found to harbor 100 different pathogens and have been shown to transmit 65 of these pathogens (Kettle, 1982). Human pathogens that have been isolated from houseflies include Campylobacter jejuni, Entamoeba histolytica, pathogenic E. coli, Salmonella typhimurium, Shigella spp., and Vibrio cholera O139 (Olsen, 1998). Michailides and Spotts (1990) found that vinegar flies and nitidulid beetles in peach and nectarine orchards were contaminated with plant pathogens and transferred them to 75 – 100 percent of injured fruit studied. Beetles were found to transfer the plant pathogens to uninjured fruit also, which caused fruit rot on 42 – 75 percent of the uninjured fruit.
Numerous studies have shown that insects and birds can carry the human pathogen E. coli O157:H7 (Janisiewicz et al., 1999; Iwasa et al., 1999; Shere et al., 1998; Rahn et al., 1997; Wallace et al., 1997). Iwasa et al. (1999) conducted a field study that found contamination of wild house flies on a cattle farm with E. coli O157:H7 which persisted over a 3-month study period; a likely source of the contamination was the cow manure that the flies were frequenting. In a controlled study, Janisiewicz and coworkers (1999) studied the potential for fruit flies to transmit E. coli O157:H7 to wounds on apples. Contact between flies inoculated with the pathogen and apples with surface wounds resulted in a high incidence of wounds contaminated with E. coli O157:H7.
Several studies have indicated that processing procedures may contribute to the microbial contamination of fruits and vegetables. A study on high-pressure washing of citrus has suggested that spray washing does not generally cause visible damage to sound fruit but will rupture fruit that has been previously physically damaged (Petracek et al., 1998). Although spray washing does not appear to compromise sound fruit, there is suggestive evidence that microorganisms can be internalized into intact fruit in a dump tank. A team of FDA scientists performed a study to assess the potential for intact oranges and grapefruit to internalize bacteria from contaminated water, using dye to represent bacteria (Merker et al., 1999). This potential internalization of pathogens from contaminated water can occur if fruit is placed in a hydrocooler or a dump tank, and also may occur on the tree during a heavy rain. The study demonstrated that infiltration of water into what appears to be intact fruit can occur. All fruit used in this study was stringently culled prior to use so that it was representative of fruit used for juicing in operations with rigorous pre-sorting systems. Uptake occurred most often when warm fruit was placed into cold water, so that the resulting pressure differential favored uptake. However, there was evidence of low levels of dye uptake in grapefruit even when there was no temperature differential. Grapefruit were generally more susceptible to infiltration than oranges. In most cases, dye was taken up through natural structures, e.g., the stem scar on fruit, but occasionally an older puncture wound that appeared to be "healed" served as the route of entry.
Buchanan and coworkers (1999) also studied the susceptibility of apples to waterborne contamination. They found that when warm apples were submerged in colder water contaminated with E. coli O157:H7, as might occur in processing operations where flume water or dump tanks are not hygienically maintained, the pathogen was occasionally internalized. These results were confirmed with dye studies in which 6 percent of warm apples immersed in cold dye solution internalized dye through open channels leading from the blossom end into the core region. Zhuang and coworkers (1995) found that tomatoes took up higher numbers of cells of Salmonella spp. from an aqueous environment when placed in water that was 15°C cooler than the tomatoes. Showalter (1979) and Bartz and Showalter (1981) found that when tomatoes were dipped into water that was colder than the fruit, creating a negative temperature differential, tomatoes took up 1 to 4 percent of the fruit weight in water from the environment; most of the water uptake appeared to be in the vascular area beneath the stem scar. In addition to the temperature differential, Bartz (1982) has shown that, with tomatoes, the amount of water uptake from the environment is partially dependent upon the depth of submersion of the fruit. The author found that infiltration of tomatoes was influenced by both the temperature differential phenomenon and hydrostatic pressure; there was a positive correlation between water uptake and depth of submersion.
Several studies have shown that cross contamination of products can occur from processing equipment and the processing environment. Eisenberg and Cichowicz (1977) noted that tomato and pineapple products can become contaminated with the mold Geotrichum candidum Link, which builds up on food contact equipment in processing plants. The authors stated that the occurrence of this mold in products can be directly related to in-plant sanitation. A survey of citrus firms in Florida (Eisenberg, 1976) found insignificant levels of Geotrichum in orange juice and grapefruit juice samples.
Data from studies on apples suggest that microorganisms can be spread within processing areas and can accumulate on processing equipment. Preliminary research at the FDA Apple Cider pilot plant in Placerville, CA, has confirmed the importance of sanitation, as one component of an overall safety strategy, in the production of quality apple juices and ciders (Keller et al., 1999). The study was undertaken to determine the quality of juice produced when little or no clean-up or sanitation of the equipment or facilities was done. In addition, apples used were not all of good quality and no culling was performed. Typical juices made under poor conditions with poor quality fruit resulted in aerobic microbial populations of over 5 logs per ml, despite initial levels on incoming apples of only 3 logs per gram (Keller et al., 1999).
Environmental sampling also was conducted as part of the FDA Apple Cider pilot study in Placerville, CA. Environmental sampling done at the beginning and end of each day for a week repeatedly demonstrated high APC counts on the conveyor belt, floor drains, hand-wash stations, the hammer mill, and on tubing used to pump pomace to the press. Air sampling was also done and showed that microorganisms can be distributed throughout a plant via aerosols that occur during clean-up and processing (Keller et al., 1999).
The State of Maryland conducted a study to determine existing manufacturing and sanitation practices among cider producers (Senkel et al., 1999). Subsequently, these cider producers were trained in safety issues, HACCP concepts and principles, sanitation procedures, and GMPs. Microbiological evaluation of in-line apples, pomace, and cider before bottling, and cider bottled before and after training was performed to determine the effectiveness of training. No pathogens were found in any of the samples. However, generic, non-pathogenic E. coli was found in 13% of in-line samples and 18% of cider samples, but not on the exterior of incoming apples. This suggests that E. coli was introduced during in-plant processing and highlights the importance of appropriate sanitation practices in juice production.
Carter (1989) noted that sanitation is important in the production of fresh-squeezed orange juice because microorganisms from the peel and equipment can instantly begin reproducing in the juice under favorable conditions. Contamination by airborne microflora can result in growth of colonies that, after several hours of extraction operation, are sufficient to cause serious quality problems in fresh orange juice.
Pathogen Survival in Fruits and Vegetables and Juices
A pathogen that has become internalized within a fruit or vegetable must be able to survive in the product until it reaches the consumer in order to become a public health hazard. Pathogen survival depends on many factors, including the physical and chemical characteristics of the fruit or vegetable, the postharvest processes applied, and consumer handling. In a market basket survey, Samish et al (1963) frequently found bacteria in tomatoes, cucumbers, peas, and beans, and less often in melons and bananas. Bacteria were rarely found in grapes, citrus fruit, olives and peaches. Several studies have shown that human pathogens can survive and grow in tomatoes and tomato products (Zhuang et al., 1995; Zhuang and Beuchat, 1996; Tsai and Ingham, 1997). Asplund and Nurmi (1991) have demonstrated that cut tomatoes can be a vector of Salmonella contamination. Golden and coworkers (1993) found that Salmonella grew rapidly on cut surfaces of cantaloupe, watermelon, and honeydew melon that were held at room temperature. Salmonella levels remained unchanged when the melons were held at refrigerated temperatures.
Fisher and Golden (1998) studied the survival of E. coli O157:H7 in different cultivars of ground apples stored at various temperatures. Although there were differences in population reduction, E. coli O157:H7 survived in all samples during storage. At refrigeration temperatures, the pathogen survived in all cultivars studied for 18 days before visible mold spoilage occurred. Survival of E. coli O157:H7 is enhanced when product is stored at refrigeration, rather than room, temperature.
Little published information is available on the natural occurrence of human pathogens in fruit. However, other microorganisms have been studied. Hill and Faville (1951) inoculated citrus fruit on the tree with Aerobacter, Xanthomonas, and Achromobacter and found that there was a 3-log increase in bacterial numbers over 5 weeks. The authors also found that one control fruit (not inoculated) had an unusually high count of yeast and molds (7,600,000 colony forming units (cfu)/ml). All other control fruit had an average count of yeast and molds of 50 cfu/ml over the study period. The authors noted that all control fruits appeared to be sound, including the one with unusually high counts. If control fruit, including the highly contaminated fruit, were used to make juice, the juice would have contained a count of 50,000 cfu/ml of yeast and molds. The authors stressed that the external appearance of the inoculated fruit gave little indication of the high counts that were present and would seldom be rejected by experienced graders.
Pao and Brown (1998) studied human pathogens associated with the surface of citrus. The study found no pathogenic bacteria of concern in packed fresh citrus fruit samples from seven commercial packinghouses. They also found no generic E. coli on fruit at the end of packinghouse procedures (dumping, washing, waxing, and hand packing), and no Salmonella at any point in the packinghouse procedure.
Several studies have demonstrated the survival of microorganisms, including human pathogens, in various juices. Miller and Kaspar (1994), Fratamico et al (1997), and Splittstoesser and coworkers (1996) found that E. coli O157:H7 survives in apple juice for up to 24 days at 4° C. Fisher and Golden (1998) noted that, when dropped apples were used to produce cider, the pH of the cider was increased by mold growth enough to allow slow growth of E. coli O157:H7 at room temperature.
Studies have also been conducted on the survival of microorganisms in orange juice. In a technical manual developed for the fresh-squeezed Florida orange juice industry, Carter (1989) noted that Lactobacillus and Leuconostoc and certain yeast and molds are considered normal microflora for fresh orange juice and stated that the presence of microorganisms in numbers in the juice establishes the difference between processed orange juice and fresh orange juice. Carter also stated that counts of 200,000 cfu/ml in fresh juice, as measured on orange serum agar, at time of packaging should be considered a practical maximum at high-temperature times of the year in order to avoid quality problems in the juice. Parish (1997) included, in a review of juice outbreaks, information on general microflora levels of orange juice made from fruit of various qualities. Juice made from sound fruit contained an average of 500 cfu/ml of juice, from dropped fruit an average of 15,000 cfu/ml of juice, from split fruit an average of 1,710,000 cfu/ml of juice, and from deteriorated fruit an average of 6,150,000 cfu/ml of juice. Fratamico and coworkers (1997) found that E. coli O157:H7 survived in orange juice for 24 days at refrigeration temperatures with very little decrease in numbers. Parish and Higgins (1989) showed that Listeria numbers declined approximately 6 logs in orange juice in 25 days at pH 3.6 and 43 days at pH 4.0 when stored at 4° C.
A May 1998 survey conducted by the Florida Department of Agriculture and Consumer Services in May 1998 of 210 small fresh juice processors found that 4 percent of samples (383 total samples) were positive for generic E. coli, indicating recent fecal contamination (Food and Drug Administration Docket # 97N-0511, Comment # 107). The survey included gift fruit shippers, small markets, retail outlets, and juice bars.
Although it has been shown that pathogens can survive in orange juice, Parish (1998) has stated that Salmonella and Listeria do not actively grow in orange juice when the pH is below 4.4. Data has been submitted to the docket of FDA's juice HACCP rule indicating that E. coli O157:H7 and Listeria do not survive in lemon and lime juices when stored at room temperature (Food and Drug Administration Docket # 97N-0511, Comment # 133).
Efficacy of Surface Interventions
Several studies have shown that surface treatments are ineffective in reducing microbial populations that have been internalized into produce. Zhuang and Beuchat (1996) demonstrated that a 15 percent solution of trisodium phosphate will completely inactivate Salmonella on the surface of tomatoes but will only result in a 2-log reduction (starting concentration = 5.5 logs) of internal populations. Pao and Davis (1999) found that immersing inoculated oranges in hot water or various chemical solutions (200 ppm chlorine, 100 ppm chlorine dioxide, 200 ppm acid anionic sanitizer, 80 ppm peroxyacetic acid, or 2% trisodium phosphate) was effective at reducing generic E. coli populations by 1.8 – 3.1 log cycles on surface areas except for the stem scar. Tested treatments reduced stem scar populations by about 1.0 log.
Published and unpublished information relevant to the subject of microbial infiltration and survival in produce has demonstrated that, under certain conditions, microorganisms can become internalized into fruits and vegetables, including citrus fruits, and can survive in that environment. Water, insects or birds, all of which may carry human pathogens, may serve as vectors resulting in the contamination of damaged or decayed sites on the rind. Microorganisms subsequently may infiltrate the produce through these damaged sites. In addition, fruit can become contaminated if warm fruit is submerged into cold, contaminated water or if vulnerable external points of fruit are immersed in contaminated water. Under certain conditions, equipment also has been shown to cross contaminate both fresh apple and orange juice during processing.
Survival of pathogens, both plant and human, has been demonstrated in both produce and juice. In laboratory studies, human pathogens have been found in or on tomatoes, cantaloupe, watermelon, honeydew melon, and apples. There appears to be no published information on human pathogens in citrus fruits; however, the presence of other bacteria internalized in citrus was noted. Numerous studies have shown that human pathogens can survive in both apple and orange juice, despite their natural acidity.
Almed, E.M., Martin, F.G., and Fluck, R.C. 1973. Damaging stresses to fresh and irradiated citrus fruit. J. Food Sci. 38: 230-233.
Asplund, K. and Nurmi, E. 1991. The growth of salmonellae in tomatoes. Int. J. Food Microbiol. 13:177-182.
Baldwin, C.H. and Goodman, R.N. 1963. Prevalence of Erwinia amylovora in apple buds as detected by phage typing. Phytopathology 53: 1299-1303.
Ballinger, W.E. and Nesbitt, W.B. 1982. Postharvest decay of muscadine grapes (Carlos) in relaiton to storage temperature, time, and stem condition. Am. J. Enol. Vitic. 33(3):173-175.
Bartz, J.A. 1982. Infiltration of tomatoes immersed at different temperatures to different depths in suspensions of Erwinia carotovora subsp. Carotovora. Plant Dis. 66:302-306.
Bartz, J.A. and Kelman, A. 1986. Reducing the potential for bacterial soft rot in potato tubers by chemical treatments and drying. Amer. Potato J. 63: 481-493.
Bartz, J.A. and Showalter, R.K. 1981. Infiltration of tomatoes by aqueous bacterial suspensions. Phytopathology 71:515-518.
Beuchat, L.R. 1996. Pathogenic microorganisms associated with fresh produce. J. Food Prot. 59(2):204-216.
Buchanan, R.L., Edelson, S.G., Miller, R.L. and Sapers, G.M. 1999. Contamination of intact apples after immersion in an aqueous environment containing Escherichia coli O157:H7. J. Food Prot. 62(5):444-450.
Carballo, S.J., Blankenship, S.M., Sanders, D.C., Ritchie, D.F. and Boyette, M.D. 1994. Comparison of packing systems for injury and bacterial soft rot on bell pepper fruit. HortTech. 4(3):269-272.
Carter, R.D. 1989. Technical Manual: Fresh-squeezed Florida orange juice production/packaging/distribution. Florida Department of Citrus, Scientific Research Department, University of Florida, 700 Experiment Station Road, Lake Alfred, FL.
Charkowski, A.O. 1999. Personal communication. United States Department of Agriculture Western Regional Research Center, 800 Buchanan Street, Albany, CA 94710.
Eisenberg, W.V. 1976. Summary of sample analysis for Geotrichum Candidum citrus survey--Orlando, Florida. Unpublished data. Food and Drug Administration, Center for Food Safety and Applied Nutrition, Office of Plant and Dairy Foods and Beverages, Division of Natural Products, 200 C Street SW, Washington, D.C.
Eisenberg, W.V. and Cichowicz, S.M. 1977. Machinery mold--indicator organism in food. Food Technol. 31:52-56.
Fisher, T.L. and Golden, D.A. 1998. Fate of Escherichia coli O157:H7 in ground apples used in cider production. J. Food Prot. 61(10):1372-1374.
Food and Drug Administration Docket #97N-0511, Comment # 107, Dockets Management Branch (HFA-305), Food and Drug Administration, 12420 Parklawn Drive, Rockville, MD.
Food and Drug Administration Docket #97N-0511, Comment # 133, Dockets Management Branch (HFA-305), Food and Drug Administration, 12420 Parklawn Drive, Rockville, MD.
Fratamico, P.M., Deng, M.Y., Strobaugh, T.P. and Palumbo, S.A. 1997. Construction and characterization of Escherichia coli O157:H7 strains expressing firefly luciferase and green fluorescent protein and their use in survival studies. J. Food Prot. 60(10):1167-1173.
Golden, D.A., Rhodehamel, E.J. and Kautter, D.A. 1993. Growth of Salmonella spp. in cantaloupe, watermelon, and honeydew melons. J. Food Prot. 56(3):194-196.
Hill, E.C. and Faville, L.W. 1951. Studies on the artificial infection of oranges with acid tolerant bacteria. Proc. Fla. State Hort. Soc. 64:174-177.
Hill, E.C. and Wenzel, F.W. 1963. Microbial populations of frozen oranges. Proc. Fla. State Hort. Soc. 76:276-281.
Iwasa, M., Sou-Ichi, M., Asakura, H., Hideaski, K. and Morimoto, Y. 1999. Detection of Escherichia coli O157:H7 from Musca domestica (Diptera: Muscidae) at a cattle farm in Japan. J. Med. Entomol. 36(1):108-112.
Janisiewicz, W.J., Conway, W.S., Brown, M.W., Sapers, G.M., Fratamico, P. and Buchanan, R.L. 1999. Fate of Escherichia coli O157:H7 on fresh-cut apple tissue and its potential for transmission by fruit flies. Appl. Environ. Microbiol. 65(1):1-5.
Keller, S.E., Merker, R.I., and Taylor, K.T. 1999. Interim report: Evaluation of foodsafety aspects of apple cider production in a small processing plant. U.S. Food and Drug Administration, Center for Food Safety and Applied Nutrition, HFH-450, 6502 South Archer Road, 4th Floor, Summit-Argo, IL 60501-1933.
Kettle, D.S. 1982. Muscidae (Houseflies, Stableflies) in Medical and Veterinary Entomology. John Wiley & Sons, New York.
Leben, C. 1972. Micro-organisms associated with plant buds. J. Gen. Microbiol. 71:327-331.
Lund, B.M. and Kelman, A. 1977. Determination of the potential for development of bacterial soft rot of potatoes. Amer. Potato J. 54:211-225.
Merker, R., Edelson-Mamel, S., Davis, V., and Buchanan, R.L. 1999. Preliminary experiments on the effect of temperature differences on dye uptake by oranges and grapefruit. U.S. Food and Drug Administration, Center for Food Safety and Applied Nutrition, 200 C Street SW, Washington, D.C. 20204.
Michailides, T.J. and Spotts, R.A. 1990. Transmission of Mucor piriformis to fruit of Prunus persica by Carpophilus spp. and Drosophila melanogaster. Plant Dis. 74:287-291.
Miller, L.G. and Kaspar, C.W. 1994. Escherichia coli O157:H7 acid tolerance and survival in apple cider. J. Food Prot. 57(6):460-464.
Olsen, A.R. 1998. Regulatory action criteria for filth and other extraneous materials. III. Review of flies and foodborne enteric disease. Regulatory Toxicol. Pharmacol. 28:199-211.
Pao, S. and Brown, G.E. 1998. Reduction of microorganisms on citrus fruit surfaces during packinghouse procedures. J. Food Prot. 61(7):903-906.
Pao, S. and Davis, C.L. 1999. Enhancing microbiological safety of fresh orange juice by fruit immersion in hot water and chemical sanitizers. J. Food Prot. 62(7):756-760.
Parish, M.E. 1997. Public health and nonpasteurized fruit juices. Crit. Rev. Microbiol. 23(2):109-119.
Parish, M.E. 1998. Food and Drug Administration Docket #97N-0511, Comment # 60, Dockets Management Branch (HFA-305), Food and Drug Administration, 12420 Parklawn Drive, Rockville, MD.
Parish, M.E. and Higgins, D.P. 1989. Survival of Listeria monocytogenes in low pH model broth systems. J. Food Prot. 52(3):144-147.
Petracek, P.D., Kelsey, D.F. and Davis, C. 1998. Response of citrus fruit to high-pressure washing. J. Amer. Soc. Hort. Sci. 123(4):661-667.
Rahn, K. Renwick, S.A., Johnson, R.P., Wilson, J.B., Clarke, R.C., Alves, D., McEwen, S., Lior, H. and Spika, J. 1997. Persistence of Escherichia coli O157:H7 in dairy cattle and the dairy farm environment. Epidemiol. Infect. 119:251-259.
Robbs, P.G., Bartz, J.A., McFie, G. and Hodge, N.C. 1996. Causes of decay of fresh-cutcelery. J. Food Sci. 61(2):444-448.
Ryall, A.L. and Pentzer, W.T. 1982. Handling, transportation and storage of fruits and vegetables, Volume 2, Fruits and tree nuts, 2nd ed. AVI Publishing Company, Westport, CT.
Samish, Z. and Etinger-Tulczynska, R. 1963. Distribution of bacteria within the tissue of healthy tomatoes. Appl. Microbiol. 11:7-10.
Samish, Z., Etinger-Tulczynska, R. and Bick, M. 1963. The microflora within the tissue of fruits and vegetables. J. Food Sci. 28:259-266.
Segall, R.H., Henry, F.E. and Dow, A.T. 1977. Effect of dump-tank water temperature on the incidence of bacterial soft rot of tomatoes. Proc. Fla. State Hort. Soc. 90:204-205.
Senkel, I.A., Henderson, R.A., Jolbitado, B. and Meng, J. 1999. Use of hazard analysis critical control point and alternative treatments in the production of apple cider. J. Food Prot. 62(7):778-785.
Seo, K.H. and Frank, J.F. 1999. Attachment of Escherichia coli O157:H7 to lettuce leaf surface and bacterial viability in response to chlorine treatment as demonstrated by using confocal scanning laser microscopy. J. Food Prot. 62(1):3-9.
Shere, J.A., Bartlett, K.J. and Kaspar, C.W. 1998. Longitudinal study of Escherichia coli O157:H7 dissemination on four dairy farms in Wisconsin. Appl. Environ. Microbiol. 64(4):1390-1399.
Sherman, M. and Allen, J.J. 1983. Impact of postharvest handling procedures on soft rot decay of bell peppers. Proc. Fla. State Hort. Soc. 96:320-322.
Showalter, R.K. 1979. Postharvest water intake by tomatoes. HortSci. 14(2):125.
Splittstoesser, D.F., McLellan, M.R. and Churey, J.J. 1996. Heat resistance of Escherichia coli O157:H7 in apple juice. J. Food Prot. 59(3):226-229.
Sugar, D. and Spotts, R.A. 1993. The importance of wounds in infection of pear fruit by Phialophora malorum and the role of hydrostatic pressure in spore penetration of wounds. Phytopathology 83:1083-1086.
Tsai, Y. and Ingham, S.C. 1997. Survival of Escherichia coli O157:H7 and Salmonella spp. in acidic condiments. J. Food Prot. 60(7):751-755.
Wallace, J.S., Cheasty, T. and Jones, K. 1997. Isolation of vero cytotoxin-producing Escherichia coli O157 from wild birds. J. Appl. Microbiol. 82:399-404.
Wells, J.M. and Butterfield, J.E. 1997. Salmonella contamination associated with bacterial soft rot of fresh fruits and vegetables in the marketplace. Plant Dis. 81:867-872.
Zhuang, R.Y. and Beuchat, L.R. 1996. Effectiveness of trisodium phosphate for killing Salmonella montevideo on tomatoes. Letters Appl. Microbiol. 22:97-100.
- Zhuang, R.Y., Beuchat, L.R. and Angulo, F.J. 1995. Fate of Salmonella montevideo on and in raw tomatoes as affected by temperature and treatment with chlorine. Appl. Environ. Microbiol. 61(6):2127-2131.