Comparison of a microbiological and a spectrophotometric method for the determination of nicotinic acid in fresh meat

The microbiological method for the determination of nicotinic acid with the aid of Leuconostoc mesenteroides ATCC 9135 was compared with a spectrophotometric method which included cleaning-up of a meat extract by thin-layer chromatography. The results obtained were in good agreement. Average recovery factors of 95–107% and reproducibilities of 2–6% (standard deviation in % of the average) indicate that the results are reliable.     

Comparison of rinsing and sanitizing procedures for reducing bacterial pathogens on fresh cantaloupes and bell peppers

Increased consumption of fruits and vegetables is linked to health benefits but also to an increase in the number of outbreaks of foodborne illness. To determine the effectiveness of different sanitizing treatments for reducing bacterial pathogens on fresh produce, fresh cantaloupes and bell peppers were harvested and inoculated with suspensions of Salmonella Typhimurium and Escherichia coli O157:H7. The inoculated fruits were treated with water wash alone or were washed and then waxed or rinsed with 200 mg/liter hypochlorite, 10% Ca(OH)2, or 2% lactic acid solutions applied by dipping for 15 s or spraying for 15 s. Preliminary experiments with chlorine treatments indicated that spraying with a 200, 600, or 1,000 mg/liter hypochlorite solution reduced populations of both pathogens by 2.1 to 2.6 and 1.5 to 2.1 log CFU for Salmonella Typhimurium and E. coli O157:H7, respectively. In general, no differences were observed between chlorine solutions without pH adjustment (pH 9.2) and those with pH adjusted to 6.0. When different wash regimes were applied to inoculated cantaloupes or bell peppers, water wash alone produced significantly lower counts of both pathogens on bell peppers in comparison to untreated controls. However, this reduction was not observed on cantaloupes, indicating a possible surface effect. Application of 2% L-lactic acid by spray was the treatment that resulted in the lowest bacterial counts on both cantaloupes and bell peppers. This treatment did not produce any deleterious change in the sensorial characteristics of the products tested. None of the pathogens studied was able to grow during refrigerated storage (5 degrees C for cantaloupes and 10 degrees C for bell peppers), although numbers close to the detection limit of the counting method were found in randomly tested individual samples at days 14 and 28 of storage, indicating that these pathogens can survive for long periods on the produce surface. These results indicate that selected produce commodities could be sanitized at the packing facility. However, these interventions should not be applied as a replacement for but only as a complement to good hygiene practices.     

Experimental comparison of excision and swabbing microbiological sampling methods for carcasses

Bovine sides, ovine carcasses, and porcine carcasses were individually inoculated by dipping in various suspensions of a marker organism (Escherichia coli K-12 or Pseudomonas fluorescens), alone or in combination with two meat-derived bacterial strains, and were sampled by two standard methods: cotton wet-dry swabbing and excision. The samples were examined for bacterial counts on plate count agar (PCA plate counts) and on violet red brilliant green agar (VRBGA plate counts) by standard International Organization for Standardization methods. Average bacterial recoveries by swabbing, expressed as a percentage of the appropriate recoveries achieved by excision, varied widely (2 to 100%). Several factors that potentially contributed to relatively low and highly variable bacterial recoveries obtained by swabbing were investigated in separate experiments. Neither the difference in size of the swabbed area (10, 50, or 100 cm2 on beef carcasses) nor the difference in time of swabbing (20 or 60 min after inoculation of pig carcasses) had a significant effect on the swabbing recoveries of the marker organism used. In an experiment with swabs preinoculated with the marker organism and then used for carcass swabbing, on average, 12% of total bacterial load was transferred inversely (i.e., from the swab to the carcass during the standard swabbing procedure). In another experiment, on average, 14% of total bacterial load was not released from the swab into the diluent during standard swab homogenization. Use of custom-made swabs with abrasive butts, around which metal pieces of pan scourers were wound, markedly increased PCA plate count recoveries from noninoculated lamb carcasses at commercial abattoirs compared with cotton swabs. In spite of the observed inferiority of the cotton wet-dry swabbing method compared with the excision method for bacterial recovery, the former is clearly preferred by the meat industry because it does not damage the carcass. Therefore, further large-scale evaluation of the two carcass sampling methods has been undertaken under commercial conditions and reported separately.     

Comparison of sampling procedures for recovery of Listeria monocytogenes from stainless steel food contact surfaces

A number of techniques exist for microbiological sampling of food processing environments in food industries. In the present study the efficacies of nine sampling procedures for the recovery of Listeria monocytogenes from food contact surfaces, including a new sampling device consisting of a miniroller, were evaluated and compared. A stainless steel table was inoculated with L. monocytogenes strain 935 (serovar 4b, human origin) and L. monocytogenes strain 437/07 (serovar 1/2b, food origin), at 10(5) CFU/100 cm(2). L. monocytogenes strain 935 was best recovered with the minirollers (recovery of up to 6.27%), while poor recoveries (<0.30%) were obtained with the towel (one-ply composite tissue), alginate swab, metallic swab, and Petrifilm methods. In the case of L. monocytogenes strain 437/07 the replicate organism detection and counting (RODAC) ALOA contact plates yielded the best recoveries (4.15%), followed by the minirollers (up to 1.52%). Overall, recovery percentages with the minirollers were higher with stomacher homogenization than with Vibromatic agitation. The recovery percentages obtained for the Listeria strain of human origin were higher than those obtained with the food strain for all sampling procedures except Petrifilm and RODAC ALOA. With the miniroller device coated with wool fiber, the recovery of L. monocytogenes can be improved from 2 to 17 times over recoveries obtained with the sponge and cotton swab. This is the first report of a miniroller device for microbiological sampling in the available literature. The novel sampling procedure is convenient to apply on surfaces, is cost-effective, and results in better recovery of L. monocytogenes than do the conventional methods.     

Development and analysis of a rumen tissue sampling procedure

A procedure for rumen tissue sampling was developed to determine treatment effects on rumen development and papillae growth in young calves and to improve repeatability in rumen tissue sampling techniques. Rumens were collected from 42 male Holstein calves from 4 separate experiments. Rumen sampling areas (n = 9) included the caudal dorsal blind sac, cranial dorsal sac, cranial ventral sac, and the caudal and ventral portions of the caudal ventral blind sac. Right and left sides of the rumen were sampled. Five 1-cm2 sections were removed from each area and measured for papillae length (n = 20/area), papillae width (n = 20/area), rumen wall thickness (n = 5/area), and number of papillae per cm2 (n = 5/area). Correlations between areas, samples, and measurements were obtained, and comparisons between experiments, areas, samples, and measurements were performed for all variables. In addition, power analyses were conducted for all variables to determine the efficacy of the procedure in detecting treatment differences. Results indicate that samples should be taken from the caudal and cranial sacs of the dorsal and ventral rumen to sufficiently represent papillae growth and development throughout the entire rumen. The procedure is capable of detecting treatment differences for papillae length and papillae width, has a decreased but acceptable capability of detecting treatment differences for rumen wall thickness, but appears limited in ability to detect treatment differences for papillae per square centimeter. In conclusion, rumen tissue sampling to determine extent of rumen development in calves can be performed in a nonbiased and repeatable manner utilizing a limited number of calves.     

Comparison of sampling methods for microbiological testing of beef animal rectal/colonal feces, hides, and carcasses

This study compared sampling methods for detecting Escherichia coli O157:H7 and Salmonella in beef cattle feces and on hides and carcasses and for enumerating E. coli biotype I counts (ECC) on carcasses. Fecal samples were collected by rectal/colonal palpation and colonal sponge swabbing. Hides were sampled by sponge swabbing three sites, hair clipping, excision, rinsing, and gauze swabbing, whereas carcasses were sampled by three-site thoracic and pattern-mark sponge swabbing and tissue excision. Overall, irrespective of sampling method, 36.7, 13.3, and 0.0% of lots contained at least one E. coli O157:H7-positive hide, fecal, and carcass sample, respectively, while the corresponding prevalence of Salmonella was 70.0, 16.7, and 6.7%, respectively. For hide sampling, excision and gauze swabbing yielded the fewest (13.3%) E. coli O157:H7-positive samples, while hair clipping and sponge swabbing yielded the most (23.3%). None of the carcass-sampling methods detected E. coli O157:H7 or differed (P > 0.05) in their ability to enumerate ECC. Colonal swabbing was the most effective (10.0%) method for detecting E. coli O157:H7 in feces. No differences (P > 0.05) in Salmonella prevalence were observed between carcass-sampling methods, although three-site sponge swabbing and tissue excision detected the most (3.3%). Hide rinsing was the most effective (P < 0.05) Salmonella detection method (63.3%), but dangers associated with its application may preclude its use by industry; there were no differences (P > 0.05) among other hide-sampling methods. No differences (P > 0.05) in Salmonella detection were observed between fecal-sampling methods. Overall, three-site sponge swabbing was the most feasible and effective sampling method for the detection of E. coli O157:H7 and Salmonella on hides and carcasses.     

Comparison of direct and indirect sampling procedures for Plodia interpunctella in a maize storage facility

Weekly sampling of the Indian meal moth, Plodia interpunctella, was conducted over 15 consecutive weeks at 19 locations within a maize storage facility. Direct sampling consisted of maize samples from two depths from the maize surface, and was compared with three indirect sampling techniques: (1) cardboard traps intended for trapping of late instar larvae and pupae; (2) unbaited sticky traps at two heights above the maize intended for trapping adults; and (3) probe traps inserted into the maize intended for trapping both larvae and adults. Temperature was recorded weekly and maize moisture content every 2 weeks at each sampled location. Total catches for the entire sampling period were highest with cardboard traps followed by maize samples, sticky traps, and probe traps. Spatial statistics were used to examine the distribution pattern of weekly catches for each sampling technique: (1) larvae in both top and bottom maize samples indicated similar aggregated distribution patterns; (2) catches with cardboard traps and sticky traps at both heights suggested a random distribution pattern; and (3) catches with probe traps were considered too low for analysis. For each weekly sampling event, the level of spatial association between sampling techniques was investigated in which the spatial distribution of larvae in top samples was compared with: (1) larvae in bottom maize samples; (2) cardboard trap catches; and (3) adults sticky traps. Catches of adults in low sticky traps were compared with: (4) adults in high sticky traps; (5) cardboard trap catches; and (6) larvae in bottom maize samples. Of the six spatial associations, only larvae in the top and bottom maize samples were significantly associated, while there was no significant spatial association involving catches with indirect sampling techniques. We used response surface regression analysis to evaluate the relative contribution of six explanatory variables in a model fitted to the abundance of larvae in maize samples (order of importance): y-coordinate of sampling locations, vertical position of samples, temperature, number of weekly sampling event, moisture content, and x-coordinate of sampling locations. Using additional response surface regression analyses with the same explanatory variables, we showed that abundance of larvae in maize samples was a poor predictor for the occurrence of P. interpunctella individuals in indirect samples. The implications of different spatial distribution patterns for different sampling techniques of P. interpunctella are discussed.     

生鲜鸭组织中重金属污染分析与安全性评价

为了解生鲜鸭组织中重金属污染状况和对其进行安全性评价,于大型超市、农贸市场和连锁店采集鸭不同部位,对Cu、Pb、As、Cd含量进行测定,参照国家食品卫生标准计算超标率,并对各组织的污染程度进行了安全性评价。结果表明:鸭肝、鸭血、鸭肾为重度污染,综合污染指数分别为4.43、4.32和4.25;鸭心和鸭肠为中度污染,综合污染指数为2.40和2.60;鸭腿肉和胸肌处于安全水平,综合污染指数为0.79和0.81。研究结果提示,国家相关部门应加强鸭可食性下水的重金属监控。     

Comparison of two field sampling procedures (En Core and field methanol extraction) for volatile organic compounds

In-situ Lasagna technology was recently evaluated at a contaminated site at Offutt Air Force Base. The site was contaminated with low levels (<30 mg/kg) of volatile organic compounds (VOCs). Originally, researchers planned to use field methanol extraction for both pre- and post-treatment sampling to evaluate the effectiveness of the technology on contaminant reduction. Precharacterization sampling, however, indicated that concentrations of some contaminants of concern were much lower than expected. Because use of methanol increases the detection limit, it was probable that post-treatment concentrations of these target contaminants would be nondetectable if methanol extraction was used. Project management, therefore, decided to use En Core samplers in addition to field methanol extraction during the pretreatment sampling event. The En Core sampling approach, while yielding a lower detection limit, uses discreet samples along the length of a core, whereas the methanol extraction approach samples the entire length of the core. The concern was that discreet samples may bias results if any "hot spots" were present. The two field sampling procedures, En Core and field methanol extraction, were performed side-by-side during the pretreatment phase of the technology evaluation in order to determine if the concern was valid for this site. Results were compared for four contaminants of concern: trichloroethylene, vinyl chloride, cis-1,2-dichloroethene, and trans-1,2-dichloroethene. The two procedures produced similar results with respect to both the concentration means and the variances, and no bias was evident. This finding supports project management's decision to use only En Core samplers post-treatment due to low concentrations of target contaminants.     

巴氏灭菌对南香果汁香气成分的影响

采用顶空-固相微萃取法提取南香鲜果汁与巴氏灭菌果汁的香气成分,用气相色谱-质谱进行定性定量分析。试验结果表明：鲜果汁与巴氏灭菌果汁分别鉴定出62和28种香气成分。南香鲜汁中的主要香气成分是己醛、2-辛醇、D-柠檬烯、（4R）-3,4-开环-5α-胆甾炕-3-酸4-羟基-4-甲基-ε-内酯等;灭菌后的南香汁中的主要香气成分为D-柠檬烯和己醛等;灭菌后果汁原有的愉悦的香气成分如内酯物质未检出;2-甲基-6-（2-丙烯基）-吡嗪的出现使果汁呈现烘烤香味,癸酮则使果汁风味变劣。     

A field study of the microbiological quality of fresh produce

The Centers for Disease Control and Prevention has reported that foodborne disease outbreaks associated with fruits and vegetables increased during the past decade. This study was conducted to characterize the routes of microbial contamination in produce and to identify areas of potential contamination from production through postharvest handling. We report here the levels of bacterial indicator organisms and the prevalence of selected pathogens in produce samples collected from the southern United States. A total of 398 produce samples (leafy greens, herbs, and cantaloupe) were collected through production and the packing shed and assayed by enumerative tests for total aerobic bacteria, total coliforms, total Enterococcus, and Escherichia coli. These samples also were analyzed for Salmonella, Listeria monocytogenes, and E. coli O157:H7. Microbiological methods were based on methods recommended by the U.S. Food and Drug Administration. For all leafy greens and herbs, geometric mean indicator levels ranged from 4.5 to 6.2 log CFU/g (aerobic plate count); less than 1 to 4.3 log CFU/g (coliforms and Enterococcus); and less than 1 to 1.5 log CFU/g (E. coli). In many cases, indicator levels remained relatively constant throughout the packing shed, particularly for mustard greens. However, for cilantro and parsley, total coliform levels increased during the packing process. For cantaloupe, microbial levels significantly increased from field through packing, with ranges of 6.4 to 7.0 log CFU/g (aerobic plate count); 2.1 to 4.3 log CFU/g (coliforms); 3.5 to 5.2 log CFU/g (Enterococcus); and less than 1 to 2.5 log CFU/g (E. coli). The prevalence of pathogens for all samples was 0, 0, and 0.7% (3 of 398) for L. monocytogenes, E. coli O157:H7, and Salmonella, respectively. This study demonstrates that each step from production to consumption may affect the microbial load of produce and reinforces government recommendations for ensuring a high-quality product.     

An assessment of sampling methods and microbiological hygiene indicators for process verification in poultry slaughterhouses

Studies to determine the appropriateness of the use of populations of indicator bacteria on poultry carcasses for process verification were undertaken in commercial slaughterhouses. Samples were collected from neck skin by excision or from whole carcass rinses and were examined for a range of presumptive process hygiene indicator bacteria. Coefficients of variation were calculated for each bacterial indicator and were significantly lower in excised samples, indicating more reproducible bacterial recovery by this sampling method. Total viable counts of aerobic bacteria, Enterobacteriaceae, and Pseudomonas in samples collected by excision had the lowest coefficients of variation when compared with other indicators and were therefore used for further study. The uncertainties associated with the quantification of each bacterial indicator were calculated and were lowest overall for total viable counts of aerobic bacteria. In general, uncertainty was higher for lower bacterial numbers. Results of microbiological testing on pooled excised neck skin samples were not significantly different from the mean of individually analyzed samples. Bacterial numbers increased by 1 log unit when cultures were stored under chilled conditions typical of those used for transporting samples to external laboratories, but the increases were not significant for Pseudomonas and aerobic bacteria when storage time was less than 17 h. Weak relationships were identified between bacterial indicator numbers and duration of processing, although cleanliness of the processing environment diminished visibly during this time. In the plants visited for this study, there was a poor relationship between presumptive bacterial indicator numbers and process hygiene. Consequently, bacterial analyses for process verification purposes may be of limited value.     

Comparison of isolation procedures for essential oils

Summary The influence of the time of distillation on the composition of the essential oils isolated from seed of ajowan, caraway, coriander, and cumin was investigated. The oils were isolated by distillation, as well as by simultaneous distillation-extraction. It was observed that the order of recovery of the oil constituents was determined by their solubility in the distillation water. Hence, the oxygenated compounds, although with higher boiling points, distilled before the hydrocarbons. In comparison, data are included for the oils obtained by solvent extraction from ground seed of the same species. In these cases the proportion of hydro carbons was higher than in the distilled oils. There was also evidence to suggest thatp-cymene in the oils of ajowan and cumin was partly an artefact of distillation.

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Vergleich von Isolierungsverfahren ätherischer ÖleII. Ajowan, Künunel, Koriander und Kreuzkümmel

Zusammenfassung Der Einfluß der Destillationsäuer auf die Zusammensetzung der ätherischen Öle von Ajowan, Kümmel, Koriander und Kreuzkümmel wurde untersucht. Die Öle wurden sowohl durch Destillation als auch durch ein Destillation-Extraktionsverfahren isoliert. Es wurde gezeigt, daß die Reihenfolge der Ölbestandteile während der Destillation bestimmt wurde von ihrer Löslichkeit im Destillationswasser, weshalb die höher siedenden sauerstoffhaltigen Komponenten schneller als die Kohlenwasserstoffe übergehen.Zum Vergleich wurden Angaben aufgenommen für Öle, die mit organischen Lösungsmitteln aus gemahlenen Früchten extrahiert worden waren. In diesen Fällen war die Menge der Kohlenwasserstoffe höher als bei den destillierten Ölen. Es gibt Hinweise dafür, daßp-Cymol in Ajowan- und Kreuzkümmelöl teilweise ein Artefakt der Destillation ist.

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Part I: Chem. Mikrobiol. Technol. Lebensm. (in press)     

A review of aerobic and psychrotrophic plate count procedures for fresh meat and poultry products

This is a review of reports that employed aerobic plate counts on fresh meat and poultry products since 1985; it lists synopses of 100 applications. A total of 15 different plating media were used, with 48 (48%) being either plate count agar (PCA) or tryptone glucose yeast extract agar. The temperature-time relations ranged from a low temperature of 20 degrees C for 120 h to 37 degrees C for 24 h. Some 29 different temperature-time combinations were used among the total of 109, with 21 (19.3%) being 35 degrees C/48 h, followed by 12 (11.0%) at 32 degrees C/48 h, 11 (10.1%) at 25 degrees C/48 h, and 9 (8.3%) at 25 degrees C/72 h. Fifty-four (49.5%) plate count applications employed incubation temperatures of 30 degrees C and below. From the 26 reports that employed psychrotrophic counts, 16 (61.5%) used PCA; 18 different temperature-time combinations were used, with 7 degrees C/10 d employed by only four. Twenty-one (80.8%) employed an incubation temperature at or <10 degrees C, and five employed an incubation temperature >10 degrees C. There is a serious need for some consensus on methodologies for aerobic and psychrotrophic counts on fresh meat and poultry products.     

An in vitro system for the comparison of excision and wet-dry swabbing for microbiological sampling of beef carcasses

An in vitro system for the comparison of wet-dry swabbing and surface tissue excision was developed to ascertain whether the commonly accepted statement of the advantage (in terms of bacterial recovery) of the tissue excision method is also legitimate when different kinds of bacteria are used. A total of 1,770 sections (2.5 by 10 cm) of bovine skin were individually inoculated on the subcutaneous fat side by spreading various suspensions of marker organisms (nalidixic acid-resistant Escherichia coli, vancomycin-resistant Enterococcus faecalis, and methicillin-resistant Staphylococcus aureus) at different concentrations and sampled by two standard methods: cotton wet-dry swabbing and excision. Most counts from cuts sampled by excision were significantly (P < 0.05) higher than the wet-dry swabs; however, no differences were observed between the control and the sampling method when sections were inoculated with bacterial solutions at a concentration of 10(3) CFU/ml and sampled by excision. For sections inoculated with bacterial solutions at a concentration of 10(3) CFU/ml, counts given as log CFU/25 cm2 ranged from 1.97 (S. aureus sampled by wet-dry swab) to 3.06 (S. aureus sampled by excision). For sections inoculated at a concentration of 10(4), counts given as log CFU/25 cm(2) ranged from 2.15 (E. faecalis sampled by wet-dry swab) to 3.19 (S. aureus sampled by excision). For sections inoculated at 10(5), counts given as log CFU/25 cm(2) ranged from 2.94 (E. faecalis, wet-dry swab) to 3.98 (S. aureus, excision), and for sections inoculated at 106, counts given as log CFU/25 cm(2) ranged from 3.53 (E. coli, wet-dry swab) to 4.69 (S. aureus, excision). The proposed system, which enabled a considerable amount of samples to be analyzed under controlled experimental conditions and a large number of data to be generated in a short time, demonstrated among the tested microorganisms that whereas the excision method recovered the highest number of bacteria, control means were always (with the exception of an inoculum of 10(3)/ml) significantly higher than means from either of the sampling methods. Our results indicate that particular attention should be paid to the diverse microflora that can contaminate carcasses in a given slaughterhouse and that it is not appropriate to generalize by saying that the destructive method is the reference technique for the bacteriological sampling of carcasses in slaughterhouses, especially when the contamination is higher than 10(3) CFU/25 cm(2).     

Comparison of microbiological risk assessment studies published

The FAO/WHO risk analysis framework and principles are in the process of being implemented in different national and international settings. The importance of a further development of international co-operation based upon agreed principles in this area is stressed in the Codex Alimentarius system, as well as under the WTO/SPS agreements. Key input in this context will come from the presentation of formalised microbiological risk assessments. The number of peer-review published microbiological risk assessments is low and the format is still variable. This paper presents a comparison of selected risk assessments in the microbiological area, and suggests a number of lessons to be learned from these.     

Accuracy of simplified sampling procedures for estimating milk composition in dairy ewes

Simplified designs of milk-composition recording, based on information from a single monthly milking, adjusted or not for interval between milkings and for milk yield, were simulated and evaluated for 2553 ewe-test-day records belonging to 155 lactations of Churra dairy ewes. Accuracy of simplified methods was evaluated by comparing estimated trait values (fat, protein, casein and total solid yields) with those observed both in a reference plan, where the two daily milkings were recorded at weekly intervals (A1), and in the official A4 milk recording (monthly records of the two daily milkings). Trait yields per lactation were estimated and adjusted to the only milking period (days in milk 30-120). Estimates of milk component traits were less precise when monthly designs, including the A4 design, were compared with a weekly sampling of both a.m. and p.m. milkings, with fat yield being the most difficult trait to estimate. All options with one daily milking every month were more accurate when the corresponding plan was based on, or began with, the a.m. milking. Adjustment for the preceding interval between milkings or milk yield did not improve sampling accuracy. The design alternating a.m. and p.m. milkings every month, without adjustment, is suggested for recoding milk component traits in dairy ewes.     

Comparison of isolation procedures for Mexican oregano oil

The influence of distillation time on the composition of Mexican oregano oil was investigated. It was observed that the order of recovery of the components was determined by their solubility when water is in contact with the plant material as in hydrodistillation and simultaneous distillation-solvent extraction, while in steam distillation the order was determined by their boiling points. The three methods produced the same composition. The oil obtained by extraction method had higher proportion of hydrocarbons and lower amount of p-cymene. As a result of this investigation it was shown that this compound was partly an artefact of distillation.     

Microscopic observation and processing validation of fruit sanitizing treatments for the enhanced microbiological safety of fresh orange juice

Studies were conducted to evaluate the infiltration of dye and bacteria into the interior of orange fruit and the impact of possible infiltration on achieving a 5-log microbial reduction during fresh juice processing. Fresh orange fruit were treated at the stem end area with dye and either Salmonella Rubislaw or Escherichia coli strains expressing green fluorescent protein. Microscopic images showed that bacterial contaminants localized at the surface or near surface areas that may be sanitized by surface treatments. Dye infiltration was not a reliable indicator of bacterial penetration in citrus fruit. To quantify the reduction of bacterial contamination, orange fruit were inoculated with E. coli and processed with and without hot water treatments. Greater than 5-log reductions were achieved in juice extracted from fruit immersed in hot water for 1 or 2 min at 80 degrees C, in comparison to the E. coli level detected in the control juice obtained by homogenization of inoculated fruit.     

A field study of the microbiological quality of fresh produce of domestic and Mexican origin

Produce is responsible for an increasingly larger proportion of foodborne disease outbreaks. In particular, the globalization of the food supply may introduce new food safety risks and allow widespread distribution of contaminated food, particularly produce. The objectives of this study were to: (i) compare the overall quality of domestic and Mexican produce throughout the packing process; (ii) examine changes in microbiological quality of both domestic and Mexican produce at each stage of production and processing; and (iii) evaluate the prevalence of select pathogens on fresh produce, including leafy green, herbs, melons, and vegetables. Furthermore, we also sought to characterize the antibiotic resistance profiles of Enterococcus faecium and Enterococcus faecalis strains isolated from fresh produce. A total of 466 produce and matching environmental swab samples was collected from various locations in packing sheds in the southern US from November 2002 through December 2003. These samples were assayed by enumerative tests for total aerobic bacteria (APC), total coliforms, total Enterococcus, and E. coli. Produce samples were also analyzed for the presence of Salmonella, Listeria monocytogenes, Shigella, and E. coli O157:H7. A total of 112 E. faecium and E. faecalis isolates were further screened for antibiotic resistance using a panel of seventeen antibiotics. Overall, the microbiological quality of fresh produce ranged from 4.0 to 7.9 log(10) CFU/g (APC); less than 1.0 log(10) to 4.5 log(10) CFU/g (coliforms); less than 1.0 log(10) to 4.0 log(10) CFU/g (E. coli); and less than 1.0 log(10) to 5.4 log(10) CFU/g (Enterococcus). No Salmonella, Shigella, or E. coli O157:H7 were detected from the 466 25-g produce samples tested. However, three domestic cabbage samples were found to be positive for L. monocytogenes. Of the Enterococcus isolates, E. faecium had a higher degree of resistance to antibiotics in general, while Enterococcus spp. isolated from Mexican produce had a higher degree of antibiotic resistance when compared to strains isolated from produce samples of domestic origin. Despite increased attention to the role of imported produce in foodborne disease, this study does not support the assumption that domestic produce is of higher microbial quality than Mexican produce.