Ionizing radiation sensitivity of Listeria monocytogenes ATCC 49594 and Listeria innocua ATCC 51742 inoculated on endive (Cichorium endiva)

Ionizing radiation inactivates the pathogenic bacteria that can contaminate leafy green vegetables. Leaf pieces and leaf homogenate of endive (Cichorium endiva) were inoculated with the pathogen Listeria monocytogenes (ATCC 49594) or Listeria innocua (ATCC 51742), a nonpathogenic surrogate bacterium. The radiation sensitivity of the two strains was similar, although L. innocua was more sensitive to the type of suspending leaf preparation. During refrigerated storage after irradiation, the population of L. monocytogenes on inoculated endive was briefly suppressed by 0.42 kilogray (kGy), a dose calibrated to achieve a 99% reduction. However, the pathogen regrew after 5 days until it exceeded the bacterial levels on the control after 19 days in storage. Treatment with 0.84 kGy, equivalent to a 99.99% reduction, suppressed L. monocytogenes throughout refrigerated storage. Doses up to 1.0 kGy had no significant effect on the color of endive leaf material, regardless of whether taken from the leaf edge or the leaf midrib. The texture of leaf edge material was unaffected by doses up to 1.0 kGy, whereas the maximum dose tolerated by leaf midrib material was 0.8 kGy. These results show that endive leaves may be treated with doses sufficient to achieve at least a 99.99% reduction of L. monocytogenes with little or no impact on the product's texture or color.     

Effect of citric acid on the radiation resistance of Listeria monocytogenes and frankfurter quality factors

Listeria monocytogenes is a common contaminant of ready-to-eat meat products, including frankfurters. Ionizing (gamma) radiation can eliminate L. monocytogenes from frankfurters. Citric acid (CA) is an antioxidant synergist and anti-microbial agent that can be applied to the surfaces of cured meat products prior to packaging. The effect of CA on the radiation resistance of L. monocytogenes that was surface-inoculated onto frankfurters was determined. The D(10) values, the radiation doses required to inactivate 90% of viable L. monocytogenes, were 0.61, 0.60, 0.54, and 0.53 kGy, on frankfurters dipped in 0, 1, 5 or 10% CA solution, respectively. CA, although an antioxidant synergist, did not increase antioxidant activity (AA) on frankfurter surfaces as determined by the ferric reducing antioxidant power (FRAP) assay. Lipid oxidation, as determined by the Thiobarbituric acid reactive substances (TBARS) assay, was not affected by CA or ionizing radiation. Color of frankfurters, determined by Hunter L, a, b, indicated that ionizing radiation induced a small, but visually imperceptible, loss of redness (a-value). Frankfurter firmness, as measured by maximum shear force, was not affected by ionizing radiation or CA. CA enhanced the lethality of ionizing radiation without negatively impacting frankfurter color, lipid oxidation, firmness, or antioxidant activity.     

Survival of Listeria monocytogenes on fresh and frozen strawberries

Cut or intact surfaces of fresh strawberries were spot inoculated with a five-strain cocktail of nalidixic-acid resistant Listeria monocytogenes (10(6) (low inoculum) and 10(8) (high inoculum) CFU per three-berry sample). Inoculated strawberries were dried for 1 h at 24 degrees C and were stored in loosely closed containers at 4 or 24 degrees C. An initial population reduction of approximately 0.6 and 1.2 log cycles, high and low inoculum, respectively, was observed on intact but not cut berries after the 1-h drying period. A decrease of 1.4 and 3.3 log cycles per intact sample was observed over 48 h for the high and low inoculum, respectively, when stored at 24 degrees C. When held at 4 degrees C, a reduction of approximately 3 log cycles per intact-berry sample was observed for both inocula over the 7-day storage period. Populations on cut surfaces remained constant at both temperatures and both inoculum densities throughout the storage period. Sliced, inoculated strawberries (6.7 log CFU/25-g sample) with or without 20% sucrose were frozen at -20+/-2 degrees C. After 28 days of frozen storage, populations of L. monocytogenes determined on tryptose phosphate agar supplemented with nalidixic acid (TPAN) had declined by 0 to 1.2 log cycles, with and without 20% sucrose, respectively. Counts on modified Oxford agar supplemented with nalidixic acid were significantly (P< or =0.05) lower (0.5 to 1.8 log CFU/g) than on TPAN indicating that some cell injury had occurred. Results of this study indicate that L. monocytogenes is capable of survival but not growth on the surface of fresh intact or cut strawberries throughout the expected shelf life of the fresh fruit and can survive on frozen strawberries for periods of at least 4 weeks. On whole strawberries held at 24 degrees C, significantly faster declines (P< or =0.05) of L. monocytogenes were observed when lower rather than higher inoculum levels were applied.     

Effectiveness of irradiation treatments in inactivating Listeria monocytogenes on fresh vegetables at refrigeration temperature

Ionizing radiation can be effective in controlling the growth of food spoilage and foodborne pathogenic bacteria. This study reports on an investigation of the effectiveness of irradiation treatment to eliminate Listeria monocytogenes on laboratory-inoculated broccoli, cabbage, tomatoes, and mung bean sprouts. Irradiation of broccoli and mung bean sprouts at 1.0 kGy resulted in reductions of approximately 4.88 and 4.57 log CFU/g, respectively, of a five-strain cocktail of L. monocytogenes. Reductions of approximately 5.25 and 4.14 log CFU/g were found with cabbage and tomato, respectively, at a similar dose. The appearance, color, texture, taste, and overall acceptability did not undergo significant changes after 7 days of postirradiation storage at 4 degrees C, in comparison with control samples. Therefore, low-dose ionizing radiation treatment could be an effective method for eliminating L. monocytogenes on fresh and fresh-cut produce.     

Effect of packaging and storage temperature on the survival of Listeria monocytogenes inoculated postprocessing on sliced salami

The survival of postprocess Listeria monocytogenes contamination on sliced salami, stored under the temperatures associated with retail and domestic storage, was investigated. Sliced salami was inoculated with low and high concentrations of L. monocytogenes before being packaged under vacuum or air. Survival of L. monocytogenes was determined after storage of sausages for 45 or 90 days for low or high sample inocula, respectively, at 5, 15, and 25 degrees C. All survival curves of L. monocytogenes were characterized by an initial rapid inactivation within the first days of storage, followed by a second, slower inactivation phase or "tailing." Greater reduction of L. monocytogenes was observed at the high storage temperature (25 degrees C), followed by ambient (15 degrees C) and chill (5 degrees C) storage conditions. Moreover, vacuum packaging resulted in a slower destruction of L. monocytogenes than air packaging, and this effect increased as storage temperature decreased. Although L. monocytogenes numbers decreased to undetectable levels by the end of the storage period, the time (in days) needed for this reduction and for the total elimination of the pathogen decreased with high temperature, aerobic storage, and high inoculum. Results of this study clearly indicated that the kinetics of L. monocytogenes were highly dependent on the interaction of factors such as storage temperature, packaging conditions, and initial level of contamination (inoculum). These results may contribute to the exposure assessment of quantitative microbial risk assessment and to the establishment of storage-packaging recommendations of fermented sausages.     

Thermal resistance of Listeria monocytogenes in inoculated and naturally contaminated raw milk

Raw whole milk inoculated with 10(5) CFU/ml of Listeria monocytogenes was thermally processed at 60-72 degrees C for a minimum holding time of 16.2 s with survival being observed at temperatures up to 67.5 degrees C. In addition, milk naturally contaminated with L. monocytogenes serotype 1 (around 10(4) CFU/ml) was pooled for 2 to 2.5 days and then run through an HTST pasteurizer at temperatures ranging from 60-78 degrees C. Viable L. monocytogenes were detected in the temperature range of 60-66 degrees C. No viable Listeria were detected after treatment at temperatures of 69 degrees C and above in any of five trials. Efficacy of pasteurization and widespread use of processing conditions well above the minimum HTST guidelines ensure the absence of Listeria in pasteurized milk products. However, survival of Listeria at sub-pasteurization temperatures (60-67.5 degrees C) is of concern with regard to heat-treated or raw-milk cheeses.     

Effect of inoculum preparation procedure and storage time and temperature on the fate of Listeria monocytogenes on inoculated salami

Although dry/semidry fermented sausages are characterized as being of low-to-moderate risk for human listeriosis on a per-serving and per-annum basis, data are lacking relative to the fate of postprocessing Listeria monocytogenes contamination during storage of such products. This study evaluated the effect of inoculum preparation and storage conditions on the fate of L. monocytogenes on vacuum-packaged salami. Commercially produced salami was sliced and inoculated (4 +/- 1.3 log CFU/ cm2) with one of four types of inocula. All inocula consisted of the same 10-strain L. monocytogenes composite, cultivated as individual strains prior to mixing for inoculation. Active cultures of individual strains were prepared (30 degrees C, 24 h) in either tryptic soy broth (containing 0.25% glucose) plus 0.6% yeast extract (TSBYE), tryptic soy broth without glucose plus 0.6% yeast extract (TSBYE-G), TSBYE-G plus 1% glucose (TSBYE+G), or in TSBYE, and then habituated (7 degrees C, 72 h) in sterile salami homogenate (10% [wt/wt] with distilled water). Inoculated salami slices were vacuum packaged, stored at 4, 12, or 25 degrees C, and analyzed (three samples per treatment in each of two replicates) periodically for surviving bacterial counts. In general, pathogen levels decreased during storage and reached levels below the detection limit (-0.4 log CFU/cm2) between 27 and 90 days of storage, depending on temperature of storage and inoculum type. Death rates (log CFU/cm2/day) were found to increase as storage temperature increased, with the exception of the acid-adapted (TSBYE+G) cells, which decreased more rapidly at 4 degrees C than at 12 or 25 degrees C. The habituated inoculum was inactivated at a faster rate than other inocula at 12 and 25 degrees C, but performed similarly to nonadapted (TSBYE-G) and partially acid-adapted (TSBYE) inocula at 4 degrees C. These data may be used to supplement existing information for use in future risk assessments.     

温度及乳酸链球菌素对单增李斯特菌的抑制作用

通过Matlab软件拟合Gompertz生长模型,研究了温度对单增李斯特菌(Listeria.monocytogenes,LM)的影响;同时,研究了不同浓度(5、10、50、100、150μg/m L)、p H(1、3、5、7、9)、温度(45、75、95、115、121℃)条件下的乳酸链球菌素对LM杀菌活性的影响,旨在为LM的监控技术发展提供理论依据。结果表明:低温的抑制效果明显,最大细胞密度减少了4.3455 lg cfu/m L;乳酸链球菌素浓度低于5μg/m L时能促进LM的生长,高于10μg/m L时,对LM有一定的杀菌作用,高于150μg/m L时,48 h之内几乎可以杀死营养肉汤中的所有LM;乳酸链球菌素对酸性有协同效应;并有较好的热稳定性。      

Bioprotective Leuconostoc strains against Listeria monocytogenes in fresh fruits and vegetables

Ten Leuconostoc mesenteroides and one Ln. citreum strains isolated from fresh fruit and vegetables were tested for their antagonistic capacity against Listeria monocytogenes. Genetic differences among strains were analyzed by Random Amplified Polymorphic DNA (RAPD). All the isolates clustered together and differed from the type strain Ln. mesenteroides ATCC 8293 as well as from Ln. fallax and Ln. citreum. Organic acids, hydrogen peroxide and bacteriocins were detected as main inhibition mechanisms. Characterization of culture supernatants from the bacteriocinogenic strains, CM135 and CM160 revealed a high resistance of antibacterial activity to temperature and pH, and a bactericidal mode of action against L. monocytogenes. Produced bacteriocins belonged to the Class IIa and sequencing of genes showed complete homology with mesentericin Y105. A study of the effect of the relative dose of pathogen and LAB on control of L. monocytogenes in wounds of Golden Delicious apples and Iceberg lettuce leaf cuts was performed. A comparison of the dose of bioprotective strain needed for a ten fold reduction of the viable pathogen concentration (ED(90)) revealed that strain CM160 was the most effective against L. monocytogenes. ED(90) values varied from 1.3.10(4) to 5.0.10(5) cfu.g(-1) or wound, at ranges of pathogen levels from 1.0.10(3) to 5.0.10(4) cfu.g(-1) of lettuce or wound of apple. The efficiency of the strains was also calculated as the ratio of the ED(90) value to the pathogen dose inoculated. The lowest ratio was found for strain CM160 at 5 to 50 cells of LAB per cell of pathogen. The strain offers potential application for prevention of the presence of L. monocytogenes in fresh fruit and vegetables.     

Strains and suspending menstrua as factors affecting death and injury of Listeria monocytogenes during freezing and frozen storage

Cell suspensions of Listeria monocytogenes strains V7, California, and Ohio in phosphate buffer solution, tryptose broth, or milk were frozen and stored at -18 degrees C. At appropriate intervals during storage, a sample was thawed at 35 degrees C and surface-plated on suitable media to allow colony formation by noninjured or noninjured plus injured cells. Degrees of death and injury were calculated from the data. Cells of L. monocytogenes were more resistant to death and injury when they were suspended in milk or tryptose broth rather than phosphate buffer solution. There was a significant (two-way ANOVA) difference in resistance to death and injury during frozen storage among strains of L. monocytogenes suspended in tryptose broth. The difference was nonsignificant when the cells were suspended in phosphate buffer solution or milk. Listeria monocytogenes strain Ohio was more resistant to death and injury during frozen storage when cells were suspended in tryptose broth rather than milk. The opposite was true for strains V7 and California. Death and injury of L. monocytogenes strains V7, California, and Ohio suspended in phosphate buffer solution were 98.7, 97.9, and 91.2% and 77.5, 51.6, and 70.2%, respectively, after 4 wk of frozen storage. The values were 67.3, 91.6, and 42.3% and 44.4, 65.6, and 32.6%, respectively, when cells were suspended in tryptose broth, and they were 37.8, 40, and 60.7% and 10.8, 66.8, and 46%, respectively, when cells were suspended in milk.     

Heat resistance of Listeria monocytogenes in vegetables: evaluation of blanching processes

The heat resistance of a Listeria monocytogenes composite (serotypes 1/2a, 1/2b, and 4b) was determined in fresh broccoli florets, sweet green peppers, onions, mushrooms, and peas using an end-point procedure in polyester pouches. The heat resistance of L. monocytogenes was higher in peas (D(60 degrees C) = 1.0 min) and mushrooms (D(60 degrees C) = 0.7 min) than in other vegetables tested (D(60 degrees C) in onions = 0.2 min) and was highest when cells were subjected to starvation before the thermal death time experiments (D(60 degrees C) of starved L. monocytogenes in mushrooms = 1.6 min). The results showed that blanching can be used as an antilisterial treatment (inactivation of 5 logs of L. monocytogenes) when the cold spot of vegetables is treated for at least 10 s at 75 degrees C or instantaneously (<1 s) at temperatures above 82 degrees C.     

Injury and death of frozen Listeria monocytogenes as affected by glycerol and milk components

A cell suspension of Listeria monocytogenes strain Scott A in phosphate buffer solution alone or with added glycerol, milk fat, lactose, or casein was frozen and stored at -18 degrees C. At suitable intervals, samples of cell suspensions were thawed at 35 degrees C and plated on suitable media to distinguish between surviving injured and noninjured cells of L. monocytogenes. Glycerol (2 or 4%) protected L. monocytogenes from death and injury during frozen storage for up to 6 mo; however, when 2% glycerol was present, 30 min of frozen storage had to elapse after completion of freezing before protection against death was evident. During short-term (2 wk or less) frozen storage, lactose, milk fat, and casein, each at 2%, provided better protection to L. monocytogenes than did 2% glycerol. During long-term frozen storage, milk components, each at 2%, protected L. monocytogenes against death and injury, but less than that provided by glycerol. Protection by lactose and milk fat against death during frozen storage was observed during 4 wk and against injury during 5 mo and 4 wk of frozen storage, respectively. Protection by casein against death and injury occurred during frozen storage for up to 6 mo. Salts that simulate milk ultrafiltrate provided almost no protection to L. monocytogenes during freezing and frozen storage. Increasing the concentration of milk fat from 2 to 4% resulted in almost no change in death of L. monocytogenes, but in a decrease in injury only during the first 24 h of frozen storage.(ABSTRACT TRUNCATED AT 250 WORDS)     

Effect of gamma irradiation on Listeria monocytogenes in frozen,artificially contaminated sandwiches

Gamma irradiation has been shown to effectively control L monocytogenes in uncooked meats but has not been extensively studied in ready-to-eat foods. The presence of Listeria in ready-to-eat foods is often due to postprocess contamination by organisms in the food-manufacturing environment. Because gamma irradiation is applied after products are packaged, the treated foods are protected from environmental recontamination. Currently, a petition to allow gamma irradiation of ready-to-eat foods is under review by the Food and Drug Administration. This study was conducted to determine if gamma irradiation could be used to control L. monocytogenes in ready-to-eat sandwiches. Ham and cheese sandwiches were contaminated with L. monocytogenes, frozen at -40 degrees C, and exposed to gamma irradiation. Following irradiation, sandwiches were assayed for L. monocytogenes. A triangle test was performed to determine if irradiated and nonirradiated sandwiches differed in sensory quality. We found that the D10-values ranged from 0.71 to 0.81 kGy and that a 5-log reduction would require irradiation with 3.5 to 4.0 kGy. The results of a 39-day storage study of sandwiches inoculated with 10(7) CFU of L monocytogenes per g indicated that counts for nonirradiated sandwiches remained fairly constant. Counts for sandwiches treated with 3.9 kGy decreased by 5 log units initially and then decreased further during storage at 4 degrees C. Sensory panelists could distinguish between irradiated and nonirradiated sandwiches but were divided on whether irradiation adversely affected sandwich quality. Our results suggest that manufacturers of ready-to-eat foods could use gamma irradiation to control L. monocytogenes and improve the safety of their products.     

Irradiation inactivation of Listeria monocytogenes in low-fat ground pork at freezing and refrigeration temperatures

Gamma radiation effectively controls Listeria monocytogenes in uncooked and in ready-to-eat foods. This study was conducted to determine if gamma radiation could be used to control L. monocytogenes in ground pork. Ground pork was contaminated with L. monocytogenes, kept at refrigeration (4 degrees C), chilling (0 degrees C), and freezing (-18 degrees C) temperatures overnight, exposed to gamma radiation and stored at 4 degrees C for 7 days, and at 0 and -18 degrees C for 60 days. Following irradiation, the meat was assayed for L. monocytogenes viable counts and lipid oxidation. A triangle test was performed to determine if sausage made from the irradiated and nonirradiated ground pork differed in sensory quality. It was observed that a 5-log reduction of L. monocytogenes viable counts would require a 3.0-kGy radiation dose. The results of a 60-day storage study of ground pork inoculated with 10(5) to 10(6) CFU of L. monocytogenes per gram indicated that counts for nonirradiated meat remained fairly constant at refrigeration, chilling, and freezing temperatures. However, irradiation of ground pork at 3.0 kGy could inactivate L. monocytogenes totally in ground pork subsequently held at all the temperatures used in this study. Lipid oxidation measurements, as determined by the thiobarbituric acid-reactive substance assay, ranged from 0.16 nmol/g for nonirradiated ground pork and 0.20 nmol/g for meat irradiated at 3.0 kGy. Sensory panelists could distinguish between irradiated and nonirradiated sausage but were divided on whether irradiation adversely affected the sausage quality. Our results suggest that gamma radiation could be useful to control L. monocytogenes in ground pork and improve the safety of ground pork products.     

Predictions of growth for Listeria monocytogenes and Salmonella during fluctuating temperature

We studied the predictive performance of a dynamic modelling approach, combined with predictions from the Food MicroModel software, applied to the growth of Listeria monocytogenes and Salmonella in pasteurised milk, chicken liver paté and minced chicken, under constant as well as fluctuating temperatures. We found that, in general, the accuracy of a prediction under fluctuation temperature was similar to that under constant temperature. Generally, there was a good agreement between predictions and observations. However, the growth of Listeria monocytogenes in pasteurised milk was inhibited largely by the natural flora present.     

Growth potential of Salmonella spp. and Listeria monocytogenes in nine types of ready-to-eat vegetables stored at variable temperature conditions during shelf-life

Growth potential (δ) is defined as the difference between the population of a microorganism at the end of shelf-life of specific food and its initial population. The determination of δ of Salmonella and Listeria monocytogenes in RTE vegetables can be very useful to determine likely threats to food safety. However, little is known on the behavior of these microorganisms in several RTE vegetables. Therefore, the aim of this study was to determine the δ of both pathogens in nine different types of RTE vegetables (escarole, collard green, spinach, watercress, arugula, grated carrot, green salad, and mix for yakisoba) stored at refrigeration (7°C) and abuse temperature (15°C). The population of aerobic microorganisms and lactic acid bacteria, including those showing antimicrobial activity has been also determined. Results indicated that L. monocytogenes was able to grow (δ≥0.5 log(10)) in more storage conditions and vegetables than Salmonella. Both microorganisms were inhibited in carrots, although a more pronounced effect has been observed against L. monocytogenes. The highest δ values were obtained when the RTE vegetables were stored 15°C/6days in collard greens (δ=3.3) and arugula (δ=3.2) (L. monocytogenes) and arugula (δ=4.1) and escarole (δ=2.8) (Salmonella). In most vegetables and storage conditions studied, the counts of total aerobic microorganisms raised significantly independent of the temperature of storage (p<0.05). Counts of lactic acid bacteria were higher in vegetables partially or fully stored at abuse temperature with recovery of isolates showing antimicrobial activity. In conclusion, the results of this study show that Salmonella and L. monocytogenes may grow and reach high populations in RTE vegetables depending on storage conditions and the definition of effective intervention strategies are needed to control their growth in these products.     

Elimination of Listeria monocytogenes from vacuum-packed dry-cured ham by E-beam radiation

The inactivation kinetics for Listeria monocytogenes Scott A (CIP 103575, serotype 4b) and Listeria innocua (NTC 11288) after E-beam radiation were studied in vacuum-packed ready-to-eat dry-cured ham to optimize the sanitation treatment of this product. A treatment of 1.12 kGy was calculated to reach the food safety objective according to the U.S. Department of Agriculture criterion. No irradiation treatment is necessary to meet the European Union microbiological criterion for this bacterium. No changes (at doses < or =4 kGy) in the 2-thiobarbituric acid reactive substances values and texture were observed. Dry-cured hams treated with 1 and 2 kGy had negligible sensory modifications (appearance, odor, and flavor). However, the application of 3 and 4 kGy resulted in an increase in the intensity of off-odors and off-flavors. Despite these effects, all irradiated vacuum-packed dry-cured hams treated at < or =4 kGy were deemed acceptable for trading.     

Effect of temperature and pH on survival of Listeria monocytogenes in coleslaw

The survival and growth of Listeria monocytogenes in fresh coleslaw, pH 3.9, and in coleslaw adjusted to pH 4.0, 5.0, 6.0 or 7.0 before inoculation was studied at three temperatures (4, 15 and 25 degrees C). L. monocytogenes was not detectable after 5 days incubation in fresh coleslaw nor in coleslaw adjusted to pH 4.0. Coleslaw at pH 5.0 was also inhibitory to L. monocytogenes at all three temperatures studied. A decline in viable numbers of L. monocytogenes in coleslaw at pH 6.0 occurred at 4 degrees C and at 15 degrees C, whereas at 25 degrees C the viable count of L. monocytogenes increased initially and remained high after incubation for 25 days. L. monocytogenes grew rapidly in coleslaw at pH 7.0 at all three temperatures studied, followed by an equally rapid decline in viable count.     

Irradiation and modified atmosphere packaging for the control of Listeria monocytogenes on turkey meat.

When radiation-sterilized ground turkey meat was inoculated with Listeria monocytogenes, packaged under mixtures of nitrogen and carbon dioxide, and irradiated with gamma-radiation doses of 0 to 3.0 kGy, there was a statistically significant (P < 0.05), but probably not a biologically significant, lower (0.39 log) predicted bacterial survival in the presence of 100% carbon dioxide than in the presence of 100% nitrogen. Possibly because all atmospheres contained oxygen and because a response surface design was used, gamma-radiation resistance was not significantly (P < 0.05) different in air than in modified atmosphere packaging (MAP) mixtures containing 5% O2 or containing 20, 40, 60, and 80% CO2 and balance N2. The antilisterial effects of MAP mixtures containing 17.2, 40.5, and 64% CO2 and balance N2 were compared to those associated with air and vacuum packaging on turkey inoculated with approximately 5 x 10(3) CFU/g. Samples were irradiated to doses of 0, 0.5, 1.0, 1.5, 2.0, and 2.5 kGy and were stored at 7 degrees C for up to 28 days. Irradiation treatments were significantly more lethal in the presence of air packaging than in either vacuum packaging or MAP, and in those samples that received >1.0 kGy, there was a concentration-dependent CO2 inhibition of L. monocytogenes multiplication and/or recovery.