Impact of cooking,cooling, and subsequent refrigeration on the growth or survival of Clostridium perfringens in cooked meat and poultry products

In January 1999, the Food Safety and Inspection Service (FSIS) finalized performance standards for the cooking and chilling of meat and poultry products in federally inspected establishments. More restrictive chilling (stabilization) requirements were adopted despite the lack of strong evidence of a public health risk posed by industry practices employing the original May 1988 guidelines (U.S. Department of Agriculture FSIS Directive 7110.3). Baseline data led the FSIS to estimate a "worst case" of 10(4) Clostridium perfringens cells per g in raw meat products. The rationale for the FSIS performance standards was based on this estimate and the assumption that the numbers detected in the baseline study were spores that could survive cooking. The assumptions underlying the regulation stimulated work in our laboratory to help address why there have been so few documented outbreaks of C. perfringens illness associated with the consumption of commercially processed cooked meat and poultry products. Our research took into account the numbers of C. perfringens spores in both raw and cooked products. One hundred ninety-seven raw comminuted meat samples were cooked to 73.9 degrees C and analyzed for C. perfringens levels. All but two samples had undetectable levels (<3 spores per g). Two ground pork samples contained 3.3 and 66 spores per g. Research was also conducted to determine the effect of chilling on the outgrowth of C. perfringens spores in cured and uncured turkey. Raw meat blends inoculated with C. perfringens spores, cooked to 73.9 degrees C, and chilled according to current guidelines or under abuse conditions yielded increases of 2.25 and 2.44 log10 CFU/g for uncured turkey chilled for 6 h and an increase of 3.07 log10 CFU/g for cured turkey chilled for 24 h. No growth occurred in cured turkey during a 6-h cooling period. Furthermore, the fate of C. perfringens in cooked cured and uncured turkey held at refrigeration temperatures was investigated. C. perfringens levels decreased by 2.52, 2.54, and 2.75 log10 CFU/g in cured turkey held at 0.6, 4.4, and 10 degrees C, respectively, for 7 days. Finally, 48 production lots of ready-to-eat meat products that had deviated from FSIS guidelines were analyzed for C. perfringens levels. To date, 456 samples have been tested, and all but 25 (ranging from 100 to 710 CFU/g) of the samples contained C. perfringens at levels of <100 CFU/g. These results further support historical food safety data that suggest a very low public health risk associated with C. perfringens in commercially processed ready-to-eat meat and poultry products.     

Evaluation of animal age and muscle type on beef log juice colour and residual GOT activity when cooked to target end-point temperature of 79.4 °C†

The effectiveness of the pink-juice test to determine 79.4 °C end-point temperature (EPT) of cooked beef logs was appraised. Logs made from five cuts of meat from three animal age groups were fabricated in triplicate to simulate products received at ports of entry and then cooked to EPTs of 78.0–81.8 °C. CIELAB L*, a*, b*, C and h ° values of internal surfaces of freshly sliced meat and pressed juices from samples were determined. Sensory ratings were made by six trained panelists to determine intensities of residual red color of the juices. Animal age and cut of meat had little effect on the CIELAB color values. Residual red color was apparent in all samples by both sensory and a* values analysis. Sensory ratings did not vary significantly (P < 0.05) by animal age or cut of meat. Average values of 3.2 (intensity range, 1–9) corresponded to an EPT slightly greater than 80 °C; absence of red color in the juices would therefore indicate an EPT in excess of the target temp of 79.4 °C. Residual glutamic-oxaloacetic transaminase activity (GOT) activity, used as a collateral test for EPT, ranged from 482.5 to 1641.8 SFU ml⁻¹ of juice and differed significantly by cut of meat (P < 0.05), but not by animal age. © 1999 Society of Chemical Industry     

Polymerase chain reaction assay for identification of chicken in meat and meat products

The aim of this study was to develop polymerase chain reaction (PCR) assay for specific detection of chicken meat using designed primer pair based on mitochondrial D-loop gene for amplification of 442 bp DNA fragments from fresh, processed and autoclaved meat and meat products. The PCR result was further verified by restriction digestion with HaeIII and Sau3AI enzymes for specific cutting site in amplified DNA fragments. The specificity of assay was cross tested with DNA of cattle, buffalo, sheep, goat, pig, duck, guinea fowl, turkey and quail, where amplification was observed only in chicken without cross reactivity with red meat species. However positive reaction was also observed in quail and turkey. In this study, no adverse effects of cooking and autoclaving were found on amplification of chicken DNA fragments. Thus, the detection limits was found to be less than 1% in admixed meat and meat products. The developed assay was found specific and sensitive for rapid identification of admixed chicken meat and meat products processed under different manufacturing conditions.     

The cytochrome c content of various poultry meats

The cytochrome c content and total haem pigments in the breast and thigh meat of broiler chickens, hens out of lay, turkeys, geese, duckling (Peking), and muscovy ducks were determined. The levels of cytochrome c in the breast and thigh meat were: for chicken 11.4 and 35.5; for hens 14.0 and 84.2; for turkeys 13.1 and 47.4; for geese 141.0 and 107.8; for duckling 111.2 and 149.9 and for muscovy ducks 81.5 and 97.3 μg per g of tissue, respectively. The correlation coefficient between cytochrome c and total haem pigments concentration was r=0.98 for breast, and r=0.85 for thigh meat. The authors postulate that the cytochrome c may play a noticeable role in the colour of fresh and processed poultry meat, but further investigations are needed to confirm this.     

CATALATIC ACTIVITY AS AN INDICATOR OF END-POINT TEMPERATURES IN BREADED, HEAT PROCESSED CHICKEN PATTIES

Adequate heat-processing of meat and poultry products to destroy harmful pathogens is important to the consumer's safety. The catalatic activity, defined as the decomposition of H₂O₂ into H₂O and O₂, has been evaluated as a potential indicator of heat treatment adequacy for chicken patties. Commercially prepared breast and leg meat patties were processed through a belt type grill to various end-point temperatures (EPTs) and their catalatic activities monitored for up to 120 min. All breast samples heated to EPTs of ≤ 69C and all leg samples heated to ≥ 68C showed positive reactions after incubation for 10 min. As the EPT increased, fewer samples were positive, indicating a decrease in the catalatic activity. For EPTs of ≥ 73C, three of 12 breasts and one of 17 leg patties showed positive activity after 30 min incubation. The catalatic activity test may offer a simple and rapid procedure for estimating the EPT at 73C with 3-4C variation for commercially processed chicken patties.     

Rosemary as antioxidant in pressure processed chicken during subsequent cooking as evaluated by electron spin resonance spectroscopy

The potential of rosemary (Rosmarinus officinalis L.) to inhibiting lipid oxidation in minced chicken breast and thigh muscle processed at 600 MPa for 10 min during subsequent heat treatment was investigated using electron spin resonance (ESR) spectroscopy and electrochemical detection of oxygen consumption. Chicken breast cooked at 95 °C was found to have significantly higher rate of formation of free radicals and oxygen consumption rate than the samples cooked at 70 °C and 120 °C and this intermediate cooking temperature was used to evaluate the effect of pressure on oxidation during subsequent cooking. Rosemary was found effective in retarding lipid oxidation since the pressurized, minced chicken breast and thigh with rosemary added showed lower rate of oxygen consumption and lower tendency of free radical formation following heat treatment than the samples without rosemary. Pressurized chicken thigh showed a higher susceptibility to oxidation than chicken breast upon subsequent heat treatment. Oxidation in pressurized and subsequently heat-treated chicken breast was from a higher tendency of radical formation concluded to be in an earlier phase of oxidation compared to thigh subjected to the same treatment.Industrial relevanceHigh-pressure processing has a great potential for microbial control of raw chicken meat as a “fresh” chill-stored, convenience product for wok cooking. While raw chicken meat is oxidatively stable, high-pressure treatment at 600 MPa and above induces lipid oxidation resulting in off-flavors during subsequent cooking. Addition of 0.1% dried rosemary to minced chicken thighs or breasts prior to high-pressure processing inhibit lipid oxidation during subsequent cooking and could form the basis for product development.     

Meat species identification and Halal authentication using PCR analysis of raw and cooked traditional Turkish foods

The method performance characteristics of commercially available PCR kits for animal species identification were established. Comminuted meat products containing different levels of pork were prepared from authentic beef, chicken, and turkey. These meat products were analysed in the raw state and after cooking for 20 min at 200 °C. For both raw and cooked meats, the PCR kit could correctly identify the animal species and could reliably detect the addition of pork at a level below 0.1%. A survey of 42 Turkish processed meat products such as soudjouk, salami, sausage, meatball, cured spiced beef and doner kebap was conducted. Thirty-six samples were negative for the presence of pork (< 0.1%) and four were found to be correctly labelled as containing pork. However, one sausage sample was labelled as containing 5% beef, but beef DNA was not detected and a meatball sample labelled as 100% beef was found to contain chicken. Another turkey meatball sample was predominantly chicken.     

Comparison of glutathione peroxidase activity,and of total and soluble selenium content in two muscles from chicken,turkey, duck,ostrich and lamb

Glutathione peroxidase activity (GSHPx), total and soluble selenium in two muscles from five species were compared (chicken, duck, turkey, ostrich and lamb). The highest GSHPx activity, found in duck muscles (4.8 U/g; 3.0 U/g), was significantly higher than that in lamb (1.8 U/g; 1.4 U/g), turkey (1.2 U/g; 0.6 U/g), chicken (1.0 U/g; 0.7 U/g), and ostrich muscles (0.9 U/g; 0.8 U/g). GSHPx activities were significantly higher in the oxidative muscles from chicken (thigh), duck (breast), turkey (thigh) and lamb (PM) than those in the corresponding glycolytic muscles (breast, thigh, breast and LD, respectively). Also the total selenium content was higher in duck muscles (149 ng/g; 139 ng/g), than in lamb (171 ng/g /PM, M. psoas major/ and 86 ng/g /LD, M. longissimus dorsi/), chicken (117 ng/g; 109 ng/g), ostrich (106 ng/g; 103 ng/g) and turkey muscles (110 ng/g; 70 ng/g). The selenium content was significantly higher in the oxidative muscles of lamb and turkey than in the corresponding glycolytic muscles. The percentage of soluble selenium in lamb PM was lower (32%) than that in all other muscles (range 48–76%). The study thus showed considerable variation, among species, of glutathione peroxidase activity, total and soluble selenium content in muscle, which may be important for the oxidative stability and nutritional value of different meat products.     

The effect of various types of poultry pre- and post-rigor meats on emulsification capacity, water-holding capacity and cooking loss

In this study, the relationship between various kinds of poultry meat (quail, partridge, chicken and turkey) on pH, emulsification capacity, water-holding capacity and cooking loss was investigated. The effect of rigor state on pH, emulsification capacity, water-holding capacity and cooking loss was also determined. To investigate these parameters, immediately after slaughter and deboning, meat parts were submitted to both pre- and post-rigor analyses. The results indicated that the emulsification capacity of quail and chicken meat was higher than the values for partridge and turkey meat. Quail meat showed the highest water-holding capacity value in the post-rigor stage. The lowest cooking loss value was found in partridge meat, in both pre- and post-rigor stages. The state of rigor had a significant (P<0.05; P0.01) effect on pH and cooking loss values, respectively.     

Occurrence of pathogens in raw and ready-to-eat meat and poultry products collected from the retail marketplace in Edmonton, Alberta, Canada

A total of 800 meat and poultry products were purchased from the retail marketplace in Edmonton, Alberta, Canada. The products consisted of raw ground beef, chicken legs, pork chops, and ready-to-eat fermented sausage, roast beef, processed turkey breast, chicken wieners, and beef wieners. The samples were analyzed to determine the prevalence of Shiga toxin-producing Escherichia coli, Salmonella, Campylobacter spp., and Listeria monocytogenes. Shiga toxin-producing E. coli 022: H8 was found in one raw ground beef sample. Salmonella and Campylobacter were found in 30 and 62% of raw chicken legs, respectively. L. monocytogenes was found in 52% of raw ground beef, 34% of raw chicken legs, 24% of raw pork chops, 4% of fermented sausages, 3% of processed turkey breast, 5% of beef wieners, and 3% of chicken wieners. The occurrence of pathogens in this study is similar to that in retail products in many other international locales.     

Antimicrobial Activity and Functionality of Reduced Sodium Chloride and Potassium Sorbate in Uncured Poultry Products

Uncured turkey and chicken breast meat products, formulated with NaCl (0.65 and 1.30%) and potassium sorbate (0 and 0.26%), were tested for antimicrobial activity and functional properties. The chopped products were inoculated (Clostridium sporogenes, 10/g) in cans and in packages and abused at 20°C. Microbial growth and gas production were rapid at both NaCl levels tested. Inclusion of potassium sorbate in the formulation delayed initiation and rate of microbial growth and gas production. Potassium sorbate also reduced (P<0.05) weight losses during cooking of the low NaCl turkey product. Rates of gas production were similar in canned and vacuum packaged products. Differences in microbial growth and gas production between chicken and turkey products were minor.     

The influence of dietary lipid source on quality characteristics of raw and processed chicken meat

The influence of dietary lipid source [animal fats (AF) and vegetable oils (VO)] on quality characteristics of raw chicken meat (breast, thigh and meat batter) and cooked breaded patties prepared using a conventional technology (CT; forming, battering, breading, frying and convection cooking) or innovative technology (IT; forming, pre-dusting, steam cooking, battering and frying) was evaluated. Overall, dietary lipid source did not influence the chemical composition of raw meat while it modified its colour (L*, a*, b*). With respect to AF, VO produced higher breast and thigh meat cooking losses as well as a lower moisture and higher protein content of cooked breaded patties. VO also determined an increase of polyunsaturated-to-saturated fatty acid ratio of both raw and processed meat. Despite the different fatty acid profiles, the oxidative status of lipids was not affected by dietary lipid source and was acceptable in both raw meat and cooked patties as indicated by peroxide and thiobarbituric acid reactive substance values. As for the processing technology, IT determined a higher moisture and lower lipid content of the cooked breaded patties. Moreover, lipolysis degree was slightly higher in the products coming from IT. Finally, patties from AF group were lighter and more yellow than products belonging to VO group whereas IT led to lighter, less red and more yellow patties in comparison to CT.     

INFLUENCE OF HEATING END-POINT TEMPERATURE ON VOLATILES FROM POULTRY MEAT - A REVIEW

During heating of muscle foods, numerous volatile flavor components are generated. Both the identity and quantity of these volatiles are influenced by cooking end-point temperature (EPT) and post-cooking storage. Methods for assessing flavor volatiles include sensory tests and gas chromatographic (GC) methods. Static headspace GC techniques either with a packed or capillary column have been used to determine the volatiles individually and they are simpler in operation compared to sensory tests. High correlations between EPTs and several compounds in heated chicken breast and leg meat patties have been obtained. Samples prepared in model systems are more uniform in EPTs as compared to processed products. Good resolution and reproducibility in the analysis of volatiles from chicken meat have been reported by using a dynamic headspace-capillary column approach. More than one half of all compounds increased linearly or quadratically as EPT increased. Controlling the heating EPT is important in ensuring the quality and stability of precooked poultry.     

Thermal properties of connective tissue in breast and leg muscles of chickens and turkeys

BACKGROUND: There is a need to characterise connective tissue of chicken and turkey as they can be involved in meat defects. This study focused on the content and thermal stability of intramuscular connective tissue. A comparison between breast and leg muscles and between 38‐day‐old chickens (Ross 502) and 110‐111‐day‐old turkeys (Nicholas 300) commercially produced in Finland was made. RESULTS: Collagen content of breast muscles was lower than that of leg muscles (approx. 2.4 mg g^?1 vs. 4.0 mg g^?1, respectively, P < 0.05), but collagen content was similar in chickens and turkeys. The percentage of soluble collagen in chicken muscles was higher than that in turkey muscles (P < 0.05). In chickens, more soluble collagen was found in leg muscles than in breast muscles (P < 0.05). Chicken breast muscles had higher onset temperature of thermal shrinkage (T_o) of intramuscular connective tissue than turkey breast muscles (P < 0.05). Chicken leg muscles had higher peak temperature of thermal shrinkage (T_p) of intramuscular connective tissue than turkey leg muscles (P < 0.05). CONCLUSION: Chickens and turkeys had similar collagen content and T_o and T_p despite the species, age and muscle difference. However, the higher collagen solubility in chickens than in turkeys indicated that collagen was less matured in chickens than in turkeys. Copyright © 2009 Society of Chemical Industry     

Presence and changes in populations of yeasts on raw and processed poultry products stored at refrigeration temperature

A study was undertaken to determine populations and profiles of yeast species on fresh and processed poultry products upon purchase from retail supermarkets and after storage at 5 degrees C until shelf life expiration, and to assess the potential role of these yeasts in product spoilage. Fifty samples representing 15 commercial raw, marinated, smoked, or roasted chicken and turkey products were analyzed. Yeast populations were determined by plating on dichloran rose bengal chloramphenicol (DRBC) agar and tryptone glucose yeast extract (TGY) agar. Proteolytic activity was determined using caseinate and gelatin agars and lipolytic activity was determined on plate count agar supplemented with tributyrin. Populations of aerobic microorganisms were also determined. Initial populations of yeasts (log10 cfu/g) ranged from less than 1 (detection limit) to 2.89, and increased by the expiration date to 0.37-5.06, indicating the presence of psychrotrophic species. Highest initial populations were detected in raw chicken breast, wings, and ground chicken, as well as in turkey necks and legs, whereas roasted chicken and turkey products contained less than 1 log10 cfu/g. During storage, yeast populations increased significantly (P < or = 0.05) in whole chicken, ground chicken, liver, heart and gizzard, and in ground turkey and turkey sausage. Isolates (152 strains) of yeasts from poultry products consisted of 12 species. Yarrowia lipolytica and Candida zeylanoides were predominant, making up 39 and 26% of the isolates, respectively. Six different species of basidiomycetous yeasts representing 24% of the isolates were identified. Most Y. lipolytica strains showed strong proteolytic and lipolytic activities, whereas C. zeylanoides was weakly lipolytic. Results suggest that yeasts, particularly Y. lipolytica, may play a more prominent role than previously recognized in the spoilage of fresh and processed poultry stored at 5 degrees C.     

Polybrominated diphenyl ethers (PBDEs) in US meat and poultry: 2012–13 levels,trends and estimated consumer exposures

ABSTRACT

Polybrominated diphenyl ethers (PBDEs) are a class of brominated flame retardants whose use has contaminated foods and caused subsequent human exposures. To address the issue of possible human exposure, samples from a 2012–13 US meat and poultry (beef, pork, chicken, turkey) study were analysed for seven PBDEs. The mean summed concentrations of the seven BDE congeners (ΣPBDE) from beef, pork, chicken and turkey were 0.40, 0.36, 0.19, and 0.76 ng g^–1 lipid weight (lw). The range of ΣPBDEs for all meat classes was 0.01–15.78 ng g^–1 lw. A comparison of this study with a 2007–08 study revealed a decline in the median ΣPBDEs for all four meat classes, a reduction of 25.9% to 70.0%, with pork, chicken and turkey PBDE residues being statistically lower relative to the 2007–08 study. BDEs 47 and 99 contributed the most to the ΣPBDE concentrations, indicating likely animal exposures to the penta-BDE formulation. Based on the reported data an estimate of US consumer daily intake of PBDEs from meat and poultry was 6.42 ng day^–1.     

POULTRY PRODUCT QUALITY. 1. Compositional Changes During Cooking of Turkey Roasts

SUMMARY: White and dark turkey roasts, averaging 7.1 and 3.1 lb respectively, were made with meat taken from selected samples of the various entries in the Pennsylvania Turkey Random Sample Meat Test. Additional róasts were made from sample birds from the University research flock. Roasts were wrapped in aluminum foil, then cooked in a Telkes oven. All roasts were cooked to an internal temperature of 170°F. There were no sex differences in cooking losses except when skin was examined separately. Differences in cooking losses were observed in the breast meat but not in the thigh meat of roasts prepared from Bronze and White turkeys. Losses were higher for breast meat than for thigh meat. There was an indication that size of bird was not a significant factor in determining percentage cooking losses for breast and thigh roasts. When fat drippings from cooked skin were analyzed for carbonyl content high skin yielding males were characterized by the high concentration of the 2-enals in relation to the methyl ketones. Low skin groups consisted mainly of methyl ketones.     

Antioxidant activities of defatted sesame meal extracts in cooked turkey breast and thigh meats

The antioxidant properties of methanolic extract of raw and roasted (at 200 °C for 60 min) defatted sesame‐meal in turkey breast and thigh meat systems were determined. The TBARS values of turkey breast and thigh meat added with 0.1% of roasted defatted sesame‐meal extract were 18.8% and 24.7%, respectively, lower than those of untreated controls after 5 days of storage. The turkey meats added with roasted defatted sesame‐meal extract had higher a* and b* values than those of controls due to the browning effects occurred in sesame seeds during roasting. The amounts of volatile hydrocarbons (pentane, hexane, heptane, and octane) and carbonyls (propanal, butanal, pentanal, hexanal and heptanal) significantly decreased by the addition of roasted defatted sesame‐meal extract. In particular, the amount of hexanal, the most predominant volatile compound in the cooked turkey meat, decreased by 74% and 83% in turkey breast and thigh meat, respectively. However, raw defatted sesame‐meal extract did not show significant antioxidant activity in turkey meats. These results indicated that heat treatment of sesame‐meal increased the antioxidant activities of methanolic extract of defatted sesame meal. Copyright © 2007 Society of Chemical Industry     

Incidence of tetracycline residues in chicken meat and liver retailed to consumers

The incidence of tetracyclines’ (TCs) residue (oxytetracycline, tetracycline, chlorotetracycline and doxycycline) in fresh chicken samples (meat and liver) collected during one year was recorded. TC residues were analysed using an HPLC-DAD method. The limit of detection for meat was 4.4, 5, 10 and 7?ng?g^?1 for OTC, TTC, CTC and DOC, respectively, compared with 5.5, 6, 12 and 9?ng?g^?1 stated for liver. The recovery of the method ranged from 91% to 70% depending upon both matrix type and tetracycline kind. The results revealed that 66 (44%) samples contained TC residues including 21 (42%) breast, 19 (38%) thigh and 26 (52%) liver samples. The corresponding contaminated ranges were 124–5812, 107–6010 and 103–8148?µg?kg^?1. A total of 12 (8%), 13 (7.33%) and 20 (13.33%) samples of breast, thigh and liver, respectively, had TC residues above the Codex maximum residue limit (MRL). Liver samples had a higher incidence and level than those found in breast or thigh samples.