Effects of pulsed electric field treatments on quality of peanut oil

The effects of pulsed electric fields (PEF) treatment on physicochemical properties of peanut oil were investigated in this paper. Compositions of fatty acid, acid value (AV), peroxide value (PV), as well as carbonyl group value (CGV) of various PEF-treated peanut oil samples with different storage time were determined by GC/MS and AOCS standard methods. GC/MS analysis showed that little change of the oil composition was observed after PEF treatment. However, after being treated by various PEF treatments and stored at 40 °C for 100 days, the biggest increment of AV was 0.69 mg g⁻¹, which was lower than that of untreated peanut oil (0.79 mg g⁻¹). The PV significantly increased from 4.8 meq kg⁻¹ untreated oil to 11.5 meq kg⁻¹ PEF treated oil (50 kV cm⁻¹). And the increase extent of CGV of oil samples during the 100 d’ storage period was decreased with increasing electric field strength. During the storage period, the differences of AV, PV, and CGV of PEF-treated sample during storage period were less than that of untreated oil, which implied that the PEF treatment could restrain the speed of lipid oxidation reaction thus extending the shelf-life of oil rich products.     

Comparison of aluminum thermal-death-time disks with a pilot-scale pasteurizer on the thermal inactivation of Escherichia coli K12 in apple cider

This study was conducted to compare thermal inactivation kinetics obtained using a pilot-scale pasteurizer and a bench-scale processing system. Pilot-scale pasteurizers are useful for product development, but comparisons on thermal inactivation kinetics with smaller scale systems are lacking. Using an Armfield pilot-scale pasteurizer and aluminum thermal-death-time (TDT) disks, the D-values and z-values of Escherichia coli K12 in apple cider were determined in the temperature range of 54–62 °C. Come-up times to 58 °C were also measured and were 35 and 61 s for the TDT disks and pasteurizer, respectively. The D-values from the TDT disks were 9.66, 4.01, 1.44 and 0.44 min at temperatures of 54, 56, 58, and 60 °C, respectively. The D-values from the pasteurizer were 3.48, 1.22, 0.10 and 0.05 min at temperatures of 56, 58, 60, and 62 °C, respectively. The z-values from the TDT disks and the pasteurizer were 4.68 and 3.60 °C, respectively. There was no significant (P > 0.05) difference in the D-values of the TDT disks and pasteurizer at 56 and 58 °C, while there was a significant (P < 0.05) difference in the D-value at 60 °C and in the z-value. This study revealed that the thermal inactivation kinetics obtained using bench scale TDT disks and an Armfield pilot-scale pasteurizer under certain conditions are similar. However, based on ease of use and other factors, TDT disks are preferable for acquiring thermal inactivation kinetics.     

Biological control of postharvest diseases of peach with Cryptococcus laurentii

Cryptococcus laurentii was evaluated for its activity in reducing postharvest gray mold decay, blue mold decay and Rhizopus decay of peach caused by Botrytis cinerea, Penicillium expansum and Rhizopus stolonifer respectively, and in reducing natural decay development of peach fruits. The concentrations of antagonist had significant effects on biocontrol effectiveness: the higher the concentrations of the antagonist, the lower the disease incidence. At concentrations of C. laurentii at 1 × 10⁹ CFU ml⁻¹, the gray mold decay was completely inhibited after 4 days incubation at 25 °C, while the control fruit had 50% decay, when inoculated with B. cinerea spores suspension of 1 × 10⁵ spores ml⁻¹; no complete control of the blue mold or Rhizopus mold was observed, when peach fruits were stored at 25 °C for 4 days (challenged with P. expansum) or 5 days (challenged with R. stolonifer) respectively, but the decay was distinctly prevented, the incidence of blue mold or Rhizopus mold was reduced by 78.6% or 80% respectively, compared with control, at challenged with P. expansum or R. stolonifer spores suspension of 5 × 10⁴ spores ml⁻¹, respectively. C. laurentii significantly reduced the natural development of decay and did not impair quality parameters of fruit following storage at 2 °C for 30 days followed by 20 °C for 7 days.     

Changes in the concentration of aflatoxin M1 during manufacture and storage of White Pickled cheese

In this study White Pickled cheese was produced from cow’s milk contaminated artificially with aflatoxin M₁ (AFM1) at two different levels, 1.5 and 3.5 μg/kg (ppb), and the effects of process stages on the AFM1 contents were investigated. Pasteurization at 72 °C for 2 min caused losses of AFM1 about 12% and 9%, respectively, in milk contaminated with 1.5 μg/kg AFM1, and 3.5 μg/l AFM1. These losses were found to be statistically significant (P < 0.01). After the cheese production, about 56% and 59% of total AFM1 remained in cheese–curd while about 32% of total AFM1 transferred to the whey for both 1.5 μg/kg and 3.5 μg/kg AFM1 contaminated milk. After 3-month storage in brine, AFM1 content of cheeses produced from 1.5 and 3.5 μg/kg AFM1 contaminated milks decreased by 2.9% and 2.8%, respectively. Changes in AFM1 content of cheese samples were found statistically insignificant (P > 0.05 and P > 0.01) for 3-month storage periods.     

Efficiency of high pressure treatment on inactivation of pathogenic microorganisms and enzymes in apple,orange, apricot and sour cherry juices

The purpose of this study was to investigate the effect of high hydrostatic pressure with a mild heat treatment on Staphylococcus aureus 485, Escherichia coli O157:H7 933 and Salmonella Enteritidis FDA in apple, orange, apricot and sour cherry juices. The effectiveness of the treatment on polyphenol oxidase activity in apple juice and pectinesterase activity in orange juice were also determined. An inoculum of microorganisms was completely inactivated at 350 MPa and 40 °C in 5 min. The residual polyphenol oxidase activity in apple juice after treatment at 450 MPa and 50 °C for 60 min was obtained as 9 ± 2.2%. The residual pectinesterase activity in orange juice after treatment at 450 MPa and 50 °C for 30 min was determined as approximately 7 ± 1.6%. It compares with 12 ± 0.2% at a treatment of 40 °C and 450 MPa for 60 min. Pressure resistant isoenzymes were thought to be responsible for the final residual activity. The inactivation is irreversible and the enzyme is not reactivated upon storage. High pressure processing constitutes an effective technology to inactivate the enzymes in fruit juices. Pressures higher than 400 MPa can be combined with mild heat (<50 °C) to accelerate enzyme inactivation.     

Potential of botanicals and biocontrol agents on growth and aflatoxin production by Aspergillus flavus infecting rice grains

The potential of certain plant extracts and biocontrol agents for the reduction of aflatoxin B₁ (AFB1) in stored rice was investigated. Among the plant extracts tested, Syzigium aromaticum (5 g/kg) showed complete inhibition of Aspergillus flavus growth and AFB1 production. Curcuma longa, Allium sativum and Ocimum sanctum also effectively inhibited the A. flavus growth (65–78%) and AFB1 production (72.2–85.7%) at 5 g/kg concentration. Among the biocontrol agents, culture filtrate of Rhodococcus erythropolis completely inhibited the AFB1 production at 25 ml/kg concentration. The other biocontrol agents, Pseudomonas fluorescens, Trichoderma virens and Bacillus subtilis showed 93%, 80% and 68% reduction of A. flavus growth and 83.7%, 72.2% and 58% reduction of AFB1 at 200 ml/kg, respectively.     

Non-thermal inactivation of Escherichia coli K12 in buffered peptone water using a pilot-plant scale supercritical carbon dioxide system with a gas–liquid porous metal contactor

This study evaluated the effectiveness of a supercritical carbon dioxide (SCCO₂) system, with a gas–liquid porous metal contactor, for reducing Escherichia coli K12 in diluted buffered peptone water. 0.1% (w/v) buffered peptone water inoculated with E. coli K12 was processed using the SCCO₂ system at CO₂ concentrations of 3.1–9.5 wt%, outlet temperatures of 34, 38, and 42 °C, a system pressure of 7.6 MPa, and a flow rate of 1 L/min. Increased CO₂ concentrations and temperatures significantly (P < 0.05) enhanced microbial reduction. A maximum reduction of 5.8-log was obtained at 8.2% CO₂ and 42 °C. To achieve a 5-log reduction of E. coli K12 in 0.1% buffered peptone water, minimum CO₂ concentrations of 9.5%, 5.5%, and 5.3% were needed at 34, 38, and 42 °C, respectively. Further reductions of cells were observed after storage for 7 days at 4 °C. But storage at 25 °C increased the number of viable cells to 8-log cfu/mL after 7 days. This study showed the potential of the pilot scale SCCO₂ system with a gas–liquid porous metal contactor for microbial inactivation in liquid food.     

Effect of organic acids,hydrogen peroxide and mild heat on inactivation of Escherichia coli O157:H7 on baby spinach

Minimally processed baby spinach contaminated with Escherichia coli O157:H7 has been associated with multiple outbreaks of foodborne illnesses recently. Chlorinated water is widely used to wash vegetables commercially, but this washing procedure has limited efficacy and can lead to the formation of carcinogenic substances. This study was conducted to determine the effects of organic acids and hydrogen peroxide alone and in binary combinations with or without mild heat (40 and 50 °C) on the inactivation of Escherichia coli O157:H7 on baby spinach. Baby spinach leaves were dip-inoculated with E. coli O157:H7 to a level of 6 log CFU/g and stored at 4 °C for 24 h before treatment. Individual washing solutions (1% and 2% lactic acid [LA], citric acid [CA], malic acid [MA], tartaric acid [TA], acetic acid [AA], hydrogen peroxide [H₂O₂] as well as binary combinations of LA, CA, MA and H₂O₂ at final concentrations of 1% were used to decontaminate spinach leaves at 22, 40 or 50 °C for 2–5 min to test their efficacy in reducing E. coli O157:H7. Chlorinated water (200 ppm free chlorine) decreased the population of E. coli O157:H7 on baby spinach by only 1.2–1.6 log CFU/g, which was not significantly different from DI water washing. Washing with 1% LA at 40 °C for 5 min was the most effective treatment achieving a 2.7 log reduction of E. coli O157:H7 which is significantly higher than chlorine washing. Washing with LA + CA or LA + HP at 40 °C for 5 min was equally effective against E. coli O157:H7, resulting in a 2.7 log reduction of E. coli O157:H7. The application of mild heat significantly enhanced the efficacy of washing solutions on the inactivation of E. coli O157:H7. There was, however, no significant difference between treatments at 40 °C for 5 min and 50 °C for 2 min. The results suggested that the use of organic acids in combination with mild heat can be a potential intervention to control E. coli O157:H7 on spinach.     

Effects of high pressure homogenization on the activity of lysozyme and lactoferrin against Listeria monocytogenes

The effects of high pressure homogenization treatment at 100 MPa (HPH), in comparison to different heat treatments, 70 °C for 30 s, 70 °C for 5 min or 100 °C for 5 min, on the activity of lysozyme and lactoferrin, were studied. The antimicrobial activities of lysozyme and lactoferrin were tested on Listeria monocytogenes inoculated in milk or cultural medium.The results indicated that antimicrobial activities of lactoferrin and lysozyme were enhanced and/or accelerated by HPH treatment. Particularly, the highest immediate inactivation values were recorded when L. monocytogenes cells were added to HPH-treated lactoferrin, processed simultaneously or separately with the target microorganism. Although to a lesser extent than HPH treatment the heat treatments applied also were able to increase the antimicrobial activity of lysozyme.     

Inactivation of foodborne pathogens in raw milk using high hydrostatic pressure

Plate counting, viability test, pulse field gel electrophoresis (PFGE) and transmission electron microscopy (TEM) were used to investigate the effect of high hydrostatic pressure (HHP) on Salmonella, Escherichia coli, Shigella and Staphyloccocus aureus in raw milk in order to determine the optimal inactivation conditions, and further understand the mechanisms of HHP on pathogens inactivation in food. The results exhibited that 300 Mpa treatment with 30 min duration at 25 °C was the optimal condition for Salmonella, E. coli, Shigella and S. aureus inactivation. Damage of the cell wall, cell membrane and cytoplasmic components by high pressure treatment can be observed in TEM micrographs. The injured cells could not be recovered, the growth rate of survivors was much lower than that of the untreated cells. PFGE showed neither corresponding DNA bands with same molecular weight nor DNA bands with same brightness could be found in the lanes between HHP treated pathogens and untreated ones. The results indicated that HHP processing can be applied to inactivate pathogens in food, the inactivation is mainly due to cell membrane damage, cell wall rupture and chromosome DNA degradation.     

Synergistic effect of high hydrostatic pressure treatment and food additives on the inactivation of Salmonella enteritidis

The synergistic effect of high hydrostatic pressure (HHP) treatment and food additives (FAs) on the inactivation of Salmonella enteritidis was investigated. At 1% concentrations, all of the FAs tested showed significant synergistic effects, and 9 of 30 FAs showed strong synergistic effects. Citric acid, adipic acid, C8-sugarester, C10-sugarester, tannin, nisin, wasabi extract, ε-polylysine, and protamine each showed a strong inactivation effect when administered alone at the 1% level. In the HHP treatment at 250 MPa for 30 min, the minimum effective concentrations of C8-sugarester, C10-sugarester, and protamine were 0.25, 0.125, and 0.06%, respectively. These results indicate that some FAs are useful for increasing the inactivation ratio of S. enteritidis in HHP treatment.     

Effects of lactic acid and lauricidin on the survival of Listeria monocytogenes,Salmonella enteritidis and Escherichia coli O157:H7 in chicken breast stored at 4 °C

Lauricidin and lactic acid were evaluated for their effects on growth and survival of Listeria monocytogenes (L55), Salmonella enteritidis (S552) and Escherichia coli O157:H7 (E19) inoculated onto raw chicken breast. Fresh, raw chicken breasts were purchased immediately after slaughter and transported on ice to the laboratory within 20 min. Each chicken breast was decontaminated by briefly dipping in 70% ethanol and passed through a flame of a Bunsen burner and then allowed to cool. The decontaminated Chicken breast was dipped in TSB broth, at room temperature (25 °C) for 15 min, containing approximately log 9 CFU/ml of L. monocytogenes, S. enteritidis or E. coli O157:H7. Initial counts of L. monocytogenes, S. enteritidis or E. coli O157:H7 counts in chicken breast immediately after dipping in TSB broth were in the range of log 7–log 8 CFU/g. After inoculation, the chicken breasts were kept at room temperature for 20 min to allow attachment. Each inoculated chicken breast (25 °C) was dipped in 0 (control – sterile water), 0.5%, 1%, 1.5% or 2% of lauricidin (w/v) or lactic acid (v/v) for 10, 20 or 30 min and then individually placed in oxygen-permeable polyethylene bags. Breasts were subjected to microbiological analyses after treatment (day 0) and after storage for 2, 5, 7, 10 and 14 d at 4 °C. Initial counts of L. monocytogenes, S. enteritidis and E. coli O157:H7, in chicken breast treated with lauricidin decreased by 2.90, 1.31 and 2.27 log CFU/g, respectively. Lauricidin was more effective in reducing L. monocytogenes population than S. enteritidis and E. coli O157:H7 population. Dipping chicken breast in lauricidin for 30 min caused a significant reduction of L. monocytogenes, S. enteritidis and E. coli O157:H7 population compared to 10 and 20 min dipping. Initial L. monocytogenes, S. enteritidis and E. coli O157:H7 counts on chicken breast treated with lactic acid decreased by 1.97, 1.71 and 2.59 log CFU/g, respectively. Lactic acid caused a higher reduction in initial S. enteritidis and E. coli O157:H7 counts compared to lauricidin.     

Survival of bacteria in less than thorough cooked,brine-injected steaks

Bacteria that may include enteric pathogens are introduced into muscle tissues when they are injected with brine. Consequently, steaks of such non-intact, non-comminuted tissues should be cooked to temperatures sufficient to render them microbiologically safe. Studies were conducted to identify the minimum safe temperature for cooking those meats. Suspensions of Escherichia coli and Listeria innocua at numbers about 8 log cfu/ml, in broth or in brines containing 2% or 5% of each of NaCl and sodium tripolyphosphate that were not supplemented or were supplemented with 2% soy protein or 2% emulsified sunflower oil were injected into the centres of 3 cm thick steaks. Groups of four steaks injected with each type of suspension were cooked to temperatures at the centres of 50, 55, 60, 65 or 70 °C. Bacteria were recovered from samples from the centres of steaks, on agars that did or did not allow resuscitation of injured cells of each organism. The results indicated that E. coli but not L. innocua was injured by the brines; that supplementing brines with protein or oil did not protect the organisms from injury or inactivation by heating; and that cooking to a central temperature > 60 ? 65 °C was sufficient to inactivate all bacteria in the meat. The centres of steaks were subsequently injected with 0.1 ml portions of five strain cocktails of E. coli O157:H7 or Listeria monocytogenes in broth containing a dye and the bacteria at numbers >8 log cfu/ml. Steaks were cooked to temperatures of 63, 64 or 65 °C, with holding for 0, 1 or 2 min after cooking before excision of all the dyed tissue from each steak and enumeration of bacteria from the tissue on resuscitating media. The results indicated that cooking to 65 °C without holding would be sufficient to reduce numbers of E. coli O157:H7 or L. monocytogenes in non-intact, non-comminuted steaks by ?7 log units.     

Efficacy of oregano oil in the inactivation of Salmonella typhimurium on lettuce

This study was conducted to determine the efficacy of oregano oil in the inactivation of Salmonella typhimurium inoculated onto iceberg lettuce. The effect of washing with oregano oil (Oreganum onites), typical of Turkey, at three different concentrations (25, 40 and 75 ppm) and four different treatment times (5, 10, 15 and 20 min) on survival of S. typhimurium inoculated to fresh cut iceberg lettuce were determined at 20 °C and compared with a 50 ppm chlorine wash at the same conditions. The spot and dip inoculation methods for applying inoculum to iceberg and romaine type lettuce were evaluated and the effects of selective and nonselective media on the recovery of S. typhimurium were also examined. Populations of S. typhimurium recovered from spot and dip inoculated lettuce were not significantly different (p > 0.05). No significant differences were found between two different media, and two different lettuce types (p > 0.05). Reductions of S. typhimurium by washing with oregano did not exceed 1.92 logarithmic units regardless of the washing times and concentrations. The effectiveness of washing lettuce with 75 ppm oregano oil on inactivation of S. typhimurium was comparable with that affected by 50 ppm chlorine. The results suggested that oregano oil might be a suitable decontamination alternative to chlorine for lettuce.     

Inactivation of Listeria monocytogenes inoculated on disposable plastic tray,aluminum foil,and paper cup by atmospheric pressure plasma

The objective of this study was to investigate the effect of atmospheric pressure plasma (APP) on Listeria monocytogenes inoculated onto disposable food containers including disposable plastic trays, aluminum foil, and paper cups. The parameters considered in APP processing were input power (75, 100, 125, and 150 W) and exposure time (60, 90, and 120 s). The bacterial reduction in the disposable plastic trays, aluminum foil, and paper cups was associated with increased input power and exposure time of APP. The D₁₀ values were calculated as 49.3, 47.7, 36.2, and 17.9 s in disposable plastic trays, 133, 111, 76.9, and 31.6 s in aluminum foil and 526, 65.8, 51.8, and 41.7 s in paper cups at 75, 100, 125, and 150 W of input power, respectively. There were no viable cells detected after 90 and 120 s of APP treatment at 150 W in disposable plastic trays. However, only three decimal reductions of viable cells were achieved in aluminum foil and paper cups at 150 W for 120 s. These results demonstrate that APP treatment is effective for inactivation of L. monocytogenes and applicable for disposable food containers. However, the type of material is crucial and appropriate treatment conditions should be considered for achieving satisfactory inactivation level.     

Importance and efficiency of in-depth antimicrobial activity for the control of listeria development with nisin-incorporated sodium caseinate films

The effect of antimicrobial sodium caseinate-based films was investigated on inhibition of Listeria innocua in cheese. Nisin was incorporated into sorbitol-plasticized sodium caseinate films at 1000 IU/cm² and the films were prepared by casting methods. Mini red Babybel® cheese was chosen as a semi-soft cheese model. The antimicrobial activity was studied based on the contact between antimicrobial films and surface-contaminated as well as in-depth contaminated cheese samples during a 7-day storage at 4 °C. The active films produced resulted in a reduction of 1.1 log CFU/g reduction in L. innocua counts in surface-inoculated cheese samples after 1 week of storage as compared to control samples. Regarding in-depth inoculated cheese samples, antimicrobial effectiveness was found to be dependent on the distance from the contact surface with the films containing nisin to the cheese matrix. The inactivation rates obtained were 1.1, 0.9 and 0.25 log CFU/g with slice 1 (distance from contact surface d = 1 mm), slice 2 (d = 2 mm) and slice 3 (d = 3 mm), respectively. Our study demonstrates the potential application of antimicrobial films as a promising method to overcome problems associated with post-process contamination, thus enhancing the safety and extending the shelf life of food products.     

Seasonal variation in the chemical composition and microbiological condition of Mediterranean horse mackerel (Trachurus mediterraneus) muscle from the North Aegean Sea (Greece)

The aim of this work was to determine the chemical composition and microbiological quality of Mediterranean horse mackerel (Trachurus mediterraneus) muscle during the year and the consequent advantages or disadvantages in processing the raw material. A total of 180 samples were examined (15 samples per month) during two years (November 2001–November 2003). Fish were caught in the coastal waters of Chalkidiki peninsula (Northern Greece). Proximate composition of the muscle during the year resulted in: water 76.8 ± 1.39%, proteins 20.3 ± 0.68%, fat 1.3 ± 1.08% and ash 1.5 ± 0.08%. In March, April and May an increase in fat content of the muscle (2.5%, 2.8% and 2.1%, respectively) and a decrease in water content of the muscle (below 75.9%) were observed. On the contrary, fat content showed a decrease in September and October (0.4% and 0.6%, respectively), while water content of the muscle increased during these months (78.2% and 77.6%, respectively). The protein content of the muscle remained at high values, while the ash content was almost constant during the year. The mean value of muscle pH was 6.38 ± 0.16; extreme values (<6 or >7) of muscle pH were not observed. Total Viable Bacteria, Shewanella putrefaciens and Pseudomonas spp. were used as microbial indices to evaluate the microbiological quality of the muscle. Mean counts of Total Viable Bacteria, S. putrefaciens and Pseudomonas spp. during the year were: 4.01 ± 0.38 log₁₀ cfu/g, 2.37 ± 0.43 log₁₀ cfu/g and 3.34 ± 0.27 log₁₀ cfu/g, respectively. The variations of the values within seasons are minimal and significant homogeneity in the chemical composition and microbiological quality of Mediterranean horse mackerel muscle is observed. This is an important advantage in processing of the raw material.     

Pseudomonas spp. and Hafnia alvei growth in UHT milk at cold storage

Gram-negative psychrotrophic bacteria isolated from samples of spoiled commercial ultra-heat treated (UHT) milk from Taiwan were comprised of 67% Pseudomonas spp. and 22% Enterobacteriaceae. Whole milk, low-fat milk, and flavored milk samples were tested. The modified Gompertz equation was used to model the data and provided a good fit for the growth of Pseudomonas spp. and Hafnia alvei at 7 °C for 14 days in both whole UHT milk and low-fat UHT milk. From this model, the estimated lag time for H. alvei was longer than that for Pseudomonas fluorescens in both whole UHT milk and low-fat UHT milk. The growth rate of H. alvei was higher than that of P. fluorescens. The pH value was significantly reduced by H. alvei than P. spp. after cultured in whole and low-fat UHT milk at 7 °C for 14 days.     

Inactivation of Salmonella,E. coli and Listeria monocytogenes in phosphate-buffered saline and apple juice by ultraviolet and heat treatments

Two strains of Escherichia coli (K-12 and O157:H7), Salmonella (enteritidis and typhimurium) and Listeria monocytogenes (AS-1 and M24-1) were individually suspended in phosphate-buffered saline (PBS) and apple juice prior to exposure to UV radiation (220–300 nm) and heating at 55 °C. The calculated decimal reduction times (D value, min) varied with suspending medium and mode of inactivation. The AS-1 and M24-1 strains of L. monocytogenes were found to be most resistant to UV in PBS (0.28–0.29 min) while the AS-1 strain was most resistant in juice (1.26 min). The AS-1 strain of L. monocytogenes and E. coli O157:H7 were most heat resistant when suspended in PBS (4.41 min) and juice (4.43 min), respectively. Results obtained from this study may be used by apple juice processors in selecting appropriate organisms for UV irradiation or heat treatment lethality validations.     

Pre-processed bovine milk quality in Trinidad: Prevalence and characteristics of bacterial pathogens and occurrence of antimicrobial residues in milk from collection centres

The study was conducted to assess the impact of the changes in the milk collection system in Trinidad (from twice daily collection to once, introduction of chilling facilities to the collection centres and transportation of milk to the processing plant in insulated truck instead of in metal churns at ambient temperature) on the microbial load and antimicrobial residue quality of the milk as well as the temperature and pH of milk, using standard methods. The presence of antimicrobial residues was detected using the Delvo test kit. Of a total of 266 milk samples from churns, the mean ± sd temperature and log₁₀ ± sd TAPC per ml was 20.36 ± 7.91 °C and 6.3 ± 1.09 respectively. For 20 milk samples from the chillers, the mean temperature and log₁₀ ± sd TAPC per ml was 15.10 ± 2.73 °C and 7.04 ± 0.33 respectively compared with corresponding values for 36 samples collected from the truck, 11.64 ± 4.22 °C and 7.11 ± 0.62 respectively (P < 0.05; X²). The mean TAPC, staphylococcal and E. coli counts per ml of milk from churns were significantly (P < 0.05; X²) higher for milk at low temperature (0–20 °C) compared with milk at high temperature (>30 °C). Eight (4.2%) of 192 milk samples tested contained antimicrobial residues. Of 168 S. aureus isolates tested, 24 (14.3%) were enterotoxigenic while 53 (45.3%) of 117 isolates tested exhibited resistance to various antimicrobial agents while of 386 isolates of E. coli tested, 3 (0.8%) were O157 strain and 129 (64.5%) of 200 isolates exhibited resistance to antimicrobial agents. It was concluded that despite the changes, the microbial load of milk was still high suggesting poor sanitary practices at the farm level. The detection of antimicrobial residues agents coupled with toxigenic S. aureus and E. coli isolates could pose health hazards to consumers.