Casein composition in Friesian herd milks was examined by quantitative column chromatography on hydroxyapatite. Whole casein was resolved into 5 fractions: (1) γ-casein + para-κ-casein; (2) κ-casein + unidentified chymosin-resistant components; (3) unidentified minor protein; (4) β-casein; (5) αs1,0- + minor αs-caseins. Protein in fractions 1, 2, 4, 5 was measured by ultraviolet spectrometry, using appropriate specific absorption coefficients. The quantitative contribution of chymosin-resistant components to the κ-casein fraction was measured by a method involving hydroxyapatite chromatography of chymosin-treated whole casein. Compositional analysis was carried out throughout a lactation cycle on a total of 24 casein samples from the milks of a winter/spring calving and autumn-calving herd. Average composition (expressed as % total casein), which was similar for both herds, was 48·7% αs-, 33·8% β-, 4·9% γ-, 9·5% κ- and 3·2% unidentified components. Lactational effects on composition were also similar for both herds and were most pronounced in late lactation where increases were recorded in γ-casein and unidentified components, and decreases in β- and αs-caseins. Fluctuations in κ-casein proportions were small and slightly higher values were obtained in early and late lactation. Casein composition also appeared to be affected to some extent by season, as shown by differences in the proportions of αs-caseins and unidentified components between mid-lactation milks from the 2 herds. Compositional variations resulted partly from the action of milk proteinase on β-casein and also, apparently, from differences in relative rates of protein biosynthesis.

The fatty-acid composition of 17 samples of New Zealand milk fat obtained throughout one dairy season is reported.

The weight percentage of butyric (C4:0) acid was significantly correlated with that of caproic (C6:0) acid and that of caprylic (C8:0) acid. Percentages of C6:0 and C8:0 showed a highly significant correlation with each other and with weight percentages of capric (C10:0) and lauric (C12:0) acids.

There was a highly significant negative correlation between palmitic (C16:0) and stearic (C18:0) acids and between C4:0 and C16:0 acids. Oleic (C18:1) acid showed significant negative correlations with C8:0, C10:0, C12:0, myristic (C14:0) and C16:0 acids.

Fifty-six Holstein dairy cows from a commercial dairy herd in the Northern part of Greece were used to determine the effect of vitamin E supplementation on immune parameters, milk composition and milk quality. Cows were assigned to one of two experimental groups: control (no vitamin E supplementation) and vitamin E supplementation. Supplementation of vitamin E started 4 weeks prior to and continued up to 12 weeks after parturition. Supplementation included daily oral administration of vitamin E at 3000 i.u./cow prepartum and was reduced to 1000 i.u./cow post partum. Blood samples were collected weekly for 8 weeks starting 4 weeks before parturition, neutrophils were isolated and the following parameters were determined in neutrophils activated by phorbol myristate acetate: total cell-associated and membrane-bound urokinase plasminogen activator (u-PA) activity and superoxide production. Milk samples were collected weekly and fat, protein, lactose, somatic cell count (SCC), plasmin and plasminogen-derived activity were determined. Activated neutrophils isolated from cows that received supplemental vitamin E had higher (P<0·01) total and membrane-bound u-PA activities during the first 3 weeks after parturition and higher (P<0·01) superoxide production during week 1 prepartum and week 1 post partum compared with the corresponding values of activated neutrophils isolated from control cows. Vitamin E supplementation had no effect (P=0·28) on plasminogen-derived activity in milk. Milk obtained from cows that received supplemental vitamin E had SCC lower by 25% (P<0·05) and plasmin lower by 30% (P<0·01) than corresponding values in milk obtained from control cows. The reduction in plasmin as a result of vitamin E supplementation is very beneficial to the dairy industry because plasmin reduces the cheese-yielding capacity of milk, affects the coagulating properties of milk and its overall ability to withstand processing during cheesemaking. In conclusion, vitamin E supplementation had positive effects on the function of bovine neutrophils and milk quality in a commercial dairy herd.

Lactobacillus helveticus and Propionibacterium freudenreichii are essential starters in Swiss cheesemaking and the release of their intracellular enzymes through autolysis could significantly influence ripening. To provide evidence of this lysis, cheese made from microfiltered thermized milk inoculated with Lb. helveticus ITGLH77, Prop. freudenreichii ITGP23 and a commercial Streptococcus thermophilus was assayed. Starter viability was determined and lysis was monitored during ripening by protein analysis with SDS-PAGE of aqueous cheese extracts and by immunoblot detection of intracellular proteins: dipeptidase (PepD) for Lb. helveticus and methylmalonyl coenzyme A mutase for Prop. freudenreichii. We verified that the species specificity of these lysis markers was towards the cytoplasms of all the species currently used in Swiss cheese. Lb. helveticus exhibited an almost complete loss of viability (99·9%) from the beginning of ripening in the cold room; concomitantly PepD appeared in the cheese extracts and was detected until the end of ripening. Damaged Lb. helveticus cells were also visualized by scanning electron microscopy. In addition, free PepD was also successfully detected in commercial Swiss-related cheeses. All these results clearly demonstrated the autolysis of Lb. helveticus in Swiss cheese. Prop. freudenreichii ITGP23 grew during warm room ripening and no loss of viability was detected after maximal growth (109 cfu/g cheese). Free methylmalonyl-coenzyme A mutase was detected at the end of ripening during cold storage, when the cheese extracts were concentrated 20-fold, demonstrating that the autolysis of Prop. freudenreichii was tardy and limited.

The reason for the reported difference in spoilage behaviour of skim and whole pasteurised milks was investigated. The rates of growth of psychrotrophic bacteria were not significantly different in the two milks and the bacterial types, all pseudomonads, present at spoilage were also similar. However, when representative spoilage organisms were cultured into freshly pasteurised skim and whole milks, skim milks exhibited predominantly bitter flavours while whole milk showed mostly sour flavours. The different spoilage behaviours can be largely explained by greater proteolysis in skim milk than in whole milk, caused by higher production of protease and greater susceptibility of the protein to protease attack. In addition, lipolysis in whole milk, caused by the substantial quantities of lipase produced by spoilage pseudomonads in this milk, also contributes to the different flavours produced during cold storage of these milk types.

The effect of varying the casein composition of artificial micelle milk on rennet coagulation time and syneresis was examined in order to determine whether either of these processes is dependent on the concentration of particular casein components. It was found that the levels of κ-and β-caseins had a significant effect on coagulation, whereas syneresis was only affected by the level of β-casein. Partial dephosphorylation of preformed micelles or the incorporation of dephosphorylated or partly dephosphorylated β-casein into artificial micelle milk was found to have an adverse effect on both coagulation and syneresis. It was concluded that the phosphate groups of casein, particularly those of β-casein, are directly involved in the micelle-micelle interactions which occur during coagulation and syneresis.

Selective dry cow therapy (SDCT) has received increasing attention in recent years owing to global concerns over agricultural use of antimicrobial drugs and development of antimicrobial resistance. The objective of this study was to evaluate the effect of SDCT on milk yield and somatic cell count (SCC) in dairy herds in the USA. Cows in four Ohio dairy herds were categorized into two groups (low-SCC and high-SCC) at dry-off based on their SCC and clinical mastitis (CM) history during the lactation preceding the dry-off. Low-SCC cows were randomly assigned to receive or not to receive intramammary antibiotics at dry-off. Milk yield and SCC of these cows during the following lactation were compared using linear mixed effects models, adjusting for parity, calving season, stage of lactation, previous lactation milk yield and herd. Milk yield of untreated and treated low-SCC cows at dry-off did not differ significantly during the following lactation. Overall, treated low-SCC cows had 16% lower SCC (approximately 35 000 cells/ml, P=0·0267) than the untreated cows during the following lactation; however, the effect was variable in different herds. Moreover the impact of treatment, or the lack thereof, on milk yield varied considerably between herds. The results suggested that in some herds treating all cows at dry-off may be beneficial while in other herds leaving healthy cows without antibiotic dry cow treatment has no negative impact on milk yield or milk quality (SCC), and in fact, may be beneficial. Further studies are needed to identify characteristics of herds where treating all cows routinely at dry-off may be needed for maintaining good udder health and where switching to selective treatment of cows at dry-off would be the optimal approach to achieve best results.

The data presented in this research communication represent the first comprehensive report on the prevalence of udder pathogens and their resistance in Slovak dairy cattle breeds. A total of 633 milk samples from 42 herds were tested. The most frequently isolated pathogens were coagulase negative staphylococci CNS or non-aureus staphylococci (NAS) followed by Escherichia (E.) coli, Staphylococcus (S.) aureus, Streptococcus (Str.) uberis and Streptococcus (Str.) agalactiae. Generally, isolated pathogens showed common resistance to aminoglycosides (streptomycin, neomycin), which are the most commonly used antibiotics to treat mastitis in Slovakia.

1. Detailed analyses for the major constituents of the colostrum and milk of four sows are reported. In all cases the initial colostrum is characterized by a very high protein, and a low lactose and fat content. As with the colostrum of other species, the transition to milk occurs progressively during the course of about 4–7 days.

2. Analyses for mineral constituents, calcium, magnesium, phosphorus and chloride are reported on a range of samples covering the whole lactation of two sows. In contrast to the ash of the colostrum of most other species, the ash of the colostrum of the sow is lower than that of normal milk, and as lactation is established there is a rise in the total ash content, and in its main constituents, calcium and phosphorus.

Six batches of Casar de Cáceres raw ewes' milk cheeses were examined throughout their ripening. Three were made in winter, the others in spring. The microbial counts in the interior of the cheeses were ∼1·5 log units higher in the winter cheeses for total viable counts, lactic streptococci and leuconostocs, and >2 log units higher for total enterobacteria, coliforms and faecal coliforms in the 60 d samples. Staphylococci were not detected after day 15 of maturation in spring cheeses, but reached 1 log unit at day 60 in the interior of winter cheeses. In the surface samples, differences in microbial counts were more marked. Values of some physicochemical indices, such as pH, % moisture content and % NaCl were also determined.

The aim of the research described here was to compare different methods of body temperature (BT) measurements in dairy cows. It was hypothesised that reticular temperature (RET) values reflect the physiological status of the animals in an equivalent way to rectal (RT) and vaginal (VT) measurements. RT, VT and RET temperatures of twelve lactating Holstein–Friesian cows were measured over five consecutive days in June and October 2013. While RT and VT were manually measured three times a day, RET was automatically recorded at 10 min intervals using a bolus in the reticulum. For comparison with RT and VT, different RET values were used: single values at the respective recording times (RET-SIN), and mean (RET-MEAN) and median (RET-MED) values of 2 h prior to RT and VT measurements. Overall, body temperatures averaged 38·1 ± 0·6, 38·2 ± 0·4, 38·7 ± 0·9, 38·5 ± 0·7 and 38·7 ± 0·5 °C for RT, VT, RET-SIN, RET-MEAN and RET-MED, respectively. RT and VT were lower than all RET measurements, while RET-SIN and RET-MED were higher than RET-MEAN (P < 0·001). RET-MEAN and RET-MED values were higher in the morning, whereas RT and VT were greatest in the evening (P < 0·001). Overall, records of RT and VT were strongly correlated (r = 0·75; P < 0·001). In contrast to RET-SIN and RET-MEAN, RET-MED was higher correlated to RT and VT. In June, coefficients were higher between all methods than in October. Relation of barn T to RT and VT was stronger when compared to RET measurements. RET-SIN was higher correlated to barn T than RET-MEAN or RET-MED. Correlation between VT and barn T was strongest (r = 0·48; P < 0·001). In summary, RET-MED showed highest correlation with VT and RT. However, single RET measurements (influenced by water or feed intake) can lead to extreme variations and differences to single VT and RT values.

A turbidimetric method, based on light reflection, was used to study acid coagulation of reconstituted skim milk at low temperature. Capillary viscosimetry, gelograph and laser granulometer techniques were also employed. Acidification of milk was produced by hydrolysis of glucono-δ-lactone. The general shape of the turbidimetric signal as a function of pH or time can be divided into three stages: a lag phase followed by a significant decrease and then a final rise. Two factors have a great influence on the development of milk turbidity, pH and temperature. Dynamic viscosity measurements can be related to the turbidimetric signal while laser granulometrie measurements cannot be correlated with changes in turbidity: the micelle size distribution remains constant until the first signs of gelation. As previous work showed, dynamic viscosity diminishes with acidification until a particular pH is reached (pH 5·9 at 15°C and pH 5·75 at 20°C). We have related this latter period to the turbidimetric lag phase. As milk turbidity became lower than its initial value (pH 5·75 at 15°C and pH 5·55 at 20°C), dynamic viscosity increased significantly. The release of material from micelles (β-casein and Ca) could explain this phenomenon. In the same way, further increase of turbidity at a particular pH value (pH 5·3 at both 15 and 20°C) coulcl be partly due to the reincorporation of soluble casein monomers in the micelle framework. As the onset of gelation was approached, turbidity still increased as a result of gel network formation.

The apparent diffusion coefficients for NaCl in Romano-type cheese salted by brining or dry salting were ∼0·23 cm2/d. A plot of the natural logarithm of % salt-in moisture against distance was almost linear, the slope of which is the distance over which the salt concentration decreases by a factor of 1/e (0·368). Such plots may be useful in predicting the concentration of NaCl at any point in the cheese after any period of brining. After 9 d brining, the water to salt flux (ratio of outflow of water to inflow of NaCl) decreased from 2·42 at the surface to ∼0·5 in the middle zone of the cheese and increased again to > 1 at greater distances from the cheese/brine interface.

1. The composition has been studied of the milk of forty-four sows in the course of sixty-eight lactations. The milk was obtained by machine milking following intravenous injection of oxytocin.

2. Definite lactational trends have been observed for all the major constituents, and the third week seems a critical stage for most of the milk components.

3. The mean values for the milk, based on the analyses of over 450 samples from the seventh to fifty-sixth day of the lactation were: fat 9·58 %, protein 6·11 %, lactose 4·62 %, ash 0·92%. Such figures are considered to be rather meaningless for most practical purposes, in view of the marked changes over the course of lactation.

4. The day-to-day variation in the composition of sow's milk has been studied. Whereas the fat value changes considerably, the non-fat constituents show a less marked variation. Difficulties in securing a representative sample of the weekly milk have been overcome by preparing a composite sample from three milMngs within the week.

5. Some preliminary work has been done on variation in the composition during the process of milking. Sequential samples show an erratic fat content, especially during the early part of the lactation. When calculated on a fat-free basis, the protein, lactose and ash contents are relatively constant during the process of milking.

Measurements of the zeta potential and particle size of casein micelles in skim milk suspensions at natural and lower pH have been made using the technique of electroacoustics. This technique requires no dilution or change of environment of the casein micelles. The zeta potential obtained at natural pH for a commercial skim milk suspension was −18 mV; it became less negative with decreasing pH. The median particle size observed at natural pH for a commercial skim milk suspension was 0·2 εm, in good agreement with previously reported values. The particle size increased as the pH was decreased.

Effective diagnostic tools for screening herds for mastitis pathogens are important in development and monitoring of mastitis control programmes. A multiplex polymerase chain reaction (PCR) assay for simultaneous detection of Staphylococcus aureus, Streptococcus agalactiae, Streptococcus dysgalactiae and Streptococcus uberis was used in preliminary studies to assess its applicability as an alternative method for monitoring mastitis caused by these organisms at the herd level. PCR was used to detect the presence of these organisms in bulk milk samples. Correlations with bulk milk somatic cell counts (BMCC), total bacteria counts and thermoduric bacteria counts were evaluated. A total of 176 bulk milk samples were collected from 42 herds on five consecutive occasions at approx. 10-d intervals. Str. uberis was the most common organism in these bulk milk samples. There was no relationship between presence of either Staph. aureus, Str. dysgalactiae or Str. uberis and BMCC, total bacteria counts or thermoduric bacteria counts. However, presence of Str. agalactiae was associated with high BMCC and total bacteria counts. The results of this study show that regular analysis of bulk milk using this multiplex PCR assay may be a useful tool for monitoring herd status with respect to Str. agalactiae, but is of less value for monitoring occurrence of Staph. aureus, Str. dysgalactiae and Str. uberis. Further investigations are needed to clarify the relationship between positive PCR results and the prevalence of infected cows in the herd.

A study was undertaken in cattle to evaluate changes in milk L-lactate in relation to mastitis. A healthy, rear quarter of the udder of each of ten cows in mid-lactation was infused with 1000 colony-forming units (cfu) of Streptococcus uberis following an afternoon milking. Foremilk samples were taken at each milking from control and treated quarters and antibiotic treatment was applied following the onset of clinical mastitis or after 72 h. One cow did not become infected. Six quarters showed clinical symptoms of mastitis within 24–40 h and this was associated with a more than 30-fold increase in milk L-lactate (to 3·3 mM) and an increase in somatic cell count (SCC) from 4·5×103 to 1×107 cells/ml. Three cows were subclinical, with cell counts ranging from 1·5×106 to 1×107 cells/ml. In these animals, milk lactate ranged from 0·7 to 1·5 mM in the infected quarters up to 40 h post-infection, compared with less than 0·1 mM in control quarters. Milk was examined from 137 cows in mid-lactation which were known to have mastitis. Foremilk samples were taken aseptically from control and infected quarters of cows on commercial farms. Mean milk L-lactate concentrations and SCC were 0·14±0·02 mM and 1·85±0·3×105 cells/ml, respectively, in control (bacteriologically negative) samples. However, L-lactate concentrations exceeded 2·5 mM in the presence of some types of infection, the level of the lactate response being closely related to the impact of the infection on SCC. L-Lactate concentrations were relatively elevated in milk samples taken post partum, declining from 0·8 to 0·14 mM over the first few days of lactation. In conclusion, milk L-lactate has potential as an indicator of clinical and subclinical mastitis in dairy cows.

This study aimed to evaluate the effect of milk fermented with Lactobacillus acidophilus 145 and Bifidobacterium longum BB536 on plasma lipids in a sample of adult women. A double-blind, placebo controlled, cross-over study (two periods of four weeks each separated by a 1-week washout period) was performed in 34 women, aged between 18 and 65 years. Group A consumed 125 g fermented milk three times a day for the first 4 weeks while group B consumed regular yoghurt under the same conditions. (Groups A and B switched products for the second treatment period). Women taking the test product with a baseline total cholesterol above 190 mg/dl showed a significant reduction in LDL cholesterol. HDL cholesterol was also reduced by the test product. We conclude that the fermented milk may help to reduce LDL levels in hypercholesterolemic adult women.

On most dairy farms teat dips are applied to the teats of cows either before or after milking in order to prevent pathogens from gaining access to the mammary gland via the teat canal. In the present experiments, a natural teat dip was developed using a fermentate containing the live bacterium Lactococcus lactis DPC 3251. This bacterium produces lacticin 3147, a two-component lantibiotic which was previously shown to effectively kill Gram-positive mastitis pathogens. Lacticin 3147 activity in the fermentate was retained at 53% of its original level following storage for 3 weeks at 4°C. In the initial experiments in vitro, 105 colony-forming units/ml (cfu/ml) of either Staphylococcus aureus, Streptococcus dysgalactiae or Streptococcus uberis were introduced into the lacticin-containing fermentate. Neither Staph. aureus nor Str. dysgalactiae could be detected after 30 min or 15 min, respectively, while Str. uberis was reduced approximately 100-fold after 15 min. Following these trials, preliminary experiments were performed in vivo on teats of lactating dairy cows. In these experiments, teats were coated with each of the challenge organisms and then dipped with the lacticin-containing fermented teat dip. Following a dip contact time of 10 min, staphylococci were reduced by 80% when compared with the undipped control teat. Streptococcal challenges were reduced by 97% for Str. dysgalactiae and by 90% for Str. uberis. These trials showed that the teat dip is able to reduce mastitis pathogens on the teats of lactating cows.

The presence of a thermolabile inhibitor of coagulase-positive staphylococci in milk was confirmed. Starter streptococci significantly suppressed the multiplication of staphylococci in milk not only by their acid production but also by some other competitive effect.

Cheesemaking trials showed that staphylococci multiplied considerably more rapidly in ‘slow’ or ‘sweet’ cheese, where the starter was inhibited by phage, than in normal cheese. Little decrease in numbers occurred in ‘sweet’ cheese even after 18 months, in contrast to the rapid decline in the normal cheese.

Staphylococci subjected in the laboratory to sublethal heat treatments had a prolonged lag phase on all media and their % recovery on selective media was significantly lower than on optimal non-selective media. It is suggested that the low survival rate of the staphylococci in cheese made from milks heated at sublethal temperatures is due to the lag in recovery of heat-shocked cells and their inability to multiply in the unfavourable cheese curd.