A study was conducted to identify the optimal temperature and time at which heat treatment of bovine colostrum would least change viscosity and IgG concentrations yet reduce bacterial count. First-milking colostrum with >50g of immunoglobulins/L (measured by colostrometer) was collected from 30 Holstein cows. Aliquots of colostrum were heated for 0, 30, 60, or 90min at 57, 60, or 63 degrees C in a water bath. Samples were examined for viscosity, IgG(1), and IgG(2) concentrations, standard plate count, coagulase-negative staphylococci, environmental streptococci, coliform, gram-negative noncoliform, Streptococcus agalactiae, and Staphylococcus aureus counts. All heat treatments reduced counts of all bacteria groups measured compared with untreated colostrum samples. Heat treatment at >or=60 degrees C denatured IgG(1) compared with untreated colostrum; however, colostral IgG(2) levels were not reduced when temperature was held at 60 degrees C for <60min. Viscosity was not affected when temperature was held at 60 degrees C for <60min. In this study, heat treatment of bovine colostrum at 60 degrees C for 30 or 60min reduced bacterial count, slightly reduced IgG concentration, and did not affect viscosity.

Newborn Holstein heifer calves were studied to compare absorption of immunoglobulin G (IgG(1) and IgG(2)), total serum protein concentration, lymphocyte counts, health scores, growth, and starter intake after receiving unheated or heat-treated colostrum. First-milking colostrum was collected from Holstein cows and frozen at -20 degrees C to accumulate a large batch. After thawing and mixing, half of the colostrum was transferred into 1.89-L plastic containers and frozen at -20 degrees C until needed for feeding. The remaining half was heated at 60 degrees C for 30 min, transferred into 1.89-L plastic containers, and then frozen at -20 degrees C until needed for feeding. Forty heifer calves weighing > or =32 kg at birth were enrolled into 1 of 2 treatment groups before suckling occurred. For the first feeding, 3.8 L of colostrum was bottle fed by 1.5 to 2 h of age. For the second and third feedings, pasteurized whole milk at 5% of birth body weight (BW) was fed. Subsequently, calves received milk replacer containing 20% crude protein and 20% fat at 10% of birth BW/d until wk 5. Milk replacer was reduced to 1 feeding of 5% birth BW until weaning at 6 wk of age. Blood samples and growth data were collected through wk 8. Batch heat-treatment of colostrum at 60 degrees C for 30 min lowered colostrum bacteria concentration while maintaining colostral IgG concentration and viscosity. Calves fed heat-treated colostrum had significantly greater IgG concentrations at 24 h and greater apparent efficiency of IgG absorption (IgG = 23.4 g/L; apparent efficiency of absorption = 33.2%) compared with calves fed unheated colostrum (IgG = 19.6 g/L; apparent efficiency of absorption = 27.7%). There was no difference between treatment groups in growth measurements, calf starter intake, lymphocyte counts, or health scores.

The objective of this study was to determine the effects of feeding heat-treated colostrum or unheated colostrum of different bacterial counts on passive transfer of immunity in neonatal dairy calves. First milking colostrum was collected from Holstein cows, frozen at -20 degrees C, and then thawed and pooled into a single batch. One-third of the pooled colostrum was transferred into plastic containers and frozen at -20 degrees C until needed for feeding (unheated-low bacteria). Another third was heat-treated at 60 degrees C for 30 min and then frozen at -20 degrees C until needed for feeding (heat-treated). The final third of colostrum was transferred into plastic containers, stored at 20 degrees C for bacteria to grow for 24 h (unheated-high bacteria), and then frozen at -20 degrees C until needed for feeding. A total of 30 Holstein bull calves weighing >or=30 kg at birth were systematically enrolled into 1 of the 3 treatment groups. Calves were separated from their dams at birth before suckling occurred. Before colostrum was fed, a jugular blood sample was collected from each calf. The first feeding consisted of 3.8 L of colostrum containing, on average, 68 g of IgG/L using an esophageal feeder between 1.5 and 2 h after birth. For the second and third feeding pasteurized whole milk at 5% of birth weight was fed. Blood samples were collected before colostrum feeding and at 24 and 48 h of age to determine serum total protein (STP) and IgG concentrations. Heat treatment of colostrum at 60 degrees C for 30 min reduced colostrum bacteria concentration yet maintained colostral IgG concentration and viscosity at similar levels to the control treatment. Calves fed heat-treated colostrum had significantly greater STP and IgG concentrations at 24 h and greater apparent efficiency of absorption (AEA) of IgG (STP = 62.5 g/L; IgG = 26.7 g/L; AEA = 43.9%) compared with calves fed unheated-low bacteria colostrum (STP = 57.0 g/L; IgG = 20.2 g/L; AEA = 35.4%) or unheated-high bacteria colostrum (STP = 56.2 g/L; IgG = 20.1 g/L; AEA = 32.4%). High bacteria load in colostrum did not interfere with total protein or IgG absorption or AEA.

No abstract

Waste milk has been fed to calves for many years, but concerns with bacterial contamination as well as possible transmission of diseases have discouraged widespread use of this feed. Pasteurization of waste milk is one option to reduce management risk while utilizing a valuable, low-cost, liquid feed source for calves. However, many farms currently pasteurizing waste milk lack a system to adequately monitor the efficiency of the process. A study was carried out to evaluate 6 on-farm pasteurization systems, including high-temperature, short-time pasteurizers and low-temperature, batch pasteurizers. Milk samples were taken pre- and postpasteurization as well as from the calf buckets and immediately frozen for later bacterial culture. Samples were collected twice daily for 15 d. Milk samples were examined for standard plate count (SPC), coagulase-negative staphylococci count, environmental streptococci count, coliform count, gram-negative noncoliform count, Streptococcus agalactiae count, and Staphylococcus aureus count. Before pasteurization, 68% of the samples had SPC <20,000 cfu/mL, and 39% of samples contained <100 cfu/mL of coliform bacteria. After pasteurization, 96% of samples had SPC <20,000 cfu/mL, and 92% had coliform counts <100 cfu/mL. Bacteria counts were significantly reduced by pasteurization, and pasteurized milk contained acceptable numbers of bacteria in >90% of samples. These results indicate that pasteurization can be very effective in lowering bacterial contamination of milk. However, bacteria numbers significantly increased after pasteurization and, in some cases, bacteria counts in milk fed to calves were similar to prepasteurization levels. Milk handling after pasteurization was identified as an important issue on the farms studied.