In several locations in the paper, the direct-fed microbial supplement was incorrectly described with respect to the number of viable yeast cells: in the abstract (page 331), in the second paragraph of Materials and Methods (page 331–332), and in the footnotes to Tables 1 and 2 (page 332). The correct description is as follows: The direct-fed microbial (DFM) supplement contained 2 × 109 viable yeast cells and 5 × 109 cfu of bacteria (Enterococcus faecium) per cow per day, top dressed in a 90-g supplement. In the Materials and Methods section (page 331), the second sentence of the second paragraph should read “The DFM consisted of a yeast and two Enterococcus faecium strains of bacteria, (Chr. Hansen, Milwaukee, WI) selected for their ability to provide the desired lactic acid concentration under ruminal conditions.” The fourth sentence should read “The 90-g supplement containing the DFM provided 2 × 109 viable yeast cells and 5 × 109 cfu of bacteria.” The authors regret the error. Milk urea concentration as an indicator of ammonia emission from dairy cow barn under restricted grazingJournal of Dairy ScienceVol. 94Issue 1PreviewBulk milk urea concentration was evaluated to assess its potential as an indicator of ammonia emission from a dairy cow barn in a situation with restricted grazing. An experiment was carried out with a herd of, on average, 52 Holstein-Friesian dairy cows. The cows were housed in a naturally ventilated barn with cubicles and a slatted floor, were fed ensiled forages and feed supplements, and each day were allowed 8.5 h of grazing. The experiment was a balanced randomized block design, replicated 3 times. Full-Text PDF Open Archive

In several locations in the paper, the direct-fed microbial supplement was incorrectly described with respect to the number of viable yeast cells: in the abstract (page 260), in the first paragraph of Materials and Methods (page 261), in the footnotes to Tables 1 through 7, and in the captions of Figures 1 to 3. The correct description is as follows: The direct-fed microbial (DFM) supplement was fed at a rate of 2 × 109 viable yeast cells and 5 × 109 cfu of bacteria per cow per day. In the Materials and Methods section (page 261), the fourth sentence of the first paragraph should read “The treatments were control (prepartum and postpartum TMR with no DFM supplementation) or DFM [control prepartum and postpartum TMR with inclusion of 2 g of DFM/cow per d (Probios TC, Chr. Hansen, Milwaukee, WI; the DFM contained 2 × 109 viable yeast cells and 5 × 109 cfu of bacteria)].” The authors regret the error. Diagnosing intramammary infections: Evaluation of definitions based on a single milk sampleJournal of Dairy ScienceVol. 94Issue 1PreviewCriteria for diagnosing intramammary infections (IMI) have been debated for many years. Factors that may be considered in making a diagnosis include the organism of interest being found on culture, the number of colonies isolated, whether or not the organism was recovered in pure or mixed culture, and whether or not concurrent evidence of inflammation existed (often measured by somatic cell count). However, research using these criteria has been hampered by the lack of a “gold standard” test (i.e., a perfect test against which the criteria can be evaluated) and the need for very large data sets of culture results to have sufficient numbers of quarters with infections with a variety of organisms. Full-Text PDF Open Access

The objective of the study was to evaluate the effect of feeding the dietary antioxidant Agrado Plus (AOX; Novus International, St. Louis, MO) in diets that contained 2% fresh fat (FF) or oxidized fat (OF) on milk production and composition and antioxidant status of cows during mid to late lactation. Forty-four mid to late lactating primiparous cows housed in a tie-stall barn were fed a diet that contained 2% FF for 15 d as adaptation period and then randomly allocated to 1 of the 4 dietary treatments (FF, FF+AOX, OF, OF +AOX) for 6 wk. Feeding AOX increased dry matter intake, 3.5% fat-corrected milk, and milk fat yield, and decreased milk protein content but not yield. Feeding OF increased milk fat yield, but decreased dry matter intake and body weight gain. Milk fat composition changed with treatments: AOX increased cis 18:1 and decreased trans-11 18:1, whereas OF decreased trans-9 and trans-11 18:1 and cis-9, trans-11 18:2 in milk. Plasma antioxidant enzymes and status were affected by treatments. Feeding OF increased superoxidase dismutase activity but decreased plasma antioxidant status, whereas AOX supplementation increased glutathione peroxidase activity across fat types and increased the antioxidant status and superoxidase dismutase activity when feeding OF diets. It can be concluded that feeding AOX improved lactation performance and the antioxidant status of the cow across fat types, and feeding OF increased milk fat yield but decreased dry matter intake, body weight gain, and antioxidant status. The negative effects of feeding OF were partially alleviated by AOX.

however was not statistically altered by PG. Serum insulin peaked significantly higher and more rapidly for cows receiving PG via drenching but not as a part of the TMR. Plasma glucose, however, tended to peak higher and more rapidly for cows receiving PG, regardless of delivery method. Results showed that rumen and blood metabolites responded similarly to liquid or dry PG drench indicating that top dressing dry PG is as effective as oral drenching liquid PG. Feeding dry PG as a part of the TMR during frequent feeding significantly altered the rumen profile toward a more glucogenic environment without stimulation of insulin.

One hundred fifty multiparous cows were balanced to 1 of 3 treatments (2 pens/trt) according to previous lactation 305-d mature equivalent yield to evaluate supplementation with yeast culture (YC; A-Max, Vi-COR, Mason, IA) and YC plus enzymatically hydrolyzed yeast (YC+EHY; Celmanax, Vi-COR) on production performance in dairy cattle. Cows entered pens at calving and remained through 14 wk postpartum. Treatment assignment to pens was random throughout the barn. Pens were identical in layout and each contained an exit alley to eliminate feed and animal mixing. The 3 treatments were control: nonsupplemented; YC: control diet with YC (56 g/d); and YC+EHY: control diet plus YC and EHY (28 g/d). Mean pen dry matter intake was similar across treatments. Cows supplemented with YC and YC+EHY produced more milk, fat-corrected milk, and energy-corrected milk than control cows (1.4 and 1.6, 1.6 and 1.8, 1.7 and 1.9 kg, respectively). Treatments YC and YC+EHY did not differ. Milk fat and lactose percentages were not affected by treatment. Milk protein percentage was higher for cows supplemented with YC+EHY than for those on YC and control treatments (2.98, 2.93, and 2.91%, respectively) with control and YC-supplemented cows not being different from each other. Differences in fat and protein yields were primarily reflective of milk yield. Treatment had no effect on milk urea nitrogen. No differences in the incidence of metabolic health were observed; however, cases of clinical mastitis for YC+EHY were less than half those for control and YC during wk 8 to 14 on trial. Somatic cell count was higher for cows fed control and YC diets compared with YC+EHY, primarily during wk 8 to 14 on trial. Supplementation of early lactation cows with YC improved milk production performance; furthermore, EHY supplementation improved milk protein percentage and mammary gland health.

Five hundred seventy-three cows, balanced by parity and 305-d mature equivalent at dry off, were assigned to 1 of 4 treatments: 1) 75% complexed trace minerals (CTM; 75C): Zn, Mn, Cu, and Co supplied at 75% of NRC (2001) guidelines by Zn-, Mn-, and Cu-specific AA complexes, and cobalt glucoheptonate; 2) 100% inorganic (100I): Zn, Mn, Cu, and Co supplied at 100% of NRC (2001) requirements by sulfate sources; 3) 100% complexed (100C): Zn, Mn, Cu, and Co supplied at 100% of NRC (2001) requirements by CTM; and 4) complexed/inorganic (C/I): Zn and Cu supplied at 100% of NRC (2001) requirements using a combination of CTM and sulfates and Co and Mn supplied with sources at 9.1 and 3.3 times NRC (2001) requirements using a combination of CTM and sulfates. All percentages of Zn, Cu, Mn, and Co relative to NRC (2001) reflect supplemental contributions and do not include basal diet contributions. Experimental periods were dry period 1, full lactation 1, dry period 2, and 200 d into the subsequent lactation. Reproductive, health, and production information was collected during both lactations. Claw evaluations were conducted at trial start, 150 d into lactation 1, at the end of lactation 1, and 150 d into lactation 2. During lactation 1, C/I cows produced more milk, fat-corrected milk, energy-corrected milk, and fat than 100I cows. During lactation 2, yields of milk, fat-corrected milk, energy-corrected milk, fat, and protein were higher for 100C and C/I cows than for 75C or 100I cows. Fat percentage was highest for 100C cows with no treatment effect on protein content. During lactations 1 and 2, C/I cows had fewer days to first estrus than cows receiving the other treatments. During lactation 2, C/I cows had fewer services per conception and days open. There were no significant effects of treatment on health. White line separation incidence was lower for 100I cows than 75C cows, whereas heel erosion was higher for the 100I cows than for the C/I cows. Fortification of trace elements with inorganic and complexed sources at or above NRC requirements improved reproductive and productive performance. In addition, cows can be supplemented with CTM at 75% of NRC requirements with no reduction in performance compared with supplementing at 100% of NRC requirements using only sulfate sources of Zn, Mn, Cu, and Co.

A double-blind field trial was conducted on a commercial dairy to study the effects of feeding a direct-fed microbial (DFM) product consisting of 2 strains of Enterococcus faecium plus Saccharomyces cerevisiae yeast on prepartum and postpartum performance of Holstein cows. Treatments consisted of the normal pre- and post-fresh TMR supplemented with the DFM (2 g/cow per d) or a placebo. Treatments started approximately 10 d prepartum and continued until about 23 d in milk (DIM). A total of 366 Holstein cows were enrolled in 1 of 2 placebo groups or 2 DFM-supplemented groups. Groups were enrolled consecutively, starting with the placebo treatment. Sample size was limited to 4 groups because the cooperating dairy prematurely terminated the study due to increased health problems in one of the groups. Blood samples were taken during the prefresh period between 2 and 10 d prior to calving and at weekly intervals from 3 to 23 DIM. Blood concentrations of nonesterified fatty acids before calving and beta-hydroxy-butyrate after calving were not affected by treatment. Supplementation with the DFM product increased milk fat percentage for the first lactation cows and increased milk protein percentage for the second and greater lactation cows during the first 85 DIM. Second-lactation cows fed the DFM product received fewer antibiotic treatments before 85 DIM than cows receiving the placebo. This validated the dairy producer's concern that cows consuming one of the diets (revealed to be the placebo diet after the study was completed) were experiencing more health problems. Most measures of milk yield were numerically increased by supplementation with the DFM product. However, differences in milk yield were not significant. Key covariates for main study outcomes included milk yield in the previous (first) lactation, body condition score prior to calving, days spent in the maternity pen, and stocking density of the pre-fresh pen.

The influence of a direct-fed microbial (DFM) on the prepartum period and the effects on production performance during the postpartum period was investigated using 64 multiparous Holstein cows. Two close-up dry cow diets were fed to two groups of 32 cows each starting 21 d precalving as follows: 1) no DFM and 2) DFM. Post-calving cows were fed a lactation ration with or without DFM supplementation.The direct-fed microbial (DFM) supplement contained 2 × 109 viable yeast cells and 5 × 109 cfu of bacteria (Enterococcus faecium) per cow per day, top dressed in a 90-g supplement [corrected].The DMI during the prepartum period was not affected by DFM supplementation. During the postpartum period, DMI, milk yield, and milk protein content were higher for cows receiving DFM supplementation compared with no DFM. Blood glucose and insulin levels were higher and NEFA levels were lower for cows receiving DFM during the postpartum period. These data suggest that targeted DFM supplementation increased DMI and milk production postpartum. Blood metabolite information would suggest this response was associated with more glucose being made available and less fatty acids being mobilized from lipid stores.

Three ruminally cannulated cows calving within 10 d of each other were fitted with indwelling ruminal pH probes 3 wk prior to expected calving dates. They were used to evaluate diurnal variation in ruminal pH pre- and post-partum and to determine the influence of daily high and low pH levels on ruminal digestion of feedstuffs. Each probe was connected to a data logger, and hourly measurements were made from 3 wk prepartum through 7 wk postpartum. Cows pre- and postpartum were fed a total mixed ration (TMR) once daily. In situ digestion of corn silage, haylage, and corn meal DM was determined for 6h prior to feeding (high pH) and then starting at 3h and continuing through 9h after feeding (low pH) for one week prior to expected calving date and for 1 and 3 wk postpartum. Weekly mean low pH was greater for cows during the prepar-tum period than during the postpartum period. There was a negative relationship between mean weekly low pH and time. Area under the curve for pH < 6 and 5.5 increased from -3 to 7 wk postpartum. In situ digestion of corn silage and haycrop silage was not affected by time pre- or postpartum or by ruminal pH. Corn meal digestion at 6h was higher at wk 1 prepartum than at wk 1 and 3 postpartum. Corn meal digestion was depressed by lower rather than higher ruminal pH. This study illustrates that there is a linear depression in ruminal pH starting 3 wk prepartum through 7 wk postpartum, suggesting that dairy cattle have a greater propensity for acidosis postpartum as intake increases. In addition, periods of low pH depressed digestibility of corn meal but not hay crop or corn silage, which suggests that energy availability may be lower.