N-acetyl-beta-D-glucosaminidase as a predictor of milk loss and recovery after clinical mastitis.

Milk samples were collected at onset of 508 episodes of clinical mastitis on a 1,700-cow dairy farm in Michigan. Daily milk production and disease events were recorded for all cows in the herd. Despite statistical association with severity of mastitis, this association was too weak for N-acetyl-beta-D-glucosaminidase (NAGase) activity to be of great value as a prognostic test for clinical mastitis. High milk NAGase activity was significantly (P less than 0.0001) associated with: increased duration of treatment; increased duration of clinical signs of mastitis; decreased daily milk production; and increased risk of the cow being culled because of mastitis. The NAGase value was combined with days in milk production, baseline milk production before mastitis onset, parity, and season of onset to predict the outcome of clinical cases as measured by the first 3 aforementioned variables. Statistical models explained little of the variability among cows in duration of treatment (R2 = 0.11), duration of clinical signs of infection (R2 = 0.11), and milk production change (R2 = 0.09).

Effect of photoperiod on milk yield and milk fat in commercial dairy herds.

Two hundred and sixteen cows stanchioned in 13 dairy herds were exposed to supplemental lighting of 16 to 16.25 h of light per day from fluorescent lamps, whereas 240 herdmates received only sunlight (9 to 12 h/day) plus lighting for usual management activities (e.g., milking and feeding). After adjustment for differences in stage of lactation, lactation number, mature equivalent, and pretrial milk yield, cows exposed to supplemental lighting produced 2.2 kg per day more milk and had .16% less milk fat than herdmate controls.

Effect of health status on culling and reproductive performance of Holstein cows.

Data were from 492 cows that calved between October 1976 and May 1977 in eight Holstein herds in Michigan. Cows were classified as those without any health-related problems during lactation; those with minor reproductive health problems not serious enough to require veterinary treatment; and those with health problems severe enough to require veterinary treatment. Among primiparous cows 4.4, 16.2, and 19.1% were culled from healthy, minor, and problem groups, whereas among multiparous cows, these percentages were 11.2, 19.1, and 31.7. Among healthy cows 33.3, 38.9, and 27.8% of total culls were classified as production, reproduction, and other. Among minor and problem cows, these percentages were 31.6, 42.1, and 26.3 and 22.6, 58.5, and 18.9. The odds of being culled were 4.3 and 5.2 times as great as for first lactation cows in minor and problem groups and 1.9 and 3.7 times as great as for older cows in the two health-problem groups. Primiparous cows in healthy group averaged 50 days to first detected estrus, 68 days to first service, and 95 days open. Least squares means for performance of primiparous cows in minor and problem groups and of multiparous cows in healthy, minor, and problem groups, as deviations from healthy cows, was days to first service, 9.1, 24.0, 2.0, 12.1, and 9.1; and days open, -7.0, 15.2, -9.1, 1.8, and 12.6. Primiparous cows with health problems were at a higher risk of being culled than multiparous cows with health problems.

Relationships among type of parturition, type of discharge from genital tract, involution of cervix, and subsequent reproductive performance in Holstein cows.

Data were from 492 Holstein cows calved between October, 1976, and May, 1977, in eight herds in Michigan. Diameter of the cervix of each cow was estimated by palpation at 8 to 21 days postpartum and again 2 wk later. Parturition and postpartum discharge from the genital tract were classified as normal or abnormal. Size of the cervix between 12 and 26 days postpartum was classified as small, medium, or large within two parity groups. Incidence of abnormal parturition and incidence of abnormal postpartum discharge were 14.1 and 38.0%. Involution of the cervix was affected by parity and type of postpartum discharge. Involution of the cervix occurred sooner postpartum in primiparous than in multiparous cows and sooner postpartum in cows with normal discharge than in cows with abnormal discharge. The greatest difference in cervix diameter between cows with normal or abnormal discharges was 10 mm at 3 wk postpartum. Days from parturition to first detected estrus and first service were extended by abnormal postpartum discharge but not by abnormal parturition. First-service conception rate was lower and days from parturition to conception were higher in cows with medium or large cervices compared to cows with small cervices. Type of postpartum discharge and size of cervix early postpartum may be useful for predicting subsequent reproductive performance in dairy cows.

Metabolic adaptations during lactogenesis. Lactose synthesis in rabbit mammary tissue during pregnancy and lactation.

PIP: Lactose biosynthesis and relevant enzymatic activity in rabbit mamma ry tissue during various stages of pregnancy and lactation are investigated by using a tissue-slice incubation method in order to understand the temporal relationships. Ovulation was induced in 27 New Zealand white rabbits and they were bred by artificial insemination. Sacrifice occurred on days 15, 24, and 29 of pregnancy, and day 2, 5, 8, 15, and 22 post partum. Nucleic acids were extracted and concentratons of DNA determined spectrophotometrically at 600 nm with diphenylamine reagent and RNA determined with orcinal reagent. The tissue incubations were made with (U-14C) glucose. (14C) lactose was then separated by paper chromatography from unchanged radioactive glucose. Enzyme analysis including determining the activities of phosphoglucomutase, UDP-glucose pyrophosphorylase, and UDP-glucose 4-epimerase. Lactose synthase was determined, as well as, hexokinase. A biphasic adaptation in the rate of lactose synthesis and in the RNA concentration was noted during lactogenesis. The 1st increase in the rate of lactose biosynthes is occurred between days 15 and 24 of pregnancy. A 2nd substantial increase was noted immediately post partum. The overall rate of lactose biosynthesis increased 12-fold from day 24 of pregnancy to day 15 of lactation post partum, and then decreased from 15 to 22 days post partum. The RNA concentration/g wet weight of tissue and the ratio of RNA/DNA closely represented the biphasic ability of the mammary-tissue slice to synthesize lactose. Increases in the activities of UDP-glucose 4-epimerase and lactose synthase were most closely correlated with increases in the rate of lactose biosynthesis. UDP-glucose pyrophosphor ylase activity was unrelated with the ability to synthesize lactose, and hexokinase and phosphoglucomutase activities were variable during pregnancy and lactation. Lactose synthase activity was present by day 15 of pregnancy, but the ability to synthesize lactose was undetected until day 24 of pregnancy.^ieng

Metabolic adaptations during lactogenesis. Fatty acid synthesis in rabbit mammary tissue during pregnancy and lactation.

1. Mammary tissue was obtained from rabbits at various stages of pregnancy and lactation and used for tissue-slice incubations (to measure the rate of fatty acid synthesis and CO(2) production) and to determine relevant enzymic activities. A biphasic adaptation in fatty acid synthetic capacity during lactogenesis was noted. 2. The first lactogenic response occurred between day 15 and 24 of pregnancy. Over this period fatty acid synthesis (from acetate) increased 14-fold and the proportions of fatty acids synthesized changed to those characteristic of milk fat (77-86% as C(8:0)+C(10:0) acids). 3. The second lactogenic response occurred post partum as indicated by increased rates of fatty acid synthesis and CO(2) production (from acetate and glucose) and increased enzymic activities. 4. Major increases in enzymic activities between mid-pregnancy and lactation were noted for ATP citrate lyase (EC 4.1.3.8), acetyl-CoA synthetase (EC 6.2.1.1), acetyl-CoA carboxylase (EC 6.4.1.2), fatty acid synthetase, glucose 6-phosphate dehydrogenase (EC 1.1.1.49), and 6-phosphogluconate dehydrogenase (EC 1.1.1.44). Smaller increases in activity occurred with glycerol 3-phosphate dehydrogenase (EC 1.1.1.8) and NADP(+)-isocitrate dehydrogenase (EC 1.1.1.42) and the activity of NADP(+)-malate dehydrogenase (EC 1.1.1.40) was negligible at all periods tested. 5. During pregnancy and lactation there was a close temporal relationship between fatty acid synthetic capacity and the activities of ATP citrate lyase (r=0.94) and acetyl-CoA carboxylase (r=0.90).

Metabolic adaptations during lactogenesis. Fatty acid and lactose synthesis in cow mammary tissue.

1. Mammary-tissue biopsies were obtained from multiparous cows at 30 and 7 days pre partum and 7 and 40 days post partum. Investigations of the effect of lactogenesis on fatty acid and lactose synthesis involved measurements of biosynthetic capacity (tissue-slice incubations in vitro) and activities of relevant enzymes. 2. Fatty acid synthesis from acetate increased over 20-fold from 30 days pre partum to 40 days post partum. Changes in the lipogenic capacity of mammary-tissue slices more closely paralleled increases in the activities of acetyl-CoA carboxylase (EC 6.4.1.2) and acetyl-CoA synthetase (EC 6.2.1.1) than of other enzymes involved in acetate incorporation into fatty acids or in NADPH generation. 3. Lactose biosynthesis by mammary-tissue slices, lactose synthetase activity (EC 2.4.1.22) and alpha-lactalbumin concentration were all negligible at 30 days pre partum but increased 2.5-4-fold between 7 days pre partum and 40 days post partum. Phosphoglucomutase (EC 2.7.5.1), UDP-glucose pyrophosphorylase (EC 2.7.7.9) and UDP-glucose 4-epimerase (EC 5.1.3.2) had substantial activities at 30 days pre partum and increased less dramatically during lactogenesis. 4. Results are consistent with acetyl-CoA carboxylase and perhaps acetyl-CoA synthetase representing the regulatory enzyme(s) in fatty acid synthesis, with lactose synthetase (alpha-lactalbumin) serving a similar function in lactose biosynthesis.