Maristela Rovai

Evaluation of udder cisterns and effects on milk yield of dairy ewes.

Nine Manchega (0.94 L/d) and 10 Lacaune (2.07 L/d) ewes at the same stage of lactation (90 d in milk) were used to study the interbreed differences in milk yield, mammary morphological traits, and machine-milking ability. Udder traits were measured after 6 h of udder filling before the start of the experiment. Cisternal area (by ultrasonography), cisternal milk (by teat cannula drainage), and alveolar milk (by machine milking after an intravenous oxytocin injection) were randomly measured 8 h after milking for 2 wk consecutively either with an intravenous injection of an oxytocin receptor blocking agent (atosiban, AT) or without (control, C) to avoid the occurrence of milk letdown before milking. Lacaune ewes had greater udder depth (22.5 +/- 0.9 vs. 19.6 +/- 0.9 cm) and cistern height (27.1 +/- 3.8 vs. 15.6 +/- 3.5 mm), whereas Manchega ewes had longer (42.7 +/- 1.5 vs. 32.7 +/- 1.5 mm) and wider teats (17.4 +/- 0.5 vs. 13.9 +/- 0.5 mm). Values per half udder for Manchega and Lacaune ewes differed in cisternal area (12.8 +/- 0.7 and 23.7 +/- 0.6 cm(2)) and cisternal milk (120 +/- 0.6 and 269 +/- 0.5 mL), but not in alveolar milk (95 +/- 0.5 and 102 +/- 0.4 mL), respectively. Cisternal area and cisternal milk were positively correlated (r = 0.79). Ratios between cisternal and alveolar milk were 56:44 and 73:27 for Manchega and Lacaune ewes, respectively. Cisternal milk volumes obtained with the AT or C treatment were similar in Manchega (111 +/- 10 vs. 122 +/- 8 mL) but differed in Lacaune ewes (239 +/- 8 vs. 299 +/- 8 mL), respectively. Consequently, alveolar milk with AT vs. C was similar in Manchega (104 +/- 8 vs. 86 +/- 7 mL) but different in Lacaune ewes (115 +/- 7 vs. 89 +/- 7 mL). Results of this experiment confirm the need for the use of an oxytocin-blocking agent for accurate evaluation of milk contained in the udder of dairy ewes. Moreover, despite the differences in daily milk yield, alveolar milk did not vary between breeds, emphasizing the role of the cisternal more than the alveolar compartment for maximizing daily milk secretion in dairy sheep.

Effect of different milking intervals on the composition of cisternal and alveolar milk in dairy cows

Effects of six different milking intervals on the distribution of milk between cistern and alveoli were studied in a randomized, incomplete Latin Square experiment with four lactating Holstein cows. Cisternal and alveolar milk was measured by udder quarter at 4, 8, 12, 16, 20 and 24-h intervals with a 3-d interperiod of regular milking. Cisternal milk was evacuated using a cannula after injection of an oxytocin-receptor blocking agent, followed by an injection of oxytocin to remove the alveolar fraction. Milk samples from each fraction and quarter were collected for analysis. Cisternal and alveolar milk increased with milking interval and represented on average 30 and 70% of the milk stored in the udder, respectively. Fat content in alveolar milk remained constant during the first 16 h, increasing rapidly thereafter, reaching its maximum at 24 h (6.95%). Fat content in cisternal milk decreased with milking interval and reached its minimum at 24 h (0.96%). Total fat yield tended to increase for cisternal milk with longer milking intervals, but it increased markedly for alveolar milk, showing that fat globules did not pass freely from alveoli to cistern between milkings. Milk protein content was greater in rear quarters than in front quarters for both milk fractions. Milk protein content increased in the cisternal milk fraction and tended to increase in the alveolar milk fraction with longer milking intervals, but values did not differ between cisternal and alveolar fractions or between front and rear quarters. Total protein yield increased with milking interval in both fractions, indicating that casein micelles passed more freely than fat globules from the alveolar to the cisternal compartment. In conclusion, the short-term effects of milking intervals in milk composition were explained by the changes observed in alveolar and cisternal milk ratio.

Extended field test on the use of visual ear tags and electronic boluses for the identification of different goat breeds in the United States.

A total of 295 goats from 4 breeds (Alpine, n = 74; Angora, n = 75; Boer-cross, n = 73; Spanish, n = 73) were used to assess the retention of 3 types of electronic ruminal boluses (B1, 20 g, n = 95; B2, 75 g, n = 100; and B3, 82 g, n = 100) according to breed and feeding conditions. Time for bolus administration, reading with a handheld reader, and animal data recording (goat identification, breed, and bolus type) were registered. Each goat was also identified with 1 flag-button plastic ear tag (4.6 g, 51 x 41 mm). Retention of boluses and ear tags was regularly monitored for 1 yr. Ruminal fluid in 5 goats from each breed and management group was obtained with an oro-ruminal probe at 2 h after feeding. Ruminal pH was measured at 24 h and at wk 1, 2, 3, and 4 and used as an indicator of feeding conditions on rumen environment. Time for bolus administration differed by bolus type (B1, 14 +/- 2 s; B2, 24 +/- 2 s; B3, 27 +/- 2 s; P < 0.05) and goat breed (Alpine, 34 +/- 3 s; Angora, 17 +/- 2 s; Boer-cross, 16 +/- 1 s; Spanish, 19 +/- 2 s; P < 0.05), although differences were due to greater times for B2 and B3 in Alpine goats. Time for bolus administration averaged 22 +/- 1 s, and overall time for bolusing, reading, and data typing was 49 +/- 1 s on average. Ruminal pH differed according to breed and feeding management (lactating Alpine, 6.50 +/- 0.07; yearling Alpine, 6.73 +/- 0.07; Angora, 6.34 +/- 0.06; Boer-cross, 6.62 +/- 0.04; Spanish, 6.32 +/- 0.08; P < 0.05), but no early bolus losses occurred; rumen pH did not differ according to bolus type (B1, 6.45 +/- 0.05; B2, 6.39 +/- 0.07; B3, 6.49 +/- 0.05; P > 0.05). At 6 mo, electronic boluses showed greater retention than ear tags (99.7 vs. 97.2%; P < 0.05). At 12 mo, bolus retention was 96.3, 100, and 97.8% for B1, B2, and B3, respectively, not differing between B1 and B3 (P = 0.562). No effect of breed and bolus type on bolus retention was detected. No goat losing, at the same time, both bolus and ear tag was observed. Ear tag retention (91.7%) was less (P < 0.05) than all types of bolus (98.1%) on average. Ear tag retention in Boer-cross (98.6%) and Alpine (96.9%) goats was greater (P < 0.05) than in Spanish (88.7%) and Angora (82.9%) and tended to differ (P = 0.095) between Spanish and Alpine. In conclusion, unlike flag-button visual ear tags and mini-boluses used here, properly designed boluses (e.g., standard bolus) met International Committee for Animal Recording and National Animal Identification System retention requirements for goat identification under US conditions and are recommended in practice.

Identifying the major bacteria causing intramammary infections in individual milk samples of sheep and goats using traditional bacteria culturing and real-time polymerase chain reaction

Use of DNA-based methods, such as real-time PCR, has increased the sensitivity and shortened the time for bacterial identification, compared with traditional bacteriology; however, results should be interpreted carefully because a positive PCR result does not necessarily mean that an infection exists. One hundred eight lactating dairy ewes (56 Manchega and 52 Lacaune) and 24 Murciano-Granadina dairy goats were used for identifying the main bacteria causing intramammary infections (IMI) using traditional bacterial culturing and real-time PCR and their effects on milk performance. Udder-half milk samples were taken for bacterial culturing and somatic cell count (SCC) 3 times throughout lactation. Intramammary infections were assessed based on bacteria isolated in ≥2 samplings accompanied by increased SCC. Prevalence of subclinical IMI was 42.9% in Manchega and 50.0% in Lacaune ewes and 41.7% in goats, with the estimated milk yield loss being 13.1, 17.9, and 18.0%, respectively. According to bacteriology results, 87% of the identified single bacteria species (with more than 3 colonies/plate) or culture-negative growth were identical throughout samplings, which agreed 98.9% with the PCR results. Nevertheless, the study emphasized that 1 sampling may not be sufficient to determine IMI and, therefore, other inflammatory responses such as increased SCC should be monitored to identify true infections. Moreover, when PCR methodology is used, aseptic and precise milk sampling procedures are key for avoiding false-positive amplifications. In conclusion, both PCR and bacterial culture methods proved to have similar accuracy for identifying infective bacteria in sheep and goats. The final choice will depend on their response time and cost analysis, according to the requirements and farm management strategy.

Thermographic variation of the udder of dairy ewes in early lactation and following an Escherichia coli endotoxin intramammary challenge in late lactation

A total of 83 lactating dairy ewes (Manchega, n=48; Lacaune, n=35) were used in 2 consecutive experiments for assessing the ability of infrared thermography (IRT) to detect intramammary infections (IMI) by measuring udder skin temperatures (UST). In experiment 1, ewes were milked twice daily and IRT pictures of the udder were taken before and after milking at 46 and 56d in milk (DIM). Milk yield was 1.46 ± 0.04 L/d, on average. Detection of IMI was done using standard bacterial culture by udder half at 15, 34, and 64 DIM. Twenty-two ewes were classified as having IMI in at least one udder half, the others being healthy (142 healthy and 24 IMI halves, respectively). Four IMI halves had clinical mastitis. No UST differences were detected by IMI and udder side, being 32.94 ± 0.04°C on average. Nevertheless, differences in UST were detected for breed (Lacaune - Manchega=0.35 ± 0.08°C), milking process moment (after - before=0.13 ± 0.11°C), and milking schedule (p.m. - a.m.=0.79 ± 0.07°C). The UST increased linearly with ambient temperature (r=0.88). In experiment 2, the UST response to an Escherichia coli O55:B5 endotoxin challenge (5 μg/udder half) was studied in 9 healthy Lacaune ewes milked once daily in late lactation (0.58 ± 0.03 L/d; 155 ± 26 DIM). Ewes were allocated into 3 balanced groups of 3 ewes to which treatments were applied by udder half after milking. Treatments were (1) control (C00, both udder halves untreated), (2) half udder treated (T10 and C01, one udder half infused with endotoxin and the other untreated, respectively), and (3) treated udder halves (T11, both udder halves infused with endotoxin). Body (vaginal) temperature and UST, milk yield, and milk composition changes were monitored by udder half at different time intervals (2 to 72 h). First local and systemic signs of IMI were observed at 4 and 6h postchallenge, respectively. For all treatments, UST increased after the challenge, peaking at 6h in T 0055 (which differed from that in C00, C01, and T10), and decreased thereafter without differences by treatment. Vaginal temperature and milk somatic cell count increased by 6h postchallenge, whereas lactose content decreased, in the endotoxin-infused udder halves. Effects of endotoxin on lactose and somatic cell count values were detectable in the infused udder halves until 72 h. In conclusion, despite the accuracy of the camera (± 0.15°C) and the moderate standard errors of the mean obtained for UST measures (± 0.05 to 0.24°C), we were unable to discriminate between healthy and infected (subclinically or clinically) udder halves in dairy ewes.

Using long-term averted goats for selective grazing in olive groves

Conditioned taste aversion (CTA) is a useful tool to modify animal feed preferences, allowing the implementation of selective grazing to control weeds in tree orchards without damaging the trees or affecting fruit production. LiCl is commonly used for inducing CTA. However, studies investigating the long-term persistence of CTA by LiCl in small ruminants are scarce. With this aim, we evaluated the efficiency of two LiCl doses (AV1 and AV2, 175 and 200 mg/kg BW, respectively) and a control (C, 0 mg/kg BW) for averting non-lactating dairy goats (n=15) to olive tree leaves. Aversion induction was reinforced on day 9 in those goats that consumed >10 g of olive leaves. Mid-term aversion effectiveness was assessed by five double-choice feeding tests (days 16, 24, 31, 38 and 53) of 30 min each, where 100 g of olive leaves were offered side-by-side with 390 g of Italian rye-grass (as-fed). Long-term aversion effectiveness was assessed in C, AV1 and AV2 goats by grazing for 30 min in paddocks with a simulated olive tree (days 59, 90, 121, 182 and 420). Moreover, C and AV2 goats were compared under on-field conditions (days 143, 211 and 363) in a commercial olive grove also for 30 min. The CTA proved to be established with a single LiCl dose in all goats and persisted for 4 and 55 days in AV1 and AV2 goats, respectively (P<0.001). However, 80% AV1 and 20% AV2 goats needed to be reinforced at day 9. When grazing under simulated olive tree and commercial olive grove conditions, the CTA goats, especially AV2 group, avoided the contact with the olive trees and minimally used a bipedal stance to feed leaves, than control goats. On average, time proportion spent consuming olive leaves and sprouts was much greater (P<0.05) for C (50.7±9.1%) than for AV1 (14.4±3.9%) and AV2 (3.1±0.9%). In conclusion, the 200 mg LiCl/kg BW dose was more effective than the 175 mg LiCl/kg BW dose for inducing an effective long-term CTA to olive tree leaves in goats.

How to Create Conditioned Taste Aversion for Grazing Ground Covers in Woody Crops with Small Ruminants

Conditioned taste aversion (CTA) is a learning behavior process where animals are trained to reject certain feed after gastrointestinal discomfort has been produced. Lithium chloride (LiCl) is the preferred agent used in livestock to induce CTA because it specifically stimulates the vomit center. In addition, LiCl is commercially available, and easy to prepare and administer using a drenching gun. Nevertheless, some factors have to be considered to obtain an effective long-lasting CTA, which allows small ruminants to graze during the cropping season. A key aspect is to use animals with no previous contact with the target plant (the plant chosen to be avoided; new feed). Due to their native neophobic feeding behavior, small ruminants can easily associate the negative feedback effects with the new feed, resulting in a strong and persistent CTA. The recommended doses are 200 and 225 mg LiCl/kg body weight (BW) for goats and sheep, respectively. To induce CTA, 100 g of the target plant should be individually offered for at least 30 min, and LiCl administered thereafter if the intake is greater than 10 g. Each time the animal eats the target plant without negative consequences, the CTA becomes weaker. Consequently, to minimize the risk of target plant consumption, it is essential to have sufficient palatable ground cover available. The presence of an alternative feed (of quality and quantity) prevents the accidental consumption of the target plant. A close monitoring of the flock is recommended to remove and re-dose any animal consuming more than 4 bites or 10 g of the target plant. At the beginning of each grazing season, check the CTA status of each animal before moving them to the crop.