The study reported in this Research Communication was conducted to investigate the molecular characterisation of buffalo SCAP gene, expression analysis, and the association between single nucleotide polymorphisms and milk production traits in 384 buffaloes. Sequence analysis revealed the SCAP gene had an open reading frame of 3837 bp encoding 1279 amino acids. A ubiquitous expression profile of SCAP gene was detected in various tissues with extreme predominance in the mammary gland during early lactation. Moreover, eleven SNPs in buffalo SCAP gene were identified, six of them (g.1717600A>G, g.1757922C>T, g.1758953G>A, g.1759142C>T, g.1760740G>A, and g.1766036T>C) were found to be significantly associated with 305-day milk yield. Thus, buffalo SCAP could sever as a candidate gene affecting milk production traits in buffalo and the identified SNPs might potentially be genetic markers.

One of the major challenges in lameness management is prompt detection, especially before visible gait disturbance. This scoping review describes the potential biomarkers for lameness in dairy cows reported in the literature, their relevance in lameness diagnosis, identifying cows at risk of developing claw lesions and monitoring recovery after treatment. Using specific keywords, a comprehensive literature search was performed in three databases: PubMed, Google Scholar and ScienceDirect to retrieve relevant articles published between 2010 and 2022. A total of 31 articles fulfilling the inclusion criteria were analysed. The categories of potential markers for lameness reported in the literature included acute phase proteins (APPs), nociceptive neuropeptides, stress hormones, proteomes, inflammatory cytokines and metabolites in serum, urine and milk. Cortisol, APPs (serum amyloid A and haptoglobin) and serum, urinary and milk metabolites were the most studied biomarkers for lameness in dairy cows. While APPs, nociceptive neuropeptides and blood cortisol analyses assisted in elucidating the pain and stress experienced by lame cows during diagnosis and after treatment, evidence-based data are lacking to support their use in identifying susceptible animals. Meanwhile, metabolomic techniques revealed promising results in assessing metabolic alterations occurring before, during and after lameness onset. Several metabolites in serum, urinary and milk were reported that could be used to identify susceptible cows even before the onset of clinical signs. Nevertheless, further research is required employing metabolomic techniques to advance our knowledge of claw horn lesions and the discovery of novel biomarkers for identifying susceptible cows. The applicability of these biomarkers is challenging, particularly in the field, as they often require invasive procedures.

The protein composition in goat milk undergoes changes throughout the different lactation periods, displaying distinct characteristics that are influenced by the dynamic nature of protein composition and concentration during the transition from colostrum secretion to mature milk. To evaluate the dynamics of whey proteins of Saanen goats during the colostral phase and the first month of lactation, 110 milk samples from 11 healthy mammary halves of seven Saanen goats were selected through a clinical evaluation. Whey was obtained by rennet coagulation of the mammary secretion. The biuret method determined total protein concentration, and their fractions were identified by 12% dodecyl sulfate-polyacrylamide gel electrophoresis. Maximum concentrations of all protein fractions were observed in the first 12 h of lactation, reducing throughout the study. Modification of the protein predominance was also observed. The transition from colostrum secretion to milk occurred 5 or 7 d postpartum.

We investigated the effect of different types of mother-young contacts (fenceline, restricted and no contact) on the health, growth performance, behaviour and physiological state of Murrah buffalo calves. A total of 24 calves were allocated to three groups of 8: NCM (no calf–mother contact), RCM (restricted calf–mother contact) and FCM (fenceline calf–mother contact). At three months of age, the FCM calves had a higher average body weight (58.6 ± 1.5 kg) than the RCM (52.8 ± 1.3 kg) and NCM (53.6 ± 1.3 kg) calves (P < 0.05). The average daily gain (ADG) at three months of age was greater in FCM (0.6 ± 0.1 kg/d) than RCM (0.5 ± 0.1 kg/d) and NCM (0.5 ± 0.1 kg/d) calves (P < 0.05). The mean immunoglobulin G (IgG) concentrations were significantly greater on d 7, 28, 42 and d 56 of sampling (P < 0.05 for all comparisons) in FCM than RCM and NCM calves. The mean cortisol levels were highest in the NCM calves followed by RCM and the lowest values were observed in FCM calves on d 0, d 7, d 28, d 42 and d 56, respectively (P < 0.05, for all recorded days). The diarrhoea score and eggs per gram of faeces (EPG) were significantly greater in the NCM group compared to the RCM and FCM groups. The time spent in cross sucking, licking inanimate objects and self-licking was greatest (P < 0.05) in NCM calves, followed by RCM calves, and was almost non-existent in the FCM group on all the recorded weeks. Time spent in backward ear position was greater (P < 0.05) in FCM than RCM and NCM calves. The average time spent in forward ear position was greatest (P < 0.05) in the RCM calves followed by NCM with the lowest time observed in FCM calves. The mean duration of time spent by calves in the asymmetrical and axial ear position differed significantly (P < 0.05) among NCM, RCM and FCM calves, P < 0.05. The full and fenceline buffalo calf–mother contact system showed higher growth rates, lower levels of stress responses, oral stereotypies and eggs per gram of faeces. In addition, ear postures may be used as a dependable, and reliable measure of positive, low arousal emotional states.

A study was made of the changes in the iodine value of milk fat from cows following the feeding of linseed oil (450g) at intervals of 6 days. Three cows in midlactation and of differing age and breed were used. The experiment consisted of a series of 3 collection periods, each of 6 days' duration, with 12 days between periods. Three doses of oil were given (6 days apart) between periods 1 and 2, the last dose of oil being given immediately before the start of period 2. The mean iodine values for the 3 periods were 35·5, 40·5 and 34·7 respectively. There was a distinct pattern of change in iodine value with time after feeding the oil, a maximum of 45·5 being attained on the second day with a subsequent decline to 38·5 on the sixth day. Analysis of variance showed that these effects were significant and due to oil-feeding, whereas changes in yield and content of fat and production of milk could be accounted for by normal decline in lactation. It was concluded that the periodic feeding of a large dose of linseed oil produces a significant increase in the iodine value of milk fat and avoids the possible disadvantages of continuous fat supplementation.

Lyphan paper M 25 can be used for pH measurements in milk and whey in the pK range 5·4—6·6. As a rule the error does not exceed 0·1 pH.

In very acid milk and whey (pH < 5·4) lyphan paper of the L series may be used. Generally the deviation does not exceed -0·2 pH. In alkaline milk and whey lyphan paper cannot be used.

In milk and whey from cows infected with mastitis M 25 may be used unless the pH exceeds 7.

This Research Paper addresses the hypothesis that using teatcups with automatic valves, without cutting off the vacuum prior to cluster removal, could increases the risk of mastitis and affect other milking variables on goats. A first trial used 46 intramammary infection (IMI)-free goats that had been milked with normal teatcups (without automatic valves) during a pre-experimental period of 8 ± 2 d postpartum. These animals were divided into two groups (n = 23), randomly assigning each group to teatcups with automatic valves (teatcups A) or without automatic valves (teatcups B) for a 20-week experimental period. During this period, several strategies were applied to increase teat exposure to pathogens in both experimental groups. In the first eight weeks of the experimental period, the new IMI rate per gland was significantly higher (P < 0·05) in the group of animals milked with teatcups A (6 of 46; 13%) than in the group milked with teatcups B (1 of 46; 2%). However, throughout the rest of the experimental period the same number of glands appeared with new IMI (n = 7) in both animal groups. SCC was higher in goats milked with teatcups A, but no significant differences were found in the remaining variables (milk production and composition, frequency of liner slips + teatcup fall-off). In a second experiment, in a crossover design (54 goats in fourth month of lactation, 2 treatments – teatcups A and B – in 2 experimental periods each lasting 1 week), no differences were observed in total milk, average milk flow, total milking time or teat thickness changes after milking between both teatcups. However, teatcups A worsened slightly the maximum milk flow. We concluded that the use of teatcups with automatic valves, without cutting off the vacuum prior to cluster removal, increases the risk of mastitis on goat livestock farms.

It was previously found that low concentrations of oleic acid in the growth medium inhibited the growth of Streptococcus cremoris strain C 13. However, a variant of this strain has now been isolated which is capable of growth in relatively high concentrations of oleic acid. This was achieved by the extended incubation of inocula of strain C 13 in milk containing various concentrations of oleic acid.

The vapour/liquid equilibrium coefficients for the steam distillation of indole and skatole from water solution over the range of concentrations 0·1 to 20–30 ppm. were found to be 2·4 and 4·7, respectively. The coefficient for indole in a cream containing 30% fat was found to be 0·31, and for skatole, in a cream containing 40% fat, 0·14. It is concluded that complete removal of indole and skatole contaminations from cream by use of steam distillation equipment is not commercially practicable.

A series of experiments is described, outlining a study of 5 factors likely to influence the efficiency and reproducibility of a standardized method used for the electronic counting of somatic cells in milk. Samples containing cells covering 5 ranges from 250000 cells/ml to 1500000 cells/ml were used and the results analysed statistically.

The residual error was given special consideration, and was found not to contribute to any significant degree to the accuracy of the method. Sample volumes of 0·5 ml and 0·1 ml used for counting were compared, and there was a decrease in accuracy using the smaller volume. The influence of individual technician skill was studied with 4 workers having differing degrees of experience, and no significant addition to the overall error was observed. The effect of agitating bulk tank milk for between 0 and 2 min before sampling was examined. Variations were considerable for agitation times of less than 1 min, but the recommended mixing time of 2 min was found to be adequate with milk quantities between 450 l and 2250 l (100 and 500 gal), and at the 5 cell-count levels chosen.

The distributions of the cell counts at the 5 levels were found to be normal with the marginal exception of samples tested at 250000 cells/ml.

All aspects of the technique, sample preparation, use and calibration of the Coulter Counter, etc, should be closely followed to ensure that no inaccuracies will result from inadequate maintenance of the machine or other equipment employed in the test.