Anne Grace Silva Siqueira Campos

Dinâmica celular e microbiológica do leite de ovelhas Santa Inês acompanhadas durante a lactação

The aim of this study was to evaluate the dynamics of intramammary infection in ewes by means of clinical examination, direct somatic cell count and the isolation of bacterial agents involved in the process during lactation, as well as the sensitivity profile of these isolates to different antimicrobials. Thirty four ewes from the Santa Ines breed, raised under semi-intensive conditions and submitted to identical sanitary and nutritional management were evaluated before and after parturition, about 10 days before parturition, 15 days after parturition (dap), 30 dap, 60 dap and 90 dap (weaning). In the respective phases a clinical exam of the mammary gland was accomplished. The direct somatic cell count (SCC) and the California Mastitis Test (CMT) were carried out in the phases postpartum (15 dap, 30 dap, 60 dap and 90 dap) as well as the bacteriological analysis which was also accomplished in the experimental phase that preceded parturition when the ewes were not milked. Milk sampling was achieved by manual means. All ewes were submitted to lentivirus serology test. The variable data of SCC were tested for normality according to Kolmogorov-Smirnov and not attended the premise of normality were transformed into log base 10 (Log10). Therefore was performed the analysis of variance and contrast of means by Tukey test with significance level of P<0.05. A descriptive study of the variables studied was done by frequency distribution (%). The average somatic cell count in negative reactions to the CMT varied 387.896,08 cells/mL to 620.611,11 cells/mL and glands reagents ranged up to 6.730.514,50 cells/mL, but there was no influence in the different stages of lactation. The results allowed to conclude that subclinical mastitis represents a sanitary concern in the breeding of Santa Ines ewes. The phase that precedes parturition is particularly worrying and deserves more attention since there is a higher bacterial isolation percentage in apparently healthy glands. In association, it was also in the first 30 days of lactation (initial phase) that a high frequency of bacterial isolation was perceived, with coagulase-negative Staphylococcus as the agent isolated in higher percentage

Efeito da administração de propileno glicol e cobalto associado à vitamina B12 sobre o perfil metabólico e a atividade enzimática de ovelhas da raça Santa Inês no periparto

The aim of this study was to evaluate the influence of the administration of propylene glycol and cobalt associated with vitamin B12 on the metabolic profile and enzymatic activity of Santa Ines ewes in the peripartum period. A total of 18 pregnant ewes, weighing around 40kg were used. Approximately 30 days before the expected date of delivery were randomly separated into three groups and administered supplements as follows: (G1/n = 6) group received propylene glycol (30mL orally daily); (G2/n = 6) group receiving cobalt (1mg cobalt chloride 1%, orally daily) associated with vitamin B12 (2mg intramuscular weekly) and (G3/n = 6) control group. Blood samples from ewes to evaluate the enzymatic and metabolic profile (glucose, β-hydroxybutyrate, BHB, NEFA, total protein, albumin, urea, creatinine, AST, GGT, ALP and CK) were taken 30 days before the date set for delivery, one week before (ante partum), delivery at 24h, 72h, 5 days, 15 days and 30 days after delivery. ketonuria was not observed in pre partum. The administration of supplements had no effect on the metabolic profile, protein and energy, and no liver disorders was observed in peripartum.

Perfil eletroforético do colostro de ovelhas suplementadas com propileno glicol e cobalto associado à vitamina B12 no final da gestação

This study aimed to evaluate the proteinogram of the colostrum of ewes submitted to administration of propylene glycol and cobalt associated with vitamin B12 in late pregnancy. Eighteen pregnant Santa Ines ewes 18 months to 5 years old were distributed by probabilistic sampling into three experimental groups, about 30 days before the expected delivery date. In group 1 (G1/n=6), daily oral doses of 30ml propylene glycol PA were administered; Group 2 (G2/n=2) received a daily oral dosage of 1mg cobalt chloride in 1% solution and 2mg of vitamin B12 intramuscularly once a week, and Group 3 (G3/n=6) was the control group. Soon after delivery 30mL of colostrum was harvested from each ewe, which were stored in appropriate containers and sent to the laboratory. After homogenization, we added to each 1000μL of colostrum 75μL solution of rennin, which was kept in a water bath at 37°C for about 20 minutes and centrifuged at 21.000G for 10 minutes in a refrigerated centrifuge. Later, the intermediate fraction, corresponding to colostrum whey, was aliquoted and kept in a -80oC ultrafreezer for subsequent determination of proteins. The determination of the total colostral protein whey was performed using a commercial reagent, observing the linearity test for colostrum. The separation of proteins was performed using the technique of electrophoresis on polyacrylamide gel containing sodium dodecyl sulfate (SDS-PAGE). Lactoferrin, IgA, albumin, IgG heavy chain (IgGCP), β-casein, IgG light chain (IgGCL), β-lactoglobulin and α-lactalbumin proteins were identified. There was no influence of the administration of supplements during late pregnancy on the concentration of proteins identified in the colostrum of the ewes.