The effect of vacuum packaging on microbiological quality of roasted chicken. Roasted chicken were subjected to two different type of packaging treatment i.e. aerobic packaging with low density polyethylene bags (con) and vacuum packaging using barrier bags (VP.). Microbiological analyses were done on 0th, 5th, 10th, 15th and 20th day at refrigeration temperature (4±1oC). Studies revealed that microbial counts in terms of total plate count, proteolytic count and yeast and mold count increased significantly (P0.05) with the advancement of storage period and were significantly higher (P0.05) for aerobically packaged product throughout the observation period however, yeast and mould count observed only on 10th, 15th and 20th day of observation period. Lactic acid bacterial counts of vacuum packaged product were significantly higher as compared to aerobically packaged sample.

Thirty Staphylococcus aureus isolates used in the study obtained from cattle (20) and goat (10) were haemolytic on blood agar. Twenty one of the isolates (14 from cattle, 7 from goats) produced a-haemolysis, 3 produced b-haemolysis (2 from cattle and 1 from goats), and 6 isolates (4 from cattle and 2 from goats) produced both a- and b-haemolysis. The haemolysins tested against erythrocytes from rabbit, cattle and horse in order to demonstrate a-, b- and d-toxins, respectively revealed that a- and b-toxins were produced by all the isolates but b toxin was produced by only 7 isolates from cattle and by 3 from goats. On titration it was recorded that highest titre was recorded for a-toxins (for cattle, 1:2560 and for goat, 1:1280) whereas the highest titres for b and d-toxins was similar (1:160) for cattle as well as goat isolates. The result obtained for qualitative and quantitative haemolysin assays correlated well with the haemolysis pattern seen on the blood agar plates.

The hooded phenotype is one of the coat color phenotype seen peculiarly in the rat. The hooded locus showing autosomal recessive inheritance is mapped to chromosome (Chr) 14 and that the hooded phenotype receives modification by hooded-modifier gene showing the linkage to the hooded locus. However, a gene responsible for either the hooded or hooded-modifier gene is not yet identified. To clarify genetic control of hooded phenotype, we carried out genetic linkage studies using BN and LEA rats. For determination of phenotypic variation, we measured ratio of pigmented coat area in parental and their Fsub(1) and Fsub(2) rats. We, then, conducted a genome-wide scan on 152 Fsub(2) rats for linkage with ratio of pigmented coat area for the dorsal, ventral and total regions. A major quantitative trait locus (QTL), D14Got40, showing highly significant linkage contributing 70-90% of the variance for hooded phenotype was detected on Chr 14, which may be correspondent to the hooded locus. In addition, another QTL, D17Rat2, showing highly significant linkage was also detected on Chr 17 in dorsal region phenotype as well as a QTL showing suggestive linkage on Chr15 in ventral region phenotype. We, further, investigated a genome-wide scan for epistatic interactions and detected significant interactions between D14Got40 and D20Mit1, and between D14Got40 and D17Rat2 in the dorsal region phenotype. These results suggest that a major QTL in Chr 14, which is possibly correspondent to the hooded locus, mainly regulates the hooded phenotype with some modifier loci, two of which show epistatic interactions with the hooded locus.

The objective of this study was to investigate the changes in synovial fluid concentration of collagen type II cleavage site (C2C) and pro collagen II C-propeptide (CPII), markers of joint cartilage degeneration and synthesis, respectively, in horses with intraarticular fracture or osteochondrosis dissecans (OCD), and to examine the relationship between arthroscopic findings and these biomarker levels. Synovial fluid was collected from 36 joints in 18 horses (6 fractures and 12 OCDs). Samples from contralateral normal joints, when available, served as controls (n=12). Concentrations of C2C and CPII were measured using enzyme-linked immunosorbant assays. Moreover, the severity of the cartilage degradation was graded arthroscopically in 16 horses, and the correlation between the C2C and CPII levels and the arthroscopic scores were investigated. Compared to the control, the concentration of C2C was increased in OCD joints but not in fracture joints, whereas the concentration of CPII was increased in fracture joints but not in OCD joints. Within each disease group there was no correlation between biomarker levels and arthroscopic findings. Therefore, although C2C and CPII have diagnostic potential further knowledge is required to provide accurate analysis.

Male Japanese black bears (Ursus thibetanus japonicus) have an explicit reproductive cycle. The objective of this study was to clarify the variation of plasma testosterone, FSH, inhibin, LH levels and testicular gonadotropin receptor mRNA expression of male bears associated with their testicular activity. Notably, this study investigated peripheral FSH concentration and localization of gonadotropin receptor mRNAs for the first time in male bears. Blood and testicular tissue samples were taken from captive, mature, male Japanese black bears during testicular active, regressive and recrudescent phases. Plasma hormone concentrations were measured by immunoassays, and gonadotropin receptor mRNA expression in the testis was investigated by in situ hybridization technique and also by real-time PCR. There were significant variations in plasma testosterone and inhibin concentrations. Changes in FSH concentration preceded these hormones with a similar tendency. Hormones started to increase during denning, and achieved the highest values at the end of the recrudescent phase for FSH and in the active phase for testosterone and inhibin. These changes in hormone concentrations were accompanied by testicular growth. In situ hybridization analysis revealed that FSH and LH receptor mRNA was possibly expressed in Sertoli cells and Leydig cells, respectively, as they are in other mammals. However, neither plasma LH concentration nor testicular gonadotropin receptor mRNA expression level varied significantly among the sampling months. These results suggest that FSH, inhibin and testosterone have roles in testicular activity in male bears. This study provides important endocrine information for comprehending seasonal reproductivity in male Japanese black bears.

The present study characterizes canine reticulocyte exosomes. Exosomes are small membrane vesicles involved in membrane remodeling that are released from reticulocytes during the final maturation step of red blood cells. The vesicles collected from reticulocyte culture supernatants by differential centrifugation contained major exosomal proteins including heat shock protein cognate 70 (Hsc70) and transferrin receptors (TfR), consistent with the definition of the exosome. In addition, the Na,K-ATPase alpha-subunit and stomatin, a lipid raft-associated protein, were extruded by the exosome pathway, possibly leading to the absence of these proteins in erythrocytes, while the major protein constituents of erythrocyte membranes, spectrin and band 3 were retained in reticulocytes and not expelled into exosomes. The Na,K-ATPase alpha-subunit, as well as TfR and about half of the stomatin contained in exosomes, was obtained in a detergent-soluble fraction that was distinct from the lipid raft micro domain. Moreover, Na,K-ATPase and a portion of stomatin were distributed differently to Hsc70, TfR, stomatin, and ganglioside Gsub(M1) in vesicles separated with sucrose density gradient centrifugation. These results demonstrate that a heterogeneous group of exosomes participates in the loss of Na,K-ATPase and membrane remodeling during reticulocyte maturation in dogs.

The study was conducted on twelve normally calved, suckled, lactating Murrah buffaloes, aged 57.9±3.2 months from 1st to 3rd parity. The animals varied from 12 to 30 days postpartum at the start of experiment and suckling was restricted to twice daily (before milking). The objective of the study was to monitor ovarian follicular changes during early postpartum in Murrah buffaloes using a real time Bmode ultrasonography. Only 3 out of 12 animals showed cyclicity during observation period. Large follicles (8 to 10 mm) were detected for the 1st time at 24.4±1.99 days, whereas 10 mm follicles were first noticed at 26.0±1.41 days. The duration of growth of dominant follicle (9.3±0.48 days) was higher than duration of its regression (7.1±0.40 days), thereby indicating that the rate of regression is faster (0.73±0.03 mm/d) as compared to rate of growth (0.64±0.02 mm/d). The duration of growth of corpus luteum formed after 1st ovulation was very short (8.67±1.44 days). The largest diameter attained by first postpartum ovulatory follicle was 13.0±1.10 mm and the calving to first postpartum ovulation interval was 52.67±8.02 days in the present study. It is concluded that very few (25%) buffaloes experience ovulations in early postpartum period (within 2 months postpartum). Low number of buffaloes displayed spontaneous resumption of postpartum cyclicity although ovaries of all the animals exhibited follicular activity.

Eight female piglets from each of three farrowed crossbred (75% Hampshire x 25% Local) gilts grouped as A, B and C were weaned at 28, 42 and 56 days respectively. Piglets of each weaned groups were divided into two sub-groups _ 'a' and 'b' consisting of 4 piglets in each. Piglets of sub-groups _ 'a' were supplemented with strategic mineral mixture while the piglets of sub-group 'b' were offered commercial mineral mixture. There was significant (P0.01) rise of serum oestradiol-17â at the pubertal oestrus compared to the levels before puberty in gilts. Oestradiol concentration did not differ significantly among piglets weaned at different days of age and between piglets supplemented with strategic and commercial mineral mixture. Serum progesterone was lowest during oestrus and highest on day 10 of the oestrus cycle in all the groups. Progesterone concentration in the piglets weaned at different days of age did not differ significantly. However, the level was found significantly (P 0.05) high in piglets supplemented with strategic mixture over the piglets supplemented with commercial mineral mixture.

Heat stress is major concern for maintaining optimum production in livestock. The improvement of productivity in dairy animals, exposed to adverse environmental conditions, is primarily focused on improving the microclimate and nutritional management of the animals. The experiment was conducted on three groups of animals comprising six adult buffaloes in each group. Two groups were exposed to heat stress in the psychrometric chamber (40oC), the third group was kept under ambient conditions as control. One of the exposed groups was offered ascorbic acid (20g/day/animal). The blood samples were taken at every 4th day up to 16th day. Samples were analyzed for the total plasma protein and plasma albumin. Results showed that as the days of exposure progressed, the level of stress increased which is evident from the elevated level of total proteins. When compared with the ascorbic acid supplemented group (7.28±0.09 gm/dl), the non-supplemented group had higher protein content (7.93±0.13 gm/dl). There was significant difference (P 0.05) in protein levels among the groups. The level of albumin also followed the same pattern as that of total protein but in heat stressed (2.42±0.17gm/ dl) and ascorbic acid supplemented animals (2.41±0.19 gm/dl), the globulin levels declined as compared to group kept at ambient conditions (2.79±0.33 gm/dl). Further, the Albumin:Globulin ratio was significantly (P 0.05) higher in heat stressed animals (2.78±0.43) and ascorbic acid supplemented animals (2.19±0.30) as compared to control group (1.61±0.37). It can be concluded that ascorbic acid supplementation would be beneficial to buffalo producers of the arid/ semi-arid regions in amelioration of stress challenge imposed by the harsh weather.

The study was conducted to determine the role of Ca2+ and K+ channels in Moringa oleifera flowers extract-induced myometrial contractility of buffalo uterus. Myometrial strips were prepared, mounted in an organ bath containing Ringer Locke solution maintained at 37oC and responses recorded using a kymograph. Moringa oleifera flowers extract (MOFE) produced quite conspicuous and concentration-dependent contractile effect on buffalo myometrium and the EC50 value was found to be 31.62 ìg/ml. Verapamil (10-12M) not only completely inhibited normal spontaneous rhythmic contractions of myometrial uterine strips but also inhibited MOFE-induced spontaneous rhythmic contractions. Ethylene glycol tetra acetic acid (EGTA; 0.1-0.2mM) reduced both the frequency and amplitude of spontaneous contractions and also produced around 28% reduction in the amplitude of MOFE-induced contractile effect. Similalrly, pinacidil (10-6M-10-5M), glibenclamide (10-5M) and 4- amino pyridine (4-AP; 1mM) pretreatments inhibited spontaneous contractions as well as the contractile effects of MOFE (250ìg/ml). Based on the results of present study, it may be inferred that both the extra- and intracellular Ca2+ are very vital for the oxytocic effect of MOFE. Functional presence of K+ ATP, K+ V and/or K+ Ca channels in buffalo myometrium and their involvement in mediating MOFEinduced contractility can not be ruled out. Moringa oleifera flowers possessed promising oxytocic activity and can be exploited in drug-development programme for evolving natural and effective oxytocic or abortifacient.