PubMed Health⌕ Search

Biomedical subjects

S M Parish

Publications and source records attributed to S M Parish.

At least 55 records · Page 3Linked to original sources

Crooked calf disease: a histological and histochemical examination of eight affected calves.

Macroscopic, histopathologic, and histochemical investigations were made on a group of eight neonatal Angus X Hereford calves, selected from an ongoing outbreak of crooked calf disease among calving heifers. Arthrogryposis of the forelimbs was seen to varying degrees in all eight animals, and torticollis was present in six calves. Histopathology, using hematoxylin and eosin stain, did not reveal any striking or consistent lesion in the affected animals; the majority of the tissues sampled were normal. Muscle samples were processed for adenosine triphosphatase (ATPase) and NADH-tetrazolium reductase (NADH-tr) histochemistry, and the data suggest that a primary myopathy is not responsible for the congenital anomalies in the affected calves.

Animals↗

Transmission of bovine leukosis virus by blood inoculation.

The experimental transmission of bovine leukosis virus (BLV)-infected whole blood was studied in 2 groups of Holstein calves. The 1st group of 4 BLV-seronegative calves was given 10 microliters of whole blood by either the IM, IV, subcutaneous, or intradermal routes. All 4 calves seroconverted to BLV within 8 weeks after they were inoculated. The 2nd group, also comprising 4 calves, was given the equivalent of 1 microliter of whole blood by the described routes. These calves seroconverted to BLV by 14 weeks after they were inoculated. The results indicated that small volumes of whole blood administered by 4 different routes were effective in the spread of BLV.

Animals↗

Properties of a respiratory syncytial virus isolated from a sheep with rhinitis.

A virus isolated from a yearling cross-bred ewe was identified as respiratory syncytial virus (RSV) by indirect immunofluorescence and by virus neutralization with bovine RSV antisera. The virus caused a mild conjunctivitis in 3-month-old lambs when inoculated alone. Although clinical signs of pneumonia were not observed, there was gross and microscopic evidence of pulmonary inflammation in the lungs of lambs inoculated with either the sheep RSV isolate alone or in conjunction with Pasteurella haemolytica. Lung lesions in the dual infection were more severe, with approximately 10% of the total lung mass affected. Lavage fluids from lambs inoculated with virus and bacteria contained approximately 3 times more inflammatory cells than from control lambs or lambs inoculated with virus only. The sheep RSV isolate was classified as a mild respiratory pathogen in lambs of this age. Speculations on the potential importance of this virus in interspecies transmission to cattle and goats were discussed.

Animals↗

Seasonal variation in passive transfer of immunoglobulin G1 to newborn calves.

Forty-eight-hour serum concentrations of immunoglobulin G1 (IgG1) were determined for 123 female calves born on 1 farm during a 12-month period and fed 2.8 L of colostrum by esophageal feeder within 2 hours of birth. Mean monthly serum IgG1 concentrations were lowest in the winter, and increased during the spring and early summer to reach their peak in September, after which they decreased. Eight of 64 calves (12.5%) born from June through October had failure of passive transer of IgG1 (serum IgG1 less than 8 mg/ml), whereas 27 of 58 (46.5%) born from November through May had failure of passive transfer.

Animals↗

Regional distribution and variation of gamma-globulin absorption from the small intestine of the neonatal calf.

125I-labeled immunoglobulin (Ig)G1 in colostral whey was used to determine the region of maximum absorption of Ig from the small intestine of the neonatal calf and the variation in Ig absorption among calves at the intestinal level. In experiment 1, 5 segments (approx 5%, 35%, 60%, 80%, and 95% of the duodenocecal length) were formed in the small intestine of 9 colostrum-deprived calves shortly after birth. These segments were injected with colostral whey containing 125I-IgG1 4 hours after birth, and uptake, transfer, and absorption (defined as uptake plus transfer) were determined for each segment 2 hours later. Raw data were adjusted for the milligrams of IgG1 injected per gram of intestinal tissue to obtain the least squares mean (LSM) value. The LSM values for absorption of IgG1 from distal segments 3, 4, and 5 were significantly greater (P less than 0.05) than those values for proximal segments 1 and 2. The region of the maximum IgG1 absorption was the lower small intestine, 60% to 80% of the duodenocecal length. There was also an indication of independence between uptake and transfer in each of the segments. Significant differences (P less than 0.05) were present among calves in the LSM values for uptake and absorption, but not for transfer. In experiment 2, thoracic ducts of 8 newborn calves were cannulated 4 to 5 hours after birth. At 6 hours after birth, colostral whey with 125I-IgG1 was injected into an intestinal segment (approx 60% to 80% of the duodenocecal length).(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Effects of chronic heat and cold stressors on plasma immunoglobulin and mitogen-induced blastogenesis in calves.

Fifty-six Holstein calves were used to investigate effects of heat and cold stressors on mitogen-induced blastogenesis of isolated peripheral blood mononuclear cells and immunoglobulins G1 and M in blood plasma. Calves were exposed to constant hot (35 degrees C), constant cold (-5 degrees C), or thermoneutral (23 degrees C) ambient conditions in environmentally-controlled chambers. Immune responses were measured soon after introduction into environmental chambers (3 days) and after various degrees of adaptation (7 and 14 days). Mortality was greater among heat- and cold-exposed calves than among thermoneutral calves. Neither heat nor cold exposure had a direct effect on blastogenesis of peripheral blood mononuclear cells by phytohemagglutinin or concanavalin A. Plasma from heat- and cold-exposed calves then was incorporated into the culture medium at a final concentration of 5% and tested in a mitogenesis assay on peripheral blood mononuclear cells from a single healthy donor. Plasma from heat-exposed calves consistently enhanced tritiated thymidine incorporation into normal peripheral blood mononuclear cells by phytohemagglutinin and concanavalin A as compared to plasma from cold-exposed calves. After heat exposure for 3 to 14 days, immunoglobulin G1 averaged 27% less in heat-exposed calves than in calves that were held at thermoneutrality, but M was unaffected. Cold exposure did not have a consistent effect on G1 or M. These data demonstrate that chronic heat and cold stressors affect calves by altering both antibody- and cell-mediated immunity.

Animals↗

Delayed-type hypersensitivity, contact sensitivity, and phytohemagglutinin skin-test responses of heat- and cold-stressed calves.

Three-week-old Holstein bull calves were used to investigate the effect of a 2-week chronic heat (35 C) or cold (-5 C) exposure on delayed-type hypersensitivity (DTH) reactions to purified protein derivative after sensitization with heat-killed Mycobacterium tuberculosis, contact sensitivity (CS) reactions to 1-fluoro-2,4-dinitrobenzene, and phytohemagglutinin (PHA) skin tests. Heat exposure reduced expression of DTH reactions by 42% and CS reactions by 38% at 24 hours after elicitation of the responses. The PHA-induced skin tests were not affected after 1 week of heat exposure, but this reaction was reduced by 20% after 2 weeks of heat exposure. The immune response of calves exposed to cold air temperatures was more complex. Cold exposure suppressed CS reactions by 39% at the end of both the 1st and 2nd weeks. The PHA response was reduced by 39% after 2 weeks of cold exposure. The DTH response depended on duration of cold exposure. The DTH reaction was increased by 42% after 1 week, but was reduced by 14% after 2 weeks. These data are consistent with the hypothesis that environmental stressors alter host resistance by affecting the immune system. Furthermore, these stress-induced changes in immune events depend on the type of immune response, the nature of the environmental stressor, and the length of time that calves are exposed to the stressor.

Animals↗

Lasalocid for improved weight gains and control of Coccidia in lambs.

Lasalocid at 25 mg/kg of feed was highly effective in reducing numbers of oocysts in feces of naturally infected ewes and lambs. Treated ewes were fed lasalocid-medicated feed before and after parturition, and the 17 lambs from these ewes also were fed medicated feed gained 5.26 kg more (P less than 0.05) than did the 17 nontreated lambs from nontreated ewes. Naturally infected lambs maintained in semiconfinement acquired coccidia infections between 23 and 64 (mean of 38) days after birth. A coccidiostat given before and during the time coccidia-naive lambs were first exposed to coccidia was necessary to achieve the greatest production response to treatment. When naturally infected feeder lambs (30.9 kg) maintained in semiconfinement were fed lasalocid-medicated feed at 25 mg/kg of feed or unmedicated feed for 91 days, no significant difference (P greater than 0.05) in rate or efficiency of gain was detected, even though lasalocid was highly effective against coccidia.

Administration, Oral↗

Whole blood leukocyte vs. separated mononuclear cell blastogenesis in calves: time-dependent changes after shipping.

The blastogenic response of peripheral blood mononuclear cells to mitogenic stimulation by concanavalin A was lower (P less than 0.01) after transporting 60 dairy calves 480 km than it was either one or two weeks later. The response was similar for phytohemagglutinin. There was a decrease (P less than 0.05) in the number of peripheral blood monocytes and neutrophils two weeks after shipping. The transportation of calves did not affect plasma IgG1 or IgM level. The mitogenic stimulation of peripheral blood leukocytes by both phytohemagglutinin and concanavalin A in whole blood cultures was more variable than with the culture of peripheral blood mononuclear cells. Technique variation, which was defined as the coefficient of variation among quadruplicate cultures, was greater than 20% for while blood assays and less than 10% for cultures of peripheral blood mononuclear cells. The variation among different calves tested at the same time and the variation within single calves tested at different times were also lower in peripheral blood mononuclear cell cultures than in whole blood mononuclear cell cultures than in whole blood assays. It is suggested that the variation among replicate cultures be reported in blastogenesis studies.

Animals↗

Azotemia in cattle.

Blood biochemical studies were performed on 21 azotemic cattle with various disease conditions. The cattle were greater than or equal to 4 months old. Blood urea nitrogen concentrations ranged from 41 to 346 mg/dl. The azotemia was determined to be of prerenal origin in 10 cattle and of renal or postrenal origin in 11 cattle. The most consistent biochemical finding was that of hypochloremia. Sixteen cattle had lower than normal concentrations of serum calcium, and 15 had serum inorganic phosphorus concentrations greater than normal. In 17 cattle, the serum concentration of inorganic phosphorus was greater than that of calcium. Plasma sodium content was lower than normal in 9 of the 21 cattle, and plasma potassium concentrations were quite variable. Most of the cattle tended to maintain a normal acid-base status or had metabolic alkalosis. It was concluded that evaluation of biochemical data does not make it possible to determine whether azotemia is prerenal, renal, or postrenal in origin.

Animals↗

Synthesis of DNA and protein by Anaplasma marginale in bovine erythrocytes during short-term culture.

Bovine erythrocytes infected with Anaplasma marginale were cultured for 1 to 5 days in a CO2 incubation chamber, pulse-labeled with [3H]thymidine and [14C]methionine, lysed, and fractionated by differential centrifugation and continuous density gradient centrifugation in Renografin. Anaplasma and associated fragments of stroma formed two distinct bands in the dense region of the gradient. Electron microscopic examination of pelleted material from the bands from cells cultured for 1 day revealed the presence of organisms that were morphologically intact or in various states of degeneration. Examination of fractions from the gradient for incorporation of label revealed that analplasma present in erythrocytes can incorporate both [3H]thymidine and [14C]methionine. Subsequent experiments demonstrated that organisms cultured for 3 and 5 days incorporated the radiolabeled compounds also, but to a lesser extent. The experiments demonstrate that it is possible to culture analplasma in vitro for short periods of time and monitor their growth characteristics.

Anaplasma↗

Inheritance of an ovine lysosomal storage disease associated with deficiencies of beta-galactosidase and alpha-neuraminidase.

Prospective and retrospective genetic studies were performed on sheep with a recently described inherited lysosomal storage disease that involves a profound deficiency of beta-galactosidase and an associated deficiency of alpha-neuraminidase. Retrospective studies of the flock of sheep in which four affected lambs were born indicated little inbreeding but the presence of a common ram in both the maternal and paternal sides of the pedigrees. When unrelated rams were used in the flock in subsequent years, no affected lambs were born. The affected lambs' parents were phenotypically normal, so the disease was investigated as a putative autosomal recessive condition in prospective breedings of related sheep over two breeding seasons. For the third breeding season, heterozygous ewes were superovulated and bred to a heterozygous ram, and the resultant embryos were transferred to recipient ewes. Later in the same breeding season, the heterozygous ewes were re-bred naturally to the heterozygous ram. Lambs were identified as affected by the development of signs of ataxia, levels of beta-galactosidase that were less than 7% of the levels in controls by spectrofluorometric assay, or the histopathologic demonstration of vacuolization of neurons. Heterozygous sheep were identified by the production of affected offspring and/or by levels of beta-galactosidase in fibroblast cultures that were approximately 50% of control levels. The phenotypic ratio of affected sheep to normal sheep and the genotypic ratio of affected to heterozygous to normal sheep were consistent, by chi-square analysis, with an autosomal recessive trait. It was concluded that this ovine lysosomal storage disease is an autosomal recessive disease.

Animals↗

Facial fibrosarcoma in two cows.

Fibrosarcoma is a common tumor affecting bone, but is uncommon in cows. Reported here are two bovine cases of facial fibrosarcoma that were very invasive.

Animals↗

Clinical and clinicopathologic characteristics of ovine GM-1 gangliosidosis.

Ovine GM-1 gangliosidosis is an inherited lysosomal storage disease. Nine lambs affected with the disease were studied to characterize clinical signs and to determine if there were any pathognomonic clinicopathologic abnormalities. Evaluation included physical, ophthalmic, and neurologic examinations, complete blood counts, serum enzyme and electrolyte analyses, urinalyses, cerebrospinal fluid analyses, blood gas analyses, roentgenograms, electromyograms, and electrocardiograms. Two affected lambs had clinicopathologic tests performed before and after the onset of clinical signs. The only consistent abnormalities recognized were nonspecific signs referable to the central nervous system; predominantly ataxia, conscious proprioceptive deficit most severe in the hind limbs, blindness, and recumbency. Lambs continued to eat and drink, though at diminished levels and with loss of body condition. It was concluded that there are no pathognomonic clinicopathologic abnormalities associated with ovine GM-1 gangliosidosis, and antemortem diagnosis requires enzyme assay of leukocytes or cultured fibroblasts, or lectin histochemistry of tissues obtained by biopsy. Lysosomal storage diseases should be considered among the differential diagnoses in young animals presenting with early neonatal death or with nonspecific neurological signs, in concert with an absence of diagnostic clinicopathologic findings.

Animals↗

Evaluation of 3 assays for failure of passive transfer in calves.

This study examined the sensitivity, specificity, predictive values, and classification accuracy of 3 commonly used screening tests for failure of passive transfer: the sodium sulfite turbidity test, the zinc sulfate turbidity test, and refractometry relative to serum immunoglobulin G1 (IgG1) concentrations determined by radial immunodiffusion. Serum samples were obtained from 242 calves ranging from 1 to 8 days of age. Using a serum concentration of 1,000 mg/dL IgG1, to define adequate passive transfer, the zinc sulfate test had a sensitivity of 1.00 and a specificity of 0.52 in the detection of inadequate passive transfer. The endpoint of the test appeared to be higher than desired; calves testing negative had mean serum IgG1 concentration of 955 mg/dL and a large proportion of calves with adequate passive transfer were misclassified as positive for failure of passive transfer. Using the qualitative zinc sulfate test, the percentage of calves correctly classified with regard to passive transfer status was less than that observed with either the sodium sulfite test or refractometry. The sensitivity of the sodium sulfite assay was 0.85 at a 1+ endpoint and 1.00 at a 2 or 3+ endpoint. The specificity of the sodium sulfite assay varied from 0.87 at a 1+ endpoint and 0.56 at a 2+ endpoint. The sensitivity and specificity of refractometry varied from 0.01 to 1.00 depending on the choice of endpoint. Refractometry correctly classified the largest proportion of calves with regard to their passive transfer status at test endpoints of 5.0 and 5.5 g/dL, 83% and 82% respectively. The highest percentages of calves correctly classified occurred with the sodium sulfite test using a 1+ endpoint (86.30%) and refractometry using a 5.0 g/dL endpoint (83.00%). A regression equation was developed that permitted calculation of an optimal endpoint for refractometric determinations of total serum protein concentration. A serum protein concentration of 5.2 g/dL was equivalent to 1,000 mg/dL serum IgG1. Optimal selection of tests for passive transfer status in calves will be governed by the prevalence of failure of passive transfer, test performance, and the anticipated costs of classification errors.

Analysis of Variance↗