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Biomedical subjects

L H Lauerman

Publications and source records attributed to L H Lauerman.

At least 37 records · Page 2Linked to original sources

Bluetongue virus in pregnant elk and their calves.

Two pregnant North American elk (Cervus canadensis), in the 3rd and 4th months of gestation, were inoculated with bluetongue (BT) virus (BTV) serotype 11. The virus was not isolated from the blood of the cows beyond postinoculation day (PID) 8, but was isolated from bone marrow and spleen samples obtained at necropsy on PID 190. Although neither cow had overt clinical signs of BT infection, fluctuations in specific neutralizing BTV antibody titers indicated viral replication. However, in 2 attempts, BTV was not recovered biologically via bites of colonized Culicoides variipennis (biting gnats) with subsequent transmission of the BTV to sheep. Bluetongue virus was isolated from the elk calves at birth and before they nursed. These calves remained latently infected, and BTV was transmitted from each calf to sheep by bites of the biting gnats. Most of the BTV biological recovery attempts resulted in suspicious BT clinical responses in sheep, but without viral isolation. However, after challenge exposure with the homologous virus, 5 of 7 recipient sheep bitten by the gnats reacted with an intensified BT clinical response that indicated viral sensitization. One calf was born weak, never attained a healthy appearance, was latently infected with BTV, and had fluctuating BTV neutralizing antibody titers. The other calf was in apparently good health, was latently infected with BTV, and was immunologically tolerant to BTV.

Animals↗

Purification and partial characterization of a macrophage cytotoxin from Pasteurella haemolytica.

A protein from Pasteurella haemolytica that was highly immunogenic and toxic toward bovine alveolar macrophages was partially purified. When isolated from culture supernatants of P haemolytica serotype 1 or serotype 6, the protein reacted on Ouchterlony immunodiffusion tests with antisera from 12 serotypes of P haemolytica, but did not cross-react with antisera to serotypes of P multocida. This indicated that the protein may be specific for P haemolytica. Bacteria were grown in dialysis culture in a brain-heart infusion and calf-serum growth medium. The protein was isolated from the medium by ultrafiltration and size-exclusion chromatography and has a molecular weight of approximately 150,000 daltons. The protein, which is highly immunogenic and has the characteristics of a virulence factor, is common to all serotypes of P haemolytica, and may be an effective agent for immunization against P haemolytica in cattle.

Antigens, Bacterial↗

Metabolic and cellular profile testing in calves maintained under feedlot conditions: protein fractions and lactate dehydrogenase isoenzymes--changes over time.

Mean concentrations for total serum protein and serum protein fractions, and mean activities for total lactate dehydrogenase (LDH) and LDH isoenzymes were determined in 114 crossbred yearling cattle during a 56-day feeding trial. These values were to be used as predictors of performance (weight gain). The mean total serum protein concentration on day 0 was high (7.27 g/dl), reached a low on days 7 and 14 (6.47 and 6.50 g/dl), and then equilibrated toward the end of the study. The mean concentration for the albumin fraction also reached a low on days 7 and 14 (2.83 and 2.84 g/dl) and then increased, remaining steady until termination of the feeding trial. The alpha-, beta-, and gamma-globulin fractions fluctuated throughout the study. The mean for total LDH activity peaked on day 21 (1,363 IU) and then remained relatively constant through day 56. Mean serum activities for the LDH3 activity peaked on day 7 (27%) and then decreased progressively to day 56 (17%). The overall trend for LDH4 and LDH5 activities seemed to be a steady increase.

Animal Feed↗

Ischemia: a cause of hepatic telangiectasis in cattle.

We histologically examined (i) 73 bovine livers condemned by packing house inspectors for telangiectasis, (ii) 15 bovine livers passed by the same inspectors as normal, and (iii) 8 livers from cattle given an injection into their mesenteric veins: 6 with a suspension of agar particles containing viable Haemophilus somnus and 2 with diluent only. The injected cattle were killed and necropsied 2 to 12 days after the inoculations. Of the 73 telangiectatic livers, 57 (78%) had thrombosed and occluded or contracted and empty portal veins (venopathies), whereas 1 of the 15 normal livers contained one microscopic focus of telangiectasis and nearby venopathy. Of the 6 livers injected with suspended particles, all had venopathies and telangiectasis and the 2 control livers had neither.

Animals↗

Laryngeal diphtheria and papillomatosis in feedlot cattle.

In a random sample of 30,444 larynges from slaughtered beef cattle, 441 (1.4%) had chronic diphtheria and 1,345 (4.4%) had papillomatosis. Both types of lesions were centered in mucous membranes over the vocal processes and medial angles of the arytenoid cartilages. Since they are found in the same anatomical locations as laryngeal contact ulcers, we hypothesize that ulcers are primary and diphtheria and papillomatosis are secondary.

Animals↗

Osteochondrosis in feedlot cattle.

Beginning in summer 1977 and continuing through four consecutive seasons, we examined lame limb joints from 106 partially fattened cattle and 28,235 pairs of occipital condyles from fully fattened cattle for osteochondrosis. Of the 106 lame cattle, nine (8.5%) had characteristic lesions, usually in their stifle joints, and of the 28,235 atlanto-occipital joints, 1063 (3.8%) had lesions on their condyles. Slices of affected articular cartilage and subjacent bone were studied radiographically and histologically. Radiographs showed subchondral defects and epiphyseal "cyst-like" lesions, and histologic sections showed disarrayed and degenerated chondrocytes. Splits occurred along osteochondral junctions or in adjacent cartilage or bone. Some bone trabeculae had been replaced by fibrous tissue that, in some areas, extended deep into epiphyses.

Animals↗

Purification and biological characterizationof endotoxin fractions from Pasteruella haemolytica.

A sequential extraction procedure was used to provide 3 endotoxin fractions from Pasteurella haemolytica with distinct biological and solubility properties. After acetone dessication, extraction with phenol, chloroform, and petroleum ether (2:5:8) provided a fraction designated rough lipopolysaccharide (LPS). Subsequent extraction of the cells with 45% phenol at 68 C yielded a fraction designated smooth LPS, which was further divided into smooth precipitate and smooth supernatant, based on sedimentation at 105,000 x g for 4 hours. Yields of the 3 fractions were 1.5%, 3%, and 5.5% of the dry weight of the cells. The polysaccharide moieties of the rough LPS amd smooth precipitate fractions were obtained by partial acid hydrolysis followed by chloroform extraction. Biological activities of all 5 fractions were compared with activities of standard LPS fractions from Serratia marcescens and Salmonella typhimurium. Results of chicken embryo lethality, the local Shwartzman's phenomenon, nonspecific resistance enhancement ot challenge exposure by S typhimurium pyrogenicity, and the Limulus amebocyte lysate assay were reported.

Animals↗

Laryngeal contact ulcers in feedlot cattle.

Of 30,444 larynges from fattened cattle at three companies, 3,985 (13.1%) had contact ulcers or ulcer scars in the mucous membranes over the vocal processes and medial angles of the arytenoid cartilages. The incidence was higher in cattle fed during fall than in cattle fed during other seasons. We hypothesize: 1. that some feedlot cattle develop acute mucositis from mixed infections with species of Pasteurella, Haemophilus, Mycoplasma, and viruses in the nose, pharynx, and larynx; 2. that reflex coughing and swallowing accelerate the rate of larynx closure; and 3. that the closures erode the swollen membrane over the vocal processes and medial angles of the arytenoid cartilages and thus produce primary contact ulcers.

Animals↗

Limb arthropathies and periarticular injuries in feedlot cattle.

Beginning summer 1977 and continuing through 4 consecutive seasons, we examined samples of at least 25, and a total of 106, lame limbs or joints from slaughtered beef cattle. Of this number about 64 (60%) were articular and 42 (40%) periarticular lesions. Fifty-three were caused by trauma and 9 by osteochondrosis. Stifle joints (40) and digital joints (19) were the most frequently affected articulations, and the humerus and femur were the most frequently fractured bones. Twenty joints, mostly stifles, had fibrinous arthritis, and Mycoplasma spp. were isolated from 11.

Animals↗

Techniques for evaluating humoral and cell-mediated immunity in mule deer fawns (Odocoileus hemionus).

Twenty mule deer fawns (Odocoileus hemionus) were removed from their dams 48 h after birth, and hand-reared. Methods for monitoring their immune capability are described. Passive humoral immunity was determined by serum protein electrophoresis. Active humoral immunity following Clostridium toxoid vaccination was determined by immunodiffusion. Cell-mediated immunity was assayed using contact sensitization to 1-nitro, 2,4-dichlorobenzene (DNCB).

Animals↗

Correlations between leukocidin production and virulence of two isolates of Fusobacterium necrophorum.

Leukocidin production by Fusobacterium necrophorum was suggested to be an important element in the development of intraabdominal and liver abscesses in mice. Leukocidin production by cultures of F necrophorum was demonstrated by an in vitro assay. One of two isolates of F necrophorum was demonstrated to produce leukocidin. The leukocidin-producing strain was observed to be more infective than the nonleukocidin-producing strain (as demonstrated by abscess formation following intraperitoneal injection of immune-suppressed and normal mice). The infectivity of the leukocidin-producing strain was increased by successive passage in immune-suppressed mice. A simultaneous increase in leukocidin production was also demonstrated. The nonleukocidin-producing strain could not be passed effectively and was relatively noninfective for mice.

Animals↗

Biological and biochemical characteristics of Fusobacterium necrophorum leukocidin.

The production of a leukocidal exotoxin by 18-hour dialysis cultures of Fusobacterium necrophorum was detected in vitro by a cytotoxicity assay, using bovine leukocytes isolated from peripheral blood. Biological characteristics were determined while maximizing the in vitro assay. Biochemical characteristics of heat stability and stability to degradative enzymes were investigated and indicated that the leukocidin is protein in nature. The characteristics indicate that this leukocidin is different from previous descriptions in the literature of the characteristics of a leukotoxin produced by F necrophorum.

Biological Assay↗

Metabolic and cellular profile testing in calves under feedlot conditions: protein fractions and lactate dehydrogenase isoenzymes--reference values.

Serum protein and lactate dehydrogenase (LDH) isoenzyme values were determined for frozen serum samples from crossbred yearling feedlot cattle on feed for 56 days. The mean percentage values for serum protein components from 114 samples were: albumin, 46.5; alpha-globulin, 10.4; beta-globulin, 18.7; gamma-globulin, 23.8. For LDH isoenzymes, they were: LDH1, 36.5; LDH2, 24.7; LDH3, 16.9; LDH4, 12.0; LDH5, 9.1. These values are compared with values from dairy cattle.

Animal Feed↗

Immunoglobulin response to bluetongue virus soluble antigen in subcutaneous chambers.

Group-specific antibodies were produced by inoculation of bluetongue virus soluble antigen into polyethylene chambers implanted subcutaneously in 8 rabbits and 2 sheep. For comparison, 5 rabbits and 1 sheep were inoculated intramuscularly with the soluble antigen in Freund's complete adjuvant. Antibodies present in the serum and chamber fluids were detected by the agar gel precipitin or serum-neutralization tests, qualitatively examined by immunoelectrophoresis and immunofluorescence, and quantitated by electroimmunodiffusion.

Animals↗