scholarly journals Evaluation of western blotting for the diagnosis of enzootic bovine leukemia

1999 ◽  
Vol 51 (4) ◽  
pp. 299-305 ◽  
Author(s):  
E.T. Gonzalez ◽  
G.A. Oliva ◽  
J. Norimine ◽  
V. Cid de la Paz ◽  
M.G. Echeverría
Keyword(s):  
Western Blotting ◽  
Post Inoculation ◽  
Infected Cattle ◽  
Serum Samples ◽  
Agar Gel ◽  
Viral Antigens ◽  
Experimental Inoculation ◽  
P24 Protein ◽  
Bovine Leukosis ◽  
Bovine Leukosis Virus

A western blotting (WB) procedure has been developed for detecting antibodies to bovine leukosis virus (BLV) in cattle sera. Two hundred and thirty three serum samples from naturally infected cattle with BLV virus and serial bleedings from experimentally BLV infected cows were used. An agar gel immunodiffusion test (AGID) was used for comparing with the results obtained by WB. The AGID positive sera showed a different degree of reactivity by WB test against the two most important viral antigens (gp51 and p24), or against one of them. Other proteins (gp30, p15, p12 and p10) were not detected with any AGID positive sera, being observed occasionally three bands corresponding to the p24 protein. Using sera obtained by BLV experimental inoculation, the antibodies directed to p24 appeared early (between the 2nd and 4th week post inoculation) and thereafter antibodies to gp51were detected in some animals. The analysis of field serum samples by AGID as compared to WB showed an agreement of 90.9%. Only 1.7% of sera were negative by AGID and positive by WB and 7.2% that were not conclusive by AGID and were defined by WB (4.2% as positive and 3.0% as negative).

Alteration in lymphocyte subpopulations in bovine leukosis virus-infected cattle

1992 ◽  
Vol 31 (1-2) ◽  
pp. 35-47 ◽  
Author(s):  
B.C. Taylor ◽  
J.L. Stott ◽  
M.A. Thurmond ◽  
J.P. Picanso
Keyword(s):  
Lymphocyte Subpopulations ◽  
Infected Cattle ◽  
Bovine Leukosis ◽  
Bovine Leukosis Virus

scholarly journals Immunodiagnosis of cattle fascioliasis using a 27 kDa Fasciola gigantica antigen

2021 ◽  
pp. 2097-2101
Author(s):  
Mohamed J. Saadh ◽  
Samer A. Tanash ◽  
Ammar M. Almaaytah ◽  
Issam J. Sa'adeh ◽  
Saed M. Aldalaen ◽  
...  
Keyword(s):  
Western Blotting ◽  
Clinical Symptoms ◽  
Characteristic Curve ◽  
Fasciola Gigantica ◽  
Enzyme Linked Immunosorbent Assay ◽  
Infected Cattle ◽  
Serum Samples ◽  
Healthy Cattle ◽  
Target Epitope ◽  
Circulating Antigens

Background and Aim: Diagnosis of fascioliasis depends on clinical symptoms and routine laboratory tests. Recently, antibodies and circulating antigens of Fasciola were used for detecting active infections. Therefore, this study aimed to identify Fasciola gigantica antigens in the sera of infected cattle using Western blotting and enzyme-linked immunosorbent assay (ELISA) for an accurate diagnosis of cattle infected with F. gigantica. Materials and Methods: Serum samples were obtained from 108, 23, and 19 cattle infected with Fasciola gigantica, Paramphistomum cervi, and Strongylids, respectively, including 57 non-infected cattle that were used as healthy cattle for the study. Western blotting and ELISA were then used to detect circulating Fasciola antigens at 27 kDa. Results: The target epitope was detected in an F. gigantica adult-worm antigen preparation, excretory/secretory products, and serum from cattle infected with F. gigantica. However, it was absent in sera from P. cervi, Strongylids, and healthy cattle. The purified 27 kDa F. gigantica (FPA-27) antigen was also detected in cattle serum using ELISA with high degrees of sensitivity and specificity (94% and 82%, respectively), and the area under the receiver operating characteristic curve was 0.89 with a highly significant correlation of p<0.0001. Conclusion: The FPA-27 is proposed to be a promising candidate for the serodiagnosis of fascioliasis in cattle.

scholarly journals Absence of Bovine Leukosis Virus in Semen of Seropositive Bulls

2002 ◽  
Vol 14 (5) ◽  
pp. 403-406 ◽  
Author(s):  
K. Yeon Choi ◽  
Don Monke ◽  
Jeffrey L. Stott
Keyword(s):  
Peripheral Blood ◽  
Detection System ◽  
Peripheral Blood Leukocytes ◽  
Chain Reaction ◽  
Agar Gel ◽  
Blood Leukocytes ◽  
Bovine Semen ◽  
Polymerase Chain ◽  
Bovine Leukosis ◽  
Bovine Leukosis Virus

A polymerase chain reaction (PCR)-based detection system was established to identify the presence of bovine leukosis virus (BLV) DNA in bovine semen. Seventy-nine bulls were included in the study. Serum, peripheral blood leukocytes, and semen were collected from each of the 79 bulls. The BLV-specific antibody was detected in serum by agar gel immunodiffusion and viral DNA in blood and semen by PCR. Serologically, 29 of the 79 bulls were BLV positive. Twenty-seven of the 29 seropositive bulls and 1 of the seronegative bulls had BLV DNA in peripheral blood leukocytes. All 79 bulls tested PCR negative for the presence of BLV in semen. This data is strong evidence that properly collected semen from BLV seropositive bulls will not contribute to dissemination of this viral infection.

Ear tattooing as a method of spread of bovine leukosis virus infection

1985 ◽  
Vol 141 (6) ◽  
pp. 647-649 ◽  
Author(s):  
M.H. Lucas ◽  
D.H. Roberts ◽  
G. Wibberley
Keyword(s):  
Virus Infection ◽  
Bovine Leukosis ◽  
Bovine Leukosis Virus

Lesions of the Enamel Organ of Developing Dog Teeth following Experimental Inoculation of Gnotobiotic Puppies with Canine Distemper Virus

1981 ◽  
Vol 18 (5) ◽  
pp. 684-689 ◽  
Author(s):  
R. R. Dubielzig ◽  
R. J. Higgins ◽  
S. Krakowka
Keyword(s):  
Canine Distemper Virus ◽  
Giant Cells ◽  
Enamel Organ ◽  
Post Inoculation ◽  
Canine Distemper ◽  
Experimental Inoculation ◽  
Enamel Epithelium ◽  
Viral Inclusions ◽  
Reduced Enamel Epithelium ◽  
Multinucleate Giant Cells

Ten 7-day-old gnotobiotic Beagle puppies were inoculated intraperitoneally with virulent canine distemper virus (R252-CDV). The dogs were killed and perfused with paraformaldehyde/glutaraldehyde from eight to 36 days after inoculation. The developing teeth of the mandibles were examined by light microscopy, and the teeth from three dogs were examined by electron microscopy. Necrosis of individual cells in the stratum intermedium of the developing tooth was the first change, detectable at day 9 post-inoculation. At day 16 post-inoculation, there was disorganization of the ameloblasts. In the stratum intermedium, multinucleate giant cells and large eosinophilic cytoplasmic viral inclusions were prominent. Ultrastructurally, these inclusions consisted of clusters of tubular aggregates typical of canine distemper virus nucleocapsids. At 28 to 36 days post-inoculation, the changes were seen in the reduced enamel epithelium. Multinucleate cells were seen, but no inclusions. Some necrotic cells were seen. In these teeth, ameloblastic cells of the root were morphologically normal. Our results suggest that distemper virus affects developing teeth by direct infection of the enamel organ.

Thyroid hormone suppression in feeder pigs following polymicrobial or porcine reproductive and respiratory syndrome virus-2 challenge

2021 ◽  
Author(s):  
J Alex Pasternak ◽  
Daniel J MacPhee ◽  
Joan K Lunney ◽  
Raymond R R Rowland ◽  
PigGen Canada ◽  
...  
Keyword(s):  
Viral Load ◽  
Thyroid Hormone ◽  
Thyroid Hormones ◽  
Average Daily Gain ◽  
Respiratory Syndrome Virus ◽  
Post Inoculation ◽  
Serum Samples ◽  
Cross Sectional ◽  
Post Exposure ◽  
Daily Gain

Abstract Thyroid hormones are powerful regulators of growth, development and basal metabolic rate and can be dysregulated under conditions of severe stress or illness. To understand the role of these hormones in porcine disease response, serum samples were obtained from 3 batches of nursery-aged pigs (n=208) exposed to a natural polymicrobial disease challenge with an array of bacterial and viral pathogens. Levels of total thyroxin (T4) and triiodothyronine (T3) assessed in sera by radioimmunoassay (RIA), decreased significantly by 14 days post exposure (DPE). Levels of T3 partially rebounded by 48 DPE, while T4 levels remain depressed. Post-exposure T3 and T4 levels were positively correlated with acute and long-term average daily gain. Cross-sectional sampling of animals maintained at the high health source farms, showed no equivalent change in either hormone when managed under standard industry conditions. To further elucidate the effect of PRRSV-infection on thyroid hormone levels, archived sera over 42 days post inoculation (DPI) from nursery pigs (N=190) challenged with one of two PRRSV2 strains by the PRRS Host Genetics Consortium (PHGC) were similarly assessed, with animals selected in a two-by-two design, to investigate biological extremes in average daily gain (ADG) and viral load. All animals showed a similar decrease in both thyroid hormones reaching a minimum at 7 DPI and returning to near pre challenge levels by 42 DPI. Post challenge T3 and T4 levels were significantly greater in high ADG groups, with no significant association with viral load or strain. The results of this study demonstrate porcine susceptibility to thyroid disruption in response to disease challenge and demonstrate a relationship between this response and growth performance.

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