Canine heartworm and heat treatment: An evaluation using a well based enzyme-linked immunosorbent assay (ELISA) and canine sera with confirmed heartworm infection status

2020 ◽  
Vol 283 ◽  
pp. 109169
Author(s):  
Jeff M. Gruntmeir ◽  
Maureen T. Long ◽  
Byron L. Blagburn ◽  
Heather S. Walden
1996 ◽  
Vol 59 (1) ◽  
pp. 6-10 ◽  
Author(s):  
PAUL C. BARTLETT ◽  
RONALD J. ERSKINE ◽  
PATRICK GASTON ◽  
PHILIP M. SEARS ◽  
HENDRICUS WILHELMUS HOUDIJK

Recent reports have indicated that the relative sensitivity and specificity of the ELISA test for detection of intramammary infection of cows with Staphylococcus aureus is not as high as originally reported. It has been suggested that antibodies measured by enzyme-linked immunosorbent assay (ELISA) more closely reflect previous infection status rather than current infection status, and that the delay in antibody formation following infection and the persistence of antibodies after elimination of infection may be responsible for some of the discrepancy observed between ELISA and bacterial culture results conducted on the same milk sample. This study (n = 209 cows) was undertaken to determine if an ELISA for S. aureus intramammary infection more closely reflects previous infection status than it does current infection status, and to ascertain whether correction of this time-delay factor substantially improves calculated values of ELISA relative sensitivity and specificity. Receiver-operator curves were constructed to compare different time-related definitions of microbiologic culture results used for comparison with ELISA results. A greater degree of curvature in receiver-operator curves indicated that ELISA results did more closely reflect culture results performed on milk samples taken 1 and 3 weeks previously. Insignificant improvement in sensitivity and specificity occurred when the database was limited to cows (n = 140) with milk production greater than 13.6 kg/day. However, values of sensitivity were all less than or equal to 90%, and values of specificity were all less than 54%.


1987 ◽  
Vol 38 (1) ◽  
pp. 83 ◽  
Author(s):  
D Munro

In 1981 a survey of the main commercial hop cultivar in Australia, Pride of Ringwood, showed that foliar symptoms were associated with the presence of carlavirus particles. The incidence of plants containing particles varied between fields from 0 to 58%. In 1982 a survey based on enzyme-linked immunosorbent assay showed that the carlaviruses were hop mosaic and hop latent viruses and that they infected 1-68% and 1-58% of plants respectively. Prunus necrotic ringspot virus infected 4-9% of plants. Arabis mosaic virus was detected in a cultivar of English origin and American hop latent virus in cultivars of recent American origin, but neither of these viruses was detected in Australian-bred hops. Virus-free plants suitable for propagation were located in cultivars Pride of Ringwood and B23, and were produced by heat treatment and meristem culture of cultivar Southern Cross.


2002 ◽  
Vol 55 ◽  
pp. 150-153 ◽  
Author(s):  
F.O. Obanor ◽  
M. Walter ◽  
N.W. Waipara ◽  
R. Cernusko

Monoclonal antibody to B cinerea (BC58) was used to develop a platetrapped antigen enzyme linked immunosorbent assay (PTAELISA) to detect and quantify Botrytis antigens in boysenberry flowers The ability of antibody BC58 to detect B cinerea in extracts from artificially infected boysenberry flowers was assessed Results showed that the antigen could be detected in latent infections Antibody BC58 sensitivity to heat treatment of the antigen incubation conditions and the detection limit were also investigated Autoclaving at 121C reduced the sensitivity of the antibody Additionally the incubation of the antigen at 4C overnight produced higher absorbance values at 405 nm than incubation at 37C for 2 h The detection and quantification of B cinerea antigen was reliable within 016 g dried mycelium per ml of PBS buffer and at least 8 x 103 spores


1989 ◽  
Vol 62 (04) ◽  
pp. 1078-1082 ◽  
Author(s):  
Burt Adelman ◽  
Patricia Ouynn

SummaryThis report describes the binding of plasminogen to fibrinogen adsorbed onto polystyrene wells. Binding was determined by enzyme linked immunosorbent assay. Both glu- and lys-plasminogen bound to immobilized fibrinogen in a dose-dependent fashion. However, more lys- than glu-plasminogen bound when equal concentrations of either were added to immobilized fibrinogen. Plasminogen binding was inhibited by epsilon aminocaproic acid indicating that binding was mediated via lysine-binding regions of plasminogen. Soluble fibrinogen added in excess of immobilized fibrinogen did not compete for plasminogen binding but fibrinogen fragments produced by plasmin digestion of fibrinogen did. Treatment of immobilized fibrinogen with thrombin caused a small but significant (p <0.01) increase in plasminogen binding. These studies demonstrate that immobilized fibrinogen binds both glu- and lys-plasminogen and that binding is mediated via lysine-binding regions. These interactions may facilitate plasminogen binding to fibrinogen adsorbed on to surfaces and to cells such as platelets which bind fibrinogen.


1995 ◽  
Vol 74 (04) ◽  
pp. 1045-1049 ◽  
Author(s):  
P Butthep ◽  
A Bunyaratvej ◽  
Y Funahara ◽  
H Kitaguchi ◽  
S Fucharoen ◽  
...  

SummaryAn increased level of plasma thrombomodulin (TM) in α- and β- thalassaemia was demonstrated using an enzyme-linked immunosorbent assay (ELISA). Nonsplenectomized patients with β-thalassaemia/ haemoglobin E (BE) had higher levels of TM than splenectomized cases (BE-S). Patients with leg ulcers (BE-LU) were found to have the highest increase in TM level. Appearance of larger platelets in all types of thalassaemic blood was observed indicating an increase in the number of younger platelets. These data indicate that injury of vascular endothelial cells is present in thalassaemic patients.


Sign in / Sign up

Export Citation Format

Share Document