An enzyme-linked immunosorbent assay for detection of bovine leukaemia virus p24 antibody in cattle

1990 ◽  
Vol 28 (1) ◽  
pp. 47-57 ◽  
Author(s):  
John B. Molloy ◽  
Peter J. Walker ◽  
F.Chris Baldock ◽  
Barry J. Rodwell ◽  
Jeff A. Cowley
2005 ◽  
Vol 59 (3-4) ◽  
pp. 363-370
Author(s):  
Tadej Malovrh ◽  
M. Pate ◽  
M. Ocepek ◽  
B. Krt

Bovine leukaemia virus (BLV) is a retrovirus that induces a chronic infection in cattle. Once infected, cattle remain virus carriers for life and start to show an antibody response within a few weeks after infection. Eradication and control of the disease are based on early diagnostics and segregation of the carriers. The choice of a diagnostic method depends on the eradication programme, money resources and characteristics of the herd to be analysed. The agar gel immunodiffusion (AGID) test has been the serological test of choice for routine diagnosis of serum samples. Nevertheless, in more recent years, the enzyme-linked immunosorbent assay (ELISA) has replaced the AGID for large scale testing. For this purpose, commercially available BLV-ELISA kits were compared to the AGID and to the polymerase chain reaction (PCR) method performed with two sets of primers, amplifying env region. The ELISA kit based on the p24 core protein was found to be less specific and served as a screening test. The ELISA kit based on the envelope glycoprotein (gpSI) served as a verification test and gave a good correlation with the AGID test and PCR method. However, ELISA showed a higher sensitivity than AGID. The p24 based ELiSA was useful for screening a large number of samples, whereas gp51 based ELISA, AGID and PCR were more important for detecting the antibody response against the individual BLV-proteins and therefore for verification of the infection with BLV.


2012 ◽  
Vol 81 (4) ◽  
pp. 353-358 ◽  
Author(s):  
Małgorzata Szewczuk ◽  
Sławomir Zych ◽  
Sylwia Katafiasz

Economic losses due to the bovine leukaemia virus infection can come from reduced milk production. The aim of this study was to evaluate molecular multiplex Polymerase Chain Reaction (multiplex PCR) test as an alternative for serologic Enzyme-linked Immunosorbent Assay (ELISA) method in diagnosing bovine leukaemia virus infections and found possible differences in milk yield in seronegative and seropositive cows. The study involved two groups of Polish Holstein-Friesian var. black and white cows (a total of 147 individuals). Animals were grouped according to their serological response to the bovine leukaemia virus antigen: control group of 71 healthy cows and second group of 76 naturally infected animals. Both multiplex PCR and ELISA proved to be very sensitive methods with sensitivity up to 100% and 97.4%, respectively. Negative effect of bovine leukaemia virus on milk yield was observed. Leucosis-free cows achieved higher milk yield (+ 322.9 kg;P≤ 0.01), protein yield (+ 5.2 kg,P≤ 0.05), and better milk yield after calculation into daily milk yield corrected for fat (+ 106.6 kg,P≤ 0.05) in comparison to seropositive cows. In infected cows a significantly higher (P≤ 0.01) fat content (4.1%) was recorded. Because ELISA test does not provide information of the infection at an early stage and is not sensitive enough to detect every infected animal, a two-step protocol allows for elimination of seropositive animals and restriction of their introduction into herds in Europe.


1994 ◽  
Vol 113 (3) ◽  
pp. 563-569 ◽  
Author(s):  
K. Knapen ◽  
P. Kerkhofs ◽  
E. Thiry ◽  
M. Mammerickx

SUMMARYSensitivity, specificity and predictive values of an enzyme-linked immunosorbent assay (ELISA) for detecting antibodies against bovine leukaemia virus (BLV) were evaluated using a representative sample of 145 serum pools, comprising from 3 to 48 individual sera. The sample was constituted according to the frequency distribution of the negative and positive pools analysed during a screening involving the whole cattle population of Belgium. Sensitivity and specificity were estimated to 88·9% and 100% and the predicted negative and positive values were 99·9% and 100%, respectively. These results indicate the use of serum pools is suitable for the detection of BLV infected herds in eradication campaigns.


2020 ◽  
Vol 11 (1) ◽  
pp. 290-293
Author(s):  
Talgat R. Yakupov ◽  
Mars M. Valiev ◽  
Farit F. Zinnatov ◽  
Azat M. Alimov ◽  
Albert K. Galiullin ◽  
...  

The article presents the results of studying the dynamics of the formation of antibodies and immune complexes, reveals the prospects for improving the early diagnosis of cattle leukaemia. Studies were conducted for 6 months on an experimental group of animals consisting of 12 cows. The titers of free and bound antibodies in blood serum and milk were determined by enzyme-linked immunosorbent assay. The results of studies showing that changes in titers of anti-leukaemia antibodies in the blood serum of cows naturally infected with BLV (bovine leukaemia virus) are significantly different from experimental infection data are adduced. In cows infected with BLV, there is no definite relationship between antibody titers in milk and in blood serum.  With sufficiently high titers of serum antibodies, antibody titers in milk can be minimal for the same cows; conversely, with low titers of serum antibodies, there can be high antibody titers in milk.  In the titers of antibodies free and bound in the immune complexes in blood serum with the development of the disease, a certain dependence is traced. With a decrease in titers of free antibodies, in most cases, an increase in titers of “bound” antibodies is observed, i.e., the degree of formation of circulating immune complexes (CECs) increases. There is no clearly defined dependence in the dynamics of changes in titers free and bound in immune complexes of antibodies in milk samples. They can remain at the same level for a long time, both at low and rather high levels.  


Sign in / Sign up

Export Citation Format

Share Document