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Biomedical subjects

J F Ferrer

Publications and source records attributed to J F Ferrer.

At least 55 records · Page 3Linked to original sources

Role of colostrum and milk in the natural transmission of the bovine leukemia virus.

The role of colostrum and milk in the transmission of the bovine leukemia virus (BLV) was examined by monitoring the development of BLV infection in calves that were fed since birth on colostrum and milk from their BLV-positive dams and then reared in complete or partial isolation from infected cattle. Twenty-one of the 25 calves raised in complete isolation remained negative for BLV until the last evaluation. At this time, 14 calves were older than 28 months of age, and seven were 16 to 20 months old. Three calves in this group became BLV positive before the age of five months, and one became so at the age of 12 months. Of the 16 calves raised in partial isolation, two were positive at the ages of 11 and 18 months, respectively. The other 14 calves remained negative during the 26 to 29 months of observation. It is not known if the six animals that became BLV positive in these two groups were infected by milk, or prenatally, or during contact with their infected dams. While only six of the 41 calves raised in isolation became infected, all 18 calves raised in contact with BLV-positive cows became infected before the age of 26 to 29 months of age, and 12 were positive at 16 to 20 months of age. Thus, it is apparent that, under natural conditions, milk-borne transmission of BLV, if it occurs at all, is much less frequent than contact transmission, despite the fact that, as shown in previous studies, infectious BLV is present in the colostrum and milk of most BLV-positive cows. Passively acquired maternal antibodies to BLV were probably responsible for the resistance of the calves to milk-borne infection.

Animals↗

Detection of bovine leukemia virus antigen in urine from naturally infected cattle.

A competitive radioimmunoassay was used to detect the major internal protein (p25) of bovine leukemia virus (BLV) in urine from infected cattle. Whole urine samples from six out of seven infected cattle were found to contain the BLV p25 antigen. Analysis of different fractions of urine indicated that p25 was present in a soluble form as well as in the high-speed pellet, but not in the low-speed pellet. Similar results were obtained with urine samples collected from a BLV-infected cow by catheterization of the bladder.

Animals↗

Detection of a precursor-like protein of bovine leukaemia virus structural polypeptides in purified virions.

Gel filtration chromatography of disrupted bovine leukaemia virus (BLV) resulted in the isolation of the 25000 mol. wt. major internal protein (p25), two previously uncharacterized proteins of mol. wt 65000 (p65) and 12000 (p12), and a mixture of p12 and a protein of mol. wt. 15000 (p15). The p65 protein does not bind to concanavalin A and its antigenicity is ether resistant. Therefore, this polypeptide is different from the previously described glycoprotein associated with BLV. Radioimmunoprecipitation and competitive radioimmunoassays indicated that the p65 protein shares antigenic determinants with the p25, p15 and p12 proteins, respectively. Furthermore, tryptic peptide mapping demonstrated that p65 contains p25, p15, p12 and a BLV protein of mol. wt. 10000 (p10). These results are consistent with the view that p65 is the precursor of gag gene-derived core proteins of BLV.

Antigens, Viral↗

An infectivity assay for bovine leukemia virus using the immunoperoxidase technique.

This report describes the development of a 7-day infectivity assay for bovine leukemia virus (BLV) which is based on the induction of the major internal virion antigen (a protein with a molecular weight of 25,000) in susceptible indicator monolayer cell cultures. In this assay, the antigen is detected in the indicator cells by the immunoperoxidase antibody technique using a specific rabbit antiserum to a BLV protein with a molecular weight of 25,000. The immunoperoxidase infectivity assay is specific, quantitative, reproducible, and more sensitive than the previously described syncytia induction assay. The immunoperoxidase infectivity assay can be applied to the detection of BLV-infected cells and provides a reliable method for the direct diagnosis of BLV infection in cattle.

Animals↗

An improved syncytia infectivity assay for the bovine leukemia virus.

Several factors that influence the sensitivity of the syncytia infectivity assay for the bovine leukemia virus (BLV) and BLV-infected lymphocytes have been examined. The use of early-passage indicator bovine embryonic spleen (BESP) cells and their pretreatment with diethylamino-ethyl-dextran (DEAE-D) was essential for optimal sensitivity. Polybrene was less effective than DEAE-D. The combination of DEAE-D and polybrene was more effective than DEAE-D alone when BLV-infected leukocytes were used as the inoculum, but not when the inoculum was a cell-free BLV preparation. Using BESP cell passages 4 to 11 as indicators, reproducible titers were obtained when aliquots of the same virus stock were assayed at different times after freezer storage. When assaying peripheral blood lymphocytes from infected cattle, optimal syncytia responses were observed consistently by inoculating 5 X 10(6) viable lymphocytes per 60-mm Falcon dish. Centrifugation of peripheral blood leukocytes from BLV-infected cattle in discontinuous bovine serum albumin gradients can be used to separate a subpopulation of infected lymphocytes. Use of this subpopulation as the inoculum, rather than unseparated buffy-coat leukocytes, greatly increases the sensitivity of the syncytia infectivity assay.

Animals↗

A critical comparison of the virus neutralizaiton, radioimmunoprecipitation and immunodiffusion tests for the serological diagnosis of BLV infection.

Several serological tests are available for the detection of antibodies to BLV. Thus far, only the virus neutralization antibody (VNA) test, the immunofluorescence test, and the immunodiffusion test with the major internal virion protein have been critically evaluated as diagnostic methods for the identification of BLV-infected cattle. Of these tests, the VNA test is the most sensitive and specific. Therefore, in the present study the VNA test has been applied to evaluate the reliability of the radioimmunoassay for BLV p25 (RIAp25) and of the immunodiffusion test with BLV-associated glycoprotein antigen (IDgp). The results show a very close agreement between the RIAp25, and the VNA test. The IDgp test is less sensitive than the RIAp25, particularly for the detection of BLV antibodies in early stages of infection. The RIAp25 is more rapid than the VNA test and does not require tissue culture techniques. Thus, the RIAp25 seems to be the most practical and sensitive available method for the serolgical diagnosis of BLV infection in cattle.

Animals↗

Natural mode of transmission of the bovine leukemia virus: role of bloodsucking insects.

The development of bovine leukemia virus (BLV) infection was studied in 14 noninfected young adult cattle exposed to 25 to 30 BLV-infected cows in an area of approximately 0.5 ha. Of 7 cattle (group 1) exposed beginning in July and August (midsummer) of 1976, 4 were infected by October, and all 7 by November (4 months' exposure). Of 7 cattle (group 2) exposed from February 1977 (midwinter), all remained negative for 3 months, and only 1 was positive after 6 months. By October 1977, however, 4 cattle in this group were infected, indicating that contact transmission of BLV is prevalent during the summer months. This, and the fact that BLV-infected lymphocytes were recovered from tabanids allowed to feed on a BLV-positive cow, supports the idea that bloodsucking insects play a major role in the spread of BLV.

Animals↗

Detection of a precursor of bovine leukemia virus structural proteins in purified virions.

Gel filtration chromatography of disrupted bovine leukemia virus (BLV) resulted in the isolation of the 25,000 dalton major virion internal protein and two previously uncharacterized virion proteins of molecular weight 65,000 and 12,000 respectively. The 65,000 dalton protein does not bind to concanavalin A and its antigenicity is ether-resistant. Therefore, this polypeptide is different from the previously described glycoprotein associated with BLV. Radiommunoprecipitation and competitive radioimmunoassays indicated that the 65,000 molecular weight polypeptide shares antigenic determinants with the 25,000, 15,000, and 12,000 dalton BLV proteins, respectively. Thus, the 65,000 dalton polypeptide may represent the precursor of these three smaller virion proteins.

Chromatography, Gel↗

An infectivity assay for the bovine leukemia virus based on the induction of the major internal virion antigen in susceptible cell cultures.

This report described the development of a 7-day infectivity assay for the bovine leukemia virus (BLV) which is based on the induction of the major internal virion antigen (p25) in susceptible indicator monolayer cell cultures. In this assay the antigen is detected in the indicator cells by the immunoperoxidase antibody technique using a monospecific anti-BLV serum. The immunoperoxidase infectivity assay (IPIA) is specific, quantitative, reproducible and more sensitive than the previously developed syncytia induction assay. The IPIA can be applied for the detection of BLV-infected cells and provides a reliable method for the direct diagnosis of BLV infection in cattle.

Antigens, Viral↗

An evaluation of the role of milk in the natural transmission of BLV.

In order to evaluate the role of milk in the transmission of BLV, the presence of the virus and viral antibodies was investigated in cattle that were born to, and nursed on, infected dams and then raised in isolation or in contact with infected animals. Only 3 of the 17 isolated cattle became infected during 25-29 months of observation. During the same period of time, all 17 cattle raised in contact with BLV-positive animals developed BLV infection. From these results, it is apparent that milk-borne transmission of BLV, if it occurs, is much less frequent than contact transmission.

Animals↗

Persistent lymphocytosis in cattle: its cause, nature and relation to lymphosarcoma.

Studies in well-characterized cattle populations strongly support the view that the bovine leukemia virus (BLV) is the causative agent of the adult (enzootic) form of bovine lymphosarcoma and persistent lymphocytosis (PL), and that host genetic factors play an important role in the development of these two conditions. On the other hand, the available information indicates that the genetic factors controlling the development of PL are frequently independent of those controlling the development of lymphosarcoma. There is no evidence that clinically normal cattle with PL harbor malignant cells or have any other clinical abnormality. In these animals lymphocytosis results from the expansion of two distinct subpopulations of non-neoplastic B lymphocytes, one of which is free of BLV. Long-term studies have shown that the large majority of cattle with PL do not develop lymphosarcoma even when kept to advanced age. These data indicate that PL is not a disease nor a preclinical stage of lymphosarcoma. Rather PL should be considered as a benign response to BLV infection which, although frequently associated with lymphosarcoma, is independant of it.

Animals↗