Antibody production in goat milk serum after virus instillation of goat mammary gland. V. Biochemical isolation and further characterization of antibodies to various influenza and mumps viruses

1970 ◽  
Vol 16 (12) ◽  
pp. 1153-1159 ◽  
Author(s):  
Arthur E. Pasieka ◽  
L. F. Guerin ◽  
Chas. A. Mitchell

This report describes the development of a method for the isolation of antibodies produced in the mammary gland and found in the milk after the instillation and propagation of various myxoviruses. Biochemical fractionation and isolation procedures have been modified and improved over our previous initial reports. The antibodies of the various influenza and mumps viruses that propagated in the gland were found to be associated with lactogammaglobulin. This report also demonstrates that the antibodies produced in the gland and thus given off in the milk are probably the same as those found in the blood if the animal were infected by conventional routes. Purification of the lactoglobulin protein fraction containing the antibody eliminated the non-specific inhibitors. These results were obtained from the various myxoviruses and mumps that propagated in the goat mammary gland.The main advantages of using the mammary gland as compared to using laboratory animals and their blood are as follows.1. Larger volumes of antibodies can be produced at one time (lactation period) against the influenza and mumps viruses for diagnostic and possibly for therapeutic uses.2. The animal (goat) does not appear to be affected whatsoever by the virus instillation and propagation techniques.3. The milk technique is therefore more humane towards laboratory animals. Invariably the laboratory animal does not have to be sacrificed.

1976 ◽  
Vol 22 (8) ◽  
pp. 1113-1119 ◽  
Author(s):  
A. E. Pasieka ◽  
F. E. Ashton ◽  
R. Wallace ◽  
F. Ota ◽  
A. Ryan ◽  
...  

Instillation of the goat's mammary gland with Neisseria gonorrhoeae colony type Tl has elicited an antibody response in the goat milk serum (GMS). Purification, and characterization of the GMS by gel filtration, electrophoresis, immunodiffusion, analytical ultracentrifugation. And serological analyses demonstrated that the active immune component was mainly in the IgA and IgG fractions (F2 and F3) of GMS.


1975 ◽  
Vol 21 (5) ◽  
pp. 655-661 ◽  
Author(s):  
Arthur E. Pasieka ◽  
L. F. Guerin ◽  
Chas. A. Mitchell

This report describes the development of a method for the production and isolation of neutralizing antibodies against rabies virus (ERA strain) and other agents in the goat mammary gland during active lactation. The rabies virus did not propagate in the gland, but neutralizing antibodies were produced by serial instillations of the antigen. This process was termed 'sham infection.' Antibodies first appeared in the milk about the 20th day and the titer increased until the 28th day. The antibodies were found to be associated with the lactogammaglobulin. The milk globulins were fractionated by gel chromatography and the fraction containing the antibody was isolated. This fraction was further purified and characterized by immunodiffusion, immunoelectrophoresis, and an analytical ultracentrifugation technique. The neutralizing antibody activity after the 29th day was associated with the milk serum IgG fraction. This active fraction was found to have a sedimentation coefficient of 6.8 Svedberg units.


Animals ◽  
2022 ◽  
Vol 12 (2) ◽  
pp. 207
Author(s):  
Xiaoyun Wu ◽  
Wondossen Ayalew ◽  
Min Chu ◽  
Jie Pei ◽  
Chunnian Liang ◽  
...  

The mammary gland is a complicated organ comprising several types of cells, and it undergoes extensive morphogenetic and metabolic changes during the female reproductive cycle. RNA editing is a posttranscriptional modification event occurring at the RNA nucleotide level, and it drives transcriptomic and proteomic diversities, with potential functional consequences. RNA editing in the mammary gland of yaks, however, remains poorly understood. Here, we used REDItools to identify RNA editing sites in mammary gland tissues in yaks during the lactation period (LP, n = 2) and dry period (DP, n = 3). Totally, 82,872 unique RNA editing sites were identified, most of which were detected in the noncoding regions with a low editing degree. In the coding regions (CDS), we detected 5235 editing sites, among which 1884 caused nonsynonymous amino acid changes. Of these RNA editing sites, 486 were found to generate novel possible miRNA target sites or interfere with the initial miRNA binding sites, indicating that RNA editing was related to gene regulation mediated by miRNA. A total of 14,159 RNA editing sites (involving 3238 common genes) showed a significant differential editing level in the LP when compared with that in the DP through Tukey’s Honest Significant Difference method (p < 0.05). According to the Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis, genes that showed different RNA editing levels mainly participated in pathways highly related to mammary gland development, including MAPK, PI3K-Akt, FoxO, and GnRH signaling pathways. Collectively, this work demonstrated for the first time the dynamic RNA editome profiles in the mammary gland of yaks and shed more light on the mechanism that regulates lactation together with mammary gland development.


1992 ◽  
Vol 267 (17) ◽  
pp. 12016-12021
Author(s):  
V.N. Subramaniam ◽  
A.R. bin Mohd Yusoff ◽  
S.H. Wong ◽  
G.B. Lim ◽  
M Chew ◽  
...  

2011 ◽  
Vol 10 (4) ◽  
pp. 1746-1754 ◽  
Author(s):  
Yalin Liao ◽  
Rudy Alvarado ◽  
Brett Phinney ◽  
Bo Lönnerdal

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