scholarly journals Formulation of Colostrum Supplements, Colostrum Replacers and Acquisition of Passive Immunity in Neonatal Calves

2001 ◽  
Vol 84 (9) ◽  
pp. 2059-2065 ◽  
Author(s):  
J.D. Quigley ◽  
R.E. Strohbehn ◽  
C.J. Kost ◽  
M.M. O’Brien
Proceedings ◽  
2019 ◽  
Vol 36 (1) ◽  
pp. 7
Author(s):  
Silva ◽  
Muller ◽  
Cavalieri ◽  
Fordyce

Late pregnant cows often experience nutritional stress in northern Australia, which reducescolostrum secretion, health, and likelihood of survival of neonatal calves [...]


2005 ◽  
Vol 2005 ◽  
pp. 210-210
Author(s):  
A. A. Sadeghi ◽  
A. Nikkhah ◽  
P. Shawrang

Neonatal calves are born with no immunoglobulins (Igs) in the blood stream and rely on Ig from colostrum through passive immunity transfer. Unfortunately, transfer of passive immunity to neonatal calves is too often inadequate, resulting in excessive rates of morbidity and mortality. Natural zeolite is characterized by framework of linked tetra hydration enclosing open cavities in the form of channels, and cages with ion exchanger and adsorption capacity. In literature, there were reported that thermally activated natural zeolite (T-zeolite) could increase colostral IgG absorption and decrease susceptibility of neonates to infections (Sadeghi et al., 2004; Stojic et al., 1995). To our knowledge, little information is available concerning the effect of thermally activated natural zeolite on colostral IgG1, IgM and IgA absorption in neonates. Our experiment was designed to investigate the effect of thermally activated natural zeolite on colostral IgG1, IgM and IgA absorption in newborn Holstein calves.


1994 ◽  
Vol 3 (5) ◽  
pp. 421-428
Author(s):  
Juha Nousiainen ◽  
Hannu Korhonen ◽  
Eeva-Liisa Syväoja ◽  
Sami Savolainen ◽  
Hannu Saloniemi ◽  
...  

Neonatal dairy calves were randomly allotted to three colostrum feeding regimens with increasing intakes of immunoglobulins (Ig) on the first day of life. The control group was fed one litre of pooled colostrum (Ig intake 19.5 g). In two experimental groups, the pooled colostrum was supplemented with 0.5 or 1.5 litres of commercial Ig-concentrate, giving a total Ig intake of 52.7 and 119.0 g, respectively. Serum IgG, IgM and IgA levels increased linearly (p < 0.001) on day 2 post partum with the increasing Ig intake. The calculated mean Ig-absorption rate was 61% and decreased linearly for IgM (p = 0.051) and IgG (p = 0.078) with increasing Ig intake. At the highest Ig intake, serum IgG remained above 10 g/l during 30 days post partum. In the experimental groups, serum IgM and IgA decreased sharply during the first week of life and were relatively constant thereafter. In the control group, however, there was an increase in serum IgM after one week post partum, perhaps due to the in situ production of Ig. With the increasing Ig intake there was a small and non-significant tendency for better live weight gain (p = 0.286) and a lower incidence of diarrhoea (p = 0.421) during the first four weeks of life. It is concluded that the Ig-product tested is well absorbed during 24 hours post partum and it can be used either as a supplement to maternal colostrum when its quality is poor, or as a substitute when colostrum is not available.


Reproduction ◽  
2000 ◽  
pp. 315-326 ◽  
Author(s):  
MH Stoffel ◽  
AE Friess ◽  
SH Hartmann

In dogs, passive immunity is conferred to fetuses and neonates by the transfer of maternal immunoglobulin G through the placenta during the last trimester of pregnancy and via the mammary gland after parturition, respectively. However, morphological evidence of transplacental transport is still lacking. The aim of the present study was to localize maternal immunoglobulin G in the labyrinthine zone and in the haemophagous zone of the canine placenta by means of immunohistochemistry and immunocytochemistry. In the labyrinthine zone, immunoglobulin G was detected in all the layers of the materno-fetal barrier including the fetal capillaries. Immunoreactivity was particularly prominent in maternal basement membrane material as well as in the syncytiotrophoblast. However, this evidence of transplacental transport of immunoglobulin G originated from a limited number of unevenly distributed maternal vessels only. In the cytotrophoblast of the haemophagous zone, immunoglobulin G was localized to phagolysosomes at various stages but was never detected within fetal vessels. The results indicate that maternal immunoglobulin G is degraded in cytotrophoblast cells of the hemophagous zone and, therefore, that transplacental transport is restricted to a subpopulation of maternal vessels in the labyrinthine zone.


Author(s):  
A.E. Chernitskiy ◽  
◽  
M.I. Retsky ◽  
A.I. Zolotarev ◽  
L.I. Efanova ◽  
...  

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