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Arkansas - Agricultural Communication Services - University of ...

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The Effect <strong>of</strong> Tasco TM Inclusion in the Prepartum Diet and<br />

Time <strong>of</strong> Sampling on the Proportions <strong>of</strong> Bovine Leukocyte Populations in<br />

Blood and Mammary Gland Secretions<br />

T. J. Wistuba, 1 E. B. Kegley, 1 T. K. Bersi, 2 D. W. Kellogg, 1 and G. F. Erf 2<br />

Story in Brief<br />

The effects <strong>of</strong> Tasco TM inclusion in the diet during the last 21 d <strong>of</strong> gestation on the proportion <strong>of</strong> bovine leukocyte<br />

populations in blood and mammary gland secretions (MGS) was investigated using flow cytometric analysis. Thirty<br />

Holstein cows were stratified by parity and randomly assigned to the Tasco TM (170 g/d) supplemented group or control<br />

diet. Tasco TM is a product derived from Ascophyllum nodosum, a brown seaweed that grows along the coast <strong>of</strong> Nova<br />

Scotia. Treatments were initiated 21 d prior to expected parturition and fed until calving. Blood samples and MGS from<br />

cows and blood samples from calves were obtained at parturition and at d 1 post partum. Proportions <strong>of</strong> bovine leukocyte<br />

populations in cows were affected by dietary treatment, but not time <strong>of</strong> sampling. In cows, supplementation <strong>of</strong><br />

Tasco TM increased the proportion <strong>of</strong> B lymphocytes (P = 0.05) in the blood. However, Tasco TM supplementation<br />

decreased the proportion <strong>of</strong> T-helper lymphocytes (P = 0.04) and tended to decrease the proportion <strong>of</strong> gd T lymphocytes<br />

(P = 0.13). The percentage <strong>of</strong> B lymphocytes tended to increase (P = 0.13) from parturition to d 1 in the MGS.<br />

Proportions <strong>of</strong> granulocytes, macrophages/monocytes and B lymphocytes in the blood <strong>of</strong> calves increased from parturition<br />

to d 1 (P < 0.04). Dietary supplementation with Tasco TM and time <strong>of</strong> sampling altered proportions <strong>of</strong> bovine leukocyte<br />

populations. The impact <strong>of</strong> Tasco TM supplementation on cow and calf health requires further investigation.<br />

Introduction<br />

Trace mineral or vitamin supplementation has been<br />

shown to improve immune response and growth performance<br />

when animals are consuming deficient or marginal levels <strong>of</strong><br />

trace minerals or vitamins. Tasco (Acadian Seaplants Ltd.;<br />

Dartmouth, Canada) is a product derived from Ascophyllum<br />

rodosum, a brown seaweed, that grows along the coast <strong>of</strong><br />

Nova Scotia. The commercial product that has been developed<br />

contains high levels <strong>of</strong> trace minerals and vitamins.<br />

Initial work using Tasco TM at Virginia Tech, Mississippi State<br />

<strong>University</strong>, and Texas Tech has shown improvements in<br />

immune cell function and hair coat scores <strong>of</strong> calves grazing<br />

fescue but no significant improvements in growth performance<br />

(Allen et al., 2001; Fike et al., 2001; and Saker et<br />

al., 2001).<br />

It has been well documented (Quigley and Drewry,<br />

1998 and Wittum and Perino, 1995) that the passive transfer<br />

<strong>of</strong> immunoglobulins in colostrum is the most important<br />

source <strong>of</strong> immunologic protection available to neonatal<br />

calves. Inadequate intake and absorption <strong>of</strong> maternal antibody<br />

has been associated with increased risk <strong>of</strong> disease and<br />

death in neonatal calves (Wittum and Perino, 1995) The concentration<br />

<strong>of</strong> immunoglobulin G (IgG) in colostrum is important<br />

in determining the degree <strong>of</strong> passive immune transfer,<br />

being linearly related to the maternal IgG concentration in<br />

calves. The objective <strong>of</strong> this study was to determine the<br />

effects <strong>of</strong> Tasco inclusion in the prepartum diet on the proportion<br />

<strong>of</strong> bovine leukocyte populations and IgG concentrations<br />

in blood and mammary gland secretions.<br />

Materials and Methods<br />

Thirty Holstein cows were stratified by parity and randomly<br />

assigned to the Tasco TM (170 g/d) supplemented group<br />

or control diet. Treatments were initiated 21 d prior to expected<br />

parturition and fed until calving. Tasco TM supplemented<br />

cows were on the diet a minimum <strong>of</strong> 8 and a maximum <strong>of</strong> 42<br />

d with a mean <strong>of</strong> 22 d. All cows were <strong>of</strong>fered 21 lb <strong>of</strong><br />

sorghum silage, ad lib hay, and 5 lb <strong>of</strong> a commercially prepared<br />

dry cow grain supplement.<br />

Blood samples from cows and calves, as well as mammary<br />

gland secretion (MGS) samples were obtained at parturition<br />

and at d 1 post partum. After calving, the cow and calf<br />

were separated before the calf nursed. Approximately two<br />

liters <strong>of</strong> bulk colostrum were collected and fed to the calf<br />

immediately after the calf was sampled. One-half liter <strong>of</strong> bulk<br />

colostrum was obtained at parturition and one day later, and<br />

centrifuged at 1000 X g at room temperature for 10 min. The<br />

supernate was removed and the pelleted cells were washed<br />

twice in phosphate-buffered saline (PBS).<br />

At parturition and one day later, peripheral blood was<br />

collected from cows and calves into vacutainer tubes containing<br />

acid citrate dextrose as an anticoagulant.<br />

Mononuclear cells were isolated by lysis <strong>of</strong> red blood cells<br />

with Tris-buffered ammonium chloride and washed twice<br />

in PBS.<br />

Samples <strong>of</strong> washed milk cells and peripheral blood<br />

mononuclear cells (1 X 10 6 /sample) were immun<strong>of</strong>luorescently<br />

labeled with a panel <strong>of</strong> mouse monoclonal antibodies<br />

specific for bovine leukocyte cell surface molecules using an<br />

1 Department <strong>of</strong> Animal Science, Fayetteville<br />

2 Department <strong>of</strong> Poultry Science, Fayetteville<br />

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