A survey was conducted in Southwestern, Punjab, Pakistan during two different seasons to assess the status of selenium of three different classes of grazing sheep. Blood plasma from lactating, non-lactating and male s...A survey was conducted in Southwestern, Punjab, Pakistan during two different seasons to assess the status of selenium of three different classes of grazing sheep. Blood plasma from lactating, non-lactating and male sheep were collected four times monthly in winter and summer seasons and analyzed for selenium concentration. Seasonal variations were found for plasma selenium concentration. Selenium concentration of plasma was higher in male sheep than those lactating and non lactating ewes during both the seasons as well as it were higher compared to the established critical value for blood plasma selenium for these ruminants. High incidence of deficiencies was found particularly for lactating ewes. These deficiencies in plasma selenium based on critical level were 35% to 15 % for lactating, 28% to 12% for non lactating ewes and 15% to 5% for male animals during winter and summer seasons, respectively. Although some differences among the three classes of sheep were found for selenium concentrations of blood plasma, but dramatic class differences could not be concluded based on this study. It was suggested based on the results obtained, pellets, glass bolus or mixture that contain selenium, should be used for supplementation for grazing sheep in the study area to maintain the plasma Se at optimum required level for the prevention of complication in livestock caused due to deficiency of this element.展开更多
An inexpensive and rapid test for determining titers of Human Immunodeficiency Virus (HIV) in plasmas was developed. Washed sheep red blood cells were applied onto HIV positive plasmas, in V-bottomed microtiter plates...An inexpensive and rapid test for determining titers of Human Immunodeficiency Virus (HIV) in plasmas was developed. Washed sheep red blood cells were applied onto HIV positive plasmas, in V-bottomed microtiter plates, to complement the HIV antigens and antibodies present in plasmas. The setup was incubated for 30 minutes at 37℃. Reciprocal of the highest dilution of each plasma which gave passive agglutination of the RBCs was read as its HIV titer. Mean HIV load of five samples, was ≥ 4096.00 ± 0.00 after one day of storage at 4℃ but it reduced to 256.00 ± 70.10, 28.80 ± 3.20, 7.20 ± 0.80 and 1.60 ± 0.98 on days 2, 3, 4 and 7, respectively. HIV antibodies were still detectable, by ELISA, in plasma dilutions that were tested negative with the new test. It was concluded that when HIV antibodies have been confirmed, or added to plasmas, passive hemagglutination test can be applied to assess their viral loads.展开更多
文摘A survey was conducted in Southwestern, Punjab, Pakistan during two different seasons to assess the status of selenium of three different classes of grazing sheep. Blood plasma from lactating, non-lactating and male sheep were collected four times monthly in winter and summer seasons and analyzed for selenium concentration. Seasonal variations were found for plasma selenium concentration. Selenium concentration of plasma was higher in male sheep than those lactating and non lactating ewes during both the seasons as well as it were higher compared to the established critical value for blood plasma selenium for these ruminants. High incidence of deficiencies was found particularly for lactating ewes. These deficiencies in plasma selenium based on critical level were 35% to 15 % for lactating, 28% to 12% for non lactating ewes and 15% to 5% for male animals during winter and summer seasons, respectively. Although some differences among the three classes of sheep were found for selenium concentrations of blood plasma, but dramatic class differences could not be concluded based on this study. It was suggested based on the results obtained, pellets, glass bolus or mixture that contain selenium, should be used for supplementation for grazing sheep in the study area to maintain the plasma Se at optimum required level for the prevention of complication in livestock caused due to deficiency of this element.
文摘An inexpensive and rapid test for determining titers of Human Immunodeficiency Virus (HIV) in plasmas was developed. Washed sheep red blood cells were applied onto HIV positive plasmas, in V-bottomed microtiter plates, to complement the HIV antigens and antibodies present in plasmas. The setup was incubated for 30 minutes at 37℃. Reciprocal of the highest dilution of each plasma which gave passive agglutination of the RBCs was read as its HIV titer. Mean HIV load of five samples, was ≥ 4096.00 ± 0.00 after one day of storage at 4℃ but it reduced to 256.00 ± 70.10, 28.80 ± 3.20, 7.20 ± 0.80 and 1.60 ± 0.98 on days 2, 3, 4 and 7, respectively. HIV antibodies were still detectable, by ELISA, in plasma dilutions that were tested negative with the new test. It was concluded that when HIV antibodies have been confirmed, or added to plasmas, passive hemagglutination test can be applied to assess their viral loads.
