Assessment of digestive enzymes activity during the fry development of rainbow trout, Oncorhynchus mykiss: from hatching to primary stages after yolk sac absorption

The aim of this study was to determine the activity of digestive enzymes during the fry development of Rainbow trout ( Oncorhynchus mykiss ), which has a remarkable role in food digestion and absorption in the first feeding. The assessment of digestive enzymes activity of gastric (pepsin), pancreatic (trypsin, chymotrypsin, α-amylase and lipase) and intestinal (alkaline phosphatase) revealed that enzymes were available on the first day after hatching (DAH) but their activity showed no significant difference from hatching to day 12 (P > 0.05). An increased activity was seen between 12 and 18 DAH and this activity was significantly higher than the first 12 days (P 0.05). These results could be used as a basis for formulating a suitable feeding and also selecting the best time for starting the feeding so that optimum nutritional values and cost-effectiveness are achieved

Comparative evaluation of antibody positive titer by ELISA and IFA in Theileria annulata vaccinated cattle in Iran

An enzyme linked immunosorbent assay (ELISA) was used to evaluate antibody positive titer in vaccinated and non-vaccinated cattle using schizont infected myeloid cells as an antigen. The result was compared with indirect fluorescent antibody level in the same animals. For this study 116 milking cows, 95 vaccinated and 21 non-vaccinated, were bleeded in order to prepare sera. They were tested with both ELISA and IFA tests. 94 sera had positive antibody titer and 22 sera were negative through ELISA test but, with IFA test, only 89 sera showed positive antibody titer and 27 were negative. Thereby, it was concluded that the sensitivity and specificity of ELISA test in comparison with IFA test was 95.5 % and 66.6 % respectively. This study generally indicated that ELISA could be an effective test for seroepidemiological investigations of bovine tropical theileriosis, and it is considered to be valid as an additional test to distinguish the vaccinated from the non vaccinated cattle in order to schedule vaccination programs

Comparative evaluation of antibody positive titer by ELISA and IFA in

An enzyme linked immunosorbent assay (ELISA) was used to evaluate antibody positive titer in vaccinated and non-vaccinated cattle using schizont infected myeloid cells as an antigen. The result was compared with indirect fluorescent antibody level in the same animals. For this study 116 milking cows, 95 vaccinated and 21 non-vaccinated, were bleeded in order to prepare sera. They were tested with both ELISA and IFA tests. 94 sera had positive antibody titer and 22 sera were negative through ELISA test but, with IFA test, only 89 sera showed positive antibody titer and 27 were negative. Thereby, it was concluded that the sensitivity and specificity of ELISA test in comparison with IFA test was 95.5 % and 66.6 % respectively. This study generally indicated that ELISA could be an effective test for seroepidemiological investigations of bovine tropical theileriosis, and it is considered to be valid as an additional test to distinguish the vaccinated from the non vaccinated cattle in order to schedule vaccination programs

Development of a Nano-ELISA system for the rapid and sensitive detection of H9N2 avian influenza

Influenza is one of the most important viral diseases that is common among the birds and the mammals and is caused by specific viruses that belong to the Orthomyxoviridae family. Migratory aquatic birds are the reservoir of the disease and there is a likelihood of the disease in any region. There are different methods for detecting the avian influenza, but by the point of detection rates, the ELISA may be one of the most important current methods. In this work we synthesized Gold nanoparticles and conjugated it with rabbit-anti-chicken IgG-HRP. An ELISA test was done to compare the bioactivity of Au-anti-chicken HRP with anti-chicken HRP in order to detect the antibody against the H9N2 subtype of avian influenza virus. Using 133 field chicken sera, the sensitivity of nano-ELISA as compared to traditional ELISA was calculated to be 100%, whereas the specificity was 92%. This method was significantly more sensitive than the traditional ELISA and didn’t require extra costs. It can therefore be concluded that the AuNP-HRP conjugate can be applicable in immune analysis procedure where a more confident result is required