Evaluation of Some Probiotics on Growth Performance and Immunity Status of Nile Tilapia.
Sherif, A. H., 1 Saker, O. A.2 and El-Sharawy, M. E.3
1- Department of fish disease, Animal health research institute. Kafr El- Sheikh provincial lab, agriculture research center.
2- Department of biochemistry, Animal health research institute. Kafr El- Sheikh
3- Department of animal production, Faculty of agriculture, Kafrelsheikh University.
Abstract
Growing concern for the high consumption of antibiotics in aquaculture has initiated a search for alternative methods of disease control by improving resistance against infectious disease which can be achieved by using of probiotics. The objective of the present study was to evaluate the influence
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Adverse environmental situations may acutely or chronically affect the health of fish, altering some of their biochemical parameters and suppressing their innate and adaptive immune responses (Giron-perez et al., 2007). Antibiotics have been used for long time as growth promoting agents but adversely affected growth and food conversion as well as multiple of drug resistant bacteria and antibiotic residues in fish meat (Wary and Davies, 2000). Therefore, using of natural feed additives to substitute antibiotic had become great interest (Kumar et al., 2003). Probiotics are defined as microbial dietary addetives that beneficially affect the host physiology by modulation immunity system, as well as improving nutritional and microbial balance in the intestinal tract (Villamil et al., 2002). Using of some kind of probiotics in aquaculture water regulated the microflora of aquaculture water, controlled pathogenic microorganisms, enhanced decomposition of the undesirable organic substances in aquaculture water, and improved ecological environment of aquaculture. In addition, the use of probiotics can increase the population of food organisms, improve the nutrition level of aquaculture animals and improve immunity of cultured animals to pathogenic microorganisms (Patterson and Burkholder …show more content…
Differential leukocytic count was calculated according to Schalm (1986). Mean Corpuscular Volume hemoglobin concentration were calculated according to the formula mentioned by Dacie and lewis (1975). Red blood cell (RBCs) and White blood cell (WBCs) counts were counted by haemocytometer according to Stoskopf (1993). In addition to MCV Mean Corpuscular Volume, MCH Mean Corpuscular Volume hemoglobin and MCHC Mean Corpuscular Volume hemoglobin concentration were calculated according to the formula mentioned by Dacie and lewis (1975).
MCV = PCV x 10 / RBCs as m/mm3.
MCH =HB contentgm/100ml x 10/ RBCs as m/mm3.
MCHC =HB contentgm/100ml x100 / PCV.
The concentration of total protein weichsellbaum (1946) and albumin (Doumas et al., 1971) were measured by colorimetric methods, While, globulin concentrations were determined by subtracting the concentration of total protein from albumin concentration. The activity of the liver enzymes, Aspartate amino transaminase (AST) and Alanine amino transaminase (ALT) was determined according to (Reitman and Frankel, 1957).
Challenge test: After 90 days of feeding, a total number of 0 fish (10 fish from each treatment) were injected I/P with the pathogenic A. hydrophila (0.3 ml of 108cells/ml), the injected fishes were kept under observation for 14 day to record the mortality rate.
Mortality rate % = No. of death in specific period x
Prelab week 1 Calculations Preparation of 1.5μmol/L mixed low-level standard dilution 150μmol/L × V1=1.5μmol/L × 10ml V1=(1.5μmol/L×10ml)/(150μmol/L)=0.1ml Conversion of milliliters to microliters (0.1ml×1000)μL= 100μL Preparation of 3μmol/L mixed low-level standard dilution 150μmol/L × V1=3μmol/L × 10ml V1=(3μmol/L×10ml)/(150μmol/L)=0.2ml Conversion of milliliters to microliters (0.2ml×1000)μL= 200μL Preparation of 3μmol/L mixed low-level standard dilution 150μmol/L × V1=7.5μmol/L × 10ml V1=(7.5μmol/L×10ml)/(150μmol/L)=0.5ml Conversion of milliliters to microliters (0.5ml×1000)μL= 500μL Preparation of the blank samples The volumetric flask will be filled to the mark with 150μmole/L of stock solution to act as blank (reference). Additional two blanks will
During the interval two patients were censored (2+ and 3+) so that at the end of the interval four patients were still at risk. Since the interval ends with the death of one of those, the chance of surviving the interval is estimated as 3/4. Also notice that at the start of the next interval (4 through 10 years), only three patients were at risk due to the death at the end of the interval. The actual curve plotted from this computation is shown in Fig. 2.3.
The goal of this experiment is to see the anti-cow antibody bind to cow serum only, and we expect to see the anti-cow antibody bind to the spot that had the cow serum. The system we used is the serum from Cow, Horse, Goat, Sheep, and Donkey, Chicken. In order to able to detect and analyze proteins based on their ability to bind to a specific antibody, the SDS-PAGE and Western Blot was performed. SDS Polyacrylamide Gel Electrophoresis (SDS-PAGE) is a very common technique used to separate proteins by molecular weight under the influence of an applied electrical field and then used to prepare for the Western Blot (#1 Lehninger). It uses a polyacrylamide gel as a support medium and sodium dodecyl sulfate (SDS), which is a detergent, to denature
The results of the gel electrophoresis are summarized in Figure 2. On the gel, both populations of fish were run and analyzed for their heterozygosity. Following the conclusion of the electrophoresis, the gel was analyzed to determine how many different alleles were present at the SFMSTR5 loci. The results of the analysis are shown in Figure 2. The gel showed that in population 1, there are three different alleles at the SFMSTR5 loci and that a majority of the fish in this population are heterozygous at this locus.
Wt. Mass Density Appearance 2-methycyclohexanol 0.75 mL 114.19 g/mol 0.93 g/mL Clear colorless liquid 85% Phosphoric acid 1.00 mL Clear
There are only eighteen deaths recorded over a period of five years. There is tenable proof of hundreds more. Over these five years, known as
Starch solution is then placed into the test tube at a quantity of 5 mL. 5 drops of Lugol’s Iodine solution is added to the test tube. If the color changes, then it is known that starches are present in the solution. Proteins are next tested. In order to do this, 5 mL of gelatin solution is added to the test tube. 10 drops of Biuret’s reagent are added to test for protein.
The investigation was carried out to identify the presence or absence of biological molecules in serum 2216. If the concentration in each test tube of the dilutions carried out will be more concentrated then the concentration of the test tube before it, then the color will be at an equal concentration with the other dilutions performed. The hypothesis was wrong because of the difference in concentrations due to the different measurements within the dilutions done. The test for starch was to add a drop of iodine solution to the pipette in the spotting tile. A reducing sugar solutions is add inside a test tube with 3 drops to then add 3 drops of benedicts and plane in a water bath.
Patients RDW, WBC, and platelets are high, (Patients chart, 2017). Labs Hgb Hct, MCV, and RBCs all relates to the red blood cells in the body. These tests are taken when patients come in complaining of dizziness, fatigue, and lack of food or fluid intakes for the past few days. These tests also amount for the total RBC cells within the body.
This paper will help others to understand what the hematology lab does and what part is play within the clinical laboratory. After reading this paper, people will be able to identify who works in a hematology lab, and what they do and why they do it. The reader will be able to understand why the hematologists who work within the lab run the tests that they perform and why and also why it is beneficial to patients for this lab to exist. Introduction
1.1 Abstract The purpose of quantitative analysis of protein using a spectrophotometer is to measure the concentration of proteins in a given sample. The experiment is conducted by laboratory method (Biuret Test) and using spectrophotometer to analyze the absorbance of reactants at 540 nm, hence determining the concentration of the proteins in a given sample. The purpose of stopped enzyme assay to study B-galactosidase is to determine the effect of temperature and concentrations of substrate on enzyme activity.
The topic of probiotic effectiveness on AAD has been recognized as need to be researched. Recent studies have concluded that probiotics can have significant relative risk reductions of 44-47% for AAD (Ouwehand et al., 2013). AAD justified as a selected topic as the rise in antibiotic use is causing a rise in AAD and its adverse effects (Pattini et al., 2013). The topic of probiotic use with antibiotic administration is a daily discussion at interdisciplinary team meetings.
5A (ii)]. Both survival rate (%) and mortality rate (%) studies
TABLE OF VARIABLES Independent Variable Method of measurement Concentration of HCl
The number of people dying during a specific period after diagnosis X 100 The number of people with the disease Source: Gordis, L. (2014). Epidemiology (5th ed.). Philadelphia, PA: Elsevier. Chapter 4,