The Application of the Immunoperoxidase (IP) Antibody Technique for the Etiological Diagnosis of Infectious Bursal Disease (IBD) in Chickens

2021 ◽  
Vol 8 (1) ◽  
pp. 36-49
Author(s):  
E. N. Okeke ◽  
G. Lang
Keyword(s):  
Bursa Of Fabricius ◽  
Antibody Technique ◽  
Background Staining ◽  
Bursal Disease ◽  
If Technique ◽  
Technical Details ◽  
Diagnostic Sensitivity And Specificity ◽  
A Site ◽  
Antigen Antibody ◽  
Virus Isolates

The Indirect IP – technique was employed in demonstrating a site where IBD antigen reacted with Its untbody in IBD-affected barya of Fabricius. In the, rabbit - wot-chicken IgG, which was conjugated to borwer dish peroxidase, was used as the Immunochemical tracers of the antigen-antibody la teraction between IBD chicken underum wad wc tions of bursa of Fabricius (BF) from IBD infected chicken. The technical details were examined and compared with the immunofluorescent (IF) and body technique. The IP – technique was simpler to perform, gave permanently stained specimens, and was answer to interpret because it was less subject to background staining than the IF - technique However both the IP and the IF — techniques were of equal diagnostic sensitivity and specificity. Some attempts made to use the IP - technique for detecting IBD teld virus isolates in cell-culture solatoh yarns were unsuccessful. The IP - technique was, however, capable of demonstrating vll-culture adapted IBD viruses lo cell monotavers. 

scholarly journals Studi Lapang: Penegakan Diagnosis Infectious Bursal Disease (IBD) Pada Ayam Broiler

2019 ◽  
Vol 3 (1) ◽  
pp. 25-30
Author(s):  
Aan Awaludin ◽  
Yudhi Ratna Nugraheni ◽  
Theo Mahiseta Syahniar ◽  
Dyah Laksito Rukmi ◽  
Agus Hadi Prayitno ◽  
...  
Keyword(s):  
Broiler Chickens ◽  
Care Management ◽  
Clinical Symptoms ◽  
Viral Disease ◽  
Bursa Of Fabricius ◽  
Infectious Bursal Disease ◽  
Bursal Disease ◽  
Commercial Farms ◽  
The One ◽  
Organ Changes

Infectious Bursal Disease (IBD), also called Gumboro, was disease which attacked cells in the bursa of fabricius, causing interference with the chicken's immune system or immunosuppressive. IBD was the one of viral disease that often attacks chickens in the field. The aim of this study was to determine the diagnosis of IBD by through at clinical symptoms and necropsy that can still be relevant on in the field. The diagnosis of IBD correctly, cheaply, easily and quickly in the field is very important to optimize the health care management and evaluation program. The method used was by observing clinical symptoms of broiler chickens in commercial farms suspected of contracting IBD and observing post-death organs (necropsy). The object of necropsy was 5 samples of broiler chickens from the farm. Data was analyzed descriptively. The results of this study was the broiler chickens that infected with IBD could be diagnosed through clinical symptoms and post-death organ changes, so that the diagnosis for IBD cases in the field used the observation of clinical symptoms and necropsy are still relevant.

scholarly journals Genome-wide analysis of differentially expressed mRNAs, lncRNAs, and circRNAs in chicken bursae of Fabricius during infection with very virulent infectious bursal disease virus

BMC Genomics ◽  
2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Xuewei Huang ◽  
Junyan Zhang ◽  
Zengsu Liu ◽  
Meng Wang ◽  
Xiaolong Fan ◽  
...  
Keyword(s):  
Signaling Pathway ◽  
Disease Virus ◽  
Infectious Bursal Disease Virus ◽  
Expression Profiles ◽  
Circular Rna ◽  
Differentially Expressed ◽  
Bursa Of Fabricius ◽  
Infectious Bursal Disease ◽  
Non Coding Rna ◽  
Bursal Disease

Abstract Background Infectious bursal disease virus (IBDV) causes acute, highly contagious, immunosuppressive, and lethal infectious disease in young chickens and mainly infects the bursa of Fabricius (BF). To investigate interactions between IBDV and its host, RNA sequencing was applied to analyze the responses of the differentially expressed transcriptional profiles of BF infected by very virulent IBDV (vvIBDV). Results In total, 317 upregulated and 94 downregulated mRNAs were found to be significantly differentially expressed in infected chickens, compared to controls. Long non-coding RNA (lncRNA) and circular RNA (circRNA) alterations were identified in IBDV-infected chickens, and significantly different expression was observed in 272 lncRNAs and 143 circRNAs. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses were performed to assess the functions of significantly dysregulated genes, which showed that the JAK-STAT signaling pathway, the NOD-like receptor signaling pathway, and apoptosis may be activated by IBDV infection. We predicted interactions between differentially expressed genes and produced lncRNA-mRNA and circRNA-miRNA-mRNA regulator network. Conclusions The present study identified the expression profiles of mRNAs, lncRNAs, and circRNAs during vvIBDV infection and provides new insights into the pathogenesis of IBDV and antiviral immunity of the host.

Apolipoprotein C-II deficiency associated with nonfunctional mutant forms of apolipoprotein C-II

1984 ◽  
Vol 62 (9) ◽  
pp. 847-852 ◽  
Author(s):  
Graham F. Maguire ◽  
J. Alick Little ◽  
Gary Kakis ◽  
W. Carl Breckenridge
Keyword(s):  
Isoelectric Focusing ◽  
Gel Electrophoresis ◽  
Sodium Dodecyl ◽  
Normal Subjects ◽  
Two Dimensional ◽  
Antibody Technique ◽  
Molecular Weights ◽  
Apolipoprotein C ◽  
Antigen Antibody ◽  
Mutant Forms

Two previously unidentified apolipoproteins (apo) designated apo C-II-X and C-II-Y have been found in plasma of homozygotes and obligate heterozygotes of a family with apo C-II deficiency. Because the plasmas of homozygotes do not activate lipoprotein lipase, apo C-II-X and C-II-Y are apparently nonfunctional. These apolipoproteins have isoelectric focusing points of 5.15 and 5.54, respectively, compared with 4.88 and 4.74 for the known isomorphs, C-II-1 and C-II-2, respectively. They have approximately similar molecular weights to apo C-II-1 and C-II-2 on two-dimensional sodium dodecyl sulphate – glycerol – polyacrylamide slab gel electrophoresis. They do not form insoluble antigen–antibody complexes with antibodies to apo C-II in single antibody immunodiffusion or electroimmunoassay systems. However, using a double-antibody technique in which immunoblotting is coupled with polyacrylamide isoelectric focusing slab gel electrophoresis, apo C-II-1, C-II-2, C-II-X, and C-II-Y have similar reactivity with antibodies to apo C-II. In this family the presence of apo C-II-X and C-II-Y discriminates obligate heterozygotes from normal subjects.

scholarly journals Simultaneous detection of vaccinal and field infectious bursal disease viruses in layer chickens challenged with a very virulent strain after vaccination

2014 ◽  
Vol 62 (2) ◽  
pp. 264-273 ◽  
Author(s):  
Ivan Dobrosavljević ◽  
Dejan Vidanović ◽  
Maja Velhner ◽  
Biljana Miljković ◽  
Branislav Lako
Keyword(s):  
Virulent Strain ◽  
Simultaneous Detection ◽  
Hypervariable Region ◽  
Vaccine Virus ◽  
Lymphoid Organs ◽  
Bursa Of Fabricius ◽  
Infectious Bursal Disease ◽  
Economic Losses ◽  
Challenge Virus ◽  
Bursal Disease

Infectious bursal disease virus is an important poultry pathogen. It is distributed worldwide and causes significant economic losses. In this study, a system was adopted for the simultaneous monitoring of vaccine and virulent strains using reverse transcription polymerase chain reaction (RT-PCR). After the decay of maternal antibodies, chickens were vaccinated at the age of 37 days with a virus of intermediate virulence and challenged at 5, 10 and 14 days post vaccination (dpv). The challenge was done with IBDV strain CH/99. Sequencing of the hypervariable region of VP2 has shown that CH/99 belongs to the very virulent group of viruses. The vaccine virus could be found in the bursa of Fabricius, spleen, thymus and bone marrow until 24 dpv. The CH/99 challenge virus was found in the bursa and lymphoid organs when chickens were challenged at 5 and 10 dpv. When challenge was performed at 14 dpv, the pathogenic virus could not be found in the bursa and other lymphoid organs.

Prevention of Avian Lymphoid Leukosis by Induction of Bursal Atrophy with Infectious Bursal Disease Viruses

1978 ◽  
Vol 15 (3) ◽  
pp. 376-382 ◽  
Author(s):  
N. F. Cheville ◽  
W. Okazaki ◽  
P. D. Lukert ◽  
H. G. Purchase
Keyword(s):  
Lymphoid Cells ◽  
Bursa Of Fabricius ◽  
Infectious Bursal Disease ◽  
Control Group ◽  
Lymphoid Leukosis ◽  
Infectious Bursal Disease Viruses ◽  
Bursal Disease ◽  
Visible Effect

Five groups of genetically susceptible chickens were inoculated at hatching with lymphoid leukosis virus; four of these were given infectious bursal viruses of varying virulence at 14 days of age and one group was not inoculated (control). All chickens in the control group developed evidence of lymphoid leukosis by 180 days. Two groups given relatively virulent bursal disease viruses, which destroyed bursal lymphoid cells, did not develop lymphoid leukosis. Treatment with avirulent vaccines had no visible effect on bursal morphology and did not significantly alter the incidence of lymphoid leukosis in two other groups, although the lime of development was delayed. Results of our study show that viral-induced destruction of the bursa of Fabricius eliminates the development of lymphoid leukosis but that infection without bursal destruction has little effect on lymphoid leukosis.

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