Standardisation Of Indirect Haemagglutination Test For Monitoring Infectious Bursal Disease Virus (Record no. 2277)

000 -LEADER
fixed length control field 02364nam a2200205Ia 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20150917154153.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 150525s1997 xx 000 0 und d
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title eng
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 0529,T
100 ## - MAIN ENTRY--AUTHOR NAME
Personal name Sajid Mahmood
110 ## - MAIN ENTRY--CORPORATE NAME
Location of meeting Dr. Muhammad Akram Muneer
245 ## - TITLE STATEMENT
Title Standardisation Of Indirect Haemagglutination Test For Monitoring Infectious Bursal Disease Virus
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Year of publication 1997
502 ## - DISSERTATION NOTE
Dissertation note Indirect haemagglutination (IHA) test was standardized and evaluated to moniter antibodies against infectious bursal disease (IBD). It was observed that oil based vaccine prepared from bursae of fäbricius of infected birds, induced a high level of antibody which were detected by agar gel precipitation test (AGPT). It was recorded Chat tannic acid, glutaraldehyde and chromium chloride had 0.0000781, 0.003906 and 0.0001562 per cent subagglutinating dilutions in normal saline solution (pH 7.2) respectively while 0.000001220, 0.0156 and 0.0025 subagglutinating dilution of the coupling agents were found in phasphate buffered saline (pH 7.2), respectively.

Indirect. haemagglutination test is sensitive and specific serological technique to study infectious bursal disease. However, antigen dilution to sensitize erythrocytes, source of erythrocytes, chemical nature of diluent, interaction temperature and time, nature and concentration of coupling agent coated erythrocytes and antiserum against IBD, had influenced the sensitivity of IHA test.

Ten percent antigen for sensitizing sheep erythrocytes, incubation temperature of 37°C for 10 minutes for antigen, tannic acid (0.005%) and erythroéyte interaction, freshly prepared sensitized erythrocytes and normal saline solution (pH 7.2) as diluent were found suitable for detecting maximum titre of anti-IBD antibodies through the IHA. Moreover it was observed that the standardized IHA proportionally showed reduction in the titre on dilution of serum. The antibody titre in the IHA was the well having serum dilution, showing resistance to bleed (flow) on tilting the plate for 5 seconds. The final results of antibody titre were achieved within 120 minutes post processing of the samples.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical Term Department of Microbiology
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Dr. Hajid
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Dr. Khushi Muhammad
710 ## - ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element Faculty of Veterinary Sciences
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Thesis
Holdings
Damaged status Collection code Permanent Location Current Location Shelving location Date acquired Full call number Accession Number Koha item type
  Veterinary Science UVAS Library UVAS Library Thesis Section 2015-05-27 0529,T 0529,T Thesis


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