Poult. Sci.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Poult Sci 2007. 86:1329-1335
© 2007 Poultry Science Association
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ahmed, Z.
Right arrow Articles by Hameed, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ahmed, Z.
Right arrow Articles by Hameed, A.

IMMUNOLOGY, HEALTH, AND DISEASE

Detection and Seroprevalence of Infectious Bronchitis Virus Strains in Commercial Poultry in Pakistan

Z. Ahmed*,1, K. Naeem* and A. Hameed{dagger}

* National Reference Laboratory for Poultry Diseases, Animal Sciences Institute, National Agricultural Research Center, Park Road, Islamabad, Pakistan; and {dagger} Department of Microbiology, Quaid-I-Azam University, Islamabad, Pakistan

1 Corresponding author: drzaheer{at}comsats.net.pk

This study was conducted to investigate the incidence of infectious bronchitis virus (IBV) in commercial broiler and layer flocks in Pakistan. Serum samples from 16 layers and 9 broiler flocks were screened against M-41, D-274, D-1466, and 4-91 strain antigens using hemagglutination inhibition assay. Overall, 88% of the flocks were seropositive for M-41 antibodies, whereas 40, 52, and 8% of the flocks were positive for D-274, D-1466, and 4-91 IBV strains, respectively. The M-41 antigen was also detected in lungs and tracheal tissues of the clinically positive infectious bronchitis cases. Phospholipase C treatment of the lung and tracheal tissue homogenates from IBV-positive chickens increased the detection limit for M-41 strain from 1.3% positive samples in simple hemagglutination assay to 30.6% positivity when the same samples were treated with phospholipase C. Similarly, reverse transcription-PCR was a much better M-41 detection tool as compared with the classical agar gel precipitation assay utilized to screen tissue homogenates from IBV-positive chickens. In conclusion, this survey clearly demonstrates that several strains of IBV are prevalent in poultry flocks in Pakistan. By utilizing such diagnostic techniques it is possible to conduct a detailed epidemiological study to determine the full economic impact of this disease.

Key Words: chicken • infectious bronchitis virus • Pakistan







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 by the Poultry Science Association.