scholarly journals Molecular characterization of highly virulent fowl adenoviruses associated with outbreaks of inclusion body hepatitis

1991 ◽  
Vol 20 (4) ◽  
pp. 597-606 ◽  
Author(s):  
K. M. Erny ◽  
D. A. Barr ◽  
K. J. Fahey
2012 ◽  
Vol 56 (1) ◽  
pp. 73-81 ◽  
Author(s):  
Arshud Dar ◽  
Susantha Gomis ◽  
Ian Shirley ◽  
George Mutwiri ◽  
Robert Brownlie ◽  
...  

2012 ◽  
Vol 7 (1) ◽  
pp. e10-e12
Author(s):  
Arshud Dar ◽  
Susantha Gomis ◽  
Ian Shirley ◽  
George Mutwiri ◽  
Robert Brownlie ◽  
...  

2020 ◽  
Vol 64 (1) ◽  
pp. 110
Author(s):  
Ahmed Elbestawy ◽  
Mahmoud Ibrahim ◽  
Haitham Hammam ◽  
Ahmed Noreldin ◽  
Amanallah Bahrawy ◽  
...  

2018 ◽  
Vol 47 (4) ◽  
pp. 384-390 ◽  
Author(s):  
Mahmoud H. A. Mohamed ◽  
Ibrahim M. El-Sabagh ◽  
Adel M. Abdelaziz ◽  
Ahmed M. Al-Ali ◽  
Mostafa Alramadan ◽  
...  

2004 ◽  
Vol 85 (7) ◽  
pp. 2015-2021 ◽  
Author(s):  
Giliane S. Trindade ◽  
Flávio G. da Fonseca ◽  
João T. Marques ◽  
Sueli Diniz ◽  
Juliana A. Leite ◽  
...  

Here is described the isolation of a naturally occurring A-type inclusion body (ATI)-negative vaccinia-like virus, Belo Horizonte virus (VBH), obtained from a mousepox-like outbreak in Brazil. The isolated virus was identified and characterized as an orthopoxvirus by conventional methods. Molecular characterization of the virus was done by DNA cross-hybridization using Vaccinia virus (VACV) DNA. In addition, conserved orthopoxvirus genes such as vaccinia growth factor, thymidine kinase and haemagglutinin were amplified by PCR and sequenced. All sequences presented high similarity to VACV genes. Based on the sequences, phenograms were constructed for comparison with other poxviruses; VBH clustered consistently with VACV strains. Attempts to amplify the ATI gene (ati) by PCR, currently used to identify orthopoxviruses, were unsuccessful. Results presented here suggest that most of the ati gene is deleted in the VBH genome.


VirusDisease ◽  
2013 ◽  
Vol 25 (1) ◽  
pp. 114-119 ◽  
Author(s):  
Dinesh Mittal ◽  
Naresh Jindal ◽  
Ashok Kumar Tiwari ◽  
Raj Singh Khokhar

1974 ◽  
Vol 18 (3) ◽  
pp. 399 ◽  
Author(s):  
J. K. Rosenberger ◽  
R. J. Eckroade ◽  
S. Klopp ◽  
W. C. Krauss

2020 ◽  
Author(s):  
Dasharath B. Shinde ◽  
Anil L Thormoth ◽  
Santosh S. Koratkar ◽  
Neeti Sharma ◽  
Ashok Rajguru ◽  
...  

Abstract Inclusion body hepatitis (IBH) is a disease of chickens characterized by acute mortality with severe anemia caused by fowl adenoviruses (FAdV). IBH is one of the most important re-emerging diseases world-wide. In India earlier IBH/ Hydropericardium Syndrome (HPS) outbreaks were mainly due to FAdV) type 4; however, in recent outbreaks, other serotypes are involved, despite regular vaccination in breeders and young chicks. The aim of the present study was isolation and molecular characterization of FAdV associated with IBH in India. A total of 193 liver samples of IBH suspected broiler chickens were collected from different regions of India. Liver samples were initially screened by histopathology and further, a total of 127 samples which microscopically showed basophilic, intra-nuclear inclusion bodies were processed for FAdV detection. A total of 69 samples were found to be positive for Hexon gene in PCR, of which 28 were sequenced. These samples showed more than 94% sequence homology with FAdV2 and 97% with FAdV11, which was confirmed by Restriction Enzyme Analysis (REA). Tissue Culture Infective Dose 50 (TCID50) and Egg Infective Dose50 (EID50) titer of isolated FAdV was found to be 106.5/ml. Pathogenicity study in SPF chicks showed 100% mortality up to Post Infection Day (PID)-6. These findings conclude that the prevalence of FAdV-11 is currently causing IBH outbreaks India. However, further genetic and pathogenic analysis of FAdV is required, which would provide useful information for the development of the efficient commercial IBH vaccine.


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