Literature DB >> 31705355

Identification and genetic analysis of infectious bursal disease viruses from field outbreaks in Kerala, India.

D Nandhakumar1, R Rajasekhar2, G Logeshwaran1, Chintu Ravishankar1, Stephy Rose Sebastian1, R Anoopraj3, K Sumod1, Binu K Mani1, G Chaithra1, Chandankar Vaidehi Deorao1, Koshy John1.   

Abstract

Recurrent infectious bursal disease (IBD) outbreaks were reported in different regions of Kerala, India. This paper reports the comparative genetic analysis of the hypervariable region of the VP2 gene of IBD virus isolates from the field outbreaks in Kerala. In phylogenetic analysis, the obtained field isolates fall into genogroup 1 and 3. In genogroup 3, all vvIBDV isolates shared a common ancestor with other south Indian isolates but isolates 9/CVASP/IBDV, 10/CVASP/IBDV, 12/CVASP/IBDV, 14/CVASP/IBDV and 17/CVASP/IBDV are most recently evolved and are diverged from the south Indian isolates. The amino acid sequence of 22 isolates was analysed, out of which 18 had conserved amino acids which were characteristic of vvIBDV. All the vvIBDV isolates obtained in the study had phenylalanine and valine at the position 240 and 294, respectively, similar to recently evolved Indian IBDV isolate (MDI14). But we observed T269A and S299N mutations in the isolate 6/CVASP/IBDV, and it is the first report of such mutations at these positions in India IBDV isolates. The isolate 11/CVASP/IBDV had a unique mutation of V225A which is not yet reported in IBDV isolates. Two isolates (15/CVASP/IBDV and 18/CVASP/IBDV) were 100% amino acid similar to intermediate plus vaccine strain. The isolates 8/CVASP/IBDV/VP2 and 19/CVASP/IBDV had amino acids unique for the intermediate vaccine with mutations observed at H253Q and V256I in 19/CVASP/IBDV, T270A and novel mutation N279Y in isolate 8/CVASP/IBDV. These two isolates had non-virulent classical heptapeptide sequence 'SWSARGS'; nevertheless, they produce field outbreaks of IBD. This is the first report of genetic characterisation of IBDV in Kerala, India.

Entities:  

Keywords:  Amino acid substitutions; Hypervariable VP2 gene; Infectious bursal disease virus (IBDV); Phylogenetic analysis; Reverse transcriptase polymerase chain reaction (RT-PCR)

Mesh:

Year:  2019        PMID: 31705355     DOI: 10.1007/s11250-019-02084-w

Source DB:  PubMed          Journal:  Trop Anim Health Prod        ISSN: 0049-4747            Impact factor:   1.559


  23 in total

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Journal:  J Virol       Date:  2001-12       Impact factor: 5.103

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5.  Virus strains from a flock exhibiting unusually high mortality due to infectious bursal disease.

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Journal:  Aust Vet J       Date:  2004-12       Impact factor: 1.281

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Authors:  J R Castón; J L Martínez-Torrecuadrada; A Maraver; E Lombardo; J F Rodríguez; J I Casal; J L Carrascosa
Journal:  J Virol       Date:  2001-11       Impact factor: 5.103

7.  Genetic characteristics of infectious bursal disease viruses from four continents.

Authors:  Daral J Jackwood; Susan Sommer-Wagner
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Authors:  D J Jackwood; B Sreedevi; L J LeFever; S E Sommer-Wagner
Journal:  Virology       Date:  2008-05-27       Impact factor: 3.616

9.  Attenuation of very virulent infectious bursal disease virus and comparison of full sequences of virulent and attenuated strains.

Authors:  D Lazarus; M Pasmanik-Chor; B Gutter; G Gallili; M Barbakov; S Krispel; J Pitcovski
Journal:  Avian Pathol       Date:  2008-04       Impact factor: 3.378

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Authors:  Camila Cristina Almeida Dias; Fernanda de Oliveira Souza; Elisa Monteiro Sant' Anna da Silva; Monique Renon Eller; Priscilla Rochele Barrios; Bernadete Miranda Dos Santos; Mauro Pires Moraes; Márcia Rogéria de Almeida
Journal:  Braz J Microbiol       Date:  2009-03-01       Impact factor: 2.476

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3.  Detection of Newcastle disease virus and assessment of associated relative risk in backyard and commercial poultry in Kerala, India.

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