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  • Agricultural Research Communication Center  (3)
  • 1
    In: Indian Journal of Animal Research, Agricultural Research Communication Center, , No. Of ( 2020-12-4)
    Abstract: Background: The present study was undertaken to diagnose and characterize canine distemper virus (CDV) isolated from dogs of southern Gujarat, India. CDV is lethal disease of canines and felines. Total of 40 different samples were collected from 18 suspected stray dogs having different clinical signs which were processed for diagnosis and characterization of CDV.Methods: All samples were processed by employing different methods like, Immunochromatography based lateral flow test (LFA), IgG based indirect enzyme linked immunosorbent assay (i-ELISA), one step RT-PCR, nested one step RT-PCR and virus isolation in MDCK cell line. Restriction endonuclease (RE) analysis was used to characterize CDV Nucleocapsid (N) gene. Conclusion: Only 04 samples (02 nasal and 02 ocular swabs) of 02 dogs found positive for LFA, while 14 serum samples out of 17 samples of 18 dogs found positive for IgG antibody. As all dogs were unvaccinated, serum samples found positive in IgG based ELISA considered for confirmative positive for CDV infection. Whereas 13 samples of 10 dogs found positive for one step RT-PCR and nested one step RT-PCR. In RE digestion, characteristic two bands were found. All representative CDV positive samples of 10 dogs showed characteristic cytopathic effect in MDCK cell line. On age group wise percent positivity was found 71.42 % (05/07) in 0 - ≤6 months, while 77.77% (07/09) in 6- ≤12 months of age group, whereas, both samples were found positive in 12 months and above group. Overall 77.77% (14/18) dogs found positive for CDV infection. To the best of our knowledge, this is the first report on study of CDV infection in dogs from Gujarat state, India.
    Type of Medium: Online Resource
    ISSN: 0976-0555 , 0367-6722
    Language: Unknown
    Publisher: Agricultural Research Communication Center
    Publication Date: 2020
    SSG: 22
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    Agricultural Research Communication Center ; 2023
    In:  Agricultural Science Digest - A Research Journal , No. Of ( 2023-10-5)
    In: Agricultural Science Digest - A Research Journal, Agricultural Research Communication Center, , No. Of ( 2023-10-5)
    Abstract: Background: Bovine papillomatosis (BP) is distributed worldwide among cattle but is relatively less common in buffaloes. Prevalence of this disease is established in buffaloes from India and Italy caused by bovine papilloma virus (BPV). The current study aimed to study the detection of bovine papilloma virus from cutaneous warts by polymerase chain reaction and confirmed by nucleotide sequencing and phylogenetic analysis. Methods: In this study a total of 10 wart samples from affected cattle were aseptically collected. Grossly, most of cutaneous warts were of variable sizes, rough or coarse in texture, grayish/blackish/flesh colored, irregular in shape (dome or button) or resembling cauliflower-like masses and elevated from skin surface by broad base. Molecular characterization of viral DNA from wart samples and partial gene sequencing, its analysis were carried out by using bioinformatics tools to establish the phylogenetic relationship. Result: In our investigation it revealed that out of total 10 cutaneous wart tissue samples, only six cattle were positive for BPV-1 while all the samples were found negative for BPV-2. The phylogenetic analysis of BPV-1gene of papilloma virus of cattle showed 100% homology with already reported sequence from china. The BPV-1 partial sequences generated in present study revealed close homology as well as with the earlier published BPV-1 sequences on NCBI.
    Type of Medium: Online Resource
    ISSN: 0976-0547 , 0253-150X
    Language: Unknown
    Publisher: Agricultural Research Communication Center
    Publication Date: 2023
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  • 3
    In: Indian Journal of Animal Research, Agricultural Research Communication Center, , No. Of ( 2023-8-7)
    Abstract: Background: Chicken Infectious Anaemia Virus (CIAV) is one of the emerging pathogen of the poultry. The Genus of this virus is Gyrovirus and the family Anelloviridae. Viral DNA contains three open reading frames (ORFs) encoding for three proteins VP1, VP2 and VP3. VP1 protein is major structural protein and is a capsid protein having major role in growth and spread of the virus. Present study was aimed for molecular detection of VP1 gene of the CIA virus in the samples collected from the outbreaks occurred at four different district of Maharashtra. Methods: Total 50 samples comprising of Spleen, bone marrow, thymus and liver, were collected. DNA extracted from those samples was used for PCR amplification targeting, VP1 gene. Selected positive purified PCR products of VP1 were subjected for Nucleotide sequencing and Phylogenetic analysis. Results: Total out of 50 pooled samples, 10 samples were positive for VP1 gene i.e. 20 %. Sequencing of coding region of four CAV positive samples was conducted. Genetic analysis showed three isolates had high similarity with Del-Ros vaccine strainfrom USA ; while one isolate shared close similarity to attenuated cloned isolate 10 of Cux-1 strain. The data also indicated Q139 and Q144 and Q394 amino acids substitutions among the VP1. Phylogenetic analysis of the sequenced viruses based on either the coding nucleotide sequence or VP1 coding sequence, suggested the circulation of III genotypes in Maharashtra.
    Type of Medium: Online Resource
    ISSN: 0976-0555 , 0367-6722
    Language: Unknown
    Publisher: Agricultural Research Communication Center
    Publication Date: 2023
    SSG: 22
    SSG: 12
    Location Call Number Limitation Availability
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