Your browser doesn't support javascript.
loading
Development of single-chain Fv against the nucleoprotein of type A influenza virus and its use in ELISA.
Sengupta, Devyani; Shaikh, Asma; Bhatia, S; Pateriya, A K; Khandia, R; Sood, R; Prakash, A; Pattnaik, B; Pradhan, H K.
Affiliation
  • Sengupta D; High Security Animal Disease Laboratory, Indian Veterinary Research Institute, Anand Nagar, Bhopal, Madhya Pradesh 462021, India.
  • Shaikh A; High Security Animal Disease Laboratory, Indian Veterinary Research Institute, Anand Nagar, Bhopal, Madhya Pradesh 462021, India.
  • Bhatia S; High Security Animal Disease Laboratory, Indian Veterinary Research Institute, Anand Nagar, Bhopal, Madhya Pradesh 462021, India. Electronic address: sandeep.bhatia@hsadl.in.
  • Pateriya AK; High Security Animal Disease Laboratory, Indian Veterinary Research Institute, Anand Nagar, Bhopal, Madhya Pradesh 462021, India.
  • Khandia R; High Security Animal Disease Laboratory, Indian Veterinary Research Institute, Anand Nagar, Bhopal, Madhya Pradesh 462021, India.
  • Sood R; High Security Animal Disease Laboratory, Indian Veterinary Research Institute, Anand Nagar, Bhopal, Madhya Pradesh 462021, India.
  • Prakash A; Department of Biotechnology and Bioinformatics, Barkatullah University, Bhopal, Madhya Pradesh 462021, India.
  • Pattnaik B; High Security Animal Disease Laboratory, Indian Veterinary Research Institute, Anand Nagar, Bhopal, Madhya Pradesh 462021, India.
  • Pradhan HK; High Security Animal Disease Laboratory, Indian Veterinary Research Institute, Anand Nagar, Bhopal, Madhya Pradesh 462021, India.
J Virol Methods ; 208: 129-37, 2014 Nov.
Article in En | MEDLINE | ID: mdl-25152529
ABSTRACT
Single chain fragment variable (ScFv) antibodies specific to the nucleoprotein (NP) of avian influenza virus (AIV) were developed using a phage display system. The variable heavy (VH) and the variable light (VL) chain gene fragments were derived from spleen cells of Balb/c mouse immunized with a recombinant NP (rNP) antigen (∼63 kDa) of H5N1 influenza virus. The VH and the VL DNA fragments were assembled through a flexible linker DNA to generate ScFv DNA that was cloned subsequently in a phagemid to express ScFv protein in Escherichia coli cells. The specific reactivity of the ScFv with the rNP antigen and viral antigen (H5N1) was confirmed by Western blot and ELISA. A competitive inhibition ELISA (CI-ELISA) was developed using the rNP and the anti-NP ScFv for detection of type-specific antibodies to AIV in chicken sera. The ScFv based CI-ELISA was compared with hemagglutination inhibition (HI) test and agar gel immunodiffusion (AGID) test over 850 sera. Sensitivity of the CI-ELISA was 100% with HI and AGID and specificity was 98.7% with HI and 100% with AGID.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viral Core Proteins / RNA-Binding Proteins / Single-Chain Antibodies / Influenza in Birds / Antibodies, Viral Type of study: Diagnostic_studies / Evaluation_studies Limits: Animals Language: En Journal: J Virol Methods Year: 2014 Document type: Article Affiliation country: India

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Viral Core Proteins / RNA-Binding Proteins / Single-Chain Antibodies / Influenza in Birds / Antibodies, Viral Type of study: Diagnostic_studies / Evaluation_studies Limits: Animals Language: En Journal: J Virol Methods Year: 2014 Document type: Article Affiliation country: India