2014Acta HorticulturaeRequires access

PREPARATION OF ANTISERUM TO RECOMBINANT COAT PROTEIN FOR DETECTING STRAWBERRY MILD YELLOW EDGE VIRUS

Hongyan Dai, Cuimei Yu, Zhihong Zhang

Open publisher page 0 citations

Abstract

Strawberry mild yellow edge virus (SMYEV) is one of the most economically important viral pathogens infecting strawberries worldwide. Immunodiagnostics is a rapid and sensitive method for detecting viruses. Preparation of antiserum against recombinant coat protein (CP) has been used for some viruses. In this paper, the full length CP gene of SMYEV, which consisted of 729 bp and encoded 242 amino acid residues, was isolated from the SMYEV isolate SY05, and then cloned into the prokaryotic expression vector pGEX-6P-1. The recombinant prokaryotic expression vector carrying the SMYEV CP gene was introduced into Escherichia coli and the fused CP protein was expressed in E. coli cells treated with IPTG. The antiserum was produced after the rabbit was immunized with the purified CP protein. Two methods, ELISA and RT-PCR, were compared for detecting SMYEV, and the results show that ELISA was as not sensitive as RT-PCR.

About this research paper

What this paper is about

Strawberry mild yellow edge virus (SMYEV) is one of the most economically important viral pathogens infecting strawberries worldwide. Immunodiagnostics is a rapid and sensitive method for detecting viruses. Preparation of antiserum against recombinant coat protein (CP) has been used for some viruses. In this paper, the full length CP gene of SMYEV, which consisted of 729 bp and encoded 242 amino acid residues, was isolated from the SMYEV isolate SY05, and then cloned into the prokaryotic expression vector pGEX-6P-1. The recombinant prokaryotic expression vector carrying the SMYEV CP gene was introduced into Escherichia coli and the fused CP protein was expressed in E. coli cells treated with IPTG. The antiserum was produced after the rabbit was immunized with the purified CP protein. Two methods, ELISA and RT-PCR, were compared for detecting SMYEV, and the results show that ELISA was as not sensitive as RT-PCR.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Strawberry mild yellow edge virus (SMYEV) is one of the most economically important viral pathogens infecting strawberries worldwide. Immunodiagnostics is a rapid and sensitive method for detecting viruses. Preparation of antiserum against recombinant coat protein (CP) has been used for some viruses. In this paper, the full length CP gene of SMYEV, which consisted of 729 bp and encoded 242 amino acid residues, was isolated from the SMYEV isolate SY05, and then cloned into the prokaryotic expression vector pGEX-6P-1. The recombinant prokaryotic expression vector carrying the SMYEV CP gene was introduced into Escherichia coli and the fused CP protein was expressed in E. coli cells treated with IPTG. The antiserum was produced after the rabbit was immunized with the purified CP protein. Two methods, ELISA and RT-PCR, were compared for detecting SMYEV, and the results show that ELISA was as not sensitive as RT-PCR.

Key concepts: Antiserum, Coat protein, Recombinant DNA, Coat, Virology, Virus, Biology, Molecular biology

Related papers

Back to paper searchBrowse research topicsOriginal source
PREPARATION OF ANTISERUM TO RECOMBINANT COAT PROTEIN FOR DETECTING STRAWBERRY MILD YELLOW EDGE VIRUS — Research Paper | ScholarLens