Abstract

Foot-and-mouth disease (FMD) is endemic in many regions of the world and is one of the most prevalent epizootic animal diseases. FMD affects livestock, such as cattle, sheep, goats and pigs, and causes enormous economic losses due to reduced productivity and trade restrictions. Preparedness and early diagnosis are essential for effective control of FMD. Many diagnostic assays are dependent on raising high-affinity, anti-FMD virus (FMDV) serotype-specific antibodies in small animals (rabbits and guinea pigs) that give broad virus coverage. Here we show that soluble, truncated forms of bovine αvβ6 bind FMDV in an authentic RGD and divalent cation dependent interaction and can be used as the trapping reagent in a FMDV sandwich ELISA. In addition, inclusion of FLAG or His tags facilitates simple purification without the loss of virus binding. We also provide evidence that when combined with a guinea pig polyclonal serum, or serotype-specific monoclonal antibodies, the integrin can be used to detect viruses representative of all FMDV serotypes. We also show that recombinant FMDV empty capsids, with stabilising disulphide bonds, can serve as an antigen in the ELISA and can therefore replace inactivated virus antigen as a positive control for the assay. Our results demonstrate the potential use of bovine αvβ6 and FMDV empty capsids in FMD diagnostic assays.

Highlights

  • Foot-and-mouth disease (FMD), caused by FMD virus (FMDV), is endemic in many regions of the world, and is one of the most prevalent epizootic animal diseases [1]

  • FMDV and empty capsids (EC) have been produced with mutations that result in stabilised capsids that are resistant to fluctuations in pH and temperature [19, 21,22,23,24]

  • To demonstrate FMDV binding to truncated αvβ6 preparations, we produced matched preparations of stabilised FMDV A22 Iraq EC with either the wild-type RGD sequence (A22ec/RGD) or a biologically inactive KGA (A22ec/KGA) in place of the RGD (Fig 1A)

Read more

Summary

Introduction

Foot-and-mouth disease (FMD), caused by FMD virus (FMDV), is endemic in many regions of the world, and is one of the most prevalent epizootic animal diseases [1]. The wells were washed three times with TBScm containing 0.05% tween and bound EC were detected by sequential incubation with a guinea pig, anti-A22 Iraq polyclonal antisera used at 1/1000 followed by a rabbit, anti-guinea pig horseradish peroxidase (HRP) conjugated secondary antibody (Sigma) used at 1/5000 for 45min each at room temperature.

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call