Abstract

African swine fever (ASF) and Classical swine fever (CSF) are both highly contagious diseases of domestic pigs and wild boar. In the last years, several cases of both diseases have been reported in the Caucasus, Russian Federation and Eastern Europe. Thus, the probability of encountering these two viruses in the same area is increasing. Since differentiation by clinical or post-mortem examination is not possible, laboratory tools for differential diagnosis are required. In the present work, we have developed a triplex bead-based assay using some of the most immunogenic antigens of each virus, for the simultaneous detection of antibodies; i.e. the VP72 and VP30 of ASF virus (ASFV) and the E2 protein of CSF virus (CSFV). The assay was firstly set up and optimized using well characterized reference serum samples specific for each pathogen. Then, a panel of 352 sera from experimentally infected animals with either ASFV or CSFV were analyzed in the multiplex assay. A collection of 253 field negative sera was also included in the study. The results of the multiplex analysis were compared to those obtained by two commercially available ELISAs for detection of antibodies against ASFV or CSFV, and considered in this study as the reference techniques. The data obtained showed values of 97.3% sensitivity and 98.3% specificity for detection of antibodies to ASFV and 95.7% of sensitivity and 99.8% specificity for detection of antibodies to CSFV. This multiplex assay allows the simultaneous and differential detection of antibodies against ASFV and CSFV, providing a valuable tool for surveillance studies. Moreover, this method is rather versatile, offering the possibility of increasing the panel of antigens from other swine diseases that could be of interest for a differential diagnosis along with ASF and CSF.

Highlights

  • African Swine Fever (ASF) is a highly infectious disease in swine population, caused by an enveloped double-stranded DNA virus, the African swine fever (ASF) virus (ASFV), which is the only member of the Asfarviridae family [1]

  • We have developed a triplex assay for detection of antibodies to ASF virus (ASFV) and CSF virus (CSFV), using immunogenic antigens of each virus: VP72 and VP30 of ASFV and E2 of CSFV, as an approach for the simultaneous detection and differential diagnosis of both diseases

  • A 1/200 dilution of serum was selected as the optimal dilution for screening purposes. This dilution showed the highest responses to ASFV and CSFV antigens while no cross-reactivity to the non-target antigens in each case

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Summary

Introduction

African Swine Fever (ASF) is a highly infectious disease in swine population, caused by an enveloped double-stranded DNA virus, the ASF virus (ASFV), which is the only member of the Asfarviridae family [1]. ASFV is composed of more than 68 structural proteins, many of which are highly immunogenic [2]. The structural viral proteins (VP) VP72 and VP30 are commonly used for diagnostic purposes [3,4,5]. ASFV infection causes a strong humoral immune. Infection with ASFV correlates with a wide range of clinical syndromes from almost unapparent disease to a hemorrhagic fever with high fatality rates (95–100%) depending on the strain virulence and the immunological characteristics of the host [8, 9]

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