Abstract

BackgroundDetection of Mycobacterium avium subspecies paratuberculosis (MAP) infection is key to the control of Johne’s disease. Immunohistochemistry is one of the methods of detection of MAP infection in tissues. However, unavailability of commercial antibodies that can detect the organism is a limiting factor for the use of immunohistochemistry. This study was aimed at developing an immunohistochemistry method to diagnose MAP in infected tissues using antibodies against MAP recombinant heat shock protein 70kd.ResultsMAP Heat shock protein 70 gene was amplified and cloned into an expression vector, Champion pET-SUMO, then expressed in E coli, purified and used to produce polyclonal rabbit antibodies against the Heat shock protein. Immunohistochemistry was performed in 35 MAP infected tissues with anti-HSP70 polyclonal antibodies. All 35 MAP infected tissues were positive for MAP within macrophages, epithelioid cells and giant cells either in clumps or singly as individual bacilli. No positive staining was seen in the three uninfected normal tissues and in MAP infected tissues where primary antibodies were substituted with PBS or pre-immune serum from the same rabbit.ConclusionAnti-HSP70 produced in this study offers an opportunity for improved diagnosis, screening of MAP in animal tissues and in studies on the pathogenesis of MAP

Highlights

  • Detection of Mycobacterium avium subspecies paratuberculosis (MAP) infection is key to the control of Johne’s disease

  • The amplification of Heat shock protein 70 (HSP70) gene resulted into a Polymerase chain reaction (PCR) product of 1872bp PCR product (Fig. 1a)

  • Optimal expression was observed between 3 and 4 h post induction. This protein was cut into a 70kd protein (HSP70) and a 13kd protein (SUMO) using Small ubiquitin like modifier (SUMO) protease (Fig. 2)

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Summary

Introduction

Detection of Mycobacterium avium subspecies paratuberculosis (MAP) infection is key to the control of Johne’s disease. Immunohistochemistry is one of the methods of detection of MAP infection in tissues. Unavailability of commercial antibodies that can detect the organism is a limiting factor for the use of immunohistochemistry. This study was aimed at developing an immunohistochemistry method to diagnose MAP in infected tissues using antibodies against MAP recombinant heat shock protein 70kd. Diagnosis of paratuberculosis or MAP infection is key to the control of Johne’s disease [4, 5]. There is continuing search for new antigens and antibodies for use in IHC detection of MAP [10]. Finding new antigens and use of recombinant DNA technology are the best hope for immunodiagnostic of paratuberculosis as it is for many other diseases

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