Abstract

Protection of cattle from alcelaphine herpesvirus-1 (AlHV-1)-induced malignant catarrhal fever (MCF) has been described previously, using an attenuated virus vaccine in an unlicensed adjuvant. The vaccine was hypothesised to induce a protective barrier of virus-neutralising antibody in the oro-nasal region, supported by the observation of high titre neutralising antibodies in nasal secretions of protected animals. Here we describe further analysis of this vaccine strategy, studying the effectiveness of the vaccine formulated with a licensed adjuvant; the duration of immunity induced; and the virus-specific antibody responses in plasma and nasal secretions. The results presented here show that the attenuated AlHV-1 vaccine in a licensed adjuvant protected cattle from fatal intranasal challenge with pathogenic AlHV-1 at three or six months. In addition, animals protected from MCF had significantly higher initial anti-viral antibody titres than animals that succumbed to disease; and these antibody titres remained relatively stable after challenge, while titres in vaccinated animals with MCF increased significantly prior to the onset of clinical disease. These data support the view that a mucosal barrier of neutralising antibody blocks infection of vaccinated animals and suggests that the magnitude of the initial response may correlate with long-term protection. Interestingly, the high titre virus-neutralising antibody responses seen in animals that succumbed to MCF after vaccination were not protective.

Highlights

  • Malignant catarrhal fever (MCF) is a fatal disease of cattle and other ungulates caused by gamma-herpesviruses of the genus macavirus, including alcelaphine herpesvirus 1 (AlHV-1) and ovine herpesvirus 2 (OvHV-2)

  • The virulent C500 strain virus was collected from cultures of bovine turbinate (BT) cells infected with a cell suspension derived from pooled lymphoid tissue from rabbits infected with AlHV-1 C500 that had developed MCF

  • Within groups 1 and 2 (Table 1) a total of 16 vaccinated animals were challenged with pathogenic AlHV-1 by the intranasal route at either 9 or 11 weeks after primary immunisation

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Summary

Introduction

Malignant catarrhal fever (MCF) is a fatal disease of cattle and other ungulates caused by gamma-herpesviruses of the genus macavirus, including alcelaphine herpesvirus 1 (AlHV-1) and ovine herpesvirus 2 (OvHV-2)[1,2]. The AlHV-1 and OvHV-2 genomes have been completely sequenced, revealing that they are highly-related viruses [3,4]. Both viruses cause MCF with similar pathology in susceptible animals that include laboratory species such as hamster and rabbit [5,6,7]. Death can occur within a few days or weeks after the first clinical signs Characteristic lesions of this disease include nonpurulent vasculitis and interstitial infiltration of lymphoid cells in most tissues, which may be associated with the presence of ulcers at epithelial surfaces [8,9]

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