Abstract

Brucella abortus and B. melitensis have been reported in several studies in animals in Zimbabwe but the extent of the disease remains poorly known. Thus, characterizing the circulating strains is a critical first step in understanding brucellosis in the country. In this study we used an array of molecular assays including AMOS-PCR, Bruce-ladder, multiple locus variable number tandem repeats analysis (MLVA) and single nucleotide polymorphisms from whole genome sequencing (WGS-SNP) to characterize Brucella isolates to the species, biovar, and individual strain level. Sixteen Brucella strains isolated in Zimbabwe at the Central Veterinary laboratory from various hosts were characterized using all or some of these assays. The strains were identified as B. ovis, B. abortus, B. canis and B. suis, with B. canis being the first report of this species in Zimbabwe. Zimbabwean strains identified as B. suis and B. abortus were further characterized with whole genome sequencing and were closely related to reference strains 1330 and 86/8/59, respectively. We demonstrate the range of different tests that can be performed from simple assays that can be run in laboratories lacking sophisticated instrumentation to whole genome analyses that currently require substantial expertise and infrastructure often not available in the developing world.

Highlights

  • Brucellosis is a worldwide infectious disease affecting a wide range of domestic and wildlife animals and humans [1]

  • This article describes the use of various assays such as AMOS, Bruce-ladder, multiple locus variable number tandem repeats analysis (MLVA), and whole genome sequencing to characterize Brucella species isolated from different animals in Zimbabwe

  • Brucellosis is caused by species in the genus Brucella, which consists of six classic species, Brucella abortus, B. melitensis, B. suis, B. ovis, B. canis, and B. neotomae [2]

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Summary

Introduction

Brucellosis is a worldwide infectious disease affecting a wide range of domestic and wildlife animals and humans [1]. The authors used biotyping and AMOS-PCR to identify Brucella isolates from commercial and communal cattle farms in Zimbabwe and reported a single B. melitensis bv. 1 was isolated from waterbuck (Kobus ellipsiprymnus) and eland (Taurotragus oryx) [16]. This complicates the control of the disease since the animals in areas bordering the National parks interact with wildlife and it is almost impossible to vaccinate wildlife. Bovine brucellosis is endemic in the country in most regions with high sero-prevalence of up to 53% reported in commercial herds as compared to 16% from small-scale farmers in Zimbabwe [17, 18]

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