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RESEARCH PRODUCT

First molecular detection of mycobacterium bovis in environmental samples from a French region with endemic bovine tuberculosis

Murielle RocheletElodie BarbierElodie BarbierAriane PayneE. GueneauMaria Laura BoschiroliA.l. BlieuxK. De CruzC. FossotAlain Hartmann

subject

0301 basic medicineGenotype040301 veterinary sciences[SDV]Life Sciences [q-bio]030106 microbiologyIndoor bioaerosolAnimals WildLocus (genetics)Applied Microbiology and BiotechnologyMicrobiology0403 veterinary scienceFeces03 medical and health sciencesGenotypeEnvironmental MicrobiologyMustelidaePrevalenceBovine tuberculosisAnimals[SDV.BV]Life Sciences [q-bio]/Vegetal Biologyquantitative real-time PCRbovine tuberculosisFeces2. Zero hungerMycobacterium bovisbiologyfungi04 agricultural and veterinary sciencesGeneral MedicineContaminationbiology.organism_classificationMycobacterium bovis3. Good healthMycobacterium tuberculosis complex[SDE]Environmental SciencesCattleindirect transmissionFranceTuberculosis BovineenvironmentBiotechnology

description

Aims The aim of the study was to determine the prevalence of Mycobacterium bovis (the causative agent of bovine tuberculosis, bTB) in environmental matrices within a French region (Cote d'Or) affected by this zoonotic disease. Methods and Results We report here the development and the use of molecular detection assays based on qPCR (double fluorescent dye labelled probe) to monitor the occurrence of Mycobacterium tuberculosis complex (MTBC) or M. bovis in environmental samples collected in pastures where infected cattle and wildlife had been reported. Three qPCR assays targeting members of the MTBC (IS1561’ and Rv3866 loci) or M. bovis (RD4 locus) were developed or refined from existing assays. These tools were validated using M. bovis spiked soil, water, and feces samples. Environmental samples were detected positive for the presence of MTBC strains and M. bovis in the environment of bTB-infected farms in the Cote d'Or region. Conclusions The development of molecular assays permitted testing of several types of environmental samples including spring water, sediment samples and soils from badger setts entrance located in the vicinity of these farms, which were repeatedly contaminated with M. bovis (up to 8.7 × 103 gene copies per g of badger sett soil). For the first time, direct spoligotyping of soil DNA enabled identification of M. bovis genotypes from environmental matrices. Significance and Impact of the Study All together, these results suggest that M. bovis occurs at low levels in environmental matrices in Cote d'Or within the bTB-infected area. Drinking contaminated water or inhaling contaminated bioaerosols might explain cattle infection in some cases. This article is protected by copyright. All rights reserved.

10.1111/jam.13090https://hal.inrae.fr/hal-02634911