Abstract

Surveillance of bovine tuberculosis (bTB) is partly based on the sanitary inspection of carcasses at the abattoir to detect bTB-like lesions which, in compliance with EU recommendations, are analysed by bacteriology and histopathology to disclose Mycobacterium bovis (or M. caprae) infection. Moreover, since 2012, a PCR method with similar sensitivity and specificity values of histopathology and bacteriology respectively is additionally employed in France, partially compensating for the weaknesses of classical diagnostic methods. We analysed a collection of bTB-like lesions from cattle presenting positive histological results albeit with negative PCR results. We present here the results of these samples, recovered from 292 animals culled between 2013 and 2016, analysed with a second line molecular diagnosis approach that consists in a combination of PCRs targeting the M. tuberculosis-M. avium complexes as well as the Mycobacterium genus and sequencing of hsp65 gene. These molecular analyses disclosed to identify the presence of non-tuberculous bacteria which could be responsible for most of these non-specific TB lesions: non tuberculous mycobacteria (24%) or Actinomycetales (56%) such as Rhodococcus equi (53%); 24% of the samples were negative. M. bovis -or any other MTBC members- was neither detected by molecular methods nor isolated in any of them at the end of the 3 months of culture. In conclusion, these results highlight the lack of specificity of histopathology and the usefulness of a first line PCR with a second line molecular diagnostic test to circumvent it. This diagnostic strategy makes it possible to reduce the number of suspect bTB cases raised at the abattoir or shortening their lock-up periods. By simplifying diagnostic schemes, the use of this tool could improve bTB surveillance and make eradication programs more efficient in the future.

Highlights

  • Bovine tuberculosis, mainly due to Mycobacterium bovis, is an important re-emergent zoonotic disease in Europe [1]

  • The bovine tuberculosis National Reference Laboratory (NRL) applies a second line molecular diagnosis method that enables the identification of mycobacterial species either on mycobacteria bacteriological isolates or directly on DNA extracted from animal samples

  • The obtained sequences were compared to the GenBank/EMBL/DDBJ databases using the BLAST program. This retrospective analysis includes all cattle cases sent to the NRL which had a negative result for Mycobacterium tuberculosis complex (MTBC) PCR but with a bTB suggestive histopathology

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Summary

Introduction

Bovine tuberculosis (bTB), mainly due to Mycobacterium bovis, is an important re-emergent zoonotic disease in Europe [1]. In a recent study on the evaluation of sensitivity and specificity of confirmatory bTB diagnostic tests, it was shown that histopathology was less specific than bacteriology, albeit as sensitive as another rapid test, a MTBC PCR introduced in France as a first line method, in parallel with bacteriology, to detect bTB infected animals [10]. The bovine tuberculosis National Reference Laboratory (NRL) applies a second line molecular diagnosis method that enables the identification of mycobacterial species either on mycobacteria bacteriological isolates or directly on DNA extracted from animal samples. This method provides rapid information about bTB or any other mycobacterial infection. In this study we summarise the results of 4 years analyses on such samples with our second line molecular diagnosis scheme, which made it possible to identify non-tuberculous bacterial agents giving rise to nonspecific bTB-like lesions, to avoid cumbersome -albeit official- diagnostic alternatives such as culture for confirming the bTB-free status of the herd, gaining diagnostic specificity and confidence for bTB status confirmation

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