Multilaboratory Evaluation of a Novel Lateral Flow Immunochromatographic Assay for Confirming Isolation of Mycobacterium bovis from Veterinary Diagnostic Specimens

Author:

Stewart Linda D.1,McCallan Lyanne2,McNair James2,McGoldrick Adrian3,Morris Rowan3,Moyen Jean-Louis4,De Juan Ferré Lucía56,Romero Beatriz5,Alonso Elena7,Parsons Sven D. C.8ORCID,Van Helden Paul8,Araújo Flábio R.9,Grant Irene R.1ORCID

Affiliation:

1. Institute for Global Food Security, School of Biological Sciences, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom

2. Veterinary Sciences Division, Agri-Food and Biosciences Institute, Belfast, Northern Ireland, United Kingdom

3. Animal and Plant Health Agency Veterinary Inspection Centre Starcross, Exeter, United Kingdom

4. Laboratoire Départemental d'Analyse et de Recherche de la Dordogne, Coulounieix-Chamiers, France

5. Centro de Vigilancia Sanitaria Veterinaria (VISAVET), Universidad Complutense, Madrid, Spain

6. Departamento Sanidad Animal, Facultad de Veterinaria, Universidad Complutense, Madrid, Spain

7. Laboratorio Regional de Sanidad Animal de la Junta de Castilla y León, León, Spain

8. DST/NRF Centre of Excellence for Biomedical Tuberculosis Research/SAMRC Centre for TB Research/Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa

9. Empresa Brasileira de Pesquisa Agropecuária (EMBRAPA Gado de Corte), Campo Grande, Brazil

Abstract

ABSTRACT A novel lateral flow immunochromatographic device (LFD) was evaluated in several veterinary diagnostic laboratories. It was confirmed to be specific for Mycobacterium bovis and M. caprae cells. The performance of the novel LFD was assessed relative to the confirmatory tests routinely applied after culture (spoligotyping or quantitative PCR [qPCR]) in each laboratory; liquid (MGIT or BacT/Alert) and/or solid (Stonebrink, Coletsos, or Lowenstein-Jensen) cultures were tested. In comparison to spoligotyping of acid-fast-positive MGIT cultures, percent agreement between positive LFD and spoligotyping results was excellent in two United Kingdom laboratories (97.7 to 100%) but lower in the Spanish context (76%), where spoligotyping was applied to MGIT cultures previously confirmed to be positive for M. tuberculosis complex (MTBC) by qPCR. Certain spoligotypes of M. bovis and M. caprae were not detected by the LFD in Spanish MGIT cultures. Compared to qPCR confirmation, the agreement between positive LFD and qPCR results was 42.3% and 50% for BacT/Alert and MGIT liquid cultures, respectively, and for solid cultures, it ranged from 11.1 to 89.2%, depending on the solid medium employed (Coletsos, 11.1%; Lowenstein-Jensen, 55.6%; Stonebrinks, 89.2%). Correlation between the novel LFD and BD MGIT TBc Identification test results was excellent when 190 MGIT cultures were tested ( r = 0.9791; P < 0.0001), with the added benefit that M. bovis was differentiated from another MTBC species in one MGIT culture by the novel LFD. This multilaboratory evaluation demonstrated the novel LFD's potential utility as a rapid test to confirm isolation of M. bovis and M. caprae from veterinary specimens following culture.

Funder

Invest Northern Ireland

Animal and Plant Health Agency

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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