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A One Health Approach Revealed the Long-Term Role of Mycobacterium Caprae As the Hidden Cause of Human Tuberculosis in a Region of Spain, 2003 to 2022.

Miguel Martinez-Lirola,Marta Herranz,Sergio Buenestado Serrano,Cristina Rodriguez-Grande, Eva Dominguez Inarra,Jose Antonio Garrido-Cardenas, Ana Maria Correa Ruiz, Maria Pilar Bermudez,Manuel Causse del Rio,Veronica Gonzalez Galan, Julia Liro Armenteros, Jose Maria Viudez Martinez,Silvia Vallejo-Godoy, Ana Belen Esteban Garcia, Maria Teresa Cabezas Fernandez,Patricia Munoz,Laura Perez Lago,Dario Garcia de Viedma

Euro surveillance/Eurosurveillance(2023)

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摘要
IntroductionMycobacterium caprae is a member of the Mycobacterium tuberculosis complex (MTBC) not routinely identified to species level. It lacks specific clinical features of presentation and may therefore not be identified as the causative agent of tuberculosis. Use of whole genome sequencing (WGS) in the investigation of a family microepidemic of tuberculosis in Almería, Spain, unexpectedly identified the involvement of M. caprae.AimWe aimed to evaluate the presence of additional unidentified M. caprae cases and to determine the magnitude of this occurrence.MethodsFirst-line characterisation of the MTBC isolates was done by MIRU-VNTR, followed by WGS. Human and animal M. caprae isolates were integrated in the analysis.ResultsA comprehensive One Health strategy allowed us to (i) detect other 11 M. caprae infections in humans in a period of 18 years, (ii) systematically analyse M. caprae infections on an epidemiologically related goat farm and (iii) geographically expand the study by including 16 M. caprae isolates from other provinces. Integrative genomic analysis of 41 human and animal M. caprae isolates showed a high diversity of strains. The animal isolates' diversity was compatible with long-term infection, and close genomic relationships existed between isolates from goats on the farm and recent cases of M. caprae infection in humans.DiscussionZoonotic circulation of M. caprae strains had gone unnoticed for 18 years. Systematic characterisation of MTBC at species level and/or extended investigation of the possible sources of exposure in all tuberculosis cases would minimise the risk of overlooking similar zoonotic events.
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