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Microbiology 145 (1999), 2519-2526
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Microbiology (1999), 145, 2519-2526.
© 1999 Society for General Microbiology


Genetics and Molecular Biology

Molecular characterization of mycobacteria isolated from seals

M. J. Zumárraga1, A. Bernardell2, R. Bastida3, V. Quse3, J. Loureiro3, A. Cataldi1, F. Bigi1, A. Alito1, M. Castro Ramos4, S. Samper5, I. Otal5, C. Martin5 and M. I. Romano1

Instituto de Biotecnología, CICV/INTA, Buenos Aires, Argentina1
Departamento de Micobacterias, DILAB SENASA, C. C. 77 Morón (1708), Buenos Aires, Argentina2
Fundación Mundo Marino, San Clemente del Tuyú, Argentina3
Laboratorio de Tuberculosis de la Dirección de Laboratorios Veterinarios (DILAVE) ‘Miguel C. Rubino’, Montevideo, Uruguay4
Departamento de Microbiología, Salud Pública y Medicina Preventiva, Facultad de Medicina, Universidad de Zaragoza, Zaragoza, Spain5

Author for correspondence: M. I. Romano. Tel: +54 1 621 1447. Fax: +54 1 481 2975. e-mail: mromano{at}cicv.inta.gov.ar

Tuberculosis (TB) was diagnosed in 10 seals from three species (Arctocephalus australis, Arctocephalus tropicalis and Otaria flavescens) found in South America. The mycobacteria isolated from these cases belonged to the Mycobacterium tuberculosis complex, as determined by RFLP using an IS6110 probe, spoligotyping, analysis of the 16S rRNA gene sequence and by PCR-restriction analysis of hsp65. Polymorphisms in gyrA, katG, oxyR and pncA were investigated in some of the isolates, as well as the presence of the MPB70 antigen. The insertion sequence IS6110 was present in three to seven copies in the genome of the mycobacteria isolated from seals. Using the IS6110 probe, six patterns (designated A, B, C, D, E and F) were identified from 10 different isolates. Patterns A and B were found for the mycobacteria isolated from two and four seals, respectively, indicating an epidemiological relationship between isolates grouped according to their IS6110 RFLP. The mycobacteria isolated from seals shared the majority of their IS6110 DNA-containing restriction fragments, and nine isolates had an identical spoligotype; only one isolate showed a minor difference in its spoligotype. In addition, none of these spoligotypes were found in other M. tuberculosis complex strains. These results suggest that the isolates from seals constitute a unique group of closely related strains. The mycobacteria isolated from seals showed polymorphisms at gyrA codon 95 and katG codon 463, as do group 1 M. tuberculosis, and M. bovis. Group 1 mycobacteria are associated with cluster cases. The spoligotypes found in the mycobacteria isolated from seals lack spacers 39–43, as does M. bovis, but the MPB70 antigen, which is highly expressed in M. bovis and minimally expressed in M. tuberculosis, was not detected in these mycobacteria. The mycobacteria isolated from seals also showed oxyR and pncA polymorphisms specific to M. tuberculosis. In conclusion, the mycobacteria that cause TB in seals in the South-Western Atlantic are a related group, and based on the combination of genetic characteristics, belong to a unique genotypic group within the M. tuberculosis complex.

Keywords: tuberculosis, Mycobacterium tuberculosis complex, spoligotyping, RFLP

Abbreviations: DR, direct repeat; PZA, pyrazinamide; Pzase, pyrazinamidase; TB, tuberculosis




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