Affiliation:
1. Centre National de Référence des Mycobactéries, Institut Pasteur,1 and
2. Servicio de Microbiologı́a, Hospital Ramón y Cajal, Madrid, Spain2
3. Clinique de Réanimation des Maladies Infectieuses, Hôpital Bichat-Claude Bernard,3 Paris, France, and
Abstract
ABSTRACT
We genetically characterized multidrug-resistant
Mycobacterium tuberculosis
complex strains which caused a nosocomial outbreak of tuberculosis affecting six human immunodeficiency virus (HIV)-positive patients and one HIV-negative staff member (E. Bouvet, E. Casalino, G. Mendoza-Sassi, S. Lariven, E. Vallée, M. Pernet, S. Gottot, and F. Vachon, AIDS 7:1453–1460, 1993). The strains showed all the phenotypic characteristics of
Mycobacterium bovis
. They presented a high copy number of IS
6110
, the spacers 40 to 43 in the direct repeat locus, and the
mtp40
fragment. They lacked the G-A mutation at position 285 in the
oxyR
gene and the C-G mutation at position 169 in the
pncA
gene. These genetic characteristics revealed that these were dysgonic, slow-growing
M. tuberculosis
strains mimicking the
M. bovis
phenotype, probably as a consequence of cellular alterations associated with the multidrug resistance. Spoligotyping and IS
6110
restriction fragment length polymorphism (RFLP) analysis confirmed that the outbreak was due to a single strain. However, the IS
6110
RFLP pattern of the strain isolated from the last patient, diagnosed three years after the index case, differed slightly from the patterns of the other six strains. A model of a possible genetic event is presented to explain this divergence. This study stresses the value of using several independent molecular markers to identify multidrug-resistant tubercle bacilli.
Publisher
American Society for Microbiology
Cited by
22 articles.
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