Affiliation:
1. Microbiology Service, Department of Laboratory Medicine, Warren G. Magnuson Clinical Center, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland
Abstract
ABSTRACT
We describe a novel molecular method for the differentiation and identification of 29 mycobacterial species. The target is the
secA1
gene that codes for the essential protein SecA1, a key component of the major pathway of protein secretion across the cytoplasmic membrane. A 700-bp region of the
secA1
gene was amplified and sequenced from 47 American Type Culture Collection strains of 29
Mycobacterium
species as well as from 59 clinical isolates. Sequence variability in the amplified segment of the
secA1
gene allowed the differentiation of all species except for the members of the
Mycobacterium tuberculosis
(MTB) complex, which had identical sequences. A range of 83.3 to 100% interspecies similarity was observed. All species could also be differentiated by their amino acid sequences as deduced from the sequenced region of the
secA1
gene, with the exception of the MTB complex. Partial sequences of
secA1
from clinical isolates belonging to nine frequently isolated species of mycobacteria revealed a very high intraspecies similarity at the DNA level (typically >99%; range, 96.0 to 100%); all clinical isolates were correctly identified. Comparison of the deduced 233-amino-acid sequences among clinical isolates of the same species showed between 99.6 and 100% similarity. To our knowledge, this is the first time a secretion-related gene has been used for the identification of the species within a bacterial genus.
Publisher
American Society for Microbiology
Cited by
60 articles.
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