Journal of Clinical Microbiology, March 2005, p. 1051-1058, Vol. 43, No. 3
0095-1137/05/$08.00+0 doi:10.1128/JCM.43.3.1051-1058.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Identification of Mycobacterium Species by secA1 Sequences
Adrian M. Zelazny,
Leslie B. Calhoun,
Li Li,
Yvonne R. Shea, and
Steven H. Fischer*
Microbiology Service, Department of Laboratory Medicine, Warren G. Magnuson Clinical Center, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland
Received 8 September 2004/
Returned for modification 27 September 2004/
Accepted 5 November 2004
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.
* Corresponding author. Mailing address: CC/DLM/Microbiology Service, Bldg. 10, Rm. 2C-385, National Institutes of Health, 10 Center Dr., MSC 1508, Bethesda, MD 20892-1508. Phone: (301) 496-4433. Fax: (301) 402-1886. E-mail: sfischer{at}cc.nih.gov.
Journal of Clinical Microbiology, March 2005, p. 1051-1058, Vol. 43, No. 3
0095-1137/05/$08.00+0 doi:10.1128/JCM.43.3.1051-1058.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Gomila, M., Ramirez, A., Lalucat, J.
(2007). Diversity of Environmental Mycobacterium Isolates from Hemodialysis Water as Shown by a Multigene Sequencing Approach. Appl. Environ. Microbiol.
73: 3787-3797
[Abstract]
[Full Text]
-
Xiong, L., Kong, F., Yang, Y., Cheng, J., Gilbert, G. L.
(2006). Use of PCR and Reverse Line Blot Hybridization Macroarray Based on 16S-23S rRNA Gene Internal Transcribed Spacer Sequences for Rapid Identification of 34 Mycobacterium Species.. J. Clin. Microbiol.
44: 3544-3550
[Abstract]
[Full Text]
-
Conville, P. S., Zelazny, A. M., Witebsky, F. G.
(2006). Analysis of secA1 Gene Sequences for Identification of Nocardia Species.. J. Clin. Microbiol.
44: 2760-2766
[Abstract]
[Full Text]
-
Adekambi, T., Stein, A., Carvajal, J., Raoult, D., Drancourt, M.
(2006). Description of Mycobacterium conceptionense sp. nov., a Mycobacterium fortuitum Group Organism Isolated from a Posttraumatic Osteitis Inflammation. J. Clin. Microbiol.
44: 1268-1273
[Abstract]
[Full Text]
-
Adekambi, T., Berger, P., Raoult, D., Drancourt, M.
(2006). rpoB gene sequence-based characterization of emerging non-tuberculous mycobacteria with descriptions of Mycobacterium bolletii sp. nov., Mycobacterium phocaicum sp. nov. and Mycobacterium aubagnense sp. nov.. Int. J. Syst. Evol. Microbiol.
56: 133-143
[Abstract]
[Full Text]
Copyright © 2005 by the American Society for Microbiology. All rights reserved.