Int J Syst Evol Microbiol 55 (2005), 1139-1147; DOI 10.1099/ijs.0.63343-0
© 2005 International Union of Microbiological Societies
Mycobacterium pseudoshottsii sp. nov., a slowly growing chromogenic species isolated from Chesapeake Bay striped bass (Morone saxatilis)
Martha W. Rhodes1,
Howard Kator1,
Alan McNabb2,
Caroline Deshayes3,
Jean-Marc Reyrat3,
Barbara A. Brown-Elliott4,
Richard Wallace, Jr4,
Kristin A. Trott5,
John M. Parker6,
Barry Lifland7,
Gerard Osterhout8,
Ilsa Kaattari1,
Kimberly Reece1,
Wolfgang Vogelbein1 and
Christopher A. Ottinger9
1 Virginia Institute of Marine Science, College of William and Mary, Gloucester Point, VA 23062, USA
2 Laboratory Services, British Columbia Centre for Disease Control, Vancouver BC, Canada V5Z 4R4
3 Avenir Group, Inserm U570, Avenir Group, Faculté de Médecine Necker-Enfants Malades, 75730 Paris Cedex 15, France
4 Mycobacteria/Nocardia Laboratory, University of Texas Health Center, Tyler, TX 75708, USA
5 Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA
6 Office of Laboratory Animal Care, University of California, Berkeley, CA 94720, USA
7 Department of Comparative Medicine, Stanford University, Stanford, CA 94305, USA
8 MIDI, Inc. Research and Development, Newark, DE 19713, USA
9 US Geological Survey, Leetown Science Center, National Fish Health Research Laboratory, Kearneysville, WV 25430, USA
Correspondence
Martha W. Rhodes
martha{at}vims.edu
A group of slowly growing photochromogenic mycobacteria was isolated from Chesapeake Bay striped bass (Morone saxatilis) during an epizootic of mycobacteriosis. Growth characteristics, acid-fastness and 16S rRNA gene sequencing results were consistent with those of the genus Mycobacterium. Biochemical reactions, growth characteristics and mycolic acid profiles (HPLC) resembled those of Mycobacterium shottsii, a non-pigmented mycobacterium also isolated during the same epizootic. Sequencing of the 16S rRNA genes, the gene encoding the exported repeated protein (erp) and the gene encoding the 65 kDa heat-shock protein (hsp65) and restriction enzyme analysis of the hsp65 gene demonstrated that this group of isolates is unique. Insertion sequences associated with Mycobacterium ulcerans, IS2404 and IS2606, were detected by PCR. These isolates could be differentiated from other slowly growing pigmented mycobacteria by their inability to grow at 37 °C, production of niacin and urease, absence of nitrate reductase, negative Tween 80 hydrolysis and resistance to isoniazid (1 µg ml1), p-nitrobenzoic acid, thiacetazone and thiophene-2-carboxylic hydrazide. On the basis of this polyphasic study, it is proposed that these isolates represent a novel species, Mycobacterium pseudoshottsii sp. nov. The type strain, L15T, has been deposited in the American Type Culture Collection as ATCC BAA-883T and the National Collection of Type Cultures (UK) as NCTC 13318T.
Published online ahead of print on 23 December 2004 as DOI 10.1099/ijs.0.63343-0.
The GenBank/EMBL/DDBJ accession numbers for the 16S rRNA and hsp65 gene sequences of Mycobacterium pseudoshottsii ATCC BAA-883T are AY570988 and AY571788, respectively.
Aligned erp gene sequences of Mycobacterium pseudoshottsii sp. nov., Mycobacterium marinum, Mycobacterium shottsii, Mycobacterium ulcerans and Mycobacterium tuberculosis are available as a supplementary figure in IJSEM Online.
This article has been cited by other articles:

|
 |

|
 |
 
C. M. Whipps, W. R. Butler, F. Pourahmad, V. G. Watral, and M. L. Kent
Molecular systematics support the revival of Mycobacterium salmoniphilum (ex Ross 1960) sp. nov., nom. rev., a species closely related to Mycobacterium chelonae
Int J Syst Evol Microbiol,
November 1, 2007;
57(11):
2525 - 2531.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. A. M. Fyfe, C. J. Lavender, P. D. R. Johnson, M. Globan, A. Sievers, J. Azuolas, and T. P. Stinear
Development and Application of Two Multiplex Real-Time PCR Assays for the Detection of Mycobacterium ulcerans in Clinical and Environmental Samples
Appl. Envir. Microbiol.,
August 1, 2007;
73(15):
4733 - 4740.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. Coutanceau, J. Decalf, A. Martino, A. Babon, N. Winter, S. T. Cole, M. L. Albert, and C. Demangel
Selective suppression of dendritic cell functions by Mycobacterium ulcerans toxin mycolactone
J. Exp. Med.,
June 11, 2007;
204(6):
1395 - 1403.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. J. Yip, J. L. Porter, J. A. M. Fyfe, C. J. Lavender, F. Portaels, M. Rhodes, H. Kator, A. Colorni, G. A. Jenkin, and T. Stinear
Evolution of Mycobacterium ulcerans and Other Mycolactone-Producing Mycobacteria from a Common Mycobacterium marinum Progenitor
J. Bacteriol.,
March 1, 2007;
189(5):
2021 - 2029.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
B. S. Ranger, E. A. Mahrous, L. Mosi, S. Adusumilli, R. E. Lee, A. Colorni, M. Rhodes, and P. L. C. Small
Globally Distributed Mycobacterial Fish Pathogens Produce a Novel Plasmid-Encoded Toxic Macrolide, Mycolactone F
Infect. Immun.,
November 1, 2006;
74(11):
6037 - 6045.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Sanguinetti, L. Novarese, B. Posteraro, S. Ranno, E. De Carolis, G. Pecorini, B. Lucignano, F. Ardito, and G. Fadda
Use of Microelectronic Array Technology for Rapid Identification of Clinically Relevant Mycobacteria
J. Clin. Microbiol.,
December 1, 2005;
43(12):
6189 - 6193.
[Abstract]
[Full Text]
[PDF]
|
 |
|
Copyright © 2005 by the International Union of Microbiological Societies.