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Journal of Clinical Microbiology, July 2007, p. 2257-2259, Vol. 45, No. 7
0095-1137/07/$08.00+0     doi:10.1128/JCM.00133-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Organisms Designated as Nocardia asteroides Drug Pattern Type VI Are Members of the Species Nocardia cyriacigeorgica{triangledown}

Patricia S. Conville* and Frank G. Witebsky

Microbiology Service, Department of Laboratory Medicine, Warren G. Magnuson Clinical Center, National Institutes of Health, U.S. Department of Health and Human Services, 10 Center Drive, MSC 1508, Bethesda, Maryland 20892-1508

Received 18 January 2007/ Returned for modification 12 April 2007/ Accepted 24 April 2007


   ABSTRACT
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Nocardia cyriacigeorgica has recently been described as an "emerging" pathogen. However, DNA-DNA hybridization results confirm that Nocardia asteroides drug pattern type VI, which has long been recognized as a common and significant pathogen in the United States, belongs to the species N. cyriacigeorgica.


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Nocardia cyriacigeorgica has recently been described as a "new" species of Nocardia capable of causing disease in humans (24). The type strain of the species was recovered from bronchial secretions of a patient with chronic bronchitis. 16S rRNA gene sequencing showed this isolate to be distinct from 17 validly described species of Nocardia; DNA-DNA hybridization showed it to be unrelated to N. abscessus (presumably DSM 44432T) (45% reassociation) and to the Nocardia asteroides type strain (presumably ATCC 19247T) (61% reassociation) (24).

In 1988, Wallace et al. described variations in the drug susceptibility patterns of 78 isolates determined biochemically to be N. asteroides (22). Most of these 78 isolates fell into one of six different susceptibility patterns; an additional miscellaneous drug pattern group included the type strain of N. asteroides (ATCC 19247T). Based largely on molecular testing, members of drug pattern types I, III, and V have subsequently been determined to belong to N. abscessus, N. nova, and N. farcinica, respectively. In the 1988 study of Wallace et al., isolates determined to belong to N. asteroides drug pattern type VI showed resistance to the penicillins and susceptibility to the broad-spectrum cephalosporins. N. asteroides drug pattern type VI has not been assigned a distinct species name; ATCC 14759 has been designated a reference strain for this drug pattern group (20).

Recently, several authors have noted the genetic similarity of N. cyriacigeorgica and N. asteroides drug pattern type VI, by using sequence analysis of the 16S rRNA gene (2, 6, 7, 16, 18) and the 65-kDa heat shock protein (HSP) gene (17), and have commented that these may in fact be the same species. To our knowledge, conclusive information concerning the conspecificity of these organisms, as determined by DNA-DNA hybridization, has not been reported.

We report here the results of sequence analysis and DNA-DNA hybridization tests of the reference strain of N. asteroides drug pattern type VI and the type strain of N. cyriacigeorgica.

Organisms. The reference strain of N. asteroides drug pattern type VI (ATCC 14759) and the type strain of N. cyriacigeorgica (DSM 44484T) were examined in this study.

Molecular methods. DNA was extracted for amplification and gene sequencing, as previously described (8). Sequencing of the 16S rRNA gene, the HSP gene, and the secA1 gene was performed as previously described (7, 8, 10). The deduced amino acid sequences of the HSP and secA1 genes for both isolates were determined with Megalign software (DNA Star, Inc., Madison, WI). Genomic DNA was extracted from both organisms, and DNA-DNA hybridization was performed as previously described (3, 4, 9). DNA-DNA hybridization was performed twice with N. cyriacigeorgica as the source of the labeled DNA and once with N. asteroides drug pattern type VI as the source of the labeled DNA. All reactions were performed in duplicate at 70°C. The relative binding ratio (RBR) [(percentage of heterologous DNA bound to hydroxyapatite/percentage of homologous DNA bound to hydroxyapatite) x 100] was calculated by the method of Brenner et al. (3). The percent divergence (calculated to the nearest 0.5%) was determined by assuming that each degree of heteroduplex instability, compared to the melting temperature of the homologous duplex, was caused by 1% unpaired bases (3).

Sequence analysis of 1,384-bp regions of the 16S rRNA gene showed the reference strain of N. asteroides drug pattern type VI to be identical to the type strain of N. cyriacigeorgica. The HSP gene sequence of N. asteroides drug pattern type VI shows 99.5% sequence similarity to that of N. cyriacigeorgica, with two base differences in a 373-bp region. The deduced amino acid sequences of the HSPs of the two organisms were identical. Comparison of a 465-bp region of the secA1 gene showed the two organisms to have 99.1% sequence similarity (four base differences); a similarity of >99.0% with this gene has been shown to indicate species identity (10). The deduced amino acid sequence of the SecA1 protein of N. asteroides drug pattern type VI was identical to that of N. cyriacigeorgica. DNA-DNA hybridization studies showed the organisms to be related, with an RBR of greater than or equal to 76.0 and percent divergence of less than or equal to 3.5 (Table 1). These values are well within the ranges established for species identity (19, 23). Thus, by currently accepted standards, N. cyriacigeorgica and isolates described as N. asteroides drug pattern type VI belong to the same species.


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  		TABLE 1. DNA relatedness of the reference strain of N. asteroides drug pattern type VI (ATCC 14759) to N. cyriacigeorgica (DSM 44484T)

 
Species formerly referred to as the "N. asteroides complex" are a heterogeneous group of organisms that are generally nonreactive on hydrolysis media and show few differences in other biochemical characteristics (5, 18). Numerous authors studying the similarities of isolates of "N. asteroides" have noted variations in susceptibility to various antibiotics (12, 13, 22) and in cell wall fatty acid components (15). Sequence analyses of "N. asteroides" isolates have confirmed the heterogeneity of isolates formerly assigned to this species and now formally designated distinct species (18).

Isolates belonging to N. asteroides drug pattern type VI are similar to each other in susceptibility to amikacin, cefamandole, cefotaxime, ceftriaxone, and imipenem and resistance to amoxicillin-clavulanic acid, ampicillin, ciprofloxacin, clarithromycin, and erythromycin (5). This organism, now named N. cyriacigeorgica, appears to be a common pathogen worldwide. In the 1988 study by Wallace et al., isolates belonging to N. asteroides drug pattern type VI comprised 35% of the 78 "N. asteroides" isolates examined. Since then, organisms of this type have been described as the most commonly isolated drug pattern type of "N. asteroides" in the southern United States (5). N. cyriacigeorgica is similarly described as a frequently isolated species in Japan (10% of 303 Nocardia isolates) and in Thailand (23.5% of 96 Nocardia isolates), as determined by chemotaxonomic and phenotypic methods. Using sequence analysis, an additional study of 121 isolates identified as "N. asteroides" from Japan and Thailand showed 27 of these isolates (22.3%) to have 16S rRNA gene sequences identical to that of the type strain of N. cyriacigeorgica. In addition, isolates of N. cyriacigeorgica have been identified by 16S rRNA gene sequence analysis from patients with disseminated disease in Canada, France, Greece, The Netherlands, and Turkey (1, 2, 11, 14, 21).

N. cyriacigeorgica, therefore, is not a "new" organism or an "emerging" pathogen; rather, it is a newly named but long-recognized agent of human disease.


   ACKNOWLEDGMENTS
 
We thank Patrick R. Murray, Department of Laboratory Medicine, Warren G. Magnuson Clinical Center, NIH, for critically reviewing the manuscript.

This research was supported by the Intramural Research Program of the NIH Warren G. Magnuson Clinical Center.

The views expressed herein are those of the authors and should not be construed as those of the U.S. Department of Health and Human Services.


   FOOTNOTES
 
* Corresponding author. Mailing address: Microbiology Service, Department of Laboratory Medicine, Warren G. Magnuson Clinical Center, National Institutes of Health, 10 Center Drive, MSC 1508, Bethesda, MD 20892-1508. Phone: (301) 496-4433. Fax: (301) 402-1886. E-mail: pconville{at}nih.gov Back

{triangledown} Published ahead of print on 2 May 2007. Back


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Journal of Clinical Microbiology, July 2007, p. 2257-2259, Vol. 45, No. 7
0095-1137/07/$08.00+0     doi:10.1128/JCM.00133-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



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