Abstract
Nocardia brasiliensis, the second most frequently isolated aerobic actinomycete in the clinical laboratory, is usually associated with localized cutaneous infections. However, 22% of 238 N. brasiliensis isolates from the United States and 12% of 66 isolates from Queensland, Australia, which had been collected over a 17-year period, were associated with extracutaneous and/or disseminated diseases. Of the 62 invasive isolates, 37 (60%) were susceptible to ciprofloxacin and/or were susceptible to clarithromycin and resistant to minocycline, compared with only 6 (3%) of 242 localized cutaneous isolates. The 43 isolates with this susceptibility pattern appeared to define a new taxon. They were similar to Nocardia asteroides complex isolates clinically in proportions from persons with pulmonary (70%), central nervous system (23%), and/or disseminated diseases (37%) in the setting of corticosteroids (74%) or AIDS (14%). This putative new taxon differed from N. brasiliensis in the hydrolysis of adenine (92 versus 4%), beta-lactamase patterns on isoelectric focusing, and the presence of two early mycolic acid-ester peaks by high-performance liquid chromatography. Restriction analysis of a 439-bp fragment of the 65-kDa heat shock protein gene revealed that N. brasiliensis and the new taxon had different restriction patterns with 8 of the 11 enzymes tested. Screening of invasive isolates of N. brasiliensis for susceptibility to ciprofloxacin will identify most isolates of the new taxon, which likely represents a new Nocardia species.
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- Arduino R. C., Johnson P. C., Miranda A. G. Nocardiosis in renal transplant recipients undergoing immunosuppression with cyclosporine. Clin Infect Dis. 1993 Apr;16(4):505–512. doi: 10.1093/clind/16.4.505. [DOI] [PubMed] [Google Scholar]
- Beaman B. L., Beaman L. Nocardia species: host-parasite relationships. Clin Microbiol Rev. 1994 Apr;7(2):213–264. doi: 10.1128/cmr.7.2.213. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Beaman B. L., Burnside J., Edwards B., Causey W. Nocardial infections in the United States, 1972-1974. J Infect Dis. 1976 Sep;134(3):286–289. doi: 10.1093/infdis/134.3.286. [DOI] [PubMed] [Google Scholar]
- Berd D. Nocardia brasiliensis infection in the United States: a report of nine cases and a review of the literature. Am J Clin Pathol. 1973 Aug;60(2):254–258. doi: 10.1093/ajcp/60.2.254. [DOI] [PubMed] [Google Scholar]
- Butler W. R., Jost K. C., Jr, Kilburn J. O. Identification of mycobacteria by high-performance liquid chromatography. J Clin Microbiol. 1991 Nov;29(11):2468–2472. doi: 10.1128/jcm.29.11.2468-2472.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Butler W. R., Kilburn J. O., Kubica G. P. High-performance liquid chromatography analysis of mycolic acids as an aid in laboratory identification of Rhodococcus and Nocardia species. J Clin Microbiol. 1987 Nov;25(11):2126–2131. doi: 10.1128/jcm.25.11.2126-2131.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Koll B. S., Brown A. E., Kiehn T. E., Armstrong D. Disseminated Nocardia brasiliensis infection with septic arthritis. Clin Infect Dis. 1992 Sep;15(3):469–472. doi: 10.1093/clind/15.3.469. [DOI] [PubMed] [Google Scholar]
- Lampe R. M., Baker C. J., Septimus E. J., Wallace R. J., Jr Cervicofacial nocardiosis in children. J Pediatr. 1981 Oct;99(4):593–595. doi: 10.1016/S0022-3476(81)80266-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lungu O., Della Latta P., Weitzman I., Silverstein S. Differentiation of Nocardia from rapidly growing Mycobacterium species by PCR-RFLP analysis. Diagn Microbiol Infect Dis. 1994 Jan;18(1):13–18. doi: 10.1016/0732-8893(94)90128-7. [DOI] [PubMed] [Google Scholar]
- McNeil M. M., Brown J. M. The medically important aerobic actinomycetes: epidemiology and microbiology. Clin Microbiol Rev. 1994 Jul;7(3):357–417. doi: 10.1128/cmr.7.3.357. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mishra S. K., Gordon R. E., Barnett D. A. Identification of nocardiae and streptomycetes of medical importance. J Clin Microbiol. 1980 Jun;11(6):728–736. doi: 10.1128/jcm.11.6.728-736.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Plikaytis B. B., Plikaytis B. D., Yakrus M. A., Butler W. R., Woodley C. L., Silcox V. A., Shinnick T. M. Differentiation of slowly growing Mycobacterium species, including Mycobacterium tuberculosis, by gene amplification and restriction fragment length polymorphism analysis. J Clin Microbiol. 1992 Jul;30(7):1815–1822. doi: 10.1128/jcm.30.7.1815-1822.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smego R. A., Jr, Gallis H. A. The clinical spectrum of Nocardia brasiliensis infection in the United States. Rev Infect Dis. 1984 Mar-Apr;6(2):164–180. doi: 10.1093/clinids/6.2.164. [DOI] [PubMed] [Google Scholar]
- Steingrube V. A., Wallace R. J., Jr, Brown B. A., Pang Y., Zeluff B., Steele L. C., Zhang Y. Acquired resistance of Nocardia brasiliensis to clavulanic acid related to a change in beta-lactamase following therapy with amoxicillin-clavulanic acid. Antimicrob Agents Chemother. 1991 Mar;35(3):524–528. doi: 10.1128/aac.35.3.524. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Steingrube V. A., Wallace R. J., Jr, Brown B. A., Zhang Y., Steele L. C., Young G., Nash D. R. Partial characterization of Nocardia farcinica beta-lactamases. Antimicrob Agents Chemother. 1993 Sep;37(9):1850–1855. doi: 10.1128/aac.37.9.1850. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Telenti A., Marchesi F., Balz M., Bally F., Böttger E. C., Bodmer T. Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysis. J Clin Microbiol. 1993 Feb;31(2):175–178. doi: 10.1128/jcm.31.2.175-178.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wallace R. J., Jr, Brown B. A., Tsukamura M., Brown J. M., Onyi G. O. Clinical and laboratory features of Nocardia nova. J Clin Microbiol. 1991 Nov;29(11):2407–2411. doi: 10.1128/jcm.29.11.2407-2411.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wallace R. J., Jr, Nash D. R., Johnson W. K., Steele L. C., Steingrube V. A. Beta-lactam resistance in Nocardia brasiliensis is mediated by beta-lactamase and reversed in the presence of clavulanic acid. J Infect Dis. 1987 Dec;156(6):959–966. doi: 10.1093/infdis/156.6.959. [DOI] [PubMed] [Google Scholar]
- Wallace R. J., Jr, Septimus E. J., Williams T. W., Jr, Conklin R. H., Satterwhite T. K., Bushby M. B., Hollowell D. C. Use of trimethoprim-sulfamethoxazole for treatment of infections due to Nocardia. Rev Infect Dis. 1982 Mar-Apr;4(2):315–325. doi: 10.1093/clinids/4.2.315. [DOI] [PubMed] [Google Scholar]
- Wallace R. J., Jr, Steele L. C., Sumter G., Smith J. M. Antimicrobial susceptibility patterns of Nocardia asteroides. Antimicrob Agents Chemother. 1988 Dec;32(12):1776–1779. doi: 10.1128/aac.32.12.1776. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wallace R. J., Jr, Steele L. C. Susceptibility testing of Nocardia species for the clinical laboratory. Diagn Microbiol Infect Dis. 1988 Mar;9(3):155–166. doi: 10.1016/0732-8893(88)90025-9. [DOI] [PubMed] [Google Scholar]
- Wallace R. J., Jr, Tsukamura M., Brown B. A., Brown J., Steingrube V. A., Zhang Y. S., Nash D. R. Cefotaxime-resistant Nocardia asteroides strains are isolates of the controversial species Nocardia farcinica. J Clin Microbiol. 1990 Dec;28(12):2726–2732. doi: 10.1128/jcm.28.12.2726-2732.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wallace R. J., Jr, Wiss K., Curvey R., Vance P. H., Steadham J. Differences among Nocardia spp. in susceptibility to aminoglycosides and beta-lactam antibiotics and their potential use in taxonomy. Antimicrob Agents Chemother. 1983 Jan;23(1):19–21. doi: 10.1128/aac.23.1.19. [DOI] [PMC free article] [PubMed] [Google Scholar]