Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 9, Number 2—February 2003
Letter

Streptomyces bikiniensis Bacteremia

On This Page
Article Metrics
12
citations of this article
EID Journal Metrics on Scopus

Cite This Article

To the Editor: Carey et al. recently reported in this journal a case of catheter-related bacteremia attributed to Streptomyces in a patient receiving holistic infusions (1). We describe the isolation of Streptomyces bikiniensis from multiple blood cultures in a single patient over the course of 1 week, further illustrating that Streptomyces is pathogenic and a cause of bacteremia even in the absence of overt clinical symptoms and risk factors.

A 14-year-old girl with osteosarcoma of the right proximal tibia came to our hospital 13 months after diagnosis for her final course of chemotherapy. At the time of diagnosis, a double-lumen central venous catheter was inserted. Her course was complicated by poor response to chemotherapy, and a limb salvage procedure was performed 3 months after diagnosis. The proximal tibia was replaced with a cadaveric bone graft. Several hours after the patient received methotrexate, a fever of 39.2°C developed. No sign of infection was observed on physical examination. Her leukocyte count was 6,300 cells/mm3 with an absolute neutrophil count of 4,914 cells/mm3. She received a single dose of acetaminophen and was without fever for the remainder of her hospitalization. A blood culture obtained from the central venous catheter at the time of fever grew Streptomyces. Repeat blood cultures obtained from both ports of the central venous catheter on day 3 and a peripheral blood culture obtained on day 4 also grew Streptomyces. Treatment with vancomycin and cotrimoxazole was started on day 4 in the hospital. The Streptomyces isolate was susceptible to vancomycin, amikacin, cotrimoxazole, erythromycin, cephazolin, and tetracycline and was resistant to ampicillin, penicillin, oxacillin, and clindamycin. A blood culture drawn from the central venous catheter on day 3 of antibiotic therapy (the 6th day in the hospital) grew Streptomyces after 9 days of incubation. All subsequent blood cultures were without growth. The central venous catheter was removed, and the patient received vancomycin intravenously for 6 weeks, without recurrence of Streptomyces bacteremia.

The bone graft was considered a potential source of infection. As most cases of disease from Streptomyces occur in the tropics, we requested information on whether the donor traveled or resided outside the United States. However, the donor had no history of travel outside the United States. All cultures taken from the donor and the graft were without growth (although this did not exclude the graft as the source of infection), and no reports of disease transmission were received from any other recipients of organs from this donor. In addition, the patient had no history of receiving infusions of holistic or alternative medicines.

The organism was initially detected in the aerobic Bact/Alert blood culture system (bioMérieux, Inc., Durham, NC) after 72 h incubation at 35°C. Presumptive identification of the pleomorphic gram-positive bacillus as Streptomyces sp. was based on phenotypic characterization by using standard conventional tests and cellular fatty acid analysis. Species identification was determined by DNA sequencing of the 16S rRNA gene. DNA sequencing reactions were performed with the Tag Dye Deoxy Terminator Cycle Sequencing Kit (Applied Biosystems, Inc., Foster City, CA), and data were generated with an ABI 377 automated instrument. The sequence data were assembled, edited, and compared with published sequences for the 16S rRNA gene of S. bikiniensis (2).

The genus Streptomyces belongs to the order Actinomycetales, which includes Mycobacterium, Nocardia, and Actinomyces. Streptomyces are gram-positive, extensively branched, filamentous bacteria that form aerial hyphae with chains of spores. Their natural habitat is soil, and each species has a defined geographic distribution. None are common in the United States. With the exception of specimens from actinomycotic mycetoma, the isolation of Streptomyces from clinical specimens frequently is considered laboratory contamination (3). Rare cases of clinical disease attributed to Streptomyces have been published, including bloodstream infection (1,4) and focal invasive infections (59). Streptomyces was not the only potential pathogen isolated from some of the clinical specimens in these studies.

Scant data are available on effective treatment of Streptomyces infection. Mycetoma caused by Streptomyces is often treated with penicillin, sulfonamides, or tetracycline; however, the cure rate is low. The recommended duration of therapy is lengthy (up to 10 months). Isolates of S. griseus referred to the Centers for Disease Control and Prevention were frequently resistant to ampicillin (80%), sulfamethoxazole (43%), cotrimoxazole (29%), and ciprofloxacin (57%) (10). Resistance to doxycycline (19%) and minocycline (10%) was lower. Vancomycin susceptibility was not tested. Resistance patterns must be interpreted cautiously because Streptomyces can synthesize antibiotics, potentially confounding results of in-vitro susceptibility testing.

The patient described in this report had no signs or symptoms of infection. The transient fever that prompted the first blood culture was probably due to the methotrexate infusion and not infection with S. bikiniensis. That the fever was of short duration despite persistently positive blood cultures supports this conclusion. The potential for causing minimal symptoms may contribute to assignment of Streptomyces as a contaminant. Clinical correlation is difficult if the infection is silent. Streptomyces isolated from blood cultures should not be dismissed as contaminants without careful consideration of the clinical situation; the isolation of Streptomyces from repeat blood cultures strongly suggests a pathogenic role.

Top

William J. Moss*Comments to Author , Jason A. Sager*, James D. Dick*, and Andrea Ruff*
Author affiliations: *Johns Hopkins University, Baltimore, Maryland

Top

References

  1. Carey  J, Motyl  M, Perlman  DC. Catheter-related bacteremia due to Streptomyces in a patient receiving holistic infusions. Emerg Infect Dis. 2001;7:10435. DOIPubMedGoogle Scholar
  2. Maidak  BL, Cole  JR, Parker  CT Jr, Garrity  GM, Larsen  N, Li  B, A new version of the RDP (Ribosomal Database Project). Nucleic Acids Res. 1999;27:1713. DOIPubMedGoogle Scholar
  3. McNeil  MM, Brown  JM. The medically important aerobic actinomycetes: epidemiology and microbiology. Clin Microbiol Rev. 1994;7:357417.PubMedGoogle Scholar
  4. Kohn  PM, Tager  M, Siegel  ML, Ashe  R. Aerobic Actinomyces septicemia. N Engl J Med. 1951;245:6404.PubMedGoogle Scholar
  5. Clarke  PRP, Warnock  GBR, Blowers  R, Wilkinson  M. Brain abscess due to Streptomyces griseus. J Neurol Neurosurg Psychiatry. 1964;27:5535. DOIPubMedGoogle Scholar
  6. Cantwell  AR Jr, Craggs  E, Swatek  F, Wilson  JW. Unusual acid-fast bacteria in panniculitis. Arch Dermatol. 1966;94:1617. DOIPubMedGoogle Scholar
  7. Shanley  JD, Snyder  K, Child  JS. Chronic pericarditis due to a Streptomyces species. Am J Clin Pathol. 1979;72:10710.PubMedGoogle Scholar
  8. Mossad  SB, Tomford  JW, Stewart  R, Ratliff  NB, Hall  GS. Case report of Streptomyces endocarditis of a prosthetic aortic valve. J Clin Microbiol. 1995;33:33357.PubMedGoogle Scholar
  9. Dunne  EF, Burman  WJ, Wilson  MJ. Streptomyces pneumonia in a patient with the human immunodeficiency virus infection: case report and review of the literature on invasive Streptomyces infectious. Clin Infect Dis. 1998;27:936. DOIPubMedGoogle Scholar
  10. McNeil  MM, Brown  JM, Jarvis  WR, Ajello  L. Comparison of species distribution and antimicrobial susceptibility of aerobic actinomycetes from clinical specimens. Rev Infect Dis. 1990;12:77883.PubMedGoogle Scholar

Top

Cite This Article

DOI: 10.3201/eid0902.020275

Related Links

Top

Table of Contents – Volume 9, Number 2—February 2003

Comments

Please use the form below to submit correspondence to the authors or contact them at the following address:

William J. Moss, Department of International Health, 615 North Wolfe Street, Baltimore, MD 21205, USA; fax: 410-502-6733

Send To

10000 character(s) remaining.

Top

Page created: December 07, 2010
Page updated: December 07, 2010
Page reviewed: December 07, 2010
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
file_external