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Case Reports in Urology
Volume 2012, Article ID 468516, 2 pages
Case Report

Actinobaculum schaalii: An Emerging Uropathogen?

1Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada V6T 2B5
2Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada V5Z 1M9

Received 20 December 2011; Accepted 26 February 2012

Academic Editors: R. Colgan, S. J. Hong, and M. Saito

Copyright © 2012 Peyman Tavassoli et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


A. schaalii is a rare uropathogen. We report urosepsis with Actinobaculum schaalii detected serendipitously in blood and urine culture in a 79-year-old with urinary tract obstruction. This paper illuminates the flaws in our current system in detecting A. schaalii and raises awareness among clinicians and laboratory teams.

1. Introduction

Actinobaculum schaalii is a small Gram-positive coccoid rod that requires CO2 for optimal growth. Also in the genus Actinobaculum are A. suis, A. urinale, and A. massiliense. A. suis is known to cause urinary tract infections (UTIs) in swine [1, 2] and human UTIs have been reported with A. urinale and A. massiliense [35]. A. schaalii, which is the focus of this paper, was first described as a cause of human UTIs in 1997, with subsequent reports [68]. Growing evidence suggests that A. schaalii may be a more common uropathogen in the elderly than previously reported, especially those with obstructive uropathy [713].

Most laboratories incubate urine cultures at 35°C in ambient air. Since A. schaalii grows slowly in aerobic conditions with no CO2 supplementation, this bacterium’s isolation and identification from urine specimens by standard laboratory methods is rare. Most laboratories do not look specifically for Actinobaculum species. Even if A. schaalii grows, this organism may be overlooked either because of overgrowth of common uropathogens or the bacteria’s resemblance to normal skin flora [7, 8, 11].

To address this problem, Bank et al. developed a TaqMan real-time quantitative PCR and assessed 252 clinical urine samples [9]. They found 22% of urine samples were positive for A. schaalii in the over 60-year-old patient population, whilst only 7% of samples were positive in the less than 60-year-old cohort [9]. Using the same diagnostic technique in a cohort of patients with kidney stones, they showed that more than 24% of urine samples were positive for A. schaalii, which was the only pathogen in more than 60% of those patients [13].

2. Case Report

A 79-year-old man with a previous history of nephrolithiasis and benign prostatic hyperplasia was admitted with fever, chills, nausea, vomiting, and diarrhea. On presentation, he had an elevated leukocyte count of 17.2 × 103 cells/μL (90% neutrophils) and an elevated creatinine and lactate (155 μmol/L and 2.6 mmol/L, resp.). His initial urinalysis tested positive for blood and leukocytes. An ultrasound of the left kidney showed left hydronephrosis and an obstructing stone in the left ureter. Empiric parenteral therapy with piperacillin-tazobactam was initiated and subsequently a left nephrostomy tube was placed. However, his condition deteriorated and the patient was transferred to the intensive care unit (ICU). A repeat urinalysis revealed 4+ polymorphonuclear cells, 4+ Gram-positive bacilli and was negative for nitrate. The initial urine culture was negative; however, an astute laboratory technologist noticed the discrepancy between the Gram-stain and the culture results. In consultation with the microbiologist, the technologist repeated the urine culture, including an anaerobic incubation. On repeat culture, the patient’s urine culture grew 10 million CFU/L of a possible anaerobic Gram-positive bacillus with the blood culture also growing anaerobic Gram-positive bacilli. Due to the unusual nature of the cultures in this urosepsis patient, the samples were sent to the reference laboratory for microorganism identification. A. schaalii was identified from blood culture. Although the care providers were informed upon initial Gram-positive bacilli observation on smear, the final bacterial identification result was released 12 days after specimen receipt. Fortunately, A. schaalii is usually sensitive to pip-tazo and the patient became stable following a short stay in ICU. Subsequently, the patient’s stone was unsuccessfully treated with extracorporeal shock wave lithotripsy (ESWL) and later definitively treated with an ureteroscopy and laser lithotripsy.

3. Discussion

A. schaalii is an emerging uropathogen mainly in elderly patients or patients with underlying urologic disease [7, 9, 13]. Although there are a few reports of nonurological infections [14, 15], the spectrum of infection primarily ranges from benign cystitis to severe pyelonephritis with urosepsis. A. schaalii has been reported in both inpatient and outpatient populations, either as an isolated organism or associated with other common uropathogens [811, 13]. Unfortunately, our routine laboratory methods will not identify A. schaalii from urine specimens as this bacterium requires CO2 and has sluggish growth in comparison to common uropathogens. For this reason, A. schaalii is identified from the blood rather than from the urine in 30% of identified cases [11].

Urologists are recommended to notify the laboratory if they are concerned about urinary infection with an unusual organism such as A. schaalii, based on risk factors or conflicting laboratory results. Accordingly, conventional laboratory methods must be modified to isolate A. schaalii from specimens upon such requests. In addition, laboratories should also consider A. schaalii as an etiology for UTI once there is no growth from the urine specimen, despite the presence of Gram-positive coccoid rods and/or leukocytes present on the urinalysis.

Another important issue relates to the susceptibility profile of A. schaalii is that it retains susceptibility to penicillins, 3rd generation cephalosporins, aminoglycosides, and nitrofurantoin. However, this organism is mainly resistant to ciprofloxacin and trimethoprim/sulfamethoxazole [11, 12], two commonly employed antibiotics in urology patients. To our knowledge, all of the A. schaalii reports and studies have been carried out in Europe with the exception of a single case report from North America [16]. Therefore, most of our clinicians are not aware of this potential uropathogen. We believe that a well-designed multicenter study is required to find out the prevalence and incidence of A. schaalii.


  1. R. L. Walker and N. J. MacLachlan, “Isolation of Eubacterium suis from sows with cystitis,” Journal of the American Veterinary Medical Association, vol. 195, no. 8, pp. 1104–1107, 1989. View at Google Scholar · View at Scopus
  2. B. Yamini and R. F. Slocombe, “Porcine abortion caused by Actinomyces suis,” Veterinary Pathology, vol. 25, no. 4, pp. 323–324, 1988. View at Google Scholar · View at Scopus
  3. G. Greub and D. Raoult, “Actinobaculum massiliae, a new species causing chronic urinary tract infection,” Journal of Clinical Microbiology, vol. 40, no. 11, pp. 3938–3941, 2002. View at Publisher · View at Google Scholar · View at Scopus
  4. F. Fendukly and B. Osterman, “Isolation of Actinobaculum schaalii and Actinobaculum urinale from a patient with chronic renal failure,” Journal of Clinical Microbiology, vol. 43, no. 7, pp. 3567–3569, 2005. View at Publisher · View at Google Scholar · View at Scopus
  5. V. Hall, M. D. Collins, R. A. Hutson, E. Falsen, E. Inganäs, and B. I. Duerden, “Actinobaculum urinale sp. nov., from human urine,” International Journal of Systematic and Evolutionary Microbiology, vol. 53, no. 3, pp. 679–682, 2003. View at Publisher · View at Google Scholar · View at Scopus
  6. P. A. Lawson, E. Falsen, E. Åkervall, P. Vandamme, and M. D. Collins, “Characterization of some Actinomyces-like isolates from human clinical specimens: reclassification of Actinomyces suis (Soltys and Spratling) as Actinobaculum suis comb. nov. and description of Actinobaculum schaalii sp. nov,” International Journal of Systematic Bacteriology, vol. 47, no. 3, pp. 899–903, 1997. View at Google Scholar · View at Scopus
  7. S. Tschudin-Sutter, R. Frei, M. Weisser, D. Goldenberger, and A. F. Widmer, “Actinobaculum schaalii—invasive pathogen or innocent bystander? A retrospective observational study,” BMC Infectious Diseases, vol. 11, no. 1, article 289, 2011. View at Google Scholar
  8. M. Reinhard, J. Prag, M. Kemp et al., “Ten cases of Actinobaculum schaalii infection: clinical relevance, bacterial identification, and antibiotic susceptibility,” Journal of Clinical Microbiology, vol. 43, no. 10, pp. 5305–5308, 2005. View at Publisher · View at Google Scholar · View at Scopus
  9. S. Bank, A. Jensen, T. M. Hansen, K. M. Søby, and J. Prag, “Actinobaculum schaalii, a common uropathogen in elderly patients, Denmark,” Emerging Infectious Diseases, vol. 16, no. 1, pp. 76–80, 2010. View at Publisher · View at Google Scholar · View at Scopus
  10. H. L. Nielsen, K. M. Søby, J. J. Christensen, and J. Prag, “Actinobaculum schaalii: a common cause of urinary tract infection in the elderly population. Bacteriological and clinical characteristics,” Scandinavian Journal of Infectious Diseases, vol. 42, no. 1, pp. 43–47, 2010. View at Publisher · View at Google Scholar · View at Scopus
  11. C. Beguelin, D. Genne, A. Vara et al., “Actinobaculum schaalii: clinical observation of 20 cases,” Clinical Microbiology and Infection, vol. 17, no. 7, pp. 1027–1031, 2011. View at Publisher · View at Google Scholar · View at Scopus
  12. V. Cattoir, A. Varca, G. Greub, G. Prod'hom, P. Legrand, and R. Lienhard, “In vitro susceptibility of Actinobaculum schaalii to 12 antimicrobial agents and molecular analysis of fluoroquinolone resistance,” Journal of Antimicrobial Chemotherapy, vol. 65, no. 12, Article ID dkq383, pp. 2514–2517, 2010. View at Publisher · View at Google Scholar · View at Scopus
  13. S. Bank, T. M. Hansen, K. M. By, L. Lund, and J. R. Prag, “Actinobaculum schaalii in urological patients, screened with real-time polymerase chain reaction,” Scandinavian Journal of Urology and Nephrology, vol. 45, no. 6, pp. 406–410, 2011. View at Google Scholar
  14. P. Haller, T. Bruderer, S. Schaeren et al., “Vertebral osteomyelitis caused by Actinobaculum schaalii: a difficult-to-diagnose and potentially invasive uropathogen,” European Journal of Clinical Microbiology and Infectious Diseases, vol. 26, no. 9, pp. 667–670, 2007. View at Publisher · View at Google Scholar · View at Scopus
  15. M. Hoenigl, E. Leitner, T. Valentin et al., “Endocarditis caused by Actinobaculum schaalii, Austria,” Emerging Infectious Diseases, vol. 16, no. 7, pp. 1171–1173, 2010. View at Publisher · View at Google Scholar · View at Scopus
  16. O. E. Larios, K. A. Bernard, K. Manickam, B. Ng, M. Alfa, and A. Ronald, “First report of Actinobaculum schaalii urinary tract infection in North America,” Diagnostic Microbiology and Infectious Disease, vol. 67, no. 3, pp. 282–285, 2010. View at Publisher · View at Google Scholar · View at Scopus