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Small colony variants of Staphylococcus aureus and pacemaker-related infection.

We describe the first known case of a device-related bloodstream infection caused by Staphylococcus aureus small colony variants. Recurrent pacemaker-related bloodstream infection within a 7-month period illustrates the poor clinical and microbiologic response to prolonged antimicrobial therapy in a patient infected with this S. aureus subpopulation.


Infections caused by Staphylococcus aureus range from mild skin infections to acute life-threatening diseases such as pneumonia, osteomyelitis, and endocarditis. However, S. aureus may also cause a chronic disease with persistent and recurrent infections. Skin and soft tissue infections, chronic osteomyelitis, and persistent infections in patients with cystic fibrosis have been associated with small colony variants, a naturally occurring subpopulation of the species S. aureus (1-6). S. aureus small colony variants are characterized as electron transport deficient bacteria because of their auxotrophism to hemin or menadione or are recognized as thymidine-dependent. These variants produce very small, mostly nonpigmented and nonhemolytic colonies. In addition, they also demonstrate various other features that are atypical for S. aureus, including reduced coagulase production, failure to use mannitol, and increased resistance to aminoglycosides and cell-wall active antibiotics (3-10). Furthermore, the ability of these variants to persist intracellularly within nonprofessional phagocytes has been described (3,5,11). Because of their fastidious growth characteristics and unusual morphologic appearance, small colony variants present a challenge both to the microbiologist and the clinician, often resulting in misidentification and misinterpretation (1,2,7,8). Prerequisite for recovering and identifying these variants is the application of extended conventional culture and identification techniques (3,5,8). We report the first case of a pacemaker-related bloodstream infection caused by S. aureus small colony variants. This case illustrates the poor clinical and microbiologic response to prolonged antimicrobial therapy in patients infected with these variants.

Case Report

A 63-year-old man was transferred to our facility with the presumptive diagnosis of endocarditis related to a pacemaker-lead infection. Past medical history included hypertension, coronary artery disease, and noninsulin-dependent diabetes mellitus. A VVI (ventricular ventricular inhibited) pacemaker had been implanted for treatment of sick sinus syndrome 9 years earlier. Six weeks before admission, this device had been removed because of a pocket infection after blunt trauma with dislocation of the device and perforation of the skin. Specimens for microbiologic culture were not obtained at this time. The pacemaker leads were left in place, a gentamicin-containing sponge was applied to the infection site, and a new pacemaker was implanted on the other side of the chest. Four weeks later, the patient sought treatment at the local hospital for a high fever (39.7[degrees]C) and chills and a subcutaneous abscess with oxacillin-susceptible S. aureus at the primary insertion site. After surgical drainage, antimicrobial therapy was initiated with intravenous cefuroxime. The remaining pacemaker leads were partially cut but not completely removed. Ten days later, spiking fever and chills unresponsive to the administration of meropenem and vancomycin developed, and the patient was transferred to our medical center for pacemaker ablation. The physical examination did not indicate auscultation abnormalities or stigmata of endocarditis. Laboratory studies were unremarkable except a C-reactive protein (CRP) level of 170 mg/L (normal value [less than or equal to] 8 mg/L) and a blood sedimentation rate of 79 mm/h. Multiple blood cultures taken on admission remained negative. Transesophageal echocardiography did not show vegetations or other evidence of endocarditis. On hospital day 6, the new pacemaker was completely removed by percutaneous ablation as were the remaining leads of the old device. Only the tip of the pacemaker lead remained fixed in the myocardium, and surgical removal involving extracorporal circulation was not attempted. The patient's condition improved rapidly, CRP level returned to normal, and on hospital day 32, the patient was transferred to the local hospital to complete a 6-week course of intravenous vancomycin and rifampin as empirical antistaphy-lococcal therapy. Before transfer, the daily vancomycin dose had been reduced to 250 nag twice a day after an elevated vancomycin serum level. Eight days later, the patient was readmitted with recurrent high fever. Blood cultures taken on readmission were again negative. After the vancomycin dose was increased to 500 mg every 12 hours, the patient promptly became afebrile. Antimicrobial therapy was discontinued after the patient had completed a 10-week course of vancomycin and rifampin. Three days later, the patient again bad spiking fever. After 6 to 48 hours of incubation, four sets of blood cultures obtained on four consecutive days yielded nonpigmented and nonhemolytic staphylococci, initially identified on the basis of a negative tube coagulation test and the API ID 32 Staph system (bioMerieux, Marcy-L'Etoile, France) as coagulase-negative staphylococci, susceptible to oxacillin (MIC 0.5 mg/mL) and vancomycin (MIC 1.0 mg/mL) but resistant to rifampin (MIC >32 mg/mL). However, the colony morphologic findings were suggestive of small colony variants of S. aureus, confirmed by polymerase chain reaction amplification of the nuc and coa genes as well as by determination of the strain's auxotrophy for hemin. The patient responded promptly to flucloxacillin, 4 g intravenously three times a day. After another 6-week course of parenteral therapy, antimicrobial therapy was discontinued, and the patient was discharged (CRP 7 mg/L, ESR 35 mm/h); he was readmitted after 6 days with chills and high fever. Antimicrobial therapy with intravenous flucloxacillin was resumed and followed by immediate defervescence. Three blood cultures taken on readmission were again positive with S. aureus small colony variants. Clonal identity of all isolates was demonstrated by pulsed-field gel electrophoresis of bacterial DNA (data not shown). A transesophageal echocardiogram showed the residual tip of the pacemaker lead fixed in the myocardial septum without vegetations. The remaining device was finally removed by open-heart surgery with use of cardiopulmonary bypass. Microbiologic culture of the pacemaker electrode performed at a different institution yielded abundant growth of staphylococci that were misidentified as S. warneri, showing the same biochemical profile as the previously isolated bacteria as determined by the ID 32 Staph system. The patient recovered completely and was discharged on the 10th postoperative day after a total hospital course of 7 months.


S. aureus small colony variants have been implicated in persistent and recurrent infections that give a poor clinical and bacteriologic response to standard antimicrobial therapy in patients with abscess, chronic osteomyelitis, and bronchopulmonary infections, particularly after prolonged exposure to antibiotics (1-6). Bloodstream infection related to an implantable intravascular device with this S. aureus variant has not been reported before. These phenotypic variants are characterized by their fastidious growth and atypical colony morphologic findings on routine media, making recovery as well as correct identification difficult for microbiologic laboratories (3,5,8). The ability to interrupt electron transport and to form a variant sub population affords S. aureus a number of survival advantages, including the ability of this subpopulation to persist intracellularly within nonprofessional phagocytes (11,12). The intracellular position may shield small colony variants from host defenses and decrease exposure to antibiotics (3,5,11). S. aureus small colony variants can be selected by gentamicin in vitro and in vivo as shown in patients with osteomyelitis after gentamicin bead placement (4,12). Chuard et al. demonstrated that, in contrast to their normal phenotype parental strain, S. aureus small colony variants that were attached to fibronectin-coated coverslips were highly resistant to cell-wall-active antimicrobial agents such as oxacillin and vancomycin (13).

In our case, findings suggest that S. aureus small colony variants might have been selected from the parent strain population with a normal phenotype after exposure to the locally applied aminoglycoside or to the prolonged administration of vancomycin. Continually positive blood cultures with the same strain as demonstrated by molecular typing and the presumable persistence of these organisms on the pacemaker lead tip may partly be explained by the poor effectiveness of vancomycin and flucloxacillin against these slow-growing organisms that were adhering to the remaining foreign body and the ability of these variants to persist intracellularly (7,8,13).

This case adds to the spectrum of persistent and relapsing infections attributed to S. aureus small colony variants and emphasizes that these variants may also play a role in intravascular device-related infections. It also illustrates that complete removal of any foreign body material is essential for the complete cure of prosthetic intravascular device-related S. aureus infection. Laboratories should be particularly alert for S. aureus small colony variants when samples are submitted from patients who have received long-term antimicrobial therapy, especially if the infection is unusually persistent or recurrent.


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(4.) von Eiff C. Bettin D, Proctor RA, Rolauffs B, Lindner N, Winkelmann W, et al. Recovery of small colony variants of Staphylococcus aureus following gentamicin bead placement for osteomyelitis. Clin Infect Dis 1997;25:1250-1.

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(6.) Seifert H, von Eiff C, Fatkenheuer G. Fatal case due to methicillin-resistant Staphylococcus aureus small colony variants in an AIDS patient. Emerg Infect Dis 1999:5:450-3.

(7.) Proctor RA, Kahl B, von Eiff C, Vaudaux PE, Lew DP, Peters G. Staphylococcal small colony variants have novel mechanisms for antibiotic resistance. Clin Infect Dis 1997;27(Suppl 1):S68-S74.

(8.) Proctor RA, Peters G. Small colony variants in staphylococcal infections: diagnostic and therapeutic implications. Clin Infect Dis 1998;27:419-23.

(9.) Kahl BC, Belling G, Reichelt R, Herrmann M, Proctor RA, Peters G. Thymidine-dependent small-colony variants of Staphylococcus aureus exhibit gross morphological and ultrastructural changes consistent with impaired cell separation. J Clin Microbiol 2003:41:410-3.

(10.) Baumert N, von Eiff C, Schaaff F, Peters G, Proctor RA, Sahl HG. Physiology and antibiotic susceptibility of Staphylococcus aureus small colony variants. Microb Drug Resist 2002;8:253-60.

(11.) Vaudaux P, Francois P, Bisognano C, Kelley WL, Lew DP, Schrenzel J, et al. Increased expression of clumping factor and fibronectin-binding proteins by hemB mutants of Staphylococcus aureus expressing small colony variant phenotypes. Infect Immun 2002;70:5428-37.

(12.) Balwit JM, van Langevelde P, Vann JM, Proctor RA. Gentamicin-resistant menadione and heroin auxotrophic Staphylococcus aureus persist within cultured eudothelial cells. J Infect Dis 1994; 170:1033-7.

(13.) Chuard C, Vaudaux PE, Proctor RA, Lew DP. Decreased susceptibility to antibiotic killing of a stable small colony variant of Staphylococcus aureus in fluid phase and on fibronectin-coated surfaces. J Antimicrob Chemother 1997;39:603-8.

Harald Seifert, * Hilmar Wisplinghoff, * Petra Schnabel, * and Christof von Eiff ([dagger])

* University of Koln, Germany; and ([dagger]) University of Munster Hospital and Clinics, Munster, Germany

Dr. Seifert is professor of clinical microbiology at the Institute for Medical Microbiology, Immunology and Hygiene at the University of Cologne, Koln, Germany. His research interests include the molecular epidemiology of nosocomial pathogens, in particular Acinetobacter species and methicillin-resistant Staphylococcus aureus, catheter-related infections, and antimicrobial resistance and its mechanisms.

Address for correspondence: Harold Seifert, Iustitut fur Medizinische Mikrobiologie, Immunologie und Hygiene, Goldenfelsstr.19-21, 50935 Koln, Germany; fax: 0049 221-4783979; email: harald.seifert
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Title Annotation:Dispatches
Author:von Eiff, Christof
Publication:Emerging Infectious Diseases
Date:Oct 1, 2003
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