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Daptomycin efficacy in the central nervous system of a patient with disseminated methicillin-resistant Staphylococcus aureus infection: a case report
© Taglietti et al.; licensee BioMed Central Ltd. 2012
Received: 9 March 2012
Accepted: 3 July 2012
Published: 31 August 2012
Staphylococcus aureus has emerged as a major nosocomial pathogen in the last decades and also represents the second most common pathogen isolated from patients in outpatient settings. Although methicillin-resistant S.aureus infections were traditionally limited to hospitals, community-associated cases of methicillin-resistant S.aureus infections have been reported. In our case, we observed an unexpected event during treatment.
A 60-year-old Caucasian man developed fever and multiple muscle and brain abscesses caused by Panton-Valentine leukocidin-negative community-associated methicillin-resistant S. aureus.
Although our patient was given antimicrobials active against the isolated methicillin-resistant S. aureus strain, it was only after the introduction of daptomycin that his skin, soft tissue and muscle lesions and also brain manifestations improved.
Staphylococcus aureus (SA) has emerged as a major nosocomial pathogen in the last decades and also represents the second most common pathogen isolated from patients in outpatient settings . SA is commonly carried asymptomatically in human anterior nares and occasionally enters the bloodstream to cause invasive diseases with a wide range of syndromes, from minor skin and soft tissue infections to life-threatening necrotizing pneumonia and toxic shock syndrome . The overall burden of staphylococcal diseases caused by antibiotic-resistant SA, particularly by methicillin-resistant S. aureus strains (MRSA), is increasing in several countries, including Italy, where MRSA accounts for 25% to 50% of all hospital-isolated SA strains and causes 52.8% of intensive care unit (ICU)-acquired infections .
Although MRSA infections were traditionally limited to hospitals, community-associated cases of MRSA (CA-MRSA) infections have been reported since the late 1990s in the USA . CA-MRSA strains are genetically and phenotypically distinct from the typical multidrug-resistant healthcare-associated MRSA. These strains are resistant to beta-lactam antibiotics, are typically susceptible to other anti-staphylococcal agents, and often encode for Panton-Valentine leukocidin (PVL) and other exotoxins and virulence factors .
The vast majority of CA-MRSA carry one of two smaller staphylococcal cassette chromosome mec(SCCmec) types, IV and V, without the additional resistance genes, and thus are in general more susceptible to non-beta-lactam antibiotics. They appear to be associated with increased transmission and hospitalization, skin and soft tissue infection and, rarely, severe diseases including necrotizing pneumonia . CA-MRSA strains have rapidly emerged worldwide and are now endemic in the USA where they are amongst the most commonly isolated pathogens in emergency departments. Furthermore, nosocomial transmission of CA-MRSA and hospital outbreaks have recently been observed in several countries .
Very few cases of infections due to CA-MRSA are reported in Italy . We describe a case of multiple muscle and brain abscesses, caused by an MRSA encoding SCCmec IV, in an apparently immunocompetent patient.
A 60-year-old Caucasian male retired nurse was admitted three years ago to our Infectious Diseases Hospital because of a three-day history of ingravescent dyspnoea, a skin abscess on his left arm and a very high fever. He had a past medical history of arterial hypertension, ischemic cardiomyopathy, cholecystectomy, lumbar discal hernia self-treated with steroids in case of lumbar pain, and an allergy to ceftriaxone.
Thirteen days prior to the present admission, our patient was admitted to an emergency room of another hospital for more severe lumbar pain; there he received intravenous steroids that improved his pain, and he was discharged on the same day. After three days, he consulted his general practitioner because of fever and the swelling of his left arm where a peripheral intravenous line was located during his previous emergency admission. With the suspicion of phlebitis, he was given piperacillin and calciparine for seven days. However, due to the persistence of the fever and arm swelling and the onset of dyspnoea, one week later he was admitted to a general hospital. His blood pressure was 100/60mmHg, pulse rate 120beats/min and temperature 39.5°C. Physical examination revealed right basal chest crepitations and an abscess on his left arm. Blood examinations showed a white blood cell count of 9.2 per mm3 with 76% neutrophils, C-reactive protein 58mg/dL (normal value <0.60mg/dL), erythrocyte sedimentation rate of 90 (normal value 0-12mm/h) and glycemia of 456mg/dL.
Red blood cells, platelet counts, and the other blood examinations were normal. A chest X-ray showed a right basal consolidation. On the second day of admission, his skin abscess was surgically drained, yielding S. aureus with a vancomycin minimum inhibitory concentration of 1μg/mL. On the same day, our patient developed chest pain and was admitted to the cardiologic ICU for an inferior ST segment elevation myocardial infarction.
On day 5, because of persisting fever and dyspnoea, our patient was transferred to the ICU of our Infectious Disease Institute. At the moment of ICU admission, he was febrile (39.8°C), confused and dyspnoic: blood and draining cultures were performed, and empiric antibiotic therapy, including meropenem (1g intravenously three times per day), linezolid (600mg intravenously twice daily) and levofloxacin (500mg intravenously twice daily), was started. Urinary antigen tests for Legionella and Streptococcus pneumoniae were negative.
His fever still persisted by day 6. A vertebral nuclear magnetic resonance (NMR) imaging study was negative for spondylodiscitis and transthoracic echocardiography showed no endocardial vegetations. On day 7, another surgical drainage of his left arm and scapular soft tissue abscesses was performed. His clinical condition was stable. Both the blood cultures and swabs performed in our Infectious Diseases Hospital yielded MRSA.
Both strains of SA isolates were methicillin-resistant. Molecular characterization was conducted by polymerase chain reaction of mec A, pvl and major enterotoxin content genes, SCCmec-typing and multilocus sequence typing (MLST); pulsed-field gel electrophoresis (PFGE) was used only to define possible relationships among the isolates. All techniques were performed as previously described [8, 9]. Strains were identical, as demonstrated by PFGE (data not shown) and belonged to the ST8 SCCmec IV.3. A further characterization to define the virulence gene content showed that the strains were PVL-negative, but possessed different superantigen toxins (enterotoxins k, q, d, j and tst), all conferring the hypervirulent behavior demonstrated by the strains. The isolated strains were susceptible to rifampin, fluoroquinolones, gentamicin, tetracycline and cotrimoxazole and were also fully susceptible to glycopeptides, linezolid, daptomycin, quinupristin/dalfopristin and tigecycline. The SA strain isolated during the previous admission to another hospital was not available to perform further microbiologic analysis.
On day 12, a whole-body computed tomography showed that the multiple brain abscesses previously described had worsened, and new brain lesions were evident. In addition, computed tomography showed the presence of left basal pneumonia and the onset of new multiple muscle abscesses (left deltoid, paravertebral, left pectoral and right psoas, gluteal and iliac). A neurosurgery consultation excluded the possibility of draining the brain abscesses. Daily administration of daptomycin 6mg/kg was started and the administration of meropenem was interrupted.
On day 22, the clinical and radiologic findings improved. Our patient became non-febrile, and erythrocyte sedimentation rate and C-reactive protein decreased. On day 38, a chest X-ray was normal, daptomycin and levofloxacin were interrupted, and our patient was discharged in good general condition. Administration of linezolid 600mg twice a day was continued for two weeks. After a two-year period, our patient is still in good health.
Skin and soft tissue and lower respiratory infections account for much of the current clinical literature about CA-MRSA. We report the case of a patient with pneumonia and multiple abscesses involving skin, soft tissue and the central nervous system caused by a PVL-negative CA-MRSA.
Notably, in our patient we observed a rapid onset and dissemination of the infection and clinical severity, similar to cases of PVL-positive CA-MRSA infections already described in the literature. Community-isolated strains, not only the PVL-positive ones, can be considered one of the most significant challenges of this epidemiological change of SA. In fact, these CA-MRSA strains, even if PVL negative, possess several virulence determinants responsible for more severe diseases than the nosocomial clones. One of these virulence determinants of CA-MRSA strains is represented by the presence of staphylococcal superantigens that, as described in the literature, may be related to steroid therapy . Our patient, as seen in the case report, had a history of lumbar discal herniation self-treated with steroids and the MRSA strain isolated possessed several superantigen toxins.
Although our patient was given antimicrobials that were active against the isolated MRSA strain, namely levofloxacin and linezolid, his clinical condition rapidly worsened. A likely explanation is the bacteriostatic effect of linezolid, the concentration-dependent activity of levofloxacin  and an aggressive virulence of the MRSA strain. In our case, the introduction of daptomycin in the antimicrobial schedule allowed fast improvement concerning skin, soft tissue and muscle lesions and also brain manifestations. Indeed, daptomycin has been shown to be effective in central nervous system infection in humans and animal models [10, 11].
CA-MRSA infection, even if PVL negative, can be rapidly aggressive with multiple lesions, including in the brain. Daptomycin seems to be effective in the treatment of these severe cases owing to its pharmacokinetic and pharmacodynamic characteristics and its fast bactericidal activity with a limited bacterial lysis [12, 13].
Written informed consent was obtained from the patient for publication of this manuscript and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
- Lowy FD: Staphylococcus aureus in fections. N Eng J Med. 1998, 339: 520-532. 10.1056/NEJM199808203390806.View ArticleGoogle Scholar
- Malacarne P, Boccalatte D, Acquarolo A, Agostini F, Anghileri A, Giardino M, Giudici D, Langer M, Livigni S, Nascimben E, Rossi C, Bertolini G: Epidemiology of nosocomial infection in 125 Italian intensive care units. Minerva Anestesiol. 2010, 76 (1): 13-23.PubMedGoogle Scholar
- Moran GJ, Krishnadasan A, Gorwitz RJ, Fosheim GE, McDougal LK, Carey RB, Talan DA, EMERGEncy ID Net Study Group: Methicillin resistant Staphylococcus aureus infections among patients in the emergency department. N Engl J Med. 2006, 355: 666-674. 10.1056/NEJMoa055356.View ArticlePubMedGoogle Scholar
- Yeung M, Balma-Mena A, Shear N, Simor A, Pope E, Walsh S, McGavin MJ: Identification of major clonal complexes and toxin producing strains among Staphylococcus aureus associated with atopic dermatitis. Microbes Infect. 2011, 13 (2): 189-197. 10.1016/j.micinf.2010.10.023.View ArticlePubMedGoogle Scholar
- Francis JS, Doherty MC, Lopatin U, Johnston CP, Sinha G, Ross T, Cai M, Hansel NN, Perl T, Ticehurst JR, Carroll K, Thomas DL, Nuermberger E, Bartlett JG: Severe community-onset pneumonia in healthy adults caused by methicillin-resistant Staphylococcus aureus carrying the Panton-Valentine leukocidin genes. Clin Infect Dis. 2005, 40: 100-107. 10.1086/427148.View ArticlePubMedGoogle Scholar
- Otter JA, French GL: Nosocomial transmission of community-associated methicillin resistant Staphylococcus aureus: an emerging threat. Lancet Infect Dis. 2006, 6: 753-755. 10.1016/S1473-3099(06)70636-3.View ArticlePubMedGoogle Scholar
- Stefani S, Bongiorno D, Cafiso V, Campanile F, Crapis M, Cristini F, Sartor A, Scarparo C, Spina D, Viale P: Pathotype and susceptibility profile of a community-acquired methicillin-resistant Staphylococcus aureus strain responsible for a case of severe pneumonia. Diagn Micr Infec Dis. 2009, 63: 100-104. 10.1016/j.diagmicrobio.2008.09.012.View ArticleGoogle Scholar
- Schlievert PM, Case LC, Strandberg KL, Abrams BB, Leung DY: Superantigen profile of Staphylococcus aureus isolates from patients with steroid-resistant atopic dermatitis. Clin Infect Dis. 2008, 46: 1562-1567. 10.1086/586746.View ArticlePubMedPubMed CentralGoogle Scholar
- Bolon MK: The newer fluoroquinolones. Infect Dis Clin N Am. 2009, 23: 1027-1051. 10.1016/j.idc.2009.06.003.View ArticleGoogle Scholar
- Gerber P, Stucki A, Acosta F, Cottagnoud M, Cottagnoud P: Daptomycin is more efficacious than vancomycin against methicillin-susceptible Staphylococcus aureus in experimental meningitis. J Antimicrob Chemoth. 2006, 57: 720-723. 10.1093/jac/dkl007.View ArticleGoogle Scholar
- Le J, Bookstaver PB, Rudisill CN, Hashem MG, Iqbal R, James CL, Sakoulas G: Treatment of meningitis caused by vancomycin-resistant Enterococcus faecium: high-dose and combination daptomycin therapy. Ann Pharmacother. 2010, 44 (12): 2001-2006. 10.1345/aph.1P333.View ArticlePubMedGoogle Scholar
- Cotroneo N, Harris R, Perlmutter N, Beveridge T, Silverman JA: Daptomycin exerts bactericidal activity without lysis of Staphylococcus aureus. Antimicrob Agents Chemother. 2008, 52 (6): 2223-2225. 10.1128/AAC.01410-07.View ArticlePubMedPubMed CentralGoogle Scholar
- Utili R, Cogo A, Cristini F, Prisco V, Sagnelli E, Tascini C, Iacoboni C, Capone A, Gattuso G, Angarano G, Petrelli E, Grossi P, Bartezaghi M, Zagni E: Clinical experience with daptomycin in Italy: results from a registry study of the treatment of Gram-positive infections between 2006 and 2009. J Chemother. 2012, 24 (2): 113-121. 10.1179/1120009X12Z.00000000023.View ArticlePubMedGoogle Scholar
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