A case report of Nocardia spp. infective endocarditis in an injection drug user
BMC Infectious Diseases volume 21, Article number: 832 (2021)
Nocardia-related endocarditis is rare. Intravenous drug use with nonsterile injection practices is a potential risk factor for nocardia infection. Disseminated nocardiosis with endovascular involvement is rarely reported in immunocompetent individuals.
A 54-year-old male was diagnosed with infective endocarditis due to Nocardia asteroides with septic emboli in the brain and spleen. The use of a matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) rapid diagnostic system was beneficial in identifying the causative organism. He was empirically treated with combination therapy consisting of three antibiotics. Antimicrobial susceptibility testing indicated that all three antibiotics had favorable minimum inhibitory concentrations (MICs). Due to his clinical status, he was not a surgical candidate. Patient passed away after discharge to hospice.
This case demonstrates unique challenges in the identification, diagnosis, and management of Nocardia-related infective endocarditis. A detailed history of injection practices should guide clinicians in assessing the risk for environmental pathogens. Valvular surgery and combination antibiotic therapy should be recommended for all eligible patients to improve the chances of survival.
The diagnosis of Nocardia-related infective endocarditis is rare, especially in the immunocompetent population. Nonsterile injection practices, such as needle washing, among persons who use drugs (PWUD) increase the risk of infection with atypical environmental pathogens. Traditionally, microbiologic identification of Nocardia spp. has been difficult due to misidentification and prolonged incubation requirements. The optimal treatment regimen for Nocardia-related infective endocarditis involves surgery for source control and combination antibiotic therapy. We report a 54-year-old male who was diagnosed with infective endocarditis due to Nocardia spp. and treated with combination of antibiotics.
A 54-year-old incarcerated male with a history of hypertension, alcohol abuse, injection drug use (IDU), and hepatitis B infection presented with fever, right-sided weakness and recurrent falls for two weeks. The patient reported injecting methamphetamine into his veins one month prior to admission and using water to clean his needles.
His vital signs were significant; he had a temperature of 99.9 F; tachycardia, with a heart rate of 120 bpm; and his blood pressure was 112/66 mmHg. The physical examination revealed bilateral weakness with pronator drift noted in the right upper extremity and dysarthria. Due to a high suspicion of stroke, magnetic resonance imaging of the brain was performed. It showed late subacute infarcts involving the left middle cerebral artery and right frontal subcortical white matter, with associated petechial hemorrhage. These findings suggested cardioembolic stroke. Transthoracic echocardiography showed severe aortic stenosis and a right to left interatrial shunt. Computed tomography of the chest, abdomen and pelvis revealed splenic infarcts.
Laboratory data revealed mild leukocytosis, with a white blood cell (WBC) count of 11.5 × 10*3/µL (reference range: 4.8–10.8 × 10*3/µL); thrombocytopenia, with a platelet count of 78 × 10*3/µL (reference range: 160–360 10*3/µL); and mild transaminitis, with an aspartate aminotransferase (AST) level of 47 IU/L (reference range: 5–40 IU/L) and alanine aminotransferase (ALT) level of 60 IU (reference range: 5–50 IU/L). Creatinine was 0.68 mg/dL (reference range: 0.5–1.50 mg/dL) and blood urea nitrogen (BUN) of 15 mg/dL (reference range: 8–24 mg/dL).
During hospitalization, he became febrile, with the body temperature reaching 102 F. Four sets of bacterial blood cultures were obtained. They were incubated with the BACTEC FX blood culture system (BD, Spark, MD). The patient was started on broad spectrum antibiotics including vancomycin and cefepime. Two sets of blood cultures turned positive on days two and three of incubation and showed gram-positive rods on examination with Gram stain. The subculture plates from these sets showed growth after only 48 h of incubation, when pinpoint white, dry colonies were observed on the aerobic blood agar plates. The organism was identified as Nocardia spp. by MALDI Biotyper CA System (MBT-CA; Bruker Daltonics, Billerica, MA) software version 3.2. 16 using pretreatment with formic acid according to the manufacturer’s instructions for clinical applications.
Due to cerebral and splenic emboli, there was high suspicion of endocarditis. Transesophageal echocardiography showed a heavily thickened and degenerated aortic valve (AV) with concomitant vegetation and abscess formation on the left coronary cusp resulting in dehiscence, perforation, and AV insufficiency. No other valves were involved. The patient’s antibiotics were switched to trimethoprim-sulfamethoxazole (TMP-SMX) 15 mg/kg/day IV divided in four doses, amikacin 21 mg/kg IV every 24 h, and imipenem-cilastatin 500 mg IV every 6 h. This antibiotic regimen was started on day 7 of admission. Repeat blood cultures remained negative. Cardiothoracic surgery was considered and a pre-surgical work-up was recommended, including digital subtraction angiography (DSA) and left heart catheterization (LHC), due to his history of tobacco use. LHC was not performed due to the patient’s worsening renal function to avoid contrast agent exposure. He ultimately developed renal failure requiring hemodialysis on the 19th day of hospitalization [Creatinine was 3.76 mg/dL, BUN of 54 mg/dL with an estimated glomerular filtration rate (eGFR) of 17 (reference range: > 60 ml/min/1.73 M*2)]. The patient’s clinical status continued to decline, with hypotension requiring vasopressors, worsening respiratory status requiring intubation, and acute renal failure requiring continuous renal replacement therapy (CRRT). Antimicrobial susceptibility testing, performed at a Nocardia reference laboratory using broth microdilution and CLSI breakpoints, showed that the organism was susceptible to amikacin, ceftriaxone, imipenem-cilastatin, linezolid, moxifloxacin, TMP-SMX, and tobramycin (Table 1). He was deemed not eligible for valvular surgery due to his worsening clinical status. After family discussion, he was transitioned to outpatient hospice care, and all antibiotics were discontinued. Patient passed away a day after discharge to a hospice care facility.
Discussion and conclusion
We report a 54-year-old male with IDU presenting with aortic valve endocarditis due to Nocardia spp. This case is unique, as it is the first published report of infective endocarditis caused by Nocardia spp. secondary to nonsterile injection practices in an immunocompetent host. The source of entry of this infection was likely secondary to nonsterile injection practices.
Nocardia spp. are ubiquitous environmental saprophytes occurring in soil, organic matter, and aquatic habitats. Microscopically, Nocardia spp. are characterized as gram-positive, beaded, branching, weakly acid-fast rods. Historically, some Nocardia spp. may be difficult to detect on standard blood culture media due to their prolonged incubation requirement 2–4 days) [1, 2]. The isolate could be recovered on fungal cultures as these are incubated for 4–6 weeks. Nocardia spp. are often misidentified as other gram-positive rods, which also leads to a delay in identification. The increased use of rapid diagnostic laboratory tests, such as MALDI-TOF MS, has significantly decreased the time to identification of this bacteria once it grows on solid agar media, as in this case . However, the complex and continuously changing taxonomy of this genus, makes difficult, particularly for Nocardia spp., to confirm the identification as different system may have a different library (2). In this case, the organism was identified as Nocardia asteroides with a score of 2.24, which is considered a good identification score. Disseminated Nocardia infection is most commonly diagnosed in patients with underlying immunocompromising conditions and is associated with a high rate of mortality (26%) [4,5,6]. The common sites of infection include the lungs, central nervous system, skin and subcutaneous tissues. The joints, bone, and heart are less commonly involved .
We conducted a literature search of English language reports in the PubMed, Ovid and EBSCO databases using the terms “endocarditis” and “nocardia”. We describe the risk factors and outcomes of 18 cases of Nocardia-related infective endocarditis in Table 2. The median patient age was 61 years. Nocardia asteroides was the most commonly reported species (61%), followed by Nocardia farcinia (11%) and other Nocardia spp. (28%) [8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24]. The most common risk factors in the reported cases were a prosthetic aortic valve (33%) [8, 13, 15,16,17], cancer (22%) [10, 18, 21, 22], and chronic obstructive pulmonary disease (COPD) (17%) [10, 11, 21]. Other pertinent risk factors included solid organ transplantation (11%) [5, 19], systemic steroid use (11%) [10, 11], and rheumatic diseases (11%) [11, 23]. Notably, the only risk factor observed in this patient was IDU, which has been reported in only two other cases [20, 24]. Certain practices, such as needle sharing, licking, washing and nonsterile injection methods, may increase the risk of infections from environmental pathogens . It is important to emphasize and educate patients about sterile practices to prevent severe infection.
The paucity of data regarding Nocardia-related infective endocarditis has hindered the ability of clinicians to determine the optimal treatment regimen and duration. Eleven patients (Table 2) received at least three drugs for infective endocarditis treatment [8, 9, 11, 13, 15, 18,19,20,21,22, 24]. Eight of these patients survived [9, 13, 15,16,17,18,19,20,21, 24]. The three patients who died did not undergo valvular surgery [8, 11, 22]. Of the seven patients [10, 12, 14,15,16,17, 23] who received less than three antibiotics, four patients survived [10, 12, 14, 16]. Irrespective of the number of antibiotics used to treat their infection, all eight patients who underwent valvular surgery survived [9, 12, 14,15,16, 18, 21, 24]. These findings indicate that valvular surgery is imperative for source control and improving outcomes in patients with a bacterial infection that is very difficult to treat. The cases in Table 2 had widely variable treatment durations, ranging from 3 weeks to 8 months. Despite the inconsistence with treatment duration and clinical success, it may be prudent to treat endocarditis due to Nocardia similarly to other serious infections caused by Nocardia spp., with combination antibiotic therapy for several months. Two agents commonly used to treat serious Nocardia infections, TMP-SMX and amikacin, have been associated with nephrotoxic effects, warranting close observation of renal function and therapeutic drug monitoring throughout the treatment period [7, 26]. Unfortunately, the use of concomitant nephrotoxic medications combined with hypoperfusion due to cardiogenic shock led to renal failure in this patient. Thus, his tenuous status lead to the determination that he was not a surgical candidate.
IDU, especially nonsterile injection practices, increases the risk of infective endocarditis caused by relatively uncommon environmental and ubiquitous pathogens, such as Nocardia spp. Hence, it is important for clinicians to suspect these organisms and obtain an appropriate history regarding injection practices. The primary treatment for endocarditis due to Nocardia is valvular surgery for source control. The reported mortality is high (60%) without valvular surgery. After source control is established, prolonged antibiotic therapy with multiple drugs is recommended, although the optimal duration is unknown.
Availability of data and materials
Data sharing is not applicable to this case report as no datasets were generated or analyzed during the current study.
Persons who use drugs
- MALDI-TOF MS:
Matrix-assisted laser desorption time of flight mass spectrometry
Injection drug use
Minimum inhibitory concentrations
Beats per minute
Millimeters of mercury
Digital subtraction angiography
Left heart catheterization
Continuous renal replacement therapy
Conville PS, Witebsky FG, et al. Nocardia, Rhodococcus, Gordonia, Actinomadura, Streptomyces, and other aerobic actinomycetes. In: Jorgensen JH, Pfaller MA, Carroll KC, et al., editors. Manual of Clinical Microbiology. 11th ed. Washington: American Society for Microbiology Press; 2015.
Brown-Elliott B, Brown JM, Conville P, et al. Clinical and laboratory features of the Nocardia spp. based on current molecular taxonomy. Clin Microbiol Rev. 2006;19:259–82.
Blosser SJ, Drake SK, Andrasko JL, et al. Multicenter matrix-assisted laser desorption ionization-time of flight mass spectrometry study for identification of clinically relevant Nocardia spp. J Clin Microbiol. 2016;54:1251–8.
Minero MV, Marin M, Cercenado E, et al. Nocardiosis at the turn of the century. Medicine (Baltimore). 2009;88(4):250–61. https://doi.org/10.1097/MD.0b013e3181afa1c8.
Smego RA Jr, Moeller MB, Gallis HA. Trimethoprim-sulfamethoxazole therapy for Nocardia infections. Arch Intern Med. 1983;143:711–8.
Uttamchandani RB, Daikos GL, Reyes RR, et al. Nocardiosis in 30 patients with advanced human immunodeficiency virus infection: clinical features and outcome. Clin Infect Dis. 1994;18:348–53.
Wilson JW. Nocardiosis: updates and clinical overview. Mayo Clin Proc. 2012;87:403–7.
Allevato PA, Eisses JF, Mezger E, et al. Nocardia asteroids with perforation of the aorta. Hum Pathol. 1985;16(7):743–6.
Antony SJ, Stivers M, Rivera JO. Endocarditis/endovascular infection with Nocardia. Infect Med. 2006;23:262–6.
Antonovich DD, Berke A, Grant-Kels JM, Fung M. Infectious eccrine hidradenitis caused by Nocardia. J Am Acad Dermatol. 2004;50(2):315–8.
Cargill JS, Boyd GJ, Weightman NC. Nocardia cyriacigeorgica: a case of endocarditis with disseminated soft-tissue infection. J of Medical Microbiol. 2010;59(2):224–30.
Castelli JB, Siciliano RF, Abdala E, Aiello VM. Infective endocarditis caused by Nocardia sp.: histological morphology as a guide for the specific diagnosis Brazil. J Infect Dis. 2011;15(4):384–6.
Daikos GL, Syriopoulou V. Successful antimicrobial chemotherapy for Nocardia asteroids prosthetic valve endocarditis. Am J Med. 2003;115:330–1.
Dhawan VK, Gadgil UG, Paliwal YK, et al. Native valve endocarditis due to a Nocardia-like organism. Clin Infect Dis. 1998;27:902–4.
Eigel P, Elert O, Hopp H, et al. Nocardial endocarditis after aortic valve replacement: reports of two cases. Scand J Thorac Cardiovasc Surg. 1998;22:289–90.
Ertl G, Schaal KP, Kochsiek K. Nocardial endocarditis of an aortic valve prosthesis. Br Heart J. 1987;57:384–6.
Falk RH, Dimock FR, Sharkey J. Prosthetic valve endocarditis resulting from Nocardia asteroides. Br Heart J. 1979;41:125–7.
Gupta S, Gulia S, Kannan RA, et al. Nocardial endocarditis in native aortic valve nocardial sepsis in a case of breast cancer. BMJ Case Rep. 2019;12: e229370. https://doi.org/10.1136/bcr-2019-229370.
Hazim AZ, Mansoor AM. Disseminated nocardiosis with infective endocarditis of a transplanted heart. BMJ Case Rep. 2018. https://doi.org/10.1136/bcr-2018-225046.
Jackson LE, Shorman M. A case of bilateral Nocardia francinia adrenal abscesses in an intravenous drug-using splenectomized patient with tricuspid endocarditis. Open Forum Infect Dis. 2018;5(7):ofy141. https://doi.org/10.1093/ofid/ofy141.
Kuretski J, Dahya V, Cason L, et al. Nocardia bacteremia and endocarditis in a patient with a sulfa allergy. Am J Med Sciences. 2016;352(5):542–3.
Majeed A, Abdullah HMA, Ullah W, Al Mohajer M. First reported case of disseminated Nocardia kroppenstedtii sp. nov. infection presenting with brain abscess and endocarditis in an immunocompromised patient with mantel cell lymphoma: challenges in diagnosis and treatment. BMJ Case Rep. 2017. https://doi.org/10.1136/bcr-2016-217337.
Vlachakis ND, Gazes PC, Hairston P. Nocardial endocarditis following mitral valve replacement. Chest. 1973;63:276–8.
Watson A, French P, Wilson M. Nocardia asteroides native valve endocarditis. Clin Infect Dis. 2001;32(4):660–1.
Peckham AM, Young EH. Opportunities to offer harm reduction to people who inject drugs during infectious encounters: narrative review. Open Forum Infect Dis. 2020;7(11):ofaa503. https://doi.org/10.1093/ofid/ofaa503.
Schlaberg R, Fisher MA, Hanson KE. Susceptibility profiles of Nocardia isolates based on current taxonomy. Antimicrob Agents Chemother. 2014;58(2):795–800.
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Enwezor, C., Russ-Friedman, C.L., Gruss, Z.P. et al. A case report of Nocardia spp. infective endocarditis in an injection drug user. BMC Infect Dis 21, 832 (2021). https://doi.org/10.1186/s12879-021-06541-6