J Bone Jt Infect 2016; 1:7-9. doi:10.7150/jbji.13863

Short Research Communication

Unusual Case of Spondylodiscitis due to Listeria monocytogenes

Guillaume Ghislain Aubin1,2, David Boutoille2,3, Romain Bourcier4, Jocelyne Caillon1,2, Didier Lepelletier1,2, Pascale Bémer1,2 *, Stéphane Corvec1,2 * Corresponding address

1. Bacteriology and Hygiene Unit, Nantes University Hospital, France.
2. EA3826, Laboratory of Clinical and Experimental Therapeutics of Infections - Nantes Medicine School, France.
3. Infectious and Tropical Diseases Unit, Nantes University Hospital, France.
4. Interventional and Diagnostic Neuroradiology, Nantes University Hospital, France.
* contributed equally to this work.

This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
How to cite this article:
Aubin GG, Boutoille D, Bourcier R, Caillon J, Lepelletier D, Bémer P, Corvec S. Unusual Case of Spondylodiscitis due to Listeria monocytogenes. J Bone Jt Infect 2016; 1:7-9. doi:10.7150/jbji.13863. Available from http://www.jbji.net/v01p0007.htm

Keywords: Spondylodiscitis, vertebral osteomyelitis, Listeria monocytogenes, MALDI-TOF, blood culture

Introduction

The diverse clinical spectrum of Listeria monocytogenes infections includes frequent clinical forms, such as meningitis or bacteremia, and uncommon manifestations, such as septic arthritis. Osteoarticular infections due to L. monocytogenes remain very rare.

Case report

A 92 year-old man was admitted to the emergency unit at Nantes University hospital for fever and acute low back pain since one week associated with a systemic inflammatory response syndrome and oliguria. His medical history included arterial hypertension, heart failure and arrhythmia, gastric ulcer and hip arthroplasty. He did not recall gastrointestinal symptoms or specific trauma to his skin. On admission, he had a temperature of 38.2°C and normal blood pressure. General examination was normal apart from low back pain and paraspinal muscle spasm. He had no sign of meningoencephalitis. Blood tests showed a total white cell count of 7.47 G.L-1 with normal neutrophil count (82.7%) and lymphopenia (7.6%) and an elevated C-reactive protein level of 190.8 mg.L-1. Three aerobic and anaerobic blood cultures (Bactec FX, Becton, Dickinson, Sparks, MD, USA) were performed on the peripheral site over the course of 24 h. The two first aerobic blood cultures were positive after 22h of incubation and yielded Gram-positive bacilli. The etiological agent of this bacteremia was identified as Listeria monocytogenes only one hour later after the Gram staining thanks to a modified driven hemolysis method using MALDI-TOF mass spectrometry [1]. After 24h of incubation, the bacterial identification was confirmed by using the hemolytic colony on blood agar plate (bioMérieux, Marcy l'Etoile, France). Esculine test was rapidly positive. According to French Listeria National center, multiplex PCR showed that this strain belonged to the serotype-associated group 4b complex (serotypes 4b, 4d, and 4e). Despite recommendations in invasive listeriosis, lumbar puncture (to objective paucisymptomatic meningoencephalitis) was not achieved in this case given the patient's age and location of infection [2]. Two days after admission, magnetic resonance imaging of the lumbar spine revealed a multifocal spondylodiscitis with global (L4-L5) and focal (L3-L4 and L5-S1) hyper intensity of the discus in T2 and abnormal hypo-intensity of the adjacent plate of the L3-L4 discus on T1 (Fig. 1). Transthoracic echocardiography did not found any evidence for infective endocarditis. Antibiotic therapy with continuous intravenous amoxicillin (200 mg/kg daily) during six days and gentamicin (5 mg/kg in one daily injection) during four days was started. In vitro susceptibility testing was performed using the disk diffusion method on Mueller-Hinton medium with 5% sheep blood (bioMérieux). This bacterium was susceptible to amoxicillin, levofloxacin, moxifloxacin, aminoglycosides, tetracycline, lincomycin, cotrimoxazole, and rifampin, according to the European Committee on Antimicrobial Susceptibility Testing (EUCAST) guidelines. After six days of intravenous therapy, given a favorable evolution, the treatment was switched to oral cotrimoxazole (30 mg/kg of sulfamethoxazole daily) for three months. Following blood cultures remained negative after the beginning of antibiotic treatment.

At the three-month clinical assessment, the patient had been recovering slowly and regaining mobility. Investigation performed to identify the source of infection found in the patient's fridge raw milk and raw milk cheese, but cultures of those food items remained negative. No predisposing condition other than his advanced age was evidenced in this patient.

 Figure 1 

Magnetic resonance imaging of the lumbar spine. A: T2 Fat suppressed - weighted magnetic resonance imaging of the lumbar spine showing global (L4-L5) or focal (L3-L4 and L5-S1) hyper intensity of the discus (little white arrows). Note the hyper intensity corresponding to the edema on the end-plate of the L3 vertebra (empty arrow). B: T1-weighted magnetic resonance showing abnormal hypo-intensity of the adjacent plate of the L3-L4 discus (empty arrows). Gadolinium injection was not performed and imaging procedure has been shortened due to the patient's pain.

J Bone Jt Infect Image (Click on the image to enlarge.)

Discussion

This case illustrates an unusual spondylodiscitis caused by L. monocytogenes in an elderly patient. L. monocytogenes is a Gram-positive, facultative intracellular bacillus that can be isolated from a large number of environmental sources such as soil, water, vegetables [3]. Listeriosis constitutes a food borne disease due to poultry, duck, beef or salmon and seafood contamination [3]. Listeria infections remain relatively rare, with an estimated 2000 cases per year in the United States and 300 cases per year in France [3]. Even though 13 serotypes have been recognized, most cases of human disease involve strains of three serotypes, i.e., serotypes 1/2a, 1/2b, and 4b [4]. In France, L. monocytogenes serotype-associated group 4b complex is the major complex causing human diseases [4]. In recent years, an increasing number of cases has been reported in Europe, essentially due to emergence of bacteremic listeriosis in immunocompromised individuals, and especially in the elderly [5]. Indeed, listeriosis currently affects debilitated patients such as those with cancer, immunosuppression, such as transplant recipients, and the elderly. Immunocompetent individuals usually present nonspecific flu-like symptoms, lymphadenopathy and gastrointestinal symptoms, whereas immunocompromised individuals may develop meningoencephalitis, bacteremia and a wide variety of focal infections [5]. Mortality of invasive listeriosis is as high as 15 to 30% [5]. Furthermore, in pregnant women, infection with L. monocytogenes may be transmitted to the fetus, leading to bacteremia and fetal loss. The majority of sporadic cases are associated with Listeria contamination of unpasteurized dairy products, although other modes of transmission may be involved. Rare epidemic cases of listeriosis have also been traced to exposure to contaminated food [4].

Spondylodiscitis due to L. monocytogenes was not already described in patient without immunodeficiency or history of spinal surgical procedure. Del Pozo et al. recently published a literature review on Listeria septic arthritis cases in the native joints of immunocompromised patients [6]. The knee was the most frequently affected joint, and two cases involved more than one joint, with no case of spondylodiscitis. Unlike other patients from Del Pozo's study, the patient did not receive any immunosuppressive therapy. As L. monocytogenes is a rare causative agent of arthritis [6-8], diagnosis can be difficult, especially when no evident sign of Listeria disease exists. Gram positive bacilli in blood culture are often considered as contamination by Corynebacterium species from the skin. Herein, bacterial identification was performed the day of blood bottle positivity by MALDI-TOF mass spectrometry. This alternative approach for rapid MALDI-TOF based identification constitutes a new step to reduce the time of identification and therefore to adapt the treatment of clinically relevant and uncommon bacteria. In this case, the antibiotic treatment was adapted 24h after sampling.

Microbiologists and physicians should be aware of L. monocytogenes infection, in light of Gram's stain results, especially in elderly and/or immunocompromised patients. The propensity for a commensal bacterium to cause unapparent bloodstream infections with septic metastasis and joint infections is of special concern for this type of patients.

As recommended by guidelines [2], treatment consisted initially in high dose of intravenous amoxicillin and gentamicin. Switch for oral antibiotics was quickly performed due to favorable evolution and difficulty of venous catheterization. Cotrimoxazole, which has good diffusion to bone tissue, has been introduced and allowed to cure the infection.

Conclusion

Antibiotic susceptibility testing, including those with a good bone diffusion remains an important step, especially with the emergence of rifampin-resistant Gram positive bacilli involved in spondylodiscitis such as L. monocytogenes or Propionibacterium acnes as recently described [9,10]. The clinicians should now consider the risk of invasive listeriosis in the elderly, since the clinical presentation may be atypical in this population.

Acknowledgements

We would like to thank the French Listeria National center (Alexandre Leclerq) for L. monocytogenes serotyping.

This work was presented at the Annual Meeting of the European Bone and Joint Infection Society (EBJIS) on September 11 to 13, 2014, in Utrecht, The Netherlands.

Competing Interests

The authors have declared that no competing interest exists.

References

1. Thomin J, Aubin GG, Foubert F, Corvec S. Assessment of four protocols for rapid bacterial identification from positive blood culture pellets by matrix-assisted laser desorption ionization-time of flight mass spectrometry (Vitek® MS). J Microbiol Methods. 2015;115:54-6

2. Hof H, Nichterlein T, Kretschmar M. Management of listeriosis. Clin Microbiol Rev. 1997;10:345-57

3. Scallan E, Hoekstra RM, Angulo FJ, Tauxe RV, Widdowson M-A, Roy SL. et al. Foodborne illness acquired in the United States-major pathogens. Emerging Infect Dis. 2011;17:7-15

4. Swaminathan B, Gerner-Smidt P. The epidemiology of human listeriosis. Microbes Infect. 2007;9:1236-43

5. Allerberger F, Wagner M. Listeriosis: a resurgent foodborne infection. Clin Microbiol Infect. 2010;16:16-23

6. Del Pozo JL, de la Garza RG, de Rada PD, Ornilla E, Yuste JR. Listeria monocytogenes septic arthritis in a patient treated with mycophenolate mofetil for polyarteritis nodosa: a case report and review of the literature. Int J Infect Dis. 2013;17:e132-3

7. Khan KM, Pao W, Kendler J. Epidural abscess and vertebral osteomyelitis caused by Listeria monocytogenes: case report and literature review. Scand J Infect Dis. 2001;33:714-6

8. Schett G, Herak P, Graninger W, Smolen JS, Aringer M. Listeria-associated arthritis in a patient undergoing etanercept therapy: case report and review of the literature. J Clin Microbiol. 2005;43:2537-41

9. Chenal-Francisque V, Charlier C, Mehvish S, Dieye H, Leclercq A, Courvalin P. et al. Highly rifampin-resistant Listeria monocytogenes isolated from a patient with prosthetic bone infection. Antimicrob Agents Chemother. 2014;58:1829-30

10. Furustrand Tafin U, Aubin GG, Eich G, Trampuz A, Corvec S. Occurrence and new mutations involved in rifampicin-resistant Propionibacterium acnes strains isolated from biofilm or device-related infections. Anaerobe. 2015;34:116-9

Author contact

Corresponding address Corresponding author: Stéphane Corvec. Institut de Biologie, Service de Bactériologie-Hygiène hospitalière, CHU de Nantes, 9 quai moncousu 44093 Nantes Cedex 01 France. Email: stephane.corvecfr; Phone: 33.2.40.08.39.55; Fax: 33.2.40.08.38.29


Published 2016-2-29