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the Creative Commons Attribution 4.0 License.
Vertebral osteomyelitis with Campylobacter jejuni – a case report and review of the literature of a very rare disease
Simone Greminger
Carol Strahm
Julia Notter
Benjamin Martens
Seth Florian Helfenstein
Jürgen Den Hollander
Manuel Frischknecht
Infections with Campylobacter species mainly cause gastrointestinal disease and are usually self-limiting. Systemic complications such as bacteremia and osteoarticular infections are rare. Here we report a very rare case of a vertebral osteomyelitis due to C. jejuni, and we reviewed the literature for similar cases, identifying six other cases. Therapy should be guided on resistance testing if available due to emerging resistance rates, especially to fluoroquinolones. Azithromycin may be a treatment option for C. jejuni spondylodiscitis.
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A 77-year-old female patient suffering from chronic lower-back pain due to scoliosis with multiple degenerative changes and discus herniation L1-S1 (last spinal infiltration more than 10 months ago) presented to a local hospital because of severe persisting diarrhea for about 7 d and acute exacerbation of lower-back pain for 2 d. The patient was under daily steroids (prednisone 10 mg) because of a rheumatic polymyalgia and suffered from secondary osteoporosis and restless legs. Their vital signs, including body temperature, were normal. Laboratory investigation revealed an inflammatory status with elevated C-reactive protein (CRP) of 376 mg L−1 (normal <8 mg L−1), elevated total white blood cell count of 17.9 G L−1 (normal range 4.0–10.0 G L−1) without left shift, thrombocytosis of 430 G L−1 (normal range 150–300 G L−1), and mild hyponatremia. Liver and kidney function were normal. Except for the pre-existing sensitivity loss in the dermatome L4 on the left side and slight abdominal tenderness, no focal neurologic deficits or further hints for other sites of infection could be found. A magnetic resonance imaging (MRI) of the lumbosacral spine showed inflammatory changes paravertebrally and inside the psoas muscle on the left side at level L3/4 without clear involvement of the intervertebral disc compartment yet, hinting at a (because of marked degenerative changes) masked spondylodiscitis with little involvement of the intervertebral space (Fig. 1). A small (1.5×1.5 cm), not drainable, abscess formation was confirmed by CT scan, revealing gas formation in the soft tissues. Two days after admission, Campylobacter jejuni could be detected in aerobic blood and stool cultures. An antimicrobial treatment with azithromycin 500 mg once daily (initially intravenously) was initiated. Antibiotic susceptibility testing showed the following minimal inhibitory concentrations (MICs): ciprofloxacin MIC 0.125 µg mL−1, erythromycin MIC 2.0 µg mL−1, imipenem MIC 0.125 µg mL−1, gentamicin MIC 0.75 µg mL−1, and amoxicillin MIC 3.0 µg mL−1. According to the European Committee on Antimicrobial Susceptibility Testing (EUCAST) criteria, this is considered susceptible to ciprofloxacin under increased drug exposure (= I) and susceptible to erythromycin under standard dosing regimen (= S) according to the EUCAST definitions of susceptibility testing categories from 2019. At the time of presentation, the former EUCAST criteria interpreted the above MICs as susceptible (= S) (EUCAST, 2023). A CT-guided fine-needle biopsy of the psoas muscle was performed: bacterial cultures showed no growth, but 16S rRNA polymerase chain reaction (PCR) analysis turned out to be positive for Campylobacter species. The antibiotic treatment was switched to oral ciprofloxacin 750 mg twice a day.
Under therapy, the diarrhea stopped quickly and inflammatory markers turned to normal range within a few weeks. Due to a significant rise of liver enzymes 23 d after initiation of treatment (ASAT/ALAT1 >2 times the upper limit, GGT >30 times the upper limit), presumably drug-induced by ciprofloxacin, azithromycin was reinitiated with consequently rapid normalization of liver parameters, so we refrained from further examination of the hepatopathy.
The patient was treated for a total of 10 weeks. MR imaging at the end of therapy showed a significant decrease in inflammatory reaction and complete resolution of the abscess formations in the psoas muscle. However, the imaging also revealed clear involvement of intervertebral disc and the adjacent vertebral bodies, so spondylodiscitis was retrospectively proven (Fig. 2). The lower-back pain also improved but did not resolve completely because of the patient's pre-existing chronic lumbar back pain syndrome. No clue regarding the environmental source of infection of the Campylobacter jejuni could be found in the patient's medical history.
We screened the PubMed database using the following keywords: “Campylobacter” AND “spondylodiscitis”; “Campylobacter” AND “vertebral osteomyelitis”; and “Campylobacter” AND “bacteremia”. A total of six cases published from 2011 to 2022 were identified. They are described in detail in Tables 1 and 2 (Feodoroff et al., 2011; Ajili et al., 2011; Tappe et al., 2012; Puljiz and Topic, 2017; Langereis et al., 2018; Nakatani et al., 2022). Most patients were elderly and had underlying comorbidities like diabetes, liver cirrhosis, or a history of chronic back disorders. If the location of the spondylodiscitis was reported, it was mostly the lumbar spine that was affected. Only half of the patients suffered from diarrhea and/or fever. Four out of six were bacteremic at the time of presentation. Two articles reported susceptibility to ciprofloxacin. The others did not list detailed data on antibiotic susceptibility. Antimicrobial treatment varied. However, most cases were treated with either fluoroquinolones or macrolides. A total treatment duration between 4–36 weeks (median 8 weeks) was reported. A favourable outcome was described in all cases but with only scarce descriptions of follow-up time.
Abbreviations: f: female, m: male, WBC: total white blood cell count, Tc: thrombocyte, CRP: C-reactive protein, G L−1: giga per litre.
Campylobacter is a genus of gram-negative curved or rode-shaped bacteria and is found in a wide range of animals: poultry (mainly C. jejuni but also C. coli), pigs (mainly C. coli), and also in pets like dogs and cats (Keller et al., 2007). Transmission to humans occurs by handling or consumption of raw, poorly cooked, or cross-contaminated food products of these animals (mainly poultry); unpasteurized cow milk; contaminated water; or by direct contact with animals (Hansson et al., 2018).
Infections in humans are mainly due to C. jejuni or C. coli (more than 90 % of all cases) and C. fetus (Hansson et al., 2018) and present as a gastrointestinal disease with mild to severe diarrhea, abdominal cramping, nausea, fever, and sometimes bloody diarrhea. In developed countries Campylobacter enteritis is the major cause of food-borne bacterial enteritis, mainly caused by C. jejuni or C. coli (Hansson et al., 2018). Incubation time varies from 1 to 7 d (mean 3 d) (Hansson et al., 2018). In immunocompetent patients, Campylobacter enteritis is usually a self-limiting disease that resolves within 1 week with no need of antibiotic treatment (Hansson et al., 2018). Antimicrobial therapy reduces duration of intestinal symptoms only by approximately 1 d (Ternhag et al., 2007). Treatment should be considered for patients with severe symptoms or those at risk of severe disease (immunocompromised, elderly, or pregnant populations) or when bacteremia is present (Hansson et al., 2018).
Campylobacter bacteremia is still considered a rare event (1 % of Campylobacter infections) (Tinévez et al., 2022) with an incidence between 0.20–1.0 cases per 100 000 population in high-income settings (Moffatt et al., 2021). Recent data showed that C. jejuni is now the most frequently detected species in patients with bacteremia in a retrospective French study (Ternhag et al., 2007). Most patients with bacteremia are elderly and have underlying medical conditions (immunodepression, hematologic malignancies, solid neoplasm, diabetes) (Tinévez et al., 2022). Cases of osteoarthritis, meningitis, intra-abdominal infection (like cholecystitis, peritonitis, colitis), endocarditis, or peri-/myocarditis are described (Tinévez et al., 2022). Rare late-onset complications of Campylobacter infection are reactive arthritis, Guillain-Barré syndrome, and irritable bowel disease (Feodoroff et al., 2011; Hansson et al., 2018).
Vertebral osteomyelitis or spondylodiscitis by C. jejuni seems to be very rare. To the best of our knowledge, there are only six cases published so far. We now describe a further case consistent with the other cases: our patient is elderly, has comorbidities, is immunocompromised, and presented with febrile diarrhea and back pain as the main symptoms. Given the constellation of MRI findings, positive blood cultures, and PCR in CT-guided biopsy of psoas abscess, we were able to prove spondylodiscitis due to Campylobacter species infection. We did not perform an additional species-specific PCR analysis because clinical findings with proven bacteremia of C. jejuni were consistent with hematogenous spondylodiscitis.
In general, Campylobacter remains susceptible to many antibiotics, but resistance is emerging, especially to fluoroquinolones: resistance rates exceed 80 % in Southeast Asia (Mason et al., 2017), but current data from the European Centre for Disease Prevention and Control (ECDC) from 2020–2021 also show high ciprofloxacin resistance rates with an average level of 64.5 % and 69.6 % (C. jejuni and C. coli, respectively) in European countries (EFSA, 2023). Intrinsic resistance to many beta-lactam (e.g. penicillin) or cephalosporin and trimethoprim antibiotics are known (Lariviere et al., 1986). Standard therapy consists of macrolides (azithromycin); fluoroquinolones (if susceptible); or amoxicillin/clavulanic acid, carbapenems, or aminoglycosides in severely ill patients who cannot tolerate oral therapy (Dai et al., 2020).
In contrast to most other published cases of vertebral osteomyelitis, we were able to perform susceptibility testing. We preferred ciprofloxacin over azithromycin due to good bioavailability, bone penetration, and broad experience in osteomyelitis treatment (Thabit et al., 2019; Berbari et al., 2015), but we nevertheless had to switch to the macrolide because of a suspected drug-induced cholestatic hepatopathy. Azithromycin bone penetration seems to be high (Landersdorfer, 2009), but it is not used in standard treatment regimens in bone and joint infections (e.g. in staphylococci; Kim et al., 2014) with the exception of atypical mycobacteria, where macrolides are often the backbone therapy in combination with other active substances (Griffith et al., 2007). Azithromycin has successfully been used as a step-down oral therapy or in combination with other antibiotics in treatment of osteomyelitis with rare or resistant pathogens like Salmonella typhi (Ayeni and Calver, 2012), Bartonella henselae (Aparicio-Casares et al., 2021), or resistant pneumococci (Riordan et al., 2008), and it may be an option for treatment in combination with rifampicin (Shirtliff et al., 1999; O'Reilly et al., 1992). Although good quality evidence is still lacking, azithromycin may be a treatment option in select cases.
Optimal treatment duration of vertebral osteomyelitis is debated, with some proposing 6 weeks (Berbari et al., 2015; Bernard et al., 2015) and others advocating a minimal duration of 8 weeks in high-risk patients (including undrained paravertebral/psoas abscesses) (Park et al., 2016). While optimal treatment duration for C. jejuni spondylodiscitis is not known, most reported cases had a favourable outcome after 4–8 weeks of therapy. Our patient was treated for a total of 10 weeks with good clinical outcome and complete resolution of the abscess in MR imaging.
In conclusion, we report a successful treatment of a rare spondylodiscitis and concomitant psoas abscess with C. jejuni with a follow-up over 4 years after completion of treatment. Although clinical data is scarce, azithromycin may occasionally be a valuable treatment option for bone infections due to its good bone penetration.
No data sets were used in this article.
SG and MF screened the literature and wrote the original manuscript. JN, BM and SFH were involved in the treatment of the patient. JDH interpreted and provided the MR images. All authors reviewed the manuscript.
The contact author has declared that none of the authors has any competing interests.
Written informed consent for publication of the case and images was obtained from the patient.
Publisher's note: Copernicus Publications remains neutral with regard to jurisdictional claims made in the text, published maps, institutional affiliations, or any other geographical representation in this paper. While Copernicus Publications makes every effort to include appropriate place names, the final responsibility lies with the authors.
This paper was edited by Aaron Tande and reviewed by two anonymous referees.
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ASAT is aspartate aminotransferase, ALAT is alanine aminotransferase, and GGT is gamma-glutamyltransferase.