Case report of Actinomyces turicensis meningitis as a complication of purulent mastoiditis

Meningitis caused by anaerobic bacteria is a rare disease therefore anaerobic culture of the cerebrospinal fluid (CSF) samples is not generally recommended. However, by these sparse cases of anaerobic meningitis certain conditions present risk factors namely, recurrent or chronic otitis media, brain abscess, necrotizing bowel lesions or peritonitis [1]. In cases of identifiable risk factors anaerobic meningitis should be kept in mind and the CSF specimen should be cultured both aerobically and anaerobically. The routine CSF sample processing lacks the anaerobic incubation that can lead to false-negative results and as a consequence to misdiagnose and therapy failure.

Actinomyces genus contains strictly anaerobic and aerotolerant, non-acid-fast, Gram-positive organisms with variable morphology, ranging from characteristic branching rods to coccobacilli arranged singly or in pairs. The most well-known species is Actinomyces israelii, however altogether 25 published Actinomyces species from human samples have been described [2]. Among these species Actinomyces turicensis was first reported in 1995 [3] and has been emerging as an important cause of infections [4]. A. turicensis is a non-pigment producing, aerotolerant member of Actinomyces genus. Its biochemical characteristics include negative reactions for the production of catalase, urease, β-N-acetyl-glucosaminidase and β-galactosidase, nitrate reduction, esculin hydrolysis, CAMP test and the fermentation of mannitol additionally, it produces α-glucosidase and ferments maltose and sucrose. Variable reactions are raffinose and trehalose fermentation [3].

Actinomyces spp. belong to the normal bacterial flora in the oral cavity, pharynx, gut and genitourinary tract [5‐10]. Actinomycosis is an uncommon infection caused by Actinomyces spp. It is characterized by an indolent, slow growing, granulomatosus disease and categorized based on the anatomical sites as orocervicofacial, thoracic and abdominopelvic forms, or in some other cases it appears as cutaneous or musculoskeletal [11‐14]. Actinomyces infections of central nervous system (CNS) such as brain abscess and meningitis are rarely diagnosed [15‐18]. To date no published reports of A. turicensis meningitis were found on online databases. We herein report the first case of A. turicensis meningitis that originated from the left mastoiditis and it was diagnosed in a patient with poor socioeconomic status.

A 43-year-old Hungarian man with poor socioeconomic living conditions was found lying on the floor unresponsively by a family member. He was taken to a regional hospital “Szent György” University Teaching Hospital, Székesfehérvár, Hungary. On admission he had low level of consciousness accompanied by stiff neck, constricted pupils and fever (38.6 °C). Alcohol abuse, smoking and epileptic seizures were found in his past medical records. Urgent skull CT scan was performed revealing left side mastoiditis but neither brain abscess nor vascular disorders were described. Blood was drawn for clinical chemistry and for bacterial culture. Relevant parameters of the blood test showed elevated white blood cell (WBC) count 24.1 10⁹/L (87.5% Neutrophils), increased C-reactive protein and procalcitonin levels (211.4 mg/L and 0.46 ng/ml, respectively). Laboratory parameters of blood and liquor are shown in Table 1. The results of the urine tests were normal.

Lumbar puncture was carried out and the CSF sample was taken to the laboratory immediately. The slightly xanthochromic CSF was cloudy showing increased WBC count (7400 cells/μl), elevated protein level (12.4 g/L), and low glucose level (< 0.6 mmol/L) compared to the elevated serum glucose level (8.1 mmol/L).

After taking blood and CSF specimens for culture Ceftriaxone (2 × 2 g), Vancomycin (2 × 1 g) and Ampicillin (6 × 2 g) were started and completed with supportive treatment.

The patient’s CSF sample was processed routinely in our Microbiology laboratory (SYNLAB Székesfehérvár, Hungary) on arrival. The Pastorex Meningitis agglutination kit (Bio-Rad) testing the CSF sample for the presence of soluble antigens of Streptococcus pneumoniae, Haemophilus influenzae type b, Neisseria meningitidis group A, group B/E.coli K1, group C, group Y/W135, and Streptococcus group B was negative. Microscopic examination showed several neutrophil granulocytes and a very few number of hardly dyed short rods or elongated cocci that seemed to be Gram-negatively stained at first examination. To exclude tuberculous meningitis Ziehl-Neelsen staining was performed, but no acid-fast bacilli were detected. At the 18–24-h and 48 h readings bacterial growth was negative both on the blood and on the chocolate culture media. Only the enrichment broth was slightly cloudy, indicating bacterial growth. On the next day, after 72 h of incubation tiny grey pinhead colonies were found on both blood and chocolate agar plates that were catalase and oxidase negative. Similar colonies were seen on the anaerobic plates. Irregular small Gram-positive bacilli and coccobacilli were observed in the microscope. The bacterium was identified as A. turicensis by VITEK 2 ANC ID Card (Biomerieux) and API Coryne (Biomerieux). The identification was verified by molecular method. PCR was performed with primers that amplified 1343 bp fragment of bacterial 16 s rRNA coding sequence [19]. PCR thermal profile was as follows: 5 min at 94 °C, 40 cycles of 94 °C for 1 min, 55 °C for 1 min and 72 °C for 1 min and a final extension at 72 °C for 2 min [20]. PCR amplicons have been purified by Qiagen PCR Purification Kit (Qiagen, GmbH, Hilden, Germany) and have been sequenced (BIOMI Kft., Gödöllő, Hungary). Analysis of nucleic acid sequence was done based on online tools of NCBI GenBank thus, the strain was identified as A. turicensis.

Antibiotic susceptibility of tested strain was performed by E-test after the European Committee on Antimicrobial Susceptibility Testing (EUCAST) recommendations. The isolated strain was susceptible to penicillin, ampicillin, imipenem, meropenem and vancomycin at concentrations ranging from 0.125 to 0. 5 mg/L.

Postoperative bleeding occurred leading to the necessity of reoperation. On the third day of postoperative period severe polyuria was presented with dilated pupils insensible to light. The skull CT scan revealed cerebral herniation, intensifying oedema and sinus thrombosis. (Figures 1 and 2). Unfortunately, there was no chance of reoperation because the patient passed away.

After 5 days of aerobic and anaerobic incubation of the blood cultures no bacterial growth was detected. Autopsy was performed that confirmed the clinical diagnosis of cerebral herniation due to the purulent meningitis and the consequent oedema in the CNS. Moreover, a greenish-yellow discharge accumulated at the brain stem and in the lateral ventricules. During histopathology an infiltration of granulocytes at the meninges was seen and suspected signs of actinomycosis was also observed.

Actinomyces spp. resides on mucous surfaces typically in the alimentary and genital tracts. On the other hand, Actinomyces spp. can rarely cause CNS infections due to the contiguous extension of neighbouring foci, such as paranasal sinusitis, or hematogenous seeding from a distant infected site such as a dental abscess, lungs and cervicofacial region although no such apparent foci are observed in one-third of cases. The typical manifestation of Actinomyces CNS infection is brain abscess, but Smego reported that 13% of CNS lesions of actinomycosis involve meningitis [17]. A. turicensis has been described as a potential pathogen mostly in genital and skin-related infections, however here we presented a case of CNS infection, namely A. turicensis meningitis as a complication of purulent mastoiditis with fatal outcome. In our patient an identical A. turicensis strain has been identified from a purulent mastoiditis and in meningitis, indicating the invasion of the pathogen from the infectious focus to CNS. There were no signs or symptoms of lung or skin actinomycosis. Anaerobes are found to be rare causative agents of meningitis but as our case report has shown it is worth to keep it in mind as possible pathogens of CNS. It may occur in patients living in poor socioeconomic conditions (e.g: homeless and alcohol abuse) and suffering from paranasal sinusitis or inflammation of other neighbouring foci. Here, we propose the need for anaerobic cultures of CSF specimens that is essential to identify Actinomyces spp. as well as other anaerob bacteria in CNS infections.