Keywords
Infection - Myroides odoratus - neurosurgery
Introduction
The bacteria belonging to the genus Myroides are nonmotile, nonfermenting, Gram negative, and rod shaped characterized by fruity
odor during growth and produce yellow-pigmented colonies on nutrient agar.[1] Bacteria of the genus Myroides are not a part of the regular human microbial flora.[2] They cause opportunistic infections in immunocompromised patients. Myroides are
ubiquitous and were found in soil and water, with M. odoratus and Myroides odoratimimus being the clinically relevant species.[3]
M. odoratus is a very rare human pathogen. Myroides spp. have been reported as a cause of cellulitis, urinary tract infection, pericardial
effusion, sepsis, and endocarditis.[2] Central nervous system (CNS) infection due to these organisms has been rarely reported
in the literature.[4] To the best of our knowledge, this is the first case report of M. odoratus-associated CNS infection in a patient with solid tumors postneurosurgery.
Case Report
A 37-year-old female with anaplastic astrocytoma in the right frontal lobe underwent
supratentorial craniectomy for a recurrent right frontal tumor in the neurosurgery
department and was discharged uneventfully [Figure 1a], [b], [c], [d]. She had a history of undergoing surgery and radiotherapy for the same disease.
She was planned for reradiation and rechallenge with temozolomide; however, after
about a month (post-2nd surgery), she complained of fever, headache, vomiting, and
neck rigidity. Her Glasgow Coma Scale = 15/15 and Karnofsky Performance Status = 70.
She had a cerebrospinal fluid (CSF) leak from the operative site and a fever of 39.4°C.
Laboratory investigations from peripheral blood indicated increased white blood cell
(WBC) count of 14.91 × 109/L (4.0–10.0); increased absolute neutrophil count of 10.74
× 109/L (2.0–7.0) at 88.6% (40.0–80.0); decreased lymphocyte count of 0.87 × 109/L
(1.0–3.0) at 5.9% (20.0–40.0); increased CSF protein = 449 mg/dL (normal: 15–45 mg/dl);
lactic dehydrogenase = 250 U/L (normal: 100–190 U/L); C-reactive protein = 10.8 mg/dl
(reference range: 0–0.33); and decreased CSF sugar level = 36 mg/dl (corresponding
random blood sugar = 78 mg/dL). She had received day 1 of salvage temozolomide before
the symptoms appeared, following which it was discontinued. Her lumbar CSF sample
was sent to the microbiology laboratory for bacterial culture and drug sensitivity,
blood sample for routine viral markers, malaria antigen testing, and the patient was
empirically started with injection vancomycin (500 mg 6 hourly) and cefoperazone–sulbactam
(2 g 12 hourly). The tests for malaria antigen detection by immune chromatographic
assay were negative; dengue-NS1 antigen, IgM, and IgG antibodies were not detected.
The viral markers for hepatitis B surface antigen, human immunodeficiency virus, and
anti-hepatitis C virus antibodies were also nonreactive. Gram staining of CSF showed
polymorphonuclear cells and Gram-negative bacilli. On culturing the CSF on blood agar
and nutrient agar for 24 h, yellow-pigmented colonies with fruity odor were obtained
[Figure 2a] and [b]. MacConkey agar did not show any growth. Gram staining of the colonies on blood
agar suggested a pure culture of Gram-negative bacilli. Identification of the isolate
was also performed on the VITEK-2 (BioMérieux, Marcy-l'Etoile, France) automated identification
system, which reported Myroides spp. and its AST MIC pattern. M. odoratus was presumptively identified by performing the desferrioxamine (250 μg-disc) susceptibility
testing; M. odoratus being desferrioxamine susceptible while the other species M. odoratimimus being nonsusceptible.[5] The minimum inhibitory concentrations (MICs) (μg/ml) were found to be ≥64, ≥16,
≥4, ≤4, 8, ≤8, ≤0.25, ≤0.25 μg/ml for amikacin, gentamicin, ciprofloxacin, piperacillin/tazobactam,
ceftazidime, cefoperazone-sulbactam, imipenem, and meropenem, respectively. However,
susceptibility interpretation is not possible due to lack of standard Clinical and
Laboratory Standards Institute (CLSI) or EUCAST interpretive breakpoints for Myroides spp. These MICs and interpretation were provided by the VITEK-2 using GN AST-N 281-NLF
cards. The VITEK-2 identification and susceptibility testing system has been used
for non-glucose-fermenting Gram-negative bacilli (including Myroides), and the results have been found to be acceptable in a study conducted by Hsieh
et al. in 2009, which reported a 100% (n = 7) concordance of GN AST-N 281-NLF cards for reporting Myroides spp. with that of conventional identification methods.[6]
Figure 1: (a-c) Contrast-enhanced coronal, sagittal, and axial view of preoperative
magnetic resonance imaging showing the tumor. (d) T2 axial image of the postoperative
magnetic resonance imaging showing tumor excision
Figure 2: Colonies of Myroides spp. seen on (a) sheep blood agar and (b) nutrient agar
Based on the culture and susceptibility results, injection vancomycin was discontinued
and the patient was treated with injection cefoperazone–sulbactam for 10 days, after
which she made a good clinical recovery and was planned for reradiation.
Discussion
Postoperative CNS infection after neurosurgery with an incidence of 0.5%–8% carries
substantial morbidity and also mortality.[7] The associated risk factors for postcraniotomy meningitis include diabetes, advanced
age, GCS <12, prolonged surgery, external ventricular drainage, lumbar drainage, use
of perioperative antibiotics, and concurrent infection.[8] Aseptic meningitis comprises 60%–75% of all cases of postoperative meningitis. However,
it is very important to promptly diagnose and treat meningitis aggressively, when
the etiology is bacterial. We used the conventional definitions to suspect bacterial
meningitis (clinical signs and symptoms, increased WBC count and protein, and reduced
glucose in CSF), which was confirmed by CSF culture. A wide range of organisms have
been implicated in postneurosurgery meningitis. Acinetobacter was the most common organism in one study.[8] The study by Srinivas et al. found Pseudomonas and other nonfermenting Gram-negative bacilli followed by Klebsiella pneumonia e to be more common.[7] Other organisms such as Staphylococcus aureus (including MRSA), Escherichia coli, Citrobacter spp., Proteus spp., Enterococcus spp., and Streptococcus agalactiae have also been reported.[9]
[10] A study conducted in the West Indies reported the isolation of M. odoratus in ventricular fluid of a 6-week-old infant with hydrocephalus who developed ventriculitis
and was managed with intraventricular cefotaxime.[4] However, Myroides spp. as a cause of postneurosurgical meningitis has rarely been reported in the literature
and this is the first time we encountered this microorganism in our setting. The source
of the organism and the mode of entry into the CSF is unknown and difficult to determine;
however, it has been hypothesized that repeated sampling of the ventricles may introduce
the infection. Myroides spp. have been reported to be among the more resistant organisms in literature, with strains
that harbor KPC-2 carbapenemase and metallo-beta-lactamases, making them resistant
to beta-lactam drugs and also carbapenems.[11] The CLSI and the The European Committee on Antimicrobial Susceptibility Testing
(EUCAST) does not provide interpretive breakpoints for Myroides spp. against antibacterials. Multidrug-resistant Myroides infection at other sites (wound, blood, bile, respiratory, etc.,) has been treated
with the few antibiotics they were susceptible to, which included meropenem, ceftazidime,
piperacillin–tazobactam, and cefoperazone.[12] The MICs for various antibiotics against our isolate were obtained by the VITEK-2
automated identification and susceptibility instrument and were found to be susceptible
to piperacillin–tazobactam, ceftazidime, cefoperazone–sulbactam, imipenem, and meropenem.
The patient was treated with intravenous cefoperazone–sulbactam and vancomycin for
10 days, after which she made a good clinical recovery and was planned for radiation.
CSF culture performed subsequently was sterile demonstrating microbiological clearance
of the organism.
M. odoratus has a role to play in the etiology of postoperative infection after neurosurgery.
Although reported to be multidrug resistant in literature, it can be treated effectively
by the use of appropriate antibiotics.
Declaration of patient consent
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images and other clinical information to be reported in the journal. The patients
understand that their names and initials will not be published and due efforts will
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