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Abstract. Actinomyces sp. are commensal, filamentous, gram-positive, acid-fast–negative bacteria that can
cause pyogranulomatous inflammation in animals and humans. Central nervous system (CNS) disease is a rare
presentation of actinomycosis and is usually due to extension from infected wounds or seeding from distant
sites. A dog with progressive, poorly localized neurologic signs had primary CNS actinomycosis without history
or evidence of previous trauma or other organ involvement. Histologically, there was a severe pyogranulomatous
meningoencephalitis with intralesional filamentous bacteria that were also visible on cytology of the cerebral
spinal fluid (CSF) postmortem. Actinomyces sp. was cultured postmortem from the CSF, confirming the diag-
nosis. This case demonstrates that Actinomyces sp. can be a causative agent of primary CNS disease in dogs.
Actinomyces sp. are gram-positive, acid-fast–negative fil- were within normal limits. Cisternal cerebrospinal fluid
amentous bacteria that cause pyogranulomatous infections in (CSF) analysis revealed neutrophilic pleocytosis with in-
dogs, cats, cattle, goats, swine, horses, foxes and human be- creased protein (Table 1). Neutrophils were nondegenerate,
ings.5 These anaerobic or microaerophilic commensal organ- and no organisms were seen on direct smears. Aerobic and
isms are found in the oral cavity of animals and humans.3 fungal CSF culture were negative for pathogens. Serologic
Cutaneous actinomycosis is the most common manifestation analyses for common infectious agents such as Cryptococcus
in dogs, especially in large breed male dogs, and Actino- sp., Toxoplasma sp., Aspergillus sp., Neospora sp., Cocci-
myces viscosus is the most frequent isolate.3–5 These infec- dioidomyces sp., Ehrlichia canis, E. platys, E. equi, and
tions are usually secondary to perforating injuries caused by Rickettsia rickettsii were negative.
bite wounds or foreign bodies. In the most common forms A provisional diagnosis of pathogen-free inflammatory
of clinical disease in the dog, the cervicofacial, abdominal, CNS disease was made, and symptomatic treatment was ini-
and thoracic regions are involved.4,7 In humans, central ner- tiated with prednisone (1 mg/kg orally twice daily). The an-
vous system (CNS) infection with Actinomyces is rare and imal showed marked clinical improvement over the next 10
usually results from extension of an adjacent focus or from days but was presented again after 2 weeks with recurrence
hematogenous seeding from a distant site.7 Risk factors in- of the initial clinical signs. A CBC revealed leukocytosis
clude dental caries or infections, recent tooth extraction, (32,900 cells/ml, normal 5 6,000–17,000 cells/ml) with neu-
head trauma, gastrointestinal tract surgery, chronic otitis, trophilia (23,359 cells/ml, normal 5 3,000–11,500 cells/ml)
mastoiditis or sinusitis, chronic osteomyelitis, tetralogy of and monocytosis (1,654 cells/ml, normal 5 150–1,350 cells/
Fallot, and Actinomyces infection of an intrauterine device.7 ml). A CSF analysis revealed increases in total nucleated
A cerebral abscess is the most common manifestation of cells and protein (Table 1). Myelography was normal. Aer-
human CNS actinomycosis. Other infrequent presentations obic and fungal cultures of the CSF were negative, and an-
are meningitis or meningoencephalitis, actinomycomas, sub- aerobic culture revealed very small numbers of Fusobacte-
dural empyema, and epidural abscesses.7 There are two un- rium nucleatum after 8 days of growth. Treatment with en-
confirmed reports of Actinomyces causing CNS disease in rofloxacin (4.5 mg/kg orally twice daily), metronidazole (8
animals: spinal meningitis in an Arctic fox and encephalitis mg/kg orally three times daily), and prednisone (0.5 mg/kg
associated with hydrocephalus in a dog.1,6 In both cases, the orally twice daily) was initiated. Intracranial magnetic res-
diagnosis of actinomycosis was assumed based on morpho- onance imaging was declined by the owner. After 1 month
logic characteristics and staining properties of the bacteria of moderate improvement, the animal acutely decompensat-
on histologic examination. Culture of Actinomyces from the ed, was presented obtunded with ataxia, vocalization, and
CNS and a definitive diagnosis has not been previously re- loss of vision following generalized seizures, and subse-
ported in domestic animals. quently died after a cardiac arrest.
A 1-year-old intact female German Shepherd Dog was On necropsy, the superficial blood vessels of the cerebral
presented to the Veterinary Medical Teaching Hospital of the cortex were hyperemic, and the cerebellum was mildly
University of California–Davis for apparent cervical pain of coned, protruding slightly through the foramen magnum.
2 months duration. All vaccinations were current, travel his- There was approximately 1 ml of purulent material in the
tory was restricted to northern California and Idaho, and the subdural space, mainly located over the brain stem. The lep-
animal had been exposed to ticks periodically. No history of tomeninges overlying the midbrain, pons, and medulla, and
trauma was noted. On physical and neurologic examination, the dura mater lining the corresponding ventral portions of
the dog was quiet and alert and had pain on movement or the calvarium were thickened, hyperemic, roughened, and
palpation of the head and neck. Results from complete blood opaque. Sagittal sections of the brain showed symmetrically
count (CBC), serum chemistry analysis, urinalysis, thoracic dilated lateral ventricles, consistent with moderate hydro-
radiographs, abdominal ultrasound examination, joint fluid cephalus. The superficial blood vessels of the spinal cord
analysis from several joints, and complete spinal radiographs were diffusely engorged. The head, including oral cavity and
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Vet Pathol 37:6, 2000 Brief Communications and Case Reports 651
Fig. 2. Brain and meninges; dog. Severe pyogranulomatous meningitis with a bacterial colony (arrow). HE. Bar 5 700 mm.