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Vet Pathol 37:650–652 (2000)

Pyogranulomatous Meningoencephalitis Due to Actinomyces sp. in a Dog

S. S. COUTO, P. J. DICKINSON, S. JANG, AND L. MUNSON

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.

Key words: Actinomyces sp.; cytology; dogs; hydrocephalus; meningoencephalitis; pyogranulomatous.

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
650
Vet Pathol 37:6, 2000 Brief Communications and Case Reports 651

Table 1. Cerebrospinal fluid (CSF) analysis of a dog


with CNS actinomycosis at presentation (sample 1) and 2
weeks after corticosteroid treatment (sample 2). Total nucle-
ated cell counts and protein levels increased following symp-
tomatic treatment.
Cisternal CSF
Normal
Parameter Sample 1 Sample 2 values
Total red blood cells (cells/ml) 9 1 0
Total nucleated cells (cells/ml) 189 3,810 0–2
Neutrophils (%) 71 80 Rare
Small mononuclear cells (%) 23 0
Large mononuclear cells (%) 6 20
Protein (mg/dl) 51 150 ,25
Gross appearance Clear Cloudy Clear

teeth, ear canals, tympanic bullae, nasal choanae, and nasal


sinuses, was examined, and no evidence of inflammation or Fig. 1. Cerebral spinal fluid: dog. Central radiating ag-
trauma was found in any of these locations. The dog also gregate of Actinomyces sp. surrounded by a corona of neu-
had multiple dark red, 0.5-cm-diameter, consolidated pul- trophils. Diff Quik. Bar 5 15 mm.
monary nodules located in the periphery of the right and left
cranial lung lobes.
Cytology smears of the CSF obtained from the subdural sidered to be associated with the actinomycosis. The single
space and stained with Diff Quik (Baxter Scientific Products, small pulmonary granuloma was a resolving lesion that was
Mc Gaw, IL) showed abundant neutrophils and a few ag- considered unrelated because of its chronicity and the ab-
gregates of degenerated neutrophils (Fig. 1). These aggre- sence of microorganisms.
gates were characterized by radiating gram-positive, acid- This case is also unusual because of the disparity of bac-
fast–negative filamentous organisms surrounded by a corona terial culture results ante- and postmortem. Fusobacterium
of elongated club-shaped neutrophils. Culture of the CSF nucleatum was not considered a contaminant and was pos-
was performed in 5% sheep blood agar with 5% carbon di- sibly a causative agent of a mixed anaerobic meningitis and
oxide at 37C, and a pure culture of Actinomyces sp. was ventriculitis, resulting in the clinical signs observed. Differ-
obtained. ent antibiotic therapies are used to treat these two anaerobic
Histologically, there was severe suppurative and granu- organisms; Fusobacterium can be treated with metronida-
lomatous meningoencephalitis and ventriculitis that involved zole, whereas penicillin derivatives are recommended for the
the brain stem and the subependymal white and gray matter treatment of Actinomyces infections. In this case, the anti-
along the lateral third and fourth ventricles (Fig. 2). Rare biotic therapy with metraonidazole could have suppressed
radiating bacterial colonies surrounded by neutrophils and a the growth of Fusobacterium, facilitating the overgrowth of
Splendore-Hoeppli reaction were found within the meninges Actinomyces, which had not been detected in antemortem
of the caudal brain stem (Fig. 3). The pulmonary nodules cultures.
were areas of bronchopneumonia, characterized by hemor- Because there was no history of trauma, a migrating fox-
rhage, and neutrophilic infiltrates surrounding small airways. tail (seed of Hordeum murinum or wild barley) was consid-
There also was a single small granuloma within the pul- ered a potential source of infection. Migrating foxtails are a
monary parenchyma, characterized by an accumulation of common cause of granulomas and abcesses due to anaerobic
epithelioid macrophages surrounded by a rim of lympho- or mixed bacterial and fungal infections in the western Unit-
cytes. No organisms were seen within this granuloma with ed States. Actinomyces hordeovulneris sp. nov. has been iso-
Giemsa, Brown and Brenn, or acid-fast (Fites Faraco) stains. lated from infections caused by migrating plant awns in Cal-
Actinomycosis of the CNS in animals has not been pre- ifornia.2 However, the present isolate of Actinomyces did not
viously confirmed by culture of the organism. In the previ- have the culture characteristics of this species.
ously reported cases of meningitis in a fox and a dog, the Hydrocephalus was common to both this case and the pre-
diagnosis was assumed based on the histologic appearance viously reported canine case and is likely secondary to
of the filamentous organisms. Furthermore, both animals had blockage of the mesencephalic aqueduct by the florid pyo-
facial or head bite wounds that probably were the source of granulomatous ventriculitis. Therefore, some of the chronic,
infection. The present case is unusual in the absence of pre- progressive, poorly localized neurologic signs may be
vious history of trauma or other sites of infection. The mul- caused by secondary hydrocephalus in dogs with CNS ac-
tifocal bronchopneumonia affected mainly cranioventral por- tinomycosis.
tions of the lungs and was interpreted to be due to aspiration, Actinomyces sp. should be considered as a potential cause
secondary to seizures. These lesions were acute and not con- of pyogranulomatous meningoencephalitis in dogs even in
652 Brief Communications and Case Reports Vet Pathol 37:6, 2000

Fig. 2. Brain and meninges; dog. Severe pyogranulomatous meningitis with a bacterial colony (arrow). HE. Bar 5 700 mm.

the absence of a positive antemortem CSF bacterial culture. Acknowledgements


Postmortem cytology of the purulent CSF was preferable to We thank Dr. R. J. Higgins for valuable assistance with
histology in identifying the causative organisms. photomicroscopy.
References
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Am J Vet Res 33:1457–1470, 1972
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Fig. 3. Meninges; dog. Higher magnification of Fig. 2, Request reprints from Dr. S. S. Couto, Anatomic Pathology
with radiating aggregate of Actinomyces sp. and Splendore- Service, Veterinary Medical Teaching Hospital, 1 Garrod
Hoeppli reaction. HE. Bar 5 70 mm. Drive, Davis, CA 95616 (USA).

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