19-year-old male rhesus macaque (Macaca
mulatta).This animal was
part of a colony housed at the Texas Biomedical Research Institute.
Clinical signs included chronic age-related arthritis in both knees and a
general decline in condition associated with cachexia, diarrhea, and
dehydration. The animal was euthanized due to poor condition.
The animal was dehydrated with low body fat but adequate muscle. Several teeth
were missing. Both knees had reduced range of motion and periarticular
Internal: The liver was enlarged with pale tan edges on several lobes. The colon was distended with fluid feces. There was multifocal, 2-5 mm diameter, slightly raised tan nodules in all lung lobes.
Multifocally, bronchial and bronchiolar walls are irregularly thickened by
large numbers of lymphocytes, plasma cells, macrophages, and eosinophils, with
fewer neutrophils and multinucleated giant cells. Airway lumens are often
enlarged and contain macrophages, granulocytes, and cross and tangential
sections of arthropod parasites. Arthropods are approximately 300-500 um in
width and characterized by a thin chitinized cuticle, jointed appendages,
striated musculature, a body cavity, digestive tract, and reproductive organs.
Many macrophages contain abundant intracytoplasmic golden-brown to black,
finely granular, birefringent pigment (mite excrement). The inflammatory cell
aggregates multifocally disrupt and/or obscure the bronchial and bronchiolar
walls, form lymphoid follicles, variably compress or extend into adjacent
alveolar tissue, and elevate the pleura (raised nodules noted grossly).
Affected bronchi and bronchioles exhibit moderate smooth muscle hypertrophy and
occasional peribronchiolar fibrosis. In less affected lung, terminal airways
and alveoli are multifocally dilated with occasional loss of alveolar septa.
Lung, rhesus macaque. Numerous 2-5mm diameter tan nodules are present within all lung lobes. (Photo courtesy of: Covance Laboratories, Inc, Madison, Wisconsin, USA.
Lung: Bronchitis/bronchiolitis, chronic
and eosinophilic, multifocal, moderate, with bronchiolectasis, smooth muscle
hyper-trophy, and mites and mite pigment, etiology consistent with Pneumonyssus
diagnoses in this animal included hepatic amyloidosis and chronic lympho-plasmacytic
Simian retrovirus and herpesvirus serology were negative.
Pneumonyssus simicola, rhesus
Pneumonyssus simicola, the lung mite of rhesus macaques, has become a
less common parasite in most managed primate colonies; the incidence of
pulmonary acariasis remains very high in feral and wild caught rhesus
monkeys. Despite extensive microscopic findings in many affected animals,
infection is typically subclinical. Sneezing, coughing, and dyspnea have been
reported.8 Antemortem diagnosis can be difficult. Radiographs are
generally not helpful; however, tracheobronchiolar lavage has been a successful
diagnostic tool, usually by identifying larva that migrates to the larynx.
False negatives are possible.1,4,5
As demonstrated in the accompanying photographs, gross findings appear as multifocal and coalescing, discrete, irregularly round to ovoid, slightly raised, light brown foci several millimeters in size. In contrast to M. tuberculosis, the lesions of Pneumonyssus simicola are typically soft and cystic, or air-filled bullae.1 Thin fibrous adhesions within the pleural cavity are commonly observed.9
Microscopic lesions consist of multifocal chronic bronchiolitis and bronchiolectasis with hyperplasia of bronchiolar smooth muscle and prominent peribronchiolar lymphoid aggregates admixed with eosinophils and pigment-laden macrophages. Adult mites, most of which are females, are normally evident in sections of affected lung. Mites are identifiable by typical arthropod characteristics; a chitinized outer cuticle, body cavity, striated musculature, jointed appendages, and sometimes other structures including brain, gastrointestinal and reproductive tract, eggs and occasionally larvae. The presence of birefringent brown to black pigment in macrophages at the periphery of affected bronchioles is a hallmark of infection and considered diagnostic even in the absence of identifiable mites.8
Bronchiolitis and bronchitis, pyogranulomatous and eosino-philic, chronic,
multifocal, moderate, with bronchiectasis and bronchiolar intraluminal
arthropods with mite pigment, rhesus macaque, Macaca mulatta.
The contributor provides an outstanding example of pulmonary acariasis
in a nonhuman primate, with numerous cross sections of well-preserved adults
and eggs scattered throughout the larger conducting airways in this section of
simicola mites are ubiquitous in wild and wild-caught Old
World primates with an incidence of nearly 100%.2,3,9 As a result,
mites and their associated lesions are considered a background incidental
finding in these animals.2,9 Previously reported
pulmonary histologic lesions are generally similar to this case with eosinophilic
to granulomatous bronchitis/bronchiolitis with variable amounts of brown to
black mite pigment within bronchi and bronchioles and moderate to marked
inflammation expanding the peribronchiolar interstitium.2,9 Other than the abundant mite pigment, conference
participants agreed that the most striking histologic lesion is the profound
bronchiectasis. Bronchiectasis is the permanent marked dilation of bronchi and
is a consequence of chronic bronchial obstruction by the parasite.
As described by the contributor, adult mites have the typical arthropod characteristics of 300-500 um width, chitinous exoskeleton, mouth parts, jointed appendages, striated musculature, a body cavity, digestive tract, reproductive structures, yolk material in yolk glands, and developing eggs.3
The highly characteristic birefringent golden brown to black crystalline mite pigment, thought to be a metabolite of digestion and excretion by the female mite, can be present in sections that lack mites and are diagnostic for the parasite.2,3,9 This pigment does not contain melanin or carbon, but rather is composed predominantly of iron. This the result of the mite feeding on host erythrocytes with digestion and excretion of blood protein, hemoglobin.9 Additionally, mite pigment is likely the cause of the majority of the inflammatory response within the lungs.2
Widespread use of the anthelmintic medication, ivermectin, during quarantine of new animals and as a part of routine colony management has markedly reduced the incidence in laboratory nonhuman primates.2,9
Pulmonary acariasis and nasopharyngeal mites occur in many other animal species. Some of the most important nasal and pneumotropic arthropod parasites of veterinary importance include Pneumo-nyssoides sp. in the lungs of New-world primates; Rhinophaga sp. in the nasal cavity of Old-world primates; Pneumo-nyssoides caninum, the nasal mite in dogs; Linguatula serrata in the nasal cavity of dogs and cats; Oestrus ovis, the nasal botfly in sheep and goats; Entonyssus sp. and Entophionyssus sp. in the trachea and lung of snakes; Cephenemyia sp. in the nasal cavity of wild cervids; Cytodites nudus in the air sacs of poultry; and Halarachne halichoeri in the nasal passages of wild sea lions.6
1. Andrade MCR, Marchevsky RS. Histopathologic findings of pulmonary acariasis in a rhesus monkeys breeding unit. Revista Brasileira de Parasitologia Veterinária. 2007; 16(4):229-234.
2. Cogswell F. Parasites of non-human primates. In: Baker DG, ed. Flynns Parasites of Laboratory Animals. 2nd ed. Ames, Iowa: Blackwell Publishing; 2007:716-717.
3. Gardiner CH, Poyton SL. An Atlas of Metazoan Parasites in Animal Tissues. Washington, DC: Armed Forces Institute of Pathology; 1999:56-58.
4. Keeling M, Wolf R. Respiratory diseases. In: Bourne G, ed. The Rhesus Monkey, Volume II: Management, Reproduction, and Pathology. New York, NY: Academic Press; 1975:70-71.
5. Lowenstine LJ, Osborn KG. Respiratory system diseases of nonhuman primates. In: Abee C, Mansfield K, Tardif S, Morris T, eds. Nonhuman Primates in Biomedical Research: Diseases. London, UK: Academic Press; 2012:467-468.
6. Pneumonyssus simicola. Joint Pathology Center Systemic Pathology (updated Oct. 2014). Retrieved from: https://www.askjpc.org/vspo/show_page.php?id=595.
7. Purcell JE, Philipp MT. Parasitic diseases of nonhuman primates: In Wolfe-Coote S, ed. The Laboratory Primate. San Diego, CA: Elsevier; 2005:589-590.
8. Stookey J, Moe J. The respiratory system. In: Benirschke K, Garner F, Jones T, eds. Pathology of Laboratory Animals, Vol. 1. New York, NY: Springer-Verlag; 1978:106-107.
9. Strait K, Else JG, Eberhard ML. Parasitic diseases of nonhuman primates. In: Abee CR, Mansfield K, Tardiff S, Morris T, eds. Nonhuman Primates in Biomedical Research: Diseases. 2nd ed. Vol. 2. San Diego, CA: Academic Press;