Psittacosis (Chlamydophila psittaci)

Published on 22/03/2015 by admin

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Chapter 219 Psittacosis (Chlamydophila psittaci)

Chlamydophila psittaci, the agent of psittacosis (also known as parrot fever and ornithosis), is primarily an animal pathogen and causes human disease oncommonly. In birds, C. psittaci infection is known as avian chlamydiosis.

Etiology

C. psittaci affects both psittacine birds (e.g., parrots, parakeets, macaws) and nonpsittacine birds (ducks, turkeys); the known host range includes 130 avian species. The life cycle of C. psittaci is the same as for Chlamydophila pneumoniae (Chapter 217). Strains of C. psittaci have been analyzed by patterns of pathogenicity, inclusion morphology in tissue culture, DNA restriction endonuclease analysis, and monoclonal antibodies, which indicate that there are 7 avian serovars. Two of the avian serovars, psittacine and turkey, are of major importance in the avian population of the USA. Each is associated with important host preferences and disease characteristics.

Diagnosis

Psittacosis can be difficult to diagnose because of the varying clinical presentations. A history of exposure to birds or association with an active case can be important clues, but as many as 20% of patients with psittacosis have no known contact. Person-to-person spread has been suggested but not proved. Other infections that cause pneumonia with high fever, unusually severe headache, and myalgia include routine bacterial and viral respiratory infections as well as Coxiella burnetii infection (Q fever), Mycoplasma pneumoniae infection, C. pneumoniae infection, tularemia, tuberculosis, fungal infections, and Legionnaires disease.

The mainstay of diagnosis remains serology using the complement fixation (CF) test, which is genus specific. According to the recommendations from the Centers for Disease Control and Prevention in 2000, a confirmed case of psittacosis requires a compatible clinical illness, usually with a reliable history of avian exposure. Laboratory confirmation may be by 1 of 3 methods: culture of C. psittaci from respiratory secretions; a ≥4-fold increase in CF or microimmunofluorescence (MIF) titer in sera collected at least 2 wk apart; or a single MIF immunoglobulin M titer of ≥1 : 16. A probable case should be epidemiologically linked to a confirmed case or have a single CF or MIF antibody titer of ≥1 : 32 in ≥1 serum sample obtained after onset of symptoms. As with the use of MIF for diagnosis of C. pneumoniae infections, cross reactions with other Chlamydia species and bacteria can occur. False-negative MIF results can occur in acutely ill patients. Early treatment of psittacosis with tetracycline can abrogate the antibody response.

The organism also can be isolated by culture from sputum or pleural fluid. Although C. psittaci will grow in the same culture systems used for isolation of Chlamydia trachomatis and C. pneumoniae, very few laboratories culture for C. psittaci, mainly because of the potential biohazard. Nucleic-acid amplification tests for detection of C. psittaci have been reported in the literature, but these are in-house assays that do not have FDA approval.