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PART II.
C. Psittaci Infection Among Humans (Psittacosis)

Copyright Notice & Disclaimer Statement


Because several diseases affecting humans can be caused by other species of Chlamydia, the disease resulting from the infection of humans with C. psittaci is frequently referred to as psittacosis.  Most C. psittaci infections in humans result from exposure to psittacine birds.

During 1987-1996, 619 cases of psittacosis in humans were reported to the Centers for Disease Control and Prevention (CDC) (2). Because the diagnosis of psittacosis can be difficult, these 619 cases represent an underestimation of the actual number of cases.  During the 1980's, public health surveillance indicated that exposure to caged pet birds accounted for 70% of the psittacosis cases for which the source of infection was known; of these, owners of companion birds or bird fanciers were the largest group of affected persons (43%).  Pet-shop employees accounted for an additional 10% of cases.  Other persons at risk include pigeon fanciers and persons whose occupation places them at risk of exposure (e.g., employees in poultry-slaughtering/processing plants, veterinarians, veterinary technicians, laboratory workers, workers in avian quarantine stations, farmers, and zoo workers).  Because human infection can result from transient exposure to infected birds or their contaminated droppings, persons with no identified avocational or occupational risk may become infected.

Transmission to Humans

Human infection with C. psittaci usually occurs through the inhalation of the organism aerosolized from respiratory secretions or dried feces of infected birds.  Other sources of exposure can include bird bites, mouth-to-beak contact, and handling the plumage and tissure of infected birds.  Brief exposures can lead to symptomatic infection; therefore, history of contact with birds may not be elicited from some patients with psittacosis.

C. psittaci from mammalian species can occasionally cause disease in humans. Certain strains of C. psittaci infect sheep, goats, and cattle, causing chronic infection of the reproductive tract, placental insufficiency, and abortion in these species. Transmission of these strains to humans exposed to birth fluids and placentas of infected animals has been reported.  Feline keratoconjunctivitis agent is a strain of C. psittaci that typically causes rhinitis and conjunctivitis in cats.  Transmission of this strain to humans appears to occur rarely.

Human-to-human transmission has been suggested, but not proven.  Standard precautions are sufficient for patients with psittacosis and specific isolation procedures (e.g., private room, negative pressure airflow, masks) are not indicated.

Clinical Signs and Symptoms

Illness onset occurs following and incubation period of 5 to 14 days. The severity of the disease resulting from C. psittaci infection ranges from inapparent to systemic illness with severe pneumonia. Although mortality rates of 15% to 20% were reported during the preantibiotic era, death occurs in <1% of properly treated patients.

Cases of symptomatic infection are typically characterized by abrupt onset of fever, chills, headache, malaise, and myalgia.  A nonproductive cough usually develops and may be accompanied by dyspnea and chest tightness. A  pulse-temperature dissociation, splenomegaly, and rash are sometimes observed and are suggestive of psittacosis in patients with community-acquired pneumonia.  Auscultatory findings may underestimate the extent of pulmonary involvement.  Radiographic findings include lobar or interstitial infiltrates.  The differential diagnosis of psittacosis-related pneumonia includes infection with Coxiella burnetti, Mycoplasma pneumodiae, Chlamydia pneumoniae, Legionella spp, and respiratory viruses (e.g., influenza). C. psittaci can affect organ systems other than the respiratory tract and result in endocarditis, myocarditis, hepatitis, and fetal death has been reported in pregnant women.

Case Definition

A patient is considered to have a confirmed case of psittacosis if

  1. C. psittaci is cultured from clinical specimens or
  2. clinical illness is compatible with chlamydiosis and the antibody titer is increased by greater than fourfold (i.e., to >32) as demonstrated by a complement-fixation (CF) or microimmunofluorescence (MIF) test for C. psittaci by either paired sera obtained at least 2 weeks apart or detection of IgM antibody (i.e., >16) by MIF against C. psittaci.

A patient is considered to have a probable case of psittacosis if there is

  1. a clinically compatible illness that is epidemiologically linked to a confirmed case or
  2. a single antibody titer >32 by MIF or CF is present in at least one serum speciment obtained after onset of symptoms.

These case definitions were established by CDC and the Council of State and Territorial Epidemiologists for epidemiologic purposes (3). They should not be used as sole criteria for establishing clinical diagnoses.

Return to Psittacosis Index

Diagnosis

Diagnosis almost always is established by using serologic methods in which paired sera are tested for Chlamydia antibodies by CF test. However, because Chlamydia CF antibody is not species specific, high CG titers also may result from C. pneumoniae and Chlamydia trachomatis infection. Acute- and convalescent-phase serum specimens should be obtained as soon as possible after onset of symptoms and greater than or equal to 2 weeks after onset of symptoms, respectively. Because treatment with tetracycline may delay or diminish the antibody response, a third serum sample may help confirm the diagnosis. All sera should be tested simultaneously at the same laboratory. If indicated by epidemiologic and clinical history, MIF assays can be used to distinguish C. psittaci infection from infection with other chlamydial species. Information about laboratory testing is often available at state laboratories. In humans, the infective agent can be isolated from sputum, pleural fluid, or clotted blood during acute illness before treatment with antibiotics.

Treatment

Tetracyclines are the drugs of choice for treating psittacosis in humans; most persons respond to oral therapy (100 mg of doxycycline administered twice a day or 500 mg of tetracycline hydrochloride administered four times a day). For initial treatment of severely ill patients, doxycycline hyclate may be administered intravenously at a dosage of 4.4 mg/kg (2 mg/lb) body weight per day divided into two daily infusions (up to 100 mg per dose). Tetracycline hydrochloride may also be given intravenously (10-15 mg/kg body weight/day divided into four daily doses), but a preparation for injection is no longer available in the United States. Remission of symptoms usually is evident within 48-72 hours. However, relapse may occur, and treatment must continue for at least 10-14 days after fever abates. Although its in vivo efficacy has not been determined, erythromycin is probably the best alternative agent for persons for whom tetracycline is contraindicated (e.g., children aged <9 years and pregnant women).

Responsibilities of Physicians

Most states require physicians to report cases of psittacosis in humans to the appropriate health authorities. Timely diagnosis and reporting may aid in identifying the source of the infection and in controlling the spread of disease. Because single-serum titers are both insensitive and nonspecific for diagnosis of psittacosis, confirmation with paired acute- and convalescent-phase sera is recommended.

Birds that are suspected sources of human infection should be referred to veterinarians for evaluation and treatment. Local and state authorities may conduct epidemiologic investigations and institute additional disease-control measures.


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