Q Fever

Cases of Q fever occur among workers whose occupations bring them in close contact with farm animals (which are often asymptomatic) or their products. Transmission is usually by inhalation of infectious aerosols that can travel long distances affecting people living downwind of an infected goat or sheep farm. The disease can also be contracted by ingesting infective raw milk.

C. burnetii is very virulent, resists inactivation, and remains viable in dust and stool for months; even a single organism can cause infection. Because of these characteristics, C. burnetii is a potential biological warfare agent.

Very rarely, the disease is transmitted from person to person.

The incubation period averages 18 to 21 days (range 9 to 28 days). Acute Q fever is often asymptomatic; in other patients, it begins abruptly with influenza-like symptoms: fever, severe headache, chills, severe malaise, myalgia, anorexia, and sweats. Fever may rise to 40° C and persist 1 to > 3 weeks.

Rarely, acute Q fever manifests as encephalitis or meningoencephalitis.

Respiratory symptoms (a dry nonproductive cough, pleuritic chest pain) appear 4 to 5 days after onset of illness. These symptoms may be particularly severe in older patients or patients who are debilitated. During examination, lung crackles are commonly noted, and findings suggesting consolidation may be present. Unlike rickettsial diseases, acute Q fever does not cause a rash.

Acute hepatic involvement, occurring in some patients, resembles viral hepatitis, with fever, malaise, hepatomegaly with right upper abdominal pain, and possibly jaundice. Headache and respiratory signs are frequently absent.

A post-Q fever fatigue syndrome has been reported to occur in up to 20% of patients with acute Q fever (1). Patients report severe fatigue, muscle pains, headache, photophobia, and/or mood and sleep changes.

Chronic Q fever may manifest within a few weeks to many years after the initial infection. People with a history of cardiac valvular defects, arterial aneurysms, or vascular grafts are at increased risk of developing chronic Q fever. Pregnancy and immunosuppression have also been linked to the development of chronic Q fever. Hepatitis may manifest as fever of unknown origin. Liver biopsy may show granulomas, which should be differentiated from other causes of liver granulomas (eg, tuberculosis, sarcoidosis, histoplasmosis, brucellosis, tularemia, syphilis).

Endocarditis resembles culture-negative subacute bacterial endocarditis; the aortic valve is most commonly affected, but vegetations may occur on any cardiac valve. Marked finger clubbing, arterial emboli, hepatomegaly, splenomegaly, and a purpuric rash may occur. Only 20 to 40 % of patients who develop Q fever endocarditis have symptoms of acute infection.

The case-fatality rate of acute Q fever is only about 1% in untreated patients. Untreated chronic Q fever endocarditis is always fatal. Adequate antibiotic treatment reduces the mortality rate for Q fever endocarditis to <5% (2). Some patients with neurologic involvement have residual impairment.

• Immunofluorescence assay (IFA) or polymerase chain reaction (PCR) of infected tissue or blood specimens

• Sometimes acute and convalescent serologic tests

Symptoms do not readily suggest the diagnosis of Q fever. Early on, Q fever resembles many infections (eg, influenza, other viral infections, salmonellosis, malaria, hepatitis, brucellosis). Later, it resembles many forms of bacterial, viral, and mycoplasmal and other atypical pneumonias. Contact with animals or animal products is an important clue.

IFA of infected tissue is the diagnostic method of choice; alternatively, enzyme-linked immunosorbent assay (ELISA) may be done. Acute and convalescent serum specimens (typically complement fixation) may be used. Antibodies to phase II antigen are used to diagnose acute disease, and antibodies to both phase I and phase II antigens are used to diagnose chronic disease.

PCR can identify the organism in biopsy or blood specimens, but negative results do not rule out the diagnosis.

C. burnetii may be isolated from clinical specimens, but only by special research laboratories; routine blood and sputum cultures are negative.

Patients with respiratory symptoms or signs require chest x-ray; findings may include atelectasis, pleural-based opacities, pleural effusion, and lobar consolidation. The gross appearance of the lungs may resemble bacterial pneumonia but, histologically, more closely resembles psittacosis and some viral pneumonias.

In acute Q fever, complete blood count may be normal, but about 30% of patients have an elevated white blood cell count. Alkaline phosphatase, aspartate aminotransferase (AST), and alanine aminotransferase (ALT) levels are mildly elevated to 2 to 3 times the normal level in typical cases. If obtained, liver biopsy specimens often show diffuse granulomatous changes.

Diagnosis of Q fever endocarditis can be difficult because blood cultures are negative and vegetative cardiac valve lesions are small and are visualized by echocardiography in only about 12% of patients (see CDC: Diagnosis and Management of Q Fever — United States, 2013: Recommendations from CDC and the Q Fever Working Group).

For acute Q fever,

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For endocarditis, treatment needs to be prolonged (months to years to lifelong), typically for at least 18 months (3

For chronic granulomatous hepatitis, the optimal regimen has not been determined.

Vaccines are effective, and in Australia, where a Q fever vaccine is commercially available, vaccination is recommended to protect people with occupational risk (eg, slaughterhouse and dairy workers, rendering-plant workers, herders, woolsorters, farmers).

Prevaccination screening with skin and blood tests should be done to identify preexisting immunity to Q fever because vaccinating people who already have immunity can cause severe local reactions.