What is Q fever?

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What is Q Fever

Q fever is a zoonotic disease caused by the bacterium Coxiella burnetii that can cause acute or chronic illness in humans, transmitted primarily through inhalation of contaminated aerosols from infected animals, particularly livestock. 1

The Causative Organism

  • Coxiella burnetii is a unique intracellular bacterium that is extremely resistant to physical stresses including heat and desiccation, allowing it to survive in the environment for months to years. 1
  • The organism is highly infectious, with as few as one organism potentially causing clinical infection. 2
  • It develops spore-like forms that contribute to its environmental persistence and makes it capable of traveling on wind currents for miles. 1, 3

Animal Reservoirs and Transmission

  • Cattle, sheep, and goats are the primary reservoirs, though infection has been confirmed in multiple vertebrate species including wildlife, domestic mammals, birds, and reptiles. 1
  • The highest numbers of organisms are shed in birth products (placenta, amniotic fluid), although viable organisms can also be shed in urine, milk, and feces of infected animals. 1, 4
  • The majority of animal infections are asymptomatic, making identification of infected animals challenging. 1

How Humans Get Infected

  • The most common mode of transmission is inhalation of infectious aerosols directly from birth fluids of infected animals or via inhalation of dust contaminated with dried birth fluids or excreta. 1
  • The bacteria can become airborne and travel considerable distances—in one outbreak, cases were documented in persons living 10 miles from the source farm. 1
  • Less common routes include ingestion of raw milk and dairy products, or contact with contaminated clothing. 1
  • Person-to-person transmission is possible but rarely reported, with rare cases documented through blood transfusion, bone marrow transplantation, and sexual transmission. 1

Clinical Manifestations

Acute Q Fever

  • Approximately 40-60% of infections are asymptomatic, with only seroconversion occurring. 1, 2
  • Symptomatic acute Q fever typically manifests 2-3 weeks after exposure as a nonspecific febrile illness, pneumonia, or hepatitis. 1
  • The most frequently reported symptoms include fever (lasting a median of 10 days untreated), fatigue, chills, myalgia, and severe debilitating headaches. 1, 5
  • Nonproductive cough occurs in approximately 50% of patients with Q fever pneumonia. 5
  • Acute Q fever has a low mortality rate (<2%) and most patients defervesce within 72 hours of doxycycline treatment. 1, 5

Chronic Q Fever

  • Chronic disease is rare (<5% of patients with acute infections) and typically manifests months to years after initial infection. 1
  • Chronic Q fever endocarditis is the most common manifestation, occurring primarily in patients with preexisting valvular heart disease, vascular grafts, or arterial aneurysms. 1
  • Unlike acute Q fever, chronic Q fever endocarditis is always fatal if untreated. 1
  • Routine blood cultures are negative in patients with chronic Q fever endocarditis, making diagnosis extremely difficult. 1
  • Vegetative lesions are visualized by echocardiography in only approximately 12% of patients. 1

Who is at Risk

Occupational Risk Factors

  • Persons whose work involves contact with animals are at increased risk, including slaughterhouse workers, veterinarians, farmers, and laboratory workers. 1
  • However, 79% of reported U.S. cases occur in patients not in previously defined high-risk occupations, and 60% occur in patients who do not report livestock contact. 1

Geographic and Demographic Factors

  • Living in a rural area or within 10 miles of a farm housing livestock increases risk. 1, 5
  • The reported incidence is higher among persons aged ≥40 years, with persons aged 60-64 years having the highest age-related risk in the United States. 1
  • Males have a higher risk for symptomatic Q fever illness than females. 1
  • Acute Q fever cases in the United States peak in the spring, correlating with livestock birthing times. 1

Diagnosis

  • Paired serum samples showing fourfold change in IgG antibody titer to C. burnetii phase II antigen by immunofluorescence assay is the gold standard for diagnosis. 5, 6
  • A single IgG titer ≥1:128 to phase II antigen in a patient ill >1 week indicates probable acute infection. 5, 6
  • PCR testing on whole blood or serum during the first 2 weeks of symptoms can provide early diagnosis. 5, 6
  • Chronic infection is distinguished by a rising phase I IgG titer. 1

Treatment

  • Doxycycline is the antibiotic of choice for Q fever. 7, 2, 4
  • For acute Q fever, a 14- to 21-day course of doxycycline is typically used. 2
  • Early treatment within the first 3 days of symptoms is most effective, and treatment should not be delayed while awaiting laboratory confirmation if Q fever is strongly suspected. 5, 6
  • For chronic infections such as endocarditis, 18 months of doxycycline supplemented with hydroxychloroquine is currently the best therapy. 2, 4

Public Health Significance

  • Q fever is a nationally notifiable disease in the United States. 1
  • The largest known outbreak involved approximately 4,000 human cases during 2007-2010 in the Netherlands, linked to dairy goat farms. 1
  • Its highly infectious nature and aerosol route of transmission make C. burnetii a possible agent of bioterrorism. 2, 8

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Q fever as a biological weapon.

Seminars in respiratory infections, 2003

Research

Is Q fever an emerging or re-emerging zoonosis?

Veterinary research, 2005

Research

Q Fever (Coxiella Burnetii).

Seminars in respiratory and critical care medicine, 2020

Guideline

Q Fever Pneumonia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Suspecting Coxiella burnetii Pneumonia (Q Fever)

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Q fever--California, Georgia, Pennsylvania, and Tennessee, 2000-2001.

MMWR. Morbidity and mortality weekly report, 2002

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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