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Brucellosis in Patients with Crimean-Congo Hemorrhagic Fever
Fazilet Duygu1, Tugba Sari1, Turan Kaya2
1Public Health Institution of Turkey, Ankara, Turkey.
Insights
Crimean-Congo hemorrhagic fever (CCHF) and brucellosis can present with similar symptoms. This study found a co-infection rate of 4.16% in patients initially diagnosed with CCHF, highlighting the need for dual screening.
Area of Science:
- Infectious Diseases
- Virology
- Bacteriology
- Epidemiology
Background:
- Crimean-Congo hemorrhagic fever (CCHF) is a severe, zoonotic viral illness transmitted by ticks, caused by a Nairovirus.
- Differential diagnosis between CCHF and other febrile illnesses, such as brucellosis, can be challenging due to overlapping clinical presentations.
Purpose of the Study:
- To determine the incidence of brucellosis in patients with a clinical suspicion of CCHF.
- To assess the diagnostic overlap and co-infection rates between CCHF and brucellosis in a Turkish cohort.
Main Methods:
- A cohort of 169 patients with an initial diagnosis of CCHF in Tokat, Turkey, during 2011 were retrospectively analyzed.
- Laboratory confirmation of CCHF involved IgM antibody detection and/or PCR.
- Brucellosis diagnosis was established using plate and standard tube agglutination (STA) tests.
Main Results:
- Of 169 patients, 120 (79%) were confirmed to have CCHF via PCR.
- Five patients (4.16%) were co-diagnosed with brucellosis, confirmed by positive agglutination tests.
- Four additional patients (2.36%) presented with negative CCHF PCR results but positive brucellosis serology.
Conclusions:
- Brucellosis and CCHF exhibit significant clinical mimicry, complicating accurate diagnosis.
- Routine screening for both brucellosis and CCHF is recommended in endemic areas for patients presenting with symptoms suggestive of either disease.
- Co-infection necessitates careful diagnostic evaluation to ensure appropriate treatment and prevent complications.
Background:
Crimean-Congo hemorrhagic fever (CCHF) is a fatal zoonotic viral disease caused by infection with a tick-borne virus of the genus Nairovirus. In this study, we investigated the incidence of brucellosis in patients diagnosed with CCHF.
Methods:
Overall, 169 patients hospitalized with an initial diagnosis of CCHF were included in 2011 in Tokat/Turkey. Immunoglobulin M (IgM) antibodies and/or PCR results were used in the laboratory diagnosis of CCHF, while plate and standard tube agglutination (STA) tests were used to diagnose brucellosis.
Results:
Overall, 120 patients (79%) with positive PCR tests were diagnosed with CCHF. Five (4.16%) were also diagnosed with brucellosis based on the positive plate and STA test results. Four patients (2.36%) had negative CCHF PCR and positive STA test results.
Conclusion:
Brucellosis and CCHF can mimic each other and that all patients with CCHF or brucellosis should be screened for both conditions.
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