Crimean‐Congo haemorrhagic fever outbreak in Northern Senegal in 2022: Prevalence of the virus in livestock and ticks, associated risk factors and epidemiological implications

Author:

Ngom Déthié1,Khoulé Aliou1,Faye Elisabeth Thérèse2,Sène Ousseynou2,Diop Sokhna Maymouna2,Sagne Samba Niang3,Diallo Mamadou Korka3,Dia Moussa2,Barry Mamadou Aliou3,Diaw Yoro4,Bocoum Mamoudou5,Ndiaye El Hadji Mamadou6,Sall Yoro6,Diop Boly6,Faye Oumar2,Faye Ousmane2,Diallo Mawlouth1,Simon‐Lorière Etienne7,Sakuntabhai Anavaj89,Fall Gamou2,Diallo Diawo1

Affiliation:

1. Institut Pasteur de Dakar, Pole of Zoology Dakar Senegal

2. Institut Pasteur de Dakar Dakar Senegal

3. Institut Pasteur de Dakar, Pole of Epidemiology, Clinical Research & Data Science Dakar Senegal

4. Departmental Service of Livestock of Podor Podor Senegal

5. Health District of Podor Podor Senegal

6. Ministère de la Santé et de l'Action Sociale (MSAS) Dakar Senegal

7. Institut Pasteur, Université de Paris, G5 Evolutionary Genomics of RNA Viruses Paris France

8. Department of Global Health, Functional Genetics of Infectious Diseases Unit, Institut Pasteur Université de Paris Paris France

9. International Vaccine Design Center (vDesC), the Institute of Medical Science The University of Tokyo (IMSUT) Tokyo Japan

Abstract

AbstractObjectiveCrimean‐Congo haemorrhagic fever (CCHF) is a severe zoonotic arboviral disease that occurs widely in Eastern and Western Europe, Asia and Africa. The disease is becoming of growing public health importance in Senegal. However, analysis of tick infestation, CCHF virus (CCHFV) circulation extent and risk factors during ongoing outbreak are scarce. A thorough outbreak investigation was carried out during a CCHF outbreak in Podor (Northern Senegal) in August 2022.MethodsTicks and blood samples were collected from animals (cattle, goats and sheep) randomly selected from confirmed CCHF human cases houses, neighbourhoods and surrounding villages. Blood samples were tested for CCHFV antibodies using a commercial enzyme‐linked immunosorbent assay (ELISA) test. Tick samples were screened for CCHFV RNA by RT‐PCR.ResultsOverall, tick infestation rate (TIR) and CCHFV seroprevalence of livestock were 52.12% (95% confidence interval (CI): 45.54%–58.64%) and 43.28% (95% CI: 36.33%–50.44%), respectively. The TIRs were 87.7% in cattle, 57.6% in sheep and 20.0% in goats. These rates were significantly associated with location, host species and tick control (p < 0.001) but not with animal age and sex (p > 0.7). CCHFV seroprevalence was 80.4% (95% CI: 67.57%–89.77%) in cattle, 35.4% (95% CI: 25.00%–47.01%) in sheep and 21.2% (95% CI: 12.11%–33.02%) in goats. Age, sex, location, animal host and presence of ticks were significantly associated to the presence of antibodies. The 950 ticks collected included among other species, Hyalomma impeltatum (48.84%) and H. rufipes (10.21%). Five pools of Hyalomma ssp. were found CCHFV RT‐PCR positive. These infected ticks included 0.86% (4/464) of H. impeltatum collected on cattle and sheep and 1.03% (1/97) of H. rufipes collected on a sheep.ConclusionsTo our knowledge, this is the first report on the extend of tick infestation and CCHFV infection in livestock during an outbreak in Senegal. The results highlight the risk of human infections and the importance of strengthening vector, animal and human surveillance as well as tick control measures in this area to prevent CCHF infections in humans.

Publisher

Wiley

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