Incidence Estimates of Acute Q Fever and Spotted Fever Group Rickettsioses, Kilimanjaro, Tanzania, from 2007 to 2008 and from 2012 to 2014

Author:

Pisharody Sruti1,Rubach Matthew P.1234,Carugati Manuela1,Nicholson William L.5,Perniciaro Jamie L.5,Biggs Holly M.1,Maze Michael J.467,Hertz Julian T.2,Halliday Jo E. B.89,Allan Kathryn J.89,Mmbaga Blandina T.410,Saganda Wilbrod1112,Lwezaula Bingileki F.1112,Kazwala Rudovick R.13,Cleaveland Sarah89,Maro Venance P.410,Crump John A.124610

Affiliation:

1. 1Division of Infectious Diseases and International Health, Department of Medicine, Duke University, Durham, North Carolina;

2. 2Duke Global Health Institute, Duke University, Durham, North Carolina;

3. 3Programme in Emerging Infectious Diseases, Duke-National University of Singapore, Singapore;

4. 4Kilimanjaro Christian Medical Centre, Moshi, Tanzania;

5. 5Centers for Disease Control and Prevention, Rickettsial Zoonoses Branch, Atlanta, Georgia;

6. 6Centre for International Health, University of Otago, Dunedin, New Zealand;

7. 7Department of Medicine, University of Otago, Christchurch, New Zealand;

8. 8Institute of Biodiversity, Animal Health and Comparative Medicine, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom;

9. 9Boyd Orr Centre for Population and Ecosystem Health, Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom;

10. 10Kilimanjaro Christian Medical University College, Moshi, Tanzania;

11. 11Mawenzi Regional Referral Hospital, Moshi, Tanzania;

12. 12Ministry of Health, Community Development, Gender, Elderly and Children, Dodoma, Tanzania;

13. 13Sokoine University of Agriculture, Morogoro, Tanzania

Abstract

ABSTRACT. Q fever and spotted fever group rickettsioses (SFGR) are common causes of severe febrile illness in northern Tanzania. Incidence estimates are needed to characterize the disease burden. Using hybrid surveillance—coupling case-finding at two referral hospitals and healthcare utilization data—we estimated the incidences of acute Q fever and SFGR in Moshi, Kilimanjaro, Tanzania, from 2007 to 2008 and from 2012 to 2014. Cases were defined as fever and a four-fold or greater increase in antibody titers of acute and convalescent paired sera according to the indirect immunofluorescence assay of Coxiella burnetii phase II antigen for acute Q fever and Rickettsia conorii (2007–2008) or Rickettsia africae (2012–2014) antigens for SFGR. Healthcare utilization data were used to adjust for underascertainment of cases by sentinel surveillance. For 2007 to 2008, among 589 febrile participants, 16 (4.7%) of 344 and 27 (8.8%) of 307 participants with paired serology had Q fever and SFGR, respectively. Adjusted annual incidence estimates of Q fever and SFGR were 80 (uncertainty range, 20–454) and 147 (uncertainty range, 52–645) per 100,000 persons, respectively. For 2012 to 2014, among 1,114 febrile participants, 52 (8.1%) and 57 (8.9%) of 641 participants with paired serology had Q fever and SFGR, respectively. Adjusted annual incidence estimates of Q fever and SFGR were 56 (uncertainty range, 24–163) and 75 (uncertainty range, 34–176) per 100,000 persons, respectively. We found substantial incidences of acute Q fever and SFGR in northern Tanzania during both study periods. To our knowledge, these are the first incidence estimates of either disease in sub-Saharan Africa. Our findings suggest that control measures for these infections warrant consideration.

Publisher

American Society of Tropical Medicine and Hygiene

Subject

Virology,Infectious Diseases,Parasitology

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