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Disease frequency of selected bacterial zoonoses in small ruminants in Tana River County, Kenya
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Disease frequency of selected bacterial zoonoses in small ruminants in Tana River County, Kenya

  1. German Federal Institute for Risk Assessment • Max-Dohrn-Straße 8-10 • 10589 Berlin, GERMANY • Phone +49 30-18412-0 • Fax +49 30-18412-99 0 99 • bfr@bfr.bund.de • www.bfr.bund.de/en GERMAN FEDERAL INSTITUTE FOR RISK ASSESSMENT Disease frequency of selected bacterial zoonoses in small ruminants in Tana River County, Kenya Martin Wainaina1,2,3, Johanna Lindahl3,4,5, Anne Mayer-Scholl1, Kristina Roesel3, Deborah Mbotha2,3, Uwe Roesler6, Delia Grace3,7, Bernard Bett3, Sascha Al Dahouk1,8 1. German Federal Institute for Risk Assessment,Berlin, Germany, 2. Dahlem Research School of Biomedical Sciences, Freie Universität Berlin (FUB), Berlin, Germany, 3. International Livestock Research Institute,Nairobi, Kenya, 4. Swedish University of Agricultural Sciences, Uppsala, Sweden, 5. Uppsala University, Uppsala, Sweden, 6. Institute for Animal Hygiene and Environmental Health, FUB, Berlin, Germany, 7. Natural Resources Institute, University of Greenwich, United Kingdom, 8. RWTH Aachen University Hospital, Aachen, Germany SAMPLE COLLECTION SITES Bacterial infections are the leading causes of non-malarial fevers in Africa. Brucellosis, leptospirosis,and Q fever are priority zoonoses in Kenya, but little information on their epidemiology is available to date. Changes in land use such as irrigation can influence the pattern of vector-borne viral and parasitic diseases. Less is known about bacterial diseases. Therefore, we implemented this longitudinal study by following up 316 small ruminants from September 2014 to June 2015. Sampling was done in pastoral, irrigated, and riverine settings in Tana River County. We aimed at estimating the disease burden, disease frequency, and associatedrisk factors for both exposure and seroconversion. Sampling ecosystems: 1. Irrigated – Bura irrigation scheme 2. Pastoral – Chifiri village 3. Riverine – Husingo village Irrigation may influence the occurrence of bacterial zoonoses such as C. burnetii. However, we did not observe this for both Leptospira spp. and Brucella spp. We also observed the possibility of prolonged periods of transmission of Brucella spp. to humans and animals. Additionally, despite determining prevalent leptospiral serovars by MAT, determining infective serovars can only be proven by bacterial cultures due to paradoxicalreactions. The high number of seropositive and seroconverting animals in the study area shows the need for surveillance and control measures to reduce animal disease burden and possible human exposure. LABORATORY ANALYSIS Serological testing: 1. Brucella spp. – Screening by ELISA and Rose Bengal tests. Confirmation by complement fixation test 2. Coxiella burnetii – phase I & II ELISA test 3. Leptospira spp. – microscopic agglutination test (MAT) Real-time PCR testing of serologically-positive animals DATA ANALYSIS First negative, later positive = seroconversion First sampling time points: 1. Seroprevalence estimations 2. Risk factors for seropositivity First time points varied Seroconversions: 1. Survival analyses 2. Serological incidence rate estimations Kenya with Tana River County in yellow and households sampled as red dots Distribution of seropositivity at first sampling time points ONE HEALTH RELEVANCE Martin Wainaina markimwa@gmail.com ● Diedersdorfer Weg 1, 12277 Berlin ● Tel: +49 30 18412-24703 BACKGROUND Leptospira spp. Coxiella burnetii Brucella spp. positive/total positive/total positive/total Total 50 /313 † 66/316 4/316 Irrigated 15/138 34/139 3/139 Pastoral 8/68 25/69 0/69 Riverine 27/107 7/108 1/108 Leptospira spp. Coxiella burnetii positive/total positive/total Total 27/263 ‡ 10/250 ‡ Irrigated 10/123 7/105 Pastoral 4/60 3/44 Riverine 13/80 0/101 Kaplan-Meier analyses: Differences in survival probabilities with time (in months) were observed for Coxiella burnetii (p=0.012), but not for Leptospira spp. (p=0.5) PCR testing: Three animals tested positive for Brucella spp. either consistently or intermittently for entire study period. One animal was also positive for C. burnetii at one time point. We detected no pathogenic leptospires. Leptospiral serovars: Serovar Ballum was the most prevalent. Evidence of paradoxical reactions was also observed. Ongoing: Estimation of seroprevalence and incidence rates using survey methods. Risk factor analyses for both seropositivity and seroconversion. Distribution of seroconversions. We observed none for Brucella spp. Animal metadata collected: species, age, sex, reproductive status A. Coxiella burnetii B. Leptospira spp. RESULTS Time † doubtful results excluded; ‡ total number depended on how many animals tested negative from the beginning
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