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Seroprevalence and risk factors for Coxiella
burnetii (Q fever) infection in humans in Bura
irrigation scheme, Tana River County, Kenya
Mwololo D.K.1, 2, Kitala P.M.1, Wanyoike S.K.3 and Bett B.2
1. Department of Public Health, Pharmacology and Toxicology, University of Nairobi, P. O. Box 29053-00625, Nairobi;
2. International Livestock Research Institute, P. O. Box 30709-00100, Nairobi
3. Veterinary Epidemiology and Economics Unit, Central Veterinary and Investigation Laboratories, Kabete, Nairobi
References
Dorko E., Kalinová Z., Tatiana Weissová T., Pilipčinec E.,(2008), Ann Agric Environ Med 15, 119–
124
Knobel D et al.(2013). American Journal of Tropical Medicine and Hygiene 88, 513–518
Maurin M. and Raoult D. (1999), Q fever. Clinical Microbiology Rev 12, 518–553
Van den Brom R., Schimmer B., Schneeberger P.M., Swart W.A., van der Hoek W ., (2013) PLoS
ONE 8 (1), e54021
Whitney A. S., Massung R. F., Candee A. J., Ailes E. C., Myer L. M., Patterson N. E., Berkelman R.
L., (2009) Clinical Infectious Diseases 48, 550-557.
Methods
• Questionnaires were administered to 85 randomly selected
households where a maximum of five individuals per household
were randomly sampled for Q fever screening.
• A commercial ELISA antibody test kit (SERION ELISA classic C.
burnetii Phase 1 IgG) was used for the detection of human
antibodies in serum directed against C. burnetii Phase 1.
• Logistic regression was used to model for potential risk factors on
univariate and multivariate analyses using R software version 3.1.1.
Conclusion: There is a need to create awareness on Q fever in the
community at Bura irrigation scheme in Tana River County. The capacity of
the hospitals in this area should also be developed to properly diagnose and
manage the disease.
• Risk factors associated (P<0.05) with individual and household
seropositivity on univariate analysis were occupation and irrigation
status (Table 2)
• Compared to farmers, pastoralists had a lower risk of Q fever
infection.
Discussion
 The community in Bura irrigation scheme does not know about Q
fever yet the reported seroprevalence is high.
 A study in western Kenya by Knobel et al. (2013) also reported a
seroprevalence closely similar to our finding.
 Studies in different sub-Saharan countries on apparently healthy
people have shown the seroprevalence to range between 1% and
37% (Kobbe et al. 2008)
 In the univariate analysis, people living in non-irrigated areas
were at lower risk of Q fever infection compared to people within
the irrigation scheme.
 Most farmers in the scheme house their livestock within the
living houses and this poses a higher risk of inhalation of infected
aerosols from sick animals.
Acknowledgements
This work falls under the project ‘Dynamic Drivers of Disease in Africa: Ecosystems,
livestock/wildlife, health and wellbeing: REF:NE/J001422/1” partly funded with support from the
Ecosystem Services for Poverty Alleviation Programme (ESPA). The ESPA program is funded by the
Department for International Development (DFID), the Economic and Social Research Council
(ESRC) and the Natural Environment Research Council (NERC).
Introduction
Q fever is a zoonotic disease caused by the bacterium Coxiella burnetii which is an obligate intracellular organism and ruminants are
considered to be the primary source of infection to humans (Van den Brom et al. 2013). Humans become infected through inhalation of
aerosols from infected ruminants such as cattle, sheep and goats and through exposure to animal products such as unpasteurized dairy
products (Whitney et al. 2009). In humans, the disease syndrome can be divided into acute and chronic forms with the acute form
manifesting as a relatively mild self-limiting febrile illness while the chronic form is a more severe disease characterized by hepatitis,
pneumonia and chronic fatigue (Dorko et al. 2008). The disease is likely to impact negatively on humans because of its public health
importance. Q fever is considered an occupational disease among farmers, abattoir workers and veterinarians, although community
outbreaks around farms with infected ruminants, especially during the kidding season, have also been reported (Maurin and Raoult 1999).
The objectives of this study were to determine the seroprevalence and risk factors for Q fever infection in humans in Bura irrigation scheme
Tana River County, Kenya.
Results
All respondents reported having never heard of Q fever before.
Table 1 shows the seroprevalence of Coxiella burnetii in different
groups of people.
Differences in the seroprevalence between different occupations as
outlined in Figure 1.
Table 1: Seroprevalence of C. burnetii in different groups of people
Table 2: Results of a univariate logistic regression model showing
significant risk factors
Category Seroprevalence (95%CI)
All tested 26.8% (18.1-35.5%)
Adults 34.2% (24.9-43.5%)
Adolescents 23.2% (14.9-31.5%)
Children 26.8% (18.1-43.5%)
Males 28% (19.2-36.8%)
Females 26% (17.4-34.6%)
0
5
10
15
20
25
30
35
40
45
Figure 1: Comparison of seroprevalence of C. burnetii antibodies among
different occupation groups.
Variable Levels Estimate 95% CI P value
Occupation Farmers Ref - -
Herdsmen 0.55 -1.12 - 2.12 0.4872
Pastoralists -1.87 -3.73 - 0.59 0.0139
Students -0.28 -0.94 - 0.37 0.4064
Other 0.21 -0.54 - 0.94 0.5759
Irrigation status Irrigated Ref - -
Non-irrigated -0.79 -1.55 -0.11 0.0292
3rd International One Health Congress, 15-18 March 2015, Amsterdam, the Netherlands

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Seroprevalence and risk factors for Coxiella burnetii (Q fever) infection in humans in Bura irrigation scheme, Tana River County, Kenya

  • 1. Seroprevalence and risk factors for Coxiella burnetii (Q fever) infection in humans in Bura irrigation scheme, Tana River County, Kenya Mwololo D.K.1, 2, Kitala P.M.1, Wanyoike S.K.3 and Bett B.2 1. Department of Public Health, Pharmacology and Toxicology, University of Nairobi, P. O. Box 29053-00625, Nairobi; 2. International Livestock Research Institute, P. O. Box 30709-00100, Nairobi 3. Veterinary Epidemiology and Economics Unit, Central Veterinary and Investigation Laboratories, Kabete, Nairobi References Dorko E., Kalinová Z., Tatiana Weissová T., Pilipčinec E.,(2008), Ann Agric Environ Med 15, 119– 124 Knobel D et al.(2013). American Journal of Tropical Medicine and Hygiene 88, 513–518 Maurin M. and Raoult D. (1999), Q fever. Clinical Microbiology Rev 12, 518–553 Van den Brom R., Schimmer B., Schneeberger P.M., Swart W.A., van der Hoek W ., (2013) PLoS ONE 8 (1), e54021 Whitney A. S., Massung R. F., Candee A. J., Ailes E. C., Myer L. M., Patterson N. E., Berkelman R. L., (2009) Clinical Infectious Diseases 48, 550-557. Methods • Questionnaires were administered to 85 randomly selected households where a maximum of five individuals per household were randomly sampled for Q fever screening. • A commercial ELISA antibody test kit (SERION ELISA classic C. burnetii Phase 1 IgG) was used for the detection of human antibodies in serum directed against C. burnetii Phase 1. • Logistic regression was used to model for potential risk factors on univariate and multivariate analyses using R software version 3.1.1. Conclusion: There is a need to create awareness on Q fever in the community at Bura irrigation scheme in Tana River County. The capacity of the hospitals in this area should also be developed to properly diagnose and manage the disease. • Risk factors associated (P<0.05) with individual and household seropositivity on univariate analysis were occupation and irrigation status (Table 2) • Compared to farmers, pastoralists had a lower risk of Q fever infection. Discussion  The community in Bura irrigation scheme does not know about Q fever yet the reported seroprevalence is high.  A study in western Kenya by Knobel et al. (2013) also reported a seroprevalence closely similar to our finding.  Studies in different sub-Saharan countries on apparently healthy people have shown the seroprevalence to range between 1% and 37% (Kobbe et al. 2008)  In the univariate analysis, people living in non-irrigated areas were at lower risk of Q fever infection compared to people within the irrigation scheme.  Most farmers in the scheme house their livestock within the living houses and this poses a higher risk of inhalation of infected aerosols from sick animals. Acknowledgements This work falls under the project ‘Dynamic Drivers of Disease in Africa: Ecosystems, livestock/wildlife, health and wellbeing: REF:NE/J001422/1” partly funded with support from the Ecosystem Services for Poverty Alleviation Programme (ESPA). The ESPA program is funded by the Department for International Development (DFID), the Economic and Social Research Council (ESRC) and the Natural Environment Research Council (NERC). Introduction Q fever is a zoonotic disease caused by the bacterium Coxiella burnetii which is an obligate intracellular organism and ruminants are considered to be the primary source of infection to humans (Van den Brom et al. 2013). Humans become infected through inhalation of aerosols from infected ruminants such as cattle, sheep and goats and through exposure to animal products such as unpasteurized dairy products (Whitney et al. 2009). In humans, the disease syndrome can be divided into acute and chronic forms with the acute form manifesting as a relatively mild self-limiting febrile illness while the chronic form is a more severe disease characterized by hepatitis, pneumonia and chronic fatigue (Dorko et al. 2008). The disease is likely to impact negatively on humans because of its public health importance. Q fever is considered an occupational disease among farmers, abattoir workers and veterinarians, although community outbreaks around farms with infected ruminants, especially during the kidding season, have also been reported (Maurin and Raoult 1999). The objectives of this study were to determine the seroprevalence and risk factors for Q fever infection in humans in Bura irrigation scheme Tana River County, Kenya. Results All respondents reported having never heard of Q fever before. Table 1 shows the seroprevalence of Coxiella burnetii in different groups of people. Differences in the seroprevalence between different occupations as outlined in Figure 1. Table 1: Seroprevalence of C. burnetii in different groups of people Table 2: Results of a univariate logistic regression model showing significant risk factors Category Seroprevalence (95%CI) All tested 26.8% (18.1-35.5%) Adults 34.2% (24.9-43.5%) Adolescents 23.2% (14.9-31.5%) Children 26.8% (18.1-43.5%) Males 28% (19.2-36.8%) Females 26% (17.4-34.6%) 0 5 10 15 20 25 30 35 40 45 Figure 1: Comparison of seroprevalence of C. burnetii antibodies among different occupation groups. Variable Levels Estimate 95% CI P value Occupation Farmers Ref - - Herdsmen 0.55 -1.12 - 2.12 0.4872 Pastoralists -1.87 -3.73 - 0.59 0.0139 Students -0.28 -0.94 - 0.37 0.4064 Other 0.21 -0.54 - 0.94 0.5759 Irrigation status Irrigated Ref - - Non-irrigated -0.79 -1.55 -0.11 0.0292 3rd International One Health Congress, 15-18 March 2015, Amsterdam, the Netherlands