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Molecular detection of Coxiella burnetii in ticks collected from animals and the environment in Uganda

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AbstractAimsCoxiella burnetii is a highly infectious organism that is easily spread through aerosols causing Q fever in humans. Ticks can harbour and transmit C. burnetii to animals, contributing to disease maintenance. Our aim was to examine the presence of C. burnetii in ticks in Uganda.Methods and ResultsIn this study, ticks were collected from five Ugandan districts and tested by real‐time PCR for C. burnetii (Coxiella outer membrane protein 1 gene). A total of 859 tick pools (9602 individual ticks) were tested, and pool positivity for C. burnetii was 5.5% (n = 47). Pooled prevalence differed by district; the highest was Luwero (7.3%), then Gulu (6.6%), and Kasese had the lowest (1.3%). However, district variation was not statistically significant (Fisher's exact = 0.07). Ticks collected from dogs and cats had the highest positivity rates [23/47, (48.9%)] followed by livestock (cattle, goats, sheep, and pigs) [18/47, (38.3%)] and vegetation [6/47, (12.8%)]. Haemaphysalis elliptica had the highest infection rates, followed by Rhipicephalus appendiculatus, Amblyomma variegatum and Rhipicephalus decoloratus had similar prevalence.ConclusionsAlthough ticks are not the primary transmitters of C. burnetii to humans, pathogen detection in ticks can be an indirect indicator of risk among animal hosts. Vulnerable populations, including occupations with close animal contact such as farming, butchery, and veterinary practice, have an increased risk of C. burnetii exposure. Veterinarians and clinicians should be aware that C. burnetii may cause human and animal illness in these regions.
Title: Molecular detection of Coxiella burnetii in ticks collected from animals and the environment in Uganda
Description:
AbstractAimsCoxiella burnetii is a highly infectious organism that is easily spread through aerosols causing Q fever in humans.
Ticks can harbour and transmit C.
 burnetii to animals, contributing to disease maintenance.
Our aim was to examine the presence of C.
 burnetii in ticks in Uganda.
Methods and ResultsIn this study, ticks were collected from five Ugandan districts and tested by real‐time PCR for C.
 burnetii (Coxiella outer membrane protein 1 gene).
A total of 859 tick pools (9602 individual ticks) were tested, and pool positivity for C.
 burnetii was 5.
5% (n = 47).
Pooled prevalence differed by district; the highest was Luwero (7.
3%), then Gulu (6.
6%), and Kasese had the lowest (1.
3%).
However, district variation was not statistically significant (Fisher's exact = 0.
07).
Ticks collected from dogs and cats had the highest positivity rates [23/47, (48.
9%)] followed by livestock (cattle, goats, sheep, and pigs) [18/47, (38.
3%)] and vegetation [6/47, (12.
8%)].
Haemaphysalis elliptica had the highest infection rates, followed by Rhipicephalus appendiculatus, Amblyomma variegatum and Rhipicephalus decoloratus had similar prevalence.
ConclusionsAlthough ticks are not the primary transmitters of C.
 burnetii to humans, pathogen detection in ticks can be an indirect indicator of risk among animal hosts.
Vulnerable populations, including occupations with close animal contact such as farming, butchery, and veterinary practice, have an increased risk of C.
 burnetii exposure.
Veterinarians and clinicians should be aware that C.
 burnetii may cause human and animal illness in these regions.

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