Evidence map›Paper›PMID 41039537›Full record

ArticleBMC veterinary research2025

Molecular characterisation of tick-borne pathogens in cattle in kenya: insights from blood, ticks, and skin swab analyses.

Dennis Getange, Samson Mukaratirwa, Joel L Bargul, Rua Khogali, John Ng'iela, James Kabii, Daniel K Masiga, Jandouwe Villinger

Abstract read
In one paragraph

Article in BMC veterinary research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. bioRxiv : the preprint server for biology · 2026
    Article
  4. Molecular characterization ofFrontiers in veterinary science · 2026
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Dennis GetangeInternational Centre of Insect Physiology and Ecology (icipe), P.O Box 30772-00100, Nairobi, Kenya. dgetange@icipe.org.
Samson MukaratirwaSchool of Life Sciences, University of KwaZulu-Natal, Westville Campus, Private Bag X54001, Durban, 4000, South Africa.
Joel L BargulInternational Centre of Insect Physiology and Ecology (icipe), P.O Box 30772-00100, Nairobi, Kenya.
Rua KhogaliInternational Centre of Insect Physiology and Ecology (icipe), P.O Box 30772-00100, Nairobi, Kenya.
John Ng'ielaInternational Centre of Insect Physiology and Ecology (icipe), P.O Box 30772-00100, Nairobi, Kenya.
James KabiiInternational Centre of Insect Physiology and Ecology (icipe), P.O Box 30772-00100, Nairobi, Kenya.
Daniel K MasigaInternational Centre of Insect Physiology and Ecology (icipe), P.O Box 30772-00100, Nairobi, Kenya.
Jandouwe VillingerInternational Centre of Insect Physiology and Ecology (icipe), P.O Box 30772-00100, Nairobi, Kenya. jandouwe@icipe.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTicks pose a major threat to livestock and human health in sub-Saharan Africa, with climate change and pastoral movements fueling their spread. Few studies have integrated multiple sample types to characterize tick-borne pathogens (TBPs) in cattle in Kenya. This knowledge gap hinders the development of effective surveillance and control strategies, leaving vulnerable populations and their livestock susceptible to these persistent threats.

methodsWe screened 280 bovine blood samples, 589 tick pools, and 284 non-invasive skin swabs from cattle in northern (Marsabit) and southern (Kajiado) Kenya by high-resolution melting analysis and Sanger sequencing of PCR products.

resultsRhipicephalus spp. (47.1%), Hyalomma spp. (30.8%), and Amblyomma spp. (22.1%) were prevalent, with Rhipicephalus evertsi only found in Kajiado and Rhipicephalus camicasi in Marsabit. In blood, Anaplasma spp. (62.9%; A. marginale, A. platys, A. ovis) and Theileria spp. (34.6%; T. velifera, T. mutans) were dominant. Tick pools harbored Coxiella burnetii, Rickettsia africae, Rickettsia aeschlimannii, Anaplasma marginale, Theileria velifera, T. ovis, and Babesia occultans, and for the first time two co-circulating Ehrlichia ruminantium strains (Welgevonden and Kumm2). Notably, C. burnetii and T. ovis were detected only in Marsabit, and T. mutans only in Kajiado. Skin swabs from tick predilection sites (ears, anal region) yielded R. africae, R. aeschlimannii, and T. velifera at low positivity, while nose swabs were negative.

conclusionsDetection of zoonotic pathogens such as C. burnetii and R. africae underscores critical public health risks, and co-infections in cattle reinforce the need for robust, integrated surveillance. Although skin swabs demonstrated limited diagnostic yield, they remain a promising non-invasive sampling approach. These findings highlight the value of targeted acarological research and coordinated control programs under a One Health framework.

Indexed as

Cattle DiseasesTick-Borne DiseasesTicksAnaplasmaAnimalsCattleKenyaSkinTheileriaAmblyommaAnaplasmaEhrlichiaQ feverRickettsiaTheileriaTick-borne pathogensTicks

Identifiers

PMID41039537
PMCPMC12492888

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.