Evidence map›Paper›PMID 41013322›Full record

SynthesisBMC infectious diseases2025

Potential zoonotic rickettsiales bacteria associated with small mammals and their ectoparasites in africa: a systematic review and meta-analysis.

Venance Theophil Msoffe, Charles M Lyimo, Moses I Olotu, Abdul S Katakweba, Rhodes H Makundi, Apia W Massawe, Gerald Misinzo, Ladslaus L Mnyone

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Venance Theophil MsoffeDepartment of Wildlife Management, College of Forestry, Wildlife and Tourism, Sokoine University of Agriculture, P.O. Box 3073, Morogoro, Tanzania. venance.msoffe@muce.ac.tz.
Charles M LyimoDepartment of Animal, Aquaculture and Range Sciences, College of Agriculture, Sokoine University of Agriculture, P.O. Box 3004, Morogoro, Tanzania.
Moses I OlotuDepartment of Biological Sciences, Mkwawa University College of Education, University of Dar es Salaam, P.O. Box 2513, Iringa, Tanzania.
Abdul S KatakwebaAfrican Centre of Excellence for Innovative Rodent Pest Management and Biosensor Technology Development, Sokoine University of Agriculture, P.O. Box 3110, Morogoro, Tanzania.
Rhodes H MakundiAfrican Centre of Excellence for Innovative Rodent Pest Management and Biosensor Technology Development, Sokoine University of Agriculture, P.O. Box 3110, Morogoro, Tanzania.
Apia W MassaweAfrican Centre of Excellence for Innovative Rodent Pest Management and Biosensor Technology Development, Sokoine University of Agriculture, P.O. Box 3110, Morogoro, Tanzania.
Gerald MisinzoDepartment of Microbiology, Parasitology and Biotechnology, College of Veterinary Medicine and Biomedical Sciences, Sokoine University of Agriculture, P.O. Box 3019, Morogoro, Tanzania.
Ladslaus L MnyoneInstitute of Pest Management, Sokoine University of Agriculture, P.O. Box 3110, Morogoro, Tanzania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The proximity of humans to small mammals and their ectoparasites at wildlife-human interfaces in Africa creates favorable conditions for the spillover of zoonotic pathogens. Anaplasmaceae and Rickettsiaceae bacteria are emerging threats due to their genomic adaptability and resilience to environmental changes. This systematic review and meta-analysis examined the distribution and prevalence of these pathogens in African small mammals and their ectoparasites. A comprehensive search across five electronic databases yielded 37 studies meeting predefined inclusion and exclusion criteria. The most frequently reported pathogens were Rickettsia felis (11 studies), Rickettsia massiliae (8 studies), and Rickettsia typhi (7 studies). A meta-analysis using a random-effects model was conducted separately for small mammals and ectoparasites. In small mammals, the highest prevalence was observed for Anaplasma spp. (15.17%; 95% CI 8-26.9%), Rickettsia helvetica (14.65%; 95% CI 9.09-22.75%), R. felis (12%; 95% CI 6.13-22.18%), R. massiliae (10.75%; 95% CI 0.6-70.55%), and Ehrlichia spp. (10.35%; 95% CI 4.13-23.66%). Among ectoparasites, the highest prevalence was found in ticks for R. africae (41.53%; 95% CI 13.53-76.33%) and R. massiliae (30.55%; 95% CI 8.96-66.29%). In fleas, R. felis (21.68%; 95% CI 8.67-44.68%) was most prevalent. This analysis underscores the importance of molecular detection tools, such as the combination of quantitative real-time polymerase chain reaction (qPCR) and sequencing for detection and identification of Rickettsiales, and highlights the dominance of R. africae, R. felis, and R. massiliae in ectoparasites, particularly in Eastern and Northern Africa. The study also underscores the impact of sample size and geographical regional differences in prevalence estimates. This review was registered in the international database of Prospectively Registered Systematic Reviews (PROSPERO) with ID: CRD42024552324.

Indexed as

Bacterial ZoonosesEctoparasitic InfestationsMammalsRickettsia InfectionsRickettsialesZoonosesAfricaAnimalsHumansPrevalenceRickettsiaTicksAfricaAnaplasmaceaeEctoparasitesRickettsiaceaeRickettsialesSmall mammals

Identifiers

PMID41013322
PMCPMC12465614

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.