# Molecular detection of hemotropic mycoplasmas (hemoplasmas) in humans and dogs living on islands and the seashore mainland of Brazil: a One Health approach

**Authors:** Louise Bach Kmetiuk, Paul Shaw, Ashley Wallington, Jobin Jose Kattoor, Mathew Johnson, Rebecca P. Wilkes, Leandro Meneguelli Biondo, Rogério Giuffrida, Vamilton Alvares Santarém, Aaronson Ramathan Freitas, Ruana Renosto Delai, Claudia Turra Pimpão, Fabiano Borges Figueiredo, Joanne B. Messick, Andrea Pires dos Santos, Alexander Welker Biondo

PMC · DOI: 10.1186/s13071-025-07234-8 · Parasites & Vectors · 2026-01-27

## TL;DR

This study investigates Mycoplasma infections in humans and dogs on islands and coastal areas of Brazil, finding a higher risk in vulnerable populations.

## Contribution

The study is the first to assess hemoplasma infections in oceanic island communities and their dogs in Brazil using qPCR and tNGS.

## Key findings

- Mycoplasma haemocanis was confirmed in 1.0% of humans and 4.5% of dogs.
- Candidatus Mycoplasma haematoparvum was detected in 7.9% of dogs.
- Human infection was associated with gender and income, while dog infection was linked to gender and forest access.

## Abstract

Although Mycoplasma spp. infection has been recently detected in other vulnerable human populations (indigenous and quilombola communities) in Brazil, no study to date has focused on traditional oceanic island communities and their dogs. To address this research gap, we assessed Mycoplasma spp. infection in humans and dogs living on the mainland seashore and oceanic islands of southern Brazil.

Humans from three oceanic islands and two coastal mainland municipalities of southern Brazil were sampled, and Mycoplasma spp. infection was determined using quantitative polymerase chain reaction (qPCR) (cycle threshold; Ct ≤ 34.4). Dog samples were collected and tested using the Canine Hemotropic Mycoplasma panel (Idexx Reference Laboratory, Sacramento, CA, USA). To ensure accurate results, samples were also subjected to targeted next-generation sequencing (tNGS), and results were used to construct phylogenetic trees. Epidemiological information was obtained to analyze associated risk factors.

A total of 19/304 (6.2%) individuals tested positive to hemoplasmas, with Mycoplasma haemocanis confirmed in 3/304 (1.0%) through 16S ribosomal RNA gene and targeted next-generation sequencing. In addition, 44/290 (15.2%) dogs were positive for hemoplasmas through qPCR testing, with 13/290 (4.5%) for M. haemocanis, 23/290 (7.9%) for Candidatus
Mycoplasma haematoparvum, and 8/290 (2.8%) for both. Statistical analysis revealed an association between human positivity and gender and income range, and dog positivity was associated with male gender and access to forest areas.

The concomitant human–dog M. haemocanis detected herein on oceanic islands together with results from previous reports on indigenous and quilombola communities, suggest that socially vulnerable populations have an increased exposure risk. Future studies should be conducted in other vulnerable populations worldwide to fully establish the extent of human–dog Mycoplasma spp. infection.

The online version contains supplementary material available at 10.1186/s13071-025-07234-8.

## Linked entities

- **Species:** Mycoplasma haemocanis (taxon 136241), Candidatus Mycoplasma haematoparvum (taxon 247278)

## Full-text entities

- **Diseases:** headaches (MESH:D006261), M. haemocanis (MESH:C566367), zoonotic diseases (MESH:D015047), Q fever (MESH:D011778), Mycoplasma haemocanis infection (MESH:D009175), pyrexia (MESH:D005334), tick bite (MESH:D064927), Chagas disease (MESH:D014355), spotted fever (MESH:D000073605), borne diseases (MESH:D017282), INFECTION (MESH:D007239), hemolytic anemia (MESH:D000743), Toxoplasma gondii (MESH:D014123), hepatosplenomegaly (MESH:C535727), seizure (MESH:D012640)
- **Chemicals:** EDTA (MESH:D004492), water (MESH:D014867), PQ477793 (-)
- **Species:** Bartonella henselae (species) [taxon 38323], Ovis aries (domestic sheep, species) [taxon 9940], Borreliella burgdorferi (Lyme disease spirochete, species) [taxon 139], Sus scrofa (pig, species) [taxon 9823], Anaplasma phagocytophilum (agent of human granulocytic ehrlichiosis, species) [taxon 948], Anaplasma platys (species) [taxon 949], Metamycoplasma hominis (species) [taxon 2098], Homo sapiens (human, species) [taxon 9606], Mycoplasma ovis (species) [taxon 171632], Toxocara (genus) [taxon 6264], Dirofilaria immitis (canine heartworm nematode, species) [taxon 6287], Mycoplasma haemofelis (species) [taxon 29501], Candidatus Mycoplasma haematoparvum (species) [taxon 247278], Mycoplasma suis (species) [taxon 57372], Candidatus Mycoplasma haematohominis (species) [taxon 1494318], Mycoplasma haemocanis (species) [taxon 136241], Ehrlichia ewingii (species) [taxon 947], Ehrlichia canis (species) [taxon 944], Canis lupus familiaris (dog, subspecies) [taxon 9615], Felis catus (cat, species) [taxon 9685]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12849347/full.md

## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC12849347/full.md

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Source: https://tomesphere.com/paper/PMC12849347