# Detection of Leishmania infantum DNA in captive wild mammals from an urban zoo in a visceral leishmaniasis–endemic area of Brazil

**Authors:** Nathália Cristina Lima Pereira, Érika Monteiro Michalsky, Daniel Moreira de Avelar, Lara Saraiva, Regina Celi Antunes Nobi, Carlyle Mendes Coelho, Humberto Espírito Santo Mello, Consuelo Latorre Fortes-Dias, Edelberto Santos Dias

PMC · DOI: 10.1371/journal.pntd.0014098 · 2026-03-20

## TL;DR

A study found Leishmania infantum DNA in a zoo maned wolf in Brazil, showing wild animals in urban areas can be exposed to visceral leishmaniasis.

## Contribution

This is the first report of Leishmania infantum DNA in a zoo-housed wild canid in a visceral leishmaniasis-endemic urban area.

## Key findings

- Leishmania infantum DNA was detected in a clinically healthy maned wolf (Chrysocyon brachyurus) at Belo Horizonte Zoo.
- The infected animal was housed in an area with high densities of Lutzomyia longipalpis, the primary VL vector.
- The findings suggest captive wildlife may be involved in local transmission cycles of visceral leishmaniasis.

## Abstract

Visceral leishmaniasis (VL) is a complex zoonotic disease transmitted to humans through the bites of Leishmania-infected phlebotomine sand flies (Diptera:Psychodidae:Phlebotominae). Its transmission dynamics are shaped by environmental, ecological, and anthropogenic factors. Rapid urbanization, landscape modification, and the rising incidence of human and canine VL in endemic cities raise concerns about parasite circulation at the human-wildlife interface, including within captive animal populations housed in urban zoological institutions.

This study was conducted at the Belo Horizonte Zoo (Minas Gerais, Brazil), located in one of city’s most VL-affected districts. We collected 31 skin biopsies and 40 blood samples from 13 captive mammal species—11 primates (Alouatta guariba, Aotus nigriceps, Ateles marginatus, Gorilla gorilla, Lagothrix lagotricha, Leontopithecus rosalia, Leontopithecus chrysopygus, Pan troglodytes, Pithecia irrorata, Saguinus imperator, Sapajus xanthosternos) and 2 carnivores (Chrysocyon brachyurus and Leopardus colocolo). Samples were screened using a complementary molecular diagnostic panel: Leishmania nested PCR (LnPCR), real time PCR (qPCR), and K26 loop-mediated isothermal amplification (K26-LAMP). Leishmania DNA was detected in the blood of a clinically healthy adult maned wolf (Chrysocyon brachyurus). Sequencing and phylogenetic analysis of the LnPCR amplicon confirmed the presence of Leishmania infantum. The animal was housed in an enclosure with documented high densities of Lutzomyia longipalpis, the primary VL vector in the region.

The detection of Leishmania infantum DNA in a zoo-housed wild canid within an VL-endemic urban area highlights the potential exposure of captive wildlife to local transmission cycles. Although infectivity and reservoir competence were not assessed, these findings underscore the importance of integrating minimally invasive molecular surveillance with entomological monitoring in zoological institutions. Such an integrated approach can strengthen One Health surveillance frameworks by enabling early detection of parasite circulation, informing risk-based management strategies, and supporting VL prevention efforts in complex urban environments.

Visceral leishmaniasis (VL) is a serious disease transmitted to humans and animals by infected sand flies. Urban expansion and the increasing incidence of VL raises concerns about parasite circulation at the interface of people, domestic and wild animals, and the environment—including wildlife in urban zoos. In this study, we analyzed 31 skin and 40 blood samples from 13 species of captive primates and carnivores at the Belo Horizonte Zoo, located in a highly VL-endemic area of Brazil. Using molecular diagnostic methods, we detected Leishmania infantum DNA in the blood of a maned wolf (Chrysocyon brachyurus), providing evidence that zoo-housed wild animals can become infected in urban endemic settings. Notably, the enclosure housing this animal exhibited a high density of Lutzomyia longipalpis, the primary vector of VL in Brazil. Although our study did not assess the infectivity of the detected parasite or the animal’s capacity to transmit it, our findings underscore the value of integrating molecular surveillance with vector monitoring in zoological institutions. Such an integrated approach aligns with the One Health framework, enabling early detection of parasite circulation at the wildlife–vector–human interface and informing both public health wildlife conservation strategies.

## Linked entities

- **Diseases:** visceral leishmaniasis (MONDO:0005445)
- **Species:** Chrysocyon brachyurus (taxon 68728), Lutzomyia longipalpis (taxon 7200), Alouatta guariba (taxon 182256), Aotus nigriceps (taxon 57175), Ateles marginatus (taxon 1529884), Gorilla gorilla (taxon 9593), Lagothrix lagotricha (taxon 9519), Leontopithecus rosalia (taxon 30588), Leontopithecus chrysopygus (taxon 58710), Pan troglodytes (taxon 9598), Pithecia irrorata (taxon 30598), Saguinus imperator (taxon 9491), Sapajus xanthosternos (taxon 174599)

## Full-text entities

- **Genes:** RBP3 (retinol binding protein 3) [NCBI Gene 5949] {aka D10S64, D10S65, D10S66, IRBP, RBPI, RP66}
- **Diseases:** zoonotic diseases (MESH:D015047), weight loss (MESH:D015431), Leishmania infection (MESH:D007896), infectious diseases (MESH:D003141), fever (MESH:D005334), disease (MESH:D004194), Infections (MESH:D007239), hepatosplenomegaly (MESH:C535727), VL (MESH:D007898), anemia (MESH:D000740), EIDs (MESH:D021821)
- **Chemicals:** tiletamine (MESH:D013992), povidone-iodine (MESH:D011206), water (MESH:D014867), ethanol (MESH:D000431), SYBR Green (MESH:C098022), Zoletil (MESH:C006131), lidocaine hydrochloride (MESH:D008012), K26 (-), ethidium bromide (MESH:D004996), agarose (MESH:D012685), EDTA (MESH:D004492), chlorhexidine (MESH:D002710), zolazepam (MESH:D015041)
- **Species:** Cephalophorus nigrifrons (black-fronted duiker, species) [taxon 129227], Legionella sp. E (species) [taxon 66964], Saguinus imperator (black-chinned emperor tamarin, species) [taxon 9491], Alouatta guariba (brown howler monkey, species) [taxon 182256], Aotus nigriceps (black-headed night monkey, species) [taxon 57175], Phlebotominae (sand flies, subfamily) [taxon 7198], Canis lupus familiaris (dog, subspecies) [taxon 9615], Leishmania amazonensis (species) [taxon 5659], Ateles marginatus (white-cheeked spider monkey, species) [taxon 1529884], Callicebus nigrifrons (black-fronted titi, species) [taxon 867334], Lutzomyia longipalpis (species) [taxon 7200], Gorilla gorilla (gorilla, species) [taxon 9593], Cerdocyon thous (common zorro, species) [taxon 9620], Lagothrix lagotricha (brown woolly monkey, species) [taxon 9519], Sapajus xanthosternos (yellow-breasted capuchin, species) [taxon 174599], Leishmania braziliensis (species) [taxon 5660], Leontopithecus chrysopygus (golden-rumped lion tamarin, species) [taxon 58710], Chrysocyon brachyurus (maned wolf, species) [taxon 68728], Pithecia irrorata (bald-faced saki, species) [taxon 30598], Leishmania infantum (species) [taxon 5671], Leontopithecus rosalia (golden lion tamarin, species) [taxon 30588], Lycalopex vetulus (hoary fox, species) [taxon 68734], Leopardus colocolo [taxon 61406], Leishmania sp. (species) [taxon 28847], Drosophila melanogaster (fruit fly, species) [taxon 7227], Trypanosoma cruzi (species) [taxon 5693], Pan troglodytes (chimpanzee, species) [taxon 9598], Speothos venaticus (bush dog, species) [taxon 68741], Homo sapiens (human, species) [taxon 9606], Diptera (flies, order) [taxon 7147]
- **Mutations:** C with 0, F59F
- **Cell lines:** JF746736.1 — Rattus norvegicus (Rat), Rat sarcoma, Cancer cell line (CVCL_L879)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13004319/full.md

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Source: https://tomesphere.com/paper/PMC13004319