Evidence map›Paper›PMID 40788895›Full record

ArticlePLoS neglected tropical diseases2025

Genetic analysis of Schistosoma mansoni in a low-transmission area in Brazil suggests population sharing between wild-hosts and humans and geographical isolation.

Karina Varella, Rosana Gentile, Roberto do Val Vilela, Silvana Carvalho Thiengo, Aline Dos Santos Moreira, José Roberto Machado-Silva, Thiago Dos Santos Cardoso, Sócrates Fraga da Costa-Neto, Beatriz de Lima Alessio Müller, Alexandre Araujo Cunha Dos Santos and 1 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Karina VarellaPrograma de Pós-Graduação em Biologia Parasitária (PPGBP), Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Manguinhos, Rio de Janeiro, Brazil.
Rosana GentileLaboratório de Biologia e Parasitologia de Mamíferos Silvestres Reservatórios, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Manguinhos, Rio de Janeiro, Brazil.
Roberto do Val VilelaLaboratório de Biologia e Parasitologia de Mamíferos Silvestres Reservatórios, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Manguinhos, Rio de Janeiro, Brazil.ORCID 0000-0003-3275-2648
Silvana Carvalho ThiengoLaboratório de Referência Nacional para Esquistossomose - Malacologia, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Manguinhos, Rio de Janeiro, Brazil.
Aline Dos Santos MoreiraPlataforma de Sequenciamento de DNA por eletroforese capilar (Sanger - RPT01A), Plataforma de Análise de Fragmentos de DNA e Microssatélites (RPT01D), Laboratório de Genômica Aplicada e Bioinovações, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Manguinhos, Rio de Janeiro, Brazil.
José Roberto Machado-SilvaLaboratório de Helmintologia Romero Lascasas Porto, Departamento de Microbiologia, Imunologia e Parasitologia, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Vila Isabel, Rio de Janeiro, Brazil.
Thiago Dos Santos CardosoLaboratório de Biologia e Parasitologia de Mamíferos Silvestres Reservatórios, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Manguinhos, Rio de Janeiro, Brazil.
Sócrates Fraga da Costa-NetoCampus Fiocruz Mata Atlântica CFMA, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
Beatriz de Lima Alessio MüllerPlataforma de Sequenciamento de DNA por eletroforese capilar (Sanger - RPT01A), Plataforma de Análise de Fragmentos de DNA e Microssatélites (RPT01D), Laboratório de Genômica Aplicada e Bioinovações, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Manguinhos, Rio de Janeiro, Brazil.
Alexandre Araujo Cunha Dos SantosPlataforma de Sequenciamento de DNA por eletroforese capilar (Sanger - RPT01A), Plataforma de Análise de Fragmentos de DNA e Microssatélites (RPT01D), Laboratório de Genômica Aplicada e Bioinovações, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Manguinhos, Rio de Janeiro, Brazil.
Arnaldo Maldonado JuniorPrograma de Pós-Graduação em Biologia Parasitária (PPGBP), Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Manguinhos, Rio de Janeiro, Brazil.

Funding

Carlos Chagas Filho Foundation for Research Support in Rio de JaneiroNational Council for Scientific and Technological Development (CNPq)Oswaldo Cruz Institute (IOC, FIOCRUZ)
6 · The paper itself

Abstract

backgroundThe fluke Schistosoma mansoni is the causative agent of intestinal schistosomiasis, a neglected tropical disease, and remains prevalent in certain regions of Brazil. In the municipality of Sumidouro, state of Rio de Janeiro, Brazil, a low-endemic area for S. mansoni, water rats (Nectomys squamipes) are naturally infected by this trematode. The S. mansoni populations infecting humans and water-rats in Sumidouro exhibit distinct patterns of cercarial emergence (chronotypes) and phenotypic differences between hosts. Previous studies have shown that the adaptation of S. mansoni populations to human hosts (diurnal chronotype) and water rats (nocturnal chronotype) could result in prezygotic isolation. To test this hypothesis, we employed the mitochondrial cytochrome c oxidase subunit 1 gene (MT-CO1) and microsatellite loci as genetic markers. PRINCIPAL

findingsWe assessed the population structure between the definitive host species and geographically distant isolates collected from two endemic localities (Pamparrão-PAM and Encanto-Soledade-ENC-SOL) in Sumidouro. Additionally, we evaluated the phylogenetic relationships between S. mansoni from Sumidouro and those from other countries. Five haplotypes of the MT-CO1 gene were identified, with haplotypes 3 and 4 exclusive to ENC-SOL, and haplotypes 1, 2, and 3 were shared between humans and water rats. Haplotype 1 was also shared with other Brazilian localities, South American countries and a single locality in West Africa. The remaining haplotypes were exclusive to Sumidouro, indicating local genetic diversity. Population structure analysis revealed no genetic differentiation associated with host species but rather geographical structuring, probably due to the sedentary habits of rodents and the limited movement of humans between localities. This finding indicates that S. mansoni populations with different chronotypes are not genetically isolated and that significant gene flow occurs between them.

conclusionsIn conclusion, our findings confirm that wild rodents contribute to the maintenance of the S. mansoni life cycle in Sumidouro and can serve as indicators of local transmission hotspots.

Indexed as

Schistosoma mansoniSchistosomiasis mansoniAnimalsBrazilElectron Transport Complex IVGenetic VariationHaplotypesHumansMicrosatellite RepeatsPhylogenyRatsSigmodontinaeElectron Transport Complex IV

Identifiers

PMID40788895
PMCPMC12338815

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Registered trials

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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.