Intragenomic diversity of the small subunit rDNA gene shows limited impact on the pathogenicity of Blastocystis infection in clinical patients

The clinical significance of Blastocystis sp. remains to be fully elucidated. This study assesses whether Blastocystis subtype diversity can affect the outcome of the infection and the occurrence of clinical manifestations in infected individuals. Stool samples from 219 Blastocystis-positive patient...

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Detalhes bibliográficos
Autores: Seijas-Pereda, Laura, Köster, Pamela Carolina, Dashti, Alejandro, Bailo-Barroso, Begoña, Guadano-Procesi, Isabel, Rescalvo-Casas, Carlos, Hernando-Gozalo, Marcos, Cuadros-González, Juan, Carmena, David, Pérez-Tanoira, Ramón
Formato: artículo
Fecha de publicación:2025
País:España
Recursos:Instituto de Salud Carlos III (ISCIII)
Repositorio:Repisalud
Idioma:inglés
OAI Identifier:oai:repisalud.isciii.es:20.500.12105/26601
Acesso em linha:https://hdl.handle.net/20.500.12105/26601
Access Level:acceso abierto
Palavra-chave:Clinical patients
Co-infection
Gastrointestinal symptoms
Pathogenicity
Spain
Virulence
Adolescent
Adult
Aged
Aged, 80 and over
Blastocystis Infections
Blastocystis
Child
Child, Preschool
Coinfection
DNA, Protozoan
DNA, Ribosomal
Feces
Female
Genetic Variation
Genotype
Humans
Infant
Male
Middle Aged
Phylogeny
Risk Factors
Sequence Analysis, DNA
Young Adult
Descrição
Resumo:The clinical significance of Blastocystis sp. remains to be fully elucidated. This study assesses whether Blastocystis subtype diversity can affect the outcome of the infection and the occurrence of clinical manifestations in infected individuals. Stool samples from 219 Blastocystis-positive patients by PCR targeting the ssu rDNA gene were fully genotyped by Sanger sequencing analyses. Co-infections by other parasitic, viral, and bacterial enteropathogens were identified by molecular and culture methods. Sequence analyses revealed the presence of six Blastocystis subtypes including ST1 (21.5 %), ST2 (17.8 %), ST3 (29.7 %), ST4 (22.8 %), ST6 (5.5 %), and ST7 (2.3 %), with a single sample harbouring a ST1+ST3 co-infection (0.5 %). Multivariate risk factor analyses using logistic regression models indicated that neither Blastocystis subtypes nor patient-associated variables including sex, country of origin, travelling history, and presence of nonspecific symptoms were positively associated with a higher likelihood of developing gastrointestinal symptoms (abdominal pain and diarrhoea). However, being of a young age (p-value: 0.003) and experiencing skin pruritus (p-value < 0.001) and eosinophilia (p-value: 0.016) were found to increase the odds of presenting gastrointestinal symptoms. Blastocystis subtypes based on variability within the ssu rDNA gene do not seem to be the main drivers of clinical manifestations in the surveyed clinical population.