Julie Guiblin, Solène Le Gal, Nathan Le Nan, Corentin Paranthoën, Lourdes Velo-Suárez, Nathalie Foucher, Maud Bernez-Romand, Anthony Madeline, Nathalie Cordonnier-Lefort, Corinne Sevin, José-Carlos Valle-Casuso, Jacques Guillot, Peggy Moreau, Gilles Nevez
{"title":"High frequency and high genetic diversity of Pneumocystis sp. in foals.","authors":"Julie Guiblin, Solène Le Gal, Nathan Le Nan, Corentin Paranthoën, Lourdes Velo-Suárez, Nathalie Foucher, Maud Bernez-Romand, Anthony Madeline, Nathalie Cordonnier-Lefort, Corinne Sevin, José-Carlos Valle-Casuso, Jacques Guillot, Peggy Moreau, Gilles Nevez","doi":"10.1093/mmy/myag043","DOIUrl":null,"url":null,"abstract":"<p><p>Twenty-two foals, aged 1-7 months, which died from interstitial pneumonia (15 foals) or unrelated illnesses and injuries (7 foals), were enrolled in this study. Sampling of the lungs was performed post-mortem for a total of 52 specimens. Pneumocystis was detected in 21/22 foals (48/52 specimens) using a Polymerase Chain Reaction (PCR) assay targeting the gene encoding the small subunit of the mitochondrial rRNA (mtSSUrRNA) of the horse-related Pneumocystis (Pneumocystis sp. 'Equus ferus caballus'). The sequencing of the PCR products was successful in 34/48 specimens. The sequences were identical to the horse-related Pneumocystis reference sequence (Genbank accession number OP738808) in 7 specimens (5 foals). Single Nucleotide Polymorphisms (SNPs) were detected in the sequences from 24 specimens (16 foals). Three alleles were determined according to these SNPs. Allele identification was successful in 10 specimens (7 foals) and unsuccessful in 21 specimens (14 foals) because of a mix of alleles. The presence of a mix of alleles highly suggests the presence of more than one strain able to infect foals. Three sequences from 2 foals did not align correctly to the reference sequence, with a percentage of identity of only 86.12%. Ultradeep sequencing of the gene encoding the large subunit of the mitochondrial rRNA (mtLSUrRNA) was performed on a subset of 5 specimens. The issued sequences were concatenated with mtSSUrRNA sequences and used for phylogenetic analysis. The phylogenetic analysis showed a shorter genetic distance of these sequences of Pneumocystis sp. 'Equus ferus caballus' with that of another species close to Pneumocystis sp. 'Sus scrofa domesticus', suggesting a putative other species able to infect foals. These results provided original and additional data on genetic diversity of Pneumocystis sp. in foals.</p>","PeriodicalId":18586,"journal":{"name":"Medical mycology","volume":" ","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2026-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical mycology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/mmy/myag043","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0
Abstract
Twenty-two foals, aged 1-7 months, which died from interstitial pneumonia (15 foals) or unrelated illnesses and injuries (7 foals), were enrolled in this study. Sampling of the lungs was performed post-mortem for a total of 52 specimens. Pneumocystis was detected in 21/22 foals (48/52 specimens) using a Polymerase Chain Reaction (PCR) assay targeting the gene encoding the small subunit of the mitochondrial rRNA (mtSSUrRNA) of the horse-related Pneumocystis (Pneumocystis sp. 'Equus ferus caballus'). The sequencing of the PCR products was successful in 34/48 specimens. The sequences were identical to the horse-related Pneumocystis reference sequence (Genbank accession number OP738808) in 7 specimens (5 foals). Single Nucleotide Polymorphisms (SNPs) were detected in the sequences from 24 specimens (16 foals). Three alleles were determined according to these SNPs. Allele identification was successful in 10 specimens (7 foals) and unsuccessful in 21 specimens (14 foals) because of a mix of alleles. The presence of a mix of alleles highly suggests the presence of more than one strain able to infect foals. Three sequences from 2 foals did not align correctly to the reference sequence, with a percentage of identity of only 86.12%. Ultradeep sequencing of the gene encoding the large subunit of the mitochondrial rRNA (mtLSUrRNA) was performed on a subset of 5 specimens. The issued sequences were concatenated with mtSSUrRNA sequences and used for phylogenetic analysis. The phylogenetic analysis showed a shorter genetic distance of these sequences of Pneumocystis sp. 'Equus ferus caballus' with that of another species close to Pneumocystis sp. 'Sus scrofa domesticus', suggesting a putative other species able to infect foals. These results provided original and additional data on genetic diversity of Pneumocystis sp. in foals.
期刊介绍:
Medical Mycology is a peer-reviewed international journal that focuses on original and innovative basic and applied studies, as well as learned reviews on all aspects of medical, veterinary and environmental mycology as related to disease. The objective is to present the highest quality scientific reports from throughout the world on divergent topics. These topics include the phylogeny of fungal pathogens, epidemiology and public health mycology themes, new approaches in the diagnosis and treatment of mycoses including clinical trials and guidelines, pharmacology and antifungal susceptibilities, changes in taxonomy, description of new or unusual fungi associated with human or animal disease, immunology of fungal infections, vaccinology for prevention of fungal infections, pathogenesis and virulence, and the molecular biology of pathogenic fungi in vitro and in vivo, including genomics, transcriptomics, metabolomics, and proteomics. Case reports are no longer accepted. In addition, studies of natural products showing inhibitory activity against pathogenic fungi are not accepted without chemical characterization and identification of the compounds responsible for the inhibitory activity.