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1.
PLoS Pathog ; 19(6): e1011418, 2023 06.
Artículo en Inglés | MEDLINE | ID: mdl-37285383

RESUMEN

It has been 49 years since the last discovery of a new virus family in the model yeast Saccharomyces cerevisiae. A large-scale screen to determine the diversity of double-stranded RNA (dsRNA) viruses in S. cerevisiae has identified multiple novel viruses from the family Partitiviridae that have been previously shown to infect plants, fungi, protozoans, and insects. Most S. cerevisiae partitiviruses (ScPVs) are associated with strains of yeasts isolated from coffee and cacao beans. The presence of partitiviruses was confirmed by sequencing the viral dsRNAs and purifying and visualizing isometric, non-enveloped viral particles. ScPVs have a typical bipartite genome encoding an RNA-dependent RNA polymerase (RdRP) and a coat protein (CP). Phylogenetic analysis of ScPVs identified three species of ScPV, which are most closely related to viruses of the genus Cryspovirus from the mammalian pathogenic protozoan Cryptosporidium parvum. Molecular modeling of the ScPV RdRP revealed a conserved tertiary structure and catalytic site organization when compared to the RdRPs of the Picornaviridae. The ScPV CP is the smallest so far identified in the Partitiviridae and has structural homology with the CP of other partitiviruses but likely lacks a protrusion domain that is a conspicuous feature of other partitivirus particles. ScPVs were stably maintained during laboratory growth and were successfully transferred to haploid progeny after sporulation, which provides future opportunities to study partitivirus-host interactions using the powerful genetic tools available for the model organism S. cerevisiae.


Asunto(s)
Criptosporidiosis , Cryptosporidium , Virus Fúngicos , Virus ARN , Animales , Saccharomyces cerevisiae/genética , ARN Viral/genética , Filogenia , Criptosporidiosis/genética , Virus ARN Bicatenario , ARN Polimerasa Dependiente del ARN/genética , Genoma Viral , ARN Bicatenario , Mamíferos
2.
Antimicrob Agents Chemother ; 65(7): e0245020, 2021 06 17.
Artículo en Inglés | MEDLINE | ID: mdl-33972245

RESUMEN

Compared to other species of Candida yeasts, the growth of Candida glabrata is inhibited by many different strains of Saccharomyces killer yeasts. The ionophoric K1 and K2 killer toxins are broadly inhibitory to all clinical isolates of C. glabrata from patients with recurrent vulvovaginal candidiasis, despite high levels of resistance to clinically relevant antifungal therapeutics.


Asunto(s)
Candida glabrata , Candidiasis Vulvovaginal , Antifúngicos/farmacología , Candida glabrata/genética , Candidiasis Vulvovaginal/tratamiento farmacológico , Farmacorresistencia Fúngica/genética , Femenino , Humanos , Ionóforos , Pruebas de Sensibilidad Microbiana , Saccharomyces cerevisiae/genética
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