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Aphanomyces astaci mtDNA: insights into the pathogen's differentiation and its genetic diversity from other closely related oomycetes.
Casabella-Herrero, Gloria; Martínez-Ríos, María; Viljamaa-Dirks, Satu; Martín-Torrijos, Laura; Diéguez-Uribeondo, Javier.
Afiliação
  • Casabella-Herrero G; Department of Mycology, Real Jardín Botánico (RJB-CSIC), Plaza Murillo 2, 28014, Madrid, Spain. Electronic address: gcasabella@rjb.csic.es.
  • Martínez-Ríos M; Department of Mycology, Real Jardín Botánico (RJB-CSIC), Plaza Murillo 2, 28014, Madrid, Spain. Electronic address: maria.mr@rjb.csic.es.
  • Viljamaa-Dirks S; Veterinary Bacteriology and Pathology, Laboratory and Research, Finnish Food Authority, Helsinki, Finland. Electronic address: satu.viljamaa-dirks@ruokavirasto.fi.
  • Martín-Torrijos L; Department of Mycology, Real Jardín Botánico (RJB-CSIC), Plaza Murillo 2, 28014, Madrid, Spain. Electronic address: lmtorrijos@rjb.csic.es.
  • Diéguez-Uribeondo J; Department of Mycology, Real Jardín Botánico (RJB-CSIC), Plaza Murillo 2, 28014, Madrid, Spain. Electronic address: dieguez@rjb.csic.es.
Fungal Biol ; 125(4): 316-325, 2021 04.
Article em En | MEDLINE | ID: mdl-33766310
ABSTRACT
The causative agent of crayfish plague, Aphanomyces astaci (Saprolegniales, Oomycota), is one of the 100 world's worst invasive alien species and represents a major threat to freshwater crayfish species worldwide. A better understanding of the biology and epidemiology of A. astaci relies on the application of efficient tools to detect the pathogen and assess its genetic diversity. In this study, we validated the specificity of two recently developed PCR-based approaches used to detect A. astaci groups. The first relies on the analysis of mitochondrial ribosomal rnnS (small) and rnnL (large) subunit sequences and the second, of sequences obtained by using genotype-specific primers designed from A. astaci whole genome sequencing. For this purpose, we tested the specificity against 76 selected isolates, including other oomycete species and the recently described species Aphanomyces fennicus, which, when used in nrITS-based specific tests for A. astaci, is known to result in a false positive. Under both approaches, we were able to efficiently and accurately identify A. astaci and its genetic groups in both pure cultures and clinical samples. We report that sequence analysis of the rnnS region alone is sufficient for the identification of A. astaci and a partial characterization of haplogroups. In contrast, the rnnL region alone is not sufficiently informative for A. astaci identification as other oomycete species present sequences identical to those of A. astaci.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aphanomyces Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aphanomyces Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article