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Identification of microsporidia host-exposed proteins reveals a repertoire of rapidly evolving proteins.
Reinke, Aaron W; Balla, Keir M; Bennett, Eric J; Troemel, Emily R.
Afiliação
  • Reinke AW; Division of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093, USA.
  • Balla KM; Division of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093, USA.
  • Bennett EJ; Division of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093, USA.
  • Troemel ER; Division of Biological Sciences, Section of Cell and Developmental Biology, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093, USA.
Nat Commun ; 8: 14023, 2017 01 09.
Article em En | MEDLINE | ID: mdl-28067236
ABSTRACT
Pathogens use a variety of secreted and surface proteins to interact with and manipulate their hosts, but a systematic approach for identifying such proteins has been lacking. To identify these 'host-exposed' proteins, we used spatially restricted enzymatic tagging followed by mass spectrometry analysis of Caenorhabditis elegans infected with two species of Nematocida microsporidia. We identified 82 microsporidia proteins inside of intestinal cells, including several pathogen proteins in the nucleus. These microsporidia proteins are enriched in targeting signals, are rapidly evolving and belong to large Nematocida-specific gene families. We also find that large, species-specific families are common throughout microsporidia species. Our data suggest that the use of a large number of rapidly evolving species-specific proteins represents a common strategy for microsporidia to interact with their hosts. The unbiased method described here for identifying potential pathogen effectors represents a powerful approach to study a broad range of pathogens.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Fúngicas / Microsporídios / Caenorhabditis elegans / Células Epiteliais / Interações Hospedeiro-Patógeno Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Fúngicas / Microsporídios / Caenorhabditis elegans / Células Epiteliais / Interações Hospedeiro-Patógeno Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article