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High-throughput anaerobic screening for identifying compounds acting against gut bacteria in monocultures or communities.
Müller, Patrick; de la Cuesta-Zuluaga, Jacobo; Kuhn, Michael; Baghai Arassi, Maral; Treis, Tim; Blasche, Sonja; Zimmermann, Michael; Bork, Peer; Patil, Kiran Raosaheb; Typas, Athanasios; Garcia-Santamarina, Sarela; Maier, Lisa.
Afiliação
  • Müller P; Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany.
  • de la Cuesta-Zuluaga J; Cluster of Excellence 'Controlling Microbes to Fight Infections', University of Tübingen, Tübingen, Germany.
  • Kuhn M; Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany.
  • Baghai Arassi M; Cluster of Excellence 'Controlling Microbes to Fight Infections', University of Tübingen, Tübingen, Germany.
  • Treis T; European Molecular Biology Laboratory, Heidelberg, Germany.
  • Blasche S; European Molecular Biology Laboratory, Heidelberg, Germany.
  • Zimmermann M; Department of Pediatrics I, University Children's Hospital Heidelberg, Heidelberg, Germany.
  • Bork P; European Molecular Biology Laboratory, Heidelberg, Germany.
  • Patil KR; Institute of Computational Biology, Helmholtz Center München, Neuherberg, Germany.
  • Typas A; Medical Research Council Toxicology Unit, University of Cambridge, Cambridge, UK.
  • Garcia-Santamarina S; European Molecular Biology Laboratory, Heidelberg, Germany.
  • Maier L; European Molecular Biology Laboratory, Heidelberg, Germany.
Nat Protoc ; 19(3): 668-699, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38092943
ABSTRACT
The human gut microbiome is a key contributor to health, and its perturbations are linked to many diseases. Small-molecule xenobiotics such as drugs, chemical pollutants and food additives can alter the microbiota composition and are now recognized as one of the main factors underlying microbiome diversity. Mapping the effects of such compounds on the gut microbiome is challenging because of the complexity of the community, anaerobic growth requirements of individual species and the large number of interactions that need to be quantitatively assessed. High-throughput screening setups offer a promising solution for probing the direct inhibitory effects of hundreds of xenobiotics on tens of anaerobic gut bacteria. When automated, such assays enable the cost-effective investigation of a wide range of compound-microbe combinations. We have developed an experimental setup and protocol that enables testing of up to 5,000 compounds on a target gut species under strict anaerobic conditions within 5 d. In addition, with minor modifications to the protocol, drug effects can be tested on microbial communities either assembled from isolates or obtained from stool samples. Experience in working in an anaerobic chamber, especially in performing delicate work with thick chamber gloves, is required for implementing this protocol. We anticipate that this protocol will accelerate the study of interactions between small molecules and the gut microbiome and provide a deeper understanding of this microbial ecosystem, which is intimately intertwined with human health.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ecossistema / Ensaios de Triagem em Larga Escala Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ecossistema / Ensaios de Triagem em Larga Escala Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article