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Spatial mapping of mobile genetic elements and their bacterial hosts in complex microbiomes.
Grodner, Benjamin; Shi, Hao; Farchione, Owen; Vill, Albert C; Ntekas, Ioannis; Diebold, Peter J; Wu, David T; Chen, Chia-Yu; Kim, David M; Zipfel, Warren R; Brito, Ilana L; De Vlaminck, Iwijn.
Afiliação
  • Grodner B; Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
  • Shi H; Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
  • Farchione O; Kanvas Biosciences, Inc, Monmouth Junction, NJ, USA.
  • Vill AC; Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
  • Ntekas I; Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
  • Diebold PJ; Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
  • Wu DT; Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
  • Chen CY; Division of Periodontology, Department of Oral Medicine, Infection, and Immunity, Harvard School of Dental Medicine, Boston, MA, USA.
  • Kim DM; Division of Periodontology, Department of Oral Medicine, Infection, and Immunity, Harvard School of Dental Medicine, Boston, MA, USA.
  • Zipfel WR; Division of Periodontology, Department of Oral Medicine, Infection, and Immunity, Harvard School of Dental Medicine, Boston, MA, USA.
  • Brito IL; Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
  • De Vlaminck I; Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Nat Microbiol ; 2024 Jun 25.
Article em En | MEDLINE | ID: mdl-38918467
ABSTRACT
The exchange of mobile genetic elements (MGEs) facilitates the spread of functional traits including antimicrobial resistance within bacterial communities. Tools to spatially map MGEs and identify their bacterial hosts in complex microbial communities are currently lacking, limiting our understanding of this process. Here we combined single-molecule DNA fluorescence in situ hybridization (FISH) with multiplexed ribosomal RNA-FISH to enable simultaneous visualization of both MGEs and bacterial taxa. We spatially mapped bacteriophage and antimicrobial resistance (AMR) plasmids and identified their host taxa in human oral biofilms. This revealed distinct clusters of AMR plasmids and prophage, coinciding with densely packed regions of host bacteria. Our data suggest spatial heterogeneity in bacterial taxa results in heterogeneous MGE distribution within the community, with MGE clusters resulting from horizontal gene transfer hotspots or expansion of MGE-carrying strains. Our approach can help advance the study of AMR and phage ecology in biofilms.

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Nat Microbiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Nat Microbiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos