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Yorodumi- EMDB-16291: Cryotomogram of individual Efs7 virions and phage attachment to a... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-16291 | |||||||||
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Title | Cryotomogram of individual Efs7 virions and phage attachment to a Enterococcus faecalis cell | |||||||||
Map data | ||||||||||
Sample |
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Biological species | Enterococcus faecalis (bacteria) | |||||||||
Method | electron tomography / cryo EM | |||||||||
Authors | Feldmueller M / Wohlfarth JC / Loessner M / Pilhofer M | |||||||||
Funding support | Switzerland, 1 items
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Citation | Journal: Nat Microbiol / Year: 2023 Title: L-form conversion in Gram-positive bacteria enables escape from phage infection. Authors: Jan C Wohlfarth / Miki Feldmüller / Alissa Schneller / Samuel Kilcher / Marco Burkolter / Susanne Meile / Martin Pilhofer / Markus Schuppler / Martin J Loessner / Abstract: At the end of a lytic bacteriophage replication cycle in Gram-positive bacteria, peptidoglycan-degrading endolysins that cause explosive cell lysis of the host can also attack non-infected bystander ...At the end of a lytic bacteriophage replication cycle in Gram-positive bacteria, peptidoglycan-degrading endolysins that cause explosive cell lysis of the host can also attack non-infected bystander cells. Here we show that in osmotically stabilized environments, Listeria monocytogenes can evade phage predation by transient conversion to a cell wall-deficient L-form state. This L-form escape is triggered by endolysins disintegrating the cell wall from without, leading to turgor-driven extrusion of wall-deficient, yet viable L-form cells. Remarkably, in the absence of phage predation, we show that L-forms can quickly revert to the walled state. These findings suggest that L-form conversion represents a population-level persistence mechanism to evade complete eradication by phage attack. Importantly, we also demonstrate phage-mediated L-form switching of the urinary tract pathogen Enterococcus faecalis in human urine, which underscores that this escape route may be widespread and has important implications for phage- and endolysin-based therapeutic interventions. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_16291.map.gz | 403.2 MB | EMDB map data format | |
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Header (meta data) | emd-16291-v30.xml emd-16291.xml | 7.6 KB 7.6 KB | Display Display | EMDB header |
Images | emd_16291.png | 118.6 KB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-16291 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-16291 | HTTPS FTP |
-Validation report
Summary document | emd_16291_validation.pdf.gz | 475.4 KB | Display | EMDB validaton report |
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Full document | emd_16291_full_validation.pdf.gz | 475 KB | Display | |
Data in XML | emd_16291_validation.xml.gz | 2.5 KB | Display | |
Data in CIF | emd_16291_validation.cif.gz | 2.9 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-16291 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-16291 | HTTPS FTP |
-Related structure data
Related structure data | C: citing same article (ref.) |
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-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_16291.map.gz / Format: CCP4 / Size: 703.1 MB / Type: IMAGE STORED AS SIGNED BYTE | ||||||||||||||||||||
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Voxel size | X=Y=Z: 13.6 Å | ||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Sample components
-Entire : Cryotomogram of individual Efs7 virions and phage attachment to a...
Entire | Name: Cryotomogram of individual Efs7 virions and phage attachment to a Enterococcus faecalis cell |
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Components |
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-Supramolecule #1: Cryotomogram of individual Efs7 virions and phage attachment to a...
Supramolecule | Name: Cryotomogram of individual Efs7 virions and phage attachment to a Enterococcus faecalis cell type: cell / ID: 1 / Parent: 0 |
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Source (natural) | Organism: Enterococcus faecalis (bacteria) |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | electron tomography |
Aggregation state | cell |
-Sample preparation
Buffer | pH: 7.3 |
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Vitrification | Cryogen name: ETHANE-PROPANE |
Sectioning | Other: NO SECTIONING |
Fiducial marker | Manufacturer: Sigma-Aldrich / Diameter: 10 nm |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 135.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 9.0 µm / Nominal defocus min: 9.0 µm |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
-Image processing
Final reconstruction | Number images used: 61 |
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