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State Key Laboratories
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Chemie GmbH
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China Beijing Tong Ren Tang Group Co Ltd
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Illumina Inc
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DSMZ
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Millipore
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Journal: bioRxiv
Article Title: Nanopore direct RNA sequencing (DRS) of MS2 bacteriophages in E.coli throughout its life cycle reveals a complex transcriptional activity to control and maintain its growth
doi: 10.1101/2025.03.30.646209
Figure Lengend Snippet: A. MS2 replication pattern. The MS2 replicase complex contains host factors EF-Tu, EF-Ts and S1 ribosomal protein. B. Schematic presentation of the MS2 full-length genomic RNA coding regions organisation and composition. NTD, N-terminal domain, CTD, C-terminal domain. The 5′ UTR of MS2 contains ∼130 nt, and the 3′ UTR of MS2 contains 171 nt. C. Growth curves of bacterial cells (DSM5695 E. coli ) infected with MS2 RNA phage at MOI = 200 (red line) and bacteria cells without infection (blue). Phages were added at t = 0. Cells were harvested at 0h, 3h, and 6h post-infection (p.i.), and RNAs were extracted. Each growth curve represents the mean values and standard deviations obtained from biological triplicates. D. MS2 plaques on the host E. coli DSM5695 at 0h, 3h, 6h, 10h p.i. Plaques were pointed with white arrows. E. Plaque PFU and size change at 0h, 3h, 6h, 10h p.i. All pair-wise comparisons (3h vs. 6h vs. 10h at each diameter) were done after observing a significant Analysis of Variance (ANOVA) test result and showed statistically significant results ( P value <0.05 after accounting for multiple comparisons), except the 3h vs. 6h (1 mm diameter) and the 3h vs. 6h (2 mm diameter) one. Data are presented as means ± standard deviation (n = 3).
Article Snippet: The
Techniques: Infection, Bacteria, Standard Deviation
Journal: bioRxiv
Article Title: Nanopore direct RNA sequencing (DRS) of MS2 bacteriophages in E.coli throughout its life cycle reveals a complex transcriptional activity to control and maintain its growth
doi: 10.1101/2025.03.30.646209
Figure Lengend Snippet: A. Read counts from nanopore direct RNA sequencing of total RNA from DSM5695 E. coli cells infected with MS2 phage at different time points (0h, 3h, 6h p.i.). B. Principal component analysis (PCA) plot of MS2 samples at 0h, 3h, 6h p.i., each with three biological replicates to visualise the batch effects. C. Differential expression patterns for four MS2 genes at different time points (0h, 3h and 6h p.i.), analysed by DESeq2 with ‘median of ratios’ to normalise the read count. Adjusted P -value (after accounting for multiple hypothesis testing using the Benjamini-Hochberg method) <0.05, *; <0.01, **. D. Coverage map for MS2 total reads at 0h, 3h, 6h p.i. E-G. MS2 raw read length distribution at 0h, 3h and 6h p.i.
Article Snippet: The
Techniques: RNA Sequencing, Infection, Expressing