Work

Corrigendum: Phenotypic and transcriptional characterization of F. tularensis LVS during transition into a viable but non-culturable state

Year: 2024

Type: erratum

Abstract: Corrigendum on: Cantlay S, Garrison NL, Patterson R, et al. Phenotypic and transcriptional characterization of F. tularensis LVS during transition into a viable but non-culturable state. Front Microbiol. 2024;15:1347488. Published 2024Feb 6. doi:10.3389/fmicb.2024.1347488 In the published article, there was an error in the legend for [Figure 6] as published. [The change in the figure legend reflects that for Fig. 6A the DEGs were identified by normalized count differences and, whilst all but two were also statistically significantly different, we wanted to change the wording to make it clear that normalized counts were used to identify and rank the genes for the nanopore experiment and the non-significant DEGs are indicated.]. The corrected legend appears below.[RNA-Seq analysis of Francisella tularensis LVS during transition to the VBNC state. F. tularensis was cultured in Chamberlain's Defined Medium (CDM) for 24 and 336 h and RNA isolated from 3 biological replicates (Nanopore) or 6 biological replicates (Illumina) was sequenced. (A) Top 20 DEG normalized count differences between the T24 and T336 Nanopore experiment samples; associated FTL identifiers and products in table, non-significant DEGs indicated with *. (B) Differences in the top 20 most significant DEGs between the T24 and T336 Illumina experiment samples; associated FTL identifiers and products in table.]The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.In the published article, there was an error in [Figure 6] as published. [The protein product names in Figure 6 did not match the FTL_RS identifiers due to a sorting error when the names were added in the figure editing process (Excel->Adobe Illustrator). These protein names were manually added using a list of genes for each analysis (nanopore and illumina) that were sorted differently from the clustered order the heatmap figure generated. We have verified that the FTL IDs associated with the heatmaps are accurate in the Figure 6_fixed image, the protein names have been sorted properly and added to the fixed version of Fig. 6]. The corrected [Figure 6] and its caption **[Figure 6

Source: Frontiers in Microbiology

DOI: 10.3389/fmicb.2024.1407526