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Comparative Genomics Hints at Dispensability of Multiple Essential Genes in Two Escherichia Coli L-form Strains

Overview
Journal Biosci Rep
Specialty Cell Biology
Date 2023 Oct 11
PMID 37819245
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Abstract

Despite the critical role of bacterial cell walls in maintaining cell shapes, certain environmental stressors can induce the transition of many bacterial species into a wall-deficient state called L-form. Long-term induced Escherichia coli L-forms lose their rod shape and usually hold significant mutations that affect cell division and growth. Besides this, the genetic background of L-form bacteria is still poorly understood. In the present study, the genomes of two stable L-form strains of E. coli (NC-7 and LWF+) were sequenced and their gene mutation status was determined and compared with their parental strains. Comparative genomic analysis between two L-forms reveals both unique adaptions and common mutated genes, many of which belong to essential gene categories not involved in cell wall biosynthesis, indicating that L-form genetic adaptation impacts crucial metabolic pathways. Missense variants from L-forms and Lenski's long-term evolution experiment (LTEE) were analyzed in parallel using an optimized DeepSequence pipeline to investigate predicted mutation effects (α) on protein functions. We report that the two L-form strains analyzed display a frequency of 6-10% (0% for LTEE) in mutated essential genes where the missense variants have substantial impact on protein functions (α<0.5). This indicates the emergence of different survival strategies in L-forms through changes in essential genes during adaptions to cell wall deficiency. Collectively, our results shed light on the detailed genetic background of two E. coli L-forms and pave the way for further investigations of the gene functions in L-form bacterial models.

Citing Articles

Implementation of Fluorescent-Protein-Based Quantification Analysis in L-Form Bacteria.

Tian D, Liu Y, Zhang Y, Liu Y, Xia Y, Xu B Bioengineering (Basel). 2024; 11(1).

PMID: 38247958 PMC: 10813599. DOI: 10.3390/bioengineering11010081.

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