Abstract
L-forms are cell wall-deficient variants of otherwise walled bacteria that maintain the ability to survive and proliferate in absence of the surrounding peptidoglycan sacculus. While transient or unstable L-forms can revert to the walled state and may still rely on residual peptidoglycan synthesis for multiplication, stable L-forms cannot revert to the walled form and are believed to propagate in the complete absence of peptidoglycan. L-forms are increasingly studied as a fundamental biological model system for cell wall synthesis. Here, we show that a stable L-form of the intracellular pathogen Listeria monocytogenes features a surprisingly intact peptidoglycan synthesis pathway including glycosyl transfer, in spite of the accumulation of multiple mutations during prolonged passage in the cell wall-deficient state. Microscopic and biochemical analysis revealed the presence of peptidoglycan precursors and functional glycosyl transferases, resulting in the formation of peptidoglycan polymers but without the synthesis of a mature cell wall sacculus. In conclusion, we found that stable, non-reverting L-forms, which do not require active PG synthesis for proliferation, may still continue to produce aberrant peptidoglycan.
Highlights
L-forms are cell wall-deficient bacterial cells that usually possess a cell wall, but can survive and multiply in the absence of this structure
By passaging a culture derived from walled L. monocytogenes EGDe in Listeria L-form medium (LLM) with high concentrations of penicillin G for more than two years, we generated a stable L-form strain that is unable to revert to the walled form
It has been recently demonstrated that unstable E. coli Lforms still show residual septal PG synthesis, which is essential for L-form multiplication and which acts as a starting point for new PG synthesis covering the complete bacterium from the onset of reversion [2,3,4]
Summary
L-forms are cell wall-deficient bacterial cells that usually possess a cell wall, but can survive and multiply in the absence of this structure. The wall-deficient state can be temporal (unstable/ transient L-forms) or permanent (stable L-forms). It has been believed that L-forms do not produce peptidoglycan (PG), or at least do not require active PG synthesis [1]. A more nuanced view on the presence and role of PG in L-forms has gained acceptance in the last decade. It has been shown that some L-form strains require PG synthesis for multiplication [2,3,4], while other L-forms can propagate in the complete absence of PG synthesis [5,6,7,8].
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