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EslB Is Required for Cell Wall Biosynthesis and Modification in Listeria monocytogenes

Lysozyme is an important component of the innate immune system. It functions by hydrolyzing the peptidoglycan (PG) layer of bacteria. The human pathogen Listeria monocytogenes is intrinsically lysozyme resistant. The peptidoglycan N-deacetylase PgdA and O-acetyltransferase OatA are two known factors...

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Autores principales: Rismondo, Jeanine, Schulz, Lisa M., Yacoub, Maria, Wadhawan, Ashima, Hoppert, Michael, Dionne, Marc S., Gründling, Angelika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847544/
https://www.ncbi.nlm.nih.gov/pubmed/33229460
http://dx.doi.org/10.1128/JB.00553-20
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author Rismondo, Jeanine
Schulz, Lisa M.
Yacoub, Maria
Wadhawan, Ashima
Hoppert, Michael
Dionne, Marc S.
Gründling, Angelika
author_facet Rismondo, Jeanine
Schulz, Lisa M.
Yacoub, Maria
Wadhawan, Ashima
Hoppert, Michael
Dionne, Marc S.
Gründling, Angelika
author_sort Rismondo, Jeanine
collection PubMed
description Lysozyme is an important component of the innate immune system. It functions by hydrolyzing the peptidoglycan (PG) layer of bacteria. The human pathogen Listeria monocytogenes is intrinsically lysozyme resistant. The peptidoglycan N-deacetylase PgdA and O-acetyltransferase OatA are two known factors contributing to its lysozyme resistance. Furthermore, it was shown that the absence of components of an ABC transporter, referred to here as EslABC, leads to reduced lysozyme resistance. How its activity is linked to lysozyme resistance is still unknown. To investigate this further, a strain with a deletion in eslB, coding for a membrane component of the ABC transporter, was constructed in L. monocytogenes strain 10403S. The eslB mutant showed a 40-fold reduction in the MIC to lysozyme. Analysis of the PG structure revealed that the eslB mutant produced PG with reduced levels of O-acetylation. Using growth and autolysis assays, we showed that the absence of EslB manifests in a growth defect in media containing high concentrations of sugars and increased endogenous cell lysis. A thinner PG layer produced by the eslB mutant under these growth conditions might explain these phenotypes. Furthermore, the eslB mutant had a noticeable cell division defect and formed elongated cells. Microscopy analysis revealed that an early cell division protein still localized in the eslB mutant, indicating that a downstream process is perturbed. Based on our results, we hypothesize that EslB affects the biosynthesis and modification of the cell wall in L. monocytogenes and is thus important for the maintenance of cell wall integrity. IMPORTANCE The ABC transporter EslABC is associated with the intrinsic lysozyme resistance of Listeria monocytogenes. However, the exact role of the transporter in this process and in the physiology of L. monocytogenes is unknown. Using different assays to characterize an eslB deletion strain, we found that the absence of EslB affects not only lysozyme resistance but also endogenous cell lysis, cell wall biosynthesis, cell division, and the ability of the bacterium to grow in media containing high concentrations of sugars. Our results indicate that EslB is, by means of a yet-unknown mechanism, an important determinant for cell wall integrity in L. monocytogenes.
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spelling pubmed-78475442021-07-25 EslB Is Required for Cell Wall Biosynthesis and Modification in Listeria monocytogenes Rismondo, Jeanine Schulz, Lisa M. Yacoub, Maria Wadhawan, Ashima Hoppert, Michael Dionne, Marc S. Gründling, Angelika J Bacteriol Research Article Lysozyme is an important component of the innate immune system. It functions by hydrolyzing the peptidoglycan (PG) layer of bacteria. The human pathogen Listeria monocytogenes is intrinsically lysozyme resistant. The peptidoglycan N-deacetylase PgdA and O-acetyltransferase OatA are two known factors contributing to its lysozyme resistance. Furthermore, it was shown that the absence of components of an ABC transporter, referred to here as EslABC, leads to reduced lysozyme resistance. How its activity is linked to lysozyme resistance is still unknown. To investigate this further, a strain with a deletion in eslB, coding for a membrane component of the ABC transporter, was constructed in L. monocytogenes strain 10403S. The eslB mutant showed a 40-fold reduction in the MIC to lysozyme. Analysis of the PG structure revealed that the eslB mutant produced PG with reduced levels of O-acetylation. Using growth and autolysis assays, we showed that the absence of EslB manifests in a growth defect in media containing high concentrations of sugars and increased endogenous cell lysis. A thinner PG layer produced by the eslB mutant under these growth conditions might explain these phenotypes. Furthermore, the eslB mutant had a noticeable cell division defect and formed elongated cells. Microscopy analysis revealed that an early cell division protein still localized in the eslB mutant, indicating that a downstream process is perturbed. Based on our results, we hypothesize that EslB affects the biosynthesis and modification of the cell wall in L. monocytogenes and is thus important for the maintenance of cell wall integrity. IMPORTANCE The ABC transporter EslABC is associated with the intrinsic lysozyme resistance of Listeria monocytogenes. However, the exact role of the transporter in this process and in the physiology of L. monocytogenes is unknown. Using different assays to characterize an eslB deletion strain, we found that the absence of EslB affects not only lysozyme resistance but also endogenous cell lysis, cell wall biosynthesis, cell division, and the ability of the bacterium to grow in media containing high concentrations of sugars. Our results indicate that EslB is, by means of a yet-unknown mechanism, an important determinant for cell wall integrity in L. monocytogenes. American Society for Microbiology 2021-01-25 /pmc/articles/PMC7847544/ /pubmed/33229460 http://dx.doi.org/10.1128/JB.00553-20 Text en Copyright © 2021 Rismondo et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Rismondo, Jeanine
Schulz, Lisa M.
Yacoub, Maria
Wadhawan, Ashima
Hoppert, Michael
Dionne, Marc S.
Gründling, Angelika
EslB Is Required for Cell Wall Biosynthesis and Modification in Listeria monocytogenes
title EslB Is Required for Cell Wall Biosynthesis and Modification in Listeria monocytogenes
title_full EslB Is Required for Cell Wall Biosynthesis and Modification in Listeria monocytogenes
title_fullStr EslB Is Required for Cell Wall Biosynthesis and Modification in Listeria monocytogenes
title_full_unstemmed EslB Is Required for Cell Wall Biosynthesis and Modification in Listeria monocytogenes
title_short EslB Is Required for Cell Wall Biosynthesis and Modification in Listeria monocytogenes
title_sort eslb is required for cell wall biosynthesis and modification in listeria monocytogenes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847544/
https://www.ncbi.nlm.nih.gov/pubmed/33229460
http://dx.doi.org/10.1128/JB.00553-20
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