Matches in SemOpenAlex for { <https://semopenalex.org/work/W4319293755> ?p ?o ?g. }
- W4319293755 abstract "Gram-positive bacterial cells are protected from the environment by a cell envelope that is comprised of a thick layer of peptidoglycan that maintains cell shape and teichoic acid polymers whose biological function remains unclear. In Bacillus subtilis, the loss of all class A penicillin-binding proteins (aPBPs), which function in peptidoglycan synthesis, is conditionally lethal. Here, we show that this lethality is associated with an alteration of lipoteichoic acids (LTAs) and the accumulation of the major autolysin LytE in the cell wall. Our analysis provides further evidence that the length and abundance of LTAs act to regulate the cellular level and activity of autolytic enzymes, specifically LytE. Importantly, we identify a novel function for the aminoacyl-phosphatidylglycerol synthase MprF in the modulation of LTA biosynthesis in both B. subtilis and Staphylococcus aureus. This finding has implications for our understanding of antimicrobial resistance (particularly to daptomycin) in clinically relevant bacteria and the involvement of MprF in the virulence of pathogens such as methicillin-resistant S. aureus (MRSA). IMPORTANCE In Gram-positive bacteria such as Bacillus subtilis and Staphylococcus aureus, the cell envelope is a structure that protects the cells from the environment but is also dynamic in that it must be modified in a controlled way to allow cell growth. In this study, we show that lipoteichoic acids (LTAs), which are anionic polymers attached to the membrane, have a direct role in modulating the cellular abundance of cell wall-degrading enzymes. We also find that the apparent length of the LTA is modulated by the activity of the enzyme MprF, previously implicated in modifications of the cell membrane leading to resistance to antimicrobial peptides. These findings are important contributions to our understanding of how bacteria balance cell wall synthesis and degradation to permit controlled growth and division. These results also have implications for the interpretation of antibiotic resistance, particularly for the clinical treatment of MRSA infections." @default.
- W4319293755 created "2023-02-07" @default.
- W4319293755 creator A5062098632 @default.
- W4319293755 creator A5069528584 @default.
- W4319293755 creator A5071259640 @default.
- W4319293755 date "2023-02-28" @default.
- W4319293755 modified "2023-10-18" @default.
- W4319293755 title "Insights into the Roles of Lipoteichoic Acids and MprF in Bacillus subtilis" @default.
- W4319293755 cites W1515069277 @default.
- W4319293755 cites W1522589910 @default.
- W4319293755 cites W1678194650 @default.
- W4319293755 cites W1931635381 @default.
- W4319293755 cites W1956166661 @default.
- W4319293755 cites W1986506035 @default.
- W4319293755 cites W2005518049 @default.
- W4319293755 cites W2026543895 @default.
- W4319293755 cites W2027572788 @default.
- W4319293755 cites W2046532579 @default.
- W4319293755 cites W2061884945 @default.
- W4319293755 cites W2066394597 @default.
- W4319293755 cites W2072217252 @default.
- W4319293755 cites W2077460182 @default.
- W4319293755 cites W2078842336 @default.
- W4319293755 cites W2087965877 @default.
- W4319293755 cites W2094133103 @default.
- W4319293755 cites W2094442395 @default.
- W4319293755 cites W2099340380 @default.
- W4319293755 cites W2101049355 @default.
- W4319293755 cites W2102454428 @default.
- W4319293755 cites W2105719418 @default.
- W4319293755 cites W2107962506 @default.
- W4319293755 cites W2108163746 @default.
- W4319293755 cites W2110162664 @default.
- W4319293755 cites W2114885447 @default.
- W4319293755 cites W2118424597 @default.
- W4319293755 cites W2118611827 @default.
- W4319293755 cites W2119619536 @default.
- W4319293755 cites W2128403490 @default.
- W4319293755 cites W2130534359 @default.
- W4319293755 cites W2130675566 @default.
- W4319293755 cites W2132284354 @default.
- W4319293755 cites W2133587620 @default.
- W4319293755 cites W2133940737 @default.
- W4319293755 cites W2143012569 @default.
- W4319293755 cites W2144025469 @default.
- W4319293755 cites W2144337101 @default.
- W4319293755 cites W2145924177 @default.
- W4319293755 cites W2146894318 @default.
- W4319293755 cites W2165629453 @default.
- W4319293755 cites W2166791780 @default.
- W4319293755 cites W2170628947 @default.
- W4319293755 cites W2171336887 @default.
- W4319293755 cites W2171571981 @default.
- W4319293755 cites W2262330728 @default.
- W4319293755 cites W2275084756 @default.
- W4319293755 cites W2334497283 @default.
- W4319293755 cites W2513563203 @default.
- W4319293755 cites W2517176893 @default.
- W4319293755 cites W2537852878 @default.
- W4319293755 cites W2560185751 @default.
- W4319293755 cites W2576814693 @default.
- W4319293755 cites W2586340362 @default.
- W4319293755 cites W2765484792 @default.
- W4319293755 cites W2890948890 @default.
- W4319293755 cites W2904481034 @default.
- W4319293755 cites W2940289922 @default.
- W4319293755 cites W2948505256 @default.
- W4319293755 cites W2969337649 @default.
- W4319293755 cites W2983594707 @default.
- W4319293755 cites W2992083765 @default.
- W4319293755 cites W2996818947 @default.
- W4319293755 cites W3001299653 @default.
- W4319293755 cites W3012427533 @default.
- W4319293755 cites W3029360949 @default.
- W4319293755 cites W3044047821 @default.
- W4319293755 cites W3084115636 @default.
- W4319293755 cites W3090466666 @default.
- W4319293755 cites W3102960110 @default.
- W4319293755 cites W3121347140 @default.
- W4319293755 cites W3128582586 @default.
- W4319293755 cites W3133440586 @default.
- W4319293755 cites W3134491518 @default.
- W4319293755 cites W3162804492 @default.
- W4319293755 cites W3205726857 @default.
- W4319293755 cites W4207021282 @default.
- W4319293755 cites W4213302333 @default.
- W4319293755 cites W4213313553 @default.
- W4319293755 cites W4220855721 @default.
- W4319293755 cites W4225787384 @default.
- W4319293755 cites W4243260669 @default.
- W4319293755 cites W4280536710 @default.
- W4319293755 doi "https://doi.org/10.1128/mbio.02667-22" @default.
- W4319293755 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36744964" @default.
- W4319293755 hasPublicationYear "2023" @default.
- W4319293755 type Work @default.
- W4319293755 citedByCount "5" @default.
- W4319293755 countsByYear W43192937552023 @default.
- W4319293755 crossrefType "journal-article" @default.
- W4319293755 hasAuthorship W4319293755A5062098632 @default.
- W4319293755 hasAuthorship W4319293755A5069528584 @default.