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Bacteria transport proteins across the plasma membrane to assemble their envelope, acquire nutrients, and establish appropriate interactions with their environment. The majority of these proteins are synthesized as precursors with a cleavable N-terminal signal sequence for recognition by the Sec machinery. In Staphylococcus aureus , a small subset of secreted precursors carries a YSIRK/GXXS motif. This motif provides a pre-translocation function by promoting the targeting of precursors to septal membranes, but the trans- acting factors that regulate such spatial distribution are not known. Here, we used immunofluorescence-microscopy to compare the spatial trafficking of Staphylococcal protein A (SpA), an abundant YSIRK/GXXS bearing precursor, between mutants of an arranged transposon library. This genetic search identified a cluster of five genes predicted to encode enzymes responsible for the synthesis of a novel surface polymer referred to as Staphylococcal surface carbohydrate, Ssc. Mutants in the ssc gene cluster no longer restrict the secretion of SpA into the cross-walls of S. aureus. ssc mutants replicate like wild-type bacteria unless grown in phosphate-limited conditions, and do not contribute to virulence when examined in a mouse model of bloodstream infection. Together, our observations suggest that S. aureus may encode a minor, phosphate-free carbohydrate, and propose a possible assembly pathway for this polymer. IMPORTANCE Gram-positive bacteria assemble peptidoglycan-linked polymers known as wall teichoic acids (WTA). Both Staphylococcus aureus and Bacillus subtilis elaborate WTAs made of poly-glycerol or poly-ribitol phosphates. WTAs contribute to cell shape maintenance, cation homeostasis, and resistance to antimicrobial compounds. Yet, B. subtilis replaces its phosphate-rich polymer with minor teichuronic acids whose functions remain elusive. S. aureus also encodes a minor wall polymer that may be required for growth under phosphate-limited condition. Here, we find that this polymer could help define the composition of the septal compartment, the site of cell division also used to recruit preproteins with a YSIRK/GXXS motif. Thus, the envelope of S. aureus may be more complex than previously thought with minor wall polymers contributing some discrete functions.
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Ibrahim et al. (2025) studied this question.
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