wall teichoic acids of staphylococcus aureus limit recognition by the drosophila peptidoglycan recognition protein-sa to promote pathogenicity墙磷壁酸的金黄色葡萄球菌限制识别果蝇肽聚糖识别protein-sa促进致病性.pdfVIP
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wall teichoic acids of staphylococcus aureus limit recognition by the drosophila peptidoglycan recognition protein-sa to promote pathogenicity墙磷壁酸的金黄色葡萄球菌限制识别果蝇肽聚糖识别protein-sa促进致病性
Wall Teichoic Acids of Staphylococcus aureus Limit
Recognition by the Drosophila Peptidoglycan
Recognition Protein-SA to Promote Pathogenicity
Magda L. Atilano1., James Yates1., Marcus Glittenberg2., Sergio R. Filipe1*, Petros Ligoxygakis2*
´ ´
1 Laboratory of Bacterial Cell Surfaces and Pathogenesis, Instituto de Tecnologia Quımica e Biologica/Universidade Nova de Lisboa, Oeiras, Portugal, 2 Genes and
Development Laboratory, Department of Biochemistry, University of Oxford, Oxford, United Kingdom
Abstract
The cell wall of Gram-positive bacteria is a complex network of surface proteins, capsular polysaccharides and wall teichoic
acids (WTA) covalently linked to Peptidoglycan (PG). The absence of WTA has been associated with a reduced pathogenicity
of Staphylococcus aureus (S. aureus). Here, we assessed whether this was due to increased detection of PG, an important
target of innate immune receptors. Antibiotic-mediated or genetic inhibition of WTA production in S. aureus led to
increased binding of the non-lytic PG Recognition Protein-SA (PGRP-SA), and this was associated with a reduction in host
susceptibility to infection. Moreover, PGRP-SD, another innate sensor required to control wild type S. aureus infection,
became redundant. Our data imply that by using WTA to limit access of innate immune receptors to PG, under-detected
bacteria are able to establish an infection and ultimately overwhelm the host. We propose that different PGRPs work in
concert to counter this strategy.
Citation: Atilano ML, Yates J, Glittenberg M, Filipe SR, Ligoxygakis P (2011) Wall Teichoic Acids of Staphylococcus aureus Limit Recognition by the Drosophila
Peptidoglycan Recognition Protein-SA to Promote Pathogenicity. PLoS Pathog 7
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