共 51 条
Wall Teichoic Acids of Staphylococcus aureus Limit Recognition by the Drosophila Peptidoglycan Recognition Protein-SA to Promote Pathogenicity
被引:42
作者:
Atilano, Magda L.
[1
]
Yates, James
[1
]
Glittenberg, Marcus
[2
]
Filipe, Sergio R.
[1
]
Ligoxygakis, Petros
[2
]
机构:
[1] Univ Nova Lisboa, Inst Tecnol Quim & Biol, Lab Bacterial Cell Surfaces & Pathogenesis, Oeiras, Portugal
[2] Univ Oxford, Dept Biochem, Genes & Dev Lab, Oxford OX1 3QU, England
基金:
英国医学研究理事会;
英国惠康基金;
关键词:
GRAM-POSITIVE BACTERIA;
TOLL PATHWAY;
SURFACE-PROTEINS;
PGRP-SD;
HOST;
BIOSYNTHESIS;
RESISTANCE;
EVASION;
ACTIVATION;
FAECALIS;
D O I:
10.1371/journal.ppat.1002421
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
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.
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页数:13
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