Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2006-1-18
pubmed:abstractText
From a forward genetic screen for phagocytosis mutants in Drosophila melanogaster, we identified a mutation that affects peptidoglycan recognition protein (PGRP) SC1a and impairs the ability to phagocytose the bacteria Staphylococcus aureus, but not Escherichia coli and Bacillus subtilis. Because of the differences in peptidoglycan peptide linkages in these bacteria, our data suggest that PGRP-SC1a is necessary for recognition of the Lys-type peptidoglycan typical of most Gram(+) bacteria. PGRP-SC1a mutants also fail to activate the Toll/NF-kappaB signaling pathway and are compromised for survival after S. aureus infection. This mutant phenotype is the first found for an N-acetylmuramoyl-l-alanine amidase PGRP that cleaves peptidoglycan at the lactylamide bond between the glycan backbone and the crosslinking stem peptides. By generating transgenic rescue flies that express either wild-type or a noncatalytic cysteine-serine mutant PGRP-SC1a, we find that PGRP-SC1a amidase activity is not necessary for Toll signaling, but is essential for uptake of S. aureus into the host phagocytes and for survival after S. aureus infection. Furthermore, we find that the PGRP-SC1a amidase activity can be substituted by exogenous addition of free peptidoglycan, suggesting that the presence of peptidoglycan cleavage products is more important than the generation of cleaved peptidoglycan on the bacterial surface for PGRP-SC1a mediated phagocytosis.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-10207004, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-10619029, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-10827080, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-10898983, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-10948168, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-11017107, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-11018014, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-11106397, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-11156609, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-11269502, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-11485985, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-11703941, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-11742401, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-11754822, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-11872802, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-11880375, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-11912488, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-11912489, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-12359879, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-12401167, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-12496260, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-12649138, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-12692550, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-12777387, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-12845326, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-14698226, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-15142531, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-15143282, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-15166147, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-15199956, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-15340057, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-15361936, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-15448690, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-15538387, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-15572450, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-15791270, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-4568761, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-7796812, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-8662762, http://linkedlifedata.com/resource/pubmed/commentcorrection/16407137-9707603
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
17
pubmed:volume
103
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
660-5
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
2006
pubmed:articleTitle
The peptidoglycan recognition protein PGRP-SC1a is essential for Toll signaling and phagocytosis of Staphylococcus aureus in Drosophila.
pubmed:affiliation
Center for Biosystems Research, University of Maryland Biotechnology Institute, 5115 Plant Sciences Building, College Park, MD 20742, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural