Please use this identifier to cite or link to this item: https://doi.org/10.1179/096805104225004833
Title: C-reactive protein: A predominant LPS-binding acute phase protein responsive to Pseudomonas infection
Authors: Ng, P.M.L. 
Jin, Z. 
Tan, S.S.H.
Ho, B.
Ding, J.L. 
Keywords: C-reactive protein
Endotoxin
Horseshoe crab
Lipopolysaccharide
Pseudomonas aeruginosa
Issue Date: 2004
Citation: Ng, P.M.L., Jin, Z., Tan, S.S.H., Ho, B., Ding, J.L. (2004). C-reactive protein: A predominant LPS-binding acute phase protein responsive to Pseudomonas infection. Journal of Endotoxin Research 10 (3) : 163-174. ScholarBank@NUS Repository. https://doi.org/10.1179/096805104225004833
Abstract: As a structural component of the outer membrane of Gram-negative bacteria, endotoxin, also known as lipopolysaccharide (LPS) exhibits strong immunostimulatory properties, rendering it a pivotal role in the pathogenesis of Gram-negative septicaemia. Our attempt to identify LPS-binding proteins from the hemolymph of the horseshoe crab led to the isolation and identification of C-reactive protein (CRP) as the predominant LPS-recognition protein during Pseudomonas infection. CRP is an evolutionarily ancient member of a superfamily of 'pentraxins'. It is a major protein in acute phase of infection in humans. Our investigation of CRP response to Pseudomonas aeruginosa unveiled a robust innate immune system in the horseshoe crab, which displays rapid suppression of a dosage of 106 CFU of bacteria in the first hour of infection and effected complete clearance of the pathogen by 3 days. Such a high dose would have been lethal to mice. Full-length CRP cDNA was cloned. Analysis of the untranslated regions suggests their crucial role in post-transcriptional regulation of CRP transcript levels. Northern blot analysis demonstrated an acute up-regulation of CRP by about 60-fold in 6-48 h of Pseudomonas infection. Taken together, our results provide new insights into the importance of CRP as a conserved molecule for pathogen recognition. © W.S. Maney & Son Ltd.
Source Title: Journal of Endotoxin Research
URI: http://scholarbank.nus.edu.sg/handle/10635/100350
ISSN: 09680519
DOI: 10.1179/096805104225004833
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