Evaluation of P1 adhesin epitopes for the serodiagnosis ofMycoplasma pneumoniaeinfections
Author:
Affiliation:
1. Department of Bacteriology; Capital Institute of Pediatrics; Beijing; China
2. The Affiliated Children's Hospital of Capital Institute of Pediatrics; Beijing; China
Publisher
Oxford University Press (OUP)
Subject
Genetics,Molecular Biology,Microbiology
Link
http://academic.oup.com/femsle/article-pdf/340/2/86/19437591/340-2-86.pdf
Reference27 articles.
1. Development of multiplex real-time PCR for the rapid detection of five bacterial causes of community acquired pneumonia;Al-Marzooq;Trop Biomed,2011
2. Interplay between mycoplasma surface proteins, airway cells, and the protean manifestations of mycoplasma-mediated human infections;Baseman;Am J Respir Crit Care Med,1996
3. Evaluation of 12 commercial tests and the complement fixation test for Mycoplasma pneumoniae specific immunoglobulin G (IgG) and IgM antibodies, with PCR used as the ‘gold standard’;Beersma;J Clin Microbiol,2005
4. Expression and immunological characterization of the carboxy-terminal region of the P1 adhesin protein of Mycoplasma pneumoniae;Chaudhry;J Clin Microbiol,2005
5. Immune response to Mycoplasma pneumoniae P1 and P116 in patients with atypical pneumonia analyzed by ELISA;Drasbek;BMC Microbiol,2004
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