Differential expression of Pmp10 in cell culture infected with Chlamydia pneumoniae CWL029

Citation
As. Pedersen et al., Differential expression of Pmp10 in cell culture infected with Chlamydia pneumoniae CWL029, FEMS MICROB, 203(2), 2001, pp. 153-159
Citations number
28
Categorie Soggetti
Microbiology
Journal title
FEMS MICROBIOLOGY LETTERS
ISSN journal
03781097 → ACNP
Volume
203
Issue
2
Year of publication
2001
Pages
153 - 159
Database
ISI
SICI code
0378-1097(20010925)203:2<153:DEOPIC>2.0.ZU;2-2
Abstract
The complete genome of Chlamydia pneumoniae contains a total of 21 genes en coding polymorphic membrane proteins (Pmp). From this large Pmp family thre e genes, pmp8, pmp10 and pmp11. were cloned and antibodies against recombin ant full-length Pmp proteins were produced. Indirect immunofluorescence mic roscopy of HEp-2 cells infected with C pneumoniae CWL029 was performed with the Pmp antibodies in combination with a Chlamydia-specific anti-lipopolys accharide (LPS) antibody, This double staining technique clearly showed tha t expression of Pmp10 was differential. Additional double staining with mon oclonal antibodies to the surface of C pneumoniae elementary bodies and the anti-LPS antibody resulted in identification of seven monoclonal antibodie s that reacted identically to the Pmp10 antibody indicating that Pmp10 is a n immunodominant protein. Finally, the molecular mechanism responsible for differential expression is suggested to be variation in the guanine residue s in the polyG tract of pmp10. (C) 2001 Federation of European Microbiologi cal Societies. Published by Elsevier Science B.V. All rights reserved.