Home LiteratureArticle Details
PMID: 9680205 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Pilus-mediated adhesion of Neisseria meningitidis: the essential role of cell contact-dependent transcriptional upregulation of the PilC1 protein.

Molecular microbiology ·Vol. 28 ·No. 6 ·1998-06-00 ·Pages 1153-63

Taha MK, Morand PC, Pereira Y, Eugène E, Giorgini D, Larribe M, Nassif X

Abstract

Pilus-mediated adherence makes an essential contribution to the pathogenesis of Neisseria meningitidis by allowing the initial localized adherence. Pili are assembled from a protein subunit called pilin. Two proteins, PilC1 and PilC2, are also key elements in the formation of pili as the production of at least one PilC protein is required for pilus assembly. In addition, PilC1 but not PilC2 modulates adhesiveness, most probably by being the adhesin. Recently, both genes have been demonstrated to be controlled by different promoters, pilC2 is expressed from a single transcription starting point (TSP), whereas pilC1 has three TSPs. One of these, PC1.1, corresponds to the unique TSP of pilC2, and two others, PC1.2 and PC1.3, are located in a region upstream of pilC1 but not pilC2. This suggests that both genes may be under the control of separate regulatory pathways. In this work, by engineering pilC1-lacZ and pilC2-lacZ transcriptional fusions, we provide evidence that expression of pilC1, but not that of pilC2, is transiently induced by bacterial cell contact. This induction required viable cells, did not need the presence of pili and relied on the expression of pilC1 from PC1.3. Destruction of this TSP by site-directed mutagenesis did not significantly diminish the piliation level or the basal expression of PilC1, but led to the loss of cell contact-dependent upregulation of pilC1 and to a dramatic decrease in bacterial adhesiveness. Taken together, these data demonstrate that cell contact-dependent upregulation of the transcription of pilC1 at PC1.3 is essential for meningococcal pilus-mediated adhesion.

MeSH Terms
Artificial Gene Fusion Bacterial Adhesion Bacterial Proteins/biosynthesis,genetics Fimbriae Proteins Fimbriae, Bacterial/genetics,physiology Fluorescent Antibody Technique Gene Deletion Gene Expression Regulation, Bacterial Immunoblotting Lac Operon Microscopy, Confocal Mutagenesis, Site-Directed Neisseria meningitidis/genetics,growth & development,pathogenicity,physiology Promoter Regions, Genetic Transcription, Genetic Up-Regulation beta-Galactosidase/metabolism
Chemicals
Bacterial Proteins pilC protein, Neisseria gonorrhoeae Fimbriae Proteins beta-Galactosidase
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Taha M K
Unité des Neisseria, Institut Pasteur, Paris, France. [email protected]
Morand P C
Pereira Y
Eugène E
Giorgini D
Larribe M
Nassif X
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
1998-06-00
Pages
1153-63
Language
English
Region
England
NLM ID
8712028
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]