The adhesin related 30-kDa protein of Mycoplasma pneumoniae exhibits size and antigen variability
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Updated: Oct 13, 2026

Biomimetic Materials to Characterize Bacteria-host Interactions
Published on: November 16, 2015
G Layh-Schmitt1, R Himmelreich, U Leibfried
1Zentrum für Molekulare Biologie Heidelberg, Universität Heidelberg, Germany.
Abstract:
Mycoplasma pneumoniae is a pathogenic bacterium colonizing epithelial cells of the human respirator tract. Using an erythrocyte binding assay we isolated a cytadsorption negative mutant designated M7 which has lost 12 of a total of 13 repetitive sequences of a proline rich C-terminal region of the adhesin related 30-kDa protein. The truncated adhesin related protein of 22 kDa showed reduced antigenicity compared to the corresponding wild-type protein. Moreover, the mutant M7 proved incapable of adhering to erythrocytes and to a human colon carcinoma cell line indicating that the repetitive C-terminal region of the 30-kDa protein is essential for effective cytadherence. The adhesin related 30-kDa protein as well as the truncated forms of the corresponding protein were accessible to carboxypeptidase Y which clearly shows surface exposure of the C-terminus of this protein.
Insights
Mycoplasma pneumoniae uses a proline-rich C-terminal region of its 30-kDa adhesin protein for cell attachment. Deleting repetitive sequences in this region prevents bacterial adherence, highlighting its importance for cytadherence.
Area of Science:
- Microbiology
- Cell Biology
- Molecular Biology
Background:
- Mycoplasma pneumoniae is a significant human respiratory pathogen.
- Bacterial adhesins are crucial for host cell colonization.
- The adhesin related 30-kDa protein of M. pneumoniae mediates cytadherence.
Purpose of the Study:
- To investigate the role of the repetitive C-terminal region of the 30-kDa adhesin protein in Mycoplasma pneumoniae cytadherence.
- To characterize a mutant with deletions in this repetitive region.
Main Methods:
- Isolation and characterization of a Mycoplasma pneumoniae mutant (M7) using an erythrocyte binding assay.
- Analysis of the adhesin related protein in the wild-type and mutant strains.
- Assessment of cytadherence to erythrocytes and a human colon carcinoma cell line.
Main Results:
- Mutant M7 lost 12 of 13 repetitive sequences in the C-terminal region of the 30-kDa adhesin protein, resulting in a truncated 22-kDa protein.
- The truncated protein exhibited reduced antigenicity.
- Mutant M7 was incapable of adhering to erythrocytes and a human colon carcinoma cell line.
- Carboxypeptidase Y accessibility confirmed surface exposure of the C-terminus.
Conclusions:
- The repetitive C-terminal region of the 30-kDa adhesin related protein is essential for Mycoplasma pneumoniae cytadherence.
- Truncation of this region significantly impairs bacterial adhesion to host cells.
- The C-terminus of the adhesin protein is surface-exposed and critical for its function.
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