Previous Article | Next Article ![]()
Journal of Bacteriology, January 2000, p. 171-178, Vol. 182, No. 1
Laboratory of Microbial Structure and
Function, Rocky Mountain Laboratories, National Institute of Allergy
and Infectious Diseases, National Institutes of Health, Hamilton,
Montana 59840, and Department of Biological Sciences, Northern Illinois
University, DeKalb, Illinois 60115
Received 1 September 1999/Accepted 15 October 1999
Neisseria gonorrhoeae is naturally competent for DNA
transformation. Under most conditions encountered in vivo, gonococci express one or more opacity (Opa) proteins on their surfaces. Recently,
it was shown that DNA preferentially binds to the surfaces of
Opa-expressing organisms compared to those of isogenic Opa-negative strains, presumably due to the numerous cationic residues in the predicted surface-exposed loops of the Opa protein. This study examined
whether Opa-DNA interactions actually influence DNA transformation of
the gonococcus. The data show that Opa-expressing gonococci are more
efficient recipients of DNA for transformation and are more susceptible
to exogenous DNase I treatment at early stages during the DNA
transformation process than non-Opa expressors. Furthermore, inhibition
of the transformation process was demonstrable for Opa+
populations when either nonspecific DNA or the polyanion heparin was
used. Overall, the data suggest that Opa expression, with its
presumptive positive surface charge contribution, promotes DNA
transformation by causing a more prolonged sequestration of donor DNA
at the cell surface, which translates into more efficient transformation over time.
0021-9193/0/$04.00+0
Opa Expression Correlates with Elevated
Transformation Rates in Neisseria gonorrhoeae
*
Mailing address: Department of Biological Sciences,
Northern Illinois University, DeKalb, IL 60115. Phone: (815)
753-7943. Fax: (815) 753-7855. E-mail: sahill{at}niu.edu.
This article has been cited by other articles:
| Appl. Environ. Microbiol. | Infect. Immun. | Eukaryot. Cell |
|---|---|---|
| Mol. Cell. Biol. | J. Virol. | Microbiol. Mol. Biol. Rev. |
| ALL ASM JOURNALS |