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Pilus- gonococcal variants. Evidence for multiple forms of piliation control
Pilus+ to pilus- transitions of gonococci (Gc) that involve rearrangement of pilin gene DNA yield the P-n phenotype, which is incapable of reversion (to pilus+). Reversion to pilus+ is found for nonpiliated Gc that have undergone no apparent pilin gene rearrangement. Among the reverting, nonpiliated...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1985
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187738/ https://www.ncbi.nlm.nih.gov/pubmed/2410533 |
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collection | PubMed |
description | Pilus+ to pilus- transitions of gonococci (Gc) that involve rearrangement of pilin gene DNA yield the P-n phenotype, which is incapable of reversion (to pilus+). Reversion to pilus+ is found for nonpiliated Gc that have undergone no apparent pilin gene rearrangement. Among the reverting, nonpiliated Gc, two distinct phenotypes (P-rp- and P-rp+) occur and are differentiated according to their synthesis (or lack) of pilin subunits; both P-rp- and P-rp+ Gc contain pilin-specific mRNA. The occurrence of these different pilus- phenotypes strongly suggests that several mechanisms can account for changes in the piliation status of Gc; one of these involves pilin gene rearrangement but the others apparently operate at posttranscriptional levels. Reverting pilus- Gc may have a pathogenic advantage in being able to reversibly alter their host cell adherence-promoting surface properties through high frequency transitions in piliation status. |
format | Text |
id | pubmed-2187738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1985 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21877382008-04-17 Pilus- gonococcal variants. Evidence for multiple forms of piliation control J Exp Med Articles Pilus+ to pilus- transitions of gonococci (Gc) that involve rearrangement of pilin gene DNA yield the P-n phenotype, which is incapable of reversion (to pilus+). Reversion to pilus+ is found for nonpiliated Gc that have undergone no apparent pilin gene rearrangement. Among the reverting, nonpiliated Gc, two distinct phenotypes (P-rp- and P-rp+) occur and are differentiated according to their synthesis (or lack) of pilin subunits; both P-rp- and P-rp+ Gc contain pilin-specific mRNA. The occurrence of these different pilus- phenotypes strongly suggests that several mechanisms can account for changes in the piliation status of Gc; one of these involves pilin gene rearrangement but the others apparently operate at posttranscriptional levels. Reverting pilus- Gc may have a pathogenic advantage in being able to reversibly alter their host cell adherence-promoting surface properties through high frequency transitions in piliation status. The Rockefeller University Press 1985-08-01 /pmc/articles/PMC2187738/ /pubmed/2410533 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Pilus- gonococcal variants. Evidence for multiple forms of piliation control |
title | Pilus- gonococcal variants. Evidence for multiple forms of piliation control |
title_full | Pilus- gonococcal variants. Evidence for multiple forms of piliation control |
title_fullStr | Pilus- gonococcal variants. Evidence for multiple forms of piliation control |
title_full_unstemmed | Pilus- gonococcal variants. Evidence for multiple forms of piliation control |
title_short | Pilus- gonococcal variants. Evidence for multiple forms of piliation control |
title_sort | pilus- gonococcal variants. evidence for multiple forms of piliation control |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187738/ https://www.ncbi.nlm.nih.gov/pubmed/2410533 |