The obligate human pathogen, Neisseria gonorrhoeae, is polyploid.
We show using several methodologies that the Gram-negative, diplococcal-bacterium Neisseria gonorrhoeae has more than one complete genome copy per cell. Gene dosage measurements demonstrated that only a single replication initiation event per chromosome occurs per round of cell division, and that th...
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doaj-77e0e4fa8cee4803a27ddd1ac0bfabeb2021-07-02T16:27:19ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852006-06-0146e18510.1371/journal.pbio.0040185The obligate human pathogen, Neisseria gonorrhoeae, is polyploid.Deborah M TobiasonH Steven SeifertWe show using several methodologies that the Gram-negative, diplococcal-bacterium Neisseria gonorrhoeae has more than one complete genome copy per cell. Gene dosage measurements demonstrated that only a single replication initiation event per chromosome occurs per round of cell division, and that there is a single origin of replication. The region containing the origin does not encode any genes previously associated with bacterial origins of replication. Quantitative PCR results showed that there are on average three genome copies per coccal cell unit. These findings allow a model for gonococcal DNA replication and cell division to be proposed, in which a minimum of two chromosomal copies exist per coccal unit within a monococcal or diplococcal cell, and these chromosomes replicate in unison to produce four chromosomal copies during cell division. Immune evasion via antigenic variation is an important mechanism that allows these organisms to continually infect a high risk population of people. We propose that polyploidy may be necessary for the high frequency gene conversion system that mediates pilin antigenic variation and the propagation of N. gonorrhoeae within its human hosts.https://doi.org/10.1371/journal.pbio.0040185 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Deborah M Tobiason H Steven Seifert |
spellingShingle |
Deborah M Tobiason H Steven Seifert The obligate human pathogen, Neisseria gonorrhoeae, is polyploid. PLoS Biology |
author_facet |
Deborah M Tobiason H Steven Seifert |
author_sort |
Deborah M Tobiason |
title |
The obligate human pathogen, Neisseria gonorrhoeae, is polyploid. |
title_short |
The obligate human pathogen, Neisseria gonorrhoeae, is polyploid. |
title_full |
The obligate human pathogen, Neisseria gonorrhoeae, is polyploid. |
title_fullStr |
The obligate human pathogen, Neisseria gonorrhoeae, is polyploid. |
title_full_unstemmed |
The obligate human pathogen, Neisseria gonorrhoeae, is polyploid. |
title_sort |
obligate human pathogen, neisseria gonorrhoeae, is polyploid. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Biology |
issn |
1544-9173 1545-7885 |
publishDate |
2006-06-01 |
description |
We show using several methodologies that the Gram-negative, diplococcal-bacterium Neisseria gonorrhoeae has more than one complete genome copy per cell. Gene dosage measurements demonstrated that only a single replication initiation event per chromosome occurs per round of cell division, and that there is a single origin of replication. The region containing the origin does not encode any genes previously associated with bacterial origins of replication. Quantitative PCR results showed that there are on average three genome copies per coccal cell unit. These findings allow a model for gonococcal DNA replication and cell division to be proposed, in which a minimum of two chromosomal copies exist per coccal unit within a monococcal or diplococcal cell, and these chromosomes replicate in unison to produce four chromosomal copies during cell division. Immune evasion via antigenic variation is an important mechanism that allows these organisms to continually infect a high risk population of people. We propose that polyploidy may be necessary for the high frequency gene conversion system that mediates pilin antigenic variation and the propagation of N. gonorrhoeae within its human hosts. |
url |
https://doi.org/10.1371/journal.pbio.0040185 |
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