Evidence map›Paper›PMID 26574512›Full record

ArticleJournal of bacteriology2015

The Gonococcal NlpD Protein Facilitates Cell Separation by Activating Peptidoglycan Cleavage by AmiC.

Elizabeth A Stohl, Jonathan D Lenz, Joseph P Dillard, H Steven Seifert

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. CRISPRi-mediated repression of threeJournal of bacteriology · 2025
    Article
  4. Article
  5. Article
  6. Mutation ofJournal of bacteriology · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Global Proteomic Analysis ofFoods (Basel, Switzerland) · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Infection and immunity · 2019
    Article
  17. Antibiotic Targets in Gonococcal Cell Wall Metabolism.Antibiotics (Basel, Switzerland) · 2018
    Review
  18. Review
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Elizabeth A StohlNorthwestern University Feinberg School of Medicine, Department of Microbiology-Immunology, Chicago, Illinois, USA.
Jonathan D LenzUniversity of Wisconsin-Madison, Department of Medical Microbiology & Immunology, Madison, Wisconsin, USA.
Joseph P DillardUniversity of Wisconsin-Madison, Department of Medical Microbiology & Immunology, Madison, Wisconsin, USA.
H Steven SeifertNorthwestern University Feinberg School of Medicine, Department of Microbiology-Immunology, Chicago, Illinois, USA h-seifert@northwestern.edu.ORCID http://orcid.org/0000-0001-8651-0375
Northwestern University · USUniversity of Wisconsin–Madison · US

Funding

Mechanisms of Gonococcal Pilin Antigenic/Phase VariationR37AI033493 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Hank S. SEIFERT · 2003 to 2026
$10.1M
Peptidoglycan metabolism and fragment releaseR01AI097157 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI DILLARD, JOSEPH P · 2012 to 2022
$5.6M
Microbial Pathogenesis &Host Responses Training ProgramT32AI055397 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI KLEIN, BRUCE STEVEN · 2003 to 2024
$5.5M
Molecular Genetics of the GonococcusR01AI044239 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SEIFERT, HANK S. · 1999 to 2014
$4.0M
Cell separation in Neisseria gonorrhoeaeR21AI099539 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI DILLARD, JOSEPH P · 2012 to 2013
$414k
Interaction in vivo between HIV and Hepatitis B VirusR21AI055379 · NIAID · MACFARLANE BURNET INST FOR RES/PUB HLTH · PI LEWIN, SHARON RUTH · 2004 to 2005
$324k
Assembly and Function of the Gonococcal PilusR56AI114821 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SEIFERT, HANK S. · 2015 to 2015
$309k
Outer membrane vesicles and peptidoglycan of Neisseria gonorrhoeaeF32AI115911 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI LENZ, JONATHAN DAVID · 2015 to 2016
$112k
NIAID NIH HHS F32 AI115911NIAID NIH HHS R01 AI044239NIAID NIH HHS R01-AI044239NIAID NIH HHS R01 AI097157NIAID NIH HHS R01-AI097157NIAID NIH HHS R21 AI055379NIAID NIH HHS R21 AI099539NIAID NIH HHS R21-AI099539NIAID NIH HHS R37 AI033493NIAID NIH HHS R37-AI033493NIAID NIH HHS R56 AI114821NIAID NIH HHS T32-AI055379NIAID NIH HHS T32 AI055397
6 · The paper itself

Abstract

unlabelledKey steps in bacterial cell division are the synthesis and subsequent hydrolysis of septal peptidoglycan (PG), which allow efficient separation of daughter cells. Extensive studies in the Gram-negative, rod-shaped bacterium Escherichia coli have revealed that this hydrolysis is highly regulated spatially and temporally. Neisseria gonorrhoeae is an obligate Gram-negative, diplococcal pathogen and is the only causative agent of the sexually transmitted infection gonorrhea. We investigated how cell separation proceeds in this diplococcal organism. We demonstrated that deletion of the nlpD gene in strain FA1090 leads to poor growth and to an altered colony and cell morphology. An isopropyl-beta-d-galactopyranoside (IPTG)-regulated nlpD complemented construct can restore these defects only when IPTG is supplied in the growth medium. Thin-section transmission electron microscopy (TEM) revealed that the nlpD mutant strain grew in large clumps containing live and dead bacteria, which was consistent with deficient cell separation. Biochemical analyses of purified NlpD protein showed that it was able to bind purified PG. Finally, we showed that, although NlpD has no hydrolase activity itself, NlpD potentiates the hydrolytic activity of AmiC. These results indicate that N. gonorrhoeae NlpD is required for proper cell growth and division through its interactions with the amidase AmiC. IMPORTANCE: N. gonorrhoeae is the sole causative agent of the sexually transmitted infection gonorrhea. The incidence of antibiotic-resistant gonococcal infections has risen sharply in recent years, and N. gonorrhoeae has been classified as a "superbug" by the CDC. Since there is a dearth of new antibiotics to combat gonococcal infections, elucidating the essential cellular process of N. gonorrhoeae may point to new targets for antimicrobial therapies. Cell division and separation is one such essential process. We identified and characterized the gonococcal nlpD gene and showed that it is essential for cell separation. In contrast to other pathogenic bacteria, the gonococcal system is streamlined and does not appear to have any redundancies.

Indexed as

AmidohydrolasesBacterial ProteinsCell DivisionMetalloproteasesNeisseria gonorrhoeaePeptidoglycanProtein BindingAmidohydrolasesBacterial ProteinsMetalloproteasesPeptidoglycan

Identifiers

PMID26574512
PMCPMC4751805
OpenAlexW2226518036

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.