Evidence map›Paper›PMID 20562302›Full record

ArticleJournal of bacteriology2010

Cyclic di-GMP signaling regulates invasion by Ehrlichia chaffeensis of human monocytes.

Yumi Kumagai, Junji Matsuo, Yoshihiro Hayakawa, Yasuko Rikihisa

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

43 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Article
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  6. Moonlighting in Rickettsiales: Expanding Virulence Landscape.Tropical medicine and infectious disease · 2022
    Review
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  13. Review
  14. Review
  15. Frontiers in cellular and infection microbiology · 2017
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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 2 countries.

Yumi KumagaiDepartment of Veterinary Biosciences, The Ohio State University, Columbus, OH 43210, USA.
Junji Matsuo
Yoshihiro Hayakawa
Yasuko Rikihisa
The Ohio State University · USAichi Institute of Technology · JP

Funding

TYPE IV SECRETION &SIGNAL TRANSDUCTION IN EHRLICHIOSISR01AI054476 · NIAID · OHIO STATE UNIVERSITY · PI RIKIHISA, YASUKO · 2004 to 2013
$3.8M
NIAID NIH HHS R01 AI054476
6 · The paper itself

Abstract

Cyclic di-GMP (c-di-GMP) is a bacterial second messenger produced by GGDEF domain-containing proteins. The genome of Ehrlichia chaffeensis, an obligatory intracellular bacterium that causes human monocytic ehrlichiosis, encodes a single protein that contains a GGDEF domain, called PleD. In this study, we investigated the effects of c-di-GMP signaling on E. chaffeensis infection of the human monocytic cell line THP-1. Recombinant E. chaffeensis PleD showed diguanylate cyclase activity as it generated c-di-GMP in vitro. Because c-di-GMP is not cell permeable, the c-di-GMP hydrophobic analog 2'-O-di(tert-butyldimethylsilyl)-c-di-GMP (CDGA) was used to examine intracellular c-di-GMP signaling. CDGA activity was first tested with Salmonella enterica serovar Typhimurium. CDGA inhibited well-defined c-di-GMP-regulated phenomena, including cellulose synthesis, clumping, and upregulation of csgD and adrA mRNA, indicating that CDGA acts as an antagonist in c-di-GMP signaling. [(32)P]c-di-GMP bound several E. chaffeensis native proteins and two E. chaffeensis recombinant I-site proteins, and this binding was blocked by CDGA. Although pretreatment of E. chaffeensis with CDGA did not reduce bacterial binding to THP-1 cells, bacterial internalization was reduced. CDGA facilitated protease-dependent degradation of particular, but not all, bacterial surface-exposed proteins, including TRP120, which is associated with bacterial internalization. Indeed, the serine protease HtrA was detected on the surface of E. chaffeensis, and TRP120 was degraded by treatment of E. chaffeensis with recombinant E. chaffeensis HtrA. Furthermore, anti-HtrA inhibited CDGA-induced TRP120 degradation. Our results suggest that E. chaffeensis invasion is regulated by c-di-GMP signaling, which stabilizes some bacterial surface-exposed proteins against proteases.

Indexed as

Bacterial AdhesionGene Expression Regulation, BacterialSignal TransductionBacterial ProteinsCell LineCelluloseCyclic GMPEhrlichia chaffeensisEscherichia coli ProteinsGene Expression ProfilingHumansMembrane ProteinsMonocytesPhosphorus-Oxygen LyasesRNA, BacterialRNA, MessengerBacterial Proteinsbis(3',5')-cyclic diguanylic acidCelluloseCyclic GMPdiguanylate cyclaseEscherichia coli ProteinsMembrane ProteinsPhosphorus-Oxygen LyasesRNA, BacterialRNA, MessengerTrans-Activators

Identifiers

PMID20562302
PMCPMC2916414
OpenAlexW2111908646

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.