Evidence map›Paper›PMID 26527639›Full record

ArticleJournal of bacteriology2016

Glutamate Limitation, BvgAS Activation, and (p)ppGpp Regulate the Expression of the Bordetella pertussis Type 3 Secretion System.

Tomoko Hanawa, Kazunari Kamachi, Hideo Yonezawa, Toshiyuki Fukutomi, Hayato Kawakami, Shigeru Kamiya

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. BopN is a Gatekeeper of theMicrobiology spectrum · 2023
    Article
  7. Conquering the host:Frontiers in microbiology · 2022
    Review
  8. Review
  9. Omics Analysis of Blood-Responsive Regulon inInternational journal of molecular sciences · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Anti-FIM and Anti-FHA Antibodies InhibitFrontiers in immunology · 2020
    Article
  14. Frontiers in cellular and infection microbiology · 2020
    Review
  15. Comparative Integrated Omics Analysis of the Hfq Regulon inInternational journal of molecular sciences · 2019
    Article
  16. Article
  17. Article
  18. 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

6 authors at 2 institutions in 1 country.

Tomoko HanawaDepartment of Infectious Diseases, Kyorin University School of Medicine, Tokyo, Japan thanawa@ks.kyorin-u.ac.jp.
Kazunari KamachiDepartment of Bacteriology II, National Institute of Infectious Diseases, Tokyo, Japan.
Hideo YonezawaDepartment of Infectious Diseases, Kyorin University School of Medicine, Tokyo, Japan.
Toshiyuki FukutomiDepartment of Pharmacology, Kyorin University School of Medicine, Tokyo, Japan.
Hayato KawakamiDepartment of Anatomy, Kyorin University School of Medicine, Tokyo, Japan.
Shigeru KamiyaDepartment of Infectious Diseases, Kyorin University School of Medicine, Tokyo, Japan.
Kyorin University · JPNational Institute of Infectious Diseases · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledBordetella pertussis is a bacterium that is considered to be highly adapted to humans, and it has not been isolated from the environment. As this bacterium does not utilize sugars, the abundant supply of glutamate in Stainer Scholte (SS) medium enables B. pertussis to grow efficiently in liquid culture in vitro, and as such, SS medium is a popular choice for laboratory experiments. However, the concentration of glutamate in the in vivo niche of B. pertussis is quite low. We investigated the bacterial response to low concentrations of glutamate to elucidate bacterial physiology via the expression of the type 3 secretion system (T3SS), and we discuss its relationship to the Bvg mode in which the two-component regulator of pathogenesis (BvgAS) is activated. Glutamate limitation induced the expression of both the T3SS apparatus and effector genes at the transcriptional level. (p)ppGpp, a modulator of the stringent response, was necessary for maximum expression of the T3SS genes. These observations indicate that the expression of the T3SS is managed by nutrient starvation. In addition, the autoaggregation ability was high in the absence of glutamate and no autoaggregation was observed in glutamate-replete medium. Taken together, glutamate-limited conditions in Bvg(+) mode elicit the high expression of T3SS genes in B. pertussis and promotes its sessile form. IMPORTANCE: Bordetella pertussis is a highly contagious pathogen that causes respiratory infectious disease. In spite of the increasing use of vaccination, the number of patients with pertussis is increasing. The proteins produced in vivo often are different from the protein profile under laboratory conditions; therefore, the development of conditions reflecting the host environment is important to understand native bacterial behavior. In the present study, we examined the effect of glutamate limitation, as its concentration in vivo is much lower than that in the culture medium currently used for B. pertussis experiments. As predicted, the T3SS was induced by glutamate limitation. These results are suggestive of the importance of regulation by nutrient conditions and in the pathogenicity of B. pertussis.

Indexed as

Bacterial ProteinsBordetella pertussisGene Expression Regulation, BacterialGlutamic AcidGuanosine PentaphosphateType III Secretion SystemsBacterial ProteinsGlutamic AcidGuanosine PentaphosphateType III Secretion Systems

Identifiers

PMID26527639
PMCPMC4751785
OpenAlexW2276715996

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.