Evidence map›Paper›PMID 28548079›Full record

ArticleNature communications2017

Design of live attenuated bacterial vaccines based on D-glutamate auxotrophy.

Maria P Cabral, Patricia García, Alejandro Beceiro, Carlos Rumbo, Astrid Pérez, Miriam Moscoso, Germán Bou

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
6.5field-weighted citation impact, top 4% 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

50 citing papers in PubMed, 70 citations in OpenAlex.

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  6. Engineering low-endotoxin lipid A in a double auxotrophFrontiers in cellular and infection microbiology · 2026
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  8. MutantMicrobiology spectrum · 2025
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  11. International journal of molecular sciences · 2025
    Review
  12. Article
  13. LpxR and PagL expression in live attenuated auxotrophicFrontiers in cellular and infection microbiology · 2025
    Article
  14. Exploring current hypervirulentFrontiers in microbiology · 2025
    Review
  15. SuperbugCurrent topics in medicinal chemistry · 2025
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  16. Microbes Saving Lives and Reducing Suffering.Microbial biotechnology · 2025
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  17. Review
  18. Article
  19. Transient infection ofApplied and environmental microbiology · 2024
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  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

7 authors at 1 institution in 1 country.

Maria P CabralMicrobiology Department, University Hospital A Coruña (CHUAC)-Biomedical Research Institute A Coruña (INIBIC), 15006 A Coruña, Spain.ORCID 0000-0002-7119-440X
Patricia GarcíaMicrobiology Department, University Hospital A Coruña (CHUAC)-Biomedical Research Institute A Coruña (INIBIC), 15006 A Coruña, Spain.
Alejandro BeceiroMicrobiology Department, University Hospital A Coruña (CHUAC)-Biomedical Research Institute A Coruña (INIBIC), 15006 A Coruña, Spain.
Carlos RumboMicrobiology Department, University Hospital A Coruña (CHUAC)-Biomedical Research Institute A Coruña (INIBIC), 15006 A Coruña, Spain.
Astrid PérezMicrobiology Department, University Hospital A Coruña (CHUAC)-Biomedical Research Institute A Coruña (INIBIC), 15006 A Coruña, Spain.
Miriam MoscosoMicrobiology Department, University Hospital A Coruña (CHUAC)-Biomedical Research Institute A Coruña (INIBIC), 15006 A Coruña, Spain.
Germán BouMicrobiology Department, University Hospital A Coruña (CHUAC)-Biomedical Research Institute A Coruña (INIBIC), 15006 A Coruña, Spain.
Universidade da Coruña · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vaccine development is a priority for global health due to the growing multidrug resistance in bacteria. D-glutamate synthesis is essential for bacterial cell wall formation. Here we present a strategy for generating effective bacterial whole-cell vaccines auxotrophic for D-glutamate. We apply this strategy to generate D-glutamate auxotrophic vaccines for three major pathogens, Acinetobacter baumannii, Pseudomonas aeruginosa and Staphylococcus aureus. These bacterial vaccines show virulence attenuation and self-limited growth in mice, and elicit functional and cross-reactive antibodies, and cellular immunity. These responses correlate with protection against acute lethal infection with other strains of the same species, including multidrug resistant, virulent and/or high-risk clones such as A. baumannii AbH12O-A2 and Ab307-0294, P. aeruginosa PA14, and community-acquired methicillin-resistant S. aureus USA300LAC. This approach can potentially be applied for the development of live-attenuated vaccines for virtually any other bacterial pathogens, and does not require the identification of virulence determinants, which are often pathogen-specific.

Indexed as

AnimalsBacteriaBacterial InfectionsBacterial VaccinesDrug DesignDrug Resistance, Multiple, BacterialFemaleGlutamic AcidHumansImmunity, CellularImmunogenicity, VaccineMaleMiceMice, Inbred BALB CMice, Inbred C57BLSequence DeletionBacterial VaccinesGlutamic AcidVaccines, Attenuated

Identifiers

PMID28548079
PMCPMC5458566
OpenAlexW2616940204

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.