Evidence map›Paper›PMID 35629400›Full record

ArticleLife (Basel, Switzerland)2022

Antimicrobial Properties of Compounds Isolated from

Camille Quenon, Thierry Hennebelle, Jean-François Butaud, Raimana Ho, Jennifer Samaillie, Christel Neut, Tamatoa Lehartel, Céline Rivière, Ali Siah, Natacha Bonneau and 5 more

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Kaempferol: A Review of Current Evidence of Its Antiviral Potential.International journal of molecular sciences · 2023
    Review
  6. Review
  7. Medicinal Values and Potential Risks Evaluation ofMolecules (Basel, Switzerland) · 2022
    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

15 authors at 3 institutions in 2 countries.

Camille QuenonUMRT 1158 BioEcoAgro, Métabolites spécialisés d'origine végétale, Université de Lille, JUNIA, Université de Liège, Université de Picardie Jules Verne, 59006 Lille, France.
Thierry HennebelleUMRT 1158 BioEcoAgro, Métabolites spécialisés d'origine végétale, Université de Lille, JUNIA, Université de Liège, Université de Picardie Jules Verne, 59006 Lille, France.
Jean-François ButaudConsultant in Forestry and Polynesian Botany, BP 52832, 98716 Pirae, Tahiti, French Polynesia.
Raimana HoEIO, UMR 241, Université de la Polynésie Française, BP 6570, 98702 Faa'a, Tahiti, French Polynesia.
Jennifer SamaillieUMRT 1158 BioEcoAgro, Métabolites spécialisés d'origine végétale, Université de Lille, JUNIA, Université de Liège, Université de Picardie Jules Verne, 59006 Lille, France.
Christel NeutInserm U1286, Laboratoire de Bactériologie, CHU Lille, Faculté des Sciences Pharmaceutiques et Biologiques, Université Lille Nord de France, 59006 Lille, France.ORCID 0000-0002-2036-6152
Tamatoa LehartelEIO, UMR 241, Université de la Polynésie Française, BP 6570, 98702 Faa'a, Tahiti, French Polynesia.
Céline RivièreUMRT 1158 BioEcoAgro, Métabolites spécialisés d'origine végétale, Université de Lille, JUNIA, Université de Liège, Université de Picardie Jules Verne, 59006 Lille, France.ORCID 0000-0002-8618-5530
Ali SiahUMRT 1158 BioEcoAgro, Métabolites spécialisés d'origine végétale, Université de Lille, JUNIA, Université de Liège, Université de Picardie Jules Verne, 59006 Lille, France.
Natacha BonneauUMRT 1158 BioEcoAgro, Métabolites spécialisés d'origine végétale, Université de Lille, JUNIA, Université de Liège, Université de Picardie Jules Verne, 59006 Lille, France.
Sevser SahpazUMRT 1158 BioEcoAgro, Métabolites spécialisés d'origine végétale, Université de Lille, JUNIA, Université de Liège, Université de Picardie Jules Verne, 59006 Lille, France.
Sébastien AnthérieuUMR-S1172, Neuroscience & Cognition INSERM, Faculté des Sciences Pharmaceutiques et Biologiques, Université Lille Nord de France, CEDEX, 59006 Lille, France.
Nicolas LebegueULR 4483-IMPECS-IMPact de l'Environnement Chimique sur la Santé humaine, CHU Lille, Institut Pasteur de Lille, Université de Lille, 59006 Lille, France.ORCID 0000-0003-4245-2833
Phila RaharivelomananaEIO, UMR 241, Université de la Polynésie Française, BP 6570, 98702 Faa'a, Tahiti, French Polynesia.
Vincent RoumyUMRT 1158 BioEcoAgro, Métabolites spécialisés d'origine végétale, Université de Lille, JUNIA, Université de Liège, Université de Picardie Jules Verne, 59006 Lille, France.
Université de Lille · FRUniversity of French Polynesia · PFInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A preliminary ethnopharmacological survey, achieved in French Polynesia, led to the collection of the most cited plants among 63 species used to treat “infectious” diseases, with a description of their medicinal uses. Bibliographical investigations and antimicrobial screening permitted the selection of the botanical species Syzygium malaccense (Myrtaceae) for phytochemical analysis. Leaves of Syzygium malaccense were usually used in mixture with rhizomes of Curcuma longa to treat infectious diseases such as cystitis. The methanolic plant extracts were tested in vitro with an agar microdilution method on 33 bacteria strains and 1 yeast to obtain their Minimal Inhibitory Concentration (MIC), and cytotoxicity against HepG2 cells were evaluated. Antimicrobial synergistic effects of methanolic plant extracts from leaves of Syzygium malaccense and rhizomes from Curcuma longa were also evaluated. The bio-guided isolation of leaf extract from Syzygium malaccense led to the identification of seven alkyl-salicylic acids (anacardic acids or ginkgolic acids C15:0, C15:1, C17:0, C17:1, C17:2, C17:3 and C19:1) described for the first time in this species. All compounds were tested against Staphylococcus aureus (18.75 < MIC < 75.0 µg/mL), Streptococcus pyogenes (2.34 < MIC < 18.75 µg/mL) and Pseudomonas aeruginosa (MIC = 150 µg/mL), and their structure−activity relationships were discussed. The methanolic extract and salicylic derivatives from S. malaccense showed an interesting antimicrobial activity against Gram+ bacteria, without toxicity on hepG2 cells at 400 μg/mL. Moreover, these antibacterial compounds have already been studied for their anti-inflammatory activity, which supports the therapeutic interest of S. malaccense against infectious diseases.

Indexed as

antimicrobialphytochemicalsalicylic compoundsSociety IslandsSyzygium malaccensetraditional medicine

Identifiers

PMID35629400
PMCPMC9147835
OpenAlexW4280582249

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.