Evidence map›Paper›PMID 31344395›Full record

ArticleFitoterapia2019

Vochysiamides A and B: Two new bioactive carboxamides produced by the new species Diaporthe vochysiae.

Sandriele Aparecida Noriler, Daiani Cristina Savi, Larissa V Ponomareva, Renata Rodrigues, Jürgen Rohr, Jon S Thorson, Chirlei Glienke, Khaled A Shaaban

Abstract read
In one paragraph

Article in Fitoterapia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Article
  2. Article
  3. EndophyticFungal systematics and evolution · 2024
    Article
  4. Studies in mycology · 2024
    Article
  5. Genomic and Untargeted Metabolomic Analysis of Secondary Metabolites in theJournal of agricultural and food chemistry · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Potential of Secondary Metabolites ofJournal of fungi (Basel, Switzerland) · 2023
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Fungal Endophytes: A Potential Source of Antibacterial Compounds.Journal of fungi (Basel, Switzerland) · 2022
    Review
  16. Article
  17. Review
  18. Potential of EndophyticJournal of microbiology and biotechnology · 2021
    Review
  19. Article
  20. Review
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

8 authors.

Sandriele Aparecida NorilerDepartment of Pathology, Universidade Federal do Parana, Av. Coronel Francisco Heráclito dos Santos, 210, CEP: 81531-970 Curitiba, PR, Brazil.
Daiani Cristina SaviDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, United States; Department of Genetics, Universidade Federal do Parana, Av. Coronel Francisco Heráclito dos Santos, 210, CEP: 81531-970 Curitiba, PR, Brazil.
Larissa V PonomarevaDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, United States; Center for Pharmaceutical Research and Innovation, College of Pharmacy, University of Kentucky, KY 40536, United States.
Renata RodriguesDepartment of Pathology, Universidade Federal do Parana, Av. Coronel Francisco Heráclito dos Santos, 210, CEP: 81531-970 Curitiba, PR, Brazil.
Jürgen RohrDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, United States.
Jon S ThorsonDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, United States; Center for Pharmaceutical Research and Innovation, College of Pharmacy, University of Kentucky, KY 40536, United States.
Chirlei GlienkeDepartment of Genetics, Universidade Federal do Parana, Av. Coronel Francisco Heráclito dos Santos, 210, CEP: 81531-970 Curitiba, PR, Brazil. Electronic address: ch.glienke@gmail.com.
Khaled A ShaabanDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, United States; Center for Pharmaceutical Research and Innovation, College of Pharmacy, University of Kentucky, KY 40536, United States. Electronic address: khaled_shaaban@uky.edu.

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
Kentucky Center for Clinical and Translational ScienceUL1TR000117 · NCATS · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2012 to 2015
$13.3M
NOVEL AUREOLIC ACID TYPE ANTITUMOR AGENTSR01CA091901 · NCI · UNIVERSITY OF KENTUCKY · PI ROHR, JURGEN T · 2001 to 2017
$3.6M
Developing Regeneration Resources for a Model AmphibianR24OD021479 · OD · UNIVERSITY OF KENTUCKY · PI THORSON, JON SCOTT, VOSS, STEPHEN RANDAL · 2016 to 2019
$2.3M
Exploring Post-Type II PKS Frame ModificationsR01GM105977 · NIGMS · UNIVERSITY OF KENTUCKY · PI ROHR, JURGEN T · 2014 to 2017
$1.1M
NCATS NIH HHS UL1 TR000117NCATS NIH HHS UL1 TR001998NCI NIH HHS R01 CA091901NIGMS NIH HHS R01 GM105977NIH HHS R24 OD021479
6 · The paper itself

Abstract

Endophytic fungi have been considered a rich source for bioactive secondary metabolites with novel chemical structures. A high diverse group of endophytes, isolated from different medicinal plants, belongs to the genus Diaporthe. In a previously study performed by our group the crude extract of strain LGMF1583 showed considerable antibacterial activity mainly against Gram-negative bacteria. Based on ITS phylogeny analysis, strain LGMF1583 was identified as belonging to Diaporthe genus and may represent a new species. In the present study, we described the new species Diporthe vochysiae based on multilocus phylogeny analysis and morphological characteristics. The species name refers to the host, from which strain LGMF1583 was isolated, the medicinal plant Vochysia divergens. In view of the biotechnological potential of strain LGMF1583, we have also characterized the secondary metabolites produced by D. vochysiae. Chemical assessment of the D. vochysiae LGMF1583 revealed two new carboxamides, vochysiamides A (1) and B (2), in addition to the known metabolite, 2,5-dihydroxybenzyl alcohol (3). In the biological activity analysis, vochysiamide B (2) displayed considerable antibacterial activity against the Gram-negative bacterium Klebsiella pneumoniae (KPC), a producer of carbapenemases, MIC of 80 μg/mL. Carbapenemases are considered a major antimicrobial resistance threat, and infections caused by KPC have been considered a public health problem worldwide, and new compounds with activity against this bacterium are nowadays even more required.

Indexed as

AmidesAnti-Bacterial AgentsAscomycotaBrazilCell Line, TumorEndophytesHumansKlebsiella pneumoniaeMolecular StructureMyrtalesPhylogenyPlants, MedicinalAmidesAnti-Bacterial AgentsCarbapenemasesDiaporthe genusMedicinal plantsSecondary metabolitesVochysia divergens

Identifiers

PMID31344395
PMCPMC7015639

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Registered trials

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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.