Evidence map›Paper›PMID 35806198›Full record

ArticleInternational journal of molecular sciences2022

The Inhibition of DNA Viruses by the Amphibian Antimicrobial Peptide Temporin G: A Virological Study Addressing HSV-1 and JPCyV.

Maria Elena Marcocci, Bianka Gabriela Jackowska, Carla Prezioso, Virginia Protto, Marta De Angelis, Francesco Saverio Di Leva, Bruno Casciaro, Alfonso Carotenuto, Maria Luisa Mangoni, Anna Teresa Palamara and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Temporins: Multifunctional Peptides from Frog Skin.International journal of molecular sciences · 2023
    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

13 authors at 5 institutions in 1 country.

Maria Elena MarcocciDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, 00185 Rome, Italy.ORCID 0000-0003-4751-4263
Bianka Gabriela JackowskaDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, 00185 Rome, Italy.ORCID 0000-0002-4416-8847
Carla PreziosoDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, 00185 Rome, Italy.ORCID 0000-0002-8377-0742
Virginia ProttoDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, 00185 Rome, Italy.
Marta De AngelisDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, 00185 Rome, Italy.ORCID 0000-0002-1916-6508
Francesco Saverio Di LevaDepartment of Pharmacy, University of Naples "Federico II", 80131 Naples, Italy.
Bruno CasciaroDepartment of Biochemical Sciences, The Istituto Pasteur-Fondazione Cenci Bolognetti, Sapienza University of Rome, 00185 Rome, Italy.ORCID 0000-0003-1295-1084
Alfonso CarotenutoDepartment of Pharmacy, University of Naples "Federico II", 80131 Naples, Italy.ORCID 0000-0001-7532-5449
Maria Luisa MangoniDepartment of Biochemical Sciences, The Istituto Pasteur-Fondazione Cenci Bolognetti, Sapienza University of Rome, 00185 Rome, Italy.ORCID 0000-0002-5991-5868
Anna Teresa PalamaraDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, 00185 Rome, Italy.ORCID 0000-0001-8330-4381
Valeria PietropaoloDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, 00185 Rome, Italy.ORCID 0000-0001-5723-8886
Giovanna De ChiaraInstitute of Translational Pharmacology, National Research Council (CNR), 00133 Rome, Italy.ORCID 0000-0002-2219-6097
Lucia NencioniDepartment of Public Health and Infectious Diseases, Sapienza University of Rome, Laboratory Affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, 00185 Rome, Italy.ORCID 0000-0003-4427-4823
Istituto Pasteur · ITUniversity of Naples Federico II · ITIstituto di Farmacologia Traslazionale · ITIstituto Superiore di Sanità · ITVita-Salute San Raffaele University · IT

Funding

Istituto Pasteur Fondazione Cenci Bolognetti grant Anna Tramontano2018Ministry of Education, Universities and Research FOE2020Ministry of Education, Universities and Research PRIN#20179JHAMZ_006Ministry of Education, Universities and Research PRIN#2017BMK8JR006Sapienza University of Rome RM11916B6A28725CSapienza University of Rome RM120172B6D0AD25
6 · The paper itself

Abstract

Herpes simplex virus type-1 (HSV-1) and John Cunningham polyomavirus (JCPyV) are widely distributed DNA viruses causing mainly asymptomatic infection, but also mild to very severe diseases, especially when these viruses reach the brain. Some drugs have been developed to inhibit HSV-1 replication in host cells, but their prolonged use may induce resistance phenomena. In contrast, to date, there is no cure for JCPyV. The search for alternative drugs that can reduce viral infections without undermining the host cell is moving toward antimicrobial peptides (AMPs) of natural occurrence. These include amphibian AMPs belonging to the temporin family. Herein, we focus on temporin G (TG), showing that it strongly affects HSV-1 replication by acting either during the earliest stages of its life cycle or directly on the virion. Computational studies have revealed the ability of TG to interact with HSV-1 glycoprotein B. We also found that TG reduced JCPyV infection, probably affecting both the earliest phases of its life cycle and the viral particle, likely through an interaction with the viral capsid protein VP1. Overall, our results are promising for the development of short naturally occurring peptides as antiviral agents used to counteract diseases related to HSV-1 and JCPyV.

Indexed as

Herpesvirus 1, HumanAmphibiansAnimalsAntimicrobial Cationic PeptidesAntimicrobial PeptidesVirus ReplicationAntimicrobial Cationic PeptidesAntimicrobial Peptidestemporinantimicrobial peptidesantiviral agentsHSV-1JCPvVtemporins

Identifiers

PMID35806198
PMCPMC9266403
OpenAlexW4283700105

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.