Evidence map›Paper›PMID 26643323›Full record

ArticleAntimicrobial agents and chemotherapy2016

The Cholestanol-Conjugated Sulfated Oligosaccharide PG545 Disrupts the Lipid Envelope of Herpes Simplex Virus Particles.

Joanna S Said, Edward Trybala, Staffan Görander, Maria Ekblad, Jan-Åke Liljeqvist, Eva Jennische, Stefan Lange, Tomas Bergström

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. ModifiedJournal of natural products · 2022
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Prophylactic Antiheparanase Activity by PG545 Is AntiviralAntimicrobial agents and chemotherapy · 2018
    Article
  13. Targeting heparin and heparan sulfate protein interactions.Organic & biomolecular chemistry · 2017
    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 at 1 institution in 1 country.

Joanna S SaidDepartment of Infectious Diseases, Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden said@microbio.gu.se tomas.bergstrom@microbio.gu.se.
Edward TrybalaDepartment of Infectious Diseases, Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden.
Staffan GöranderDepartment of Infectious Diseases, Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden.
Maria EkbladDepartment of Infectious Diseases, Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden.
Jan-Åke LiljeqvistDepartment of Infectious Diseases, Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden.
Eva JennischeDepartment of Medical Biochemistry and Cell Biology, Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden.
Stefan LangeDepartment of Infectious Diseases, Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden.
Tomas BergströmDepartment of Infectious Diseases, Institute of Biomedicine, University of Gothenburg, Göteborg, Sweden said@microbio.gu.se tomas.bergstrom@microbio.gu.se.
University of Gothenburg · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herpes simplex virus (HSV) and many other viruses, including HIV, initiate infection of host cells by binding to glycosaminoglycan (GAG) chains of cell surface proteoglycans. Although GAG mimetics, such as sulfated oligo- and polysaccharides, exhibit potent antiviral activities in cultured cells, the prophylactic application of these inhibitors as vaginal microbicides failed to protect women upon their exposure to HIV. A possible explanation for this failure is that sulfated oligo- and polysaccharides exhibit no typical virucidal activity, as their interaction with viral particles is largely electrostatic and reversible and thereby vulnerable to competition with GAG-binding proteins of the genital tract. Here we report that the cholestanol-conjugated sulfated oligosaccharide PG545, but not several other sulfated oligosaccharides lacking this modification, exhibited virucidal activity manifested as disruption of the lipid envelope of HSV-2 particles. The significance of the virus particle-disrupting activity of PG545 was also demonstrated in experimental animals, as this compound, in contrast to unmodified sulfated oligosaccharide, protected mice against genital infection with HSV-2. Thus, PG545 offers a novel prophylaxis option against infections caused by GAG-binding viruses.

Indexed as

Administration, IntravaginalAnimalsAntiviral AgentsDisease Models, AnimalFemaleHerpes GenitalisHerpesvirus 2, HumanLipidsMice, Inbred C57BLOligosaccharidesSaponinsVirionAntiviral AgentsLipidsOligosaccharidesPG 545phosphomannopentaose sulfateSaponins

Identifiers

PMID26643323
PMCPMC4750709
OpenAlexW2190711022

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.