Evidence map›Paper›PMID 27353268›Full record

ArticleAntimicrobial agents and chemotherapy2016

Macrolones Are a Novel Class of Macrolide Antibiotics Active against Key Resistant Respiratory Pathogens In Vitro and In Vivo.

Hana Čipčić Paljetak, Donatella Verbanac, Jasna Padovan, Miroslava Dominis-Kramarić, Željko Kelnerić, Mihaela Perić, Mihailo Banjanac, Gabrijela Ergović, Nerrisa Simon, John Broskey and 2 more

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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

9 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Evading resistance at the double.Nature chemical biology · 2024
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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

12 authors at 2 institutions in 2 countries.

Hana Čipčić PaljetakGlaxoSmithKline Research Centre Zagreb, Zagreb, Croatia hana.paljetak@mef.hr.
Donatella VerbanacGlaxoSmithKline Research Centre Zagreb, Zagreb, Croatia.
Jasna PadovanGlaxoSmithKline Research Centre Zagreb, Zagreb, Croatia.
Miroslava Dominis-KramarićGlaxoSmithKline Research Centre Zagreb, Zagreb, Croatia.
Željko KelnerićGlaxoSmithKline Research Centre Zagreb, Zagreb, Croatia.
Mihaela PerićGlaxoSmithKline Research Centre Zagreb, Zagreb, Croatia.
Mihailo BanjanacGlaxoSmithKline Research Centre Zagreb, Zagreb, Croatia.
Gabrijela ErgovićGlaxoSmithKline Research Centre Zagreb, Zagreb, Croatia.
Nerrisa SimonGlaxoSmithKline, Collegeville, Pennsylvania, USA.
John BroskeyGlaxoSmithKline, Collegeville, Pennsylvania, USA.
David J HolmesGlaxoSmithKline, Collegeville, Pennsylvania, USA.
Vesna Eraković HaberGlaxoSmithKline Research Centre Zagreb, Zagreb, Croatia.
GlaxoSmithKline (Croatia) · HRGlaxoSmithKline (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As we face an alarming increase in bacterial resistance to current antibacterial chemotherapeutics, expanding the available therapeutic arsenal in the fight against resistant bacterial pathogens causing respiratory tract infections is of high importance. The antibacterial potency of macrolones, a novel class of macrolide antibiotics, against key respiratory pathogens was evaluated in vitro and in vivo MIC values against Streptococcus pneumoniae, Streptococcus pyogenes, Staphylococcus aureus, and Haemophilus influenzae strains sensitive to macrolide antibiotics and with defined macrolide resistance mechanisms were determined. The propensity of macrolones to induce the expression of inducible erm genes was tested by the triple-disk method and incubation in the presence of subinhibitory concentrations of compounds. In vivo efficacy was assessed in a murine model of S. pneumoniae-induced pneumonia, and pharmacokinetic (PK) profiles in mice were determined. The in vitro antibacterial profiles of macrolones were superior to those of marketed macrolide antibiotics, including the ketolide telithromycin, and the compounds did not induce the expression of inducible erm genes. They acted as typical protein synthesis inhibitors in an Escherichia coli transcription/translation assay. Macrolones were characterized by low to moderate systemic clearance, a large volume of distribution, a long half-life, and low oral bioavailability. They were highly efficacious in a murine model of pneumonia after intraperitoneal application even against an S. pneumoniae strain with constitutive resistance to macrolide-lincosamide-streptogramin B antibiotics. Macrolones are the class of macrolide antibiotics with an outstanding antibacterial profile and reasonable PK parameters resulting in good in vivo efficacy.

Indexed as

AnimalsAnti-Bacterial AgentsBacterial ProteinsDisease Models, AnimalDrug Resistance, BacterialEscherichia coliHaemophilus influenzaeKetolidesLincosamidesMacrolidesMaleMethyltransferasesMiceMice, Inbred C57BLPneumonia, PneumococcalProtein BiosynthesisAnti-Bacterial AgentsBacterial ProteinsErmA protein, BacteriaKetolidesLincosamidesMacrolidesMethyltransferasesProtein Synthesis InhibitorsStreptogramin Btelithromycin

Identifiers

PMID27353268
PMCPMC4997857
OpenAlexW2463264282

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.