Evidence map›Paper›PMID 40462653›Full record

ArticleThe Journal of antimicrobial chemotherapy2025

A novel azithromycin resistance mutation in Mycoplasma genitalium induced in vitro.

Teck-Phui Chua, Jennifer Danielewski, Catriona S Bradshaw, Dorothy A Machalek, Suzanne M Garland, Jose L Huaman, Jørgen S Jensen, Gerald L Murray

Abstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Drug resistance ofFrontiers in cellular and infection microbiology · 2026
    Review
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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

8 authors.

Teck-Phui ChuaDepartment of Obstetrics, Gynaecology, and Newborn Health, University of Melbourne, Parkville, Victoria, Australia.
Jennifer DanielewskiCentre for Women's Infectious Diseases, The Royal Women's Hospital, Parkville, Victoria, Australia.
Catriona S BradshawMelbourne Sexual Health Centre, Alfred Health, Carlton, Victoria, Australia.
Dorothy A MachalekThe Kirby Institute, University of New South Wales, Sydney, New South Wales, Australia.
Suzanne M GarlandDepartment of Obstetrics, Gynaecology, and Newborn Health, University of Melbourne, Parkville, Victoria, Australia.
Jose L HuamanDepartment of Obstetrics, Gynaecology, and Newborn Health, University of Melbourne, Parkville, Victoria, Australia.
Jørgen S JensenResearch Unit for Reproductive Microbiology, Statens Serum Institut, Copenhagen, Denmark.ORCID 0000-0002-7464-7435
Gerald L MurrayDepartment of Obstetrics, Gynaecology, and Newborn Health, University of Melbourne, Parkville, Victoria, Australia.ORCID 0000-0003-3330-4433

Funding

Australian Government Research Training Program ScholarshipAustralian Research Council Industrial Transformation Research Hub for Antimicrobial Resistance IH190100021NHMRC Investigator APP1197951
6 · The paper itself

Abstract

backgroundMycoplasma genitalium is a sexually transmitted bacterium of increasing concern due to issues around antimicrobial resistance. Resistance is typically mediated by SNPs; however, the difficulty of isolation and culture of M. genitalium limits the ability to analyse the impact of individual mutations.

objectivesThe aim of this study was to generate and characterize antibiotic-resistant M. genitalium mutants in vitro to understand the development of macrolide resistance in this bacterium.

methodsSequential MIC assays for azithromycin were performed using the laboratory strain of M. genitalium (G37) grown in Hayflick medium. Bacteria were enumerated by droplet digital PCR (ddPCR) targeting mgpB, and a new ddPCR assay was established to detect specific mutations in the 23S rRNA gene. MICs of selected macrolide antibiotics were determined in Hayflick medium. Whole genome sequencing (WGS) was performed on the Oxford Nanopore MinION.

resultsAfter eight passages in azithromycin, a novel 23S rRNA gene mutation, G2057A (Escherichia coli numbering), was detected. The mutant did not display a detectable growth defect and had elevated MICs to azithromycin (8-fold), josamycin (8-fold) and erythromycin (16- to 32-fold). WGS did not identify other mutations likely to contribute to reduced macrolide susceptibility.

conclusionsA novel 23S rRNA gene mutation was identified in M. genitalium. This variation is found in Mycoplasma hominis, which is intrinsically resistant to certain macrolides. While this mutation has not been observed clinically in M. genitalium, these findings have expanded our understanding of resistance mechanisms within the Mollicutes, in particular the propensity for M. genitalium to develop resistance, even in low concentrations of antibiotic, and the interaction of azithromycin with the ribosome.

Indexed as

Anti-Bacterial AgentsAzithromycinDrug Resistance, BacterialMutationMycoplasma genitaliumHumansMacrolidesMicrobial Sensitivity TestsMycoplasma InfectionsRNA, Ribosomal, 23SWhole Genome SequencingAnti-Bacterial AgentsAzithromycinMacrolidesRNA, Ribosomal, 23S

Identifiers

PMID40462653
PMCPMC12209806

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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.