Evidence map›Paper›PMID 42129501›Full record

ArticleScientific reports2026

Real-time monitoring of metabolic plasticity in Mycoplasma gallisepticum under varying nutrient conditions via DART-HRMS.

Marco Bottinelli, Carmela Zacometti, Andrea Massaro, Annalucia Tondo, Davide Prataviera, Beatrice Colò, Micaela Picchi, Miklós Gyuranecz, Roberto Piro, Alessandra Tata and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Marco Bottinelli *Mycoplasma Unit, WOAH Reference Laboratory for Avian Mycoplasmosis (M. gallisepticum, M. synoviae), SCT-1 Verona, Istituto Zooprofilattico Sperimentale delle Venezie, Buttapietra, Italy.
Carmela Zacometti *Laboratorio di Chimica Sperimentale, SCS8, Istituto Zooprofilattico Sperimentale delle Venezie, Vicenza, Italy.
Andrea MassaroLaboratorio di Chimica Sperimentale, SCS8, Istituto Zooprofilattico Sperimentale delle Venezie, Vicenza, Italy.
Annalucia TondoMycoplasma Unit, WOAH Reference Laboratory for Avian Mycoplasmosis (M. gallisepticum, M. synoviae), SCT-1 Verona, Istituto Zooprofilattico Sperimentale delle Venezie, Buttapietra, Italy.
Davide PratavieraMycoplasma Unit, WOAH Reference Laboratory for Avian Mycoplasmosis (M. gallisepticum, M. synoviae), SCT-1 Verona, Istituto Zooprofilattico Sperimentale delle Venezie, Buttapietra, Italy.
Beatrice ColòMycoplasma Unit, WOAH Reference Laboratory for Avian Mycoplasmosis (M. gallisepticum, M. synoviae), SCT-1 Verona, Istituto Zooprofilattico Sperimentale delle Venezie, Buttapietra, Italy.
Micaela PicchiMycoplasma Unit, WOAH Reference Laboratory for Avian Mycoplasmosis (M. gallisepticum, M. synoviae), SCT-1 Verona, Istituto Zooprofilattico Sperimentale delle Venezie, Buttapietra, Italy.
Miklós GyuraneczHUN-REN Veterinary Medical Research Institute, Budapest, Hungary.
Roberto PiroLaboratorio di Chimica Sperimentale, SCS8, Istituto Zooprofilattico Sperimentale delle Venezie, Vicenza, Italy.
Alessandra TataLaboratorio di Chimica Sperimentale, SCS8, Istituto Zooprofilattico Sperimentale delle Venezie, Vicenza, Italy. atata@izsvenezie.it.
Salvatore CataniaMycoplasma Unit, WOAH Reference Laboratory for Avian Mycoplasmosis (M. gallisepticum, M. synoviae), SCT-1 Verona, Istituto Zooprofilattico Sperimentale delle Venezie, Buttapietra, Italy.

Funding

National Research, Development and Innovation Office of Hungary TKP2021-EGA-01National Research, Development and Innovation Office of Hungary. RRF-2.3.1-21-2022-00001
6 · The paper itself

Abstract

Mycoplasmas are known for being fastidious, with scientists still struggling to propagate them in vitro. Improving their culture is vital for future research, despite limited metabolomics studies available. This study explored the chemical composition changes in four liquid media (A, B, C, D) inoculated with Mycoplasma gallisepticum (MG), aiming to uncover overlooked metabolic features. We used Direct Analysis in Real Time High-Resolution Mass Spectrometry (DART-HRMS) across five time points over 71 h. Integration of DART-HRMS data with statistical analysis showed that media A and D initially contained higher glucose levels, which declined over time. Lactic acid levels rose in all media, with signals reaching saturation at the latest time points. Subsequent pathway enrichment analysis revealed an unexpected overexpression of arginine metabolism. Spermidine accumulation in certain media suggests a potential link to inhibited biofilm formation, opening questions about polyamine function in MG. Histidinal accumulation indicated an unpredicted amino acid synthesis capability in a mycoplasma and MG's inability to convert arginine into glutamic acid. Additionally, MG was observed to utilize creatine when present. These findings highlight the importance of metabolomics in understanding enigmatic microorganisms like mycoplasmas, reaffirming that environmental factors drive alternative metabolic routes in MG and opening new research avenues.

Indexed as

Culture MediaMass SpectrometryMetabolomicsMycoplasma gallisepticumArginineGlucoseArginineCulture MediaGlucoseDART-HRMSMediumMetabolismMetabolomicsMycoplasma gallisepticum

Identifiers

PMID42129501
PMCPMC13365527

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.