Evidence map›Paper›PMID 42157423›Full record

ReviewMedical gas research2026

Sensing the host atmosphere: carbon dioxide regulates virulence and drug response in medically relevant fungi.

Thaís P Mello, Lívia S Ramos, Marta H Branquinha, André L S Santos

Abstract readReview
In one paragraph

Review in Medical gas research, 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

4 authors.

Thaís P MelloLaboratório de Estudos Avançados de Microrganismos Emergentes e Resistentes (LEAMER), Departamento de Microbiologia Geral, Instituto de Microbiologia Paulo de Góes (IMPG), Centro de Ciências da Saúde (CCS), Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, Brazil.
Lívia S RamosLaboratório de Estudos Avançados de Microrganismos Emergentes e Resistentes (LEAMER), Departamento de Microbiologia Geral, Instituto de Microbiologia Paulo de Góes (IMPG), Centro de Ciências da Saúde (CCS), Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, Brazil.
Marta H BranquinhaLaboratório de Estudos Avançados de Microrganismos Emergentes e Resistentes (LEAMER), Departamento de Microbiologia Geral, Instituto de Microbiologia Paulo de Góes (IMPG), Centro de Ciências da Saúde (CCS), Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, Brazil.
André L S SantosLaboratório de Estudos Avançados de Microrganismos Emergentes e Resistentes (LEAMER), Departamento de Microbiologia Geral, Instituto de Microbiologia Paulo de Góes (IMPG), Centro de Ciências da Saúde (CCS), Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, Brazil.ORCID 0000-0003-0821-8592

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carbon dioxide (CO 2 ) is a pivotal environmental signal that influences the physiology, development and pathogenic potential of fungi. Beyond its role as a metabolic by-product, CO 2 functions as a conserved signaling molecule that enables fungal pathogens to sense and adapt to host niches. This review synthesizes current knowledge on how fluctuations in CO 2 concentration modulate growth dynamics, morphogenesis, virulence-associated attributes and antifungal susceptibility in clinically important yeasts and filamentous fungi. In Candida species, particularly Candida albicans , physiological CO 2 levels encountered in host tissues (~5%) act as a potent morphogenetic signal, driving the yeast-to-hypha transition, promoting biofilm formation and inducing metabolic reprogramming; processes tightly linked to tissue invasion and persistence. CO 2 exposure also alters membrane composition and stress response pathways, thereby modulating susceptibility to antifungal agents. In Cryptococcus neoformans , elevated CO 2 concentrations promote capsule biosynthesis and enlargement, alongside extensive remodeling of surface architecture and membrane composition. These CO 2 -driven adaptations strengthen resistance to host immune defenses and are associated with increased tolerance to antifungals. In Aspergillus species, CO 2 availability influences growth, mycotoxin biosynthesis and developmental trajectories by shifting the balance between asexual and sexual reproduction, with downstream effects on virulence and antifungal responsiveness. In Scedosporium / Lomentospora species, CO 2 promotes conidial germination and developmental transitions that may indirectly impact antifungal susceptibility and pathogenic fitness. Collectively, these findings highlight environmental CO 2 as a pivotal and dynamic regulator of fungal biology, offering key insights into host-pathogen interactions, informing the prediction of antifungal susceptibility profiles and supporting the rational optimization of therapeutic strategies in clinical settings.

Indexed as

Antifungal AgentsCarbon DioxideFungiHost-Pathogen InteractionsAnimalsHumansVirulenceAntifungal AgentsCarbon Dioxideantifungal resistancebiofilmcarbon dioxidehost environmentmorphogenesisproliferation

Identifiers

PMID42157423
PMCPMC13456448

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Registered trials

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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.