Evidence map›Paper›PMID 38816572›Full record

ArticleArchives of microbiology2024

Increased Brucella abortus asRNA_0067 expression under intraphagocytic stressors is associated with enhanced virB2 transcription.

Adrian Muñoz-Bucio, Beatriz Arellano-Reynoso, Félix J Sangari, Rodrigo Sieira, Patricia Thébault, Clara Espitia, Juan M García Lobo, Asunción Seoane, Francisco Suárez-Güemes

Abstract read
In one paragraph

Article in Archives of microbiology, 2024. 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. Review
  2. Review
  3. ThemicroLife · 2025
    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

9 authors.

Adrian Muñoz-BucioFacultad de Medicina Veterinaria y Zootecnia, Departamento de Microbiología e Inmunología. Circuito Exterior S/N, Universidad Nacional Autónoma de México, CDMX, Ciudad Universitaria, Coyoacán, 04510, Mexico.ORCID http://orcid.org/0000-0003-3557-973X
Beatriz Arellano-ReynosoFacultad de Medicina Veterinaria y Zootecnia, Departamento de Microbiología e Inmunología. Circuito Exterior S/N, Universidad Nacional Autónoma de México, CDMX, Ciudad Universitaria, Coyoacán, 04510, Mexico.ORCID http://orcid.org/0000-0002-3067-2719
Félix J SangariInstituto de Biomedicina y Biotecnología de Cantabria (IBBTEC), Universidad de Cantabria-CSIC-SODERCAN, C. Albert Einstein 22, 39011, Santander, Cantabria, Spain.ORCID http://orcid.org/0000-0002-3298-6076
Rodrigo SieiraFundación Instituto Leloir-IIBBA CONICET, Av. Patricias Argentinas 435CABA, CP. 1405, Buenos Aires Argentina, Argentina.ORCID http://orcid.org/0000-0002-4495-563X
Patricia ThébaultLaboratoire Bordelais de Recherche en Informatique (LaBRI), UMR 5800, CNRS, Bordeaux INP, Université de Bordeaux, 33400, Talence, France.ORCID http://orcid.org/0000-0003-2276-4573
Clara EspitiaDepartamento de Inmunología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México MX, CDMX, Circuito Escolar 33, Ciudad Universitaria, Coyoacán, 04510, Mexico.ORCID http://orcid.org/0000-0001-7731-4049
Juan M García LoboInstituto de Biomedicina y Biotecnología de Cantabria (IBBTEC), Universidad de Cantabria-CSIC-SODERCAN, C. Albert Einstein 22, 39011, Santander, Cantabria, Spain.ORCID http://orcid.org/0000-0002-9187-0671
Asunción SeoaneInstituto de Biomedicina y Biotecnología de Cantabria (IBBTEC), Universidad de Cantabria-CSIC-SODERCAN, C. Albert Einstein 22, 39011, Santander, Cantabria, Spain.ORCID http://orcid.org/0000-0001-9415-9394
Francisco Suárez-GüemesFacultad de Medicina Veterinaria y Zootecnia, Departamento de Microbiología e Inmunología. Circuito Exterior S/N, Universidad Nacional Autónoma de México, CDMX, Ciudad Universitaria, Coyoacán, 04510, Mexico. fsg@unam.mx.ORCID http://orcid.org/0000-0003-0118-2494

Funding

DGAPA-PAPIIT (UNAM) IN218421
6 · The paper itself

Abstract

Intracellular pathogens like Brucella face challenges during the intraphagocytic adaptation phase, where the modulation of gene expression plays an essential role in taking advantage of stressors to persist inside the host cell. This study aims to explore the expression of antisense virB2 RNA strand and related genes under intracellular simulation media. Sense and antisense virB2 RNA strands increased expression when nutrient deprivation and acidification were higher, being starvation more determinative. Meanwhile, bspB, one of the T4SS effector genes, exhibited the highest expression during the exposition to pH 4.5 and nutrient abundance. Based on RNA-seq analysis and RACE data, we constructed a regional map depicting the 5' and 3' ends of virB2 and the cis-encoded asRNA_0067. Without affecting the CDS or a possible autonomous RBS, we generate the deletion mutant ΔasRNA_0067, significantly reducing virB2 mRNA expression and survival rate. These results suggest that the antisense asRNA_0067 expression is promoted under exposure to the intraphagocytic adaptation phase stressors, and its deletion is associated with a lower transcription of the virB2 gene. Our findings illuminate the significance of these RNA strands in modulating the survival strategy of Brucella within the host and emphasize the role of nutrient deprivation in gene expression.

Indexed as

Brucella abortusGene Expression Regulation, BacterialAnimalsBacterial ProteinsMacrophagesRNA, AntisenseRNA, BacterialStress, PhysiologicalTranscription, GeneticBacterial ProteinsRNA, AntisenseRNA, BacterialAntisense RNAsBrucella abortusIntraphagocytic adaptationStressorsvirB2

Identifiers

PMID38816572
PMCPMC11139718

What OpenQuestion holds

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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.