Evidence map›Paper›PMID 38655087›Full record

ArticleFrontiers in microbiology2024

A bioinformatic approach to identify confirmed and probable CRISPR-Cas systems in the

Jetsi Mancilla-Rojano, Víctor Flores, Miguel A Cevallos, Sara A Ochoa, Julio Parra-Flores, José Arellano-Galindo, Juan Xicohtencatl-Cortes, Ariadnna Cruz-Córdova

Open access · goldAbstract read
In one paragraph

Article in Frontiers in 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
0.9field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Advances in phage therapy forFrontiers in microbiology · 2026
    Review
  2. Whole-genome sequencing ofMicrobial genomics · 2025
    Article
  3. Comprehensive Approaches to CombattingAntibiotics (Basel, Switzerland) · 2024
    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

8 authors at 5 institutions in 3 countries.

Jetsi Mancilla-RojanoPosgrado en Ciencias Biológicas, Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico, Mexico.
Víctor FloresDepartment of Biochemistry, University of Cambridge, Cambridge, United Kingdom.
Miguel A CevallosCentro de Ciencias Genómicas, Programa de Genómica Evolutiva, Universidad Nacional Autónoma de México, Cuernavaca, Mexico.
Sara A OchoaLaboratorio de Investigación en Bacteriología Intestinal, Unidad de Enfermedades Infecciosas, Hospital Infantil de México Federico Gómez, Secretaría de Salud, Mexico, Mexico.
Julio Parra-FloresDepartment of Nutrition and Public Health, Universidad del Bío-Bío, Chillán, Chile.
José Arellano-GalindoUnidad de Investigación en Enfermedades Infecciosas, Hospital Infantil de México Federico Gomez, Mexico, Mexico.
Juan Xicohtencatl-CortesLaboratorio de Investigación en Bacteriología Intestinal, Unidad de Enfermedades Infecciosas, Hospital Infantil de México Federico Gómez, Secretaría de Salud, Mexico, Mexico.
Ariadnna Cruz-CórdovaPosgrado en Ciencias Biológicas, Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico, Mexico.
Secretaria de Salud · MXHospital Infantil de México Federico Gómez · MXUniversidad Nacional Autónoma de México · MXUniversity of Bío-Bío · CLUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The Methods: Acb complex genomes available in the NCBI and BV-BRC databases, the identification and characterization of CRISPR-Cas systems were performed using CRISPRCasFinder, CRISPRminer, and CRISPRDetect. Sequence types (STs) were determined using the Oxford scheme and ribosomal multilocus sequence typing (rMLST). Prophages were identified using PHASTER and Prophage Hunter. Results: A total of 293 genomes representing six Acb species exhibited CRISPR-related sequences. These genomes originate from various sources, including clinical specimens, animals, medical devices, and environmental samples. Sequence typing identified 145 ribosomal multilocus sequence types (rSTs). CRISPR-Cas systems were confirmed in 26.3% of the genomes, classified as subtypes I-Fa, I-Fb and I-Fv. Probable CRISPR arrays and Discussion: This study elucidates CRISPR-Cas systems and defense mechanisms within the Acb complex, highlighting their diverse distribution and interactions with prophages and other genetic elements. This study also provides valuable insights into the evolution and adaptation of these microorganisms in various environments and clinical settings.

Indexed as

Acinetobacter baumanniiAcinetobacter calcoaceticus–Acinetobacter baumannii complexcas genesCRISPR systemsprophages

Identifiers

PMID38655087
PMCPMC11035748
OpenAlexW4394618542

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.