Evidence map›Paper›PMID 40126549›Full record

ArticleThe Journal of antimicrobial chemotherapy2025

Validation of a modified rapid test to detect the cefazolin inoculum effect in methicillin-susceptible Staphylococcus aureus from bloodstream infections in hospitals from North and Latin America.

Sara I Gomez-Villegas, Sandra Rincon, Lina P Carvajal, J Manuel Matiz-González, Diana Panesso, Truc T Tran, Erika Flores, Jacob Dziadula, Rodrigo Baptista, Tanis C Dingle and 9 more

Abstract readValidation Study
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. Development of a rapid diagnostic test for the cefazolin inoculum effect in methicillin-susceptible Staphylococcus aureus: Cefinase disk direct (CDD) test.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Article
  2. Article
  3. 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

19 authors.

Sara I Gomez-VillegasBrigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Sandra RinconMolecular Genetics and Antimicrobial Resistance Unit, Universidad El Bosque, Bogota, Colombia.
Lina P CarvajalMolecular Genetics and Antimicrobial Resistance Unit, Universidad El Bosque, Bogota, Colombia.
J Manuel Matiz-GonzálezMolecular Genetics and Antimicrobial Resistance Unit, Universidad El Bosque, Bogota, Colombia.
Diana PanessoMolecular Genetics and Antimicrobial Resistance Unit, Universidad El Bosque, Bogota, Colombia.
Truc T TranCenter for Infectious Diseases, Houston Methodist Research Institute, Houston, TX, USA.
Erika FloresCenter for Infectious Diseases, Houston Methodist Research Institute, Houston, TX, USA.
Jacob DziadulaCenter for Infectious Diseases, Houston Methodist Research Institute, Houston, TX, USA.
Rodrigo BaptistaCenter for Infectious Diseases, Houston Methodist Research Institute, Houston, TX, USA.
Tanis C DingleAlberta Precision Laboratories, Public Health Laboratory, Calgary, Alberta, Canada.
Jennifer Dien BardDepartment of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, CA, USA.ORCID 0000-0003-0524-9473
April AbbottDepartment of Laboratory Medicine, Deaconess Health System, Evansville, IN, USA.
Carey-Ann D BurnhamDepartment of Pathology & Immunology, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
Stephanie FritzDepartment of Pediatrics, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.ORCID 0000-0002-8602-5879
Lars F WestbladeDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.
Susan Butler-WuKeck School of Medicine, University of Southern California, Los Angeles, CA, USA.
William R MillerCenter for Infectious Diseases, Houston Methodist Research Institute, Houston, TX, USA.ORCID 0000-0002-1518-2973
Cesar A AriasCenter for Infectious Diseases, Houston Methodist Research Institute, Houston, TX, USA.
Jinnethe ReyesMolecular Genetics and Antimicrobial Resistance Unit, Universidad El Bosque, Bogota, Colombia.ORCID 0000-0002-1722-0734

Funding

Project 3: Functional Microbiome and Host Signatures in Transition from Commensal to pathogenP01AI152999 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI SAVIDGE, TOR C. · 2020 to 2025
$12.0M
VENOUS: A translational study of enterococcal bacteremiaR01AI148342 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ARIAS, CESAR AUGUSTO · 2020 to 2024
$3.9M
The LiaFSR system and antimicrobial peptide resistance in enterococciR01AI134637 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Cesar Augusto Arias · 2018 to 2026
$3.7M
Clinical Impact of the Cefazolin Inoculum EffectR01AI173138 · NIAID · METHODIST HOSPITAL RESEARCH INSTITUTE · PI Cesar Augusto Arias · 2023 to 2026
$2.6M
POR Program on Genomic Prediction of Antimicrobial Resistance in VREK24AI121296 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ARIAS, CESAR AUGUSTO · 2016 to 2025
$1.5M
Antimicrobial Resistance Training Program in the Texas Medical Center (AMR-TPT)T32AI179595 · NIAID · METHODIST HOSPITAL RESEARCH INSTITUTE · PI Cesar Augusto Arias · 2024 to 2026
$1.0M
National Institute of Allergy and Infectious Diseases K24AI121296NIAID NIH HHS K24 AI121296NIAID NIH HHS P01 AI152999NIAID NIH HHS R01 AI134637NIAID NIH HHS R01 AI148342NIAID NIH HHS R01 AI173138NIAID NIH HHS T32 AI179595NIH HHS
6 · The paper itself

Abstract

backgroundThe cefazolin inoculum effect (CzIE), defined here as a cefazolin MIC at high inoculum (107 colony-forming units/mL)  ≥16 mg/L in MSSA, has been associated with less favourable clinical outcomes. However, detection of this phenotype is challenging in the clinical microbiology laboratory. We previously described modification of a rapid nitrocefin test using ampicillin disks rather than ampicillin powder for induction of the Staphylococcus aureus β-lactamase (BlaZ).

objectiveEvaluate the performance of the modified rapid nitrocefin test in a blinded fashion using MSSA isolates recovered from patients with bacteraemia.

methodsWe evaluated 200 MSSA isolates recovered from Latin American (LA) and North American (NA) hospitals (67 and 133 from NA and LA, respectively). The CzIE was determined using the modified rapid nitrocefin test with ampicillin disks and compared with MIC determination at high inoculum (gold standard). All isolates were subjected to whole-genome sequencing on an Illumina Hi-Seq platform. Performance metrics were calculated for the complete dataset and according to specific BlaZ types.

resultsThe prevalence of the CzIE was 53% (105/200). Compared with the gold standard, the modified nitrocefin rapid test had a sensitivity of 96% and a specificity of 91.6%, with an overall accuracy of 94%. There were no false-positive results among blaZ-negative MSSA strains.

conclusionsThe modified nitrocefin rapid test exhibited a robust performance to detect the CzIE in isolates from the Americas. This methodology is inexpensive and can be implemented in clinical microbiology laboratories around the world, including those with limited resources.

Indexed as

Anti-Bacterial AgentsBacteremiaCefazolinStaphylococcal InfectionsStaphylococcus aureusbeta-LactamasesHospitalsHumansLatin AmericaMicrobial Sensitivity TestsNorth AmericaSensitivity and SpecificityWhole Genome SequencingAnti-Bacterial Agentsbeta-LactamasesCefazolin

Identifiers

PMID40126549
PMCPMC12159742

What OpenQuestion holds

Textmetadata
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.