Evidence map›Paper›PMID 42251401›Full record

ArticleAnnals of clinical microbiology and antimicrobials2026

A longitudinal analysis of Clostridioides difficile virulence profiles across three geographic regions in Israel (2020-2022).

Orna Schwartz, Avi Peretz, Maya Azrad

Abstract read
In one paragraph

Article in Annals of clinical microbiology and antimicrobials, 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

3 authors.

Orna SchwartzAzrieli Faculty of Medicine, Bar Ilan University, Safed, Israel.
Avi PeretzAzrieli Faculty of Medicine, Bar Ilan University, Safed, Israel.
Maya AzradClinical Microbiology Laboratory, Tzafon Medical Center, Poriya, Israel. mazrad@tzmc.gov.il.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClostridioides difficile infection (CDI) is one of the leading infectious diarrhea worldwide. C. difficile pathogenicity is mediated by various virulence factors, including toxins and biofilm formation. This study included 313 C. difficile isolates that were previously collected from four medical centers. We aimed to investigate the prevalence, distribution, and associations of virulence factors in C. difficile strains from both healthcare-associated (HA)- and community-acquired (CA)-CDI patients across Israel from 2020 to 2022.

methodsMulti-locus sequence typing (MLST) and whole-genome sequencing (WGS) were performed for strain classification and virulence gene detection. Toxin and biofilm production were also characterized.

resultsSequence type (ST) 42 (12.5%) and ST2 (11.5%) were the most prevalent strains. Toxin production patterns were significantly associated with setting of infection acquisition (p < 0.0001). Isolates producing both toxin A and B were 2.5-fold more common among HA-CDI strains, while toxin-A-producers were more frequent in CA-CDI. Biofilm was produced by 96.9% of isolates, with strong biofilm-producing strains significantly more prevalent in hospitals (p < 0.001). Furthermore, isolates producing both toxins A and B were predominantly moderate or strong biofilm producers (p < 0.0001). agrD presence was significantly associated with ST, toxin production patterns and biofilm-production capacity (p < 0.0001 for ST and biofilm, p = 0.0016 for toxins).

conclusionsThis study revealed a high diversity of C. difficile strains in Israel and demonstrated that virulence factor patterns differ significantly across STs and the acquisition setting. The differences between HA-CDI and CA-CDI isolates in some virulence factors underscores the importance of continuous epidemiological surveillance to guide tailored treatment and prevention strategies.

Indexed as

Clostridioides difficileClostridium InfectionsVirulence FactorsBacterial ProteinsBacterial ToxinsBiofilmsCommunity-Acquired InfectionsCross InfectionEnterotoxinsFemaleHumansIsraelLongitudinal StudiesMaleMultilocus Sequence TypingPrevalenceBacterial ProteinsBacterial ToxinsEnterotoxinsVirulence FactorsAntibiotic susceptibilityC. difficileStrainsVirulence genesWGS

Identifiers

PMID42251401
PMCPMC13651375

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.