» Articles » PMID: 33504843

Cytotoxic Escherichia Coli Strains Encoding Colibactin, Cytotoxic Necrotizing Factor, and Cytolethal Distending Toxin Colonize Laboratory Common Marmosets (Callithrix Jacchus)

Overview
Journal Sci Rep
Specialty Science
Date 2021 Jan 28
PMID 33504843
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Cyclomodulins are virulence factors that modulate cellular differentiation, apoptosis, and proliferation. These include colibactin (pks), cytotoxic necrotizing factor (cnf), and cytolethal distending toxin (cdt). Pathogenic pks+, cnf+, and cdt+ E. coli strains are associated with inflammatory bowel disease (IBD) and colorectal cancer in humans and animals. Captive marmosets are frequently afflicted with IBD-like disease, and its association with cyclomodulins is unknown. Cyclomodulin-encoding E. coli rectal isolates were characterized using PCR-based assays in healthy and clinically affected marmosets originating from three different captive sources. 139 E. coli isolates were cultured from 122 of 143 marmosets. The pks gene was detected in 56 isolates (40%), cnf in 47 isolates (34%), and cdt in 1 isolate (0.7%). The prevalences of pks+ and cnf+ E. coli isolates were significantly different between the three marmoset colonies. 98% of cyclomodulin-positive E. coli belonged to phylogenetic group B2. Representative isolates demonstrated cyclomodulin cytotoxicity, and serotyping and whole genome sequencing were consistent with pathogenic E. coli strains. However, the presence of pks+, cnf+, or cdt+ E. coli did not correlate with clinical gastrointestinal disease in marmosets. Cyclomodulin-encoding E. coli colonize laboratory common marmosets in a manner dependent on the source, potentially impacting reproducibility in marmoset models.

Citing Articles

Diarrheagenic in Stool Specimens Collected from Patients Attending Primary Healthcare Facilities in Ethiopia: Whole-Genome Sequencing-Based Molecular Characterization.

Wolde D, Eguale T, Medhin G, Feleke Haile A, Alemayehu H, Mihret A Int J Mol Sci. 2024; 25(19).

PMID: 39408580 PMC: 11476756. DOI: 10.3390/ijms251910251.


Designing multi-epitope vaccine against important colorectal cancer (CRC) associated pathogens based on immunoinformatics approach.

Motamedi H, Mahdizade Ari M, Shahlaei M, Moradi S, Farhadikia P, Alvandi A BMC Bioinformatics. 2023; 24(1):65.

PMID: 36829112 PMC: 9951438. DOI: 10.1186/s12859-023-05197-0.


Role of adherent invasive in pathogenesis of inflammatory bowel disease.

Zheng L, Duan S, Dai Y, Wu S World J Clin Cases. 2022; 10(32):11671-11689.

PMID: 36405271 PMC: 9669839. DOI: 10.12998/wjcc.v10.i32.11671.


Analysis of gut microbiome profiles in common marmosets (Callithrix jacchus) in health and intestinal disease.

Sheh A, Artim S, Burns M, Molina-Mora J, Lee M, Dzink-Fox J Sci Rep. 2022; 12(1):4430.

PMID: 35292670 PMC: 8924212. DOI: 10.1038/s41598-022-08255-4.

References
1.
Wilson M, Jiang Y, Villalta P, Stornetta A, Boudreau P, Carra A . The human gut bacterial genotoxin colibactin alkylates DNA. Science. 2019; 363(6428). PMC: 6407708. DOI: 10.1126/science.aar7785. View

2.
Marini R, Taylor N, Liang A, Knox K, Pena J, Schauer D . Characterization of hemolytic Escherichia coli strains in ferrets: recognition of candidate virulence factor CNF1. J Clin Microbiol. 2004; 42(12):5904-8. PMC: 535218. DOI: 10.1128/JCM.42.12.5904-5908.2004. View

3.
El-Aouar Filho R, Nicolas A, De Paula Castro T, Deplanche M, De Carvalho Azevedo V, Goossens P . Heterogeneous Family of Cyclomodulins: Smart Weapons That Allow Bacteria to Hijack the Eukaryotic Cell Cycle and Promote Infections. Front Cell Infect Microbiol. 2017; 7:208. PMC: 5440457. DOI: 10.3389/fcimb.2017.00208. View

4.
Kaper J, Nataro J, Mobley H . Pathogenic Escherichia coli. Nat Rev Microbiol. 2004; 2(2):123-40. DOI: 10.1038/nrmicro818. View

5.
Garcia A, Fox J . The rabbit as a new reservoir host of enterohemorrhagic Escherichia coli. Emerg Infect Dis. 2004; 9(12):1592-7. PMC: 3034324. DOI: 10.3201/eid0912.030223. View