Shiga Toxin-Producing Escherichia coli (STEC): Unveiling Pathogenic Mechanisms and Exploring Therapeutic Targets

Escherichia coli

Introduction

Shiga toxin-producing Escherichia coli (STEC) strains lurk within the vast and often beneficial world of E. coli. These pathogenic bacteria possess a stealthy ability to cause severe illness, highlighting the importance of understanding their virulence mechanisms. This review sheds light on STEC and their arsenal of weaponry, focusing on Shiga toxins and the ensuing pathological consequences.

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Shiga Toxins: Unveiling the Molecular Machete


STEC strains wield a potent weapon – Shiga toxins (Stx). These toxins, categorized into Stx1 and Stx2, are structurally similar yet display varying degrees of cytotoxicity. Stx exerts its deleterious effects through a well-orchestrated process:


1.Intimate Attachment: STEC harbors intimin, an outer membrane adhesin, facilitating intimate attachment to host intestinal epithelial cells via interaction with host cell receptors.


2.Endocytosis and Retrograde Trafficking: The bound Stx is endocytosed by the host cell and undergoes retrograde trafficking via the Golgi apparatus.


3.Ribosomal Shutdown: Stx disrupts protein synthesis by inactivating ribosomal RNA in the endoplasmic reticulum, leading to cellular dysfunction and death.


The potency of Stx lies in its ability to target the globally essential cellular process of protein synthesis. This indiscriminate attack on intestinal epithelial cells disrupts barrier function, electrolyte homeostasis, and nutrient absorption, leading to the characteristic symptoms of STEC infection.


A toxic environment: a growing understanding of how microbial communities affect Escherichia coli O157:H7 Shiga toxin expression


Beyond Cytotoxicity: The Spectrum of STEC-Mediated Disease


STEC infection extends beyond localized intestinal damage. Released Stx can enter the bloodstream, leading to systemic complications:


Hemolytic-Uremic Syndrome (HUS): Stx has a particular affinity for the glomerular endothelium in the kidneys. The damage caused by Stx triggers HUS, characterized by hemolytic anemia, thrombocytopenia, and acute kidney injury.


Neurological Complications: In severe cases, Stx can traverse the blood-brain barrier, leading to neurological complications like encephalopathy and seizures.


Unveiling the Pathogen's Arsenal: Additional Virulence Factors


While Stx is undoubtedly the centerpiece of STEC pathogenesis, several other virulence factors contribute to disease severity:


Shiga toxin-converting bacteriophages (Stx phages): These lysogenic phages integrate into the STEC genome, encoding Stx production.


Secreted Autoaggregative Signaling Molecules (SAAs): SAAs promote bacterial aggregation, facilitating colonization and enhancing cell-to-cell contact for efficient Stx delivery.


Enterocyte effacement proteins: These proteins contribute to the formation of attaching and effacing (A/E) lesions, further compromising the intestinal barrier.


Understanding the intricate interplay between these virulence factors is crucial for developing targeted therapeutic interventions.



Conclusion


STEC strains, disguised amongst the commensal E. coli population, pose a significant public health threat. Their arsenal, with Shiga toxins as the centerpiece, disrupts intestinal function and can lead to life-threatening complications. Deciphering the intricate mechanisms of Stx action and the interplay with other virulence factors paves the way for the development of novel diagnostics, therapeutic strategies, and preventive measures to combat STEC infections.

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