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Strong contact points between adjacent cells anchor them to each other, forming tissues. Such anchoring junctions are of two types –  adherens junctions and desmosomes. Adherens junctions are abundant in tissues such as  epithelium and endothelium, forming a continuous zone of adhesion called the adhesion belt. In other tissues, such as  heart muscle, they appear as clusters, linking the cells to produce coordinated heart muscle contraction.
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Laminins are heterotrimeric proteins with high molecular mass found in the extracellular matrix. Each laminin molecule is composed of three chains, viz. alpha, beta, and gamma, coded by five, four, and three paralogous genes, respectively. Laminins are categories based on the compositions of the three chains.
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Related Experiment Video

Updated: Mar 16, 2026

Cefoperazone-treated Mouse Model of Clinically-relevant Clostridium difficile Strain R20291
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Clostridium difficile Adhesins.

Séverine Péchiné1, Cécile Denève-Larrazet1, Anne Collignon2

  • 1Unité Bactéries Pathogènes et Santé (UBaPS), Faculté de Pharmacie, Université Paris-Sud, Université Paris-Saclay, 92290, Châtenay Malabry, France.

Methods in Molecular Biology (Clifton, N.J.)
|August 11, 2016
PubMed
Summary

Clostridium difficile adherence to host cells is crucial for intestinal infection. This study details methods to investigate bacterial colonization factors and their adhesive properties.

Keywords:
AdherenceAdhesinsClostridium difficileIntestinal colonizationSurface proteins

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In Vitro Assay of Bacterial Adhesion onto Mammalian Epithelial Cells
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Area of Science:

  • Microbiology
  • Infectious Diseases
  • Gastroenterology

Background:

  • Clostridium difficile causes a range of intestinal diseases, from mild diarrhea to severe colitis.
  • Infection pathogenesis involves spore germination, bacterial multiplication, and toxin production (TcdA, TcdB, CDT).
  • Bacterial adhesins are key factors for C. difficile colonization in the gut.

Purpose of the Study:

  • To describe methods for studying Clostridium difficile adherence to host cells.
  • To present techniques for evaluating bacterial colonization in vivo.
  • To demonstrate the adhesive properties of specific surface proteins.

Main Methods:

  • In vitro assays using epithelial cells to assess C. difficile adherence.
  • In vivo studies in animal models to analyze intestinal colonization.
  • Methods to characterize adhesive surface proteins like Cwp66, GroEL, and FbpA.

Main Results:

  • Established protocols for in vitro and in vivo adherence studies.
  • Demonstrated adhesive capabilities of C. difficile surface proteins.
  • Provided a framework for identifying novel colonization factors.

Conclusions:

  • Adherence mechanisms are critical for C. difficile pathogenesis.
  • The described methods facilitate the study of bacterial colonization factors.
  • Understanding adherence is vital for developing therapeutic strategies against C. difficile infections.