Expression of the VapD protein by Helicobacter pylori during intracellular infection

Alejandro Flores-Alanis1, Gabriela Delgado1, Carlos Santiago-Olivares1

  • 1Departamento de Microbiología y Parasitología, Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico City, Mexico.

Insights

Helicobacter pylori persists inside host cells, aided by virulence-associated protein D (VapD). This study confirms VapD protein expression and intracellular localization during H. pylori infection, supporting its role in chronic infections.

Area of Science:

  • Microbiology
  • Cell Biology
  • Infectious Diseases

Background:

  • Helicobacter pylori establishes chronic infections by persisting intracellularly.
  • The virulence-associated protein D (VapD) gene is upregulated during intracellular H. pylori infection.
  • Previous studies linked VapD to bacterial persistence, but its protein expression and localization were unconfirmed.

Purpose of the Study:

  • To detect and localize the VapD protein during H. pylori intracellular infection within eukaryotic cells.

Main Methods:

  • Co-culture of H. pylori strain 26695 with AGS cells.
  • Immunofluorescence microscopy using polyclonal antibodies against VapD.
  • Confocal microscopy to confirm intracellular localization.
  • Use of H. pylori strain Tx30a (vapD-deficient) as a negative control.

Main Results:

  • VapD protein expression was detected specifically in AGS cells infected with H. pylori strain 26695.
  • Confocal microscopy confirmed intracellular localization of VapD, coinciding with bacterial presence.
  • A high percentage of infected cells showed positive VapD signals.

Conclusions:

  • This study provides the first direct evidence of VapD protein expression during H. pylori intracellular infection.
  • Confirms VapD production at the protein level, supporting its role in the intracellular survival of H. pylori.
  • Reinforces the association of VapD with the intracellular lifestyle of H. pylori, a key factor in chronic infections.

Related Concept Videos

Peptic Ulcer01:27

Peptic Ulcer

Peptic ulcers are erosive lesions of the gastric or duodenal lining, most commonly caused by Helicobacter pylori infection. This Gram-negative, helical bacterium has adapted to survive the stomach’s acidic environment by producing urease, which converts urea into ammonia and carbon dioxide. The ammonia neutralizes gastric acid in the bacterium’s immediate environment, allowing colonization of the gastric mucosa. H. pylori attaches to mucus-secreting epithelial cells, penetrates the...
23
Regulation of Bacterial Virulence01:28

Regulation of Bacterial Virulence

Pathogenic bacteria employ a range of regulatory mechanisms to modulate the expression of virulence genes in response to environmental and host-derived signals. These mechanisms ensure that virulence factors are expressed only under favorable conditions, thereby optimizing infection and survival strategies.Mechanisms of Virulence RegulationKey regulatory strategies include:Two-Component Systems: These consist of a membrane-bound sensor kinase and a cytoplasmic response regulator. Environmental...
14
Immune Response Against Viral Pathogens01:29

Immune Response Against Viral Pathogens

The immune system's response to viral infections is a complex and coordinated process involving natural killer (NK) cells, T cell-mediated responses, and antibody-mediated responses.
NK Cells
NK cells are a crucial part of our innate immune system, acting as the first line of defense against viral infections. These cells can recognize and kill infected cells without prior exposure to the virus, effectively slowing down the spread of infection. Additionally, NK cells produce proinflammatory...
2.5K
Pathophysiology of Peptic Ulcer Disease: Injurious Factors01:22

Pathophysiology of Peptic Ulcer Disease: Injurious Factors

Peptic ulcers are sores on the stomach's inner lining and the upper small intestine, which are the result of disruptions in the mucosal layer that houses parietal cells which produce gastric acid, and chief cells which secrete pepsinogen.
In the antrum region, G cells secrete the gastrin hormone that binds to gastrin-cholecystokinin-B (CCK2) receptors on parietal and enterochromaffin-like (ECL) cells in the fundic glands. Simultaneously, the vagus nerve releases acetylcholine, which binds...
1.5K
Peptic Ulcer Disease III: Clinical Manifestations and Diagnostic Studies01:28

Peptic Ulcer Disease III: Clinical Manifestations and Diagnostic Studies

Peptic ulcer disease (PUD) presents with diverse symptoms depending on the location and severity of the ulcer. Clinical manifestations of peptic ulcer include dull pain and a burning sensation in the mid-epigastric region.
Few clinical manifestations differentiate gastric ulcers from duodenal ulcers. Distinctions in the location, timing, and pain relief are crucial for healthcare providers in differentiating between gastric and duodenal ulcers during clinical assessments.
766
Treating Helicobacter pylori in Peptic Ulcers: Antimicrobial Therapy01:16

Treating Helicobacter pylori in Peptic Ulcers: Antimicrobial Therapy

Helicobacter pylori, a resilient gram-negative bacterium, can thrive in the stomach's harsh, acidic environment. Infection with H. pylori leads to a cascade of events within the stomach lining. One of the critical disruptions caused by this bacterium is the interference with somatostatin production, a hormone responsible for regulating acid secretion. This interference tips the balance, escalating acid secretion and diminishing bicarbonate levels. This imbalance compromises the defensive...
2.0K