Vesicles as carriers of virulence factors in parasitic protozoan diseases

Ana Claudia Torrecilhas1, Robert I Schumacher, Maria Júlia M Alves

  • 1Departamento de Ciências Biológicas, Campus Diadema, Universidade Federal de São Paulo, UNIFESP, São Paulo, SP, Brazil.

Microbes and Infection
|August 16, 2012
PubMed

Insights

Pathogenic trypanosomatids shed vesicles containing molecules crucial for infection, challenging the view of these structures as mere cellular waste. Understanding vesicle origin and composition is key to their biological function and therapeutic potential.

Area of Science:

  • * Cell biology
  • * Parasitology
  • * Immunology

Background:

  • * Shed vesicles, including exosomes and microparticles, are researched for cell communication and therapeutic applications.
  • * Pathogenic trypanosomatids were previously thought to release vesicles as metabolic waste.
  • * Apicomplexa parasites circulate host-derived vesicles with bound antigens.

Purpose of the Study:

  • * To review how pathogenic trypanosomatids utilize shed vesicles for host interaction.
  • * To compare vesicle shedding mechanisms between trypanosomatids and Apicomplexa.
  • * To highlight the importance of vesicle origin and composition in determining function.

Main Methods:

  • * Literature review of studies on parasitic vesicles.
  • * Comparative analysis of vesicle-mediated interactions in trypanosomatids and Apicomplexa.
  • * Discussion of molecular composition and biological roles of shed vesicles.

Main Results:

  • * Trypanosomatids shed vesicles containing molecules vital for establishing infection.
  • * These vesicles are not merely cellular waste but active participants in host-parasite interactions.
  • * Parasite-derived vesicles play a significant role in modulating the host environment.

Conclusions:

  • * Shed vesicles are critical for trypanosomatid pathogenesis.
  • * Understanding vesicle biology offers insights into host-parasite communication.
  • * Knowledge of vesicle origin and composition can unlock their diagnostic and therapeutic potential.

Related Concept Videos

Intralumenal Vesicles and Multivesicular Bodies01:38

Intralumenal Vesicles and Multivesicular Bodies

Intraluminal vesicles (ILVs) are small vesicles 50-80 nm in diameter formed during the maturation of early endosomes. A specialized endosome containing numerous ILVs is called a multivesicular body (MVB). ILVs contain internalized molecules such as antigens, nucleic acids, proteins, and metabolites. Some of these molecules are released from the MVBs inside exosomes and are transported to other cells. Other MVBs contain molecules that are retained in the ILVs and are later degraded within the...
Overview of Secretory Vesicles01:33

Overview of Secretory Vesicles

Secretory vesicles, also known as dense core vesicles (DCVs), are membrane-bound vesicles that transport secretory proteins, such as hormones or neurotransmitters. Regulated secretory vesicles transport proteins from the trans-Golgi network to the exterior of the cell. Proteins present in regulated secretory vesicles are required to be rapidly exocytosed in large amounts upon a specific stimulus.
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
Diversity of Protists II01:27

Diversity of Protists II

Alveolates are a group of organisms recognized by the presence of alveoli, which are cytoplasmic sacs located beneath the cell membrane. While their function remains uncertain, alveoli may help regulate water balance by controlling how much water enters and leaves the cell. In dinoflagellates, these structures may serve as armor plates. There are three major types of alveolates: ciliates, which move using cilia; dinoflagellates, which use flagella for movement; and apicomplexans, which are...
Intracellular Movement of Viruses and Bacteria01:10

Intracellular Movement of Viruses and Bacteria

Intracellular bacteria and viruses often comprise a group of highly infectious pathogens that can cause several diseases. Bacterial pathogens include those belonging to the genus Rickettsia responsible for conditions such as rocky mountain spotted fever and the Mediterranean spotted fever; Chlamydia, a genus responsible for a sexually transmitted disease; Coxiella burnetii, an agent responsible for Q fever. Viral pathogens include vaccinia—a poxvirus, and herpes simplex virus—a virus that...
Vesicular Tubular Clusters01:45

Vesicular Tubular Clusters

After budding out from the ER membrane, some COPII vesicles lose their coat and fuse with one another to form larger vesicles and interconnected tubules called vesicular tubular clusters or VTCs. These clusters constitute a compartment at the ER-Golgi interface known as ERGIC (Endoplasmic Reticulum Golgi Intermediate Compartment). The ERGIC is a mobile membrane-bound cargo transport system that sorts proteins secreted from ER and delivers them to the Golgi.
With the help of motor proteins such...
Colonisation of Pathogens01:25

Colonisation of Pathogens

Pathogen colonization of host tissues is a critical step in the development of infectious diseases. Various pathogenic microorganisms, including bacteria, fungi, viruses, and protozoa, have evolved complex strategies to attach to, invade, and persist within host environments. These mechanisms enable pathogens to establish infections, evade immune responses, and resist antimicrobial treatments.Attachment to Host CellsIn bacteria, colonization typically begins with adherence to host epithelial...