UPSC MainsBOTANY-PAPER-I202110 Marks150 Words
Q1.

What are prions? How are these different from viroids? How are prions transmitted?

How to Approach

This question requires a comparative understanding of prions and viroids, both non-conventional infectious agents. The answer should begin by defining prions, then viroids, highlighting their structural and compositional differences. Subsequently, it should detail the transmission mechanisms of prions. A concise, structured approach focusing on composition, structure, replication, and transmission will be effective. The answer should be factual and avoid overly complex biological jargon.

Model Answer

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Introduction

Prions and viroids represent unique challenges to our understanding of infectious agents, as they deviate significantly from the conventional virus-host paradigm. Discovered in the 1980s, these acellular entities are responsible for several neurodegenerative diseases in animals and humans. While both are infectious and cause disease, they differ fundamentally in their composition and mode of replication. Understanding these differences is crucial for developing effective diagnostic and therapeutic strategies. This answer will delineate the nature of prions and viroids, contrasting their characteristics and detailing prion transmission pathways.

Prions: Infectious Proteins

Prions, short for "proteinaceous infectious particles," are misfolded proteins that have the ability to induce normal proteins to adopt the same misfolded shape. This misfolding leads to the formation of aggregates that accumulate in the brain, causing neurodegenerative diseases. The prion protein (PrP) exists in two forms: a normal, cellular form (PrPC) and an abnormal, infectious form (PrPSc). PrPSc is resistant to degradation and triggers the conversion of PrPC to PrPSc, initiating a chain reaction.

Viroids: Infectious RNA

Viroids are the smallest known infectious agents, consisting solely of a small, circular, single-stranded RNA molecule. Unlike viruses, they lack a protein coat. Viroids replicate autonomously within host cells, utilizing the host's RNA polymerase to amplify their RNA genome. They primarily infect plants, causing a variety of diseases characterized by stunted growth and leaf abnormalities.

Key Differences: Prions vs. Viroids

The fundamental difference lies in their composition. Prions are composed entirely of protein, while viroids are composed solely of RNA. This difference dictates their replication mechanisms. Prions propagate by converting normal proteins, whereas viroids replicate using the host's enzymatic machinery. Furthermore, prions primarily affect animals (including humans), while viroids are known to infect only plants.

Feature Prions Viroids
Composition Misfolded protein (PrPSc) Small, circular RNA
Protein Coat Absent Absent
Replication Conversion of normal proteins (PrPC to PrPSc) Host RNA polymerase-mediated replication
Host Range Animals (including humans) Plants
Disease Examples Creutzfeldt-Jakob Disease (CJD), Bovine Spongiform Encephalopathy (BSE) Potato Spindle Tuber Disease, Citrus Exocortis Disease

Prion Transmission

Prion transmission can occur through several routes:

  • Sporadic: Prions arise spontaneously due to the misfolding of normal proteins. This is the most common form of CJD in humans.
  • Inherited: Genetic mutations in the PRNP gene (encoding PrP) increase the likelihood of misfolding and prion disease.
  • Acquired: This occurs through exposure to prion-contaminated materials. Examples include:
    • Iatrogenic: Transmission through medical procedures, such as contaminated surgical instruments or corneal transplants.
    • Consumption of contaminated meat: Variant CJD (vCJD) is linked to the consumption of beef from cattle infected with BSE ("mad cow disease").

Prions are remarkably resistant to conventional sterilization methods, such as autoclaving and irradiation, requiring specialized procedures for inactivation.

Conclusion

In conclusion, prions and viroids represent fascinating and challenging infectious agents. While both are acellular and cause disease, their fundamental differences in composition – protein versus RNA – dictate their replication strategies and host ranges. Prion transmission, particularly through sporadic, inherited, and acquired routes, poses significant public health concerns, necessitating stringent surveillance and preventative measures. Further research into the mechanisms of prion misfolding and viroid replication is crucial for developing effective therapies and mitigating the risks associated with these unique pathogens.

Answer Length

This is a comprehensive model answer for learning purposes and may exceed the word limit. In the exam, always adhere to the prescribed word count.

Additional Resources

Key Definitions

PrPC
Normal, cellular prion protein found throughout the body, particularly in the brain. It is involved in various cellular processes, but its exact function is not fully understood.
Neurodegenerative Disease
A condition characterized by the progressive loss of structure or function of neurons, including the death of neurons. These diseases often worsen over time and can affect movement, memory, and thinking.

Key Statistics

As of 2023, approximately 365 cases of variant Creutzfeldt-Jakob Disease (vCJD) have been reported worldwide, primarily in the United Kingdom.

Source: World Health Organization (WHO) - Knowledge cutoff 2023

The estimated incidence of Creutzfeldt-Jakob Disease (CJD) is approximately 1-2 cases per million people per year globally.

Source: Creutzfeldt-Jakob Disease Foundation - Knowledge cutoff 2023

Examples

Kuru

Kuru is a prion disease historically found among the Fore people of Papua New Guinea. It was transmitted through the practice of endocannibalism, where they consumed the brains of deceased relatives as part of funeral rituals.

Frequently Asked Questions

Are prions considered living organisms?

No, prions are not considered living organisms. They lack nucleic acids (DNA or RNA) and cannot reproduce independently. They are simply misfolded proteins that can induce other proteins to misfold.

Topics Covered

BiologyMicrobiologyPrionsViroidsInfectious Diseases