UPSC MainsZOOLOGY-PAPER-I201415 Marks
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Q7.

What is Parasitism? Give an account of the life cycle of Wucheraria bancrofti and add a note on the pathogenicity and control of the disease caused by this parasite.

How to Approach

This question requires a detailed understanding of parasitism, specifically focusing on *Wuchereria bancrofti*, the causative agent of lymphatic filariasis. The answer should begin with a clear definition of parasitism, followed by a comprehensive description of the parasite's life cycle. Crucially, it must then address the pathogenicity of the disease and outline control measures. A structured approach – definition, life cycle (stages, vectors), pathogenicity (clinical manifestations), and control (preventive & curative) – is recommended. Use of diagrams (though not possible in text format) should be mentally visualized while writing.

Model Answer

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Introduction

Parasitism is a symbiotic relationship between organisms where one organism, the parasite, benefits at the expense of the other, the host. This interaction can range from mild inconvenience to severe disease and even death for the host. Lymphatic filariasis, commonly known as elephantiasis, is a debilitating parasitic disease affecting millions globally, primarily in tropical and subtropical regions. It is caused by thread-like filarial worms, with *Wuchereria bancrofti* being the most prevalent species responsible for approximately 90% of cases. Understanding the life cycle, pathogenicity, and control strategies of this parasite is crucial for effective public health interventions.

What is Parasitism?

Parasitism is a type of symbiotic relationship, specifically an association between two different organisms where one organism (the parasite) benefits by deriving nutrients at the expense of the other organism (the host). Parasites can be ectoparasites (living on the surface of the host, e.g., ticks) or endoparasites (living inside the host, e.g., *Wuchereria bancrofti*). The relationship is often harmful to the host, causing varying degrees of damage and disease.

Life Cycle of *Wuchereria bancrofti*

The life cycle of *Wuchereria bancrofti* is complex, involving both human and mosquito vectors. It can be broadly divided into the following stages:

  • Infective Stage: Third-stage larvae (L3)
  • Vector: *Culex*, *Anopheles*, and *Aedes* mosquitoes
  • Human Host: The cycle unfolds within the human lymphatic system.

The life cycle can be described in the following steps:

  1. Mosquito Ingestion: A mosquito ingests microfilariae (L1 larvae) during a blood meal from an infected human.
  2. Development in Mosquito: Within the mosquito, microfilariae migrate to the thoracic muscles and develop into second-stage larvae (L2). They then molt into infective third-stage larvae (L3). This process takes approximately 10-14 days.
  3. Transmission to Human: When the infected mosquito takes a blood meal from a human, the L3 larvae are deposited onto the skin and enter the human body through the bite wound.
  4. Migration and Maturation: L3 larvae migrate to the lymphatic vessels and mature into adult worms (male and female). This maturation process takes about 6-12 months.
  5. Reproduction: Adult worms reside in the lymphatic vessels, primarily in the lower limbs, and reproduce sexually, releasing microfilariae into the lymphatic system and bloodstream.
  6. Microfilariae Circulation: Microfilariae exhibit nocturnal periodicity, meaning they are most abundant in the peripheral blood during the night. This nocturnal pattern is linked to the feeding habits of the mosquito vectors.

Pathogenicity of *Wuchereria bancrofti*

The pathogenicity of *Wuchereria bancrofti* is primarily due to the inflammatory response triggered by the presence of adult worms in the lymphatic vessels and the subsequent lymphatic obstruction. The clinical manifestations can be categorized into:

  • Acute Lymphangitis: Characterized by fever, chills, and inflammation of the lymphatic vessels.
  • Chronic Lymphoedema: The most common manifestation, resulting from lymphatic obstruction and accumulation of lymph fluid in the tissues, leading to swelling of the limbs, scrotum (hydrocele in males), and breasts.
  • Tropical Pulmonary Eosinophilia (TPE): A less common manifestation, characterized by nocturnal cough, wheezing, and eosinophilia (increased eosinophils in the blood).
  • Elephantiasis: Severe, chronic lymphoedema leading to thickening and hardening of the skin and subcutaneous tissues.

The damage caused by the parasite is not directly due to tissue destruction but rather to the host's immune response and the resulting lymphatic damage.

Control of Lymphatic Filariasis

The control of lymphatic filariasis relies on a combination of preventive and curative strategies:

  • Mass Drug Administration (MDA): The cornerstone of filariasis control programs. It involves administering anti-filarial drugs (diethylcarbamazine (DEC), ivermectin, and albendazole) to the entire population at risk, regardless of whether they are infected.
  • Vector Control: Reducing mosquito populations through measures such as insecticide spraying, larviciding, and environmental management (e.g., eliminating mosquito breeding sites).
  • Improved Sanitation: Reducing mosquito breeding sites through improved drainage and waste management.
  • Patient Management: Providing supportive care to patients with lymphoedema and hydrocele, including hygiene education, skin care, and physiotherapy.
  • Disease Surveillance: Monitoring the prevalence of infection through blood surveys and identifying areas where MDA needs to be intensified.

The Global Programme to Eliminate Lymphatic Filariasis (GPELF), launched by the World Health Organization (WHO) in 2000, aims to eliminate lymphatic filariasis as a public health problem by 2030.

Conclusion

*Wuchereria bancrofti* remains a significant public health challenge in many tropical and subtropical countries. A thorough understanding of its life cycle and pathogenicity is essential for implementing effective control strategies. The success of the GPELF hinges on sustained MDA programs, robust vector control measures, and comprehensive patient care. Continued research into novel diagnostic tools and therapeutic interventions is also crucial for achieving the ultimate goal of eliminating lymphatic filariasis globally.

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

Microfilariae
Immature larvae of filarial worms, found in the blood or lymphatic system of infected individuals. They are the form ingested by mosquitoes.
Nocturnal Periodicity
The phenomenon where microfilariae exhibit peak density in the peripheral blood during the night, coinciding with the feeding activity of mosquito vectors.

Key Statistics

Approximately 51 million people are currently infected with lymphatic filariasis globally, with over 1.6 billion people at risk of infection (WHO, 2023 - knowledge cutoff).

Source: World Health Organization (WHO)

Approximately 90% of lymphatic filariasis cases are caused by *Wuchereria bancrofti* (WHO, 2022 - knowledge cutoff).

Source: World Health Organization (WHO)

Examples

MDA in India

India has been actively implementing MDA programs since 2004, using a triple drug therapy (DEC, albendazole, and ivermectin) to eliminate lymphatic filariasis. Significant progress has been made, with a substantial reduction in the prevalence of infection in many endemic areas.

Frequently Asked Questions

Can lymphatic filariasis be cured?

While there is no cure for the existing lymphatic damage (lymphoedema), the infection can be stopped by killing the adult worms with anti-filarial drugs. Early treatment can prevent further progression of the disease.

Topics Covered

BiologyZoologyParasitologyParasitesFilariasisPublic Health