How is Asia-like Artemisinin Resistance Emerging in Africa?

Context:

  • A recent global genetic study has revealed the emergence of artemisinin resistance in Africa, showing patterns similar to early resistance signals observed earlier in Southeast Asia.
  • This development poses a serious threat to global malaria elimination efforts, especially as Africa accounts for the majority of malaria cases and deaths worldwide.

Key Highlights:

Scientific Background / Drug Details

  • Artemisinin, derived from the Artemisia annua plant, was discovered in China under Project 523, led by Tu Youyou.
  • Artemisinin-based Combination Therapies (ACTs) are the global first-line treatment against Plasmodium falciparum malaria.

Genetic Findings

  • Resistance is linked to mutations in the kelch13 gene of the malaria parasite.
  • The study analysed 1.1 lakh parasite samples from 73 countries over 43 years.
  • 492 unique kelch13 mutations were identified.
  • High prevalence regions in Africa:
    • Rwanda
    • Uganda
    • Tanzania
    • Eritrea
    • Sudan
    • Ethiopia

Nature of Resistance in Africa

  • Unlike Southeast Asia, where resistance spread via imported mutant strains, African resistance appears to be independently emerging.
  • Kelch13 mutations allow parasites to enter a slow-growth survival mode, reducing drug effectiveness.

Contributing Factors

  • Incomplete treatment adherence
  • Use of single-drug therapies
  • Weak genetic surveillance systems
  • Reduced malaria funding
  • COVID-19 disruptions leading to fewer post-2019 samples and data gaps

Significance / Concerns

  • Threatens the efficacy of ACTs, the backbone of malaria control.
  • Risk of large-scale treatment failure in Africa.
  • Could reverse decades of progress in malaria reduction.

Relevant Prelims Points:

  • Issue: Emerging artemisinin resistance in Africa.
  • Causes:
    • Genetic mutations in kelch13 gene
    • Drug pressure from widespread ACT use
    • Poor monitoring and misuse of antimalarials
  • Government / Global Initiatives:
    • WHO Global Malaria Programme
    • Roll Back Malaria Partnership
  • Benefits of ACTs:
    • High efficacy
    • Reduced mortality
  • Challenges:
    • Drug resistance
    • Weak health systems
    • Surveillance gaps
  • Impact:
    • Increased malaria burden
    • Global health security risk

Relevant Mains Points:

  • Key Concepts & Definitions:
    • Plasmodium falciparum: Deadliest malaria parasite species.
    • Genetic Surveillance: Monitoring pathogen mutations to track resistance.
  • Static + Current Linkages:
    • Role of WHO in resistance monitoring.
    • Lessons from Southeast Asia’s resistance spread.
  • International Dimensions:
    • Need for cross-border data sharing.
    • Global funding cooperation.
  • Way Forward:
    • Strengthen genetic surveillance networks in Africa.
    • Ensure strict treatment adherence.
    • Monitor resistance to partner drugs in ACTs.
    • Diversify antimalarial drug strategies.
    • Restore funding and post-pandemic data collection mechanisms.

UPSC Relevance (GS-wise):

  • GS Paper 3: Science & Technology (Biotechnology, Drug Resistance), Environment & Ecology (Disease burden).
  • GS Paper 2: International Relations (Global health cooperation, WHO).
  • Prelims: Drugs, diseases, genetic mutations, international health initiatives.
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