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Gene's role in malaria drug resistance proved

In research supported by the National Institute of Allergy and Infectious Diseases (NIAID), David A. Fidock, Ph.D., has proved conclusively that the malaria-causing parasite Plasmodium falciparum became resistant to the anti-malarial drug chloroquine through mutations in a single parasite gene. Paradoxically, this gene acts as both a shield and a chink in the armor of P. falciparum by making the parasite less susceptible to chloroquine, but more susceptible to some other anti-malarials. Dr. Fidock and members of his laboratory at the Albert Einstein College of Medicine published their findings in this week's edition of the journal Science as part of a special issue that also includes publication of the genetic sequence of Anopheles gambiae, a mosquito that transmits malaria.

Chloroquine helped control or eliminate malaria throughout much of the world when it became widely used in the years following World War II. Chloroquine-resistant (CQR) P. falciparum emerged in Southeast Asia and South America in the 1950s and spread through much of Africa within two decades. Compared with chloroquine, drugs to treat CQR malaria are more expensive and cause more side effects while working less effectively. Resurgent malaria brings death and suffering to hundreds of millions and seriously impedes economic growth throughout malarious regions.

"Dr. Fidock's work provides direct and conclusive evidence of what was formerly only suspected; namely, that mutations in a single gene give P. falciparum the ability to resist chloroquine," says Michael Gottlieb, Ph.D., chief of NIAID's parasitology and international programs branch. "Curiously, the presence of this gene, named pfcrt, also appears to make P. falciparum more susceptible to two other anti-malarial drugs, artemisinin and quinine," he adds.

The gene finding has potentially important implications for malaria treatment and control, notes Dr. Gottlieb. "If we can develop further the methods we h
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Contact: Anne A. Oplinger
aoplinger@niaid.nih.gov
301-402-1663
NIH/National Institute of Allergy and Infectious Diseases
2-Oct-2002


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