Nitric Oxide Synthase 2Lambaréné(G‐954C), Increased Nitric Oxide Production, and Protection against Malaria
Author(s) -
Jürgen F. J. Kun,
Benjamin Mordmüller,
Douglas J. Perkins,
Jürgen May,
Odile MercereauPuijalon,
Michael Alpers,
J. Brice Weinberg,
Peter G. Kremsner
Publication year - 2001
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/322037
Subject(s) - nitric oxide , malaria , nitric oxide synthase , ex vivo , biology , polymorphism (computer science) , immunology , microbiology and biotechnology , in vivo , allele , genetics , gene , endocrinology
A point mutation in the promoter of the nitric oxide synthase 2 gene (NOS2), termed NOS2(Lambaréné) (NOS2-G954C), protects heterozygous carriers against severe malaria as effectively as the sickle cell trait. In a prospective longitudinal study, 841 individual infections of initially 200 children (151 wild-type vs. 49 NOS2(Lambaréné) carriers) were monitored for 4 years, to assess the rates of malarial attacks in the 2 groups; carriers of the NOS2(Lambaréné) polymorphism were significantly less likely to experience malarial attacks than were others (P=.002). The distribution of the NOS2(Lambaréné) polymorphism was investigated in malaria-endemic areas. It was found to be present with the highest frequency in Africa and at a lower frequency in Asia. Ex vivo studies showed that cells isolated from people with this polymorphism have a 7-fold higher baseline NOS activity, compared with the levels detected in cells from subjects with the wild-type gene (P=.003).
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