TY - JOUR KW - Animals KW - Disease Models, Animal KW - Epoxide Hydrolases KW - Fish Diseases KW - Genetic Predisposition to Disease KW - Humans KW - leprosy KW - Tuberculosis KW - Zebrafish AU - Tobin DM AU - Vary J AU - Ray J AU - Walsh G AU - Dunstan SJ AU - Bang N AU - Hagge D AU - Khadge S AU - King M AU - Hawn TR AU - Moens C AU - Ramakrishnan L AB -

Exposure to Mycobacterium tuberculosis produces varied early outcomes, ranging from resistance to infection to progressive disease. Here we report results from a forward genetic screen in zebrafish larvae that identify multiple mutant classes with distinct patterns of innate susceptibility to Mycobacterium marinum. A hypersusceptible mutant maps to the lta4h locus encoding leukotriene A(4) hydrolase, which catalyzes the final step in the synthesis of leukotriene B(4) (LTB(4)), a potent chemoattractant and proinflammatory eicosanoid. lta4h mutations confer hypersusceptibility independent of LTB(4) reduction, by redirecting eicosanoid substrates to anti-inflammatory lipoxins. The resultant anti-inflammatory state permits increased mycobacterial proliferation by limiting production of tumor necrosis factor. In humans, we find that protection from both tuberculosis and multibacillary leprosy is associated with heterozygosity for LTA4H polymorphisms that have previously been correlated with differential LTB(4) production. Our results suggest conserved roles for balanced eicosanoid production in vertebrate resistance to mycobacterial infection.

BT - Cell C1 - http://www.ncbi.nlm.nih.gov/pubmed/20211140?dopt=Abstract DA - 2010 Mar 05 DO - 10.1016/j.cell.2010.02.013 IS - 5 J2 - Cell LA - eng N2 -

Exposure to Mycobacterium tuberculosis produces varied early outcomes, ranging from resistance to infection to progressive disease. Here we report results from a forward genetic screen in zebrafish larvae that identify multiple mutant classes with distinct patterns of innate susceptibility to Mycobacterium marinum. A hypersusceptible mutant maps to the lta4h locus encoding leukotriene A(4) hydrolase, which catalyzes the final step in the synthesis of leukotriene B(4) (LTB(4)), a potent chemoattractant and proinflammatory eicosanoid. lta4h mutations confer hypersusceptibility independent of LTB(4) reduction, by redirecting eicosanoid substrates to anti-inflammatory lipoxins. The resultant anti-inflammatory state permits increased mycobacterial proliferation by limiting production of tumor necrosis factor. In humans, we find that protection from both tuberculosis and multibacillary leprosy is associated with heterozygosity for LTA4H polymorphisms that have previously been correlated with differential LTB(4) production. Our results suggest conserved roles for balanced eicosanoid production in vertebrate resistance to mycobacterial infection.

PY - 2010 SP - 717 EP - 30 T2 - Cell TI - The lta4h locus modulates susceptibility to mycobacterial infection in zebrafish and humans. VL - 140 SN - 1097-4172 ER -