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Draft genome of the filarial nematode parasite Brugia malayi
Authors:Ghedin Elodie  Wang Shiliang  Spiro David  Caler Elisabet  Zhao Qi  Crabtree Jonathan  Allen Jonathan E  Delcher Arthur L  Guiliano David B  Miranda-Saavedra Diego  Angiuoli Samuel V  Creasy Todd  Amedeo Paolo  Haas Brian  El-Sayed Najib M  Wortman Jennifer R  Feldblyum Tamara  Tallon Luke  Schatz Michael  Shumway Martin  Koo Hean  Salzberg Steven L  Schobel Seth  Pertea Mihaela  Pop Mihai  White Owen  Barton Geoffrey J  Carlow Clotilde K S  Crawford Michael J  Daub Jennifer  Dimmic Matthew W  Estes Chris F  Foster Jeremy M  Ganatra Mehul  Gregory William F  Johnson Nicholas M  Jin Jinming  Komuniecki Richard  Korf Ian
Affiliation:Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA. GhedinE@dom.pitt.edu
Abstract:Parasitic nematodes that cause elephantiasis and river blindness threaten hundreds of millions of people in the developing world. We have sequenced the approximately 90 megabase (Mb) genome of the human filarial parasite Brugia malayi and predict approximately 11,500 protein coding genes in 71 Mb of robustly assembled sequence. Comparative analysis with the free-living, model nematode Caenorhabditis elegans revealed that, despite these genes having maintained little conservation of local synteny during approximately 350 million years of evolution, they largely remain in linkage on chromosomal units. More than 100 conserved operons were identified. Analysis of the predicted proteome provides evidence for adaptations of B. malayi to niches in its human and vector hosts and insights into the molecular basis of a mutualistic relationship with its Wolbachia endosymbiont. These findings offer a foundation for rational drug design.
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