Location: Animal Parasitic Diseases Laboratory
Title: Comparative genomics of the major parasitic wormsAuthor
BEASELY, HELEN - Wellcome Trust Sanger Institute | |
BENNETT, HAYLEY - Wellcome Trust Sanger Institute | |
COGHLAN, AVRIL - Wellcome Trust Sanger Institute | |
COTTON, JAMES - Wellcome Trust Sanger Institute | |
DOYLE, STEPHEN - Wellcome Trust Sanger Institute | |
GORDON, DARIA - Wellcome Trust Sanger Institute | |
HARSHA, BHAVANA - Wellcome Trust Sanger Institute | |
HUCKVALE, THOMAS - Wellcome Trust Sanger Institute | |
LOMAX, JANE - Wellcome Trust Sanger Institute | |
HOLROYD, NANCY - Wellcome Trust Sanger Institute | |
REID, ADAM - Wellcome Trust Sanger Institute | |
RIBEIRO, DIOGO - Wellcome Trust Sanger Institute | |
RINALDI, GABRIEL - Wellcome Trust Sanger Institute | |
SHAFIE, MYRIAM - Wellcome Trust Sanger Institute | |
STANLEY, ELEANOR - Wellcome Trust Sanger Institute | |
TRACEY, ALAN - Wellcome Trust Sanger Institute | |
BERRIMAN, MATTHEW - Wellcome Trust Sanger Institute | |
HALLSWORTH-PEPIN, KYMBERLIE - Washington University School Of Medicine | |
MARTIN, JOHN - Washington University School Of Medicine | |
OZERSKY, PHILIP - Washington University School Of Medicine | |
ROSA, BRUCE - Washington University School Of Medicine | |
TYAGI, RAHUL - Washington University School Of Medicine | |
ZHANG, XU - Washington University School Of Medicine | |
MITREVA, MAKEDONKA - Washington University School Of Medicine | |
LAETSCH, DOMINIK - University Of Edinburgh | |
KOUTSOVOULOS, GEORGIOS - University Of Edinburgh | |
KUMAR, SUJAI - University Of Edinburgh | |
KAUR, GAGANJOT - University Of Edinburgh | |
BLAXTER, MARK - University Of Edinburgh | |
HOWE, KEVIN - European Molecular Biology Laboratory | |
LEACH, ANDREW - European Molecular Biology Laboratory | |
MUTOWO, PRUDENCE - European Molecular Biology Laboratory | |
RAWLINGS, NEIL - European Molecular Biology Laboratory | |
KUO, TZU-HAO - Biodiversity Research Center, Academia Sinica (BRCAS) | |
LEE, TRACY - Biodiversity Research Center, Academia Sinica (BRCAS) | |
KE, HUEI-MIEN - Biodiversity Research Center, Academia Sinica (BRCAS) | |
TSAI, ISHENG - Biodiversity Research Center, Academia Sinica (BRCAS) | |
WHEELER, NICOLAS - Iowa State University | |
DAY, TIM - Iowa State University | |
ZAMANIAN, MOSTAFA - University Of Wisconsin | |
BEECH, ROBIN - McGill University - Canada | |
PARKINSON, JOHN - University Of Toronto | |
SESHADRI, SWAPNA - University Of Toronto | |
KIKUCHI, TAISEI - University Of Miyazaki | |
MAIZELS, RICK - University Of Glasgow | |
PARTONO, FELIX - University Of Indonesia Faculty Of Medicine | |
BABAYAN, SIMON - University Of Glasgow | |
ALLEN, JUDITH - University Of Edinburgh | |
O'BOYLE, NOEL - Nextmove Software Ltd | |
WANG, LIAN-CHEN - Chang Gung University | |
OSUNA, ANTONIO - Universidad De Granada | |
CRUZ-BUSTOS, TERESA - Universidad De Granada | |
SAMBLAS, MERCEDES - Universidad De Granada | |
CUELLAR, CARMEN - Complutense University Of Madrid (UCM) | |
COOPER, PHILIP - University Of London | |
DEVANEY, EILEEN - University Of Glasgow | |
HARCUS, YVONNE - University Of Edinburgh | |
HODGKINSON, JANE - Liverpool University | |
BAH, GERMANUS - Institute Of Agricultural Research For Development (IRAD) | |
TANYA, VINCENT - Institute Of Agricultural Research For Development (IRAD) | |
EBERHARD, MARK - Centers For Disease Control And Prevention (CDC) - United States | |
ASANO, KAZUHITO - Showa University School Of Medicine | |
RODRIGUEZ, PILAR - University Of La Laguna | |
SATO, HIROSHI - Yamaguchi University | |
GILLEARD, JOHN - University Of Calgary | |
MATTHEWS, JACQUELINE - The Moredun Group | |
COOK, JOSEPH - University Of New Mexico | |
TOLDEO, RAFAEL - Universidad De Valencia | |
SCHOLZ, TOMAS - Biology Centre Of The Ascr Of The Czech Republic, Vvi | |
SCHNYDER, MANUELA - University Of Zurich | |
ALLAN, FIONA - Natural History Museum - London | |
EMERY, AIDAN - Natural History Museum - London | |
OLSON, PETER - Natural History Museum - London | |
ROLLINSON, DAVID - Natural History Museum - London | |
CASTILLO, ESTELA - Universidad De La República | |
KALBE, MARTIN - Max Planck Institute For Evolutionary Biology | |
EOM, KEESEON - Chungbuk National University College Of Medicine | |
HORAK, PETR - Charles University, Czech Republic | |
MITREVA, MAKEDONKA - Washington University School Of Medicine | |
HAWDON, JOHN - George Washington University Medical Center | |
Urban, Joseph | |
Hill, Dolores | |
Zarlenga, Dante | |
BISSET, STEWART - Agresearch | |
PFARR, KENNETH - University Of Bonn | |
MAKEPEACE, BENJAMIN - University Of Liverpool | |
TAYLOR, DAVID - University Of Edinburgh |
Submitted to: Nature Genetics
Publication Type: Peer Reviewed Journal Publication Acceptance Date: 8/16/2018 Publication Date: 11/5/2018 Citation: Beasely, H., Bennett, H.M., Coghlan, A., Cotton, J., Doyle, S.R., Gordon, D., Harsha, B., Huckvale, T., Lomax, J., Holroyd, N., Reid, A.J., Ribeiro, D., Rinaldi, G., Shafie, M., Stanley, E., Tracey, A., Berriman, M., Hallsworth-Pepin, K., Martin, J., Ozersky, P., Rosa, B.A., Tyagi, R., Zhang, X., Mitreva, M., Laetsch, D.R., Koutsovoulos, G., Kumar, S., Kaur, G., Blaxter, M., Howe, K.L., Leach, A.R., Mutowo, P., Rawlings, N., Kuo, T., Lee, T.J., Ke, H., Tsai, I.J., Wheeler, N.J., Day, T.A., Zamanian, M., Beech, R.N., Parkinson, J., Seshadri, S.L., Kikuchi, T., Maizels, R.M., Partono, F., Babayan, S., Allen, J.E., O'Boyle, N., Wang, L., Osuna, A., Cruz-Bustos, T., Samblas, M.G., Cuellar, C., Cooper, P.J., Devaney, E., Harcus, Y., Hodgkinson, J., Bah, G., Tanya, V.N., Eberhard, M.L., Asano, K., Rodriguez, P.F., Sato, H., Gilleard, J.S., Matthews, J.B., Cook, J., Toldeo, R., Scholz, T., Schnyder, M., Allan, F., Emery, A., Olson, P.D., Rollinson, D., Castillo, E., Kalbe, M., Eom, K.S., Horak, P., Mitreva, M., Hawdon, J.M., Urban Jr, J.F., Hill, D.E., Zarlenga, D.S., Bisset, S.A., Pfarr, K., Makepeace, B., Taylor, D.W. 2018. Comparative genomics of the major parasitic worms. Nature Genetics. 5:163-174. https://doi.org/10.1038/s41588-018-0262-1. DOI: https://doi.org/10.1038/s41588-018-0262-1 Interpretive Summary: Over a quarter of the human population is infected with parasitic worms made up of many species of roundworms and flatworms. These infections are generally chronic and rarely lethal, but they represent diseases of poverty that impede economic development. Notably, there is relatively little research investment for these infections that make up eight of the World Health Organization's list of 20 most neglected tropical diseases of humans and that have a costly impact on the livestock industry worldwide. A limited spectrum of drugs are available to treat these infections and resistance is common in farm animals. Repeated mass drug administration in human populations increases the risk of resistance to human. There are no vaccines for humans, few for animals, and the commonly-used anti-plant-parasitic compounds may have negative environmental impact. Comparing the genome biology of parasitism between the broad category of roundworms and flatworms could reveal common strategies employed to subvert host defenses and that exacerbate the response to infection increasing the intensity of disease. In this study, a combined 36 published genomes with new assemblies for 31 roundworm and 14 for flatworm species were analyzed as part of the largest genome comparison to date of parasitic and non-parasitic worms. The data was used to identify gene families associated with the evolution of major parasitic groups, and to accelerate the search for novel control strategies and interventions, including a mined-dataset of more than 1.4 million genes that can be used to predict new drug targets and drugs. This work has broad application to the development of tools to manage these infections in humans, livestock and plants. Technical Abstract: Parasitic nematodes (roundworms) and platyhelminths (flatworms) cause debilitating chronic infections of humans and animals, decimate crop production and are a major impediment to socioeconomic development. Here we compare the genomes of 81 nematode and platyhelminth species, including those of 76 parasites. From 1.4 million genes, we identify gene family births and hundreds of large expanded gene families at key nodes in the phylogeny that are relevant to parasitism. Examples include gene families that modulate host immune responses, enable parasite migration though host tissues or allow the parasite to feed. We use a wide-ranging in silico screen to identify and prioritize new potential drug targets and compounds for testing. We also uncover lineage-specific differences in core metabolism and in protein families historically targeted for drug development. This is the broadest comparative study to date of the genomes of parasitic and non-parasitic worms. It provides a transformative new resource for the research community to understand and combat the diseases that parasitic worms cause. |