Abstract
MalariaGEN is a data-sharing network that enables groups around the world to work together on the genomic epidemiology of malaria. Here we describe a new release of curated genome variation data on 7,000 Plasmodium falciparum samples from MalariaGEN partner studies in 28 malaria-endemic countries. High-quality genotype calls on 3 million single nucleotide polymorphisms (SNPs) and short indels were produced using a standardised analysis pipeline. Copy number variants associated with drug resistance and structural variants that cause failure of rapid diagnostic tests were also analysed. Almost all samples showed genetic evidence of resistance to at least one antimalarial drug, and some samples from Southeast Asia carried markers of resistance to six commonly-used drugs. Genes expressed during the mosquito stage of the parasite life-cycle are prominent among loci that show strong geographic differentiation. By continuing to enlarge this open data resource we aim to facilitate research into the evolutionary processes affecting malaria control and to accelerate development of the surveillance toolkit required for malaria elimination.
Original language | English |
---|---|
Article number | 42 |
Pages (from-to) | 1-31 |
Number of pages | 31 |
Journal | Wellcome Open Research |
Volume | 6 |
DOIs | |
State | Published - 2021 |
Externally published | Yes |
Keywords
- Data resource
- Drug resistance
- Evolution
- Genomic epidemiology
- Genomics
- Malaria
- Plasmodium falciparum
- Population genetics
- Rapid diagnostic test failure
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In: Wellcome Open Research, Vol. 6, 42, 2021, p. 1-31.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - An open dataset of Plasmodium falciparum genome variation in 7,000 worldwide samples
AU - Gen, Malaria
AU - Ahouidi, Ambroise
AU - Ali, Mozam
AU - Almagro-Garcia, Jacob
AU - Amambua-Ngwa, Alfred
AU - Amaratunga, Chanaki
AU - Amato, Roberto
AU - Amenga-Etego, Lucas
AU - Andagalu, Ben
AU - Anderson, Tim J.C.
AU - Andrianaranjaka, Voahangy
AU - Apinjoh, Tobias
AU - Ariani, Cristina
AU - Ashley, Elizabeth A.
AU - Auburn, Sarah
AU - Awandare, Gordon A.
AU - Ba, Hampate
AU - Baraka, Vito
AU - Barry, Alyssa E.
AU - Bejon, Philip
AU - Bertin, Gwladys I.
AU - Boni, Maciej F.
AU - Borrmann, Steffen
AU - Bousema, Teun
AU - Branch, Oralee
AU - Bull, Peter C.
AU - Busby, George B.J.
AU - Chookajorn, Thanat
AU - Chotivanich, Kesinee
AU - Claessens, Antoine
AU - Conway, David
AU - Craig, Alister
AU - D'Alessandro, Umberto
AU - Dama, Souleymane
AU - Day, Nicholas PJ
AU - Denis, Brigitte
AU - Diakite, Mahamadou
AU - Djimdé, Abdoulaye
AU - Dolecek, Christiane
AU - Dondorp, Arjen M.
AU - Drakeley, Chris
AU - Drury, Eleanor
AU - Duffy, Patrick
AU - Echeverry, Diego F.
AU - Egwang, Thomas G.
AU - Erko, Berhanu
AU - Fairhurst, Rick M.
AU - Faiz, Abdul
AU - Fanello, Caterina A.
AU - Fukuda, Mark M.
AU - Gamboa, Dionicia
AU - Ghansah, Anita
AU - Golassa, Lemu
AU - Goncalves, Sonia
AU - Hamilton, William L.
AU - Harrison, G. L.Abby
AU - Hart, Lee
AU - Henrichs, Christa
AU - Hien, Tran Tinh
AU - Hill, Catherine A.
AU - Hodgson, Abraham
AU - Hubbart, Christina
AU - Imwong, Mallika
AU - Ishengoma, Deus S.
AU - Jackson, Scott A.
AU - Jacob, Chris G.
AU - Jeffery, Ben
AU - Jeffreys, Anna E.
AU - Johnson, Kimberly J.
AU - Jyothi, Dushyanth
AU - Kamaliddin, Claire
AU - Kamau, Edwin
AU - Kekre, Mihir
AU - Kluczynski, Krzysztof
AU - Kochakarn, Theerarat
AU - Konaté, Abibatou
AU - Kwiatkowski, Dominic P.
AU - Kyaw, Myat Phone
AU - Lim, Pharath
AU - Lon, Chanthap
AU - Loua, Kovana M.
AU - Maïga-Ascofaré, Oumou
AU - Malangone, Cinzia
AU - Manske, Magnus
AU - Marfurt, Jutta
AU - Marsh, Kevin
AU - Mayxay, Mayfong
AU - Miles, Alistair
AU - Miotto, Olivo
AU - Mobegi, Victor
AU - Mokuolu, Olugbenga A.
AU - Montgomery, Jacqui
AU - Mueller, Ivo
AU - Newton, Paul N.
AU - Nguyen, Thuy
AU - Nguyen, Thuy Nhien
AU - Noedl, Harald
AU - Nosten, François
AU - Noviyanti, Rintis
AU - Nzila, Alexis
AU - Ochola-Oyier, Lynette I.
AU - Ocholla, Harold
AU - Oduro, Abraham
AU - Omedo, Irene
AU - Onyamboko, Marie A.
AU - Ouedraogo, Jean Bosco
AU - Oyebola, Kolapo
AU - Pearson, Richard D.
AU - Peshu, Norbert
AU - Phyo, Aung Pyae
AU - Plowe, Chris V.
AU - Price, Ric N.
AU - Pukrittayakamee, Sasithon
AU - Randrianarivelojosia, Milijaona
AU - Rayner, Julian C.
AU - Ringwald, Pascal
AU - Rockett, Kirk A.
AU - Rowlands, Katherine
AU - Ruiz, Lastenia
AU - Saunders, David
AU - Shayo, Alex
AU - Siba, Peter
AU - Simpson, Victoria J.
AU - Stalker, Jim
AU - Su, Xin zhuan
AU - Sutherland, Colin
AU - Takala-Harrison, Shannon
AU - Tavul, Livingstone
AU - Thathy, Vandana
AU - Tshefu, Antoinette
AU - Verra, Federica
AU - Vinetz, Joseph
AU - Wellems, Thomas E.
AU - Wendler, Jason
AU - White, Nicholas J.
AU - Wright, Ian
AU - Yavo, William
AU - Ye, Htut
N1 - Funding Information: Grant information: The sequencing, analysis, informatics and management of the Community Project are supported by Wellcome Funding Information: This study was conducted by the MalariaGEN Plasmodium falciparum Community Project, and was made possible by clinical parasite samples contributed by partner studies, whose investigators are represented in the author list and in the associated data release (https://www.malariagen.net/resource/26). This research was supported in part by the Intramural Research Programme of the NIH, NIAID. In addition, the authors would like to thank the following individuals who contributed to partner studies, making this study possible: Dr Eugene Laman for work in sample collection in the Republic of Guinea; Dr Abderahmane Tandia and Dr Yacine Deh and Dr Samuel Assefa for work in sample collection in Mauritania; Dr Ibrahim Sanogo for work in sample collection in Mali; Dr James Abugri and Dr Nicholas Amoako for work coordinating sample collection in Ghana. Genome sequencing was undertaken by the Wellcome Sanger Institute and we thank the staff of the Wellcome Sanger Institute Sample Logistics, Sequencing, and Informatics facilities for their contribution. The authors would like to thank Erin Courtier for her assistance with the journal submission. The views expressed here are solely those of the authors and do not reflect the views, policies or positions of the U.S. Government or Department of Defense. Material has been reviewed by the Walter Reed Army Institute of Research. There is no objection to its presentation and/or publication. The opinions or assertions contained herein are the private views of the author, and are not to be construed as official, or as reflecting true views of the Department of the Army or the Department of Defense. The investigators have adhered to the policies for protection of human subjects as prescribed in AR 70?25. PR is a staff member of the World Health Organization. PR alone is responsible for the views expressed in this publication and they do not necessarily represent the decisions, policy or views of the World Health Organization. Funding Information: through Sanger Institute core funding (098051), a Strategic Award (090770/Z/09/Z) and the Wellcome Centre for Human Genetics core funding (203141/Z/16/Z), by the MRC Centre for Genomics and Global Health which is jointly funded by the Medical Research Council and the Department for International Development (DFID) (G0600718; M006212), and by the Bill & Melinda Gates Foundation (OPP1204628). Funding Information: This study was conducted by the MalariaGEN Plasmodium falciparum Community Project, and was made possible by clinical parasite samples contributed by partner studies, whose investigators are represented in the author list and in the associated data release (https://www.malariagen.net/resource/26). This research was supported in part by the Intramural Research Programme of the NIH, NIAID. In addition, the authors would like to thank the following individuals who contributed to partner studies, making this study possible: Dr Eugene Laman for work in sample collection in the Republic of Guinea; Dr Abderahmane Tandia and Dr Yacine Deh and Dr Samuel Assefa for work in sample collection in Mauritania; Dr Ibrahim Sanogo for work in sample collection in Mali; Dr James Abugri and Dr Nicholas Amoako for work coordinating sample collection in Ghana. Genome sequencing was undertaken by the Wellcome Sanger Institute and we thank the staff of the Wellcome Sanger Institute Sample Logistics, Sequencing, and Informatics facilities for their contribution. The authors would like to thank Erin Courtier for her assistance with the journal submission. The views expressed here are solely those of the authors and do not reflect the views, policies or positions of the U.S. Publisher Copyright: © 2021. MalariaGEN et al.
PY - 2021
Y1 - 2021
N2 - MalariaGEN is a data-sharing network that enables groups around the world to work together on the genomic epidemiology of malaria. Here we describe a new release of curated genome variation data on 7,000 Plasmodium falciparum samples from MalariaGEN partner studies in 28 malaria-endemic countries. High-quality genotype calls on 3 million single nucleotide polymorphisms (SNPs) and short indels were produced using a standardised analysis pipeline. Copy number variants associated with drug resistance and structural variants that cause failure of rapid diagnostic tests were also analysed. Almost all samples showed genetic evidence of resistance to at least one antimalarial drug, and some samples from Southeast Asia carried markers of resistance to six commonly-used drugs. Genes expressed during the mosquito stage of the parasite life-cycle are prominent among loci that show strong geographic differentiation. By continuing to enlarge this open data resource we aim to facilitate research into the evolutionary processes affecting malaria control and to accelerate development of the surveillance toolkit required for malaria elimination.
AB - MalariaGEN is a data-sharing network that enables groups around the world to work together on the genomic epidemiology of malaria. Here we describe a new release of curated genome variation data on 7,000 Plasmodium falciparum samples from MalariaGEN partner studies in 28 malaria-endemic countries. High-quality genotype calls on 3 million single nucleotide polymorphisms (SNPs) and short indels were produced using a standardised analysis pipeline. Copy number variants associated with drug resistance and structural variants that cause failure of rapid diagnostic tests were also analysed. Almost all samples showed genetic evidence of resistance to at least one antimalarial drug, and some samples from Southeast Asia carried markers of resistance to six commonly-used drugs. Genes expressed during the mosquito stage of the parasite life-cycle are prominent among loci that show strong geographic differentiation. By continuing to enlarge this open data resource we aim to facilitate research into the evolutionary processes affecting malaria control and to accelerate development of the surveillance toolkit required for malaria elimination.
KW - Data resource
KW - Drug resistance
KW - Evolution
KW - Genomic epidemiology
KW - Genomics
KW - Malaria
KW - Plasmodium falciparum
KW - Population genetics
KW - Rapid diagnostic test failure
UR - http://www.scopus.com/inward/record.url?scp=85103577104&partnerID=8YFLogxK
U2 - 10.12688/wellcomeopenres.16168.2
DO - 10.12688/wellcomeopenres.16168.2
M3 - Article
AN - SCOPUS:85103577104
SN - 2398-502X
VL - 6
SP - 1
EP - 31
JO - Wellcome Open Research
JF - Wellcome Open Research
M1 - 42
ER -