Plasmodium cynomolgi genome sequences provide insight into Plasmodium vivax and the monkey malaria clade

Shin‐Ichiro Tachibana(Osaka University), Steven A. Sullivan(New York University), Satoru Kawai(Dokkyo Medical University), Shota Nakamura(Osaka University), Hyunjae R. Kim(New York University), N. Goto(Osaka University), Nobuko Arisue(Osaka University), Nirianne Palacpac(Osaka University), Hajime Honma(Osaka University), Masanori Yagi(Osaka University), Takahiro Tougan(Osaka University), Yuko Katakai(Corporation for Production and Research of Laboratory Primates), Osamu Kaneko(Nagasaki University), Toshihiro Mita(Juntendo University), Kiyoshi Kita(The University of Tokyo), Yasuhiro Yasutomi(National Institute of Biomedical Innovation, Health and Nutrition), Patrick L Sutton(New York University), Rimma Shakhbatyan(New York University), Toshihiro Horii(Osaka University), Teruo Yasunaga(Osaka University), John W. Barnwell(Center for Global Health), Ananías A. Escalante(Arizona State University), Jane M. Carlton(New York University), Kazuyuki Tanabe(Osaka University)
Nature Genetics
August 3, 2012
Cited by 196Open Access
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Abstract

Jane Carlton, Kazuyuki Tanabe and colleagues report the draft genome sequences of three Plasmodium cynomolgi strains isolated from infected monkeys. Their comparative genomic analysis with P. vivax and P. knowlesi offers insights into these simian malaria parasites. P. cynomolgi, a malaria-causing parasite of Asian Old World monkeys, is the sister taxon of P. vivax, the most prevalent malaria-causing species in humans outside of Africa. Because P. cynomolgi shares many phenotypic, biological and genetic characteristics with P. vivax, we generated draft genome sequences for three P. cynomolgi strains and performed genomic analysis comparing them with the P. vivax genome, as well as with the genome of a third previously sequenced simian parasite, Plasmodium knowlesi. Here, we show that genomes of the monkey malaria clade can be characterized by copy-number variants (CNVs) in multigene families involved in evasion of the human immune system and invasion of host erythrocytes. We identify genome-wide SNPs, microsatellites and CNVs in the P. cynomolgi genome, providing a map of genetic variation that can be used to map parasite traits and study parasite populations. The sequencing of the P. cynomolgi genome is a critical step in developing a model system for P. vivax research and in counteracting the neglect of P. vivax.


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