HOME > About Nagasaki University > Research information > Ass. Prof. Richard Culleton et al. reported the genomes of Plasmodium malariae and Plasmodium ovale in International Journal for Parasitology.

Ass. Prof. Richard Culleton et al. reported the genomes of Plasmodium malariae and Plasmodium ovale in International Journal for Parasitology.

July. 13, 2016

In collaboration with colleagues in China and Saudi Arabia, the Malaria Unit at Nekken present a landmark new publication; the genomes of Plasmodium malariae and Plasmodium ovale published for the first time. These two species of malaria parasite are responsible for a large burden of disease throughout the tropics. Despite their importance as human pathogens their genomes have not been available until now, due to difficulties in obtaining sufficient quantities of DNA. The publication of these genomes will aid with the development of new drugs and vaccines against these neglected tropical pathogens.


Genome-scale comparison of expanded gene families in Plasmodium ovale wallikeri and Plasmodium ovale curtisi with Plasmodium malariae and with other Plasmodium species

Abstract

Malaria in humans is caused by six species of Plasmodium parasites, of which the nuclear genome sequences for the two Plasmodium ovale spp., P. ovale curtisi and P. ovale wallikeri, and Plasmodium malariae have not yet been analyzed. Here we present an analysis of the nuclear genome sequences of these three parasites, and describe gene family expansions therein. Plasmodium ovale curtisi and P. ovale wallikeri are genetically distinct but morphologically indistinguishable and have sympatric ranges through the tropics of Africa, Asia and Oceania. Both P. ovale spp. show expansion of the surfin variant gene family, and an amplification of the Plasmodium interspersed repeat (pir) superfamily which results in an approximately 30% increase in genome size. For comparison, we have also analyzed the draft nuclear genome of P. malariae, a malaria parasite causing mild malaria symptoms with a quartan life cycle, long-term chronic infections, and wide geographic distribution. Plasmodium malariae shows only a moderate level of expansion of pir genes, and unique expansions of a highly diverged transmembrane protein family with over 550 members and the gamete P25/27 gene family. The observed diversity in the P. ovale wallikeri and P. ovale curtisi surface antigens, combined with their phylogenetic separation, supports consideration that the two parasites be given species status.

Article:http://www.sciencedirect.com/science/article/pii/S0020751916301357