Affiliations 

  • 1 Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom
  • 2 Genomics Institute Singapore, Singapore
  • 3 The Francis Crick Institute, 1 Midland Road, London NW1 1AT, United Kingdom
  • 4 Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom; The Francis Crick Institute, 1 Midland Road, London NW1 1AT, United Kingdom
  • 5 King Abdullah University of Science and Technology, Thuwal, Saudi Arabia
  • 6 Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom; Genomics Institute Singapore, Singapore
  • 7 Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom; Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom. Electronic address: taane.clark@lshtm.ac.uk
Int J Parasitol, 2018 03;48(3-4):191-196.
PMID: 29258833 DOI: 10.1016/j.ijpara.2017.09.008

Abstract

Plasmodium knowlesi, a common parasite of macaques, is recognised as a significant cause of human malaria in Malaysia. The P. knowlesi A1H1 line has been adapted to continuous culture in human erythrocytes, successfully providing an in vitro model to study the parasite. We have assembled a reference genome for the PkA1-H.1 line using PacBio long read combined with Illumina short read sequence data. Compared with the H-strain reference, the new reference has improved genome coverage and a novel description of methylation sites. The PkA1-H.1 reference will enhance the capabilities of the in vitro model to improve the understanding of P. knowlesi infection in humans.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.