Affiliations 

  • 1 Department of Parasitology, Faculty of Medicine, Universiti Malaya, 50603 Kuala Lumpur, Malaysia
  • 2 Vector Borne Disease Sector, Disease Control Division, Ministry of Health Malaysia, 62590 Putrajaya, Malaysia
  • 3 Sarawak Health Department, Ministry of Health Malaysia, 93050 Kuching, Sarawak, Malaysia
  • 4 Sabah Health Department, Ministry of Health Malaysia, 88590 Kota Kinabalu, Sabah, Malaysia
  • 5 Public Health Laboratory Kota Kinabalu, Ministry of Health Malaysia, 88850 Kota Kinabalu, Sabah, Malaysia
Trop Biomed, 2022 Dec 01;39(4):504-510.
PMID: 36602208 DOI: 10.47665/tb.39.4.006

Abstract

The Plasmodium knowlesi secreted protein with an altered thrombospondin repeat (PkSPATR) is an important protein that helps in the parasite's invasion into the host cell. This protein has been regarded as one of the potential vaccine candidates against P. knowlesi infection. This study investigates the genetic diversity and natural selection of PkSPATR gene of P. knowlesi clinical isolates from Malaysia. PCR amplification of the full length PkSPATR gene was performed on 60 blood samples of infected P. knowlesi patients from Peninsular Malaysia and Malaysian Borneo. The amplified PCR products were cloned and sequenced. Sequence analysis of PkSPATR from Malaysia showed higher nucleotide diversity (CDS p: 0.01462) than previously reported Plasmodium vivax PvSPATR (p = 0.0003). PkSPATR from Peninsular Malaysia was observed to have slightly higher diversity (CDS p: 0.01307) than those from Malaysian Borneo (CDS p: 0.01212). Natural selection analysis on PkSPATR indicated significant purifying selection. Multiple amino acid sequence alignment revealed 69 polymorphic sites. The phylogenetic tree and haplotype network did not show any distinct clustering of PkSPATR. The low genetic diversity level, natural selection and absence of clustering implied functional constrains of the PkSPATR protein.

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