Affiliations 

  • 1 Malaria, Centre for Disease Control, Malaria, Schistosomiasis and Leishmaniasis Control Program, State Ministry of Health, Nyala, Sudan
  • 2 Department of Biology, Faculty of Exact and Applied Sciences, University of N'djamena, N'djamena, Chad
  • 3 Department of Biology, Faculty of Education, Omdurman Islamic University, Omdurman, Sudan
  • 4 Genetics and Molecular Biology Laboratory, Department of Zoology, Faculty of Science, University of Khartoum, Khartoum, Sudan
  • 5 Department of Molecular Genetics, Institute of Molecular Biology, University of Nyala, Nyala, Sudan
  • 6 National Public Health Reference Laboratory, Ministry of Health, Mogadishu, Somalia
  • 7 Faculty of Infectious Diseases, London School of Hygiene and Tropical Medicine, London, UK
  • 8 Department of Medical Microbiology & Parasitology, School of Medical Sciences, Universiti Sains Malaysia, 16150, Kubang Kerian, Kelantan, Malaysia. zeehaida@usm.my
  • 9 Department of Zoology, Faculty of Science and Technology, Omdurman Islamic University, Omdurman, Sudan. Khalid541983@yahoo.com
Sci Rep, 2020 07 30;10(1):12822.
PMID: 32733079 DOI: 10.1038/s41598-020-69756-8

Abstract

In remote areas of malaria-endemic countries, rapid diagnostic tests (RDTs) have dramatically improved parasitological confirmation of suspected malaria cases, especially when skilled microscopists are not available. This study was designed to determine the frequency of Plasmodium falciparum isolates with histidine-rich protein 2 (pfhrp2) gene deletion as one of the possible factors contributing to the failure of PfHRP2-based RDTs in detecting malaria. A total of 300 blood samples were collected from several health centres in Nyala City, Western Sudan. The performance of PfHRP2-based RDTs in relation to microscopy was examined and the PCR-confirmed samples were investigated for the presence of pfhrp2 gene. A total of 113 out of 300 patients were P. falciparum positive by microscopy. Among them, 93.81% (106 out of 113) were positives by the PfHRP2 RDTs. Seven isolates were identified as false negative on the basis of the RDTs results. Only one isolate (0.9%; 1/113) potentially has pfhrp2 gene deletion. The sensitivity and specificity of PfHRP2-based RDTs were 93.81% and 100%, respectively. The results provide insights into the pfhrp2 gene deletion amongst P. falciparum population from Sudan. However, further studies with a large and systematic collection from different geographical settings across the country are needed.

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