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. 2023 Nov 10;15(1):96.
doi: 10.1186/s13073-023-01247-7.

Rapid profiling of Plasmodium parasites from genome sequences to assist malaria control

Affiliations

Rapid profiling of Plasmodium parasites from genome sequences to assist malaria control

Jody E Phelan et al. Genome Med. .

Abstract

Background: Malaria continues to be a major threat to global public health. Whole genome sequencing (WGS) of the underlying Plasmodium parasites has provided insights into the genomic epidemiology of malaria. Genome sequencing is rapidly gaining traction as a diagnostic and surveillance tool for clinical settings, where the profiling of co-infections, identification of imported malaria parasites, and detection of drug resistance are crucial for infection control and disease elimination. To support this informatically, we have developed the Malaria-Profiler tool, which rapidly (within minutes) predicts Plasmodium species, geographical source, and resistance to antimalarial drugs directly from WGS data.

Results: The online and command line versions of Malaria-Profiler detect ~ 250 markers from genome sequences covering Plasmodium speciation, likely geographical source, and resistance to chloroquine, sulfadoxine-pyrimethamine (SP), and other anti-malarial drugs for P. falciparum, but also providing mutations for orthologous resistance genes in other species. The predictive performance of the mutation library was assessed using 9321 clinical isolates with WGS and geographical data, with most being single-species infections (P. falciparum 7152/7462, P. vivax 1502/1661, P. knowlesi 143/151, P. malariae 18/18, P. ovale ssp. 5/5), but co-infections were identified (456/9321; 4.8%). The accuracy of the predicted geographical profiles was high to both continental (96.1%) and regional levels (94.6%). For P. falciparum, markers were identified for resistance to chloroquine (49.2%; regional range: 24.5% to 100%), sulfadoxine (83.3%; 35.4- 90.5%), pyrimethamine (85.4%; 80.0-100%) and combined SP (77.4%). Markers associated with the partial resistance of artemisinin were found in WGS from isolates sourced from Southeast Asia (30.6%).

Conclusions: Malaria-Profiler is a user-friendly tool that can rapidly and accurately predict the geographical regional source and anti-malarial drug resistance profiles across large numbers of samples with WGS data. The software is flexible with modifiable bioinformatic pipelines. For example, it is possible to select the sequencing platform, display specific variants, and customise the format of outputs. With the increasing application of next-generation sequencing platforms on Plasmodium DNA, Malaria-Profiler has the potential to be integrated into point-of-care and surveillance settings, thereby assisting malaria control. Malaria-Profiler is available online (bioinformatics.lshtm.ac.uk/malaria-profiler) and as standalone software ( https://github.com/jodyphelan/malaria-profiler ).

Keywords: Diagnostics; Drug resistance; Genomics; Malaria; Plasmodium parasites; Whole genome sequencing.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Population structure of Plasmodium. a Circular maximum likelihood tree of 51 human and 24 non-human Plasmodium isolates using mitochondrial sequences shows perfect clustering of species as expected. This indicates the presence of a species-specific sequence which is exploited in the k-mer-based speciation function. Pf P. falciparum, Pv P. vivax, Pk P. knowlesi, Pcyn P. cynomolgi, Pm P. malariae, Poc P. ovale curtesi. b P. falciparum principal component analysis showing clustering by geographic region specifically separation between Southeast Asia and Oceania and Africa. c P. vivax principal component analysis showing clustering by geographic region. d P. knowlesi principal component analysis showing clustering by region (Peninsular (Pen-Pk) vs. Borneo Malaysia), and within Borneo based on host (Macaca fascularis (Mf-Pk) and Macaca nemestrina (Mn-Pk))
Fig. 2
Fig. 2
Example of Malaria-Profiler report outputs. a Thai isolate confirmed to be P. falciparum from Southeast Asia, with a complex drug resistance profile (accession no. ERR248945). b A traveller isolate sequenced on Oxford Nanopore Technology and determined to be from East Africa and with chloroquine, Sulfadoxine and Pyrimethamine resistance (accession no. ERR11254081)

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